Sample records for zinc complexes influencia

  1. Influencia de distintos medios agresivos en la acción protectora de las pinturas ricas en zinc

    Abreu, C. M.


    Full Text Available The aim of the present work is to determine the influence that different atmospheric agents have in steel protection by zinc rich paints based on inorganic silicate binder. The presence of pollutants in the atmosphere has been simulated by periodical deposition of sulphate and/or chloride solutions on the surface of the samples. With the aim of determining the validity of immersion tests, usually used in these types studies, the samples were kept in a controlled atmosphere at 20°C and 60% RH. These exposition conditions could represent a relative dry atmosphere allowing the zinc corrosion. Electrochemical impedance spectroscopy was employed to follow the time evolution of the studied paints. The corresponding impedance spectra were modeled using an electrical equivalent circuit approach. This methodology allows establishing that pollutants as well as weathering conditions define the protecting mechanism of these zinc rich paints. The results show a fast evolution towards a barrier-type protecting mechanism.

    En este trabajo se pretende determinar la influencia de distintos agentes corrosivos atmosféricos en la protección anticorrosiva que ejercen las pinturas ricas en zinc de base silicato inorgánico. Sobre las muestras pintadas, y una vez han curado, se depositan periódicamente disoluciones de sulfato y de cloruro, tanto de forma independiente como conjunta. Con objeto de determinar la validez de los ensayos de inmersión, habitualmente utilizados en este tipo de estudios, las pinturas se exponen en cámara de humedad a 20°C y 60% de humedad relativa, lo que sería equiparable a ambientes naturales relativamente secos y que, sin embargo, permiten la corrosión del zinc. La evolución de las pinturas se estudia mediante espectroscopia de impedancia electroquímica. Los espectros obtenidos se interpretan en función de modelos de circuitos equivalentes. Esta metodología permite establecer que el mecanismo de protección est

  2. Chirality sensing with stereodynamic biphenolate zinc complexes.

    Bentley, Keith W; de Los Santos, Zeus A; Weiss, Mary J; Wolf, Christian


    Two bidentate ligands consisting of a fluxional polyarylacetylene framework with terminal phenol groups were synthesized. Reaction with diethylzinc gives stereodynamic complexes that undergo distinct asymmetric transformation of the first kind upon binding of chiral amines and amino alcohols. The substrate-to-ligand chirality imprinting at the zinc coordination sphere results in characteristic circular dichroism signals that can be used for direct enantiomeric excess (ee) analysis. This chemosensing approach bears potential for high-throughput ee screening with small sample amounts and reduced solvent waste compared to traditional high-performance liquid chromatography methods.

  3. Anti-ulcer activity of a slow-release zinc complex, zinc monoglycerolate (Glyzinc).

    Rainsford, K D; Whitehouse, M W


    A slow-release zinc complex, zinc monoglycerolate (ZMG) was examined for its potential gastroprotective activity in various gastric ulcer models. These models comprised (a) oral or parenteral non-steroidal anti-inflammatory drugs (NSAIDs) given to rats whose gastrointestinal mucosa was pre-sensitized by prior development of arthritis, oleyl alcohol-induced inflammation and cold exposure, (b) oral ethanol (12.5-100%) with and without added 4% HCl, (c) intraperitoneal reserpine (5 mg kg-1) in arthritic and normal rats and in normal mice, (d) oral NSAIDs given to mice in which acid and pepsin production was stimulated by co-administration of intraperitoneal bethanechol chloride (5 mg kg-1) to enhance ulcer development, and (e) NSAIDs given to carrageenan-inflamed rats to determine effects of ZMG on paw inflammation. In these models, ZMG given orally was effective in preventing development of gastric lesions, except with propionic acid NSAIDs; the effective doses being apparently dependent on the severity of the mucosal injury. In many of the models ZMG was superior to zinc sulphate and other zinc salts or metal ion complexes investigated but was slightly more effective or equipotent compared with zinc acexamate. ZMG did not impair the anti-oedemic effects of NSAIDs. ZMG is thus an effective agent in preventing ulcer development in a wide range of model systems and may be more effective than zinc salts because of the controlled slow-release of zinc from the complex.

  4. A Photoluminescence Study of the Changes Induced in the Zinc White Pigment by Formation of Zinc Complexes.

    Artesani, Alessia; Gherardi, Francesca; Nevin, Austin; Valentini, Gianluca; Comelli, Daniela


    It is known that oil paintings containing zinc white are subject to rapid degradation. This is caused by the interaction between the active groups of binder and the metal ions of the pigment, which gives rise to the formation of new zinc complexes (metal soaps). Ongoing studies on zinc white paints have been limited to the chemical mechanisms that lead to the formation of zinc complexes. On the contrary, little is known of the photo-physical changes induced in the zinc oxide crystal structure following this interaction. Time-resolved photoluminescence spectroscopy has been applied to follow modifications in the luminescent zinc white pigment when mixed with binder. Significant changes in trap state photoluminescence emissions have been detected: the enhancement of a blue emission combined with a change of the decay kinetic of the well-known green emission. Complementary data from molecular analysis of paints using Fourier transform infrared spectroscopy confirms the formation of zinc carboxylates and corroborates the mechanism for zinc complexes formation. We support the hypothesis that zinc ions migrate into binder creating novel vacancies, affecting the photoluminescence intensity and lifetime properties of zinc oxide. Here, we further demonstrate the advantages of a time-resolved photoluminescence approach for studying defects in semiconductor pigments.

  5. Effect of the ratio of zinc amino acid complex to zinc sulfate on the performance of Holstein cows

    Nayeri, A; Upah, N C; Sucu, E; Sanz-Fernandez, M V; DeFrain, J M; Gorden, P J; Baumgard, L H


    Multiparous (n=70) and primiparous (n=66) Holstein cows were balanced by 305-d previous mature-equivalent milk yield and parity and assigned to 1 of 3 dietary treatments to evaluate the ratio of zinc sulfate to zinc amino acid complex (CZ...

  6. Mononuclear Phenolate Diamine Zinc Hydride Complexes and Their Reactions With CO2.

    Brown, Neil J; Harris, Jonathon E; Yin, Xinning; Silverwood, Ian; White, Andrew J P; Kazarian, Sergei G; Hellgardt, Klaus; Shaffer, Milo S P; Williams, Charlotte K


    The synthesis, characterization, and zinc coordination chemistry of the three proligands 2-tert-butyl-4-[tert-butyl (1)/methoxy (2)/nitro (3)]-6-{[(2'-dimethylaminoethyl)methylamino]methyl}phenol are described. Each of the ligands was reacted with diethylzinc to yield zinc ethyl complexes 4-6; these complexes were subsequently reacted with phenylsilanol to yield zinc siloxide complexes 7-9. Finally, the zinc siloxide complexes were reacted with phenylsilane to produce the three new zinc hydride complexes 10-12. The new complexes 4-12 have been fully characterized by NMR spectroscopy, mass spectrometry, and elemental analyses. The structures of the zinc hydride complexes have been probed using VT-NMR spectroscopy and X-ray diffraction experiments. These data indicate that the complexes exhibit mononuclear structures at 298 K, both in the solid state and in solution (d8-toluene). At 203 K, the NMR signals broaden, consistent with an equilibrium between the mononuclear and dinuclear bis(μ-hydrido) complexes. All three zinc hydride complexes react rapidly and quantitatively with carbon dioxide, at 298 K and 1 bar of pressure over 20 min, to form the new zinc formate complexes 13-15. The zinc formate complexes have been analyzed by NMR spectroscopy and VT-NMR studies, which reveal a temperature-dependent monomer-dimer equilibrium that is dominated by the mononuclear species at 298 K.

  7. The effect of different complexing agents on the properties of zinc sulfide thin films deposited from aqueous solutions


    The zinc sulfide (ZnS) thin films were prepared on glass substrates by chemical bath deposition using the aqueous solutions of zinc chloride, thiourea, pH regulator and complexing agent (ammonia and hydrazine hydrate, trisodium citrate or sodium hydroxide). The calculations of boundary conditions for formation of zinc sulfide and zinc hydroxide were made at various zinc salt concentrations with different complexing agents. The structural, morphology and optical properties of the ZnS thin film...

  8. Zinc surface complexes on birnessite: A density functional theory study

    Kwon, Kideok D.; Refson, Keith; Sposito, Garrison


    Biogeochemical cycling of zinc is strongly influenced by sorption on birnessite minerals (layer-type MnO2), which are found in diverse terrestrial and aquatic environments. Zinc has been observed to form both tetrahedral (Zn{sup IV}) and octahedral (Zn{sup VI}) triple-corner-sharing surface complexes (TCS) at Mn(IV) vacancy sites in hexagonal birnessite. The octahedral complex is expected to be similar to that of Zn in the Mn oxide mineral, chalcophanite (ZnMn{sub 3}O{sub 7} {center_dot} 3H{sub 2}O), but the reason for the occurrence of the four-coordinate Zn surface species remains unclear. We address this issue computationally using spin-polarized Density Functional Theory (DFT) to examine the Zn{sub IV}-TCS and Zn{sup VI}-TCS species. Structural parameters obtained by DFT geometry optimization were in excellent agreement with available experimental data on Zn-birnessites. Total energy, magnetic moments, and electron-overlap populations obtained by DFT for isolated Zn{sup IV}-TCS revealed that this species is stable in birnessite without a need for Mn(III) substitution in the octahedral sheet and that it is more effective in reducing undersaturation of surface O at a Mn vacancy than is Zn{sub VI}-TCS. Comparison between geometry-optimized ZnMn{sub 3}O{sub 7} {center_dot} 3H{sub 2}O (chalcophanite) and the hypothetical monohydrate mineral, ZnMn{sub 3}O{sub 7} {center_dot} H{sub 2}O, which contains only tetrahedral Zn, showed that the hydration state of Zn significantly affects birnessite structural stability. Finally, our study also revealed that, relative to their positions in an ideal vacancy-free MnO{sub 2}, Mn nearest to Zn in a TCS surface complex move toward the vacancy by 0.08-0.11 {angstrom}, while surface O bordering the vacancy move away from it by 0.16-0.21 {angstrom}, in agreement with recent X-ray absorption spectroscopic analyses.

  9. The Zinc-Schiff Base-Novicidin Complex as a Potential Prostate Cancer Therapy

    Milosavljevic, Vedran; Haddad, Yazan; Merlos Rodrigo, Miguel Angel; Moulick, Amitava; Polanska, Hana; Hynek, David; Heger, Zbynek; Kopel, Pavel; Adam, Vojtech


    Prostate cancer cells control energy metabolism by chelating intracellular zinc. Thus, zinc delivery has been a popular therapeutic approach for prostate cancer. Here, we propose the use of the membrane-penetrating peptide Novicidin connected to zinc-Schiff base as a carrier vehicle for the delivery of zinc to prostate cells. Mass spectrometry, electrochemistry and spectrophotometry confirmed the formation/stability of this complex and provided insight regarding the availability of zinc for complex interactions. This delivery system showed minor toxicity in normal PNT1A cells and high potency towards PC3 tumor cells. The complex preferentially penetrated PC3 tumor cells in contrast to confinement to the membranes of PNT1A. Furthermore, zinc uptake was confirmed in both cell lines. Molecular analysis was used to confirm the activation of zinc stress (e.g., ZnT-1) and apoptosis (e.g., CASP-1). Our results strongly suggest that the zinc-Schiff base-Novicidin complex has great potential as a novel anticancer drug. PMID:27727290

  10. Optoelectronic Properties of Color-Tunable Mixed Ligand-Based Light-Emitting Zinc Complexes

    Singh, Devender; Bhagwan, Shri; Saini, Raman Kumar; Tanwar, Vijeta; Nishal, Vandna


    A series of mixed ligand-based zinc complexes (Zn1-Zn5); [(8-hydroxyquinolinato)(2-(2-hydroxyphenyl)benzimidazolato)zinc(II)] (Zn1), [(5-chloro-8-hydroxyquinolinato)(2-(2-hydroxyphenyl)benzimidazolato)zinc(II)] (Zn2), [(5,7-dichloro-8-hydroxyquinolinato)(2-(2-hydroxyphenyl)benzimidazolato)zinc(II)] (Zn3), [(2-methyl-8-hydroxyquinolinato)(2-(2-hydroxyphenyl)benzimidazolato)zinc(II)] (Zn4) and [(5,7-dimethyl-8-hydroxyquinolinato)(2-(2-hydroxyphenyl)benzimidazolato)zinc(II)] (Zn5) were synthesized and characterized. The photophysical properties of zinc complexes were examined by ultraviolet-visible absorption and photoluminescence emission spectroscopy. All prepared metal complexes produced intense luminescence on excitation with a UV light source. In this study, the color-tunable characteristics of metal complexes were investigated by introducing the electron-donating and electron-withdrawing groups on the 8-hydroxyquinoline ligand. The emission spectra of metal complexes showed emission wavelength at 500 nm for [ZnHBI(q)], 509 nm for [ZnHBI(Clq)], 504 nm for [Zn(HBI)(Cl2q)], 496 nm for [ZnHBI (Meq)] and 573 nm for [ZnHBI(Me2Q)] materials. A temperature-dependent PL spectrum was used to study the emission profile of zinc complex and observed that variation in the temperature altered the position and the intensity of emission peak. The synthesized metal complex also exhibited good thermal stability (>300°C). Photophysical characteristics of color-tunable light-emitting zinc complexes suggested that these materials could be efficiently used for emissive display device applications.

  11. Computational protocol for predicting the binding affinities of zinc containing metalloprotein-ligand complexes.

    Jain, Tarun; Jayaram, B


    Zinc is one of the most important metal ions found in proteins performing specific functions associated with life processes. Coordination geometry of the zinc ion in the active site of the metalloprotein-ligand complexes poses a challenge in determining ligand binding affinities accurately in structure-based drug design. We report here an all atom force field based computational protocol for estimating rapidly the binding affinities of zinc containing metalloprotein-ligand complexes, considering electrostatics, van der Waals, hydrophobicity, and loss in conformational entropy of protein side chains upon ligand binding along with a nonbonded approach to model the interactions of the zinc ion with all the other atoms of the complex. We examined the sensitivity of the binding affinity predictions to the choice of Lennard-Jones parameters, partial atomic charges, and dielectric treatments adopted for system preparation and scoring. The highest correlation obtained was R2 = 0.77 (r = 0.88) for the predicted binding affinity against the experiment on a heterogenous dataset of 90 zinc containing metalloprotein-ligand complexes consisting of five unique protein targets. Model validation and parameter analysis studies underscore the robustness and predictive ability of the scoring function. The high correlation obtained suggests the potential applicability of the methodology in designing novel ligands for zinc-metalloproteins. The scoring function has been web enabled for free access at as BAPPL-Z server (Binding Affinity Prediction of Protein-Ligand complexes containing Zinc metal ions).

  12. Zinc

    ... slow wound healing, poor sense of taste and smell, diarrhea, and nausea. Moderate zinc deficiency is associated ... nose, as it might cause permanent loss of smell. In June 2009, the US Food and Drug ...

  13. Defect Chemistry and Microstructure of Complex Perovskite Barium Zinc Niobate

    Peng, Ping


    This dissertation presents a systematic study of the characterization of the phase transitions, microstructures, defects and transport properties of undoped and doped complex perovskite barium zinc niobate (BZN). Complex perovskite BZN is a paraelectric material while its parent material barium titanate is ferroelectric. With codoping of (Zn + 2Nb) into Ti site, BaTiO_3 shows three distinguished features. First, the Curie temperature is lowered; second, the three phase transitions (cubic-tetragonal-orthorhombic-rhombohedral) coalesce; and lastly, the transition becomes diffuse showing a typical 2nd order phase transition compared with 1st order in undoped BaTiO_3. Complex microchemical ordering is another characteristic of BZN. Stoichiometric BZN shows a mixture of two types of ordering schemes. 1:1, 1:2 ordered microdomains and the disordered matrix co-exist. The 1:1 type ordering involves an internal charge imbalance which inhibits the growth of 1:1 type of ordered microdomains. The 1:2 type ordering is consistent with the chemical composition of BZN. These ordering patterns can be modified by either adjustment of the Zn/Nb ratio or by doping. The defect structure of the stoichiometric BZN is closely related to that of BaTiO_3. Stoichiometric BZN is an insulator with wide band gap (~ 3.70 eV). Undoped BZN has a high oxygen vacancy concentration which comes from three possible sources, such as unavoidable acceptor impurities, due to their natural abundance, Zn/Nb ratio uncertainty due to processing limitations, and high temperature ZnO loss due to sintering process. The oxygen vacancy concentration for undoped BZN lays in the neighborhood of 1500 ppm (atm.). The compensation defects for various dopants have also been identified. Both electrons and holes conduct by a small polaron mechanism. Various thermodynamic parameters, such as enthalpies of oxidation and reduction, mass action constants for intrinsic electronic disorder, oxidation and reduction have been

  14. Toxic and nontoxic components of botulinum neurotoxin complex are evolved from a common ancestral zinc protein

    Inui, Ken [Department of Food and Cosmetic Science, Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri 099-2493 (Japan); Japan Society for the Promotion of Science, 1-8 Chiyoda-ku, Tokyo 102-8472 (Japan); Sagane, Yoshimasa [Department of Food and Cosmetic Science, Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri 099-2493 (Japan); Miyata, Keita [Department of Food and Cosmetic Science, Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri 099-2493 (Japan); Japan Society for the Promotion of Science, 1-8 Chiyoda-ku, Tokyo 102-8472 (Japan); Miyashita, Shin-Ichiro [Department of Food and Cosmetic Science, Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri 099-2493 (Japan); Suzuki, Tomonori [Department of Bacteriology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558 (Japan); Shikamori, Yasuyuki [Agilent Technologies International Japan, Ltd. Takaura-cho 9-1, Hachioji-shi, Tokyo 192-0033 (Japan); Ohyama, Tohru; Niwa, Koichi [Department of Food and Cosmetic Science, Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri 099-2493 (Japan); Watanabe, Toshihiro, E-mail: [Department of Food and Cosmetic Science, Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri 099-2493 (Japan)


    Highlights: Black-Right-Pointing-Pointer BoNT and NTNHA proteins share a similar protein architecture. Black-Right-Pointing-Pointer NTNHA and BoNT were both identified as zinc-binding proteins. Black-Right-Pointing-Pointer NTNHA does not have a classical HEXXH zinc-coordinating motif similar to that found in all serotypes of BoNT. Black-Right-Pointing-Pointer Homology modeling implied probable key residues involved in zinc coordination. -- Abstract: Zinc atoms play an essential role in a number of enzymes. Botulinum neurotoxin (BoNT), the most potent toxin known in nature, is a zinc-dependent endopeptidase. Here we identify the nontoxic nonhemagglutinin (NTNHA), one of the BoNT-complex constituents, as a zinc-binding protein, along with BoNT. A protein structure classification database search indicated that BoNT and NTNHA share a similar domain architecture, comprising a zinc-dependent metalloproteinase-like, BoNT coiled-coil motif and concanavalin A-like domains. Inductively coupled plasma-mass spectrometry analysis demonstrated that every single NTNHA molecule contains a single zinc atom. This is the first demonstration of a zinc atom in this protein, as far as we know. However, the NTNHA molecule does not possess any known zinc-coordinating motif, whereas all BoNT serotypes possess the classical HEXXH motif. Homology modeling of the NTNHA structure implied that a consensus K-C-L-I-K-X{sub 35}-D sequence common among all NTNHA serotype molecules appears to coordinate a single zinc atom. These findings lead us to propose that NTNHA and BoNT may have evolved distinct functional specializations following their branching out from a common ancestral zinc protein.

  15. Zinc Pyrithione: A Topical Antimicrobial With Complex Pharmaceutics.

    Schwartz, James R


    Zinc pyrithione (ZPT) is an active material that has been used for over 50 years to effectively treat dandruff and seborrheic dermatitis (D/SD). It has become the most common material for that purpose, its use has expanded to include other skin benefits such as skin hygiene. However, there is much about ZPT that is unappreciated. It is a rationally developed molecule that was modeled after the naturally occurring antimicrobial aspergillic acid. The molecular basis for its antifungal activity has been elucidated. The efficacy of ZPT originates from two attributes. First, it has a very broad antimicrobial spectrum of activity, including fungi, gram-positive and -negative bacteria. Second, the material has very low solubility, resulting in formulation and delivery as a particulate material, which has distinct performance advantages. The particles are deposited and retained on the target skin surfaces even when delivered from rinse-off products. These particles slowly release molecularly active material to interact with the surface fungal and bacteria cells to control their population, functioning as slow-release reservoirs to provide extended and persistent benefits. This particulate nature, though, results in complex pharmaceutics to realize the full efficacy benefits; it is common to see products with the same ZPT level having widely varying levels of clinical performance. Several product matrix-determined factors directly impact resultant benefits: ZPT must be retained on the skin surface achieving uniform spatial distribution laterally as well as within hair follicles (especially on scalp); ZPT must be maintained as a physically stable dispersion in product; ZPT must be maintained in a chemically active form as there are many chemical reactions that can occur that can harm ZPT bioactivity. The benefits achievable by employing ZPT require significant pharmaceutics expertise to realize the full benefits of this active material.

  16. Synthesis of zinc sulphide nanoparticles from thermal decomposition of zinc N-ethyl cyclohexyl dithiocarbamate complex

    Abdullah, Nurul Hidayah [Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Zainal, Zulkarnain, E-mail: [Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Silong, Sidik [UiTM Negeri Sembilan, Kampus Kuala Pilah, Pekan Parit Tinggi, 72000 Kuala Pilah, Negeri Sembilan (Malaysia); Tahir, Mohamed Ibrahim Mohamed; Tan, Kar-Ban [Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Chang, Sook-Keng [Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia)


    Synthesis of nanostructured semiconductor materials from various single source precursors has been massively explored for potential applications in modern technology. Thermal decomposition method has been employed to prepare nanoparticles zinc sulphide from zinc N-ethyl cyclohexyl dithiocarbamate precursor. Effect of heat treatment at different calcination duration on the structural, morphological, compositional and band gap properties of zinc sulphide were investigated. The obtained samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and energy dispersive X-ray (EDX) analysis. XRD showed the precursor was decomposed to hexagonal zinc sulphide after 2–6 h of calcination duration at 400 °C. The sizes of zinc sulphide (ZnS) nanoparticles obtained from TEM analysis were about 6–11 nm. The existence of the hexagonal ZnS phase is not affected by the calcination duration, while only a slight difference in the crystallinity and crystallite size of ZnS is observed from XRD analysis. EDX analyses reveal that the as-prepared ZnS nanoparticles have an approximate composition of Zn and S close to 1:1, giving a possible composition of ZnS. Besides, direct band gap energy of ZnS was found to be around 3.78–3.95 eV. - Highlights: • Zinc N-ethyl cyclohexyl dithiocarbamate was used as single source precursor. • No surfactant was used in the preparation of ZnS nanoparticles. • Pure phase nanostructured ZnS is obtained. • A good stoichiometric sample with an average atomic ratio of Zn:S close to 1:1.

  17. The impact of tertiary wastewater treatment on copper and zinc complexation.

    Constantino, C; Gardner, M; Comber, S D W; Scrimshaw, M D; Ellor, B


    Tightening quality standards for European waters has seen a move towards enhanced wastewater treatment technologies such as granulated organic carbon treatment and ozonation. Although these technologies are likely to be successful in degrading certain micro-organic contaminants, these may also destroy compounds which would otherwise complex and render metals significantly less toxic. This study examined the impact of enhanced tertiary treatment on the capacity of organic compounds within sewage effluents to complex copper and zinc. The data show that granulated organic carbon treatment removes a dissolved organic carbon (DOC) fraction that is unimportant to complexation such that no detrimental impact on complexation or metal bioavailability is likely to occur from this treatment type. High concentrations of ozone (>1 mg O3/mg DOC) are, however, likely to impact the complexation capacity for copper although this is unlikely to be important at the concentrations of copper typically found in effluent discharges or in rivers. Ozone treatment did not affect zinc complexation capacity. The complexation profiles of the sewage effluents show these to contain a category of non-humic ligand that appears unaffected by tertiary treatment and which displays a high affinity for zinc, suggesting these may substantially reduce the bioavailability of zinc in effluent discharges. The implication is that traditional metal bioavailability assessment approaches such as the biotic ligand model may overestimate zinc bioavailability in sewage effluents and effluent-impacted waters.

  18. [Zinc].

    Couinaud, C


    Zinc is indispensable for life from bacteria to man. As a trace element it is included in numerous enzymes or serves as their activator (more than 80 zinc metallo-enzymes). It is necessary for nucleic acid and protein synthesis, the formation of sulphated molecules (insulin, growth hormone, keratin, immunoglobulins), and the functioning of carbonic anhydrase, aldolases, many dehydrogenases (including alcohol-dehydrogenase, retinal reductase indispensable for retinal rod function), alkaline phosphatase, T cells and superoxide dismutase. Its lack provokes distinctive signs: anorexia, diarrhea, taste, smell and vision disorders, skin lesions, delayed healing, growth retardation, delayed appearance of sexual characteristics, diminished resistance to infection, and it may be the cause of congenital malformations. Assay is now simplified by atomic absorption spectrophotometry in blood or hair. There is a latent lack prior to any disease because of the vices of modern eating habits, and this increases during stress, infections or tissue healing processes. Its lack is accentuated during long-term parenteral feeding or chronic gastrointestinal affections. Correction is as simple as it is innocuous, and zinc supplements should be given more routinely during surgical procedures.

  19. A Zinc Morpholine Complex Prevents HCl/Ethanol-Induced Gastric Ulcers in a Rat Model.

    Salama, Suzy M; Gwaram, Nura Suleiman; AlRashdi, Ahmed S; Khalifa, Shaden A M; Abdulla, Mahmood A; Ali, Hapipah M; El-Seedi, Hesham R


    Zinc is a naturally occurring element with roles in wound healing and rescuing tissue integrity, particularly in the gastrointestinal system, where it can be detected in the mucosal and submucosal layers. Zinc chelates are known to have beneficial effects on the gastrointestinal mucosa and in cases of gastric ulcer. We synthesized complexes of zinc featuring a heterocyclic amine binding amino acids then investigated their ability to enhance the gastric self-repair. Zinc-morpholine complex, Zn(L)SCN, namely showed strong free-radical scavenging, promotion of the DNA and RNA polymerases reconstruction and suppression of cell damage. The complex's mode of action is proposed to involve hydrogen bond formation via its bis(thiocyanato-k)zinc moiety. Zn(L)SCN complex had potent effects on gastric enzymatic activity both in vitro and in vivo. The complex disrupted the ulcerative process as demonstrated by changes in the intermediate metabolites of the oxidative pathway - specifically, reduction in the MDA levels and elevation of reduced glutathione together with an attenuation of oxidative DNA damage. Additionally, Zn(L)SCN restored the gastric mucosa, inhibited the production of pro-inflammatory cytokines (IL-6, TNF and the caspases), and preserved the gastric mucous balance. Zn(L)SCN thus exhibited anti-oxidative, anti-inflammatory and anti-apoptotic activities, all of which have cytoprotective effects on the gastric lining.

  20. Synthesis, characterization, and antibacterial activities of a novel nanohydroxyapatite/zinc oxide complex.

    Zhou, G.; Li, Yubao; Xiao, W.; Zhang, L.; Zuo, Y.; Xue, J.; Jansen, J.A.


    Nanohydroxyapatite (n-HA)/zinc oxide (ZnO) complex was synthesized by a direct precipitation method, and the antibacterial capability and antibacterial mechanism of this complex were investigated in this article. Transmission electron microscope (TEM), Fourier transform infrared, X-ray photoelectron

  1. Unique Ligand-Based Oxidative DNA Cleavage by Zinc(II) Complexes of Hpyramol and Hpyrimol

    Maheswari, P.U.; Barends, S.; Özalp-Yaman, S.; de Hoog, P.; Casellas, H.; Teat, S.J.; Massera, C.; Lutz, M.; Spek, A.L.; van Wezel, G.P.; Gamez, P.; Reedijk, J.


    The zinc(II) complexes reported here have been synthesised from the ligand 4-methyl-2-N-(2-pyridylmethyl)aminophenol (Hpyramol) with chloride or acetate counterions. All the five complexes have been structurally characterised, and the crystal structures reveal that the ligand Hpyramol gradually unde

  2. A role for dZIP89B in Drosophila dietary zinc uptake reveals additional complexity in the zinc absorption process.

    Richards, Christopher D; Warr, Coral G; Burke, Richard


    Dietary zinc is the principal source of zinc in eukaryotes, with its uptake and distribution controlled by a complex network of numerous membrane-spanning transport proteins. Dietary absorption is achieved by members of the SLC39A (ZIP) gene family, which encode proteins that are generally responsible for the movement of zinc into the cytosol. ZIP4 is thought to be the primary mammalian zinc uptake gene in the small intestine, with mutations in this gene causing the zinc deficiency disease Acrodermatitis enteropathica. In Drosophila, dual knockdown of the major dietary zinc uptake genes dZIP42C.1 (dZIP1) and dZIP42C.2 (dZIP2) results in a severe sensitivity to zinc-deficient media. However, the symptoms associated with ZIP4 loss can be reversed by zinc supplementation and dZIP42C.1 and 2 knockdown has minimal effect under normal dietary conditions, suggesting that additional pathways for zinc absorption exist in both mammals and flies. This study provides evidence that dZIP89B is an ideal candidate for this role in Drosophila, encoding a low-affinity zinc uptake transporter active in the posterior midgut. Flies lacking dZIP89B, while viable and apparently healthy, show indications of low midgut zinc levels, including reduced metallothionein B expression and compensatory up-regulation of dZIP42C.1 and 2. Furthermore dZIP89B mutants display a dramatic resistance to toxic dietary zinc levels which is abrogated by midgut-specific restoration of dZIP89B activity. We postulate that dZIP89B works in concert with the closely related dZIP42C.1 and 2 to ensure optimal zinc absorption under a range of dietary conditions.

  3. Anti-inflammatory, antinociceptive and ulcerogenic activity of a zinc-diclofenac complex in rats

    Santos L.H.


    Full Text Available We investigated the anti-inflammatory, antinociceptive and ulcerogenic activity of a zinc-diclofenac complex (5.5 or 11 mg/kg in male Wistar rats (180-300 g, N = 6 and compared it to free diclofenac (5 or 10 mg/kg and to the combination of diclofenac (5 or 10 mg/kg and zinc acetate (1.68 or 3.5 mg/kg. The carrageenin-induced paw edema and the cotton pellet-induced granulomatous tissue formation models were used to assess the anti-inflammatory activity, and the Hargreaves model of thermal hyperalgesia was used to assess the antinociceptive activity. To investigate the effect of orally or intraperitoneally (ip administered drugs on cold-induced gastric lesions, single doses were administered before exposing the animals to a freezer (-18ºC for 45 min in individual cages. We also evaluated the gastric lesions induced by multiple doses of the drugs. Diclofenac plus zinc complex had the same anti-inflammatory and antinociceptive effects as diclofenac alone. Gastric lesions induced by a single dose administered per os and ip were reduced in the group treated with zinc-diclofenac when compared to the groups treated with free diclofenac or diclofenac plus zinc acetate. In the multiple dose treatment, the complex induced a lower number of the most severe lesions when compared to free diclofenac and diclofenac plus zinc acetate. In conclusion, the present study demonstrates that the zinc-diclofenac complex may represent an important therapeutic alternative for the treatment of rheumatic and inflammatory conditions, as its use may be associated with a reduced incidence of gastric lesions.

  4. Zinc complexes as fluorescent chemosensors for nucleic acids: new perspectives for a "boring" element.

    Terenzi, Alessio; Lauria, Antonino; Almerico, Anna Maria; Barone, Giampaolo


    Zinc(II) complexes are effective and selective nucleic acid-binders and strongly fluorescent molecules in the low energy range, from the visible to the near infrared. These two properties have often been exploited to quantitatively detect nucleic acids in biological samples, in both in vitro and in vivo models. In particular, the fluorescent emission of several zinc(II) complexes is drastically enhanced or quenched by the binding to nucleic acids and/or upon visible light exposure, in a different fashion in bulk solution and when bound to DNA. The twofold objective of this perspective is (1) to review recent utilisations of zinc(II) complexes as selective fluorescent probes for nucleic acids and (2) to highlight their novel potential applications as diagnostic tools based on their photophysical properties.

  5. Thermokinetics of the Formation Reaction of Zinc Histidine Complex

    GAO,Sheng-Li(高胜利); CHEN,San-Ping(陈三平); HU,Rong-Zu(胡荣祖); SHI,Qi-Zhen(史启祯)


    The enthalpy change of reaction of zinc chloride with L-α-histidine in the temperature range of 25-50 ℃ has been determined by a microcalorimeter. On the basis of experimental and calculated results, three thermodynamics parameters (the activation enthalpy, the activation entropy, the activation free energy), the rate constant and three kinetic parameters (the activation energy, the pre-exponential constant and the reaction order) of the reaction, and the standard enthalpy of formarion of Zn(His)2+ (aq.) are obtained. The results showed that the title reaction easily took place at the studied temperature.

  6. Spontaneous resolution of a bis(eta(1)-methylcyclopentadienyl)zinc complex

    Olsson, S.; Lennartson, A.


    Two crystalline complexes of bis(eta(1)-methylcyclopentadienyl)zinc, [Zn(C5H4Me)(2)(py)(2)] (1), where py is pyridine, and [Zn(C5H4Me)(2)(teeda)], 2, where teeda is N,N,N',N'-tetraethylethylenediamine have been isolated. The crystal structures of 1 and 2 are the first crystal structures for Zn(C5H4......Me)(2) complexes reported in the literature; both structures display eta(1)-coordination of the methylcyclopentadienyl ring to zinc, and both compounds display chirogenic alpha-carbon atoms. While 1 forms racemic crystals, 2 undergoes spontaneous resolution and crystals of 2 are thus enantiomerically...

  7. The self-aggregation of chiral threonine-linked porphyrins and their zinc(Ⅱ) complexes


    The self-aggregation of chiral threonine-linked porphyrins and their zinc(Ⅱ) complexes in water-alcohol system and water-alcohol-NaCl system has been studied by circular dichroism (CD),UV-Vis absorption spectra and fluorescence spectra methods.The experiment results indicate that chiral threonine-linked porphyrins and their zinc(Ⅱ) complexes have two different kinds of aggregates in water-alcohol system and water-alcohol-NaCl system.And the porphyrins may form highly organized and orientated aggregates in water-alcohol-NaCl system.The aggregates in water-alcohol-NaCl system may have helical structures.

  8. Superoxide disproportionation driven by zinc complexes with various steric and electrostatic properties.

    Wada, Akira; Jitsukawa, Koichiro; Masuda, Hideki


    Attractive models: Synthetic Zn(II) complexes were investigated as models of copper-zinc superoxide dismutase. Superoxide underwent a unique disproportionation reaction in the electrostatic sphere of the complexes (see picture; bpy=2,2'-bipyridyl). The effectiveness of the Zn(II) complexes in inducing the disproportionation of superoxide depended on both the Lewis acidity and the coordination geometry of the Zn center.

  9. Preparation and Electronic Property Investigation of Zinc(II)-Schiff Base Complexes in the Confined Space

    Peng Shang; Lei Zhang


    Metal-Schiff base complexes have attracted continued research interest regarding their intriguing and useful features, while the electronic properties of these complexes in the confined space have not been sufficiently addressed in previous studies. In this work, a new zinc(II)-Schiff base complex bis(N-dodecyl salicylideneiminato)Zn(II) (1) was synthesized and subsequently loaded in an inorganic solid host. A large red shift (~40 nm) of the absorption onset was recorded, when the microenviro...

  10. Competitive Complexation of Copper and Zinc by Sequentially Extracted Humic Substances from Manure Compost

    LIU Shuai; WANG Xu-dong; LU Li-lan; DIAO Shi-rong; ZHANG Jun-feng


    Chicken manure with similar content of copper and zinc was chosen to conduct a composting experiment to investigate the changes of organic carbon and humus substance complexed copper (HS-Cu) and zinc (HS-Zn), which were extracted by water (H2O), sodium hydroxide (NaOH), and sodium pyrophate-NaOH mixture (Na4P2O7-NaOH), sequentially. Distributions of copper and zinc in fulvic acids (FA) and humic acids (HA) in the three extracts were studied. During manure composting, the concentrations of copper and zinc increased from about 500 mg kg-' in the raw material to 1100 mg kg-1 in the final products. HS-Cu in H2O, NaOH, and Na4P2O7-NaOH extracts occupied 6.7, 26.7, and 19% averagely of total copper and HS-Zn represented 2.7, 13.7, and 17% averagely of total zinc in compost, respectively. In water extracts, both HA and FA mainly complexed with Cu and the mole ratio of Cu to Zn was 2.8 in HA fractions and was 2.6 in FA fractions, respectively. HA mainly complexed with copper, so that the ratios of HA-Cu to HA-Zn averaged 3.4 in NaOH extracts. FA had a similar potential to complex with copper and zinc, so that the ratio of FA-Cu to FA-Zn was close to 1. In Na4P2O7-NaOH extracts, HA or FA had a similar potential to complex with copper and zinc. The ratio of HS-Cu to HS-Zn was close to 1. With manure composting, Na4P2O7-NaOH extractable HS-Zn increased to a level as high as HS-Cu. This indicated that more and more stable complexes of HS-Zn were formed in the late decomposition period. The competition between copper and zinc to be complexed with humic substance became weaker and weaker with the decomposition process.

  11. Nonlinear optical response of tetra and mono substituted zinc phthalocyanine complexes

    Fashina, Adedayo; Nyokong, Tebello, E-mail:


    The nonlinear absorption properties of 6 mono-substituted and 3 symmetric zinc phthalocyanine complexes have been studied in dimethylsulfoxide (DMSO) using 10 ns pulses at 532 nm. The non linear absorption of the complexes has been studied using the Z-scan technique. The study showed that both the singlet and triplet excited states contribute to the non linear absorption behavior. The nonlinear third-order susceptibility and second-order hyperpolarizability values of the complexes are reported. It was observed that two of the symmetric phthalocyanine complexes (5-α substituted with aminophenoxy and 9-β substituted with carboxyphenoxy) showed better and promising optical nonlinearity when compared to the other complexes studied. - Highlights: • Nonlinear absorption properties of zinc phthalocyanine are reported • Singlet and triplet excited states contribute to the non linear absorption. • Symmetrically tetra substituted phthalocyanines showed better optical nonlinearity.

  12. Fabrication of an Organic Light-Emitting Diode from New Host π Electron Rich Zinc Complex

    Jafari, Mohammad Reza; Janghouri, Mohammad; Shahedi, Zahra


    A new π electron rich zinc complex was used as a fluorescent material in organic light-emitting diodes (OLEDs). Devices with a structure of indium tin oxide/poly (3,4-ethylenedi-oxythiophene):poly(styrenesulfonate) (PEDOT: PSS) (50 nm)/polyvinylcarbazole (60 nm)/Zn: %2 porphyrin derivatives (45 nm)/Al (150 nm) were fabricated. Porphyrin derivatives accounting for 2 wt.% in the π electron rich zinc complex were used as a host. The electroluminescence (EL) spectra of porphyrin derivatives indicated a red shift, as π electron rich zinc complex EL spectra. The device (4) has also a luminance of 3420 cd/m2 and maximum efficiency of 1.58 cd/A at 15 V, which are the highest values among four devices. The result of Commission International del'Eclairage (CIE) (X, Y) coordinate and EL spectrum of device (3) indicated that it is more red shifted compared to other devices. Results of this work indicate that π electron rich zinc complex is a promising host material for high efficiency red OLEDs and has a simple structure compared to Alq3-based devices.

  13. Zebra reaction or the recipe for the synthesis of heterodimeric zinc complexes.

    Jędrzkiewicz, D; Ejfler, J; John, Ł; Szafert, S


    A series of asymmetric heterodimeric zinc complexes have been synthesized in a direct reaction between conformationally flexible chiral/achiral homodimers. The cooperative activity of steric factors and coordination codes resulted in an intriguing chiral self-sorting process. Herein, we are reporting our recent exploration of the first example of such a type of reaction.

  14. Enantioselective Conjugate Addition of Grignard Reagents to Enones Catalyzed by Chiral Zinc(II) Complexes

    Jansen, Johan F.G.A.; Feringa, Bernard


    Various chiral zinc(II) complexes catalyze the asymmetric 1,4-addition of Grignard reagents to α,β-unsaturated ketones with high chemoselectivities (yields of 1,4-adducts, 83-99%), high regioselectivities (1,4/1,2 ratios up to 499) and modest enantioselectivities (ee up to 33%). A study of several f

  15. Studies on the Interaction between Zinc-Hydroxybenzoite Complex and Genomic DNA

    Hacali Necefoglu


    Full Text Available Zinc-Hydroxybenzoite ([Zn (H206] (p-HO-C6H4COO22H20 complex which wassynthesized and characterized by instrumental methods and the DNA samples which hadbeen isolated from cattle were allowed to interact at 37 oC for different time periods. Theinteraction of genomic DNA with this complex has been followed by agarose gelelectrophoresis at 50 V for 2 h. When DNA samples were allowed to interact with this metalcomplex, it was found that band intensities changed with the concentrations of the complex.In the result of interaction between this complex and genomic DNA samples, it wasdetermined that the intensities of bands were changed at the different concentrations of thecomplex. The brightness of the bands was increased and mobility of the bands wasdecreased, indicating the occurrence of increased covalent binding of the metal complexwith DNA. In this study it was concluded that the damage effect of ascorbate was reducedby Zinc-Hydroxybenzoite.

  16. Studies on cluster, salt and molecular complex of zinc-quinolinate

    Prithiviraj Khakhlary; Jubaraj B Baruah


    Reactions of zinc halides with 8-hydroxyquinoline (hydroxQ) in equimolar ratio were carried out in different solvents. Respective solvates of tetranuclear clusters, namely [Zn4(oxyQ)6X2].(solvent)2, (when X=Cl, Solvent=dimethylformamide (1), dimethylacetamide (2) and dimethysulphoxide (3); X = Br, solvent = dimethylformamide (4), oxyQ=quinolinate anion) were obtained. Bond parameters of these isostructural clusteres 1–4 are compared from their single crystal structures. Anhydrous form of the cluster have porous packing and is thermally stable below 250° C. Surface area of the clusters 1 and 4 are 8.933 and 6.172 m2/g, respectively. Complexes 1 and 4 can be reversibly hydrated, which is reflected in colour changes. The reaction of zinc chloride with 8-hydroxyquinoline in equimolar ratio followed by crystallization from water gave salt (HhydroxQ)2 [ZnCl4] (5) and a similar reaction followed by crystallization from 3-methylpyridine (3mepy) resulted in the molecular complex [Zn(oxyQ)2(3mepy)]. [Zn(oxyQ)2(3mepy)2].3H2O (6). Complex 5 is formed from a hydrolytic equilibrium of water with zinc chloride yielding tetrachloro zinc anion and zinc hydroxide. Taking advantage of this reaction, a composite material of ZnO@complex 5 exhibiting dual fluorescence at 450 and 575 nm on excitation at 390 nm was prepared. Fluorescence emission properties of all the complexes in solid state are compared with fluorescence emission of the ligand

  17. Structural and Functional Studies of the Protamine 2-Zinc Complex from Syrian Gold Hamster (Mesocricetus Auratus) Spermatids and Sperm

    Dolan, Cheryl E. [Univ. of California, Davis, CA (United States)


    The research described in this dissertation consists of four major areas: (1) sequence analysis of protamine 2 from Muroid rodents to identify potential zinc-binding domain(s) of protamine 2; (2) structural studies of the protamine 2-zinc complex from Syrian Gold hamster sperm and spermatids to elucidate the role of zinc during spermiogenesis; (3) structural studies of an unique protamine 2-zinc complex from chinchilla sperm; and (4) Nuclear Magnetic Resonance (NMR) studies of soluble complexes of hairpin oligonucleotides with synthetic arginine-rich peptides or protamine 1 isolated from bull sperm. First, zinc was quantitated in spermatids and sperm by Proton-Induced X-ray Emission (PIXE) to determine whether zinc is present in the early stages of spermiogenesis. The PIXE results revealed the zinc content varies proportionately with the amount of protamine 2 in both spermatid and sperm nuclei. An exception was chinchilla sperm containing twice the amount of protamine 2 than zinc. Further analyses by PIXE and X-ray Absorption Spectroscopy (XAS) of zinc bound to protamines isolated from hamster sperm confirmed the majority of the zinc is bound to protamine and identified the zinc ligands of protamine 2 in hamster spermatids and sperm in vivo. These studies established that zinc is bound to the protamine 2 precursor in hamster spermatids and the coordination of zinc by protamine 2 changes during spermiogenesis. Finally, the sequence analysis combined with the XAS results suggest that the zinc-binding domain in protamine 2 resides in the amino-terminus. Similar analyses of chinchilla sperm by XAS were performed to clarify the unusual PIXE results and revealed that chinchilla has an atypical protamine 2-zinc structure. Two protamine 2 molecules coordinate one zinc atom, forming homodimers that facilitate the binding of protamine 2 to DNA and provide an organizational scheme that would accommodate the observed species-specific protamine stoichiometry in mammalian sperm

  18. Antibacterial and antifungal activity of zinc(II complexes with some 2-methylbenzimidazole derivatives

    Podunavac-Kuzmanović Sanja O.


    Full Text Available Zinc(II chloride reacts with 2-methylbenzimidazole derivatives to give complexes of the formula ZnL2Cl2-nH2O, where L=2-methylbenzimidazole l-benzyl-2-methylbenzimida-zole and l-(4-methylbenzyl-2-methylbenzimidazole n=0, 0.5 or 1. All the ligands and their zinc(II complexes were evaluated for their in vitro antimicrobial activity against Pseudomonas aeruginosa Bacillus sp., Staphylococcus aureus, Sarcina lutea and Candida pseudotropicalis. It was found that the majority of the investigated compounds displayed in vitro antimicrobial activity against very persistent microorganisms, except for the starting ligand, 2-methylbenzimidazole and its zinc(II complex which were active only against gram-negative bacteria. None of the compounds was significantly effective against Candida pseudotropicalis, except for l-(4-methylbenzyl-2-methylbenzimidazoleandits complex, which very slightly or slightly inhibited the yeast growth. The minimum inhibitory concentration (MIC was determined for all the ligands and their complexes. The effect of ligand and complex structure on the antimicrobial activity was discussed.

  19. Zinc(II) complexes of carboxamide derivatives: Crystal structures and interaction with calf thymus DNA

    Biplab Mondal; Buddhadeb Sen; Ennio Zangrando; Pabitra Chattopadhyay


    Two mononuclear zinc(II) complexes of newly designed carboxamide derivatives, formulated as [Zn(L1)3](ClO4)2 (1) and [Zn(L2)3](ClO4)2 (2) [where L1 = -(furan-2-ylmethyl)-2-pyridinecarboxamide and L2 = -(thiophen-2-ylmethyl)-2-pyridine-carboxamide], have been isolated in pure form in the reaction of perchlorate salts of Zn(II) with ligands L1 and L2, respectively. The two complexes were characterized by physicochemical and spectroscopic tools, and by X-ray crystal structures of both ligands and the complex 1. In complex 1, zinc(II) is chelated by three ligands with a distorted octahedral geometry. The DNA-binding properties of zinc complexes 1 and 2 have been investigated by spectroscopic methods and viscosity measurements. The results suggest that both complexes 1 and 2 bind to DNA in an intercalation mode between the uncoordinated furan or thiophene chromophore and the base pairs of DNA.

  20. Synthesis, characterization, thermal and DNA-binding properties of new zinc complexes with 2-hydroxyphenones.

    Mrkalić, Emina; Zianna, Ariadni; Psomas, George; Gdaniec, Maria; Czapik, Agnieszka; Coutouli-Argyropoulou, Evdoxia; Lalia-Kantouri, Maria


    The neutral mononuclear zinc complexes with 2-hydroxyphenones (ketoH) having the formula [Zn(keto)2(H2O)2] and [Zn(keto)2(enR)], where enR stands for a N,N'-donor heterocyclic ligand such as 2,2'-bipyridine (bipy), 1,10-phenanthroline (phen) or 2,2'-dipyridylamine (dpamH), have been synthesized and characterized by IR, UV and (1)H NMR spectroscopies. The 2-hydroxyphenones are chelated to the metal ion through the phenolate and carbonyl oxygen atoms. The crystal structures of [bis(2-hydroxy-4-methoxy-benzophenone)(2,2'-bipyridine)zinc(II)] dimethanol solvate and [bis(2-hydroxy-benzophenone)(2,2'-bipyridine)zinc(II)] dimethanol solvate have been determined by X-ray crystallography. The thermal stability of the zinc complexes has been investigated by simultaneous TG/DTG-DTA technique. The ability of the complexes to bind to calf-thymus DNA (CT DNA) has been studied by UV-absorption and fluorescence emission spectroscopy as well as viscosity measurements. UV studies of the interaction of the complexes with DNA have shown that they can bind to CT DNA and the corresponding binding constants to DNA have been calculated and evaluated. The complexes most probably bind to CT DNA via intercalation as concluded by studying the viscosity of a DNA solution in the presence of the complexes. Competitive studies with ethidium bromide (EB) have shown that the reported complexes can displace the DNA-bound EB, suggesting strong competition with EB for the intercalation site.

  1. Synthesis, Characterization and Biological Activity of an Intramolecular Stacking Zinc(Ⅱ) Complex

    GAO, Enjun; LIU, Lei; ZHU, Mingchang; WU, Qiong


    The synthesis, crystallographic analysis and spectroscopic study of a zinc(Ⅱ) complex [Zn(bipy)(pmal)(H2O)]· 2H2O (bipy=2,2'-bipyfidine, pmal=phenylmalonic acid) were carded out. The complex has been investigated by the methods of X-ray crystallography, elemental analysis and IR spectra. The binding ability of the Zn(Ⅱ) complex to calf thymus (CT-DNA) was characterized by measuring the effects on the UV spectroscopy and fluorescence spectra of DNA. The agarose gel electrophoresis experimental results suggest that the ligand planaxity of complex has a significant effect on cleaving the pBR322 plasmid DNA.

  2. Enantiomer separation by complexation SFC on immobilized Chirasil-nickel and Chirasil-zinc.

    Schurig, V; Fluck, M


    The use of complexation SFC for enantiomer separation of Lewis base selectands on chiral nickel(II)- and zinc(II)-bis[(3-heptafluorobutanoyl)-10-methylene-(1R)-camphora te] chemically bonded to poly(dimethylsiloxane) (Chirasil-nickel and Chirasil-zinc) and employed as Lewis acid selectors is described. The method is especially suited for less volatile and configurationally labile racemates. The variation of the experimental parameters temperature T, pressure p and density rho of the mobile phase carbon dioxide on the retention factor k, relative retention r and chiral separation factor alpha is studied, providing insights into the mechanisms of chiral recognition under supercritical conditions. For mecoprop methyl ester (methyl 2-(4-chloro-2-methylphenoxy)propanoate) an unusual increase of alpha at increased temperature is observed on Chirasil-nickel. Supercritical carbon dioxide does not inadvertently affect the complexation equilibria between Lewis donor selectands and the Lewis acid metal selectors during complexation SFC.

  3. Zinc complexes of the antibacterial drug oxolinic acid: structure and DNA-binding properties.

    Tarushi, Alketa; Psomas, George; Raptopoulou, Catherine P; Kessissoglou, Dimitris P


    The neutral mononuclear zinc complexes with the quinolone antibacterial drug oxolinic acid in the absence or presence of a nitrogen donor heterocyclic ligand 2,2'-bipyridine or 1,10-phenanthroline have been synthesized and characterized. The experimental data suggest that oxolinic acid is on deprotonated mode acting as a bidentate ligand coordinated to the metal ion through the ketone and one carboxylato oxygen atoms. The crystal structures of (chloro)(oxolinato)(2,2'-bipyridine)zinc(II), 2, and bis(oxolinato)(1,10-phenanthroline)zinc(II), 3, have been determined with X-ray crystallography. The biological activity of the complexes has been evaluated by examining their ability to bind to calf-thymus DNA (CT DNA) with UV and fluorescence spectroscopies. UV studies of the interaction of the complexes with DNA have shown that they can bind to CT DNA and the DNA-binding constants have been calculated. Competitive studies with ethidium bromide (EB) have shown that complex 3 exhibits the ability to displace the DNA-bound EB indicating that it binds to DNA in strong competition with EB.

  4. Spectroscopic study on the photophysical properties of chlorine substituted tetraphenylporphyrinhistidine and its zinc (Ⅱ) complexes

    ZHANG Huijuan; FENG Juan; AI Xicheng; ZHANG Xingkang; YU Zhongheng; ZHANG Jianping


    The photophysical properties of ortho-Cl, meta-Cl and para-Cl substituted tetraphenylporphyrin-histidine and their zinc (Ⅱ) complexes have been studied by means of steady-state absorption and fluorescence spectroscopies, as well as time-resolved fluorescence spectroscopy. For the cases of both free-base and zinc complexes, it was found that the ortho-chlorine substitution onto the phenyl rings significantly altered the fluorescence quantum yield, the fluorescence lifetime and the ratio between radiative and nonradiative deactivation rates of the porphyrin chromophore, i.e. the photophysical parameters were quite differentfrom those of meta- and para-substi- tuted compounds. On the other hand, however, the introduction of covalently-linked histidine did not exert much effects onthe photophysical behavior of the porphyrin chromophore. The results are interpreted in terms of the steric effect and the heavy-atom effect from the chlorine atoms substituted onto the phenyl rings.

  5. Fluorescent zinc-terpyridine complex containing coordinated peroxo counter ion in aqueous medium

    S Kapoor; M S Sastry


    We describe a mixed ligand-zinc (10) complex containing coordinated peroxo ion and 2,2'2"-terpyridine and exhibiting fluorescence in the visible region (473 nm) on excitation at 390 nm in aqueous medium at room temperature. We also discuss the unusual phenomenon of enhancement of this fluorescence intensity on addition of some transition metal ions (35, 310, 40 and 39 electronic configurations).

  6. Synthesis, characterization and biological evaluation of Rutin-zinc(II) flavonoid -metal complex.

    Ikeda, Norma Estefania Andrades; Novak, Estela Maria; Maria, Durvanei Augusto; Velosa, Adélia Segin; Pereira, Regina Mara Silva


    Synthesis of compounds analogous to natural products from secondary metabolites, such as flavonoids, is a promising source of novel drugs. Rutin (quercetin-3-O-rutinoside) is a natural flavone, which has, in its chemical structure, different sites for coordination with transition metals and the complexation with these metals enhances its biological properties. Rutin-zinc(II), a flavonoid-metal complex, was synthesized and characterized by UV-VIS, FT-IR, elemental analysis and (1)H NMR. The antioxidant and antitumor activities, as well as the cytotoxicity and in vivo toxicity of this complex were evaluated and compared with the free rutin. Rutin-zinc(II) has not shown any cytotoxicity against normal cells (fibroblasts and HUVECs) or toxicity in BALB/c mice, but has shown antioxidant activity in vitro and cytotoxicity against leukemia (KG1, K562 and Jurkat), multiple myeloma (RPMI8226) and melanoma (B16F10 and SK-Mel-28) cell lines in vitro. In Ehrlich ascites carcinoma model, Rutin-zinc(II) modulated the mitochondrial membrane potential and the expression of genes related to cell cycle progression, angiogenesis and apoptosis.

  7. Zinc complexes developed as metallopharmaceutics for treating diabetes mellitus based on the bio-medicinal inorganic chemistry.

    Yoshikawa, Yutaka; Yasui, Hiroyuki


    Biological trace metals such as iron, zinc, copper, and manganese are essential to life and health of humans, and the success of platinum drugs in the cancer chemotherapy has rapidly grown interest in developing inorganic pharmaceutical agents in medicinal chemistry, that is, medicinal inorganic chemistry, using essential elements and other biological trace metals. Transition metal complexes with unique chemical structures may be useful alternatives to the drugs available to address some of the incurable diseases. In this review, we emphasize that metal complexes are an expanding of interest in the research field of treatment of diabetes mellitus. Especially, orally active anti-diabetic and anti-metabolic syndrome zinc complexes have been developed and progressed since the discovery in 2001, where several highly potent anti-diabetic zinc complexes with different coordination structures have quite recently been disclosed, using experimental diabetic animals. In all of the complexes discussed, zinc is found to be biologically active and function by interacting with some target proteins related with diabetes mellitus. The design and screening of zinc complexes with higher activity is not efficient without consideration of the translational research. For the development of a clinically useful metallopharmaceutics, the research of zinc complexes on the long-term toxicity including side effects, clear-cut evidence of target molecule for the in vivo pharmacological action, and good pharmacokinetic property are essential in the current and future studies.

  8. Thermodynamic Complexation of Dopamine with Zinc(Ⅱ) in Media with Different Dielectric Constants



    The complexation of zinc(Ⅱ) with dopamine has been investigated by spectrophotometric measurements in mixed solvent system at an ionic strength of 0.2 mol·dm-3 sodium chloride, at (15±0.1), (25±0.1), (35±0.1 )℃ in a pH range of ca. 6 to ca. 7 with a high ratio of ligand to metal. The effect of solvent systems on protonation and complexation was discussed. Linear relationships were observed by plotting Ig K versus I/D, where K and D show stability and dielectric constants, respectively.

  9. New complexes of heteroaromatic N-oxides with europium, uranyl and zinc ions

    Zbigniew Hnatejko


    New solid complexes of europium,uranyl and zinc ions with N-oxides of 4-chloro-2,6-dimethylpyridine,quinoline and 4-methoxyquinaldinic acid in presence different anions were obtained and characterized by elemental and TG analyses,IR and luminescence spectra.The compounds are crystalline,hydrated or anhydrous salts with colours typical of metal ions.Thermal studies showed that in hydrated salts lattice or coordination water molecules are present.A role of different anions in the formation of various types of the complexes is presented.

  10. A Rac1-GDP Trimer Complex Binds Zinc with Tetrahedral and Octahedral Coordination, Displacing Magnesium

    Prehna,G.; Stebbins, E.


    The Rho family of small GTPases represent well characterized signaling molecules that regulate many cellular functions such as actin cytoskeletal arrangement and the cell cycle by acting as molecular switches. A Rac1-GDP-Zn complex has been crystallized in space group P3{sub 2}21 and its crystal structure has been solved at 1.9 {angstrom} resolution. These trigonal crystals reveal the unexpected ability of Rac1 to coordinate Zn atoms in a tetrahedral fashion by use of its biologically relevant switch I and switch II regions. Upon coordination of zinc, the switch I region is stabilized in the GDP-bound conformation and contributes to a Rac1 trimer in the asymmetric unit. Zinc coordination causes switch II to adopt a novel conformation with a symmetry-related molecule. Additionally, zinc was found to displace magnesium from its octahedral coordination at switch I, although GDP binding remained stable. This structure represents the first reported Rac1-GDP-Zn complex, which further underscores the conformational flexibility and versatility of the small GTPase switch regions.

  11. A Rac1--GDP trimer complex binds zinc with tetrahedral and octahedral coordination, displacing magnesium

    Prehna, G.; Stebbins, C


    The Rho family of small GTPases represent well characterized signaling molecules that regulate many cellular functions such as actin cytoskeletal arrangement and the cell cycle by acting as molecular switches. A Rac1-GDP-Zn complex has been crystallized in space group P3221 and its crystal structure has been solved at 1.9 {angstrom} resolution. These trigonal crystals reveal the unexpected ability of Rac1 to coordinate Zn atoms in a tetrahedral fashion by use of its biologically relevant switch I and switch II regions. Upon coordination of zinc, the switch I region is stabilized in the GDP-bound conformation and contributes to a Rac1 trimer in the asymmetric unit. Zinc coordination causes switch II to adopt a novel conformation with a symmetry-related molecule. Additionally, zinc was found to displace magnesium from its octahedral coordination at switch I, although GDP binding remained stable. This structure represents the first reported Rac1-GDP-Zn complex, which further underscores the conformational flexibility and versatility of the small GTPase switch regions.

  12. Zinc transport complexes contribute to the homeostatic maintenance of secretory pathway function in vertebrate cells.

    Ishihara, Kaori; Yamazaki, Tomohiro; Ishida, Yoko; Suzuki, Tomoyuki; Oda, Kimimitsu; Nagao, Masaya; Yamaguchi-Iwai, Yuko; Kambe, Taiho


    Zinc transporters play important roles in a wide range of biochemical processes. Here we report an important function of ZnT5/ZnT6 hetero-oligomeric complexes in the secretory pathway. The activity of human tissue-nonspecific alkaline phosphatase (ALP) expressed in ZnT5(-)ZnT7(-/-) cells was significantly reduced compared with that expressed in wild-type cells as in the case of endogenous chicken tissue-nonspecific ALP activity. The inactive human tissue-nonspecific ALP in ZnT5(-)ZnT7(-/-) cells was degraded by proteasome-mediated degradation without being trafficked to the plasma membrane. ZnT5(-)ZnT7(-/-) cells showed exacerbation of the unfolded protein response as did the wild-type cells cultured under a zinc-deficient condition, revealing that both complexes play a role in homeostatic maintenance of secretory pathway function. Furthermore, we showed that expression of ZnT5 mRNA was up-regulated by the endoplasmic reticulum stress in various cell lines. The up-regulation of the hZnT5 transcript was mediated by transcription factor XBP1 through the TGACGTGG sequence in the hZnT5 promoter, and this sequence was highly conserved in the ZnT5 genes of mouse and chicken. These results suggest that zinc transport into the secretory pathway is strictly regulated for the homeostatic maintenance of secretory pathway function in vertebrate cells.

  13. Synthesis and structures of bis-ligated zinc complexes supported by tridentate ketoimines that initiate L-lactide polymerization.

    Gerling, Kimberly A; Rezayee, Nomaan M; Rheingold, Arnold L; Green, David B; Fritsch, Joseph M


    Eight bis-ligated, homoleptic, zinc complexes were synthesized through the reaction of NNO Schiff base ketoimines bearing varying substituents with diethyl zinc in an inert atmosphere glovebox at room temperature and isolated in 62-95% yield. The complexes were characterized with (1)H, (13)C, and (19)F nuclear magnetic resonance spectroscopy, absorbance spectroscopy, high resolution mass spectrometry, elemental analysis, and single crystal X-ray crystallography. The complexes were shown to adopt distorted octahedral coordination geometry around zinc. The (1)H and (19)F NMR spectra of complexes 1-7 showed stable zinc coordination at 300 K while the effect of steric encumbrance and two trifluoromethyl groups in complex 8 was investigated with variable temperature NMR. The bis-ligated zinc complexes were effective initiators for the ring opening polymerization of L-lactide into poly-L-lactic acid (PLLA). With [L-lac]/[Zn complex] = 50, the bis-ligated zinc complexes yielded percentage conversion of 14-98% with polymerization times varying from 15-1440 min, where the longest reaction times were required when two trifluoromethyl groups were present. The addition of 4-fluorophenol co-catalyst resulted in up to a 5-fold increase in the percentage conversion in toluene solution and up to a 14-fold increase in bulk melt polymerization with reductions in the poly-dispersity index values for the isolated PLLA. Addition of 4-fluorophenol to complex 1 was studied with (1)H and (19)F NMR and appeared to yield an in situ generated zinc alkoxide complex.

  14. Coordination chemistry and reactivity of zinc complexes supported by a phosphido pincer ligand.

    D'Auria, Ilaria; Lamberti, Marina; Mazzeo, Mina; Milione, Stefano; Roviello, Giuseppina; Pellecchia, Claudio


    The preparation and characterization of new Zn(II) complexes of the type [(PPP)ZnR] in which R = Et (1) or N(SiMe(3))(2) (2) and PPP is a tridentate monoanionic phosphido ligand (PPP-H = bis(2-diphenylphosphinophenyl)phosphine) are reported. Reaction of ZnEt(2) and Zn[N(SiMe(3))(2)](2) with one equivalent of proligand PPP-H produced the corresponding tetrahedral zinc ethyl (1) and zinc amido (2) complexes in high yield. Homoleptic (PPP)(2) Zn complex 3 was obtained by reaction of the precursors with two equivalents of the proligand. Structural characterization of 1-3 was achieved by multinuclear NMR spectroscopy ((1)H, (13)C, and (31)P) and X-ray crystallography (3). Variable-temperature (1)H and (31)P NMR studies highlighted marked flexibility of the phosphido pincer ligand in coordination at the metal center. A DFT calculation on the compounds provided theoretical support for this behavior. The activities of 1 and 2 toward the ring-opening polymerization of ε-caprolactone and of L- and rac-lactide were investigated, also in combination with an alcohol as external chain-transfer agent. Polyesters with controlled molecular parameters (M(n), end groups) and low polydispersities were obtained. A DFT study on ring-opening polymerization promoted by these complexes highlighted the importance of the coordinative flexibility of the ancillary ligand to promote monomer coordination at the reactive zinc center. Preliminary investigations showed the ability of these complexes to promote copolymerization of L-lactide and ε-caprolactone to achieve random copolymers whose microstructure reproduces the composition of the monomer feed.

  15. Structural and antimicrobial properties of irradiated chitosan and its complexes with zinc

    Khan, Azam; Mehmood, Shaukat; Shafiq, Muhammad; Yasin, Tariq; Akhter, Zareen; Ahmad, Shabir


    The aim of this research was to evaluate the structural and antimicrobial properties of irradiated chitosan and its complexes with zinc. Chitosan having a molecular weight (Mη) of 220 kDa was exposed to gamma rays in dry, wet and solution forms. The chitosan-zinc complexes were prepared by varying the Mη of chitosan and Zn content. Viscometeric analysis revealed a sharp decrease in the Mη of chitosan irradiated in solution form even at lower doses compared with the dry and wet forms. X-ray diffraction patterns demonstrated variation in the crystallinity of chitosan upon exposure to gamma rays. The antibacterial response of the irradiated chitosan and its complexes against gram-positive and gram-negative bacteria demonstrated wide spectrum of effective antimicrobial activities, which increased with the dose. Additionally, the complexes exhibited excellent antifungal activity with no growth of Aspergallious fumigatus and Fusarium solani even after two weeks. These results suggested that the irradiated chitosan and its complexes with Zn can be used as antimicrobial additives for various applications.

  16. A zinc complex of heparan sulfate destabilises lysozyme and alters its conformation

    Hughes, Ashley J. [Institute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB (United Kingdom); Diamond Light Source Ltd., Diamond House, Didcot, Oxfordshire OX11 0DE (United Kingdom); Hussain, Rohanah [Diamond Light Source Ltd., Diamond House, Didcot, Oxfordshire OX11 0DE (United Kingdom); Cosentino, Cesare; Guerrini, Marco [Istituto di Chimica e Biochimica ' G. Ronzoni' , Via G. Colombo 81, Milano 20133 (Italy); Siligardi, Giuliano [Diamond Light Source Ltd., Diamond House, Didcot, Oxfordshire OX11 0DE (United Kingdom); Yates, Edwin A., E-mail: [Institute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB (United Kingdom); Rudd, Timothy R., E-mail: [Institute of Integrative Biology, University of Liverpool, Liverpool L69 7ZB (United Kingdom); Istituto di Chimica e Biochimica ' G. Ronzoni' , Via G. Colombo 81, Milano 20133 (Italy)


    Highlights: Black-Right-Pointing-Pointer Zinc-heparan sulfate complex destabilises lysozyme, a model amyloid protein. Black-Right-Pointing-Pointer Addition of zinc, without heparan sulfate, stabilises lysozyme. Black-Right-Pointing-Pointer Heparan sulfate cation complexes provide alternative protein folding routes. -- Abstract: The naturally occurring anionic cell surface polysaccharide heparan sulfate is involved in key biological activities and is implicated in amyloid formation. Following addition of Zn-heparan sulfate, hen lysozyme, a model amyloid forming protein, resembled {beta}-rich amyloid by far UV circular dichroism (increased {beta}-sheet: +25%), with a significantly reduced melting temperature (from 68 to 58 Degree-Sign C) by fluorescence shift assay. Secondary structure stability of the Zn-heparan sulfate complex with lysozyme was also distinct from that with heparan sulfate, under stronger denaturation conditions using synchrotron radiation circular dichroism. Changing the cation associated with heparan sulfate is sufficient to alter the conformation and stability of complexes formed between heparan sulfate and lysozyme, substantially reducing the stability of the protein. Complexes of heparan sulfate and cations, such as Zn, which are abundant in the brain, may provide alternative folding routes for proteins.

  17. Possible identification of zinc-vacancy-donor-impurity complexes in zinc telluride by optically detected magnetic resonance

    Bittebierre, J.; Cox, R. T.


    Application of the optically detected magnetic resonance (ODMR) technique to donor-acceptor recombination luminescence in donor-doped ZnTe crystals shows the presence of two acceptor centers having noncubic symmetry. One of these centers, labeled At, has precisely trigonal symmetry C3. In terms of a spin Hamiltonian for an effective spin S=1/2, its g factors are gzz=2.664 and gxx=gyy~=0, where z corresponds to a direction. The other center, labeled Am, has mirror symmetry CS, with gzz=2.540 and gxx~=gyy~=0.25, where the z axis is inclined at 6.7° to in a \\{110\\} plane. The g factors are interpreted by considering the effect of a low-symmetry crystal field on a J=(3/2) (Γ8) hole in ZnTe. Hyperfine splittings of magnitude 190×10-4 cm-1 for At and 180×10-4 cm-1 for Am are observed in the ODMR spectra and attributed to interactions with three equivalent or nearly equivalent Te nuclei. Center At is observed in chlorine-doped ZnTe; center Am is observed in aluminum-doped ZnTe and is very likely the acceptor called AC, known by its bound-exciton line at 2.369 eV. It is proposed that these single-acceptor centers are double-acceptor-single-donor pairs and, more precisely, that the double-acceptor constituent is the zinc vacancy. That is, the trigonal center At is VZnClTe and the mirror-symmetry center Am is VZnAlZn. If this interpretation is correct, the electronic properties of vacancy centers in ZnTe are remarkably different from those of the well-known VZn-donor-impurity associates (the ``A centers'') in ZnSe and ZnS. Whereas the latter centers are very deep centers with large pseudo-Jahn-Teller distortions, centers At and Am in ZnTe are of shallow or intermediate depth, retain the full symmetry of the vacancy-impurity complex, and have unquenched orbital angular momentum. Finally, it is suggested that the detection of zinc-vacancy acceptors in donor-doped ZnTe may help one to understand the difficulty of producing n-type material.

  18. Novel polystyrene-anchored zinc complex:Efficient catalyst for phenol oxidation

    Alekha Kumar Sutar a; Yasobanta Das ab; Sasmita Pattnaik a; Anita Routaray a; Nibedita Nath a; Prasanta Rath b; Tungabidya Maharana c


    The novel recyclable free -ONNO- tetradentate Schiff base ligand N,N′-bis(2-hydroxy-3-methox-ybenzaldehyde)4-methylbenzene-1,2-diamine (3-MOBdMBn) was synthesized. Complexation of this ligand with zinc (3-MOBdMBn-Zn) was performed, and the catalytic activity of the complex was evaluated. The polymer-supported analog of this complex (P-3-MOBdMBn-Zn) was synthesized, and its catalytic activity was studied. These free and polymer-anchored zinc complexes were prepared by the reactions of metal solutions with one molar equivalent of unsupported 3-MOBdMBn or P-3-MOBdMBn in methanol under nitrogen. The catalytic activity of 3-MOBdMBn-Zn and P-3-MOBdMBn-Zn was evaluated in phenol oxidation. The activity of P-3-MOBdMBn-Zn was signif-icantly affected by the polymer support, and the rate of phenol conversion was around 50%for polystyrene-supported 3-MOBdMBn. The experimental results indicated that the reaction rate was affected by the polymer support, and the rate of phenol conversion was 1.64 μmol/(L·s) in the presence of polystyrene-supported 3-MOBdMBn.

  19. PIAS1-modulated Smad2/4 complex activation is involved in zinc-induced cancer cell apoptosis.

    Yang, N; Zhao, B; Rasul, A; Qin, H; Li, J; Li, X


    Prostate cancer is one of the most frequently diagnosed cancers among men. Dietary intake of nutrients is considered crucial for preventing the initiation of events leading to the development of carcinoma. Many dietary compounds have been considered to contribute to cancer prevention including zinc, which has a pivotal role in modulating apoptosis. However, the mechanism for zinc-mediated prostate cancer chemoprevention remains enigmatic. In this study, we investigated the therapeutic effect of zinc in prostate cancer chemoprevention for the first time. Exposure to zinc induced apoptosis and resulted in transactivation of p21(WAF1/Cip1) in a Smad-dependent and p53-independent manner in prostate cancer cells. Smad2 and PIAS1 proteins were significantly upregulated resulting in dramatically increased interactions between Smad2/4 and PIAS1 in the presence of zinc in LNCaP cells. Furthermore, it was found that the zinc-induced Smad4/2/PIAS1 transcriptional complex is responsible for Smad4 binding to SBE1 and SBE3 regions within the p21(WAF1/Cip1) promoter. Exogenous expression of Smad2/4 and PIAS1 promotes zinc-induced apoptosis concomitant with Smad4 nuclear translocation, whereas endogenous Smad2/4 silencing inhibited zinc-induced apoptosis accompanying apparent p21(WAF1/Cip1) reduction. Moreover, the knockdown of PIAS1 expression attenuated the zinc-induced recruitment of Smad4 on the p21(WAF1/Cip1) promoter. The colony formation experiments demonstrate that PIAS1 and Smad2/4 silencing could attenuate zinc apoptotic effects, with a proliferation of promoting effects. We further demonstrate the correlation of apoptotic sensitivity to zinc and Smad4 and PIAS1 in multiple cancer cell lines, demonstrating that the important roles of PIAS1, Smad2, and Smad4 in zinc-induced cell death and p21(WAF1/Cip1) transactivation were common biological events in different cancer cell lines. Our results suggest a new avenue for regulation of zinc-induced apoptosis, and provide a

  20. Molecular modeling of zinc paddlewheel molecular complexes and the pores of a flexible metal organic framework.

    Alzahrani, Khalid A H; Deeth, Robert J


    A new all-atom first-principles force field (FF) is constructed for the bimetallic, four-bladed zinc paddlewheel (ZPW) motif. Zinc-ligand interactions are described via Morse functions and the angular geometry at the metal centers is modeled with a pure ligand-ligand repulsion term. The ZPW-FF is principally based on 15 DFT-optimized model systems of general formula ZnPR.nL, where ZnP is the base Zn2(O2CR)4 unit, R = H, CH3 or CF3, L = NH3 or pyridine, and n = 0, 1 or 2. It correctly generates the distorted tetrahedral coordination of the uncapped [Zn2(O2CR)4] species in their ground states as well as giving reasonable structures and energies for the higher symmetry D4h transition state conformations. The zinc-ligand Morse function reference distance, r 0 , is further refined against 30 complexes located in the Cambridge Structural Database and this FF is applied to pore models of the flexible metal-organic framework (MOF) [Zn(bdc)2(dabco)]n (bdc = 1,4-benzendicarboxylate; dabco = 1,4-diazabicyclo(2.2.2)octane). A single pore model reproduces the unit cell of the evacuated MOF system while a 3×3 grid model is necessary to provide good agreement with the observed pronounced structural changes upon adsorption of either dimethylformamide or benzene.

  1. Comparison of zinc complexation properties of dissolved organic matter from surface waters and wastewater treatment plant effluents

    CHENG Tao


    Unlike natural organic matter(NOM), wastewater organic matter(WWOM) from wastewater treatment plant effluents has not been extensively studied with respect to complexation reactions with heavy metals such as copper or zinc. In this study, organic matter from surface waters and a wastewater treatment plant effluent were concentrated by reverse osmosis(RO) method. The samples were treated in the laboratory to remove trace metals and major cations. The zinc complexing properties of both NOM and the WWOM were studied by square wave anodic stripping voltammetry(SWASV). Experimental data were compared to predictions using the Windermere Humic Aqueous Model(WHAM) Version VI. We found that the zinc binding of WWOM was much stronger than that of NOM and not well predicted by WHAM. This suggests that in natural water bodies that receive wastewater treatment plant effluents the ratio of WWOM to NOM must be taken into account in order to accurately predict free zinc activities.

  2. Electrochemical and optical characterization of cobalt, copper and zinc phthalocyanine complexes.

    Lee, Jaehyun; Kim, Se Hun; Lee, Woosung; Lee, Jiwon; An, Byeong-Kwan; Oh, Se Young; Kim, Jae Pil; Park, Jongwook


    New phthalocyanine (Pc) derivatives that include the alkyl group in ligand were synthesized based on three core metals such as zinc (Zn), copper (Cu), and cobalt (Co). Electrochemical behaviors and optical properties of the new phthalocyanine derivatives with ligand and different core metal were investigated by using cyclic voltammetry, UV-Visible (UV-Vis) spectroscopy and photoluminescence (PL) spectroscopy. In UV-Vis data, maximum values of 2H, Co, Cu, and Zn complexes were 708 nm and 677 nm, 686 nm, 684 nm, respectively.

  3. Dipyridylamide ligand dependent dimensionality in luminescent zinc 2,4-pyridinedicarboxylate coordination complexes

    Wudkewych, Megan J.; LaDuca, Robert L.


    Zinc nitrate, 2,4-pyridinedicarboxylic acid (2,4-pdcH2), and a hydrogen-bonding capable dipyridylamide ligand were combined in aqueous solution and subjected to hydrothermal reaction conditions. Three new crystalline coordination complexes were generated; their dimensionality depends crucially on the dipyridylamide length and geometric disposition of the pyridyl nitrogen donors. The three new phases were structurally characterized via single-crystal X-ray diffraction. {[H23-pina][Zn(2,4-pdc)2(H2O)2]·H2O} (1, 3-pina = 3-pyridylisonicotinamide) is a salt with protonated dipyridylamide cations and coordination complex anions. {[Zn2(2,4-pdc)2(H2O)4(3-pna)]·3H2O}n (2, 3-pna = 3-pyridylnicotinamide) shows a system of two-fold interpenetrated ruffled (6,3) coordination polymer layers. {[Zn(2,4-pdc)(H2O)2(3-pmna)]n (3, 3-pmna = 3-pyridylmethylnicotinamide) manifests a simple 1D chain topology. Luminescence was observed for two of the zinc complexes; this behavior is attributed to π-π* or π-n molecular orbital transitions. Thermal decomposition properties of the new phases are also probed.

  4. Interaction of Small Zinc Complexes with Globular Proteins and Free Tryptophan

    Joann M. Butkus


    Full Text Available A series of eight water soluble anionic, cationic, and neutral zinc(II complexes were synthesized and characterized. The interaction of these complexes with bovine serum albumin (BSA, human serum albumin (HSA, lysozyme, and free tryptophan (Trp was investigated using steady-state fluorescence spectroscopy. Static and dynamic fluorescence quenching analysis based on Stern-Volmer kinetics was conducted, and the decrease in fluorescence intensity of the Trp residue(s can be ascribed predominantly to static quenching that occurs when the Zn complex binds to the protein and forms a nonfluorescent complex. The role played by the nature of the ligand, the metal, and complex charge in quenching Trp fluorescence was investigated. The binding association constants (Ka ranged from 104 to 1010 M−1 and indicate that complexes with planar aromatic features have the strongest affinity for globular proteins and free Trp. Complexes with nonaromatic features failed to interact with these proteins at or in the vicinity of the Trp residues. These interactions were studied over a range of temperatures, and binding was found to weaken with the increase in temperature and was exothermic with a negative change in entropy. The thermodynamic parameters suggest that binding of Zn complexes to the proteins is a highly spontaneous and favorable process.

  5. An in vitro study of interactions between insulin-mimetic zinc(II) complexes and selected plasma components.

    Enyedy, Eva Anna; Horváth, László; Gajda-Schrantz, Krisztina; Galbács, Gábor; Kiss, Tamás


    The speciations of some potent insulin-mimetic zinc(II) complexes of bidentate ligands: maltol and 1,2-dimethyl-3-hydroxypyridinone with (O,O) and picolinic acid with (N,O) coordination modes, were studied via solution equilibrium investigations of the ternary complex formation in the presence of small relevant bioligands of the blood serum such as cysteine, histidine and citric acid. Results show that formation of the ternary complexes, especially with cysteine, is favoured at physiological pH range in almost all systems studied. Besides these low molecular mass binders, serum proteins among others albumin and transferrin can bind zinc(II) or its complexes. Accordingly, the distribution of zinc(II) between the small and high molecular mass fractions of the serum was also studied by ultrafiltration. Modelling calculations relating to the distribution of zinc(II), using the stability constants of the ternary complexes studied and those of the serum proteins reported in the literature, confirmed the ultrafiltration results, namely, the primary role of albumin in zinc(II) binding among the low and high molecular mass components of the serum.

  6. Dual Effect of Curcumin-Zinc Complex in Controlling Diabetes Mellitus in Experimentally Induced Diabetic Rats.

    Al-Ali, Khalil; Abdel Fatah, Hala Salah; El-Badry, Yaser Abdel-Moemen


    Ultrasound-assisted extraction of curcumin from Curcuma longa was performed in an ultrasonic bath at 30°C using ethanol for 40 min. A successful attempt has been made to prepare curcumin-zinc (Zn) complex using a simple chemical procedure. The complex formation and its stoichiometry were characterized using elemental analysis, Fourier transform (FT)-IR and UV spectroscopy which revealed the interaction of Zn(II) ion (M) with curcumin (ligand, L) to proceed via (ML) complex type formation. Oral administration of curcumin-Zn complex at a concentration of 150 mg/kg body weight/rat/d for 45 d in streptozotocin-induced diabetic rats in comparison to curcumin and/or Zn administration exerted a hypoglycemic effect. A significant reduction in blood glucose, glycosylated hemoglobin (Hb)A1c, and lipid profile parameters with an excellent improvement in plasma insulin levels have been attained. Also, the reduced activities of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), urea, and creatinine in the diabetic rats treated with the complex exhibited the non-toxic nature of the curcumin-Zn complex. Finally, the larger extent of the complex in hyperglycemic improvement in comparison to curcumin and/or Zn supplementation was interpreted by its dual action on glucose and insulin maintenance.

  7. Zinc and Gold Complexes in the Treatment of Breast Cancer / Kompleksi Cinka I Zlata U Lecenju Karcinoma Dojke

    Benazic Sasa


    Full Text Available Metals are essential components in indispensable biochemical processes for living organisms. This review article highlights the metals zinc and gold in the development and treatment of breast cancer. Metal compounds off er many advantages as therapeutics due to their ability to coordinate ligands in a three-dimensional configuration. In aqueous solution, they form positively charged ions that can bind to negatively charged biological molecules. Metal complexes that contain metal ions such as zinc(II and gold have received considerable attention as potential anticancer agents. Zinc is an essential trace element that plays a critical role in a wide range of cellular processes that include structural, signalling, catalytic and regulatory functions. Zinc acts as a key structural component in many proteins and enzymes, including transcription factors, cellular signalling proteins, and DNA repair enzymes, and perturbed levels of zinc in tissues may play a role in cancer aetiology and outcome. Unlike zinc, gold is feasible as a component of compounds for effective anticancer therapy. Some progress in anticancer therapy may include interactions between zinc and gold.

  8. Synthesis and Characterization of Zinc β-Diketonate Complex Extended to the Macromolecular Polymers

    Mohammed A. Al-Anber


    Full Text Available A mononuclear complex of [Zn(tta2(H2O2] (3 (tta = deprotonated of 1-thenoyl-4,4,4-trifluoro­acetone (1 has been prepared by the reaction of 1-thenoyl-4,4,4-trifluoro­acetone (H-tta: 1 with Zn(OAc2.4H2O (OAc = O2CMe in a 2:1 molar ratio. Complex 3 can be extended to form a coordination polymers of general formula [Zn(tta2(X]n (X = 4,4'-bipy (4, pz (5 by the reaction of zinc atom in 3 with s-donor ligand such as 4,4-bipyridine (4,4'-bipy and pyrazin (pz. The reaction completion was controlled via FTIR and elemental analysis.

  9. Antibacterial and Antifungal Studies on Some Schiff Base Complexes of Zinc(II).

    Joseyphus, R Selwin; Nair, M Sivasankaran


    Two Schiff base ligands L1and L2 were obtained by the condensation of glycylglycine respectively with imidazole-2-carboxaldehyde and indole-3-carboxaldehyde and their complexes with Zn(II) were prepared and characterized by microanalytical, conductivity measurement, IR, UV-Vis., XRD and SEM. The molar conductance measurement indicates that the Zn(II) complexes are 1: 1electrolytes. The IR data demonstrate the tetradentate binding of L1and tridentate binding of L2. The XRD data show that Zn(II) complexes with L1and L2 have the crystallite sizes of 53 and 61nm respectively. The surface morphology of the complexes was studied using SEM. The in vitro biological screening effects of the investigated compounds were tested against the bacterial species Staphylococcus aureus, Escherichia coli, Klebsiella pneumaniae, Proteus vulgaris and Pseudomonas aeruginosa and fungal species Aspergillus niger, Rhizopus stolonifer, Aspergillus flavus, Rhizoctonia bataicola and Candida albicans by the disc diffusion method. A comparative study of inhibition values of the Schiff base ligands and their complexes indicates that the complexes exhibit higher antimicrobial activity than the free ligands. Zinc ions are proven to be essential for the growth-inhibitor effect. The extent of inhibition appeared to be strongly dependent on the initial cell density and on the growth medium.

  10. Intracellular distribution of fluorescent copper and zinc bis(thiosemicarbazonato) complexes measured with fluorescence lifetime spectroscopy.

    Hickey, James L; James, Janine L; Henderson, Clare A; Price, Katherine A; Mot, Alexandra I; Buncic, Gojko; Crouch, Peter J; White, Jonathan M; White, Anthony R; Smith, Trevor A; Donnelly, Paul S


    The intracellular distribution of fluorescently labeled copper and zinc bis(thiosemicarbazonato) complexes was investigated in M17 neuroblastoma cells and primary cortical neurons with a view to providing insights into the neuroprotective activity of a copper bis(thiosemicarbazonato) complex known as Cu(II)(atsm). Time-resolved fluorescence measurements allowed the identification of the Cu(II) and Zn(II) complexes as well as the free ligand inside the cells by virtue of the distinct fluorescence lifetime of each species. Confocal fluorescent microscopy of cells treated with the fluorescent copper(II)bis(thiosemicarbazonato) complex revealed significant fluorescence associated with cytoplasmic puncta that were identified to be lysosomes in primary cortical neurons and both lipid droplets and lysosomes in M17 neuroblastoma cells. Fluorescence lifetime imaging microscopy confirmed that the fluorescence signal emanating from the lipid droplets could be attributed to the copper(II) complex but also that some degree of loss of the metal ion led to diffuse cytosolic fluorescence that could be attributed to the metal-free ligand. The accumulation of the copper(II) complex in lipid droplets could be relevant to the neuroprotective activity of Cu(II)(atsm) in models of amyotrophic lateral sclerosis and Parkinson's disease.

  11. Synthesis, crystal structure and luminescence properties of acenaphthene benzohydrazide based ligand and its zinc(II) complex

    Kumar, Mukesh; Roy, Soumyabrata; Faizi, Md. Serajul Haque; Kumar, Santosh; Singh, Mantu Kumar; Kishor, Shyam; Peter, Sebastian C.; John, Rohith P.


    The complex compound of zinc(II) supported by (Z)-2-hydroxy-N‧-(1-oxoacenaphthylen-2(1H) ylidene)benzohydrazide ligand (H2L1) has been reported and discussed. The reaction of zinc acetate with H2L1 ligand leads to the formation of a mononuclear zinc(ii) complex, [Zn(HL1)2H2O]. The ligand, H2L1 has been characterized by elemental analysis, 1H, 13C and 1Hsbnd COSY -NMR, IR and ESI-MS, while the complex was characterized by elemental analysis, IR, and ESI-MS. The crystal structures of the free ligand H2L1 and the complex have also been determined by single crystal X-ray diffraction. The ligand chelates with metal centre with a nitrogen atom of imino moiety and an oxygen atom of enolic group. The complex shows distorted trigonal bipyramidal geometry around the metal centre with oxygen atoms lying in the equatorial plane and imino nitrogen atoms along the axial direction. The DFT/TD-DFT calculations were performed on both the ligand and its zinc complex to get insight into the structural, electronic and optical properties. The photoluminescence, fluorescence properties of the complex have been investigated.

  12. Microwave-assisted synthesis and complexation of luminescent cyanobipyridyl-zinc(II) bis(thiolate) complexes with intrinsic and ancillary photophysical tunability.

    Bagley, Mark C; Lin, Zhifan; Pope, Simon J A


    A series of cyanobipyridine-derived zinc(II) bis(thiolate) complexes are prepared rapidly and efficiently by a microwave-assisted cross-coupling/complexation sequence and display luminescence that can be modulated using intrinsic functionality and ancillary ligands.

  13. Synthesis and antibacterial activity of cephradine metal complexes : part II complexes with cobalt, copper, zinc and cadmium.

    Sultana, Najma; Arayne, M Saeed; Afzal, M


    Cephradine, the first generation cephalosporin, is active against a wide range of Gram-positive and Gram-negative bacteria including penicillinase-producing Staphylococci. Since the presence of complexing ligand may affect the bioavailability of a metal in the blood or tissues, therefore, in order to study the probable interaction of cephradine with essential and trace elements present in human body, cephradine has been reacted with cobalt, copper, zinc and cadmium metal halides in L:M ratio of 2:1 in methanol and the products recrystallized from suitable solvents to pure crystals of consistent melting points. Infrared and ultraviolet studies of these complexes were carried out and compared with ligand. Magnetic susceptibility studies of these complexes were also carried out showing their paramagnetic behavior. From the infra red studies and elemental analysis of the complexes, it has been shown that the drug molecule serves as a bidentate ligand coordinating through both its carboxylate at C-3 and beta-lactam nitrogen and the metal having a square planar or octahedral geometry. To evaluate the changes in microbiological activity of cephradine after complexation, antibacterial studies were carried out by observing the changes in MIC (minimum inhibitory concentration) of the complexes and compared with the parent drug by measuring the zone of inhibition of complexes and compared with the parent cephalosporin against both Gram-positive and Gram-negative organisms. For MIC observation, serial dilution method was employed and zone series were determined by disk diffusion method. Our investigations reveal that formation of complexes results in decrease in antibacterial activity of cephradine and MIC values are increased.

  14. Influence of Water Deficit on Iron and Zinc Uptake by Matricaria chamomilla L. Influencia del Deficit Hídrico en la Absorción de Hierro y Zinc por Matricaria chamomilla L.

    Alireza Pirzad


    Full Text Available Iron and zinc deficiency are a yield-limiting factor with major implications for field crop production in many agricultural regions of the world; this production is essential source of Fe and Zn in human and animal diets. Two experiments were conducted under greenhouse conditions to evaluate Fe and Zn uptake by German chamomile (Matricaria chamomilla L. grown under several drought conditions. Treatments were arranged in four irrigation regimes (95%, 80%, 65%, and 50% field capacity and six irrigation disruptions (stem formation, flower onset, full bloom, first harvest, second harvest, and control without disruption based on a randomized complete block design with five and four replicates in experiments 1 and 2, respectively. In Experiment 1, the irrigation regimes had no significant effect on Fe and Zn uptake by German chamomile, which reached total means of Fe (39.68 mg kg4 and Zn (29.15 mg kg4. In Experiment 2, the highest amount of Fe (39.0 mg kg4 was obtained from irrigation disruption at first harvest; this is similar to the results of irrigation disruption at flower onset and full bloom. However, irrigation disruption in stem formation (21.3 mg kg4, second harvest (12.95 mg kg4, and the control (7.79 mg kg4 had a decreasing trend of Fe uptake. The maximum value of Zn (40.0 mg kg4 occurred at irrigation disruption at the full bloom stage, which was also similar to irrigation disruption at flower onset and stem formation. However, later irrigation disruptions at the first and second harvest stages caused lower amounts of Zn uptake by chamomile. Therefore, the lowest Zn values were obtained from irrigation disruption at second harvest (5.0 mg kg4 and the control (5.5 mg kg4. Regressions between both Fe or Zn uptake and irrigation showed a binomial function.La deficiencia de hierro y zinc es un factor limitante de la producción con grandes implicaciones para producción de cultivo en terreno en muchas regiones agrícolas del mundo como

  15. Comparison of copper and zinc in vitro bioaccessibility from cyanobacteria rich in proteins and a synthetic supplement containing gluconate complexes: LC-MS mapping of bioaccessible copper complexes.

    Wojcieszek, Justyna; Witkoś, Katarzyna; Ruzik, Lena; Pawlak, Katarzyna


    An analytical procedure was proposed to estimate bioaccessibility of copper and zinc in Spirulina Pacifica tablets with respect to that of copper and zinc in gluconate complexes. Spirulina is the common name for diet supplements produced primarily from two species of cyanobacteria, namely Arthrospira platensis and Arthrospira maxima. Spirulina tablets are an excellent source of proteins, vitamins and minerals. To obtain information about the bioavailability of these elements, an in vitro bioaccessibility test was performed by application of a two-step protocol which simulated the gastric (pepsin) and intestinal (pancreatin) digestion. The species obtained were investigated by size exclusion chromatography on a chromatograph coupled to a mass spectrometer with inductively coupled plasma (SEC-ICP-MS) and an on-capillary liquid chromatograph coupled to an electrospray mass spectrometer (μ-HPLC-ESI-MS). Both copper and zinc were found to be highly bioaccessible in Spirulina tablets (90-111%) and those containing gluconate complexes (103% for Cu and 62% for Zn). In Spirulina tablets, copper was found to form two types of complex: (1) polar ones with glycine and aspartic acid and (2) more hydrophobic ones containing amino acids with cyclic hydrocarbons (phenylalanine, histidine, proline and tyrosine). Zinc and copper were also proved to form complexes during the digestion process with products of pepsin digestion, but the stability of these complexes is lower than that of the complexes formed in Spirulina. The results proving the involvement of proteins in the enhancement of copper and zinc bioaccessibility will be useful for the design of new copper and zinc supplements.

  16. An effective approach for generating a three-Cys2His2 zinc-finger-DNA complex model by docking

    Rajasekaran M


    Full Text Available Abstract Background Determination of protein-DNA complex structures with both NMR and X-ray crystallography remains challenging in many cases. High Ambiguity-Driven DOCKing (HADDOCK is an information-driven docking program that has been used to successfully model many protein-DNA complexes. However, a protein-DNA complex model whereby the protein wraps around DNA has not been reported. Defining the ambiguous interaction restraints for the classical three-Cys2His2 zinc-finger proteins that wrap around DNA is critical because of the complicated binding geometry. In this study, we generated a Zif268-DNA complex model using three different sets of ambiguous interaction restraints (AIRs to study the effect of the geometric distribution on the docking and used this approach to generate a newly reported Sp1-DNA complex model. Results The complex models we generated on the basis of two AIRs with a good geometric distribution in each domain are reasonable in terms of the number of models with wrap-around conformation, interface root mean square deviation, AIR energy and fraction native contacts. We derived the modeling approach for generating a three-Cys2His2 zinc-finger-DNA complex model according to the results of docking studies using the Zif268-DNA and other three crystal complex structures. Furthermore, the Sp1-DNA complex model was calculated with this approach, and the interactions between Sp1 and DNA are in good agreement with those previously reported. Conclusions Our docking data demonstrate that two AIRs with a reasonable geometric distribution in each of the three-Cys2His2 zinc-finger domains are sufficient to generate an accurate complex model with protein wrapping around DNA. This approach is efficient for generating a zinc-finger protein-DNA complex model for unknown complex structures in which the protein wraps around DNA. We provide a flowchart showing the detailed procedures of this approach.

  17. Synthesis, structural characterization and biological activity of a trinuclear zinc(II) complex: DNA interaction study and antimicrobial activity

    Bhaskar Biswas; Niranjan Kole; Moumita Patra; Shampa Dutta; Mousumi Ganguly


    A trinuclear zinc(II) complex [Zn3L2(-O2CCH3)2(H2O)2]·H2O·2CH3OH (1) was synthesized from an in situ reaction between zinc acetate and a Schiff base ligand (H2L = 2-((2-hydroxyphenylimino) methyl)-6-methoxyphenol). The ligand was prepared by (1:1) condensation of ortho-vanillin and ortho-aminophenol. The ligand and zinc(II) complex were characterized by elemental analysis, Fourier Transform Infrared (FTIR), 1H-Nuclear Magnetic Resonance (NMR), UV-Vis spectroscopy, Powder X-ray Diffraction (PXRD) and thermogravimetric analysis. 1 crystallizes in P-1 space group with = 11.9241(3) Å, = 12.19746 Å, = 20.47784 Å with unit cell volume is 2674.440 (Å)3. Binding property of the complex with calf thymus DNA (CT-DNA) has been investigated using absorption and emission studies. Thermal melting and viscosity experiments were further performed to determine the mode of binding of 1 with CT-DNA. Spectroscopic and viscosity investigations revealed an intercalative binding mode of 1 with CT-DNA. The ligand and its zinc complex were screened for their biological activity against bacterial species and fungi. Activity data show that the metal complex has more antibacterial and antifungal activity than the parent Schiff base ligand and against those bacterial or fungi species.

  18. Crystal structures of three complexes of zinc chloride with tri-tert-butylphosphane

    Aaron D. Finke


    Full Text Available Under anhydrous conditions and in the absence of a Lewis-base solvent, a zinc chloride complex with tri-tert-butylphosphane as the μ-bridged dimer is formed, viz. di-μ-chlorido-bis[chloridobis(tri-tert-butylphosphanezinc], [ZnCl4(C12H27P2], (1, which features a nearly square-shaped (ZnCl2 cyclic core and whose Cl atoms interact weakly with C—H groups on the phosphane ligand. In the presence of THF, monomeric dichlorido(tetrahydrofuran-κO(tri-tert-butylphosphane-κPzinc, [ZnCl2(C4H8O(C12H27P] or [P(tBu3(THFZnCl2], (2, is formed. This slightly distorted tetrahedral Zn complex has weak C—H...Cl interactions between the Cl atoms and phosphane and THF C—H groups. Under ambient conditions, the hydrolysed complex tri-tert-butylphosphonium aquatrichloridozincate 1,2-dichloroethane monosolvate, (C12H28P[ZnCl3(H2O]·C2H4Cl2 or [HPtBu3]+ [(H2OZnCl3]−·C2H4Cl2, (3, is formed. This complex forms chains of [(H2OZnCl3]− anions from hydrogen-bonding interactions between the water H atoms and Cl atoms that propagate along the b axis.

  19. Zinc deficiency in infants and children: a review of its complex and synergistic interactions.

    Krebs, Nancy F; Miller, Leland V; Hambidge, K Michael


    Zinc deficiency is estimated to contribute to over half a million deaths per year in infants and children under 5 years of age. This paper reviews the features of mild-to-moderate zinc deficiency, which include growth faltering, deficits in immune function and altered integrity and function of the gastro-intestinal tract. Sub-clinical features include oxidative stress and a pro-inflammatory state. The homeostatic response to low dietary zinc intake by increasing absorption is limited, especially if the source of zinc is of poor bioavailability, and conservation of endogenous intestinal losses is a critical component of adaptation. Owing to low zinc intakes, older breastfed infants, especially those of low birthweight, are predictably at risk of zinc deficiency if complementary food choices are unfortified and/or low in zinc. Host factors such as young age, poor intra-uterine zinc accretion owing to poor maternal status and/or prematurity, and gastro-intestinal dysfunction also potently predispose to zinc deficiency. Environmental enteropathy, which is prevalent in low-resource settings, may substantially impair zinc absorption and/or increase endogenous losses, and thus lead to relatively high zinc requirements. Emerging evidence highlights common features between chronic inflammation and zinc deficiency, and each may exacerbate the other. More investigations of zinc homeostasis in populations in low-resource settings are needed to better quantify absorption capacity and losses. Effective preventive strategies must address potentially higher zinc requirements as well as the underlying context that perpetuates a vicious cycle of zinc deficiency and multiple adverse outcomes.

  20. Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.

    Dawkins, Michael J C; Middleton, Ewart; Kefalidis, Christos E; Dange, Deepak; Juckel, Martin M; Maron, Laurent; Jones, Cameron


    The first examples of essentially two-coordinate, monomeric zinc hydride complexes, LZnH (L = -N(Ar)(SiR3)) (Ar = C6H2{C(H)Ph2}2R'-2,6,4; R = Me, R' = Pr(i) (L'); R = Pr(i), R' = Me (L*); R = Pr(i), R' = Pr(i) (L(†))) have been prepared and shown by crystallographic studies to have near linear N-Zn-H fragments. The results of computational studies imply that any PhZn interactions in the compounds are weak at best. Preliminary reactivity studies reveal the compounds to be effective for the stoichiometric hydrozincation and catalytic hydrosilylation of carbonyl compounds.

  1. Synthesis and characterization of ZnO nanoparticles by thermal decomposition of a curcumin zinc complex

    Mutasim I. Khalil


    Full Text Available ZnO nanoparticles were generated by thermal decomposition of a binuclear zinc (II curcumin complex as single source precursor. Thermal behavior of the precursor showed a considerable weight loss at about 374 °C by an exothermic reaction with a maximum weight loss rate of 14%/min. Complete decomposition of precursor was observed within 49 min with a heating rate of 10 °C/min. Synthesized nanoparticles have been characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy and selected area electron diffraction microscopy. Results revealed monodispersed hexagonal zincite structure with an average size of 117 ± 4 nm.

  2. Mechanochemical synthesis and in vitro anti-Helicobacter pylori and uresase inhibitory activities of novel zinc(II)-famotidine complex.

    Amin, Muhammad; Iqbal, Mohammad S; Hughes, Roy W; Khan, Safyan A; Reynolds, Paul A; Enne, Virve I; Sajjad-ur-Rahman; Mirza, Akmal S


    The mechanochemical synthesis and characterization of a zinc complex with famotidine is described. The complex was characterized by microanalysis and a number of spectroscopic techniques. The complex was of M:L dihydrate type. Derivatization of famotidine with zinc appears to enhance the activity of the drug by inhibiting the growth of Helicobacter pylori (two reference and 34 clinical isolates). The complex inhibited the growth of H. pylori in an MIC range of 1-8 microg mL(-1). The anti-H. pylori activity of the zinc-famotidine complex against antibiotic-resistant strains was nearly comparable to that of antibiotic-susceptible strains. The complex was found to be far less toxic than the parent drug, as demonstrated by its higher LD(50) value. In the human urease enzyme inhibition assay the complex exhibited significant inhibition. The new complex appears to be more useful in eradicating both the antibiotic-susceptible and antibiotic-resistant strains of H. pylori.

  3. Preparation and Electronic Property Investigation of Zinc(II-Schiff Base Complexes in the Confined Space

    Peng Shang


    Full Text Available Metal-Schiff base complexes have attracted continued research interest regarding their intriguing and useful features, while the electronic properties of these complexes in the confined space have not been sufficiently addressed in previous studies. In this work, a new zinc(II-Schiff base complex bis(N-dodecyl salicylideneiminatoZn(II (1 was synthesized and subsequently loaded in an inorganic solid host. A large red shift (~40 nm of the absorption onset was recorded, when the microenvironment of 1 changed from the solvent ethanol to the inorganic solid medium, evidencing the confined space effect. The marked shift of the absorption onset was associated with a band-gap reduction between the highest occupied molecular orbital (HOMO and the lowest unoccupied molecular orbital (LUMO. Theoretical calculation results showed that the confined space effect is distance dependent and exerts a more profound influence on the HOMO than the LUMO within an effective distance range. An initial study implied that the confined space effect is also accompanied with the electron density variation.

  4. Purification and characterization of a native zinc-binding high molecular weight multiprotein complex from human seminal plasma.

    Yadav, Vikash Kumar; Kumar, Vijay; Chhikara, Nirmal; Kumar, Sanjay; Manral, Pallavi; Kashav, Tara; Saini, Savita; Srinivasan, A; Singh, Sarman; Singh, Tej P; Yadav, Savita


    The seminal plasma comprises secretions from various accessory sex glands. During fertilization spermatozoa undergo complex sequences of precisely timed events that are regulated by the activation of different intracellular signaling pathways. The precision and efficacy of these pathways are often influenced by the assembly and interactions of multiprotein complexes, thereby directing the flow of regulatory information. Our knowledge about these protein complexes present in human seminal plasma (HuSP) is limited. Here we report the identification and characterization of a native high molecular weight zinc-binding multiprotein complex from HuSP by utilizing 2-DE followed by MS. Twenty-six proteins representing isoforms and/or fragments of 11 different proteins were found to be assembled in this complex. Prostate-specific antigen, zinc α2-glycoprotein, prostatic acid phosphatase, and prolactin inducible protein were the major proteins of this complex. Dynamic light scattering experiments revealed changes in aggregation pattern accompanied with deviation from physiological pH and in presence of SDS. However, no significant changes were observed in the presence of physiological ligands such as zinc and fructose. The present study will be useful and contribute to guide the future studies performed for elucidation of biological significance of this native complex in HuSP.

  5. Gastroprotection studies of Schiff base zinc (II derivative complex against acute superficial hemorrhagic mucosal lesions in rats.

    Shahram Golbabapour

    Full Text Available BACKGROUND: The study was carried out to assess the gastroprotective effect of the zinc (II complex against ethanol-induced acute hemorrhagic lesions in rats. METHODOLOGY/PRINCIPAL FINDING: The animals received their respective pre-treatments dissolved in tween 20 (5% v/v, orally. Ethanol (95% v/v was orally administrated to induce superficial hemorrhagic mucosal lesions. Omeprazole (5.790×10(-5 M/kg was used as a reference medicine. The pre-treatment with the zinc (II complex (2.181×10(-5 and 4.362×10(-5 M/kg protected the gastric mucosa similar to the reference control. They significantly increased the activity levels of nitric oxide, catalase, superoxide dismutase, glutathione and prostaglandin E2, and decreased the level of malondialdehyde. The histology assessments confirmed the protection through remarkable reduction of mucosal lesions and increased the production of gastric mucosa. Immunohistochemistry and western blot analysis indicated that the complex might induced Hsp70 up-regulation and Bax down-regulation. The complex moderately increased the gastroprotectiveness in fine fettle. The acute toxicity approved the non-toxic characteristic of the complex (<87.241×10(-5 M/kg. CONCLUSION/SIGNIFICANCE: The gastroprotective effect of the zinc (II complex was mainly through its antioxidant activity, enzymatic stimulation of prostaglandins E2, and up-regulation of Hsp70. The gastric wall mucus was also a remarkable protective mechanism.

  6. Topical erythromycin-zinc acetate complex lotion versus topical erythromycin gel in treatment of mild to moderate acne vulgaris

    Hayder R. Al-Hamamy


    Full Text Available Introduction: Topical antibiotics are the main step in the treatment of mild to moderate acne vulgaris. Erythromycin is one of the effective topical therapies for this disease. Zinc sulfate 5% solution was reported to be effective in treatment of acne vulgaris and rosacea. Aim: To compare the effectiveness and side effects of topical erythromycin in combination with zinc and erythromycin alone in treatment of mild to moderate acne vulgaris. Material and Methods: This single, blind, therapeutic, comparative study was done in the Department of Dermatology – Baghdad Teaching Hospital, Baghdad, Iraq; from May 2012 – August 2013.Scoring of acne was carried out and the patients were examined every two weeks for 10 weeks of treatment. One month after stopping drugs, patients were evaluated for drug complications and disease recurrence. Eighty patients fulfilling enrollment criteria were included in this study. Patients were divided into two groups: Group A (40 patients treated twice daily with topical erythromycin-zinc complex lotion and Group B (40 patients treated twice daily with topical 2% erythromycin gel. Results: Both topical erythromycin-zinc lotion and erythromycin gel were statistically an effective therapy starting after 6 weeks treatment and up to 4 weeks after stopping treatment. Erythromycin-zinc lotion was more effective and act earlier than erythromycin gel starting from 4 weeks of therapy till the end of treatment (after 10 week and even after 4 weeks after stopping the treatment (p value <0.0001. Conclusions: Erythromycin-zinc complex lotion was an effective and well tolerated topical therapy for mild to moderate inflammatory acne vulgaris and was more effective than erythromycin gel alone.

  7. Synthesis and characterization of heteroleptic copper and zinc complexes with saccharinate and aminoacids. Evaluation of SOD-like activity of the copper complexes.

    Santi, Eduardo; Viera, Inés; Mombrú, Alvaro; Castiglioni, Jorge; Baran, Enrique J; Torre, María H


    Five new copper and zinc heteroleptic complexes with saccharin and aminoacids with general stoichiometry Na(2)[M(sac)(2)(aa)(2)].nH(2)O (M denotes Cu or Zn, sac the saccharinate ion, and aa the aminoacids) were synthesized and characterized by elemental and thermogravimetric analysis, conductimetric measurements and IR, Raman and UV-vis spectroscopies. In all the complexes, copper and zinc ions coordinated with the aminoacids through the terminal amine and carboxylate residues and with saccharin through the heterocyclic nitrogen atom. Besides, the superoxide dismutase-like activity of the heteroleptic copper complexes was evaluated and compared with the homoleptic copper amino acid complexes with the aim to observe the influence of the saccharin coordination.

  8. Synthesis, characterization and anticancer activity of kaempferol-zinc(II) complex.

    Tu, Lv-Ying; Pi, Jiang; Jin, Hua; Cai, Ji-Ye; Deng, Sui-Ping


    According to the previous studies, the anticancer activity of flavonoids could be enhanced when they are coordinated with transition metal ions. In this work, kaempferol-zinc(II) complex (kaempferol-Zn) was synthesized and its chemical properties were characterized by UV-VIS, FT-IR, (1)H NMR, elemental analysis, electrospray mass spectrometry (ES-MS) and fluorescence spectroscopy, which showed that the synthesized complex was coordinated with a Zn(II) ion via the 3-OH and 4-oxo groups. The anticancer effects of kaempferol-Zn and free kaempferol on human oesophageal cancer cell line (EC9706) were compared. MTT results demonstrated that the killing effect of kaempferol-Zn was two times higher than that of free kaempferol. Atomic force microscopy (AFM) showed the morphological and ultrastructural changes of cellular membrane induced by kaempferol-Zn at subcellular or nanometer level. Moreover, flow cytometric analysis indicated that kaempferol-Zn could induce apoptosis in EC9706 cells by regulating intracellular calcium ions. Collectively, all the data showed that kaempferol-Zn might be served as a kind of potential anticancer agent.

  9. Spin interaction in octahedral zinc complexes of mono- and diradical Schiff and mannich bases.

    Orio, M; Philouze, C; Jarjayes, O; Neese, F; Thomas, F


    The four Schiff bases 2-tert-butyl-4-methoxy-6-[(pyridin-2-ylmethylimino)methyl]phenol, 2,4-di-tert-butyl-6-[(pyridin-2-ylmethylimino)methyl]phenol, 2-tert-butyl-4-methoxy-6-(quinolin-8-yliminomethyl)phenol, and 2,4-di-tert-butyl-6-(quinolin-8-yliminomethyl)phenol) as well as one Mannich base, N,N',N,N'-bis[(2-hydroxy-3,5-di-tert-butylbenzyl)(2-pyridylmethyl)]ethylenediamine, and their zinc bis-phenolate complexes 1-5, respectively, have been prepared. The complexes 4 and 5 have been characterized by X-ray diffraction crystallography, showing a zinc ion within an octahedral environment, with a cis orientation of the phenolate moieties. 1-5 exhibit in their cyclic voltammetry curves two anodic reversible waves attributable to the successive oxidation of the phenolates into phenoxyl radicals. Bulk electrolysis at ca. +0.1 V affords the zinc-coordinated monophenoxyl radical species (1(*))(+)-(5(*))(+) characterized by UV-vis absorption bands at 400-440 nm. The more stable radicals are (3(*))(+) and (4(*))(+) (half-life higher than 90 min at 298 K), likely due to the increased charge delocalization within the quinoline moieties. These species exhibit a significant additional near-IR band (epsilon > 1650 M(-1) cm(-1)) attributed to a CT transition. In the two-electron-oxidized species (1(**))(2+)-(5(**))(2+) the radical spins present a weak magnetic coupling. EPR reveals an antiferromagnetic exchange interaction for (1(**))(2+)-(4(**))(2+), whereas an unusual ferromagnetic exchange coupling is operative in (5(**))(2+). The weak magnitude of experimental |J| values (within the 1-5 cm(-1) range) as well as their sign could be well reproduced by DFT calculations at the B3LYP level. The small energy gap between the ground and the first excited spin states allows us to investigate the zero-field splitting (ZFS) of the triplet by EPR spectroscopy. This parameter is found to be axial for all systems, with |D| values of 0.0163 cm(-1) for (1(**))(2+), 0.0182 cm(-1) for (2

  10. Superiority of zinc complex of acetylsalicylic acid to acetylsalicylic acid in preventing postischemic myocardial dysfunction.

    Korkmaz, Sevil; Atmanli, Ayhan; Li, Shiliang; Radovits, Tamás; Hegedűs, Peter; Barnucz, Enikő; Hirschberg, Kristóf; Loganathan, Sivakkanan; Yoshikawa, Yutaka; Yasui, Hiroyuki; Karck, Matthias; Szabó, Gábor


    The pathophysiology of ischemic myocardial injury involves cellular events, reactive oxygen species, and an inflammatory reaction cascade. The zinc complex of acetylsalicylic acid (Zn(ASA)2) has been found to possess higher anti-inflammatory and lower ulcerogenic activities than acetylsalicylic acid (ASA). Herein, we studied the effects of both ASA and Zn(ASA)2 against acute myocardial ischemia. Rats were pretreated with ASA (75 mg/kg) or Zn(ASA)2 (100 mg/kg) orally for five consecutive days. Isoproterenol (85 mg/kg, subcutaneously [s.c.]) was applied to produce myocardial infarction. After 17-22 h, animals were anesthetized with sodium pentobarbital (60 mg/kg, intraperitoneally [i.p.]) and both electrical and mechanical parameters of cardiac function were evaluated in vivo. Myocardial histological and gene expression analyses were performed. In isoproterenol-treated rats, Zn(ASA)2 treatment normalized significantly impaired left-ventricular contractility index (Emax 2.6 ± 0.7 mmHg/µL vs. 4.6 ± 0.5 mmHg/µL, P < 0.05), increased stroke volume (30 ± 3 µL vs. 50 ± 6 µL, P < 0.05), decreased systemic vascular resistance (7.2 ± 0.7 mmHg/min/mL vs. 4.2 ± 0.5 mmHg/min/mL, P < 0.05) and reduced inflammatory infiltrate into the myocardial tissues. ECG revealed a restoration of elevated ST-segment (0.21 ± 0.03 mV vs. 0.09 ± 0.02 mV, P < 0.05) and prolonged QT-interval (79.2 ± 3.2 ms vs. 69.5 ± 2.5 ms, P < 0.05) by Zn(ASA)2. ASA treatment did not result in an improvement of these parameters. Additionally, Zn(ASA)2 significantly increased the mRNA-expression of superoxide dismutase 1 (+73 ± 15%), glutathione peroxidase 4 (+44 ± 12%), and transforming growth factor (TGF)-β1 (+102 ± 22%). In conclusion, our data demonstrate that oral administration of zinc and ASA in the form of bis(aspirinato)zinc(II) complex is superior to ASA in preventing electrical

  11. Comparison and analysis on the serum-binding characteristics of aspirin-zinc complex and aspirin.

    Zhang, Hua-Xin; Zhang, Qun; Wang, Hong-Lin; Li, Li-Wei


    This study was designed to compare the protein-binding characteristics of aspirin-zinc complex (AZN) with those of aspirin itself. AZN was synthesized and interacted with a model transport protein, human serum albumin (HSA). Three-dimensional fluorescence, ultraviolet-visible and circular dichroism (CD) spectra were used to characterize the interaction of AZN with HSA under physiological conditions. The interaction mechanism was explored using a fluorescence quenching method and thermodynamic calculation. The binding site and binding locality of AZN on HSA were demonstrated using a fluorescence probe technique and Förster non-radiation energy transfer theory. Synchronous fluorescence and CD spectra were employed to reveal the effect of AZN on the native conformation of the protein. The HSA-binding results for AZN were compared with those for aspirin under consistent experimental conditions, and indicated that aspirin acts as a guide in AZN when binding to Sudlow's site I, in subdomain IIA of the HSA molecule. Moreover, compared with aspirin, AZN showed greater observed binding constants with, but smaller changes in the α-helicity of, HSA, which proved that AZN might be easier to transport and have less toxicity in vivo. Copyright © 2017 John Wiley & Sons, Ltd.

  12. Syntheses and Structures of Blue Luminescent Zinc(Ⅱ) Complexes with 2,6-Bis(imino)pyridyl Ligands

    FAN Rui-qing; ZHU Dong-sheng; MU Ying; SU Qing


    @@ Luminescent coordination compounds with nitrogen-containing ligands have attracted much attention due to their good performance in sensor and electroluminescent device techniques[1-17]. To develop new luminescent materials, a large number of d10 metal complexes, especially zinc complexes, with the nitrogen-containing ligands have been synthesized and their luminescence behaviour have been studied[1-11]. It has been found that for a given complex, the size of the π-conjugated system of the ligand and the electronic effect of substituents at the ligand are important factors for modulating its luminescent properties[5,8,9].

  13. Synthesis and structural determination of zinc complexes based on an anilido-aldimine ligand containing an O-donor pendant arm: zinc alkoxide derivative as an efficient initiator for ring-opening polymerization of cyclic esters.

    Wang, Chao-Hsiang; Li, Chen-Yu; Huang, Bor-Hunn; Lin, Chu-Chieh; Ko, Bao-Tsan


    Zinc complexes bearing the anilido-aldiminate AA(OMe) ligand (AA(OMe)-H = (E)-2,6-diisopropyl-N-(2-(((2-methoxyethyl)imino)methyl)phenyl)aniline) were synthesized in a stepwise method and were structurally characterized. The reaction of AA(OMe)-H (1) with one equivalent of diethyl zinc (ZnEt2) furnishes a three-coordinated and mononuclear zinc complex [(AA(OMe))ZnEt] (2). Further reaction of 2 with a stoichiometric amount of benzyl alcohol (BnOH) affords a four-coordinated and dinuclear zinc benzylalkoxide complex [(AA(OMe))Zn(μ-OBn)]2 (3). In the presence of two equivalents of AA(OMe)-H with ZnEt2, a homoleptic and four-coordinated zinc complex [(AA(OMe))2Zn] (4) is formed. The geometry around the zinc centres of 3 and 4 are both distorted tetrahedrals, while 2 adopts a different coordination mode with a slightly distorted trigonal planar geometry. The variable-temperature (1)H NMR studies of 3 illustrate that 3 exhibits a dinuclear structure in solution at low temperature as well as in the solid state. While raising the temperature, it drifts towards dissociation to form a mononuclear zinc benzylalkoxide species, which coexists in solution. The ring-opening polymerizations of ε-caprolactone (ε-CL) and β-butyrolactone (β-BL) catalyzed by complexes 3 and 4 are investigated. The ε-CL and β-BL polymerizations initiated by zinc alkoxide 3 were demonstrated to have living characteristics and to proceed in a controlled manner with narrow polydispersity indices (PDIs high monomer-to-initiator ratio (1200/1) initiated by 3 has also been reported.

  14. Industrialization of New Process to Electrolysis Zinc from Zinc Chloride and Ammonia Complex%氯化锌氨络合物制锌新工艺的工业化实践

    邓良勋; 吴保庆


    用氯化铵与含氧化锌原料反应生成氯化锌氨络合物,净化后电解制取阴极锌.介绍了该流程的原理及工业试生产的有关情况.%The zinc chloride and ammonia complex was produced by reacting ammonium chloride with zinc oxide containing raw materials, after purification which was used to produce cathode zinc via electrolysis process.The principles of this process and industrialization pilot production were introduced in detail.

  15. A Metal-Amino Acid Complex-Derived Bifunctional Oxygen Electrocatalyst for Rechargeable Zinc-Air Batteries.

    Ding, Yanjun; Niu, Yuchen; Yang, Jia; Ma, Liang; Liu, Jianguo; Xiong, Yujie; Xu, Hangxun


    Bifunctional oxygen electrocatalyst: A metal-amino acid complex is developed to prepare high-performance mesoporous carbon electrocatalyst for both oxygen reduction and oxygen evolution reactions. Such prepared catalyst can be used to assemble rechargeable zinc-air batteries with excellent durability. This work represents a new route toward low-cost, highly active, and durable bifunctional electrocatalysts for cutting-edge energy conversion devices.

  16. Zinc triggers a complex transcriptional and post-transcriptional regulation of the metal homeostasis gene FRD3 in Arabidopsis relatives.

    Charlier, Jean-Benoit; Polese, Catherine; Nouet, Cécile; Carnol, Monique; Bosman, Bernard; Krämer, Ute; Motte, Patrick; Hanikenne, Marc


    In Arabidopsis thaliana, FRD3 (FERRIC CHELATE REDUCTASE DEFECTIVE 3) plays a central role in metal homeostasis. FRD3 is among a set of metal homeostasis genes that are constitutively highly expressed in roots and shoots of Arabidopsis halleri, a zinc hyperaccumulating and hypertolerant species. Here, we examined the regulation of FRD3 by zinc in both species to shed light on the evolutionary processes underlying the evolution of hyperaccumulation in A. halleri. We combined gene expression studies with the use of β-glucuronidase and green fluorescent protein reporter constructs to compare the expression profile and transcriptional and post-transcriptional regulation of FRD3 in both species. The AtFRD3 and AhFRD3 genes displayed a conserved expression profile. In A. thaliana, alternative transcription initiation sites from two promoters determined transcript variants that were differentially regulated by zinc supply in roots and shoots to favour the most highly translated variant under zinc-excess conditions. In A. halleri, a single transcript variant with higher transcript stability and enhanced translation has been maintained. The FRD3 gene thus undergoes complex transcriptional and post-transcriptional regulation in Arabidopsis relatives. Our study reveals that a diverse set of mechanisms underlie increased gene dosage in the A. halleri lineage and illustrates how an environmental challenge can alter gene regulation. © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.

  17. Synthesis, crystal structure and spectroscopic properties of a supramolecular zinc(II) complex with N2O2 coordination sphere.

    Dong, Wen-Kui; Zhang, Li-Sha; Sun, Yin-Xia; Zhao, Meng-Meng; Li, Gang; Dong, Xiu-Yan


    A new hexa-coordinated zinc(II) complex, namely [ZnL(H2O)2]n, with N2O2 coordination sphere (H2L=4,4'-dibromo-6,6'-dichloro-2,2'-[ethylenedioxybis(nitrilomethylidyne)]diphenol) has been synthesized and structurally characterized by elemental analyses, IR, UV-vis spectra and TG-DTA analyses, etc. Crystallographic data are monoclinic, space group P2(1)/c, a=24.634(2)Å, b=10.144(1)Å, c=7.9351(6)Å, β=91.371(2)°, V=1982.4(3)Å(3), Dc=2.099 g/cm(3), Z=4. The zinc(II) complex exhibits a slightly distorted octahedral geometry with halogen-substituted Salen-type bisoxime forming the basal N2O2 coordination sphere and two oxygen atoms from two coordinated water molecules in the axial position. The hydrogen-bonding and π-π stacking interactions have stabilized the zinc(II) complex molecules to form a self-assembling infinite dual metal-water chain-like structure with the nearest Zn⋯Zn distance of 4.954(4)Å.

  18. Main group chemistry of 9-hydroxophenalenone: Syntheses and structural characterization of the alkaline earth and zinc complexes

    Arup Mukherjee; Prinson P Samuel; Carola Schulzke; Swadhin K Mandal


    Herein, we report the synthesis and characterization of 9-hydroxophenalenone based alkaline earth and zinc complexes.The reaction of 9-hydroxophenalenone (HO,O-PLY (1)) with one equivalent of KN(SiMe3)2 and MI2 in THF yields heteroleptic complexes [(O,O-PLY)M(THF)]I [M= Mg (2), Ca (3), Sr (4), Ba (5); n = 1-4], while use of two equivalents of KN(SiMe3)2 in THF (with respect to PLY) produces homoleptic complex (O,O-PLY)2Mg(THF)2 (6). Moreover, reaction between two equivalents of 1 with one equivalent of ZnMe2 in THF produces complex (O,O-PLY)2Zn(THF)2 (7). All these complexes were characterized by NMR spectroscopy and elemental analyses. The solid state structures of complexes 2, 6 and 7 were established by single crystal X-ray diffraction analysis.

  19. Synthesis and crystal structure of 5-(4'-carboxyphenyl)-10,15,20-tri(4¢-t-butylphenyl)porphinato zinc(II) complex

    P Bhyrappa; C Arunkumar; J J Vittal


    Synthesis and crystal structure of 5-(4'-carboxyphenyl)-10,15,20-tri(4'--butylphenyl)porphinato zinc(II) have been presented. The title complex shows interesting hydrogen-bonded dimeric structure in the solid state.

  20. Silica-grafted diethylzinc and a silsesquioxane-based zinc alkyl complex as catalysts for the alternating oxirane-carbon dioxide copolymerization

    Duchateau, Robbert; van Meerendonkt, Wouter J.; Huijser, Saskia; Staal, Bastiaan B. P.; van Schilt, Marcus A.; Gerritsen, Gijsbert; Meetsma, Auke; Koning, Cor E.; Kemmere, Maartje F.; Keurentjes, Jos T. F.


    A novel zinc silsesquioxane complex ([(c-C5H9)(7)Si7O11(OSiMePh2)](2)Zn4Me4 (1)) has been used as a model compound for silica-grafted zinc catalysts in the copolymerization of cyclohexene oxide and CO2. Complex 1 exists as a dimer in the solid state and is moderately active in the copolymerization,

  1. Complexation of zinc in organic soils--EXAFS evidence for sulfur associations.

    Karlsson, Torbjörn; Skyllberg, Ulf


    Even if it is generally accepted that associations with natural organic matter (NOM) to a great extent determine the bioavailability and mobility of trace metals in soils and waters, the knowledge about the identity of NOM functional groups involved is still limited. In this study, extended X-ray absorption fine structure (EXAFS) spectroscopy was used to determine the coordination chemistry of zinc (Zn) in two organic soils (500-10,000 microg Zn g(-), pH 5.6-7.3). In both soils Zn was coordinated by a mixture of oxygen/nitrogen (O/N) and sulfur (S) ligands in the first coordination shell. In average, 0.4-0.9 S atoms were located at a distance of 2.29-2.33 angstom, well in agreement with a 4-fold coordination with thiolates (RS-) in proteins. In addition 2.7-3.7 O/N atoms were located at 1.99-2.04 angstrom. The improved merit of fit by inclusion of S atoms was shown to be significant after adjusting for the improvement caused merely by increasing the number of fitting parameters. Two second shell Zn-C distances were used in our model: 3.0-4.2 carbon (C) atoms, associated to first shell O/N, were encountered at an average distance of 2.84 amgstrom, and 0.4-0.9 C atoms, associated to first shell S, were encountered at an average distance of 3.32 angstrom. These Zn-C distances are well in agreement with distances determined in well-defined organic molecules. It is concluded that Zn forms mainly inner-sphere complexes with a mixture of 4-fold coordination with S and O/N ligands and 6-fold coordination with O ligands in organic soils.

  2. Synthesis, characterization and thermal behavior of antibacterial and antifungal active zinc complexes of bis (3(4-dimethylaminophenyl)-allylidene-1,2-diaminoethane

    Montazerozohori, Morteza, E-mail: [Department of Chemistry, Yasouj University, Yasouj 75918-74831 (Iran, Islamic Republic of); Zahedi, Saeedeh [Department of Chemistry, Yasouj University, Yasouj 75918-74831 (Iran, Islamic Republic of); Naghiha, Asghar [Department of Animal Sciences, Faculty of Agriculture, Yasouj University, Yasouj (Iran, Islamic Republic of); Zohour, Mostafa Montazer [Genetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan (Iran, Islamic Republic of)


    In this work, synthesis of a new series of zinc halide/pseudohalide complexes of a bidentate Schiff base ligand entitled as bis (3-(4-dimethylaminophenyl)-allylidene)-1,2-diaminoethane(L) is described. The ligand and its zinc complexes were characterized by various techniques such as elemental analysis, FT-IR, UV–visible, {sup 1}H and {sup 13}C NMR spectra, cyclic voltammetry, and conductometry. Accordingly ZnLX{sub 2} (X = Cl{sup −}, Br{sup −}, I{sup −}, SCN{sup −} and N{sub 3}{sup −}) was suggested as molecular formula of the complexes. Redox behaviors of ligand and its zinc complexes were investigated by cyclic voltammetry method. Furthermore, the ligand and its zinc halide/pseudohalide complexes were tested for their in vitro antibacterial activities against two gram positive bacteria (Staphylococcus aureus and Bacillus subtilis) and two gram negative bacteria (Escherichia coli and Pseudomonas aeruginosa). Also in vitro antifungal activities of them against Candida albicans and Aspergillus niger were investigated. The results indicated that all compounds are antibacterial and antifungal active. Thermal behaviors of ligand and its zinc complexes were studied from room temperature to 1100 °C under argon atmosphere. It was found that the ligand and zinc iodide are decomposed completely via three and four steps respectively while other zinc complexes leave out the metal or organometallic compounds as final residuals after 3–4 decomposition steps at above temperature range. Moreover evaluation of some thermo-kinetic parameters such as activation energy (∆E{sup ⁎}), enthalpy (∆H{sup ⁎}), entropy (∆S{sup ⁎}) and Gibbs free energy change (∆G{sup ⁎}) of the thermal decomposition steps were performed based on the Coats–Redfern relation. - Highlights: • Some novel complexes of Zn(II) with a bidentate Schiff base ligand have been synthesized. • Redox behavior of ligand and zinc complexes was investigated by cyclic voltammetry. • The

  3. Oral administration of Bis(aspirinato)zinc(II) complex ameliorates hyperglycemia and metabolic syndrome-like disorders in spontaneously diabetic KK-A(y) mice: structure-activity relationship on zinc-salicylate complexes.

    Yoshikawa, Yutaka; Adachi, Yusuke; Yasui, Hiroyuki; Hattori, Masakazu; Sakurai, Hiromu


    In recent years, the number of patients suffering from diseases, such as cancer, apoplexy, osteoporosis, hypertension, and type 2 diabetes mellitus is increasing worldwide. Type 2 diabetes, a lifestyle-related disease, is recognized as a serious disease. Various types of pharmaceutics for diabetes have been used. Since the relationship between diabetes and biometals such as vanadium, copper, and zinc ions has been recognized for many years, we have been developing the anti-diabetic metal complexes as new candidates. We found that several zinc(II) (Zn) complexes exhibit glucose-lowering activity for treating type 2 diabetes. High doses of salicylates have been known to reverse hyperglycemia and hyperinsulinemia in type 2 diabetic patients. These findings strongly suggest that the combined use of Zn and salicylates achieves the synergism in treating type 2 diabetes. Because aspirin, acetyl salicylic acid, has a chelating ability, we used it as a ligand to Zn. Several Zn-salicylate complexes were prepared and their biological activities were examined in this study. The complexes with an electron-withdrawing group in the ligand exhibited higher in vitro insulinomimetic activity than those of Zn complexes with an electron-donating group in the ligand. When bis(aspirinato)Zn (Zn(asp)₂) complex was orally administered on KK-A(y) mice with hereditary type 2 diabetes, the diabetic state was improved. In addition, this complex exhibited normalizing effects on serum adiponectin level and high blood pressure in metabolic syndrome. In conclusion, Zn(asp)₂ complex is newly proposed as a potent anti-diabetic and anti-metabolic syndrome agent.

  4. Designing ancillary ligands for heteroleptic/homoleptic zinc complex formation: synthesis, structures and application in ROP of lactides.

    Jędrzkiewicz, D; Ejfler, J; Gulia, N; John, Ł; Szafert, S


    Synthesis and characterization of a series of new amino-phenol/naphthol ligands (L(1,2)-H) have been developed and their respective zinc complexes ( 1 and 2-Zn ) have been synthesized. The molecular structures of L(1)-H and 1, 2-Zn were explored in detail by NMR, single-crystal X-ray studies and DFT calculations, which confirmed the existence of complexes as stabile dimers both in a solution and in the solid state. All complexes mediate the ring-opening polymerization (ROP) of lactide highly efficiently, at room temperature, in a controlled fashion. The influence of the architecture of the ligand on the desired homo/heteroleptic complex formation, as well as the relationship between the initiator design and the catalytic activity have been investigated.

  5. Highly microporous carbons derived from a complex of glutamic acid and zinc chloride for use in supercapacitors

    Dong, Xiao-Ling; Lu, An-Hui; He, Bin; Li, Wen-Cui


    The selection of carbon precursor is an important factor when designing carbon materials. In this study, a complex derived from L-glutamic acid and zinc chloride was used to prepare highly microporous carbons via facile pyrolysis. L-glutamic acid, a new carbon precursor with nitrogen functionality, coordinated with zinc chloride resulted in a homogeneous distribution of Zn2+ on the molecular level. During pyrolysis, the evaporation of the in situ formed zinc species creates an abundance of micropores together with the inert gases. The obtained carbons exhibit high specific surface area (SBET: 1203 m2 g-1) and a rich nitrogen content (4.52 wt%). In excess of 89% of the pore volume consists of micropores with pore size ranging from 0.5 to 1.2 nm. These carbons have been shown to be suitable for use as supercapacitor electrodes, and have been tested in 6 M KOH where a capacitance of 217 F g-1 was achieved at a current density of 0.5 A g-1. A long cycling life of 30 000 cycles was achieved at a current density of 1 A g-1, with only a 9% loss in capacity. The leakage current through a two-electrode device was measured as 2.3 μA per mg of electrode and the self-discharge characteristics were minimal.

  6. Synthesis, characterization and thermal behavior of antibacterial and antifungal active zinc complexes of bis (3(4-dimethylaminophenyl)-allylidene-1,2-diaminoethane.

    Montazerozohori, Morteza; Zahedi, Saeedeh; Naghiha, Asghar; Zohour, Mostafa Montazer


    In this work, synthesis of a new series of zinc halide/pseudohalide complexes of a bidentate Schiff base ligand entitled as bis (3-(4-dimethylaminophenyl)-allylidene)-1,2-diaminoethane(L) is described. The ligand and its zinc complexes were characterized by various techniques such as elemental analysis, FT-IR, UV-visible, (1)H and (13)C NMR spectra, cyclic voltammetry, and conductometry. Accordingly ZnLX2 (X=Cl(-), Br(-), I(-), SCN(-) and N3(-)) was suggested as molecular formula of the complexes. Redox behaviors of ligand and its zinc complexes were investigated by cyclic voltammetry method. Furthermore, the ligand and its zinc halide/pseudohalide complexes were tested for their in vitro antibacterial activities against two gram positive bacteria (Staphylococcus aureus and Bacillus subtilis) and two gram negative bacteria (Escherichia coli and Pseudomonas aeruginosa). Also in vitro antifungal activities of them against Candida albicans and Aspergillus niger were investigated. The results indicated that all compounds are antibacterial and antifungal active. Thermal behaviors of ligand and its zinc complexes were studied from room temperature to 1100 °C under argon atmosphere. It was found that the ligand and zinc iodide are decomposed completely via three and four steps respectively while other zinc complexes leave out the metal or organometallic compounds as final residuals after 3-4 decomposition steps at above temperature range. Moreover evaluation of some thermo-kinetic parameters such as activation energy (∆E*), enthalpy (∆H*), entropy (∆S*) and Gibbs free energy change (∆G*) of the thermal decomposition steps were performed based on the Coats-Redfern relation.

  7. New dinuclear copper(II) and zinc(II) complexes for the investigation of sugar-metal ion interactions.

    Bera, Manindranath; Patra, Ayan


    We have studied the binding interactions of biologically important carbohydrates (D-glucose, D-xylose and D-mannose) with the newly synthesized five-coordinate dinuclear copper(II) complex, [Cu(2)(hpnbpda)(μ-OAc)] (1) and zinc(II) complex, [Zn(2)(hpnbpda)(μ-OAc)] (2) [H(3)hpnbpda=N,N'-bis(2-pyridylmethyl)-2-hydroxy-1,3-propanediamine-N,N'-diacetic acid] in aqueous alkaline solution. The complexes 1 and 2 are fully characterized both in solid and solution using different analytical techniques. A geometrical optimization was made of the ligand H(3)hpnbpda and the complexes 1 and 2 by molecular mechanics (MM+) method in order to establish the stable conformations. All carbohydrates bind to the metal complexes in a 1:1 molar ratio. The binding events have been investigated by a combined approach of FTIR, UV-vis and (13)C NMR spectroscopic techniques. UV-vis spectra indicate a significant blue shift of the absorption maximum of complex 1 during carbohydrate coordination highlighting the sugar binding ability of complex 1. The apparent binding constants of the substrate-bound copper(II) complexes have been determined from the UV-vis titration experiments. The binding ability and mode of binding of these sugar substrates with complex 2 are indicated by their characteristic coordination induced shift (CIS) values in (13)C NMR spectra for carbon atoms C1, C2, and C3 of sugar substrates.

  8. Synthesis and Crystal Structure of Zinc(Ⅱ) Complex with Isonicotinate Containing a Three-dimensional Hydrogen-bond Network


    A zinc complex, [Zn(iso)2(H2O)4](iso=C6H4NO2-), was synthesized and characterized by elemental analysis, thermal analysis and IR spectrum studies. The crystal structure of the complex was determined by X-ray diffraction. The crystal crystallizes in the triclinic system, molecular formula ZnC12H16N2Os, Mr=381.64, space group P1 with a = 6.338(1 ), b =6.919(1), c=9.277(1), a =96.28(1),β =104.91(1 ),γ =112.85(1)°, V=352.12(9)A3, Z=1, Dc=l.80g·cm-3 and F(000)=196, μ =l.791mm-1. The crystal structure was solved by direct methods for final R=0.0204 and Rw=0.0542 for 1258 observed reflections with [Fo>4 σ (Fo)]. The crystal structure reveals that zinc ion is trans-octahedral with two pyridyl nitrogens and two aque oxygens at the equational positions and two aqua oxygens at the axial positions. The complex forms a three-dimensional network through intermolecular hydrogen bonds.

  9. Spectral and Electroluminescent Properties of Binuclear Zinc Complexes with Halogen-Substituted Derivatives of 1,2,4-Triazole

    Kopylova, T. N.; Degtyarenko, K. M.; Samsonova, L. G.; Gadirov, R. M.; Gusev, A. N.; Shul'gin, V. F.; Meshkova, S. B.


    Spectral properties of binuclear zinc complexes in chloroform solutions and polyvinylcarbazole (PVC) films are investigated. It is demonstrated that incorporation of a halogen atom (chlorine or bromine) in a ligand benzene ring leads to a small shift of the spectrum toward the red region and a reduction of the fluorescence quantum yield. The fluorescence and phosphorescence spectra at T = 77K are investigated. The fluorescence undergoes a blue shift of about 30 nm and multiply increases in the intensity, and the phosphorescence is observed at 540-580 nm. The phosphorescence lifetime is estimated. The electroluminescent properties of metal complexes in structures with thermal vacuum spin coating of complexes and in PVC films are investigated.

  10. Syntheses, structural variations and fluorescence studies of two dinuclear zinc(II) complexes of a Schiff base ligand with an extended carboxylate side arm

    Shit, Shyamapada; Sasmal, Ashok; Dhal, Piu; Rizzoli, Corrado; Mitra, Samiran


    A potentially tetradentate Schiff base ligand containing carboxylic acid group, HL, (E)-2-((pyridin-2-yl)methyleneamino)-5-chlorobenzoic acid is synthesized and characterized. Reaction of HL with hydrated zinc(II) trichloroacetate and zinc(II) trifluoroacetate under similar reaction condition yields two discrete dinuclear complexes, [Zn(L)(Cl)]2 (1) and [Zn(L)(CF3COO)]2 (2) and characterized by different physicochemical methods. Single crystal X-ray structural characterization reveals different ligating properties of the coordinated anionic ligand (L-) in its zinc(II) complexes. The side arm carboxylate of L- shows μ1,3-carboxylato-bridging mode in 1 and connects zinc(II) atoms in syn-anti fashion while it exhibits a μ1,1-carboxylato-bridging mode in 2. The metal ions display distorted square pyramidal geometries in both the structures and associated with different degrees of distortions. The fluorescence spectra of HL and its zinc(II) complexes recorded in methanol at room temperature which reveal the enhancement of emission intensity for the complexes compared to that of the free ligand. Thermogravimetric analyses (TGA) reveal high thermal stabilities of the complexes.

  11. Zinc-prolinamide complex catalyzed direct asymmetric aldol reactions in the presence of water


    An efficient direct asymmetric aldol reaction with zinc triflate and prolinamides as combined catalysts is reported.A series of chiral prolinamides have been designed and used in the direct aldol reaction resulting in the desired products with excellent yields(up to 94% yield) and high enantioselectivities(up to 96% ee).Water was found to play a significant role in the formation of the aldol products,which suggests a new strategy in the design of new organic catalysts.

  12. The complex interface chemistry of thin-film silicon/zinc oxide solar cell structures.

    Gerlach, D; Wimmer, M; Wilks, R G; Félix, R; Kronast, F; Ruske, F; Bär, M


    The interface between solid-phase crystallized phosphorous-doped polycrystalline silicon (poly-Si(n(+))) and aluminum-doped zinc oxide (ZnO:Al) was investigated using spatially resolved photoelectron emission microscopy. We find the accumulation of aluminum in the proximity of the interface. Based on a detailed photoemission line analysis, we also suggest the formation of an interface species. Silicon suboxide and/or dehydrated hemimorphite have been identified as likely candidates. For each scenario a detailed chemical reaction pathway is suggested. The chemical instability of the poly-Si(n(+))/ZnO:Al interface is explained by the fact that SiO2 is more stable than ZnO and/or that H2 is released from the initially deposited a-Si:H during the crystallization process. As a result, Zn (a deep acceptor in silicon) is "liberated" close to the silicon/zinc oxide interface presenting the inherent risk of forming deep defects in the silicon absorber. These could act as recombination centers and thus limit the performance of silicon/zinc oxide based solar cells. Based on this insight some recommendations with respect to solar cell design, material selection, and process parameters are given for further knowledge-based thin-film silicon device optimization.

  13. Effect of glucosamine conjugation to zinc(II) complexes of a bis-pyrazole ligand: syntheses, characterization and anticancer activity.

    Bhattacharyya, Sudipta; Sarkar, Amrita; Dey, Suman Kr; Mukherjee, Arindam


    The bis(3,5-dimethyl-1H- pyrazol-1yl)acetic acid (bdmpza) ligand was conjugated with tert-butyl-N-(2-aminoethyl) carbonate, methyl-2-amino-4-(methylthio)butanoate and 1,3,4,6-tetra-O-acetyl-β-d-glucosamine hydrochloride via amide coupling method to form three ligands L1-L3 which were then reacted with Zn(II) salts to form four zinc complexes (1-4). The complexes were characterized by (1)H NMR, (13)C NMR, electrospray ionization mass spectrometry (ESI-MS), FT-IR, CHN analyses. Complexes 1, 2 and 4 were also characterized by single crystal X-ray diffraction. It was found that Zn(II) salts could selectively remove the acetyl group from anomeric position leaving everything else intact. The cytotoxicity studies of the ligand and the complexes showed that the conjugation to acetylated glucosamine enhances cytotoxic ability although the complexes become more hydrophilic. Cytotoxicity studies in human breast adenocarcinoma (MCF-7), human cervical cancer (HeLa WT) and human lung adenocarcinoma (A549) showed that the acetylated glucosamine conjugation to the bis-pyrazole ligated Zn(II) complex led to 2-4 fold increase in cytotoxicity (IC50 values ca. 57-80μM) against HeLa WT and MCF-7 cell lines. The Zn(II) complex bearing the acetylated glucosamine inhibits the cell cycle in the G2/M phase of MCF-7 cell line. ICP-MS data shows more accumulation of Zn(II) inside the cell upon use of complex 4 as compared to Zn(II) salts or the other presented complexes. Further studies suggest that the mitochondrial transmembrane potential changes in the presence of complex 4 and caspase-7 is activated by Zn(II) salts but the activation is much more by complex 4 and hence there is apoptosis and dose dependent chromatin condensation/nuclear fragmentation as observed by microscopy.

  14. Synthesis and DNA cleavage activities of mononuclear macrocyclic polyamine zinc(II), copper(II), cobalt(II) complexes which linked with uracil.

    Wang, Xiao-Yan; Zhang, Ji; Li, Kun; Jiang, Ning; Chen, Shan-Yong; Lin, Hong-Hui; Huang, Yu; Ma, Li-Jian; Yu, Xiao-Qi


    Mononuclear macrocyclic polyamine zinc(II), copper(II), cobalt(II) complexes, which could attach to peptide nucleic acid (PNA), were synthesized as DNA cleavage agents. The structures of these new mononuclear complexes were identified by MS and (1)H NMR spectroscopy. The catalytic activities on DNA cleavage of these mononuclear complexes with different central metals were subsequently studied, which showed that copper complex was better catalyst in the DNA cleavage process than zinc and cobalt complexes. The effects of reaction time, concentration of complexes were also investigated. The results indicated that the copper(II) complexes could catalyze the cleavage of supercoiled DNA (pUC 19 plasmid DNA) (Form I) under physiological conditions to produce selectively nicked DNA (Form II, no Form III produced) with high yields. The mechanism of the cleavage process was also studied.

  15. Theoretical and experimental evaluation of structural and optical properties of novel zinc-benzimidazole metal complex doped in polystyrene matrices

    Praveen, P. A.; Babu, R. Ramesh


    A novel zinc incorporated benzimidazole metal complex (diacetobis (1H-benzimidazole) Zn(II)) is synthesized by a simple chemical route. The structure of the obtained complex is predicted using FTIR and EPR spectroscopy and further confirmed using semiempirical simulation of vibrational frequencies. Theoretical energy gap of the complex is about 3.2 eV and the hyperpolarizability calculations show that the third harmonic generation dominates over other mechanisms in the complex. Recorded absorption spectrum of the complex shows a broad absorption band between 200 and 300 nm corresponding to π-π transitions. To evaluate the third order nonlinear optical properties experimentally, the complex is doped into a polystyrene matrix with different weight percentages and fabricated as freestanding films. The films are subjected to Z-scan analysis and from the open and closed aperture scans the samples are found to have a reverse saturable absorption and self focusing effect. The calculated third order susceptibilities are of the order of 10-4 esu, which is one of the largest values reported in literature.

  16. Design, synthesis and characterization of zinc-morin, a metal flavonol complex and evaluation of its antidiabetic potential in HFD-STZ induced type 2 diabetes in rats.

    Sendrayaperumal, V; Iyyam Pillai, S; Subramanian, S


    The present study deals with the synthesis, characterization of zinc-morin complex and evaluation of its antidiabetic efficacy in High Fat Diet (HFD)-fedStreptozotocin (STZ) induced diabetic rats. Oral administration of zinc-morin complex to diabetic rats (5mg/kg body weight/day) for a period of 30 days resulted in the decreased levels of blood glucose and HbA1c. Oral administrations of the zinc-morin complex for 30 days significantly improved hyperglycemia, glucose intolerance, and insulin resistance. The elevated levels of lipid peroxides declined and the antioxidant competence was found to be improved in diabetic rats treated with the complex. The status of the lipid and lipoprotein profile in the serum was normalized upon treatment. Levels of TNFα decreased upon treatment with the complex. The altered levels of adipokines such as adiponectin and leptin were normalized upon treatment with the complex. In conclusion, the present study indicates that the zinc-morin complex possesses antidiabetic, antidyslipidemic and antioxidant potentials in HFD-fedSTZ induced diabetic rats.

  17. Synthesis, X-ray crystal structures and thermal analyses of some new antimicrobial zinc complexes: New configurations and nano-size structures.

    Masoudiasl, A; Montazerozohori, M; Naghiha, R; Assoud, A; McArdle, P; Safi Shalamzari, M


    Some new five coordinated ZnLX2 complexes, where L is N3-Schiff base ligand obtained by condensation reaction between diethylenetriamine and (E)-3-(2-nitrophenyl)acrylaldehyde and X (Cl(-), Br(-), I(-), N3(-) and NCS(-)), were synthesized and characterized by FT-IR, (1)H and (13)CNMR, UV-visible, ESI-mass spectra and molar conductivity measurements. The structures of zinc iodide and thiocyanate complexes were determined by X-ray crystallographic analysis. The X-ray results showed that the Zn (II) center in these complexes is five-coordinated in a distorted trigonal-bipyramidal configuration. Zinc iodide and thiocyanate complexes crystallize in the monoclinic and triclinic systems with space groups of C2/c and P1- with eight and two molecules per unit cell respectively. The crystal packing of the complexes consists of intermolecular interactions such as C-H(…)O and C-H(…)I, C-H(···)S, N(…)O, together with π-π stacking and some other unexpected interactions. The mentioned interactions cause three-dimensional supramolecular structure in the solid state. Zinc complexes were also prepared in nano-structure by sonochemical method confirmed by XRD, SEM and TEM analyses. Moreover, ZnO nanoparticles were synthesized by direct thermolysis of zinc iodide complex. Furthermore, antimicrobial and thermal properties of the compounds were completely investigated.

  18. Peptide-based FeS4 complexes: the zinc ribbon fold is unsurpassed to stabilize both the FeII and FeIII states.

    Jacques, Aurélie; Latour, Jean-Marc; Sénèque, Olivier


    Whereas Zn(Cys)4 zinc fingers exist with different protein folds, only the zinc ribbon fold is found in rubredoxin Fe(Cys)4 sites. To assess the significance of this observation, we have investigated the binding and stability of Fe(2+) and Fe(3+) ions by a set of four peptides designed to model Zn(Cys)4 zinc fingers with various folds, i.e. zinc ribbon, treble clef and a loosened zinc ribbon fold. All peptides were shown by means of UV-Vis and CD spectroscopies to form stable 1 : 1 Fe(II)/peptide complexes with binding constants higher than 10(7) M(-1) at pH 7. Their oxidation into Fe(III) complexes and the stability of the latter were compared. The UV-Vis absorption and CD spectroscopic properties of the Fe(II) and Fe(III) complexes were analysed with respect to the structures of the zinc analogues in order to get insight into the local arrangement of the Fe(Cys)4 core around the metal ion. The chemical stability of these complexes was rationalized according to the shielding from the solvent provided by the various peptide folds to the FeS4 core. In addition, we showed that whereas UV-visible spectra inform only on the FeS4, the information derived from the corresponding CD spectra extend to the Cβ orientation and the peptide fold. The results presented here demonstrate that while the zinc ribbon fold is not strictly required to obtain a Fe(Cys)4 site, it affords a drastically superior protection of the site toward external redox agents. This finding brings new clues to engineer stable and redox-active Fe(Cys)4 sites in de novo proteins.

  19. Large fluorescence response by alcohol from a bis(benzoxazole)-zinc(II) complex: the role of excited state intramolecular proton transfer.

    Wang, Junfeng; Chu, Qinghui; Liu, Xiumin; Wesdemiotis, Chrys; Pang, Yi


    The formation of a bis(HBO) anion is known to turn on the fluorescence to give red emission, via controlling the excited-state intramolecular proton transfer (ESIPT). The poor stability of the formed anion, however, hampered its application. The anion stability is found to be greatly improved by attaching the anion to Zn(2+) cation (i.e., forming zinc complex), whose emission is at λem ≈ 550 and 760 nm. Interestingly, addition of methanol to the zinc complex induces a remarkable red fluorescence (λem ≈ 630 nm, φfl ≈ 0.8). With the aid of spectroscopic studies ((1)H NMR, UV-vis, fluorescence, and mass spectra), the structures of the zinc complexes are characterized. The emission species is identified as a dimer-like structure. The study thus reveals an effective fluorescence switching mechanism that could further advance the application of ESIPT-based sensors.

  20. Syntheses and solid state structures of zinc (II) complexes with Bi-dentate -(Aryl)imino-acenapthenone (Ar-BIAO) ligands

    Srinivas Anga; Supriya Rej; Kishor Naktode; Tigmansu Pal; Tarun K Panda


    We have synthesized five zinc complexes of molecular formulae [ZnCl2(2,6-dimethylphenyl-BIAO)]2 (1a), [ZnBr2(2,6-dimethylphenyl-BIAO)]2 (1b), [ZnI2(2,6-dimethylphenyl-BIAO)]2(1c), [ZnBr2(mes-BIAO)]2(2b) and [ZnBr2(dipp-BIAO)] (3b) with rigid unsymmetrical iminoacenaphthenone ligands, (2,6-dimethylphenyl-BIAO) (1), (mesityl-BIAO) (2) and (2,6-diisopropylphenyl-BIAO) (3). The zinc complex 1a was prepared by the reaction of ZnCl2 and neutral (mesityl-BIAO) (1). However, complexes 1b, 2b and 3b were obtained by the treatment of ZnBr2 and neutral ligands 1-3 respectively in 1:1 molar ratio in dichloromethane at ambient temperature. In a similar reaction of ZnI2 with (2,6-dimethylphenyl-BIAO) (1) in dichloromethane the corresponding iodo-complex 1c was obtained in good yield. All the zinc (II) complexes are characterized by FT-IR, 1H and 13C{1H} NMR spectroscopic techniques. The solid state structures of the complexes 1a, 1b, 1c, 2b and 3b are confirmed by single crystal X-ray diffraction analysis. The molecular structures of complexes 1a, 1b, 1c and 2b reveal the dimeric nature of the complexes and subsequently the centre atom zinc is penta-coordinated to adopt distorted trigonal bipyramidal geometry around it. In contrast, the complex 3b is in monomeric in nature due to bulkier size of the ligand and zinc ion is tetra coordinated to adopt distorted tetrahedral geometry.

  1. (Pyridine)(tetrahydroborato)zinc complex, (Zn(BH{sub 4}){sub 2}(py)), as a new stable, efficient and chemoselective reducing agent for reduction of carbonyl compounds

    Zeynizadeh, Behzad; Faraji, Fariba [Urima Univ., Urima (Iran, Islamic Republic of)


    (Pyridine)(tetrahydroborato)zinc complex, (Zn(BH{sub 4}){sub 2}(py)), as a stable white solid, was prepared quantitatively by complexation of an equimolar amount of zinc tetrahydroborate and pyridine at room temperature. This reagent can easily reduce variety of carbonyl compounds such as aldehydes, ketones, acyloins, {alpha}-diketones and {alpha},{beta}-unsaturated carbonyl compounds to their corresponding alcohols in good to excellent yields. Reduction reactions were performed in ether or THF at room temperature or under reflux conditions. In addition, the chemoselective reduction of aldehydes over ketones was accomplished successfully with this reducing agent.

  2. Synthesis aspects, structural, spectroscopic, antimicrobial and room temperature ferromagnetism of zinc iodide complex with Schiff based ligand

    Shakila, K.; Kalainathan, S.


    In this paper, we report the successful growth of complex compound of zinc iodide with thiocarbamide by slow evaporation method. The single crystal XRD study reveals that the crystal belongs to monoclinic system with centrosymmetric space group and powder XRD analysis shows that the perfect crystalline nature of the crystal. The presence of functional group and element were confirmed from FT-IR and EDAX analysis. Optical absorbance of the grown crystal was studied by UV-Vis spectrophotometer. The optical constants were calculated from the optical absorbance data such as refractive index (n), extinction coefficient (K) and reflectance (R). The optical band gap (Eg) of thiocarbamide zinc iodide crystal is 4.22 eV. The magnetic properties of grown crystal have been determined by Vibrating Sample Magnetometry (VSM). Room temperature magnetization revealed a ferromagnetic behaviour for the grown crystal. The antibacterial and antifungal activities of the title compound were performed by well diffusion method and MIC method against the standard bacteria like Staphylococcus aureus, Escherichia coli, Klebsiella pneumonia and against fungus like Aspergillus niger, Rhizopus sps and Penicillium sps. Thermal behaviour of the crystal has been investigated using thermogravimetric analysis (TGA) and differential thermal analysis (DTA).

  3. Potential effect on the cathodic efficiency of a Zinc electrodeposition in a cyanide free alkaline bath; Influencia del potencial sobre el rendimiento catodico en la electrodeposicion de cinc en un bano alcalino exento de cianuro

    Diez, J. A.; Muller, C.; Grande, H.


    The aim of this work has been the study of the potential advantages of ursin a potentiostatic method in galvanizing industrial processes. The behaviour of cyanide-free alkaline zinc bath has been analyzed using the process cathodic efficiency as control parameter. By anodic re dissolution (Q{sub 0}x/Q{sub r}ed measurement), the potential range of maximum cathodic efficiency has been set. Finally, the method has been scaled up to a semi-pilot plant in order to check the stability of the results and as a previous step to industry implementation. At this scale, the cathodic efficiency has been measured by weight loss tests. (Author) 22 refs.

  4. Characteristic differences in the formation of complex coacervate core micelles from neodymium and zinc-based coordination polymers.

    Yan, Yun; Besseling, Nicolaas A M; de Keizer, Arie; Stuart, Martien A Cohen


    In this paper we compare the formation of complex coacervate core micelles (C3Ms) from two different tricompontent mixtures, namely neodymium, the bisligand L2EO4 and the poly(cation)-block-poly(neutral) diblock copolymer P2MVP41-b-PEO205, and zinc, L2EO4 and P2MVP41-b-PEO205 mixed systems. Three sets of titration experiments were carried out for each system: (i) titration of diblock copolymer P2MVP41-b-PEO205 with the stoichiometric mixture of metal ions and bisligands, (ii) titration of a mixture of diblock copolymer and bisligand with metal ions, and (iii) titration of a mixture of diblock copolymer and metal ions with bisligands. In all the above three cases, micelles are found to form either in a broad range of charge ratios or in a broad range of metal/bisligand ratios. Upon addition of Nd2-(L2EO4)3 coordination polymer to P2MVP41-b-PEO205 solution, and upon addition of Nd3+ to a mixture of L2EO4 and P2MVP41-b-PEO205, micelles are found to form immediately after the first addition, whereas micelles show up in the similar zinc system only after a certain threshold Zn-(L2EO4) or Zn2+ concentration. This difference can be traced to the different structures of the Nd2-(L2EO4)3 and Zn-(L2EO4) coordination compounds. At very low concentrations, Zn-(L2EO4) are ring-like oligomers, but Nd2-(L2EO4)3 are larger networks. The network structure favors the formation of coacervate micellar core with P2MVP41-b-PEO205. Moreover, excess of Nd3+ ions will break up the C3Ms, while the same amount of Zn2+ has hardly any effect on the C3Ms. The breakdown of C3Ms by Nd3+ is due to the charge inversion of the coordination complex with increasing [Nd3+]/[L2EO4] ratio, which results in repulsive interaction between the coordination complex and the diblock copolymer, whereas no such interaction can occur in the zinc system.

  5. Synthetic, spectral and solution studies on imidazolate-bridged copper(II)-copper(II) and copper(II)-zinc(II) complexes

    Subodh Kumar; R N Patel; P V Khadikar; K B Pandeya


    Synthesis, spectral and solution studies on 2-ethyl imidazolate-bridged (2-EtIm) homo-binuclear copper(II)-copper(II) and hetero-binuclear copper(II)-zinc(II) homologue are described. Magnetic moment values of homo-binuclear complexes indicate that the imidazolate group can mediate antiferromagnetic interactions. Optical spectra of hetero-binuclear complex at varying H values suggest that the imidazolate-bridged complex is stable over the H-range 7 15-10 0.

  6. Synthesis, Spectral Characterization, and Biochemical Evaluation of Antidiabetic Properties of a New Zinc-Diosmin Complex Studied in High Fat Diet Fed-Low Dose Streptozotocin Induced Experimental Type 2 Diabetes in Rats

    Veerasamy Gopalakrishnan


    Full Text Available In view of the established antidiabetic properties of zinc, the present study was aimed at evaluating the hypoglycemic properties of a new zinc-diosmin complex in high fat diet fed-low dose streptozotocin induced experimental type 2 diabetes in rats. Zinc-diosmin complex was synthesized and characterized by various spectral studies. The complexation between zinc ions and diosmin was further evidenced by pH-potentiometric titrations and Job’s plot. Diabetic rats were orally treated with zinc-diosmin complex at a concentration of 20 mg/kg b.w./rat/day for 30 days. At the end of the experimental period, the rats were subjected to oral glucose tolerance test. In addition, HOMA-IR and various biochemical parameters related to glucose homeostasis were analyzed. Treatment with zinc-diosmin complex significantly improved the glucose homeostasis in diabetic rats. Treatment with zinc-diosmin complex significantly improved insulin sensitivity, at least in part, through enhancing protein metabolism and alteration in the levels of muscle and liver glycogen. The assay of clinical marker enzymes revealed the nontoxic nature of the complex. Determination of renal tissue markers such as blood urea and serum creatinine indicates the renoprotective nature of the complex. These findings suggest that zinc-diosmin complex is nontoxic and has complimentary potential to develop as an antihyperglycemic agent for the treatment of diabetes mellitus.

  7. Zinc(II) and Cadmium(II) complexes with N4-coordinate pyrazole based ligand: Syntheses, characterization and structure

    Solanki, Ankita; Sadhu, Mehul H.; Kumar, Sujit Baran; Mitra, Partho


    A series of six new mononuclear zinc(II) complexes of the type [Zn(X)(dbdmp)]Y (1-6) (X = N3-/NCO-/NCS-, Y = ClO4-/PF6-, and dbdmp = N,N-diethyl-N‧,N‧-bis((3,5-dimethyl-1H-pyrazol-1-yl)methyl)ethane-1,2-diamine), two binuclear cadmium(II) complexes [{Cd(dbdmp)}2(μ-N3)2](Y)2 (7-8) and three mononuclear cadmium(II) complexes [Cd(NCO)(dbdmp)]Y (Y = ClO4-/PF6-) (9-10) and [Cd(NCS)2(dbdmp)] (11) have been synthesized and characterized by physico-chemical methods. Crystal structures of the complexes [Zn(N3)(dbdmp)]ClO4 (1), [{Cd(dbdmp)}2(μ-N3)2](ClO4)2 (7), [Cd(NCO)(dbdmp)]ClO4 (9) and [Cd(NCS)2(dbdmp)] (11) have been solved by single crystal X-ray diffraction studies and showed that [Zn(N3)(dbdmp)]ClO4 (1) and [Cd(NCO)(dbdmp)]ClO4 (9) have distorted trigonal bipyramidal geometry, [Cd(NCS)2(dbdmp)] (11) and [(dbdmp)Cd(μ-N3)]2(ClO4)2 (7) have distorted octahedral geometry.

  8. Comments on "Synthesis aspects, structural, spectroscopic, antimicrobial and room temperature ferromagnetism of zinc iodide complex with Schiff based ligand" by K. Shakila and S. Kalainathan, Spectrochim. Acta 135 A (2015) 1059-1065

    Srinivasan, Bikshandarkoil R.; Nadkarni, V. S.


    Shakila and Kalainathan report on the synthetic and structural aspects of a zinc iodide complex with Schiff based ligand, which exhibits room temperature ferromagnetism. In this comment, many points of criticism, concerning the characterization of this so called zinc iodide complex of Schiff based ligand are highlighted to prove that the title paper is completely erroneous.

  9. Cadmium complexes bearing (Me2)N^E^O(-) (E = S, Se) organochalcogenoalkoxides and their zinc and mercury analogues.

    Pop, Alexandra; Bellini, Clément; Şuteu, Răzvan; Dorcet, Vincent; Roisnel, Thierry; Carpentier, Jean-François; Silvestru, Anca; Sarazin, Yann


    Heteroleptic zinc and cadmium complexes of the type [{(Me2)N^E^O(R2)}M-Nu]n (M = Zn, Cd; E = S, Se; R = CH3, CF3; Nu = N(SiMe3)2, I, Cl; n = 1-2) were prepared by reacting the alcohol proteo-ligands {(Me2)N^E^O(R2)}H with [M(N(SiMe3)2)2] (M = Zn, Cd) or [XMN(SiMe3)2] (M = Zn, X = Cl; M = Cd, X = I) in an equimolar ratio. These group 12 metal complexes were characterised in solution by multinuclear NMR spectroscopy and their solid-state structures were determined by X-ray diffractometry. The ligands {(Me2)N^E^O((CH3)2)}(-) bearing CH3 groups in α position to the alkoxide behave as κ(2)-O,E-bidentate moieties (E = S, Se) and form centro-symmetric dinuclear O-bridged heteroleptic alkoxo-amido complexes both with zinc and cadmium, with four-coordinate metal centres resting in tetrahedral environments. By contrast, complexes supported by the CF3-substituted {(Me2)N^E^O((CF3)2)}(-) crystallise as tetrahedral mononuclear species, with tridentate κ(3)-N,O,E-coordinated ligands. These structural differences resulting from changes in the ligand skeleton and in the electron-donating properties of the alkoxide were also observed in solution. Attempts to prepare congeneric heteroleptic mercury complexes from [Hg(N(SiMe3)2)2] unexpectedly only afforded homoleptic bis(alkoxide)s such as [{(Me2)N^S^O((CF3)2)}2Hg]. Owing to the strong Hg-C bond, treatment of [PhHgN(SiMe3)2] with {(Me2)N^S^O((CF3)2)}H afforded the heteroleptic, T-shaped [{(Me2)N^S^O((CF3)2)}HgPh] mercuric alkoxide upon elimination of hexamethyldisilazane. [{(Me2)N^S^O((CF3)2)}2Hg] and [{(Me2)N^S^O((CF3)2)}HgPh] constitute very rare examples of structurally characterised mercuric alkoxides.

  10. Exploring zinc coordination in novel zinc battery electrolytes.

    Kar, Mega; Winther-Jensen, Bjorn; Forsyth, Maria; MacFarlane, Douglas R


    The coordination of zinc ions by tetraglyme has been investigated here to support the development of novel electrolytes for rechargeable zinc batteries. Zn(2+) reduction is electrochemically reversible from tetraglyme. The spectroscopic data, molar conductivity and thermal behavior as a function of zinc composition, between mole ratios [80 : 20] and [50 : 50] [tetraglyme : zinc chloride], all suggest that strong interactions take place between chloro-zinc complexes and tetraglyme. Varying the concentration of zinc chloride produces a range of zinc-chloro species (ZnClx)(2-x) in solution, which hinder full interaction between the zinc ion and tetraglyme. Both the [70 : 30] and [50 : 50] mixtures are promising electrolyte candidates for reversible zinc batteries, such as the zinc-air device.

  11. Complexes cobalt(II, zinc(II and copper(II with some newly synthesized benzimidazole derivatives and their antibacterial activity



    Full Text Available The preparation and properties of some complexes of cobalt(II, zinc(II and copper(II with several newly synthesized benzimidazole derivatives (L are reported. The complexes, of the general formula [MCl2L2] (M=Co(II, Zn(II and [CuCl2L(H2O], have a tetrahedral structure. The complexes were characterized by elemental analysis, molar conductivity, magnetic susceptibility measurements, IR and absorption electronic spectra. The antibacterial activitiy of the benzimidazoles and their complexes was evaluated against Erwinia carotovora subsp. carotovora and Erwinia amylovora. The complexes were found to be more toxic than the ligands.

  12. Bioavailability and Electroreactivity of Zinc Complexed to Strong and Weak Organic Ligands.

    Kim, Ja-Myung; Baars, Oliver; Morel, François M M


    Laboratory experiments have established the importance of complexation by organic ligands in determining the bioavailability of trace metals to marine phytoplankton, while electrochemical measurements with field samples have demonstrated that a large fraction of bioactive trace metals are complexed to strong organic ligands in seawater. Using the model organic ligands, EDTA and histidine, we show a quantitative correspondence between the bioavailability of Zn to the diatom Thalassiosira weissflogii, and its reduction at -1.2 V (vs Ag/AgCl) on a hanging mercury drop electrode. Equilibrium calculations and polarographic data indicate that Zn bound in inorganic complexes and the 1:1 Zn-histidine complex, but not in the 1:2 Zn-histidine complex or the Zn-EDTA complexes, is taken up by the organism and reduced at the electrode surface, confirming a previous report of the bioavailability of weak Zn complexes. Electrochemical measurements of Zn speciation in seawater do not generally reveal the presence of weak (and potentially bioavailable) complexes; but such measurements (particularly by Anodic Stripping Voltammetry) should nonetheless often provide good estimates of the bioavailable Zn concentrations. These results can likely be generalized to other bioactive divalent trace metals.

  13. Complex nanospherulites of zinc oxide and native amorphous boron in the lunar regolith from Mare Crisium

    Mokhov, A. V.; Kartashov, P. M.; Gornostaeva, T. A.; Asadulin, En. E.; Bogatikov, O. A.


    During the study of tea-colored impact glass fragments from the sample of lunar regolith delivered to Earth by the Luna 24 automatic station by transmission electron microscopy, the composition variations of the previously described high-carbonaceous film, the presence of at least three composition types of glasses, and unusual nanospherulites with Zn-B-N-O composition were discovered. As a part of a nonuniform high-carbonaceous oxygen-bearing film, sites enriched in either Na, S, Si, or Ca were detected. All these sites, as well as the whole film, are electron-amorphous; however, crystalline graphite was also found. Two types of nanospherulites are composed of amorphous ZnO and regular interstratifications of crystalline ZnO and amorphous boron layers with insignificant participation of adsorbed nitrogen. It is supposed that the formation of zinc-boron nanospherulites was caused by a fast-flowing explosive process and probably was modulated by high-frequency acoustic oscillations in a cloud of evaporated high-temperature ionized gas during the impact event.

  14. Efficient catalytic phosphate ester cleavage by binuclear zinc(II) pyrazolate complexes as functional models of metallophosphatases.

    Penkova, Larysa V; Maciag, Anna; Rybak-Akimova, Elena V; Haukka, Matti; Pavlenko, Vadim A; Iskenderov, Turganbay S; Kozłowski, Henryk; Meyer, Franc; Fritsky, Igor O


    A series of dizinc(II) complexes based on the pyrazolate ligands 3-[(1E)-N-hydroxyethanimidoyl]-4-methyl-1H-pyrazole-5-carboxylic acid (H(3)L(1)), (1E,1'E)-1,1'-(4-methyl-1H-pyrazole-3,5-diyl)diethanone dihydrazone (HL(2)), (E,E)-(4-methyl-1H-pyrazole-3,5-diyl)bis(methylmethanone) dioxime (H(3)L(3)), (E,E)-(4-phenyl-1H-pyrazole-3,5-diyl)bis(phenylmethanone) dioxime (H(3)L(4)), and 1H-pyrazole-3,5-dicarboxylic acid (H(3)L(5)) have been synthesized and investigated as functional models of phosphoesterases, focusing on correlations between the hydrolytic activity and molecular parameters of the bimetallic core. Speciation of the various dizinc complexes in solution has been determined potentiometrically, and the structures in the solid state have been established by X-ray crystallography. The hydrolysis of two phosphoesters, an RNA model 2-hydroxypropyl-p-nitrophenyl phosphate (HPNP) and the pesticide paraoxon-ethyl (POE), promoted by the dinuclear phosphoesterase model complexes has been investigated in DMSO/buffered water (1:1) at 50 degrees C as a function of complex concentration, substrate concentration, and pH. Drastic differences in the hydrolytic activities of [Zn(2)(HL(1))(2)](0), [Zn(2)(L(2))(2)](2+), [Zn(2)(H(2)L(3))(2)](2+), and [Zn(2)(HL(5))(2)](2-) are observed and can be attributed to molecular peculiarities. Pyrazolate-bridged dinuclear zinc(II) complexes seem to provide a sufficient number of coordination sites for both activating the substrate and generating the nucleophile, where the phosphate esters are preferentially bound in a bidentate bridging fashion (in the case of HPNP) and in a monodentate fashion (in the case of POE).

  15. Hybrid scorpionate/cyclopentadienyl magnesium and zinc complexes: synthesis, coordination chemistry, and ring-opening polymerization studies on cyclic esters.

    Garcés, Andrés; Sánchez-Barba, Luis F; Alonso-Moreno, Carlos; Fajardo, Mariano; Fernández-Baeza, Juan; Otero, Antonio; Lara-Sánchez, Agustín; López-Solera, Isabel; Rodríguez, Ana María


    The reaction of the hybrid scorpionate/cyclopentadienyl lithium salt [Li(bpzcp)(THF)] [bpzcp = 2,2-bis(3,5-dimethylpyrazol-1-yl)-1,1-diphenylethylcyclopentadienyl] with 1 equiv of RMgCl proceeds cleanly to give very high yields of the corresponding monoalkyl kappa(2)-NN-eta(5)-C(5)H(4) magnesium complexes [Mg(R)(kappa(2)-eta(5)-bpzcp)] (R = Me 1, Et 2, (n)Bu 3, (t)Bu 4, CH(2)SiMe(3) 5, CH(2)Ph 6). Hydrolysis of the hybrid lithium salt [Li(bpzcp)(THF)] with NH(4)Cl/H(2)O in ether cleanly affords the two previously described regioisomers: (bpzcpH) 1-[2,2-bis(3,5-dimethylpyrazol-1-yl)-1,1-diphenylethyl]-1,3-cyclopentadiene (a) and 2-[2,2-bis(3,5-dimethylpyrazol-1-yl)-1,1-diphenylethyl]-1,3-cyclopentadiene (b). Subsequent reaction of the bpzcpH hybrid ligand with ZnR(2) quantitatively yields the monoalkyl kappa(2)-NN-eta(1)(pi)-C(5)H(4) zinc complexes [Zn(R){kappa(2)-eta(1)(pi)-bpzcp}] (R = Me 7, Et 8, (t)Bu 9, CH(2)SiMe(3) 10). Additionally, magnesium alkyls 1, 2, 4, and 5 can act as excellent cyclopentadienyl and alkyl transfers to the zinc metal center and yield zinc alkyls 7-10 in good yields. The single-crystal X-ray structures of the derivatives 4, 5, 7, and 10 confirm a 4-coordinative structure with the metal center in a distorted tetrahedral geometry. Interestingly, whereas alkyl magnesium derivatives 4 and 5 present a eta(5) coordination mode for the cyclopentadienyl fragment, zinc derivatives 7 and 10 feature a peripheral eta(1)(pi) arrangement in the solid state. Furthermore, the reaction of the hybrid lithium salt [Li(bpzcp)(THF)] with 1 equiv of ZnCl(2) in tetrahydrofuran (THF) affords very high yields of the chloride complex [ZnCl{kappa(2)-eta(1)(pi)-bpzcp}] (11). Compound 11 was used as a convenient starting material for the synthesis of the aromatic amide zinc compound [Zn(NH-4-MeC(6)H(4)){kappa(2)-eta(1)(pi)-bpzcp}] (12), by reaction with the corresponding aromatic primary amide lithium salt. Alternatively, aliphatic amide and alkoxide derivatives were

  16. Syntheses, structures and luminescence behaviour of some zinc(II) complexes containing acetate and tetradentate Schiff bases

    Ashis Kumar Maji; Subhasis Roy; Somnath Choubey; Rajarshi Ghosh; Barindra Kumar Ghosh


    Two mononuclear compounds of the types pentacoordinated [Zn(L1)(OAc)]PF6·H2O (1) and hexacoordinated [Zn(L2)(OAc)]PF6 (2) [L1 = N,N′-(bis(pyridin-2-yl)formylidene)-1,3-propanediamine; L2 = N,N′-(bis(pyridin-2-yl)benzylidene)-1,4-butanediamine] have been synthesized using one-pot reactions of a 1:1:1 molar ratio of Zn(OAc)2.2H2O, L1/L2, ammonium hexafluorophosphate in MeOH at room temperature. Compounds 1 and 2 are characterized on the basis of microanalytical, spectroscopic, thermal and other physicochemical results. Single crystal X-ray structural study reveals that the zinc(II) centre in 1 is coordinated by four N atoms of the Schiff base L1 and one O atom of terminal acetate with a ZnN4O chromophore, whereas in 2, the zinc(II) centre is bound by four N atoms of the tailored Schiff base L2 and two O atoms of the chelated acetate. In the crystalline state, mononuclear units in 1 are engaged in weak cooperative intermolecular O-H⋯O and C-H⋯F hydrogen bonds affording a 1D chain. The individual units of 2 are packed by ⋯ and anion⋯ interactions to form a 2D sheet structure. The complexes show reasonable thermal stabilities and display intraligand → ∗ fluorescence in solid state at room temperature.

  17. Complexing ability of (-)-cytisine--synthesis, spectroscopy and crystal structures of the new copper and zinc complexes.

    Przybył, Anna K; Kubicki, Maciej; Jastrzab, Renata


    For the first time the NMR spectra of quinolizidine alkaloid with Cu(II) are studied. Structures of new complexes of (-)-cytisine with Cu(+2) and Zn(+2) cations are visualized, discussed in detail and characterized by spectroscopic methods: ESI-MS, NMR, UV-vis, EPR and crystallographic methods. In solution metal coordinates through the protonated nitrogen atoms of secondary amino groups (in piperidine ring) of cytisine molecule. While in solid state the most stable structures of the complexes are those in which the coordination of Cu(II) and Zn(II) salts is realized solely through the lactam carbonyl oxygen atom.

  18. Excited state intramolecular proton transfer (ESIPT) in six-coordinated zinc(ii)-quinoxaline complexes with ligand hydrogen bonds: their fluorescent properties sensitive to axial positions.

    Sakai, Ken-Ichi; Takahashi, Sami; Kobayashi, Ataru; Akutagawa, Tomoyuki; Nakamura, Takayoshi; Dosen, Masaaki; Kato, Masako; Nagashima, Umpei


    Zinc(ii)-quinoxaline complexes, [Zn(hqxc)(2)(py)(2)] and [Zn(hqxc)(2)(DMSO)(2)] (hqxc = 3-hydroxy-2-quinoxalinecarboxylate, py = pyridine, DMSO = dimethyl sulfoxide), were prepared and characterized by X-ray crystallography and fluorescence spectroscopy. In both complexes, the zinc ion is six-coordinated by two equatorial bidentate hqxc ligands with an intramolecular hydrogen bond and two axial monodentate ligands such as pyridine or DMSO. In spite of similar coordination geometries, there is a remarkable difference between their solid-state fluorescent properties. The pyridine complex is strongly fluorescent (fluorescence quantum yield Phi = 0.22), giving rise to a significantly Stokes-shifted spectrum. From its thin film photopumped by a nitrogen gas laser, amplified spontaneous emission was observed. These results suggest that the fluorescence occurs by way of excited-state intramolecular proton-transfer (ESIPT) in the hydrogen bond of hqxc. On the other hand, the DMSO complex shows fluorescent intensity (Phi = 0.08) lower than that of the pyridine complex, and shows normal emission in addition to ESIPT emission. From IR measurements for these complexes, it is concluded that axial ligands influence the hydrogen bond strength of the equatorial hqxc ligand via zinc and thus the ESIPT efficiency.

  19. Magnesium, zinc, aluminium and gallium hydride complexes of the transition metals.

    Butler, Michael J; Crimmin, Mark R


    The preparation and applications of heterobimetallic complexes continue to occupy researchers in the fields of organometallic, main group, and coordination chemistry. This interest stems from the promise these complexes hold as precursors to materials, reagents in synthesis and as new catalysis. Here we survey and organise the state-of-the-art understanding of the TM-H-M linkage (M = Mg, Zn, Al, Ga). We discuss the structure and bonding in these complexes, their known reactivity, and their largely unrealised potential in catalysis.

  20. Metal complexes as templates: syntheses, structures, and luminescent properties of two zinc phosphonocarboxylates with ABW-zeolite topology.

    Chen, Zhenxia; Yang, Haiyang; Deng, Mingli; Ling, Yun; Weng, Linhong; Zhou, Yaming


    Two novel zinc phosphonocarboxylates, Zn(3)(pbc)(2)(bpy)(H(2)O)·H(2)O (1) and Zn(2)(pbc)(2)·Zn(bpy)(H(2)O)(4)·2H(2)O (2) (pbc = 4-phosphono-benzoic acid, bpy = 2,2'-bipyridine), were hydrothermally synthesized and structurally characterized. Both of them exhibit zeolitic ABW topology in which double-zigzag inorganic chains are cross-linked by the organic parts. It is notable that the metal complex Zn(bpy)(H(2)O)(x) plays different roles in the two compounds. In 1, the Zn(bpy)(H(2)O) units coordinate with the phosphonate and carboxylate oxygen atoms and participate in the construction of the three-dimensional framework. In 2, the in situ generated [Zn(bpy)(H(2)O)(4)](2+) cation acts as a template, which directs the ABW-type open-framework by strong hydrogen bonds. It is the first example where a metal complex is used as a template in the synthesis of metal phosphonates. The luminescent properties of 1 and 2 are also investigated.

  1. An exploratory investigation of polar organic compounds in waters from a lead–zinc mine and mill complex

    Rostad, Colleen E.; Schmitt, Christopher J.; Schumacher, John G.; Leiker, Thomas J.


    Surface water samples were collected in 2006 from a lead mine-mill complex in Missouri to investigate possible organic compounds coming from the milling process. Water samples contained relatively high concentrations of dissolved organic carbon (DOC; greater than 20 mg/l) for surface waters but were colorless, implying a lack of naturally occurring aquatic humic or fulvic acids. Samples were extracted by three different types of solid-phase extraction and analyzed by electrospray ionization/mass spectrometry. Because large amounts of xanthate complexation reagents are used in the milling process, techniques were developed to extract and analyze for sodium isopropyl xanthate and sodium ethyl xanthate. Although these xanthate reagents were not found, trace amounts of the degradates, isopropyl xanthyl thiosulfonate and isopropyl xanthyl sulfonate, were found in most locations sampled, including the tailings pond downstream. Dioctyl sulfosuccinate, a surfactant and process filtering aid, was found at concentrations estimated at 350 μg/l at one mill outlet, but not downstream. Release of these organic compounds downstream from lead-zinc mine and milling areas has not previously been reported. A majority of the DOC remains unidentified.

  2. Photo- and electroluminescent properties of zinc(II) complexes with tetradentate Schiff bases, derivatives of salicylic aldehyde

    Vashchenko, A. A.; Lepnev, L. S.; Vitukhnovskii, A. G.; Kotova, O. V.; Eliseeva, S. V.; Kuz'mina, N. P.


    It is studied how the introduction of various substituents into the composition of organic ligands affects the photoluminescence spectra of new zinc(II) complexes with tetradentate Schiff bases H2L (derivatives of salicylic aldehyde (H2SAL1, H2SAL2) and o-vanillin (H2MO1, H2MO2) with ethylenediamine and o-phenylenediamine) in the form of bulk solids and thin films. It is demonstrated that the emission spectra of bulk solid complexes without o-phenylenediamine bridges (ZnSAL1 and ZnMO1) contain additional long-wavelength bands compared to the spectra of corresponding thin films. In the case of films obtained from [ZnSAL1]2 dimer complexes, the long-wavelength band is dominant. At the same time, the photoluminescence spectra of ZnSAL2 and ZnMO2 complexes with o-phenylenediamine bridges are similar in the case of solid samples and thin films. The electroluminescent properties of organic light-emitting diodes (OLEDs) with the ITO/α-NPD/ZnL/Ca:Al structure are studied. The bathochromic shift of the electroluminescence peaks of OLEDs with respect to the photoluminescence spectra of bulk solid samples and thin films is probably related to the formation of exciplexes at the α-NPD/ZnL interface. The electroluminescence spectra of OLEDs based on [ZnSAL1]2 show a hypsochromic shift of the emission maximum, which can be caused by a shift of the recombination region into the α-NPD layer.

  3. Complexes of myo-Inositol-Hexakisphosphate (IP6) with Zinc or Lanthanum for the Decorporation of Radiocesium.

    Ogawa, Kazuma; Aoki, Miho; Fukuda, Tadahisa; Kadono, Sumi; Kiwada, Tatsuto; Odani, Akira


    Radioactive nuclides leak into the surrounding environment after nuclear power plant disasters, such as the Chernobyl accident and the Fukushima Daiichi Nuclear Power Plant disaster. Cesium-137 ((137)Cs) (t1/2=30.1 year), a water-soluble radionuclide with a long physical half-life, contaminates aquatic ecosystems and food products. In humans, (137)Cs concentrates in muscle tissue and has a long biological half-life, indicating it may be harmful. myo-Inositol-hexakisphosphate (IP6) is a compound found in grain, beans, and oil seeds. IP6 has the ability to form insoluble complexes with metals, including lanthanum (La) and zinc (Zn). We hypothesized that La-IP6 and Zn-IP6 may promote the elimination of (137)Cs from the body through the adsorption of La-IP6 and Zn-IP6 to (137)Cs in the gastrointestinal tract. Therefore, in this study, we evaluated the adsorptive capacity of La-IP6 and Zn-IP6 complexes with (137)Cs in vitro and in vivo. La-IP6 and Zn-IP6 complexes were stable in acidic solution (pH 1.2) at 37°C. In vitro binding assays indicated that La-IP6 and Zn-IP6 complexes adsorbed (137)Cs, with the adsorption capacity of Zn-IP6 to (137)Cs greater than that of La-IP6. To evaluate the usefulness of La-IP6 and Zn-IP6 in vivo, La-IP6 or Zn-IP6 was administrated to mice after intravenous injection of (137)Cs. However, the biodistribution of (137)Cs in the La-IP6 treated group and the Zn-IP6 treated group was nearly identical to the non-treated control group, indicating that La-IP6 and Zn-IP6 were not effective at promoting the elimination of (137)Cs in vivo.

  4. Novel Zinc(II) Complexes of Heterocyclic Ligands as Antimicrobial Agents: Synthesis, Characterisation, and Antimicrobial Studies

    Yamgar, Ramesh S.; Nivid, Y.; Nalawade, Satish; Mandewale, Mustapha; Atram, R. G.; Sawant, Sudhir S.


    The synthesis and antimicrobial activity of novel Zn(II) metal complexes derived from three novel heterocyclic Schiff base ligands 8-[(Z)-{[3-(N-methylamino)propyl]imino}methyl]-7-hydroxy-4-methyl-2H-chromen-2-one, 2-[(E)-{[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]imino}methyl]phenol, and (4S)-4-{4-[(E)-(2-hydroxybenzylidene)amino]benzyl}-1,3-oxazolidin-2-one have been described. These Schiff base ligands and metal complexes are characterised by spectroscopic techniques. According to these data, we propose an octahedral geometry to all the metal complexes. Antimicrobial activity of the Schiff base ligand and its metal complexes was studied against Gram negative bacteria: E. coli and Pseudomonas fluorescens, Gram positive bacteria: Staphylococcus aureus, and also against fungi, that is, C. albicans and A. niger. Some of the metal complexes show significant antifungal activity (MIC < 0.2 μg/mL). The “in vitro” data has identified [Zn(NMAPIMHMC)2]·2H2O, [Zn(TMPIMP)2]·2H2O, and [Zn(HBABO)2]·2H2O as potential therapeutic antifungal agents against C. albicans and A. niger. PMID:24707242

  5. Coordination Chemistry of Polyaromatic Thiosemicarbazones 2: Synthesis and Biological Activity of Zinc, Cobalt, and Copper Complexes of 1-(Naphthalene-2-ylethanone Thiosemicarbazone

    Marc-Andre LeBlanc


    Full Text Available A novel thiosemicarbazone from 2-acetonaphthone (represented as acnTSC has been synthesized and its basic coordination chemistry with zinc(II, cobalt(II, and copper(II explored. The complexes were characterized by elemental analysis and various spectroscopic techniques and are best formulated as [M(acnTSC2Cl2] with the metal likely in an octahedral environment. The anticancer activity of the complexes was determined against a panel of human colon cancer cells (HCT-116 and Caco-2. The compounds bind to DNA via an intercalative mode with binding constants of 9.7×104 M-1, 1.8×105 M-1, and 9.5×104 M-1 for the zinc, cobalt, and copper complexes, respectively.

  6. Radical pathway in catecholase activity with zinc-based model complexes of compartmental ligands.

    Guha, Averi; Chattopadhyay, Tanmay; Paul, Nanda Dulal; Mukherjee, Madhuparna; Goswami, Somen; Mondal, Tapan Kumar; Zangrando, Ennio; Das, Debasis


    Four dinuclear and three mononuclear Zn(II) complexes of phenol-based compartmental ligands (HL(1)-HL(7)) have been synthesized with the aim to investigate the viability of a radical pathway in catecholase activity. The complexes have been characterized by routine physicochemical studies as well as X-ray single-crystal structure analysis: [Zn(2)(H(2)L(1))(OH)(H(2)O)(NO(3))](NO(3))(3) (1), [Zn(2)L(2)Cl(3)] (2), [Zn(2)L(3)Cl(3)] (3), [Zn(2)(L(4))(2)(CH(3)COO)(2)] (4), [Zn(HL(5))Cl(2)] (5), [Zn(HL(6))Cl(2)] (6), and [Zn(HL(7))Cl(2)] (7) [L(1)-L(3) and L(5)-L(7) = 2,6-bis(R-iminomethyl)-4-methylphenolato, where R= N-ethylpiperazine for L(1), R = 2-(N-ethyl)pyridine for L(2), R = N-ethylpyrrolidine for L(3), R = N-methylbenzene for L(5), R = 2-(N-methyl)thiophene for L(6), R = 2-(N-ethyl)thiophene for L(7), and L(4) = 2-formyl-4-methyl-6-N-methylbenzene-iminomethyl-phenolato]. Catecholase-like activity of the complexes has been investigated in methanol medium by UV-vis spectrophotometric study using 3,5-di-tert-butylcatechol as model substrate. All complexes are highly active in catalyzing the aerobic oxidation of 3,5-di-tert-butylcatechol (3,5-DTBC) to 3,5-di-tert-butylbenzoquinone (3,5-DTBQ). Conversion of 3,5-DTBC to 3,5-DTBQ catalyzed by mononuclear complexes (5-7) is observed to proceed via formation of two enzyme-substrate adducts, ES1 and ES2, detected spectroscopically, a finding reported for the first time in any Zn(II) complex catalyzed oxidation of catechol. On the other hand, no such enzyme-substrate adduct has been identified, and 3,5-DTBC to 3,5-DTBQ conversion is observed to be catalyzed by the dinuclear complexes (1-4) very smoothly. EPR experiment suggests generation of radicals in the presence of 3,5-DTBC, and that finding has been strengthened by cyclic voltammetric study. Thus, it may be proposed that the radical pathway is probably responsible for conversion of 3,5-DTBC to 3,5-DTBQ promoted by complexes of redox-innocent Zn(II) ion. The ligand

  7. In vitro DNA binding studies of the sweetening agent saccharin and its copper(II) and zinc(II) complexes.

    Icsel, Ceyda; Yilmaz, Veysel T


    The interactions of fish sperm DNA (FS-DNA) with the sodium salt of sweetener saccharin (sacH) and its copper and zinc complexes, namely [M(sac)2(H2O)4]·2H2O (M=Cu(II) or Zn(II)) were studied by using UV-Vis titration, fluorometric competition, thermal denaturation, viscosity and gel electrophoresis measurements. The intrinsic binding constants (Kb) obtained from absorption titrations were estimated to be 2.86 (±0.06)×10(4)M(-1) for Na(sac), 6.67 (±0.12)×10(4)M(-1) for Cu-sac and 4.01 (±0.08)×10(4)M(-1) for Zn-sac. The Cu-sac complex binds to FS-DNA via intercalation with a KA value of 50.12 (±0.22)×10(4)M(-1) as evidenced by competitive binding studies with ethidium bromide. Moreover, competition experiments with Hoechst 33258 are indicative of a groove binding mode of Na(sac) and Zn-sac with binding constants of 3.13 (±0.16)×10(4)M(-1) and 5.25 (±0.22)×10(4)M(-1), respectively. The spectroscopic measurements indicate a moderate DNA binding affinity of Na(sac) and its metal complexes. The suggested binding modes are further confirmed by the thermal denaturation and viscosity measurements. In addition, Cu-sac and Zn-sac show weak ability to damage to pBR322 supercoiled plasmid DNA.

  8. Synthesis and Uncommon Structural Characterization of Novel Zinc and Cadmium Complexes with Imino Nitroxide Radical

    WANG Shu-Ping; GAO Dong-Zhao; LIAO Dai-Zheng; JIANG Zong-Hui; YAN Shi-Ping


    Two novel complexes {[Zn(IM4py)2(tp)(H2O)]·2H2O}n 1 and {[Cd(IM4py)2(tp)- (H2O)]·1.25H2O}n 2 (IM4py=2-(4'-pyridinyl)-4,4,5,5-tetramethylimidazoline-1-oxyl and tp=terephthalate dianion) have been synthesized and characterized by elemental analyses, IR spectrum and single-crystal X-ray diffraction. Crystal data for complex 1: monoclinic, space group C2/c, a=20.648(7), b=12.130(4), c=14.036(4) (A), β=106.351(5)°, C32H42N6O9Zn, Mr=720.09, V=3373.3(2) (A)3, Z=4, Dc=1.418 g/cm3, μ(MoKα)= 0.790 mm-1, F(000)=1512, the final R=0.0407 and Wr=0.0894 for 3480 independent reflections with Rint=0.0432. Crystal data for complex 2: monoclinic, space group C2/c, a=21.332(6), b=12.063(3), c=14.246(4) (A), β=106.704(4)°, C32H40.50N6O8.25Cd, Mr=753.60, V=3511.2(2) (A)3, Z=4, Dc=1.426 g/cm3, μ(MoKα)= 0.679 mm-1, F(000)=1554, the final R=0.0419 and Wr=0.0961 for 3627 independent reflections with Rint=0.0440. The framework structures of complexes 1 and 2 are 3-D networks via the hydrogen bonds among 1-D chains. The notable characteristics of the two complexes are that the coordination polyhedron of Zn(Ⅱ) adopts a rare distorted five-coordinate square pyramidal geometry in 1, and the Cd(Ⅱ) complex exhibits an unusual distorted seven-coordinate pentagonal bipyramid in 2.

  9. Structural Determination of Bis-histidinopeptide Zinc Complexes by 15N NMR (HMBC) Spectra

    ZHOU,Cheng-He; Juan F.Miravet; M.Isabel Burguete; Santiago V.Luis; BAI,Xue; YUAN,Yong


    @@ Polynitrogen receptors such as bis-histidine peptides possess strong ability to bind metals, which play much important roles in medicinal, bioinorganic, bioorganic, biomimetic and supramolecular chemistry. In order to investigate the interaction of these hosts with a variety of neutral, cationic and anionic guests, several techniques, for example, NMR,potentiometric tirations and monocrystal X-ray diffraction have been employed. Among them NMR is a powerful technique for unraveling the structure of polynitrogen receptors as long as they are in solution where the rapid tumbling of molecules averages out the anisotropies such as chemical shift and dipole-dipole interactions. General 1H NMR approach has been widely used for the study of host-guest interaction, but it is difficult for the accurate measurement in complexes structures, particularly metal complexes structures in which how the polynitrogen receptors bind metal, and which nitrogen binds metal and so on.

  10. The role of zinc on the chemistry of complex intermetallic compounds

    Xie, Weiwei [Iowa State Univ., Ames, IA (United States)


    Combining experiments and electronic structure theory provides the framework to design and discover new families of complex intermetallic phases and to understand factors that stabilize both new and known phases. Using solid state synthesis and multiple structural determinations, ferromagnetic β-Mn type Co8+xZn12–x was analyzed for their crystal and electronic structures.

  11. Application of a topical biomimetic electrical signaling technology to photo-aging: a randomized, double-blind, placebo-controlled trial of a galvanic zinc-copper complex.

    Chantalat, Jeannette; Bruning, Elizabeth; Sun, Ying; Liu, Jue-Chen


    The first signs of facial skin photo-aging often occur in the skin of the periorbital area and include sagging, loss of firmness and definition, and sallowness. Epidermal wounds have been shown to alter the trans-epithelial electrical potential creating an electric signal that directs cell migration in epithelial wound healing; this electric field declines sharply with age. A topical galvanic zinc-copper complex, which couples elemental zinc and copper to create a biomimetic electric field, has demonstrated anti-inflammatory activity and extracellular matrix improvement in vitro, including collagen and elastin production. To evaluate the efficacy and tolerability of a galvanic zinc-copper complex on photo-aging parameters in a randomized, double-blind, placebo-controlled clinical trial. In this eight-week study, women (40-65 years) with mild to moderate photo-aging were randomized to use placebo or 1 of 3 galvanic zinc-copper complex compositions (gel and activating moisturizer). Efficacy evaluations included clinical grading, specialized clinical imaging, and subject self-assessments performed at baseline, 15-30 minutes after product application and after 1, 2, 4, and 8 weeks. Tolerability was based on adverse events and clinical grading of irritation. Significance was set at P?0.05 versus baseline and between treatment groups. The study was completed by 124 women. Compositions containing the galvanic zinc-copper complex showed statistically significant clinical improvements versus placebo and baseline rapidly (15-30 min) after application and through week 8. Clinical grading showed significant improvement versus placebo in skin radiance and under-eye dark circles 15-30 minutes after first application with continued improvement through week 8, and in overall photo-damage, fine lines, lifted appearance of the eyes, and under-eye wrinkles starting after two weeks and continuing through week 8. Test compositions were well tolerated. This galvanic zinc-copper complex

  12. N,N’-diisopropylthiourea and N,N’-dicyclohexyl-thiourea zinc(II complexes as precursors for the synthesis of ZnS nanoparticles

    J. Raftery


    Full Text Available The single X-ray crystal structures of zinc (II complexes of N,N’-diisopropylthiourea and N,N’ dicyclohexylthiourea weredetermined.These complexes, similar to other alkylthioureas, were found to be effective as precursors for the preparation of hexadecylamine-capped ZnS nanoparticles. The complexes are air-stable, easy to prepare and inexpensive. They pyrolyse cleanly to give high-quality ZnS nanoparticles, which show quantum confinement effects in their absorption spectra and close to band-edge emission. Their broad diffraction patterns are typicalof nanosized particles while their transmission electronmicroscopy images showed agglomerates of needle-like platelet nanoparticles.

  13. Synthesis and physico-chemical characterization of zinc(II, nickel(II and cobalt(II complexes with 2-phenyl-2-imidazoline

    Podunavac-Kuzmanović Sanja O.


    Full Text Available Chlorides and nitrates of zinc(II, nickel(II and cobalt(II react with 2-phenyl-2-imidazoline to give complexes of the type [ML2X2]·nH2O (M=Zn, Ni or Co; L=2-phenyl-2-imidazoline; X=Cl or NO3; n=0, 1 or 2. The complexes were synthesized and characterized by elemental analysis of the metal molar conductivity, magnetic susceptibility measurements and IR spectra. The molar conductances of the zinc(II complexes in DMF solutions indicate that the complexes behave as non-electrolytes. The values of magnetic conductivity in the case of nickel(II complexes indicate that one of the coordinated anions (chloride or nitrate has been replaced by DMF molecule. The molar conductivity values of cobalt(II complexes indicate the partial substitution of coordinated anions with solvent molecules. The room temperature effective magnetic moments and IR data of the complexes suggest that all Zn(II, Ni(II and Co(II complexes have a tetrahedral configuration, which is realized by participation of the pyridine nitrogen of two organic ligand molecules, and two chloride or nitrate anions typical for these classes of organic ligands.

  14. Preparation of Zinc Oxide (ZnO) Thin Film as Transparent Conductive Oxide (TCO) from Zinc Complex Compound on Thin Film Solar Cells: A Study of O2 Effect on Annealing Process

    Muslih, E. Y.; Kim, K. H.


    Zinc oxide (ZnO) thin film as a transparent conductive oxide (TCO) for thin film solar cell application was successfully prepared through two step preparations which consisted of deposition by spin coating at 2000 rpm for 10 second and followed by annealing at 500 °C for 2 hours under O2 and ambient atmosphere. Zinc acetate dehydrate was used as a precursor which dissolved in ethanol and acetone (1:1 mol) mixture in order to make a zinc complex compound. In this work, we reported the O2 effect, reaction mechanism, structure, morphology, optical and electrical properties. ZnO thin film in this work shows a single phase of wurtzite, with n-type semiconductor and has band gap, carrier concentration, mobility, and resistivity as 3.18 eV, 1.21 × 10-19cm3, 11 cm2/Vs, 2.35 × 10-3 Ωcm respectively which is suitable for TCO at thin film solar cell.

  15. Synthesis and molecular structure of a zinc complex of the vitamin K3 analogue phthiocol

    Kathawate, Laxmi; Sproules, Stephen; Pawar, Omkar; Markad, Ganesh; Haram, Santosh; Puranik, Vedavati; Salunke-Gawali, Sunita


    The complex [Zn(phthiocol)2(H2O)2]; 1, where phthiocol is 2-hydroxy-3-methyl-1,4-naphthoquinone, has been synthesized and characterized by elemental analysis, FT-IR, 1H NMR, UV-vis spectroscopy, thermogravimetric (TG) analysis, electrochemical and single crystal X-ray diffraction studies. The νCO stretch shifts to lower frequencies upon complexation of phthiocol to Zn2+. 1H NMR spectra show an upfield shift of the benzenoid ring protons in 1. There is a bathochromic shift of the LMCT band in the UV-vis spectra of 1. Single crystal X-ray structure of 1 show distorted octahedral geometry around Zn2+. Two phthiocol ligands are in plane with the metal, while water molecules are trans to this plane. Coordination of deprotonated phthiocol ligands is 'trans, trans' to Zn2+. Intra as well as intermolecular interactions are observed in 1. Molecules of 1 show three dimensional network through CH⋯O and OH⋯O interactions. Additional anodic peaks are observed in cyclic voltammogram of phthiocol ligand due to oxidation of reduced species formed during reduction. One-electron reduction of 1 is shown to be reversible and DFT studies define this redox event as ligand-centered.

  16. Influencia mental a distancia sobre los organismos vivientes

    Bonilla, Ernesto


    Este articulo revisa estudios relacionados con la influencia mental a distancia sobre los organismos vivientes, incluyendo las sugestiones mentales de sueno y despertar, la influencia mental a grandes...

  17. Iron and zinc complexation in wild-type and ferritin-expressing wheat grain: implications for mineral transport into developing grain

    Neal, Andrew L; Geraki, Kalotina; Borg, Søren


    We have used synchrotron-based X-ray fluorescence and absorption techniques to establish both metal distribution and complexation in mature wheat grains. In planta, extended X-ray absorption fine structure (EXAFS) spectroscopy reveals iron phytate and zinc phytate structures in aleurone cells...... of ferritin-expressing grains is quite different from that in wild-type grain. This may explain why the raised levels of minerals transported to the developing grain accumulate within the crease region of the transgenic grain....

  18. Carboxylated dithiafulvenes and tetrathiafulvalene vinylogues: synthesis, electronic properties, and complexation with zinc ions

    Yunfei Wang


    Full Text Available A class of carboxyl and carboxylate ester-substituted dithiafulvene (DTF derivatives and tetrathiafulvalene vinylogues (TTFVs has been synthesized and their electronic and electrochemical redox properties were characterized by UV–vis spectroscopic and cyclic voltammetric analyses. The carboxyl-TTFV was applied as a redox-active ligand to complex with Zn(II ions, forming a stable Zn-TTFV coordination polymer. The structural, electrochemical, and thermal properties of the coordination polymer were investigated by infrared spectroscopy, cyclic voltammetry, powder X-ray diffraction, and differential scanning calorimetric analyses. Furthermore, the microscopic porosity and surface area of the Zn-TTFV coordination polymer were measured by nitrogen gas adsorption analysis, showing a BET surface of 148.2 m2 g−1 and an average pore diameter of 10.2 nm.

  19. Self-assembly of a helical zinc-europium complex: speciation in aqueous solution and luminescence

    Emmanuel eDeiters


    Full Text Available Two new tridentate(NNO-bidentate(NN compartmental ligands, HL5 and HL6, are synthesized from pyridine and benzimidazole synthons. They react in aqueous solution under physiological conditions with ZnII, LnIII, or a mixture thereof, to yield complexes of different stoichiometries, 1:3, 2:2, 2:3, 1:1:3, the speciation of which is established by UV-visible titrations and ESI mass spectrometry. Photophysical studies of the EuIII-containing solutions in Tris-HCl 0.1 M (pH = 7.4 show that lanthanide luminescence arises from a unique N6O3 coordination site with pseudo D3 symmetry. Relevant parameters such as crystal field splitting, lifetime, radiative lifetime and intrinsic quantum yield perfectly match those reported for dinuclear 4f-4f helicates in which the EuIII ion has the same coordination environment.

  20. Metal-Based Biologically Active Compounds: Synthesis, Spectral, and Antimicrobial Studies of Cobalt, Nickel, Copper, and Zinc Complexes of Triazole-Derived Schiff Bases

    Kiran Singh


    Full Text Available A series of cobalt, nickel, copper, and zinc complexes of bidentate Schiff bases derived from the condensation reaction of 4-amino-5-mercapto-3-methyl/ethyl-1,2,4-triazole with 2,4-dichlorobenzaldehyde were synthesized and tested as antimicrobial agents. The synthesized Schiff bases and their metal complexes were characterized with the aid of elemental analyses, magnetic moment measurements, spectroscopic and thermogravimetric techniques. The presence of coordinated water in metal complexes was supported by infrared and thermal gravimetric studies. A square planar geometry was suggested for Cu(II and octahedral geometry proposed for Co(II, Ni(II, and Zn(II complexes. The Schiff bases and their metal complexes have been screened for antibacterial (Pseudomonas aeruginosa, Bacillus subtilis and antifungal activities (Aspergillus niger, A. flavus. The metal complexes exhibited significantly enhanced antibacterial and antifungal activity as compared to their simple Schiff bases.

  1. Mechanistic implications in the phosphatase activity of Mannich-based dinuclear zinc complexes with theoretical modeling.

    Sanyal, Ria; Zhang, Xuepeng; Kundu, Priyanka; Chattopadhyay, Tanmay; Zhao, Cunyuan; Mautner, Franz A; Das, Debasis


    An "end-off" compartmental ligand has been synthesized by an abnormal Mannich reaction, namely, 2-[bis(2-methoxyethyl)aminomethyl]-4-isopropylphenol yielding three centrosymmetric binuclear μ-phenoxozinc(II) complexes having the molecular formula [Zn2(L)2X2] (Zn-1, Zn-2, and Zn-3), where X = Cl(-), Br (-), and I (-), respectively. X-ray crystallographic analysis shows that the ZnO3NX chromophores in each molecule form a slightly distorted trigonal-bipyramidal geometry (τ = 0.55-0.68) with an intermetallic distance of 3.068, 3.101, and 3.083 Å (1-3, respectively). The spectrophotometrical investigation on their phosphatase activity established that all three of them possess significant hydrolytic efficiency. Michaelis-Menten-derived kinetic parameters indicate that the competitiveness of the rate of P-O bond fission employing the phosphomonoester (4-nitrophenyl)phosphate in 97.5% N,N-dimethylformamide is 3 > 1 > 2 and the kcat value lies in the range 9.47-11.62 s(-1) at 298 K. Theoretical calculations involving three major active catalyst forms, such as the dimer-cis form (D-Cis), the dimer-trans form (D-Trans), and the monoform (M-1 and M-2), systematically interpret the reaction mechanism wherein the dimer-cis form with the binuclear-bridged hydroxide ion acting as the nucleophile and one water molecule playing a role in stabilizing the leaving group competes as the most favored pathway.

  2. Russian Nesting Doll Complexes of Molecular Baskets and Zinc Containing TPA Ligands.

    Zhiquan, Lei; Polen, Shane; Hadad, Christopher M; RajanBabu, T V; Badjić, Jovica D


    In this study, we examined the structural and electronic complementarities of convex 1-Zn(II), comprising functionalized tris(2-pyridylmethyl)amine (TPA) ligand, and concave baskets 2 and 3, having glycine and (S)-alanine amino acids at the rim. With the assistance of (1)H NMR spectroscopy and mass spectrometry, we found that basket 2 would entrap 1-Zn(II) in water to give equimolar 1-Zn⊂2in complex (K = (2.0 ± 0.2) × 10(3) M(-1)) resembling Russian nesting dolls. Moreover, C3 symmetric and enantiopure basket 3, containing (S)-alanine groups at the rim, was found to transfer its static chirality to entrapped 1-Zn(II) and, via intermolecular ionic contacts, twist the ligand's pyridine rings into a left-handed (M) propeller (circular dichroism spectroscopy). With molecular baskets embodying the second coordination sphere about metal-containing TPAs, the here described findings should be useful for extending the catalytic function and chiral discrimination capability of TPAs.

  3. Differential effects of zinc and magnesium ions on mineralization activity of phosphatidylserine calcium phosphate complexes.

    Wu, Licia N Y; Genge, Brian R; Wuthier, Roy E


    Mg(2+) and Zn(2+) are present in the mineral of matrix vesicles (MVs) and biological apatites, and are known to influence the onset and progression of mineral formation by amorphous calcium phosphate (ACP) and hydroxyapatite (HAP). However, neither has been studied systematically for its effect on mineral formation by phosphatidylserine-Ca(2+)-Pi complexes (PS-CPLX), an important constituent of the MV nucleation core. Presented here are studies on the effects of increasing levels of Mg(2+) and Zn(2+) on the process of mineral formation, either when present in synthetic cartilage lymph (SCL), or when incorporated during the formation of PS-CPLX. Pure HAP and PS-CPLX proved to be powerful nucleators, but ACP took much longer to induce mineral formation. In SCL, Mg(2+) and Zn(2+) had significantly different inhibitory effects on the onset and amount of mineral formation; HAP and PS-CPLX were less affected than ACP. Mg(2+) and Zn(2+) caused similar reductions in the rate and length of rapid mineral formation, but Zn(2+) was a more potent inhibitor on a molar basis. When incorporated into PS-CPLX, Mg(2+) and Zn(2+) caused significantly different effects than when present in SCL. Even low, subphysiological levels of Mg(2+) altered the inherent structure of PS-CPLX and markedly reduced its ability to induce and propagate mineral formation. Incorporated Zn(2+) caused significantly less effect, low (<20 microM) levels causing almost no inhibition. Levels of Zn(2+) present in MVs do not appear to inhibit their nucleational activity.

  4. Separation of copper, iron, and zinc from complex aqueous solutions for isotopic measurement

    Borrok, D.M.; Wanty, R.B.; Ridley, W.I.; Wolf, R.; Lamothe, P.J.; Adams, M.


    The measurement of Cu, Fe, and Zn isotopes in natural samples may provide valuable information about biogeochemical processes in the environment. However, the widespread application of stable Cu, Fe, and Zn isotope chemistry to natural water systems remains limited by our ability to efficiently separate these trace elements from the greater concentrations of matrix elements. In this study, we present a new method for the isolation of Cu, Fe, and Zn from complex aqueous solutions using a single anion-exchange column with hydrochloric acid media. Using this method we are able to quantitatively separate Cu, Fe, and Zn from each other and from matrix elements in a single column elution. Elution of the elements of interest, as well as all other elements, through the anion-exchange column is a function of the speciation of each element in the various concentrations of HCl. We highlight the column chemistry by comparing our observations with published studies that have investigated the speciation of Cu, Fe, and Zn in chloride solutions. The functionality of the column procedure was tested by measuring Cu, Fe, and Zn isotopes in a variety of stream water samples impacted by acid mine drainage. The accuracy and precision of Zn isotopic measurements was tested by doping Zn-free stream water with the Zn isotopic standard. The reproducibility of the entire column separation process and the overall precision of the isotopic measurements were also evaluated. The isotopic results demonstrate that the Cu, Fe, and Zn column separates from the tested stream waters are of sufficient purity to be analyzed directly using a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS), and that the measurements are fully-reproducible, accurate, and precise. Although limited in scope, these isotopic measurements reveal significant variations in ??65Cu (- 1.41 to + 0.30???), ??56Fe (- 0.56 to + 0.34???), and ??66Zn (0.31 to 0.49???) among samples collected from different

  5. Dynamic Assembly Inclusion Complexes of Tweezer-type Bis(zinc porphyrin) with 5,15-Di(4-pyridyl)porphyrin Derivatives

    ZHOU,Zai-Chun; YANG,Yi; ZHU,Yi-Zhou; ZHENG,Jian-Yu


    Dynamic assembly inclusion complexes of tweezer-type bis(zinc porphyrin) (1) with di(4-pyridyl)porphyrin derivatives have been designed and constructed. The complexes are induced by Zn-N coordination, and the weak binding allows the large-size di(4-pyridyl)poiphyrin guests in random rotation. Dynamic characteristics of these assemblies, such as ligand exchange and dynamic fluorescence quenching, have been investigated by 'H NMR, UV-Vis and fluorescence spectra. The stability of such assembly has pronounced dependence on the size-matching effect and thermal effect.

  6. Zinc finger domain of Su(Hw) protein is required for the formation of functional Su(Hw)-dependent insulator complex.

    Golovnin, A K; Molodina, V V; Georgiev, P G; Melnikova, L S


    This study is devoted to clarifying the role of Mod(mdg4)-67.2 and Su(Hw) proteins in the interaction between Su(Hw)-dependent insulator complexes and identifying the specific domains of the Su(Hw) protein required for insulation or mutual neutralization of insulators. Using genetic techniques and experiments in yeast two-hybrid system, we have demonstrated that the zinc finger domain of the Su(Hw) protein is involved in forming a functional insulator complex and cannot be replaced with the DNA-binding domain of the GAL4 protein.

  7. Influencia del zinc administrado a pacientes críticos con nutrición parenteral sobre los niveles de zinc plasmático, proteína C reactiva, interleuquina-6 y receptor soluble de interleuquina-6 Influence of zinc administered by total parenteral nutrition on plasmatic zinc levels, on reactive C protein, on serum interleukin-6 and on serum interleukin-6 soluble receptor, in critical patients

    A. M.ª Menéndez


    Full Text Available Objetivos: Estudiar, en pacientes críticos, la respuesta de los niveles de Zn en plasma (ZnPl, de IL-6 sérica, del IL-6sR y de la PCR en relación al Zn administrado en la NPT, para evitar la deficiencia o el exceso de Zn. Métodos: 17 pacientes que recibieron NPT, por pancreatitis aguda o luego de una cirugía abdominal mayor. Al inicio (To y a la finalización (Tf de la NPT (6 a 21 días se determinó en suero: IL-6 y IL-6 sR (ELISA; PCR (inmunoturbidimetría; ZnPl y Zn en NPT (Espectrometría de Absorción Atómica. Características físicas: edad, años (promedio ± DE y rangos: 60,6 ± 11,7 (37-77; BMI (kg/m²: 26,0 ± 3,4 (19,9-34,0. Resultados: Promedio ± DE (y rangos: aporte de Zn en la NPT: 6,1 ± 2,0 mg/día (2,8 a 10,8; parámetros bioquímicos, a To y Tf, respectivamente: Zn Pl (μg/dl: 104 ± 46 (35-177; 120 ± 55 (52-229; IL-6 (pg/mL 93 ± 74 (10-262; 117 ± 180 (7-761; IL6sR (pg/mL: 1012 ± 322 (589-1.855; 1.269 ± 451 (631-2.195; PCR (mg/L: 71 ± 63 (2-196; 65 ± 43 (0-137. Dos pacientes, que fallecieron, incrementaron más de 4 veces los niveles de IL6, mantuvieron altos niveles de IL-6sR, pero disminuyendo los de PCR, recibiendo 4,2 y 5,2 mg/d de Zn. El 60% de los pacientes con evolución clínica favorable presentó una disminución de los niveles de IL6. Conclusiones: en los pacientes críticos, con evolución favorable, dosis de Zn de 2,8 a 10,8 mg/d en la NPT no exacerbaron la respuesta inflamatoria, evaluada mediante los niveles de IL-6, IL6sR y PCR.Objectives: To study the interrelationship between serum Interleukin-6 (IL-6, serum Interleukin-6 soluble Receptor (IL-6 sR, C-Reactive Protein (C-RP, plasmatic Zinc levels (PlZn and their response in relation to Zn administered by TPN, in critical patients. Methods: 17 patients, receiving TPN as a consequence of acute pancreatitis (n = 4 or after a major abdominal surgery due to intestinal cancer (n = 7, intestinal fístula (n = 3, intestinal obstruction (n = 2 or

  8. Spectroscopic, crystal structural and electrochemical studies of zinc(II)-Schiff base complex obtained from 2,3-diaminobenzene and 2-hydroxy naphthaldehyde.

    Ouari, Kamel; Bendia, Sabrina; Weiss, Jean; Bailly, Corinne


    Mononuclear zinc(II) complex, [Zn(II)L], where L is a dianionic ligand, has been synthesized and characterized by elemental analysis, electronic, IR and NMR [(1)H, (13)C, DEPT, (1)H-(1)H COSY, ROESY, HSQC and HMBC] spectroscopic techniques. Structural analysis of the complex by single crystal X-ray crystallography shows the presence of a distorted square planar coordination geometry (NNOO) of the metal center. The crystal of the title complex C28H18N2O2Zn belongs to the orthorhombic system with space group Pmn21. Electrochemical behavior of the Zn(II)L complex has been investigated by cyclic voltammetry on glassy carbon and platinum electrodes in DMF at 100 mV/s scan rate.

  9. NMR investigation of dynamic processes in complexes of nickel(II) and zinc(II) with iminodiacetate, n-methyliminodiacetate and n-ethyliminodiacetate

    Wagner, M.R.


    Analysis of oxygen-17 bulk water relaxation rates with an aqueous solution of 1:1 Ni(II):ida reveals that two rate-limiting processes are involved with solvent exchange. Analysis of carbon-13 longitudinal relaxation rates of the bis-ligand complexes with zinc(II) are used to determine molecular tumbling rates and methyl rotation rates. The carbon-13 transverse relaxation rates for the carbons in the bis-ligand complex with Ni(II) are adequately fitted to the Solomon-Bloembergen equation. Three carboxylate carbon peaks are seen with the /sup 13/C spectrum of the 1:2 Ni(II):ida complex, which coalesce into a single peak above about 360 K. The mechanism and rate of ligand exchange are determined for the complexes Zn(II)L/sub 2//sup -2/ (L = mida, eida) in aqueous solution by total lineshape analysis of the proton spectrum at 500 MHz.

  10. Synthesis and characterization of mixed ligand complexes of Zn(II) and Co(II) with amino acids: Relevance to zinc binding sites in zinc fingers

    P Rabindra Reddy; M Radhika; P Manjula


    Mixed ligand complexes of Zn(II) and Co(II) with cysteine, histidine, cysteinemethylester, and histidinemethylester have been synthesized and characterized by elemental analysis, conductivity, magnetic susceptibility measurements, and infrared, 1H NMR, TGA and FAB mass spectra. In these complexes, histidine, and histidinemethylester act as bidentate ligands involving amino and imidazole nitrogens in metal coordination. Similarly, cysteine, and cysteinemethylester also act as bidentate ligands coordinating through thiol sulphur and amino nitrogen. Tetrahedral geometry has been proposed for Zn(II) and Co(II) complexes based on experimental evidence.

  11. Synthesis and characterization of a new zinc(II) complex with tetradentate azo-thioether ligand: X-ray structure, DNA binding study and DFT calculation

    Mondal, Apurba Sau; Pramanik, Ajoy Kumar; Patra, Lakshman; Manna, Chandan Kumar; Mondal, Tapan Kumar


    A new zinc(II) complex, [Zn(L)(H2O)](ClO4) (1) with azo-thioether containing NSNO donor ligand, 3-(2-(2-((pyridin-2-ylmethyl)thio)phenyl)hydrazono)pentane-2,4-dione (HL) is synthesized and characterized by several spectroscopic techniques. The distorted square based pyramidal (DSBP) geometry is confirmed by single crystal X-ray structure. The ability of the complex to bind with CT DNA is investigated by UV-vis method and the binding constant is found to be 4.16 × 104 M-1. Competitive binding study with ethidium bromide (EB) by fluorescence method suggests that the zinc(II) complex efficiently displaces EB from EB-DNA. The Stern-Volmer dynamic quenching constant, Ksv is found to be 1.2 × 104 M-1. Theoretical calculations by DFT and TDDFT/CPCM methods are used to interpret the electronic structure and UV-vis spectrum of the complex.

  12. Elimination of the copper-zinc interference in anodic stripping voltammetry by addition of a complexing agent.

    Brandes Marques, A L; Chierice, G O


    The addition of cyanide and Triton X-100 suppress the formation of the CuZn intermetallic compound in ASV making it possible to determine traces of zinc(II) in the presence of an excess of copper ions. The precision of the method (5%) and the accuracy (error of 1.4%) in sea water are satisfactory.

  13. Mixed metal copper(II)-nickel(II) and copper(II)-zinc(II) complexes of multihistidine peptide fragments of human prion protein.

    Jószai, Viktória; Turi, Ildikó; Kállay, Csilla; Pappalardo, Giuseppe; Di Natale, Giuseppe; Rizzarelli, Enrico; Sóvágó, Imre


    Mixed metal copper(II)-nickel(II) and copper(II)-zinc(II) complexes of four peptide fragments of human prion protein have been studied by potentiometric, UV-vis and circular dichroism spectroscopic techniques. One peptide contained three histidyl residues: HuPrP(84-114) with H85 inside and H96, H111 outside the octarepeat domain. The other three peptides contained two histidyl residues; H96 and H111 for HuPrP(91-115) and HuPrP(84-114)H85A while HuPrP(84-114)H96A contained the histidyl residues at positions 85 and 111. It was found that both histidines of the latter peptides can simultaneously bind copper(II) and nickel(II) ions and dinuclear mixed metal complexes can exist in slightly alkaline solution. One molecule of the peptide with three histidyl residues can bind two copper(II) and one nickel(II) ions. H85 and H111 were identified as the major copper(II) and H96 as the preferred nickel(II) binding sites in mixed metal species. The studies on the zinc(II)-PrP peptide binary systems revealed that zinc(II) ions can coordinate to the 31-mer PrP peptide fragments in the form of macrochelates with two or three coordinated imidazol-nitrogens but the low stability of these complexes cannot prevent the hydrolysis of the metal ion in slightly alkaline solution. These data provide further support for the outstanding affinity of copper(II) ions towards the peptide fragments of prion protein but the binding of nickel(II) can significantly modify the distribution of copper(II) among the available metal binding sites.

  14. A simple and sensitive spectrofluorimetric method for the determination of furosemide using zinc(II)-1,4-bis(imidazol-1-ylmethyl)benzene complexes.

    Liu, Yali; Wang, Huijuan; Wang, Jian; Li, Yuanfang


    A novel spectrofluorometric method for the determination of furosemide (FUR) is described. The method is based on enhancement of fluorescence emission of FUR in the presence of zinc (II) complexes of 1,4-bis(imidazol-1-ylmethyl)benzene. Under optimum conditions, the enhanced fluorescence intensity is linearly related to the concentration of FUR. The proposed method has been successfully applied to the determination of FUR in pharmaceutical preparations. The possible mechanism of this reaction is discussed briefly based on data from fluorescence spectroscopy, UV-vis absorption and infrared spectroscopy. Copyright © 2012 John Wiley & Sons, Ltd.

  15. Syntheses, Characterizations, Crystal Structures and Antibacterial Activities of Two Zinc(Ⅱ) Complexes with a Schiff Base Derived from o-Vanillin and p-Toluidine


    Two new zinc(Ⅱ) complexes, [Zn2L2aCl4]·2[ZnL(CH3OH)Cl2] 1 and [ZnL2(NO3)2] 2,were synthesized by reacting ZnX2·nH2O (X = Cl-, NO3-) and a Schiff base ligand 2-[(4-me-thylphenylimino)methyl]-6-methoxyphenol (C15H15NO2, L) which was obtained by the condensation of o-vanillin (2-hydroxy-3-methoxybenzaldehyde) with p-toluidine. Both 1 and 2 were characterized by single-crystal X-ray diffraction technique, elemental analysis, molar conductance, FT-IR, UV-Vis,1H-NMR spectra and thermogravimetric analysis. The Schiff base ligand and its zinc(Ⅱ) complexes have been tested in vitro to evaluate their antibacterial activity against bacteria, viz., Escherichia Coli,Staphylococcus aureus and Bacillus Subtilis. The results show that these complexes have higher activity than the corresponding free Schiff base ligand against the same bacteria.

  16. Cobalt, nickel, copper and zinc complexes with 1,3-diphenyl-1H-pyrazole-4-carboxaldehyde Schiff bases: antimicrobial, spectroscopic, thermal and fluorescence studies.

    Singh, Kiran; Kumar, Yogender; Puri, Parvesh; Kumar, Mahender; Sharma, Chetan


    Two new Schiff bases of 1,3-diphenyl-1H-pyrazole-4-carboxaldehyde and 4-amino-5-mercapto-3-methyl/H-1,2,4-triazole [HL(1-2)] and their Cobalt, Nickel, Copper and Zinc complexes have been synthesized and characterized by elemental analyses, spectral (UV-vis, IR, (1)H NMR, Fluorescence) studies, thermal techniques and magnetic measurements. A square planar geometry for Cu(II) and octahedral geometry for Co(II), Ni(II) and Zn(II) complexes have been proposed. In order to evaluate the biological activity of Schiff bases and to assess the role of metal ion on biological activity, the pyrazole Schiff bases and their metal complexes have been studied in vitro antibacterial against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and antifungal against Aspergillus niger, and Aspergillus flavus. In most of the cases higher activity was exhibited upon coordination with metal ions.

  17. The synthesis and characterization of complexes of zinc(II, cadmium(II, platinum(II and palladium(II with potassium 3-dithiocarboxy-3-aza-5-aminopentanoate



    Full Text Available Complexes of zinc(II, cadmium(II, platinum(II and palladium(II with a new polydentate dithiocarbamate ligand, 3-dithiocarboxy-3-aza-5-aminopentanoate (daap-, of the type M(daap2·nH2O (M = Zn(II, Cd(II, n = 2, or M = Pt(II, Pd(II, n = 0, have been prepared and characterized by elemental analysis, IR and UV/VIS spectroscopy, as well as magnetic measurements. The spectra of the complexes suggest a bidentate coordination of the daap- ligand to the metal ions via the sulfur atoms of the deprotonated dithiocarbamato group. The fact that under the same experimental conditions its S-methyl ester does not form complexes could be taken as proof of the suggested coordination mode.

  18. Zinc(II) complexes containing bis-benzimidazole derivatives as a new class of apoptosis inducers that trigger DNA damage-mediated p53 phosphorylation in cancer cells.

    Liu, Shenggui; Cao, Wenqiang; Yu, Lianling; Zheng, Wenjie; Li, Linlin; Fan, Cundong; Chen, Tianfeng


    In the present study, two zinc(II) complexes containing bis-benzimidazole derivatives, Zn(bpbp)Cl2 (1) and [Zn(bpbp)2](ClO4)2·CH3CH2OH·H2O (2) (bpbp = 2,6-bis(1-phenyl-1H-benzo[d]imidazol-2-yl)pyridine), have been designed, synthesized and evaluated for their in vitro anticancer activities. The underlying molecular mechanisms through which they caused the cancer cell death were also elucidated. The complexes were identified as potent antiproliferative agents against a panel of five human cancer cell lines by comparing with cisplatin. Complex 2 demonstrated dose-dependent growth inhibition on MCF-7 human breast carcinoma cells with IC50 at 2.9 μM. Despite this potency, the complexes possessed great selectivity between human cancer cells and normal cells. Induction of apoptosis in MCF-7 cells by complex 2 was evidenced by accumulation of sub-G1 cell population, DNA fragmentation and nuclear condensation. Further investigation on intracellular mechanisms revealed that complex 2 was able to induce p53-dependent apoptosis in cancer cells by triggering DNA damage. On the basis of this evidence, we suggest that Zn(II) complexes containing bis-benzimidazole derivatives may be candidates for further evaluation as chemotherapeutic agents for human cancers.

  19. Syntheses and crystal structures of two mixed-ligand dimeric zinc complexes containing a dithiol ligand and an open chain crown ether ligand with terminal quinolyl groups

    Li, Cheng-Juan; Dou, Jian-Min; Li, Da-Cheng; Wang, Da-Qi


    Two mixed-ligand zinc complexes Zn(L)(H 2O)(mnt) ( 1) and Zn(L)(H 2O)(i-mnt) ( 2) (where L=2,6-bis(8'-quinoylyloxymethyl)pyridine, mnt =1,2-dicyanoethylene-1,2-ditholate and i-mnt =1,1-dicyanoethylene-2,2-ditholate) have been synthesized and characterized by elemental analysis, FT-IR spectra, and single-crystal X-ray diffraction. Complexes 1 and 2 both crystallize in the monoclinic system, space group C2/ c and each displays a distorted trigonal bipyramidal around zinc atom. The coordination sphere of Zn is NO 2S 2 type, where the dithiol ligand (mnt or i-mnt) and one terminal quinolyl group of L act as the chelate S, S and N, O donor sets, respectively, besides the coordination water molecules. Furthermore, there are intramolecular H-bonds occurred between the coordination water molecule and the N2, N3 atoms of the L and the molecules of 1 and 2 both form the dimers through the intermolecular π-π stacking interactions.

  20. A novel zinc finger protein Zfp277 mediates transcriptional repression of the Ink4a/arf locus through polycomb repressive complex 1

    Negishi, Masamitsu; Saraya, Atsunori; Mochizuki, Shinobu


    . METHODOLOGY/PRINCIPAL FINDINGS: We examined the function of Zinc finger domain-containing protein 277 (Zfp277), a novel zinc finger protein that interacts with the PcG protein Bmi1. Zfp277 binds to the Ink4a/Arf locus in a Bmi1-independent manner and interacts with polycomb repressor complex (PRC) 1 through......BACKGROUND: Polycomb group (PcG) proteins play a crucial role in cellular senescence as key transcriptional regulators of the Ink4a/Arf tumor suppressor gene locus. However, how PcG complexes target and contribute to stable gene silencing of the Ink4a/Arf locus remains little understood...... direct interaction with Bmi1. Loss of Zfp277 in mouse embryonic fibroblasts (MEFs) caused dissociation of PcG proteins from the Ink4a/Arf locus, resulting in premature senescence associated with derepressed p16(Ink4a) and p19(Arf) expression. Levels of both Zfp277 and PcG proteins inversely correlated...

  1. Administration of zinc complex of acetylsalicylic acid after the onset of myocardial injury protects the heart by upregulation of antioxidant enzymes.

    Korkmaz-Icöz, Sevil; Atmanli, Ayhan; Radovits, Tamás; Li, Shiliang; Hegedüs, Peter; Ruppert, Mihály; Brlecic, Paige; Yoshikawa, Yutaka; Yasui, Hiroyuki; Karck, Matthias; Szabó, Gábor


    We recently demonstrated that the pre-treatment of rats with zinc and acetylsalicylic acid complex in the form of bis(aspirinato)zinc(II) [Zn(ASA)2] is superior to acetylsalicylic acid in protecting the heart from acute myocardial ischemia. Herein, we hypothesized that Zn(ASA)2 treatment after the onset of an acute myocardial injury could protect the heart. The rats were treated with a vehicle or Zn(ASA)2 after an isoproterenol injection. Isoproterenol-induced cardiac damage [inflammatory infiltration into myocardial tissue, DNA-strand breakage evidenced by TUNEL-assay, increased 11-dehydro thromboxane (TX)B2-levels, elevated ST-segment, widened QRS complex and prolonged QT-interval] was prevented by the Zn(ASA)2 treatment. In isoproterenol-treated rats, load-independent left ventricular contractility parameters were significantly improved after Zn(ASA)2. Furthermore, Zn(ASA)2 significantly increased the myocardial mRNA-expression of superoxide dismutase-1, glutathione peroxidase-4 and decreased the level of Na(+)/K(+)/ATPase. Postconditioning with Zn(ASA)2 protects the heart from acute myocardial ischemia. Its mechanisms of action might involve inhibition of pro-inflammatory prostanoids and upregulation of antioxidant enzymes.

  2. Design, synthesis and physico-chemical investigation of a dinuclear zinc(II) complex with a novel ‘end-off’ compartmental ligand

    Anil D Naik; Vidyanand K Revankar


    A novel dinucleating pentadentate Schiff base, resulting from the condensation of 2,6-diformyl--cresol and N-methyl-indolyl-3-thiohydrazide, and its Zn complex have been prepared and characterized on the basis of elemental analysis, IR, UV-Visible, 1H NMR and 13C NMR studies. The ligand is acyclic and consists of a phenolate head unit, with two inbuilt azomethine shoulders and two indole thiohydrazide arms forming SNONS coordinating sites. NMR and IR spectral studies show that the ligand exists in thioketo form. Each Zn ion in the dinuclear core is in tetrahedral environment with endogenous phenolate bridging and exogenous acetate bridging. The zinc complex in DMF exhibits fluorescence.

  3. New tetradentate N,N,N,N-chelating α-diimine ligands and their corresponding zinc and nickel complexes: synthesis, characterisation and testing as olefin polymerisation catalysts.

    Li, Lidong; Gomes, Clara S B; Gomes, Pedro T; Duarte, M Teresa; Fan, Zhiqiang


    A series of zinc complexes of the general formula {[ZnCl(ArN=C(An)-C(An)=NAr)](+)}(2)[Zn(2)Cl(6)](2-) (where Ar = 2-(1-benzyl-1H-1,2,3-triazol-4-yl)phenyl 2a, 2-(1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)phenyl 2b, 2-(1-phenyl-1H-1,2,3-triazol-4-yl)phenyl 2c; An = acenaphthene backbone) were prepared by the condensation of acenaphthenequinone with the corresponding o-triazolyl-substituted anilines (2-(1-benzyl-1H-1,2,3-triazol-4-yl)aniline 1a, 2-(1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)aniline 1b, 2-(1-phenyl-1H-1,2,3-triazol-4-yl)aniline 1c) which were formed by the copper(I)-catalyzed Huisgen[3+2] dipolar cycloaddition between 2-ethynylaniline and the corresponding azides in high yields, using anhydrous ZnCl(2) as the metal template, in boiling glacial acetic acid. Zinc complexes of the type [ZnCl(ArN=C(An)-C(An)=NAr)](+)[ZnCl(3)(NCCH(3))](-) (4a-c) were synthesized by crystallisation of the corresponding complexes 2a-c in acetonitrile, at -20 °C. After removal of zinc dichloride from complexes 2a-c by the addition of potassium oxalate, in dichloromethane, the tetradentate N,N,N,N-chelating α-diimine ligands of the type ArN=C(An)-C(An)=NAr (5a-c) were obtained. The new ligand precursors and zinc complexes were characterised by elemental analysis, (1)H and (13)C{(1)H} NMR spectroscopy, two-dimensional NMR spectroscopy, and X-ray diffraction. Reaction of the ligand precursors 5a-c with [NiBr(2)(DME)], in dichloromethane, gave nickel complexes of the type [NiBr(2)(ArN=C(An)-C(An)=NAr)] (6a-c). The results of single crystal X-ray diffraction characterisation and magnetic susceptibility measurements demonstrated that nickel complexes 6a-c possess octahedral geometries around the nickel atoms with variable configurations, the Br atoms of which can be ionized when dissolved in methanol. In preliminary catalytic tests, complexes 6a-c revealed to be active as catalysts for the polymerisation of norbornene and styrene, when activated by cocatalyst MAO. The characterisation

  4. Synthesis, Crystal Structure and Fluorescence Property of a Five- and Six-coordinated Trinuclear Zinc(II) Complex:{[ZnL(OAc)]2Zn}·CH3COCH3

    DONG,Wen-Kui; ZHANG,Yan-Ping; ZHAO,Chun-Yu; TANG,Xiao-Lu; L(U),Zhong-Wu; ZOU,Zheng


    A novel linear trinuclear zinc(II) complex, {[ZnL(OAc)]2Zn}·CH3COCH3 (H2L: ethylenedioxybis(5-bromo-2-hydroxybenzylideneamino)), has been synthesized and structurally characterized. X-ray crystal structure of the complex reveals that three zinc(II) ions are coordinated by two tetradentate L2- units and two acetate ions acting as bridging groups. The coordination geometry around the terminal Zn(1) or Zn(1)#1 atom approaches a distorted square pyramid. The coordination sphere of the central Zn(2) atom constitutes a slightly distorted octahedral geometry. The blue-green emission from the zinc(II) complex can be observed, where the maximum emission wavelength is at 464 nm.

  5. Zinc naphthalenedicarboxylate coordination complex: A promising anode material for lithium and sodium-ion batteries with good cycling stability.

    Fei, Hailong; Feng, Wenjing; Xu, Tan


    It is important to discover new, cheap and environmental friendly electrode materials with high capacity and good cycling stability for lithium and sodium-ion batteries. Zinc 1,4-naphthalenedicarboxylate was firstly found to be stable anode materials for lithium and sodium-ion batteries. The discharge capacity can be up to 468.9mAhg(-1) after 100 cycles at a current density of 100mAg(-1) for lithium-ion batteries, while the second discharge capacity of 320.7mAhg(-1) was achieved as anode materials for sodium-ion batteries. A possible electrochemical reaction mechanism was discussed.

  6. Novel Zinc(II) Complexes [Zn(atc-Et)2] and [Zn(atc-Ph)2]: In Vitro and in Vivo Antiproliferative Studies

    Lopes, Erica de O.; de Oliveira, Carolina G.; da Silva, Patricia B.; Eismann, Carlos E.; Suárez, Carlos A.; Menegário, Amauri A.; Leite, Clarice Q. F.; Deflon, Victor M.; Pavan, Fernando R.


    Cisplatin and its derivatives are the main metallodrugs used in cancer therapy. However, low selectivity, toxicity and drug resistance are associated with their use. The zinc(II) (ZnII) thiosemicarbazone complexes [Zn(atc-Et)2] (1) and [Zn(atc-Ph)2] (2) (atc-R: monovalent anion of 2-acetylpyridine N4-R-thiosemicarbazone) were synthesized and fully characterized in the solid state and in solution via elemental analysis, Fourier transform infrared (FTIR), ultraviolet-visible (UV-Vis) and proton nuclear magnetic resonance (1H NMR) spectroscopy, conductometry and single-crystal X-ray diffraction. The cytotoxicity of these complexes was evaluated in the HepG2, HeLa, MDA-MB-231, K-562, DU 145 and MRC-5 cancer cell lines. The strongest antiproliferative results were observed in MDA-MB-231 and HepG2 cells, in which these complexes displayed significant selective toxicity (3.1 and 3.6, respectively) compared with their effects on normal MRC-5 cells. In vivo studies were performed using an alternative model (Artemia salina L.) to assure the safety of these complexes, and the results were confirmed using a conventional model (BALB/c mice). Finally, tests of oral bioavailability showed maximum plasma concentrations of 3029.50 µg/L and 1191.95 µg/L for complexes 1 and 2, respectively. According to all obtained results, both compounds could be considered as prospective antiproliferative agents that warrant further research. PMID:27213368

  7. Bis(3-methyl-2-pyridyl)ditelluride and pyridyl tellurolate complexes of zinc, cadmium, mercury: Synthesis, characterization and their conversion to metal telluride nanoparticles.

    Kedarnath, G; Jain, Vimal K; Wadawale, Amey; Dey, Gautam K


    Treatment of an acetonitrile solution of metal chloride with bis(3-methyl-2-pyridyl)ditelluride, [Te(2)(pyMe)(2)], in the same solvent yielded complexes of composition [MCl(2){Te(2)(pyMe)(2)}] (M = Zn or Cd) whereas reactions of [MCl(2)(tmeda)] with NaTepyR (R = H or Me) gave tellurolate complexes of the general formula [M(TepyR)(2)] (M = Cd or Hg). When the cadmium complex [Cd(Tepy)(2)] was crystallized in the presence of excess tmeda, [Cd(Tepy)(2)(tmeda)] was formed exclusively. These complexes were characterized by elemental analyses, uv-vis, (1)H NMR data. The crystal structures of [ZnCl(2){Te(2)(pyMe)(2)}] and [Cd(Tepy)(2)(tmeda)] were established by single crystal X-ray diffraction. In the former zinc is coordinated to nitrogen atoms of the pyridyl group, while in the latter the coordination environment around tetrahedral cadmium is defined by the two neutral nitrogen atoms of tmeda, and two pyridyl tellurolate ligands. Thermal behavior of some of these complexes was studied by thermogravimetric analysis. Pyrolysis of [M(Tepy)(2)] in a furnace or in coordinating solvents such as hexadecylamine/tri-n-octylphosphine oxide (HDA/TOPO) at 350 and 160 degrees C, respectively gave MTe nanoparticles, which were characterized by uv-vis, photoluminiscence, XRD, EDAX and TEM.

  8. Synthesis, characterization, spectroscopic and theoretical studies of new zinc(II), copper(II) and nickel(II) complexes based on imine ligand containing 2-aminothiophenol moiety

    Shafaatian, Bita; Mousavi, S. Sedighe; Afshari, Sadegh


    New dimer complexes of zinc(II), copper(II) and nickel(II) were synthesized using the Schiff base ligand which was formed by the condensation of 2-aminothiophenol and 2-hydroxy-5-methyl benzaldehyde. This tridentate Schiff base ligand was coordinated to the metal ions through the NSO donor atoms. In order to prevent the oxidation of the thiole group during the formation of Schiff base and its complexes, all of the reactions were carried out under an inert atmosphere of argon. The X-ray structure of the Schiff base ligand showed that in the crystalline form the SH groups were oxidized to produce a disulfide Schiff base as a new double Schiff base ligand. The molar conductivity values of the complexes in dichloromethane implied the presence of non-electrolyte species. The fluorescence properties of the Schiff base ligand and its complexes were also studied in dichloromethane. The products were characterized by FT-IR, 1H NMR, UV/Vis spectroscopies, elemental analysis, and conductometry. The crystal structure of the double Schiff base was determined by single crystal X-ray diffraction. Furthermore, the density functional theory (DFT) calculations were performed at the B3LYP/6-31G(d,p) level of theory for the determination of the optimized structures of Schiff base complexes.

  9. Fundamental insights into conformational stability and orbital interactions of antioxidant (+)-catechin species and complexation of (+)-catechin with zinc(II) and oxovanadium(IV)

    Yasarawan, Nuttawisit; Thipyapong, Khajadpai; Sirichai, Somsak; Ruangpornvisuti, Vithaya


    Conformational stability of (+)-catechin species in water has been examined with density functional theory, associated with the polarizable continuum model (PCM) of solvation. Factors such as electron delocalization, lone-pair electron donation and intramolecular hydrogen bonding substantially contribute to the conformational stabilization. Upon deprotonation, the HOMO and LUMO energies for (+)-catechin are both elevated; the energy gaps for the deprotonated species are narrower than the energy gap for the neutral species. The preferential deprotonation occurs at the C3'-, C5-, C7- and C4'-OH groups successively. The pKa value at 9.3 predicted for the most acidic OH group agrees well with previous experimental data; however the values are overestimated for the less acidic OH groups due to limitations of the PCM for charged solutes and/or complex nature of true deprotonation pathways. Formation of hydrogen radicals should be promoted at high pH values following the bond dissociation enthalpies. Complexation of (+)-catechin with either zinc(II) or oxovanadium(IV) is favored at the 1:1 metal-to-ligand (M:L) mole ratio, with the oxovanadium(IV) complex showing higher reaction preference. At M:L = 1:2, formation of two isomeric complexes are plausible for each type of metal ion. Effects of stoichiometry and isomerism on the computational spectral features of the possibly formed metal complexes have been described.

  10. Chemical-Biological Properties of Zinc Sensors TSQ and Zinquin: Formation of Sensor-Zn-Protein Adducts versus Zn(Sensor)2 Complexes.

    Nowakowski, Andrew B; Meeusen, Jeffrey W; Menden, Heather; Tomasiewicz, Henry; Petering, David H


    Fluorescent zinc sensors are the most commonly used tool to study the intracellular mobile zinc status within cellular systems. Previously, we have shown that the quinoline-based sensors Zinquin and 6-methoxy-8-p-toluenesulfonamido-quinoline (TSQ) predominantly form ternary adducts with members of the Zn-proteome. Here, the chemistries of these sensors are further characterized, including how Zn(sensor)2 complexes may react in an intracellular environment. We demonstrate that these sensors are typically used in higher concentrations than needed to obtain maximum signal. Exposing cells to either Zn(Zinquin)2 or Zn(TSQ)2 resulted in efficient cellular uptake and the formation of sensor-Zn-protein adducts as evidenced by both a fluorescence spectral shift toward that of ternary adducts and the localization of the fluorescence signal within the proteome after gel filtration of cellular lysates. Likewise, reacting Zn(sensor)2 with the Zn-proteome from LLC-PK1 cells resulted in the formation of sensor-Zn-protein ternary adducts that could be inhibited by first saturating the Zn- proteome with excess sensor. Further, a native SDS-PAGE analysis of the Zn-proteome reacted with either the sensor or the Zn(sensor)2 complex revealed that both reactions result in the formation of a similar set of sensor-Zn-protein fluorescent products. The results of this experiment also demonstrated that TSQ and Zinquin react with different members of the Zn-proteome. Reactions with the model apo-Zn-protein bovine serum albumin showed that both Zn(TSQ)2 and Zn(Zinquin)2 reacted to form ternary adducts with its apo-Zn-binding site. Moreover, incubating Zn(sensor)2 complexes with non-zinc binding proteins failed to elicit a spectral shift in the fluorescence spectrum, supporting the premise that blue-shifted emission spectra are due to sensor-Zn-protein ternary adducts. It was concluded that Zn(sensors)2 species do not play a significant role in the overall reaction between these sensors and

  11. Influence of zinc concentration on structure, complex permittivity and permeability of Ni–Zn ferrites at high frequency

    Jiang, Nan-Nan; Yang, Yang; Zhang, Yu-Xiang [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710119 (China); Zhou, Jian-Ping, E-mail: [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710119 (China); Liu, Peng [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710119 (China); Deng, Chao-Yong [Department of Electronic Science, Key Laboratory of Functional Composite Materials of Guizhou Province, Guizhou University, Guiyang 550025 (China)


    Polycrystalline soft magnetic nickel–zinc ferrites with chemical composition Ni{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4}, where x=0, 0.2, 0.4, 0.6, 0.65, 0.7, 0.75, and 0.8, were prepared by solid state reaction method. We researched the effect of zinc concentration on the lattice parameter, crystal morphology and electromagnetic properties at high frequency. Results show that ε′ and ε″ decline with increasing frequency until they reach almost constants over 3 MHz to 1 GHz. The dielectric constant achieves a maximum when the Zn concentration is 0.8. The value of ε′ slightly declines with increasing frequency in the range of 2–18 GHz. The spectra of the permeability displays a relaxation resonance for the ferrites with x=0, 0.2, and 0.4 in 3 MHz to 1 GHz frequency range. The permeability is ruled by Snoek's law, which results in the values of μ′ decreased fast below 2 GHz and smaller than 1 above 2 GHz. The value of μ′ reaches maximum and μ″ shows minimum for the samples around x=0.75 in 2–18 GHz range. The magnetic permeability μ′ decreases in an external magnetic field, and shows two resonance peaks corresponding to domain wall and spin rotation resonance. The resonance peaks shift to higher frequency with increasing the external magnetic field. But the permeability has no clear response for magnetic field when zinc concentration is much higher. - Graphical abstract: (a) Resonance frequencies for the domain wall and spin components as a function of external magnetic field and (b) illustration of magnetization process. - Highlights: • A detailed study on permittivity and permeability of Ni–Zn ferrites in 3 MHz to 18 GHz. • Magnetic field inspires two resonance peaks in permeability. • The resonance peaks shift to higher frequency with the magnetic field.

  12. Synthesis, spectral characterization and biological activity of zinc(II) complexes with 3-substituted phenyl-4-amino-5-hydrazino-1, 2, 4-triazole Schiff bases.

    Singh, A K; Pandey, O P; Sengupta, S K


    New Zn(II) complexes have been synthesized by the reactions of zinc(II) acetate with Schiff bases derived from 3-substituted phenyl-4-amino-5-hydrazino-1, 2, 4-triazole and benzaldehyde, 2-hydroxyacetophenone or indoline-2,3-dione. All these complexes are soluble in DMF and DMSO; low molar conductance values indicate that they are non-electrolytes. Elemental analyses suggest that the complexes have 1:1 stoichiometry of the type [ZnL(H(2)O)(2)], [ZnL'(OAc)(2)(H(2)O)(2)] (L=dianionic Schiff bases derived from 3-(substituted phenyl)-4-amino-5-hydrazino-1, 2, 4-triazole and 2-hydroxyacetophenone or indoline-2,3-dione; L'=neutral Schiff bases derived from 3-(substituted phenyl)-4-amino-5-hydrazino-1, 2, 4-triazole and benzaldehyde) and they were characterized by FT-IR, (1)H NMR, (13)C NMR and FAB mass. All these Schiff bases and their complexes have also been screened for their antibacterial activities against Bacillus subtilis, Escherichia coli and antifungal activities against Colletotrichum falcatum, Aspergillus niger, Fusarium oxysporium and Carvularia pallescence by petriplates methods.

  13. A new route for visible/near-infrared-light-driven H2 production over titania: Co-sensitization of surface charge transfer complex and zinc phthalocyanine

    Zhang, Xiaohu; Peng, Bosi; Peng, Tianyou; Yu, Lijuan; Li, Renjie; Zhang, Jing


    This work introduces a new strategy for visible/near-infrared (NIR) light responsive H2 production over TiO2 nanoparticles co-sensitized with zinc phthalocyanine derivative (Zn-tri-PcNc) and surface ligand-to-metal charge transfer (LMCT) complex, which is in situ formed on the TiO2 nanoparticles' surfaces by using ascorbic acid (AA). The in situ formed surface LMCT complex (AA-TiO2) exhibits obvious visible-light-responsive photoactivity (126.2 μmol/h) for H2 production with a high apparent quantum yield (AQY) of 16.1% at 420 nm monochromatic light irradiation. Moreover, the co-sensitized TiO2 nanoparticles (Zn-tri-PcNc-TiO2-AA) shows a much higher photoactivity (162.2 μmol/h) for H2 production than the surface LMCT complex, and broader spectral responsive region (400-800 nm) with a relatively high AQY value (0.97%) at 700 nm monochromatic light irradiation. The present result reveals a possible substitute for the conventional Ru(II)-bipyridyl complexes or organic dyes as sensitizer of semiconductors in the field of solar fuel conversion.

  14. Zinc complexing ligands in rivers in pristine peatland areas in Borneo, and rivers with agricultural and industrial anthropogenic influence in Tropical South East Asia: Elucidating the connection to oceanic regional and global distributions of Zinc ligands and bioavailable Zinc

    Carrasco, G. G.; Chen, M.


    Organic complexing ligands dominate the chemical speciation of Zn in seawater globally, affecting its bioavailability and regulating its micronutrient role. We have shown that intermediate water masses in the West Pacific indicate a connection between point sources related to marginal seas, riverine matter, benthic fluxes, and continental shelves, with ligand concentrations and binding strengths evolving along water mass trajectories. Here we will present results from recent studies in tropical South East Asia that explore rivers in pristine peatland areas in Borneo, and rivers near and around agricultural and industrial anthropogenic influence in Borneo, Singapore and Malaysia, with the aim of elucidating the importance of relatively fresh natural and agricultural land-based plant material and industrial anthropogenic material in the organic matter mix that the ligands are a part of. These results track the ligand concentration and binding strength of different sources of Zn complexing ligands obtained using ASV and modern comprehensive mathematical methods We will compare records of humic substances from coral cores near the mouth of these rivers, with the goal of ascertaining a possible link of humic substance concentrations and metal complexing ligands in the region. We will compare the results from these large sources of organic matter with the ligands observed in continental shelves, where the organic matter has suffered biochemical processes, with ligands observed in the West Pacific, after decades of bacterial respiration while travelling along water masses. We aim to compare these ligand in order to assess the relevance of these sources of complexing ligands to regulate regional and global distribution of Zn ligands and its bioavailable concentrations.

  15. Binding of Cationic Bis-porphyrins Linked with p- or m-Xylylenediamine and Their Zinc(II Complexes to Duplex DNA

    Tadayuki Uno


    Full Text Available Spectroscopic, viscometric, and molecular docking analysis of binding of cationic bis-porphyrins linked with p- or m-xylylenediamine (H2pXy and H2mXy and their zinc(II complexes (ZnpXy and ZnmXy to duplex DNA are described. H2pXy and H2mXy bound to calf thymus DNA (CTDNA stronger than unichromophoric H2TMPyP, and showed exciton-type induced circular dichroism spectra of their Soret bands. The H2TMPyP-like units of the metal-free bis-porphyrins did not intercalate into CTDNA, and thus the binding mode is outside binding with intramolecular stacking. ZnpXy showed favorable binding to A·T over G·C region, and should lie in the major groove of A·T region.

  16. Formation of a unique zinc carbamate by CO2 fixation: implications for the reactivity of tetra-azamacrocycle ligated Zn(II) complexes.

    Notni, Johannes; Schenk, Stephan; Görls, Helmar; Breitzke, Hergen; Anders, Ernst


    The macrocyclic ligand [13]aneN 4 ( L1, 1,4,7,10-tetra-azacyclotridecane) was reacted with Zn(II) perchlorate and CO 2 in an alkaline methanol solution. It was found that, by means of subtle changes in reaction conditions, two types of complexes can be obtained: (a) the mu 3 carbonate complex 1, {[Zn( L1)] 3(mu 3-CO 3)}(ClO 4) 4, rhombohedral crystals, space group R3 c, with pentacoordinate zinc in a trigonal bipyramidal enviroment, and (b) an unprecedenced dimeric Zn(II) carbamate structure, 2, [Zn( L2)] 2(ClO 4) 2, monoclinic crystals, space group P2 1/ n. The ligand L2 (4-carboxyl-1,4,7,10-tetra-azacyclotridecane) is a carbamate derivative of L1, obtained by transformation of a hydrogen atom of one of the NH moieties into carbamate by means of CO 2 uptake. In compound 2, the distorted tetrahedral Zn(II) coordinates to the carbamate moiety in a monodentate manner. Most notably, carbamate formation can occur upon reaction of CO 2 with the [Zn L1] (2+) complex, which implicates that a Zn-N linkage is cleaved upon attack of CO 2. Since complexes of tetra-azamacrocycles and Zn(II) are routinely applied for enzyme model studies, this finding implies that the Zn-azamacrocycle moiety generally should no longer be considered to play always only an innocent role in reactions. Rather, its reactivity has to be taken into account in respective investigations. In the presence of water, 2 is transformed readily into carbonate 1. Both compounds have been additionally characterized by solid-state NMR and infrared spectroscopy. A thorough comparison of 1 with related azamacrocycle ligated zinc(II) carbonates as well as a discussion of plausible reaction paths for the formation of 2 are given. Furthermore, the infrared absorptions of the carbamate moiety have been assigned by calculating the vibrational modes of the carbamate complex using DFT methods and the vibrational spectroscopy calculation program package SNF.

  17. A new air-stable zinc complex based on a 1,2-phenylene-diimino-2-cyanoacrylate ligand as an efficient catalyst of the epoxide-CO2 coupling.

    Fuchs, M A; Staudt, S; Altesleben, C; Walter, O; Zevaco, T A; Dinjus, E


    A novel zinc complex based on a diethyl 1,2-phenylene-diimino-2-cyanoacrylate ligand is a very efficient catalyst in the conversion of epoxides with CO2 to organic carbonates, in the case of propylene carbonate also under mild reaction conditions. Using cyclohexene oxide leads to the formation of alternating aliphatic polycarbonates in good yields.

  18. Synthesis, Crystal Structure and Luminescent Properties of a Novel Zinc(Ⅱ) Complex of N-Acetyl-L-glutamic Acid and Imidazole Ligands

    CHENG Meng-Qi; MA Lu-Fang; WANG Li-Ya; WANG Jian-Ge


    A novel complex (Zn(Im)2(A-glu)·0.5H2O (Im = imidazole, A-glu = N-acetyl- L-glutamic acid) has been synthesized from the reaction of A-glu with Zn(CH3COO)2(2H2O in the presence of Im at 65 ℃, and structurally characterized by single-crystal X-ray diffraction. The complex crystallizes in tetragonal, space group P43212 with a = b = 8.9078(6), c = 43.458(6) (A), C26H36N10O11Zn2, Mr = 795.39, V = 3448.3(6) (A)3, Dc = 1.532 g/cm3, Z = 4, μ(MoK() = 1.461 mm(1, F(000) = 1640, the final R = 0.0453 and wR = 0.0992. X-ray analysis reveals that the crystal structure is constructed by mixed ligands. A-glu adopts the bis-monodentate coordination mode linking two adjacent metal ions to form a one-dimensional chain. Zinc(Ⅱ) ions are four-coordinated with a distorted tetrahedral geometry. Luminescent properties of the complex have been inves- tigated.

  19. Synthesis and characterization of an effective organic/inorganic hybrid green corrosion inhibitive complex based on zinc acetate/Urtica Dioica

    Salehi, E.; Naderi, Reza; Ramezanzadeh, B.


    This study aims at synthesis and characterization of an effective corrosion inhibitive complex based on zinc acetate/Urtica Dioica (ZnA-U.D) for corrosion protection of mild steel in chloride solution. The chemical structure and morphology of the complex were characterized by Fourier transform infrared spectroscopy (FT-IR), UV-vis, thermal gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The corrosion protection performance of the mild steel samples dipped in 3.5 wt.% NaCl solutions with and without ZnA-U.D extract was investigated by visual observations, open circuit potential (OCP) measurements, electrochemical impedance spectroscopy (EIS) and polarization test. Results revealed that the ZnA successfully chelated with organic inhibitive compounds (i.e Quercetin, Quinic acid, Caffeic acid, Hystamine and Serotonin) present in the U.D extract. The electrochemical measurements revealed the effective inhibition action of ZnA-U.D complex in the sodium chloride solution on the mild steel. The synergistic effect between Zn2+ and organic compounds present in the U.D extract resulted in protective film deposition on the steel surface, which was proved by SEM and XPS analyses.

  20. Synthesis, Crystal Structure and Kinetic Mechanism of Thermal Decomposition of a Zinc(II) Complex with N-Salicylidene-p-toluidine

    ZHAO Guo-Liang; WEN Yi-Hang; YU Yu-Ye


    The title complex, Zn(C14H13NO)2Cl2 1, has been synthesized by the reaction of zinc chloride with Schiff base ligand N-salicylidene-p-toluidine and its structure was determined by single-crystal X-ray diffraction. The crystal is of monoclinic, space group Cc with a = 14.896(3), b = 12.506(2), c = 15.352(3)(A), β = 114.711(4)o, V = 2598.0(8) (A)3, C28H26ZnCl2N2O2, Mr = 558.80, Z = 4, Dc = 1.429 g/cm3, μ = 1.179 mm-1, Flack parameter = 0.027(19), F(000) = 1152, R = 0.0709 and wR = 0.1041 for 3117 observed reflections (I > 2σ(I)). In complex 1, the center Zn ion is four-coordinated by two O atoms from two Schiff base ligands and two Cl atoms in a distorted tetrahedral geometry. Additionally, the thermal decomposition of complex 1 as well as its kinetic mechanisms and equations is studied under the non-isothermal integral and differential methods in air by TG-DTG curves.

  1. A mononuclear zinc(II) complex with piroxicam: crystal structure, DNA- and BSA-binding studies; in vitro cell cytotoxicity and molecular modeling of oxicam complexes.

    Jannesari, Zahra; Hadadzadeh, Hassan; Amirghofran, Zahra; Simpson, Jim; Khayamian, Taghi; Maleki, Batool


    A new mononuclear Zn(II) complex, trans-[Zn(Pir)2(DMSO)2], where Pir(-) is 4-hydroxy-2-methyl-N-2-pyridyl-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide (piroxicam), has been synthesized and characterized. The crystal structure of the complex was obtained by the single crystal X-ray diffraction technique. The interaction of the complex with DNA and BSA was investigated. The complex interacts with FS-DNA by two binding modes, viz., electrostatic and groove binding (major and minor). The microenvironment and the secondary structure of BSA are changed in the presence of the complex. The anticancer effects of the seven complexes of oxicam family were also determined on the human K562 cell lines and the results showed reasonable cytotoxicities. The interactions of the oxicam complexes with BSA and DNA were modeled by molecular docking and molecular dynamic simulation methods.

  2. A mononuclear zinc(II) complex with piroxicam: Crystal structure, DNA- and BSA-binding studies; in vitro cell cytotoxicity and molecular modeling of oxicam complexes

    Jannesari, Zahra; Hadadzadeh, Hassan; Amirghofran, Zahra; Simpson, Jim; Khayamian, Taghi; Maleki, Batool


    A new mononuclear Zn(II) complex, trans-[Zn(Pir)2(DMSO)2], where Pir- is 4-hydroxy-2-methyl-N-2-pyridyl-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide (piroxicam), has been synthesized and characterized. The crystal structure of the complex was obtained by the single crystal X-ray diffraction technique. The interaction of the complex with DNA and BSA was investigated. The complex interacts with FS-DNA by two binding modes, viz., electrostatic and groove binding (major and minor). The microenvironment and the secondary structure of BSA are changed in the presence of the complex. The anticancer effects of the seven complexes of oxicam family were also determined on the human K562 cell lines and the results showed reasonable cytotoxicities. The interactions of the oxicam complexes with BSA and DNA were modeled by molecular docking and molecular dynamic simulation methods.

  3. Los mecanismos de influencia en el liderazgo

    Arango Cardona, Patricia


    Este trabajo tiene como objetivo fundamental identificar las tácticas de influencia que utiliza el señor Carlos Pérez, gerente y socio principal de G. & M., en su trato cotidiano con sus colaboradores, así como la reacción de estos últimos ante dichas tácticas.

  4. Thermodynamics of mixed-ligand complex formation of zinc nitrilotriacetate with amino acids and dipeptides in solution

    Pyreu, Dmitrii, E-mail: [Department of Inorganic and Analytic Chemistry, Ivanovo State UniversityErmak 39, Ivanovo 153025 (Russian Federation); Gruzdev, Matvey; Kumeev, Roman [G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences, Ivanovo (Russian Federation); Gridchin, Sergei [Ivanovo State University of Chemistry and Technology, Ivanovo (Russian Federation)


    Highlights: • Stable mixed ligand complexes of ZnNta with amino acids and dipeptides. • Histamine-like coordination mode of His in the complex ZnNtaHis. • Glycine-like coordination of Lys and Orn in the complexes ZnNtaL and ZnNtaHL • NH{sub 2}, CO-coordination mode of GlyGly in the complex ZnNtaGG. • NH{sub 2}, N{sup −} or NH2, N{sup −}, COO-coordination modes of GlyGly in the complex ZnNtaGGH{sub −1}. - Abstract: The isothermal calorimetry, pH-potentiometric titration and {sup 1}H and {sup 13}C NMR methods has been used to study the mixed-ligand complex formation in the systems Zn{sup 2+}–Nta{sup 3–}–L{sup −} (L = His, Orn, Lys, GlyGly, AlaAla) in aqueous solution at 298.15 K and the ionic strength of I = 0.5 (KNO{sub 3}). The thermodynamic parameters of formation of the mixed complexes have been determined. The relationship between the probable coordination modes of the complexone and amino acid or dipeptide molecules in the mixed-ligand complex and the thermodynamic parameters has been discussed.

  5. Reactivity of Cys4 Zinc Finger Domains with Gold(III) Complexes : Insights into the Formation of "Gold Fingers"

    Jacques, Aurélie; Lebrun, Colette; Casini, Angela; Kieffer, Isabelle; Proux, Olivier; Latour, Jean-Marc; Sénèque, Olivier


    Gold(I) complexes such as auranofin or aurothiomalate have been used as therapeutic agents for the treatment of rheumatoid arthritis for several decades. Several gold(I) and gold(III) complexes have also shown in vitro anticancer properties against human cancer cell lines, including cell lines resis

  6. Reactivity of Cys4 Zinc Finger Domains with Gold(III) Complexes : Insights into the Formation of "Gold Fingers"

    Jacques, Aurélie; Lebrun, Colette; Casini, Angela; Kieffer, Isabelle; Proux, Olivier; Latour, Jean-Marc; Sénèque, Olivier


    Gold(I) complexes such as auranofin or aurothiomalate have been used as therapeutic agents for the treatment of rheumatoid arthritis for several decades. Several gold(I) and gold(III) complexes have also shown in vitro anticancer properties against human cancer cell lines, including cell lines

  7. A series of Zn-4f heterometallic coordination polymers and a zinc complex containing a flexible mixed donor dicarboxylate ligand.

    Feng, Xun; Feng, Yu-Quan; Liu, Lang; Wang, Li-Ya; Song, Hong-Liang; Ng, Seik-Weng


    A new zinc compound, together with a corresponding series of Zn-4f heterometallic coordination polymers, namely, [Zn(H2PBDA)(PBDA)]n (1), {[Ln2(PBDA)2·2H2O] [Zn2(PBDA)2Cl2]}n [H2PBDA = 3-(pyridin-3-yl-oxy) benzene-1,2-dicarboxylic acid, and Ln = Pr(2), Nd(3), Eu(4), Gd(5), Dy(6), Ho(7), Er(8)] have been hydrothermally synthesized and characterized systematically. Polymers 2-8 feature two-dimensional (2D) 4,4 networks, containing the original 1D heterometallic double stranded chains composed of [Ln2Zn2(PBDA)2] entities. The extensive hydrogen bonding and π-π stacking interactions were observed to stabilize the extended architectures. The luminescence emission spectra of the polymers vary depending on the lanthanide(III) ion present. Informative magnetic susceptibility measurements show that the same carboxylate bridging fashion of the PBDA ligand results in the different magnetic properties occurring within the heterometallic coordination polymers. In addition, polymer 6 exhibits an interesting slow magnetic relaxation behavior at lower temperatures.

  8. The Fruitless gene in Nasonia displays complex sex-specific splicing and contains new zinc finger domains.

    Bertossa, Rinaldo C; van de Zande, Louis; Beukeboom, Leo W


    The transcription factor Fruitless exerts a broad range of functions during Drosophila development, the most apparent of which is the determination of sexual behavior in males. Although fruitless sequences are found in other insect orders, little is known about fruitless structure and function outside Diptera. We have performed a thorough analysis of fruitless transcripts in the haplo-diploid wasp Nasonia vitripennis and found both sex-specific and non-sex-specific transcripts similar to those found in Drosophila. In Nasonia, however, a novel, large fruitless transcript is present in females only. Putative binding sites for sex-specific splicing factors found in Nasonia fruitless and doublesex as well as Apis mellifera doublesex transcripts were sufficient to identify a corresponding female-specific fruitless exon in A. mellifera, suggesting that similar factors in both hymenopteran species could be responsible for sex-specific splicing of both genes. Furthermore, new C(2)H(2) zinc finger domains found in Nasonia fruitless transcripts were also identified in the fruitless locus of major holometabolous insect species but not in drosophilids. Conservation of important domains and sex-specific splicing in Diptera and Hymenoptera support the hypothesis that fruitless is an ancient gene and has conserved functions in insects. Considerable divergences in other parts of the gene are expected to underlie species-specific differences and may help to explain diversity observed in insect sexual behaviors.

  9. Synthesis, X-ray, and Spectroscopic Study of Dissymmetric Tetrahedral Zinc(II) Complexes from Chiral Schiff Base Naphthaldiminate Ligands with Apparent Exception to the ECD Exciton Chirality.

    Enamullah, Mohammed; Makhloufi, Gamall; Ahmed, Rifat; Joy, Baitul Alif; Islam, Mohammad Ariful; Padula, Daniele; Hunter, Howard; Pescitelli, Gennaro; Janiak, Christoph


    Bidentate enantiopure Schiff base ligands, (R or S)-N-1-(Ar)ethyl-2-oxo-1-naphthaldiminate (R- or S-N^O), diastereoselectively provide Λ- or Δ-chiral-at-metal four-coordinated Zn(R- or S-N^O)2 {Ar = C6H5; Zn-1R or Zn-1S and p-C6H4OMe; Zn-2R or Zn-2S}. Two R- or S-N^O-chelate ligands coordinate to the zinc(II) in a tetrahedral mode and induce Λ- or Δ-configuration at the zinc metal center. In the solid state, the R- or S-ligand diastereoselectively gives Λ- or Δ-Zn configuration, respectively, and forms enantiopure crystals. Single crystal structure determinations show two symmetry-independent molecules (A and B) in each asymmetric unit to give Z' = 2 structures. Electronic circular dichroism (ECD) spectra show the expected mirror image relationship resulting from diastereomeric excess toward the Λ-Zn for R-ligands and Δ-Zn for S-ligands in solution. ECD spectra are well reproduced by TDDFT calculations, while the application of the exciton chirality method, in the common point-dipole approximation, predicts the wrong sign for the long-wavelength couplet. A dynamic diastereomeric equilibrium (Λ vs Δ) prevails for both R- and S-ligand-metal complexes in solution, respectively, evidenced by (1)H NMR spectroscopy. Variable temperature (1)H NMR spectra show a temperature-dependent shift of the diastereomeric equilibrium and confirm Δ-Zn configuration (for S-ligand) to be the most stable one and favored at low temperature. DSC analyses provide quantitative diastereomeric excess in the solid state for Zn-2R and Zn-2S, which is comparable to the results of solution studies.

  10. Unsymmetrical Mesoporphyrinic Complexes of Copper (II) and Zinc (II). Microwave-Assisted Synthesis, Spectral Characterization and Cytotoxicity Evaluation

    Rica Boscencu


    New unsymmetrical mesoporphyrinic complexes, namely 5-(4-hydroxyphenyl)-10,15,20–tris-(4-carboxymethylphenyl)–21,23-Zn(II)-porphine and 5-(4-hydroxyphenyl)-10,15,20–tris-(4-carboxymethylphenyl)–21,23-Cu(II)-porphine, were synthesized using a microwave irradiation method. The structures of the porphyrinic complexes were confirmed using FT-IR, UV–Vis, EPR and NMR spectral data. The spectral absorption and emission properties of the porphyrinic complexes were studied in organic solvents of diffe...

  11. Deciphering the Conformational Choreography of Zinc Coordination Complexes with Standard and Novel Proton NMR Techniques Combined with DFT Methods.

    Pucheta, Jose Enrique Herbert; Prim, Damien; Gillet, Jean Michel; Farjon, Jonathan


    The presence of water has been shown to deeply impact the stability and geometry of Zn complexes in solution. Evidence for tetra- and penta-coordinated species in a pyridylmethylamine-Zn(II) model complex is presented. Novel (1) H NMR tools such as T1 -filtered selective exchange spectroscopy and pure shifted gradient-encoded selective refocusing as well as classical 2D ((1) H-(1) H) exchange spectroscopy, diffusion-ordered spectroscopy and T1 ((1) H) measurements, in combination with density functional theory methods allow the full conformational dynamics of a pyridylmethylamine-Zn(II) complex to be revealed. Four conformers and two families of complexes depending on the hydration states are elucidated.

  12. Unsymmetrical Mesoporphyrinic Complexes of Copper (II and Zinc (II. Microwave-Assisted Synthesis, Spectral Characterization and Cytotoxicity Evaluation

    Rica Boscencu


    Full Text Available New unsymmetrical mesoporphyrinic complexes, namely 5-(4-hydroxyphenyl-10,15,20–tris-(4-carboxymethylphenyl–21,23-Zn(II-porphine and 5-(4-hydroxyphenyl-10,15,20–tris-(4-carboxymethylphenyl–21,23-Cu(II-porphine, were synthesized using a microwave irradiation method. The structures of the porphyrinic complexes were confirmed using FT-IR, UV–Vis, EPR and NMR spectral data. The spectral absorption and emission properties of the porphyrinic complexes were studied in organic solvents of different polarities and the influence of solvent polarity on the wavelengths of the absorbance and fluorescence band maxima is described. The cytotoxicity evaluation of the porphyrinic complexes was performed on human colon adenocarcinoma cell line HT29 for different doses and incubation times. The obtained result indicates a lack of or low toxicity for both compounds, thus recommending them for further testing in light activation protocols.

  13. Anion-tuned self-assembly of zinc(II) fluconazole complexes: Crystal structures, luminescent and thermal properties

    Zhang, Lei; Ling, Yun; Peng, Feng; Du, Miao


    Four novel fluconazole-bridged Zn(II) complexes, [Zn(HFlu)Cl 2(DMF)] 2 ( 1), {[Zn(HFlu) 2(H 2O) 2](NO 3) 2·2DMF} n ( 2), {[Zn(HFlu) 2(H 2O) 2](NO 3) 2} n ( 3) and {[Zn(HFlu)(SCN) 2]·H 2O} n ( 4) [HFlu = 2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)-propan-2-ol], have been synthesized and structurally characterized by X-ray diffraction method. The structure of dimeric complex 1 consists of 20-membered macrometallacyclic ring-like structure, in which the Zn(II) ion is in a five-coordinated distorted trigonal bipyramidal geometry with the Zn⋯Zn distance of 10.265(3) Å across the cis HFlu ligand. Complex 2 shows infinite 1-D macrocyclic double chain structure with the central Zn(II) ions being six-coordinated by four HFlu ligands and two apical water molecules and with the intrachain Zn⋯Zn distance of 10.722(3) Å across the trans HFlu ligand. The crystal structure of complex 3 is analogous to that of complex 2 with the intrachain Zn⋯Zn distance of 10.654(2) Å. The structure of complex 4 consists of infinite 1-D coordination polymeric chain with the tetrahedral coordination geometry of Zn(II) ion and with the intrachain Zn⋯Zn distance of 11.173(2) Å across the cis HFlu ligand. Complexes 1- 4 show the similar fluorescence emission to the free HFlu ligand at ambient temperature and the thermal stabilities of the complexes have also been investigated.

  14. Coordination chemistry of sugar-phosphate complexes with palladium(II), rhenium(V) and zinc(II)

    Steinborn, Christian Martin


    As described before, some studies dealing with coordination chemistry of sugar phosphates are available but no analogous complexes of Zn{sup II} have been investigated yet. The primary goal of this work is, therefore, to fill this gap. In order to stay close to the active sites of enzymes such as class-II-aldolase, the simple metal fragment Zn{sup II}(dien) is used. NMR spectroscopy is used primarily as analytical method since it enables the investigation of both complex equilibria in solution and pH dependence of metal-binding sites. Since this approach is challenging due to the fast metal-ligand exchange and the absence of CIS values, it is necessary to improve the significance of NMR data collected from sugar-phosphate complexes with Zn{sup II}. Hence, further experiments are performed with molecules similar to sugar phosphates such as reducing and methylated sugars or polyols. Beside NMR spectroscopy, crystal-structure analysis will be used to get more detailed information about the binding pattern of the complexes. Additionally, sugar-phosphate complexes of Pd{sup II} are investigated. Further experiments are conducted, on the one hand, to synthesise more sugarphosphate complexes with ReVON2 fragments, and, on the other hand, to grow crystals confirming the theory about mixed sugar-core-phosphate chelation.

  15. Gastroprotective and antidepressant effects of a new zinc(II)-curcumin complex in rodent models of gastric ulcer and depression induced by stresses.

    Mei, Xueting; Xu, Donghui; Xu, Sika; Zheng, Yanping; Xu, Shibo


    Curcumin, a yellow pigment found in the rhizome of Curcuma loga, has been used to treat a variety of digestive and neuropsychiatric disorders since ancient times in China. Curcumin can chelate various metal ions to form metallocomplexes of curcumin which show greater effects than curcumin alone. This study investigated the antiulcerogenic and antidepressant effects of a Zn(II)-curcumin complex on cold-restraint stress (CRS)-induced gastric ulcers in rats, and on the forced swimming test (FST), tail suspension test (TST) and 5-hydroxy-l-tryptophan (5-HTP)-induced head twitch test in mice. CRS disrupted the rat mucosal barrier and induced gastric ulcers by decreasing the activities of the antioxidant enzymes, and increasing H(+)-K(+)-ATPase activity and malondialdehyde (MDA) level. Pretreatment with Zn(II)-curcumin (12, 24, and 48mg/kg) dose-dependently reversed these trends, reduced gastric lesions and H(+)-K(+)-ATPase activity, and increased antioxidant activities compared with control groups. Zn(II)-curcumin significantly increased HSP70 mRNA, and attenuated increased iNOS mRNA in the mucosa. Zn(II)-curcumin (17, 34, and 68mg/kg) also significantly decreased immobility time in the FST and TST, and enhanced 5-HTP-induced head twitches in mice. These results demonstrate that the Zn(II)-curcumin complex showed significant gastroprotective and antidepressant effects compared with curcumin alone via a synergistic effect between curcumin and zinc.

  16. A novel SPE-HPLC method for simultaneous determination of selected sulfonated phthalocyanine zinc complexes in mouse plasma following cassette dosing.

    Jiang, Zhou; Shao, Jingwei; Chen, Meili; Wang, Jian; Jia, Lee


    Sulfonated phthalocyanine zinc complexes (ZnPcSn) are a mixture of polymolecules with different number of the sulfonic groups. They are typical photosensitizers for photodynamic therapy (PDT). Analysis of the sulfonic phthalocyanine complexes in blood is a global technical challenge to developing this kind of photosensitizers into clinics. To circumvent the problem, we aimed at developing a novel solid-phase extraction (SPE)-HPLC method, which was primarily composed of (1) the SPE material that has both the aliphatic benzene group and hydrophilic ethylenediamino group bonded to the silica surface typically for retaining those hydrophobic compounds with some degree of hydrophilic anionic (negatively charged) functionality; and (2) the RP-Amide C16 HPLC column packed with palmitamidopropylsilane for both reversed-phase and anion exchange separation. The method was validated in terms of recovery, precision and accuracy for pharmacokinetic study with the photosensitizer following its intravenous cassette dosing to mice. The present study is the first report on using an SPE-HPLC mode to simultaneously determine the phthalocyanine-based polymolecule photosensitizer in blood. The study will aid in clinical development of photosensitizers.

  17. Solvolysis mechanisms of RNA phosphodiester analogues promoted by mononuclear zinc(II) complexes: mechanisic determination upon solvent medium and ligand effects.

    Zhang, Xuepeng; Zhu, Yajie; Gao, Hui; Zhao, Cunyuan


    The solvolysis mechanisms of RNA phosphodiester model 2-(hydroxypropyl)-4-nitrophenyl phosphate (HpPNP) catalyzed by mononuclear zinc(II) complexes are investigated in the paper via a theoretical approach. The general-base-catalyzed (GBC) and specific-base-catalyzed (SBC) mechanisms are thoroughly discussed in the paper, and the calculations indicate a SBC mechanism (also named as the direct nucleophilic attack mechanism) when the cyclization of HpPNP is promoted by the Zn:[12]aneN3 complex ([12]aneN3 = 1,5,9-triazacyclododecane). The ligand effect is considered by involving two different catalysts, and the results show that the increasing size catalyst provides a lower energy barrier and a significant mechanistic preference to the SBC mechanism. The solvent medium effect is also explored, and reduced polarity/dielectric constant solvents, such as light alcohols methanol and ethanol, are more favorable. Ethanol is proven to be a good solvent medium because of its low dielectric constant. The computational results are indicative of concerted pathways. Our theoretical results are consistent with and well interpret the experimental observations and, more importantly, provide practical suggestions on the catalyst design and selection of reaction conditions.

  18. Synthesis and characterization of bis (acetylacetonato κ-O, O') [zinc(ii)/copper(ii)] hybrid organic-inorganic complexes as solid metal organic precursors.

    Rooydell, Reza; Wang, Ruey-Chi; Brahma, Sanjaya; Ebrahimzadeh, Farzaneh; Liu, Chuan-Pu


    We have synthesized novel metal organic hybrid mixed compounds of bis (acetylacetonato κ-O, O') [zinc(ii)/copper(ii)]. Taking C10H14O4Zn0.7Cu0.3 (Z0.7C0.3AA) as an example, the crystals are composed of Z0.7C0.3AA units and uncoordinated water molecules. Single-crystal X-ray diffraction results show that the complex Z0.7C0.3AA crystallizes in the monoclinic system, space group P21/n. The unit cell dimensions are a = 10.329(4) Å, b = 4.6947(18) Å, and c = 11.369(4) Å; the angles are α = 90°, β = 91.881(6)°, and γ = 90°, the volume is 551.0(4) Å(3), and Z = 2. In this process, the M(ii) ions of Zn and Cu mix and occupy the centers of symmetrical structural units, which are coordinated to two ligands. The measured bond lengths and angles of O-M-O vary with the ratio of metal species over the entire series of the complexes synthesized. The chemistry of the as-synthesized compounds has been characterized using infrared spectroscopy, mass spectroscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy analysis, and the morphology of the products has been characterized using scanning electron microscopy. The thermal decomposition of the Z0.7C0.3AA composites measured by thermogravimetric analysis suggests that these complexes are volatile. The thermal characteristics of these complexes make them attractive precursors for metal organic chemical vapor deposition.

  19. Five-Coordinate Zinc(II Complex: Synthesis, Characterization, Molecular Structure, and Antibacterial Activities of Bis-[(E-2-hydroxy-N′-{1-(4-methoxyphenylethylidene}benzohydrazido]dimethylsulfoxidezinc(II Complex

    Zhi-Qiang Liu


    Full Text Available The titled Zn(II complex was synthesized by reacting the compound (E-2-hydroxy-N′-{1-(4-methoxyphenylethylidene}benzohydrazide with zinc(II acetate dihydrate in alkaline DMSO and ethanol solution under reflux condition for 28 hours. The resulting solid was filtered and recrystallized from the mixture of ethanol and DMSO. The hydrazone Schiff base and its Zn(II complex were characterized using 1H, 13C NMR, FTIR, UV-Vis spectroscopy, and single crystal X-ray diffraction analysis. Meanwhile, their antibacterial activities were examined using disc diffusion method. The spectral studies showed that the hydrazone Schiff base underwent keto-enol tautomerization, forming a bidentate ligand (N,O towards Zn(II ion. Surprisingly, on top of the two hydrazone Schiff base molecules which coordinated to the Zn metal center, an additional DMSO molecule was found attached to the Zn metal center in the crystal data, resulting in a 5-coordinate distorted trigonal bipyramidal Zn(II complex. Both hydrazone Schiff base and its Zn(II complexes were found to exhibit low antibacterial activity even when the concentrations were increased to 800 ppm.

  20. Novel zinc(II) and copper(II) complexes of a Mannich base derived from lawsone: Synthesis, single crystal X-ray analysis, ab initio density functional theory calculations and vibrational analysis.

    Neves, Amanda P; Vargas, Maria D; Téllez Soto, Claudio A; Ramos, Joanna M; Visentin, Lorenzo do C; Pinheiro, Carlos B; Mangrich, Antônio S; de Rezende, Edivaltrys I P


    Zinc(II) and copper(II) complexes of a tridentate Mannich base L1 derived from 2-hydroxy-1,4-naphthoquinone, pyridinecarboxyaldehyde and 2-aminomethylpyridine, [ZnL1Cl(2)]·H(2)O 1 and [CuL1Cl(2)]·2H(2)O 2, have been synthesized and fully characterized. The structure of complex 1 has been elucidated by a single crystal X-ray diffraction study: the zinc atom is pentacoordinate and the coordination geometry is a distorted square base pyramid, with a geometric structural parameter τ equal to 0.149. Vibrational spectroscopy and ab initio DFT calculations of both compounds have confirmed that the two complexes exhibit similar structures. Full assignment of the vibrational spectra was also supported by careful analysis of the distorted geometries generated by the normal modes. Copyright © 2012 Elsevier B.V. All rights reserved.

  1. Novel Bis-β-diketone-type Ligand and Its Copper and Zinc Complexes for Two-photon Biological Imaging

    ZHOU Shuang-sheng; XUE Xuan; WEI Dong; JIANG Bo; WANG Jia-feng; LU Cheng-hua


    A curcumin derivative ligand,1,7-bis(3-methoxyl-4-oxyethylacetate)phenyl-1,6-heptadiene-3,5-diketone (diethyl acetatecurcumin,abbreviated as HL),and its Cu(Ⅱ) and Zn(Ⅱ) complexes have been synthesized and characterized by elemental analyses,infrared(IR),1H NMR and molar conductivity.The experimental results show that the resulting complexes bear strong two-photon excited fluorescence(TPEF) in N,N-dimethyformamide solvent,which has been proven to be potentially useful for two-photon microscopy imaging in living cells.In addition,cytotoxicity tests show that the low-micromolar concentrations of metal-ligand complex(ML2) did not cause significant reduction in cell viability over a pcriod of,at least,24 h and should be safe for further biological studies.

  2. Synthesis and Characterization of Some New Complexes of Magnesium (II and Zinc (II with the Natural Flavonoid Primuletin

    Ştefania Felicia Bǎrbuceanu


    Full Text Available Two new metal complexes formulated as [Mg(L2(H2O2]·H2O (1 and [Zn(L2(H2O2]·0.5H2O (2, where HL = 5-hydroxyflavone (primuletin, have been synthesized and characterized by elemental and thermal analyses, molar conductance, IR, UV-Vis, 1H- and 13C-NMR, fluorescence and mass spectra. In solid state, complexes had shown higher fluorescence intensities comparing to the free ligand, and this behavior is appreciated as a consequence of the coordination process.

  3. 烟酸锌配合物的合成及结构表征%Synthesis and Crystal Structure of the Nicotinate Zinc Complex

    康海霞; 傅玉琴


    应用水热合成法合成了烟酸锌配合物,通过X-射线单晶衍射对其进行了结构表征,并通过XRD对其纯度进行了分析.X-射线单晶衍射表明,该配合物属正交晶系,空间群为Pbca,晶胞参数为a=1.4229(3) nm, b=0.69191(12) nm, c=0.85012(15) nm,α=90°,β=118.2020(10)°,γ=90°, Z=2, V =737.6(2)樻3, Mr =381.64, Dc =1.718 mg/m 3,μ=1.710 mm -1, F(000)=392,最终R 1=0.0189, wR 2=0.0532.晶体结构表明,该配合物中中心锌原子是六配位,形成了一个稍微畸变的正八面体构型,通过氢键的作用,标题化合物形成了复杂的三维的网状结构.%The nicotinate zinc complex is synthesized and characterized by X-Ray single crystal diffraction.It crystallizes in Orthorhombic, space group Pbca with a=1.4229 (3) nm, b=0.69191 (12) nm, c=0.85012 (15) nm, alpha=90 deg, beta =118.2020(10) deg, gamma =90 deg, Z =2, V =737.6(2) Å3, Mr =381.64, Dc =1.718 mg/m3 ,μ=1.710 mm-1 , F(000)=392.The Final R1=0.0189, wR2=0.0532.Crystal structure shows that the coordination environment around the Zinc can be described as a slightly distorted octahed-ron.The title compound forms a complex three-dimensional network structure through hydrogen bonding.

  4. Highly selective and sensitive DNA assay based on electrocatalytic oxidation of ferrocene bearing zinc(II)-cyclen complexes with diethylamine.

    Shiddiky, Muhammad J A; Torriero, Angel A J; Zeng, Zhanghua; Spiccia, Leone; Bond, Alan M


    A highly selective and sensitive electrochemical biosensor has been developed that detects DNA hybridization by employing the electrocatalytic activity of ferrocene (Fc) bearing cyclen complexes (cyclen = 1,4,7,10-tetraazacyclododecane, Fc[Zn(cyclen)H(2)O](2)(ClO(4))(4) (R1), Fc(cyclen)(2) (R2), Fc[Zn(cyclen)H(2)O](ClO(4))(2) (R3), and Fc(cyclen) (R4)). A sandwich-type approach, which involves hybridization of a target probe hybridized with the preimmobilized thiolated capture probe attached to a gold electrode, is employed to fabricate a DNA duplex layer. Electrochemical signals are generated by voltammetric interrogation of a Fc bearing Zn-cyclen complexes that selectively and quantitatively binds to the duplex layers through strong chelation between the cyclen complexes and particular nucleobases within the DNA sequence. Chelate formation between R1 or R3 and thymine bases leads to the perturbation of base-pair (A-T) stacking in the duplex structure, which greatly diminishes the yield of DNA-mediated charge transport and displays a marked selectivity to the presence of the target DNA sequence. Coupling the redox chemistry of the surface-bound Fc bearing Zn-cyclen complex and dimethylamine provides an electrocatalytic pathway that increases sensitivity of the assay and allows the 100 fM target DNA sequence to be detected. Excellent selectivity against even single-base sequence mismatches is achieved, and the DNA sensor is stable and reusable.

  5. Synthesis, crystal structure and computational chemistry research of a Zinc(II complex: [Zn(Pt(Biim2

    Teng Fei


    Full Text Available The title metal-organic coordination complex [Zn(pt(Biim2] (pt=phthalic acid, benzene-1,2-dicarboxylate, Biim=2,2'-biimidazole 1 has been obtained by using hydrothermal synthesis and characterized by single-crystal X-ray diffraction. The complex crystallizes in monoclinic, space group P21/n with a = 8.5466(15 Å, b = 11.760(2 Å, c = 20.829(4 Å, β = 95.56(2º, V = 2083.5(6 Å3, Mr =497.78, Dc = 1.587 g/cm3, μ(MoKα = 1.226 mm−1, F(000 = 1016, Z = 4, the final R = 0.0564 and wR = 0.1851 for 3656 observed reflections (I > 2σ(I. The elemental analysis, IR, TG and the theoretical calculation were also investigated.

  6. One- and Two-photon Excited Fluorescence of Zinc(Ⅱ), Cadmium(Ⅱ) Complexes Containing Phenothiazine Ligand


    A new ligand, 10-ethylphenothiazinyl - 3 - yl - methylene thiosemicarbazon (HL) and its complexes ML2 (M=Zn2+, Cd2+), which exhibit intensive two-photon excited (TPE) fluorescence at 800 nm laser pulses in femtosecond regime, were synthesized and characterized.The measured power dependence of the fluorescence signals provided direct evidence for TPE.All of them exhibited a large two-photon absorptive cross section and, more importantly from the application point of view, high photochemical/photothermal stability.

  7. Availability of zinc and the ligands citrate and histidine to wheat: does uptake of entire complexes play a role?

    Gramlich, Anja; Tandy, Susan; Frossard, Emmanuel; Eikenberg, Jost; Schulin, Rainer


    Organic ligands in soils affect the availability of trace metals such as Zn to plants. This study investigated the effects of two of these ligands, citrate and histidine, on Zn uptake by wheat under hydroponic conditions. Uptake of (65)Zn in the presence of these ligands was compared to uptake in the presence of EDTA at the same free Zn concentration (Zn(2+) ~ 50 nM). In the presence of citrate Zn root uptake was enhanced ~3.5 times and in the presence of histidine, by a factor of ~9, compared to the EDTA treatments. Citrate uptake was slightly reduced in the treatment containing ligands and Zn compared to the treatment containing the same ligand concentration but no Zn. In addition, a higher uptake of Zn than of citrate was observed. This suggests that the enhanced Zn uptake was primarily due to increased supply of Zn(2+) by diffusion and dissociation of Zn-citrate complexes at the root surface. Histidine uptake was much higher than citrate uptake and not influenced by the presence of Zn. As histidine forms stronger complexes with Zn than citrate, the results suggest that the enhancement of Zn uptake in the presence of histidine was in part due to the uptake of undissociated Zn-histidine complexes.

  8. A Novel Two-dimensional Homochiral Zinc(II) Complex Constructed Based on In Situ Ligand Formation%A Novel Two-dimensional Homochiral Zinc(II) Complex Constructed Based on In Situ Ligand Formation

    ZHAO Xiu-Qin; GUO Chang; HUANG Rong-Yi; XU Heng; LIU Guang-Xiang; WU Gen-Hua


    A novel zinc(II) complex, Zn(IBT)2 (1, H1BT = 5-(4-((1H-imidazol-1-yl)methyl)- phenyl)-2H-tetrazole) has been synthesized with Zn(NO3)2·6H2O, 4-(imidazol-l-ylmethyl)benzonnitrile (IBN) and NaN3 by the hydrothermal method, and characterized by elemental analysis, IR and single-crystal X-ray diffraction. Crystallographic data for 1: C22H18N12Zn, Mr = 515.85, orthorhombic, Pbcn, a = 16.0567(15), b = 9.5316(9), c = 14.6107(14) A, V= 2236.1(4) A3, Z= 4, Dc = 1.532 g/cm3,μ = 1.138 mm-1, F(000) = 1056, R = 0.0350 and wR = 0.0888 for 1438 observed reflections (I 〉 2σ(I)) and the goodness-of-fit S = 1.002 on F2. The crystal structural analysis revealed that complex 1 exhibits a rare two-dimensional homochiral wave-like layer structure. In addition, the photoluminescence of complex 1 was studied in the solid state at room temperature together with its theoretical analysis.

  9. The influence of green microstructure and sintering parameters on precipitation process during copper-nickel-zinc ferrites sintering; Influencia de la microestructura en verde y de las variables de sinterizacion en el proceso de precipitacion producido durante la sinterizacion de ferritas de cobre-niquel-cinc

    Barba, A.; Clausell, C.; Jarque, J. C.; Monzo, M.


    Microstructural changes that occur during heat treatment of copper-nickel-zinc ferrites have been studied. The process of precipitation of the two types of crystals that occur during the sintering process has been analyzed. It is found that this process depends on dry relative density of the press specimens and on the following sintering parameters: sintering temperature, sintering time and cooling rate of the thermal cycle. Crystal precipitates characterization have been done by scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) analysis, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). These techniques have allowed to determine the nature of these crystals, which in this case correspond to zinc and copper oxides. It has been used two chemical reactions to explain the bulk precipitation and subsequent re-dissolution of these crystal precipitates during sintering. (Author)

  10. Post-synthetic modification of mesoporous zinc-adeninate framework with tris(2,2′-biprydine) ruthenium(II) complex and its electrochemiluminescence

    Park, Ji Eun; Shin, Ik Soo [Dept. of Chemistry, Soongsil University, Seoul (Korea, Republic of); Oh, Hye Jae; An, Ji Hyun [Dept. of Chemistry Education, Seoul National University, Seoul (Korea, Republic of)


    Herein we report a redox-active metal-organic framework (MOF) via post-synthetic cation exchange with tris(2,2′-biprydine) ruthenium(II) complex (Ru(bpy){sub 3}{sup 2+}). A porous anionic zinc-adeninate framework (bMOF-100) is spacious enough to easily entrap 2.43 of Ru(bpy){sub 3}{sup 2+} cations within the mesopore. The encapsulation supported the framework structure preventing any distortion from a rapid solvent evaporation under SEM observation. Ru(bpy){sub 3}{sup 2+}@bMOF-100 was then immobilized on the surface of glassy carbon electrode, and its electrocatalytic and electrochemiluminescent (ECL) properties were investigated in aqueous and organic solution. Especially, Ru(bpy){sub 3}{sup 2+}@bMOF-100 showed the excellent electrochemical properties of Ru(bpy){sub 3}{sup 2+}, but gradual decomposition of the MOF structure was observed under electrochemical measurements because of the sluggish oxidation of adeninate ligand.

  11. Unusual self-assembled 1D tape of tetramers and water-nitrate clusters trapped in a zinc(II) complex: Synthesis, characterization, luminescence and catalytic properties

    Ma, De-Yun; Guo, Hai-Fu; Dong, Ji; Xu, Jun


    Unusual tetramers and water-nitrate clusters have been observed in a mononuclear zinc(II) complex of [Zn(4-cpa)(phen)2(H2O)]·(H2O)·(NO3)] (1), (4-Hcpa = 4-chlorophenoxyacetic acid, phen = 1,10-phenanthroline), which was synthesized under hydrothermal conditions and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), powder X-ray diffraction, UV-vis absorption spectra and single-crystal X-ray diffraction. The crystal structure analysis of 1, reveals that the nitrate anions, water molecules and carboxylate oxygen atoms (O3) pack to form a one-dimensional infinite tape parallel to the c-axis. The uncoordinated carboxylate oxygen atoms (O3) of 4-cpa ligands, water molecules and nitrate anions interact via hydrogen bonds and extend 1 into a water-anion-cation tape, which are finally connected into a 3D supramolecular structure via π⋯π stacking interactions. Excitation (λex = 310 nm) and luminescence data observed at room temperature show that 1 emits bright blue fluorescence. Moreover, 1 has a remarkable activity for degradation of methyl orange in a photo-assisted Fenton-like process.

  12. Syntheses, spectral, electrochemical and thermal studies of mononuclear manganese(III) complexes with ligands derived from 1,2-propanediamine and 2-hydroxy-3 or 5-methoxybenzaldehyde: Self-assembled monolayer formation on nanostructure zinc oxide thin film

    Habibi, Mohammad Hossein; Askari, Elham; Amirnasr, Mehdi; Amiri, Ahmad; Yamane, Yuki; Suzuki, Takayoshi


    Mononuclear Mn(III) complexes have been prepared via the Mn(II) reaction of an equimolar of Schiff-bases derived from reaction of 2-hydroxy-3-methoxybenzaldehyde or 2-hydroxy-5-methoxybenzaldehyde with 1,2-diaminopropane. Axial ligands L include: pyridine (py) and H 2O. The resulting complexes have been characterized by FT-IR and UV-vis spectroscopy. The crystal structures of the complexes were determined and indicate that in the solid state the complex adopts a slightly distorted octahedral environment of the imine N and hydroxo O with the two axial ligands. The electrochemical reduction of these complexes at a glassy carbon electrode in acetonitrile solution indicates that the first reduction process corresponding to Mn III-Mn II is electrochemically quasi-reversible. Thermal stability of these complexes was determined by TG and DTG. Layers of these complexes were formed on nanostructure zinc oxide thin film and a red shift was observed when zinc oxide thin film is modified by complex.

  13. The biological inorganic chemistry of zinc ions.

    Krężel, Artur; Maret, Wolfgang


    The solution and complexation chemistry of zinc ions is the basis for zinc biology. In living organisms, zinc is redox-inert and has only one valence state: Zn(II). Its coordination environment in proteins is limited by oxygen, nitrogen, and sulfur donors from the side chains of a few amino acids. In an estimated 10% of all human proteins, zinc has a catalytic or structural function and remains bound during the lifetime of the protein. However, in other proteins zinc ions bind reversibly with dissociation and association rates commensurate with the requirements in regulation, transport, transfer, sensing, signalling, and storage. In contrast to the extensive knowledge about zinc proteins, the coordination chemistry of the "mobile" zinc ions in these processes, i.e. when not bound to proteins, is virtually unexplored and the mechanisms of ligand exchange are poorly understood. Knowledge of the biological inorganic chemistry of zinc ions is essential for understanding its cellular biology and for designing complexes that deliver zinc to proteins and chelating agents that remove zinc from proteins, for detecting zinc ion species by qualitative and quantitative analysis, and for proper planning and execution of experiments involving zinc ions and nanoparticles such as zinc oxide (ZnO). In most investigations, reference is made to zinc or Zn(2+) without full appreciation of how biological zinc ions are buffered and how the d-block cation Zn(2+) differs from s-block cations such as Ca(2+) with regard to significantly higher affinity for ligands, preference for the donor atoms of ligands, and coordination dynamics. Zinc needs to be tightly controlled. The interaction with low molecular weight ligands such as water and inorganic and organic anions is highly relevant to its biology but in contrast to its coordination in proteins has not been discussed in the biochemical literature. From the discussion in this article, it is becoming evident that zinc ion speciation is

  14. Self-assembled nanostructures of amphiphilic zinc(II) salophen complexes: role of the solvent on their structure and morphology.

    Oliveri, Ivan Pietro; Malandrino, Graziella; Di Bella, Santo


    This contribution explores the effect of several solvent properties, such as volatility, polarity, and Lewis basicity on the formation of molecular self-assembled nanostructures in the solid state, obtained either by casting of related solutions or by complete solvent evaporation, using seven solvents representative of common classes of coordinating organic solvents, of an amphiphilic Zn(II) Schiff-base complex. In all cases, the existence of well-defined X-ray diffraction patterns, for both the cast and powder samples, indicates a strong tendency towards the molecular self-assembly of such complexes. While nanostructures formed in acetone, THF, pyridine, and DMF have a lamellar organization, those formed in ACN, ethanol, and DMSO exhibit a 2D columnar square structure. Field emission scanning electron microscopy analysis indicates that nanostructures formed in volatile acetone, THF, ACN, and ethanol solvents show a fibrous morphology, while those formed in less volatile pyridine, DMF, and DMSO have a ribbon appearance. Overall, the results indicate that while the formation of such nanostructures is independent of the Lewis basicity of the solvent, the solvent polarity affects their structure - more polar solvents favour higher symmetry structures - and the solvent volatility influences their morphology and ordering in the cast films - lower volatility of the solvent parallels the formation of much more ordered structures. Therefore, the appropriate choice of solvent allows control of the structure, morphology, and ordering of these molecular assemblies.

  15. Structural study of the zinc and cadmium complexes of a type 2 plant (Quercus suber) metallothionein: insights by vibrational spectroscopy.

    Domènech, Jordi; Tinti, Anna; Capdevila, Mercè; Atrian, Silvia; Torreggiani, Armida


    Zn- and Cd-complexes of Quercus suber metallothionein (QsMT) were obtained by in vivo-synthesis, in order to obtain physiologically representative aggregates, and characterized by spectrometric and spectroscopic methods. The secondary structure elements and the coordination environments of the metal binding sites of the two aggregates were determined, as well as the main metal-containing species formed. The results obtained from the analysis of the Raman and IR spectra reveal that these metal-MT complexes predominantly contain beta-sheet elements (about 60%), whereas they lack alpha-helices. These structural features slightly depend on the divalent metal bound. In particular, Cd(II) binding to QsMT induces a slight increase of the beta-sheet percentage, as well as a decrease in beta-turn elements with respect to Zn(II) binding. Conversely, the in vivo capability of QsMT to inglobe metal and sulfide ions is metal-depending. Spectroscopic vibrational data also confirm the presence of sulfide ligands in the metal clusters of both Zn- and Cd-QsMT, while the participation of the spacer His residue in metal coordination was only found in Cd-QsMT, in agreement with the CD results. Overall data suggest different coordination environments for Zn(II) and Cd(II) ions in QsMT.




    Full Text Available Five new molybdato (four and hydrogenomolybdato (one adducts and complexes have been synthesized and studied by infrared spectroscopy. The suggested structures are all discrete, the molybdate anion behaving as a trichelating, a monochelating, a bridging, a tetrachelating and a bichelating ligand. The environment around Zn, Co, Cd is tetrahedral or trigonal bipyramidal also for Zn - while being octahedral for Sb. The Cd pentanuclear adduct has a two metallic components structure, a tetranuclear anionic one with a tetrachelating molybdate, the second being a neutral dehydrated adduct component. The suggested structure for the hydrogenomolybdato adduct is discrete, the hydrogenomolybdate being present as a hydrogen bonded dimer behaves as a bridging bidentate ligand. The water molecules can be considered as a coordinating ligand or lattice. When secondary interactions through hydrogen bonds involving the water molecules are considered supramolecular architectures are obtained.

  17. Experimental research on ore dressing of one complex copper and zinc polymetallic ore from Inner Mongolia%内蒙古某铜锌复杂多金属矿石选矿试验研究

    刘先鹏; 刁玉东; 董丽梅


    A flotation experimental research is carried out according to the property of the ores from one complex copper and zinc polymetallic mine in Inner Mongolia.Through a preferential flotation flowsheet,that is to recover cop-per prior to zinc,a fairly good closed circuit test index is obtained:the copper grade in copper concentrate is 26.98%with the recovery rate of 83 .56%;the zinc grade in zinc concentrate is 50 .59%with the recovery rate of 76 .84%.%针对内蒙古某铜锌复杂多金属矿矿石性质,进行了浮选试验研究。通过采用优先浮选流程,即先选铜,再选锌,获得了较好的试验指标:铜精矿铜品位26.98%、铜回收率83.56%,锌精矿锌品位50.59%、锌回收率76.84%。

  18. Zinc-bromine battery development

    Richards, Lew; Vanschalwijk, Walter; Albert, George; Tarjanyi, Mike; Leo, Anthony; Lott, Stephen


    This report describes development activities on the zinc-bromine battery system conducted by Energy Research Corporation (ERC). The project was a cost-shared program supported by the U.S. Department of Energy and managed through Sandia. The project began in September 1985 and ran through January 1990. The zinc-bromine battery has been identified as a promising alternative to conventional energy storage options for many applications. The low cost of the battery reactants and the potential for long life make the system an attractive candidate for bulk energy storage applications, such as utility load leveling. The battery stores energy by the electrolysis of an aqueous zinc bromide salt to zinc metal and dissolved bromine. Zinc is plated as a layer on the electrode surface while bromine is dissolved in the electrolyte and carried out of the stack. The bromine is then extracted from the electrolyte with an organic complexing agent in the positive electrolyte storage tank. On discharge the zinc and bromine are consumed, regenerating the zinc bromide salt.

  19. Thermal, Spectral, Fluorescence, and Antimicrobial Studies of Cobalt, Nickel, Copper, and Zinc Complexes Derived from 4-[(5-Bromo-thiophen-2-ylmethylene-amino]-3-mercapto-6-methyl-5-oxo-[1,2,4]triazine

    Kiran Singh


    Full Text Available A new series of cobalt, nickel, copper, and zinc complexes of bidentate Schiff base derived from the condensation of 5-bromothiophene-2-carboxaldehyde with 4-amino-3-mercapto-6-methyl-5-oxo-[1,2,4]triazine were synthesized. Physical (magnetic measurements, molar conductance, TG, spectral (UV-Vis, IR, 1HNMR, fluorescence, ESR, and analytical data have established the structures of synthesized Schiff base and its metal complexes. The presence of coordinated water in metal complexes was confirmed by IR and TG studies. The Schiff base exhibits a strong fluorescence emission, contrast to this partial fluorescence quenching phenomena is observed in its metal complexes. A square planar geometry for Cu(II and octahedral geometry for Co(II, Ni(II and Zn(II complexes have been proposed. The Schiff base and its metal complexes have been screened for antibacterial (Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and antifungal activities (Aspergillus niger, A. flavus.

  20. Various ways to reduce zinc oxide levels in S-SBR rubber compounds

    Heideman, G.; Noordermeer, Jacobus W.M.; Datta, Rabin; van Baarle, Ben


    Because of environmental concerns, the zinc content in rubber compounds has come under scrutiny. The research described in this article encompasses zinc-oxide, various zinc-complexes and alternative metal oxides as activators for sulphur vulcanisation. Regarding zinc complexes, it can be concluded

  1. Rapid Isolation and Determination of Flavones in Biological Samples Using Zinc Complexation Coupled with High-Performance Liquid Chromatography

    Chenghe Sun


    Full Text Available Chlorophyll-type contaminants are commonly encountered in the isolation and determination of flavones of plant aerial plant parts. Heme is also a difficult background substance in whole blood analysis. Both chlorophyll and heme are porphyrin type compounds. In this study, a rapid method for isolating flavones with 5-hydroxyl or ortho-hydroxyl groups from biological samples was developed based on the different solubilities of porphyrin-metal and flavone-metal complexes. It is important that other background substances, e.g., proteins and lipids, are also removed from flavones without an additional processing. The recoveries of scutellarin, baicalin, baicalein, wogonoside and wogonin, which are the primary constituents of Scutellaria baicalensis (skullcaps were 99.65% ± 1.02%, 98.98% ± 0.73%, 99.65% ± 0.03%, 97.59% ± 0.09% and 95.19% ± 0.47%, respectively. As a sample pretreatment procedure, this method was coupled to high-performance liquid chromatography (HPLC with good separation, sensitivity and linearity and was applied to determine the flavone content in different aerial parts of S. baicalensis and in dried blood spot samples.

  2. Influencia de los productos de la reacción entre lípidos oxidados (4,5 (E)-epoxy-2(E)-heptenal y 4,5 (E)-epoxy- 2 (E) -decenal) y lisina sobre la utilización de zinc y calcio: ensayos en células Caco-2

    Seiquer, Isabel; Navarro, María Pilar


    The influence of the presence of brown products from the reaction between two oxidized lipids (4,5 (E)-epoxy-2(E)-heptenal, EH, and 4,5 (E)-epoxy-2 (E)-decenal, ED) and lysine (EH-L and ED-L) on zinc and calcium utilization was studied, and compared with a fructosyl-lysine mixture (F-L). Assays were carried out in Caco-2 cells grown in bicameral chambers. The Zn transported across the cell monolayer was significantly lower in the presence of the EH-L, ED-L and F-L samples, specially with E...

  3. 复合氨基酸络合铁、锌对肥育猪铁、锌吸收代谢的影响%Effects of Iron and Zinc Complex Amino Acid Chelate on Absorption Metabolism of Iron and Zinc of Finishing Pigs

    詹康; 占今舜; 赵国琦; 霍永久


    本试验旨在研究复合氨基酸络合铁、锌对肥育猪血液生化指标,血清中免疫球蛋白含量,毛发中铁、锌含量及铁、锌表观消化率的影响。选择体重[(55.63±1.33)kg]相近的“杜×长×大”肥育猪36头,随机分至对照组和2个试验组,每组3个重复,每个重复4头猪。对照组饲喂铁、锌含量均为100 mg/kg(由硫酸亚铁、硫酸锌提供)的基础饲粮,试验1组饲喂铁、锌含量均为50 mg/kg(由硫酸亚铁、硫酸锌提供)+50 mg/kg(由复合氨基酸络合铁、锌提供)的基础饲粮,试验2组饲喂铁、锌含量均为100 mg/kg(由复合氨基酸络合铁、锌提供)的基础饲粮。结果表明:1)3组间的红细胞数量、血细胞压积、血清免疫球蛋白A和免疫球蛋白M含量无显著差异( P>0.05)。2)试验2组的血红蛋白含量和血清免疫球蛋白 G含量显著高于对照组( P<0.05)。3)试验2组毛发中铁含量显著高于对照组( P<0.05),试验2组毛发中锌含量显著高于试验1组和对照组( P<0.05);4)试验2组粪中铁含量和试验2组、试验1组粪中锌含量显著低于对照组( P<0.05);3组间铁和锌表观消化率无显著差异( P>0.05)。由此可见,添加复合氨基酸络合铁、锌可显著增加肥育猪血红蛋白、血清免疫球蛋白G含量及毛发中铁、锌含量,显著降低粪中铁、锌含量。%To study the effects of iron and zinc complex amino acid chelate on blood biochemical indexes,im-munoglobulin content in serum,iron and zinc contents in hair and apparent digestibility of iron and zinc of fin-ishing pigs,thirty-six finishing pigs( Duroc × Landrace × Yorkshire ) with an average initial body weight of (55.63±1.33)kg were selected and randomly allotted to three groups. There were three replicates per group and four pigs in each replicate. Pigs of the control group fed a basal diet with 100 mg

  4. Dinuclear cadmium(II), zinc(II), and manganese(II), trinuclear nickel(II), and pentanuclear copper(II) complexes with novel macrocyclic and acyclic Schiff-base ligands having enantiopure or racemic camphoric diamine components.

    Jiang, Jue-Chao; Chu, Zhao-Lian; Huang, Wei; Wang, Gang; You, Xiao-Zeng


    Four novel [3 + 3] Schiff-base macrocyclic ligands I-IV condensed from 2,6-diformyl-4-substituted phenols (R = CH(3) or Cl) and enantiopure or racemic camphoric diamines have been synthesized and characterized. Metal-ion complexations of these enantiopure and racemic [3 + 3] macrocyclic ligands with different cadmium(II), zinc(II), manganese(II), nickel(II), and copper(II) salts lead to the cleavage of Schiff-base C horizontal lineN double bonds and subsequent ring contraction of the macrocyclic ligands due to the size effects and the spatial restrictions of the coordination geometry of the central metals, the steric hindrance of ligands, and the counterions used. As a result, five [2 + 2] and one [1 + 2] dinuclear cadmium(II) complexes (1-6), two [2 + 2] dinuclear zinc(II) (7 and 8), and two [2 + 2] dinuclear manganese(II) (9 and 10) complexes together with one [1 + 1] trinuclear nickel(II) complex (11) and one [1 + 2] pentanuclear copper(II) complex (12), bearing enantiopure or racemic ligands, different substituent groups in the phenyl rings, and different anionic ligands (Cl(-), Br(-), OAc(-), and SCN(-)), have been obtained in which the chiral carbon atoms in the camphoric backbones are arranged in different ways (RRSS for the enantiopure ligands in 1, 2, 4, 5, and 7-10 and RSRS for the racemic ligands in 3, 6, 11, and 12). The steric hindrance effects of the methyl group bonded to one of the chiral carbon atoms of camphoric diamine units are believed to play important roles in the formation of the acyclic [1 + 1] trinuclear complex 11 and [1 + 2] dinuclear and pentanuclear complexes 6 and 12. In dinuclear cadmium(II), zinc(II), and manganese(II) complexes 1-10, the sequence of separations between the metal centers is consistent with that of the ionic radii shortened from cadmium(II) to manganese(II) to zinc(II) ions. Furthermore, UV-vis, circular dichroism, (1)H NMR, and fluorescence spectra have been used to characterize and compare the structural

  5. Poder e influencia en el liderazgo transformacional

    Pichicata R., David Stiven; Cicua N., Nicolás


    Como proyecto de grado, el presente trabajo consiste en una revisión teórica de los conceptos de liderazgo, poder e influencia, junto con las posibles relaciones que entre ellos se pueden presentar. Para ello, cada concepto es definido de manera individual, y con base en ello, se identifica la dependencia que tienen estos conceptos entre sí y la importancia dentro del desarrollo del liderazgo transformacional actual. Para lograr lo propuesto, se llevó a cabo la revisión de una parte de la lit...

  6. Niveles de vitamina A y zinc en pacientes de cirugía gastroenterológica: Relación con la inflamación y la aparición de complicaciones postoperatorias Vitamin A and zinc levels in gastroenterological surgical patients: Relation with inflammation and postoperative complications

    L. B. Zago; E. Danguise; C. A. González Infantino; M. E. Río; Callegari, M.


    Introducción: Se acepta que la depleción aún moderada de algunos nutrientes puede afectar la evolución del paciente quirúrgico. Objetivo: Evaluar la influencia de los niveles plasmáticos de retinol y de zinc preoperatorios sobre la evolución postoperatoria; evaluar la influencia de la inflamación sobre los niveles de ambos marcadores. Métodos: Se determinaron los niveles plasmáticos de retinol y zinc en 50 pacientes previo a ser sometidos a cirugías gastroenterológicas programadas. Para carac...

  7. Copper(II) and zinc(II) complexes of the peptides Ac-HisValHis-NH2 and Ac-HisValGlyAsp-NH2 related to the active site of the enzyme CuZnSOD.

    Bóka, Beáta; Myari, Alexandra; Sóvágó, Imre; Hadjiliadis, Nick


    Copper(II) and zinc(II) complexes of the peptides Ac-HisValHis-NH2 and Ac-HisValGlyAsp-NH2 related to the active site of the enzyme CuZnSOD were studied by potentiometric and spectroscopic (UV-Vis, CD and EPR) techniques. The results reveal that both ligands have effective metal binding sites, but the tripeptide is a much stronger complexing agent than the tetrapeptide. The formation of a macrochelate via the coordination of the imidazolyl residues is suggested in the copper(II)-Ac-HisValHis-NH2 system in the acidic pH range, while a 4N complex predominates at physiological pH. The interaction of Ac-HisValHis-NH2 with zinc(II) results in the formation of a precipitate indicating polynuclear complex formation. Both copper(II)-Ac-HisValHis-NH2 and copper(II)-HisValHis systems exhibit catalytic activity toward the dismutation of superoxide anion at physiological pH, but the saturated coordination sphere of the metal ions in both systems results in low reactivity as compared to the native enzyme.

  8. Preparation of Zinc (II and Cadmium (II Complexes of the Tetradentate Schiff Base Ligand 2-((E-(2-(2-(pyridine-2-yl- ethylthioethyliminomethyl-4-bromophenol (PytBrsalH

    Roya Kabiri


    Full Text Available We describe the synthesis and characterization of two new zinc (II andcadmium (II complexes of the tetradentate dissymmetric Schiff base ligand 2-((E-(2-(2-(pyridine-2-ylethylthioethyliminomethyl-4-bromophenol (PytBrsalH, prepared from 1-(2-pyridyl-3-thia-5-aminopentane (pyta and 5-bromosalicylaldehyde. The complexeswere synthesized by treating an ethanolic solution of the ligand with equimolar amounts ofappropriate metal salts in 1 M methanolic solution of NaOH or alternatively, by a moredirect route in which the two reactants are added to a solution of the ligand immediatelyafter formation of the latter and prior to any isolation. The complexes were characterizedby elemental analysis, FTIR, 1H-NMR, electronic spectra and molar conductivity.According to obtained data, the probable coordination geometries of zinc and cadmium inthese complexes with mixed N, S and O donor atoms are tetrahedral- and octahedral-like,respectively. Both complexes were found to be 1:1 electrolyte systems in acetonitrile.

  9. Monitoring of meteorology and air quality at influence area of COMPERJ (Rio de Janeiro Petrochemical Complex); Monitoramento meteorologico e da qualidade do ar na regiao de influencia do COMPERJ (Complexo Petroquimico do Rio de Janeiro)

    Albuquerque, Edler Lins de; Villa, Felipe de Santana; Lyra, Diogenes Ganghis Pimentel de [CETREL-LUMINA Solucoes Ambientais, Salvador, BA (Brazil); Secron, Marcelo; Iorio, Patricia Freire; Mendes, Marcos Faistauer [PETROBRAS, Rio de Janeiro, RJ (Brazil)


    Rio de Janeiro Petrochemical Complex (COMPERJ) will be installed in the north region of Itaborai city. The start of COMPERJ operations is foreseen to 2012. Because of the intensification of industrialization and urbanization processes, the implantation of COMPERJ will bring environmental modifications for Itaborai city and neighbors areas. Thus, meteorological and air quality monitoring was initiated in February of 2007 with the intention of carrying out a characterization of air pollution in this area, before COMPERJ operations. In this work are presented the results found in campaigns performed of February of 2007 until April of 2008. The meteorological monitoring disclosed that the meteorological parameters have varied enough throughout the months, but these are representative of a global behavior of the studied area. Monitoring of air quality has shown that atmospheric levels of monitored pollutants has been generally below of Brazilian air quality standards. This fact corroborates the basic aspect of the present study: identification of the concentrations 'background' in the studied area. Throughout the period of monitoring, the primary air quality standard for ozone has been reached. Observations of meteorological parameters indicate that this fact is associated to the emissions originated from Sao Goncalo, Niteroi and Rio de Janeiro cities. (author)

  10. DNA- and BSA-binding studies and anticancer activity against human breast cancer cells (MCF-7) of the zinc(II) complex coordinated by 5,6-diphenyl-3-(2-pyridyl)-1,2,4-triazine

    Anjomshoa, Marzieh; Fatemi, Seyed Jamilaldin; Torkzadeh-Mahani, Masoud; Hadadzadeh, Hassan


    Binding studies of a mononuclear zinc(II) complex, [Zn(dppt)2Cl2] (dppt is 5,6-diphenyl-3-(2-pyridyl)-1,2,4-triazine), with DNA and bovine serum albumin (BSA) have been investigated under physiological conditions. The binding properties of the complex with fish sperm DNA (FS-DNA) have been investigated by UV-Vis absorption, thermal denaturation, competitive DNA-binding studies with ethidium bromide (EB) by fluorescence, and gel electrophoresis techniques. The competitive study with (EB) shows that the complex can displace EB from the DNA-EB system and compete for the DNA-binding sites with EB, which is usually characteristic of the intercalative interaction of compounds with DNA. The value of the fluorescence quenching constant (Ksv) was obtained as 3.1 × 104 M-1, indicating that this complex shows a high quenching efficiency and a significant degree of binding to DNA. Moreover, the intercalative binding mode has also been verified by the results of UV-Vis absorption, thermal denaturation and gel electrophoresis. The value of Kb at room temperature was calculated to be 1.97 × 105 M-1, indicating that the complex possesses strong tendency to bind with DNA. This value is very greater than to the values obtained for other zinc(II) complexes. The interaction of the complex with BSA has been studied by UV-Vis absorption, fluorescence and circular dichroism (CD) spectroscopic techniques. The results indicate that the complex has a quite strong ability to quench the fluorescence of BSA and the binding reaction is mainly a static quenching process. The quenching constants (KSV), the binding constants (Kb), the number of binding sites at different temperatures, the binding distance between BSA and the complex (r), and the thermodynamic parameters (ΔHo, ΔSo and ΔGo) between BSA and the complex were calculated. The complex exhibits good binding propensity to BSA showing relatively high binding constant values. The positive ΔHo and ΔSo values indicate that the

  11. DNA- and BSA-binding studies and anticancer activity against human breast cancer cells (MCF-7) of the zinc(II) complex coordinated by 5,6-diphenyl-3-(2-pyridyl)-1,2,4-triazine.

    Anjomshoa, Marzieh; Fatemi, Seyed Jamilaldin; Torkzadeh-Mahani, Masoud; Hadadzadeh, Hassan


    Binding studies of a mononuclear zinc(II) complex, [Zn(dppt)2Cl2] (dppt is 5,6-diphenyl-3-(2-pyridyl)-1,2,4-triazine), with DNA and bovine serum albumin (BSA) have been investigated under physiological conditions. The binding properties of the complex with fish sperm DNA (FS-DNA) have been investigated by UV-Vis absorption, thermal denaturation, competitive DNA-binding studies with ethidium bromide (EB) by fluorescence, and gel electrophoresis techniques. The competitive study with (EB) shows that the complex can displace EB from the DNA-EB system and compete for the DNA-binding sites with EB, which is usually characteristic of the intercalative interaction of compounds with DNA. The value of the fluorescence quenching constant (Ksv) was obtained as 3.1×10(4)M(-1), indicating that this complex shows a high quenching efficiency and a significant degree of binding to DNA. Moreover, the intercalative binding mode has also been verified by the results of UV-Vis absorption, thermal denaturation and gel electrophoresis. The value of Kb at room temperature was calculated to be 1.97×10(5)M(-1), indicating that the complex possesses strong tendency to bind with DNA. This value is very greater than to the values obtained for other zinc(II) complexes. The interaction of the complex with BSA has been studied by UV-Vis absorption, fluorescence and circular dichroism (CD) spectroscopic techniques. The results indicate that the complex has a quite strong ability to quench the fluorescence of BSA and the binding reaction is mainly a static quenching process. The quenching constants (KSV), the binding constants (Kb), the number of binding sites at different temperatures, the binding distance between BSA and the complex (r), and the thermodynamic parameters (ΔH(o), ΔS(o) and ΔG(o)) between BSA and the complex were calculated. The complex exhibits good binding propensity to BSA showing relatively high binding constant values. The positive ΔH(o) and ΔS(o) values indicate that

  12. Transcriptional activation is a conserved feature of the early embryonic factor Zelda that requires a cluster of four zinc fingers for DNA binding and a low-complexity activation domain.

    Hamm, Danielle C; Bondra, Eliana R; Harrison, Melissa M


    Delayed transcriptional activation of the zygotic genome is a nearly universal phenomenon in metazoans. Immediately following fertilization, development is controlled by maternally deposited products, and it is not until later stages that widespread activation of the zygotic genome occurs. Although the mechanisms driving this genome activation are currently unknown, the transcriptional activator Zelda (ZLD) has been shown to be instrumental in driving this process in Drosophila melanogaster. Here we define functional domains of ZLD required for both DNA binding and transcriptional activation. We show that the C-terminal cluster of four zinc fingers mediates binding to TAGteam DNA elements in the promoters of early expressed genes. All four zinc fingers are required for this activity, and splice isoforms lacking three of the four zinc fingers fail to activate transcription. These truncated splice isoforms dominantly suppress activation by the full-length, embryonically expressed isoform. We map the transcriptional activation domain of ZLD to a central region characterized by low complexity. Despite relatively little sequence conservation within this domain, ZLD orthologs from Drosophila virilis, Anopheles gambiae, and Nasonia vitripennis activate transcription in D. melanogaster cells. Transcriptional activation by these ZLD orthologs suggests that ZLD functions through conserved interactions with a protein cofactor(s). We have identified distinct DNA-binding and activation domains within the critical transcription factor ZLD that controls the initial activation of the zygotic genome.

  13. Further Aspects of Ochratoxin A-Cation Interactions: Complex Formation with Zinc Ions and a Novel Analytical Application of Ochratoxin A-Magnesium Interaction in the HPLC-FLD System

    Miklós Poór


    Full Text Available Ochratoxin A (OTA is a mycotoxin produced by different Aspergillus and Penicillium species. Since its mechanism of action is not fully understood yet, it is important to gain further insight into different interactions of OTA at the molecular level. OTA is found worldwide in many foods and drinks. Moreover, it can also be detected in human and animal tissues and body fluids, as well. Therefore, the development of highly sensitive quantitative methods for the determination of OTA is of utmost importance. OTA most likely forms complexes with divalent cations, both in cells and body fluids. In the present study, the OTA-zinc interaction was investigated and compared to OTA-magnesium complex formation using fluorescence spectroscopy and molecular modeling. Our results show that zinc(II ion forms a two-fold higher stable complex with OTA than magnesium(II ion. In addition, based on the enhanced fluorescence emission of OTA in its magnesium-bound form, a novel RP-HPLC-fluorescence detector (FLD method was also established. Our results highlight that the application of magnesium chloride in alkaline eluents results in an approximately two-fold increase in sensitivity using the HPLC-FLD technique.

  14. Synthesis and characterization of cobalt(II), nickel(II), copper(II) and zinc(II) complexes with Schiff base derived from 4-amino-3-mercapto-6-methyl-5-oxo-1,2,4-triazine.

    Singh, Kiran; Barwa, Manjeet Singh; Tyagi, Parikshit


    A few (1:1) and (1:2) metal complexes of cobalt(II), nickel(II), copper(II) and zinc(II) have been isolated with ligand derived from the condensation of 4-amino-3-mercapto-6-methyl-5-oxo-1,2,4-triazine with 2-acetylpyridine (L(1)) and characterized by elemental analysis, conductivity measurements, infrared, electronic, (1)H NMR spectral data, magnetic and thermogravimetric analyses. Due to insolubility in water and most of the common organic solvents and infusibility at higher temperatures, all the complexes are thought to be polymeric in nature. A square-planar geometry was suggested for copper(II) and octahedral proposed for cobalt(II), nickel(II) and zinc(II). Some of the chemically synthesized compounds have been screened in vitro against the three Gram-positive (Staphylococcus aureus, Staphylococcus epidermidis and Bacillus subtilis) and two Gram-negative (Salmonella typhi and Escherichia coli) organisms. It is observed that the coordination of metal ion has pronounced effect on the microbial activities of the ligand. The metal complexes have higher antimicrobial effect than the free ligands.


    Dr.Nilima Thosar*, Dr. Manoj Chandak, Dr.Manohar Bhat, Dr.Silpi Basak


    Background: Endodontic treatment of primary teeth is required to eliminate microorganisms from the infected root canals having complex root canal anatomy. Objectives: To assess the antifungal effect of zinc oxide paste with tea tree oil, thyme oil, peppermint oil on candida albicans and to compare it with zinc oxide eugenol paste. Materials and methods: Zinc oxide pastes containing essential oils used in the present study were zinc oxide tea tree oil paste (ZOT); zinc oxide thyme oil ...

  16. Lessons from a “Failed” Experiment: Zinc Silicates with Complex Morphology by Reaction of Zinc Acetate, the Ionic Liquid Precursor (ILP Tetrabutylammonium Hydroxide (TBAH, and Glass

    Andreas Taubert


    Full Text Available At elevated temperatures, the ionic liquid precursor (ILP tetrabutylammonium hydroxide reacts with zinc acetate and the glass wall of the reaction vessel. While the reaction of OH- with the glass wall is not surprising as such and could be considered a failed experiment, the resulting materials are interesting for a variety of applications. If done on purpose and under controlled conditions, the reaction with the glass wall results in uniform, well-defined hemimorphite Zn4Si2O7(OH2·nH2O and willemite Zn2SiO4 microcrystals and films. Their morphology can be adjusted by variation of the reaction time and reaction temperature. The hemimorphite can be transformed to Zn2SiO4 via calcination. The process is therefore a viable approach for the fabrication of porous films on glass surfaces with potential applications as catalyst support, among others.

  17. Integrated criteria document Zinc

    Cleven RFMJ; Janus JA; Annema JA; Slooff W


    This report contains information on zinc and zinc compounds concerning standards, emissions, exposure levels and effect levels. It includes a risk evaluation and presents proposals for maximum permissible concentrations of zinc in the environment. This study indicates that the concentration of zinc

  18. Cobalt(II), nickel(II), copper(II), zinc(II) and hafnium(IV) complexes of N'-(furan-3-ylmethylene)-2-(4-methoxyphenylamino)acetohydrazide.

    Emam, Sanaa M; El-Saied, Fathy A; Abou El-Enein, Saeyda A; El-Shater, Heba A


    Cobalt(II), nickel(II), copper(II), zinc(II) and hafnium(IV) complexes of furan-2-carbaldehyde 4-methoxy-N-anilinoacetohydrazone were synthesized and characterized by elemental and thermal (TG and DTA) analyses, IR, UV-vis and (1)H NMR spectra as well as magnetic moment and molar conductivity. Mononuclear complexes are obtained with 1:1 molar ratio except complexes 3 and 9 which are obtained with 1:2 molar ratios. The IR spectra of ligand and metal complexes reveal various modes of chelation. The ligand behaves as a neutral bidentate one and coordination occurs via the carbonyl oxygen atom and azomethine nitrogen atom. The ligand behaves also as a monobasic tridentate one and coordination occurs through the enolic oxygen atom, azomethine nitrogen atom and the oxygen atom of furan ring. Moreover, the ligand behaves as a neutral tridentate and coordination occurs via the carbonyl oxygen, azomethine nitrogen and furan oxygen atoms as well as a monobasic bidentate and coordination occurs via the enolic oxygen atom and azomethine nitrogen atom. The electronic spectra and magnetic moment measurements reveal that all complexes possess octahedral geometry except the copper complex 10 possesses a square planar geometry. The thermal studies showed the type of water molecules involved in metal complexes as well as the thermal decomposition of some metal complexes.

  19. Update on zinc biology.

    Solomons, Noel W


    Zinc has become a prominent nutrient of clinical and public health interest in the new millennium. Functions and actions for zinc emerge as increasingly ubiquitous in mammalian anatomy, physiology and metabolism. There is undoubtedly an underpinning in fundamental biology for all of the aspects of zinc in human health (clinical and epidemiological) in pediatric and public health practice. Unfortunately, basic science research may not have achieved a full understanding as yet. As a complement to the applied themes in the companion articles, a selection of recent advances in the domains homeostatic regulation and transport of zinc is presented; they are integrated, in turn, with findings on genetic expression, intracellular signaling, immunity and host defense, and bone growth. The elements include ionic zinc, zinc transporters, metallothioneins, zinc metalloenzymes and zinc finger proteins. In emerging basic research, we find some plausible mechanistic explanations for delayed linear growth with zinc deficiency and increased infectious disease resistance with zinc supplementation. Copyright © 2013 S. Karger AG, Basel.

  20. Factores humanos y su influencia en la productividad

    Mirza Cequea; Miguel Núñez Bottini


    La productividad es un concepto de naturaleza multidimensional en la que influyen ciertas características y comportamientos del individuo, dicha influencia implica procesos psicológicos y psicosociales complejos de cuantificar que constituyen los factores humanos. El objetivo general de la investigación, es analizar los factores humanos y su influencia en la productividad, vista desde la perspectiva de tres unidades diferentes; individuo, grupo y organización. Para tal fin, se plantearon ...

  1. Hemimorphite Ores: A Review of Processing Technologies for Zinc Extraction

    Chen, Ailiang; Li, Mengchun; Qian, Zhen; Ma, Yutian; Che, Jianyong; Ma, Yalin


    With the gradual depletion of zinc sulfide ores, exploration of zinc oxide ores is becoming more and more important. Hemimorphite is a major zinc oxide ore, attracting much attention in the field of zinc metallurgy although it is not the major zinc mineral. This paper presents a critical review of the treatment for extraction of zinc with emphasis on flotation, pyrometallurgical and hydrometallurgical methods based on the properties of hemimorphite. The three-dimensional framework structure of hemimorphite with complex linkage of its structural units lead to difficult desilicification before extracting zinc in the many metallurgical technologies. It is found that the flotation method is generally effective in enriching zinc minerals from hemimorphite ores into a high-grade concentrate for recovery of zinc. Pure zinc can be produced from hemimorphite or/and willemite with a reducing reagent, like methane or carbon. Leaching reagents, such as acid and alkali, can break the complex structure of hemimorphite to release zinc in the leached solution without generation of silica gel in the hydrometallurgical process. For optimal zinc extraction, combing flotation with pyrometallurgical or hydrometallurgical methods may be required.

  2. Stepwise preparation and characterization of molecular wires made of zinc octaethylporphyrin complexes bridged by 4, 4'-bipyridine on HOPG

    Ferreira, Quirina; Alcacer, LuIs; Morgado, Jorge, E-mail:, E-mail:, E-mail: [Instituto de Telecomunicacoes, Instituto Superior Tecnico, Avenida Rovisco Pais, P-1049-001 Lisboa (Portugal)


    Molecular-scale devices can be made using a step-by-step procedure, in a controllable and highly versatile way. In this report, we describe the growth of molecular wires (MW) from zinc (II) octaethylporphyrin (ZnOEP) assembled on highly oriented pyrolytic graphite (HOPG) by a step-by-step approach using 4, 4'-bipyridine (BP) to bridge the porphyrin units, via coordination of the nitrogen atom to zinc. In order to gain an insight into the molecular self-organization of these wires, we carried out a detailed scanning tunnelling microscopy (STM) analysis of each monolayer, using a solid/liquid interface technique, up to a complete ZnOEP/BP/ZnOEP/BP/ZnOEP-assembled structure. The electrical properties of the MWs were assessed by scanning tunnelling spectroscopy (STS) and by current-sensing atomic force microscopy (CS-AFM), showing an increase of electrical resistance with the length of the MW.

  3. Mixed effect of the supporting electrolyte and the zinc anode in the electrochemical homocoupling of 2-bromopyridines catalyzed by nickel complexes in an undivided cell.

    de França, Kelnner W R; Oliveira, Jadson de Lira; Florêncio, Tupolevck; da Silva, Aderivaldo P; Navarro, Marcelo; Léonel, Eric; Nédélec, Jean-Yves


    [reactions: see text] Nickel-catalyzed electroreductive homocoupling of 2-bromomethylpyridines and 2-bromopyridine has been investigated in an undivided cell in the presence of a zinc sacrificial anode. A series of reactions were performed with various types and concentrations of supporting electrolyte. It was observed that a key step in this process is the formation of an arylzinc through a nickel-zinc transmetalation. This intermediate can be transformed back to the reactive arylnickel species to afford the homocoupling as the final product. The back process from the arylzinc intermediate is, however, suppressed in the presence of high concentration (0.2 M) of tetraalkylammonium salts. On the contrary, with NaI, the formation of the dimer is not prevented, whatever the NaI concentration.

  4. 2-氨甲基吡啶配体锌配合物的合成、晶体结构及催化性能%Synthesis, Crystal Structure and Catalytic Performance of Zinc Complex Containing 2-(Aminomethyl) pyridine Ligand

    刘超; 卓馨; 张虎; 刘新华


    以2-氨甲基吡啶为配体与醋酸锌反应合成了一种新型锌金属配合物[Zn( AMPy)2(OAc)]2·[ Zn( OAc)4]( AMPy=2-氨甲基吡啶),通过核磁共振谱、红外光谱、元素分析和X射线单晶衍射对其结构进行了表征.晶体结构显示,该配合物属于三斜晶系,空间群为 P1,晶胞参数为 a=1.07360(19) nm, b=1.2491(2) nm, c=1.8976(3) nm,α=83.809(2)°,β=89.595(2)°,γ=65.708(2)°, V=2.3039(7) nm3, Z=2;配合物分子由3个不同的配位Zn离子通过分子内氢键连成一个完整的分子,分子间氢键再将其连成一个二维网状结构.研究了该金属配合物在Henry催化反应方面的性能,并优化出最佳催化条件.%A novel zinc metal complex [ Zn ( AMPy ) 2 ( OAc ) ] 2 [ Zn ( OAc ) 4 ] [ AMPy=2-( aminomethyl ) pyridine] was synthesized by the reaction of zinc acetate to 2-( aminomethyl) pyridine ligand. The structure of the complex was characterized by 1 H NMR, IR, elemental analysis and X-ray single crystal diffraction. The crystal structural analyses show that the complex belongs to triclinic system, space group is P1 with a=1. 07360(19) nm, b=1. 2491(2) nm, c=1. 8976(3) nm, α=83. 809(2)°, β=89. 595(2)°, γ=65. 708(2)°, V=2. 3039(7) nm3, Z=2. The complex molecular consists of three different coordinated zinc ions which are connected by intramolecular hydrogen bonds into a total molecular, and 2D network structure is further formed by intermolecular hydrogen bonds. The catalytic performance of the metal complex in Henry reaction was studied, and the optimum catalytic conditions were obtained. The results show that the complex exhibits a high catalytic performance with 9%( molar fraction) of catalyst loading, methanol as solvent and reaction at room temperature for 20 h.

  5. ErbB2-Driven Breast Cancer Cell Invasion Depends on a Complex Signaling Network Activating Myeloid Zinc Finger-1-Dependent Cathepsin B Expression

    Rafn, Bo; Nielsen, Christian Thomas Friberg; Andersen, Sofie Hagel;


    signaling network activates the transcription of cathepsin B gene (CTSB) via myeloid zinc finger-1 transcription factor that binds to an ErbB2-responsive enhancer element in the first intron of CTSB. This work provides a model system for ErbB2-induced breast cancer cell invasiveness, reveals a signaling...... network that is crucial for invasion in vitro, and defines a specific role and targets for the identified serine-threonine kinases....

  6. Structural, MALDI-TOF-MS, magnetic and spectroscopic studies of new dinuclear copper(II), cobalt(II) and zinc(II) complexes containing a biomimicking μ-OH bridge.

    Núñez, Cristina; Bastida, Rufina; Macías, Alejandro; Valencia, Laura; Neuman, Nicolás I; Rizzi, Alberto C; Brondino, Carlos D; González, Pablo J; Capelo, José Luis; Lodeiro, Carlos


    The Py(2)N(4)S(2) octadentate coordinating ligand afforded dinuclear cobalt, copper and zinc complexes and the corresponding mixed metal compounds. The overall geometry and bonding modes have been deduced on the basis of elemental analysis data, MALDI-TOF-MS, IR, UV-vis and EPR spectroscopies, single-crystal X-Ray diffraction, conductivity and magnetic susceptibility measurements. In the copper and zinc complexes, a μ-hydroxo bridge links the two metal ions. In both cases, the coordination geometry is distorted octahedral. Magnetic and EPR data reveal weakly antiferromagnetic high spin Co(II) ions, compatible with a dinuclear structure. The magnetic characterization of the dinuclear Cu(II) compound indicates a ferromagnetically coupled dimer with weak antiferromagnetic intermolecular interactions. The intra-dimer ferromagnetic behaviour was unexpected for a Cu(II) dimer with such μ-hydroxo bridging topology. We discuss the influence on the magnetic properties of non-covalent interactions between the bridging moiety and the lattice free water molecules.

  7. Method of capturing or trapping zinc using zinc getter materials

    Hunyadi Murph, Simona E.; Korinko, Paul S.


    A method of trapping or capturing zinc is disclosed. In particular, the method comprises a step of contacting a zinc vapor with a zinc getter material. The zinc getter material comprises nanoparticles and a metal substrate.

  8. Zinc: the neglected nutrient.

    Shambaugh, G E


    Zinc was first recognized as essential for animals at the University of Illinois School of Agriculture in 1916, when it was found that zinc-deficient baby pigs were runty, developed dermatitis on their legs, and were sterile. Zinc deficiency was first recognized in man by Dr. Ananda Prasad of Detroit 26 years ago when he measured serum and hair zinc levels in young male Egyptian dwarfs who had failed to mature and were small in stature. By simply adding zinc to their regular diet, they grew in height and became sexually mature. It is now recognized that dwarfism in males is frequent around the Mediterranean, where wheat is the staple of life and has been grown for 4,000 years on the same soil, thereby resulting in the depletion of zinc. Professor Robert Henkin first suggested that zinc deficiency might cause hearing-nerve impairment. Assay of the soft tissues of the cochlea and vestibule revealed a zinc level higher than that of any other part of the body. Previously, the eye was considered to have the highest level of zinc of any organ. To diagnose zinc deficiency clinically, we use serum zinc assays made at the Mayo Clinic Trace Element Laboratory. With zinc supplementation in patients who are marginally zinc deficient, there has been improvement in tinnitus and sensorineural hearing loss in about one-third of elderly adults. We believe zinc deficiency is one causation of presbycusis; by recognizing and correcting it, a progressive hearing loss can be arrested.

  9. Kinetics of the dissolution of zinc sulfide in an oxidizing slag

    Gupta, Suresh K.


    A new concept has been developed for the production of zinc from zinc and complex zinc concentrates. It is a two-stage process involving oxidation of zinc sulfide to oxide and dissolution into slag and the fuming of zinc from the slag by injecting carbonaceous materials into it to produce zinc vapors which can be subsequently condensed in a lead-splash condenser such as those used in the Imperial Smelting Process (ISP). In this paper, the effects of the quantity of air, temperature, and concentrate feed rate have been discussed on the production of zinc-rich slag, which is the first stage of the proposed process.

  10. Effect of 2-Amino-Benzothiazole Zinc Complex on the Growth and Development of Cotton Bollworm%2-氨基苯并噻唑锌配合物对棉铃虫生长发育的影响

    张海玲; 王树芳; 张优优; 王玉平; 柴连琴


    选取数百条正常三龄棉铃虫,分成5组,分别饲喂含不同剂量的2-氨基苯并噻唑锌配合物的人工配制饲料,期间测量每条虫的体重,直至生长到六龄使用血细胞计数板对血细胞进行计数,再测定血浆中的T-SOD活性.结果显示:与对照组相比,饲喂含低剂量2-氨基苯并噻唑锌配合物饲料的棉铃虫的血细胞数目较多,T-SOD活力较强;饲喂含高剂量配合物饲料的棉铃虫受到严重抑制,几乎处于不生长状态.以上结果表明低剂量2-氨基苯并噻唑锌配合物对棉铃虫生长发育有促进作用,而高剂量的则有抑制作用.%Hundreds of normal third instar cotton bollworms were selected and divided into five groups. They were fed with the artificial feed with different doses of 2-amino benzothiazole zinc complex solution. During the period, the weight of each cotton bollworm was measured. The number of the blood cells was calculated, using the blood cell counting plate. Then the activity of the T-SOD was determinated. Compared with the control group, the cotton bollworms fed with low dose of 2-amino benzothiazole zinc complex feed have more blood cells and a higher activity of T-SOD. Cotton bollworms fed with high dose of the complex were seriously inhibited and almost no growth in the state was shown. It suggested that low dose of 2-amino benzothiazole zinc complex promoted the growth and development of cotton bollworms, while high dose inhibited that.

  11. Partial substitution, with their chelated complexes, of the inorganic zinc, copper and manganese in sow diets reduced the laminitic lesions in the claws and improved the morphometric characteristics of the hoof horn of sows from three Greek herds.

    Varagka, Nikoleta; Lisgara, Marina; Skampardonis, Vassilis; Psychas, Vassilis; Leontides, Leonidas


    Hoof lesions in sows have been associated with lameness and poor hoof horn quality. The mechanical strength and quality of hoof horn is determined by the density and diameter of horn tubules, which were recently associated with the severity of lesions on the hoof wall of sows. Histologic changes that have previously been described in cases of bovine laminitis, have also been observed in the dermis and epidermis of the sows' claws. Trace elements, particularly zinc, copper and manganese, occupy important roles as enzyme catalysts in the process of keratin synthesis which determines the quality and the integrity of the hoof epidermis. Therefore, the objective of this study was to investigate the effect of diet supplementation with chelated zinc, copper and manganese, partially substituting their inorganic form, on sow claw health and hoof horn quality assessed by macroscopic, histologic and morphometric examination. Clinically, the total claw lesion score was significantly lower in claws of sows which received the "organic" diet compared to those of sows on the "inorganic" diet. Histologically, lamellar hyperplasia was the most frequently recorded change in the epidermis of the sows' claws regardless of the diet's mineral source. The claws of the sows which received the organic diet were more likely to have none or less histologic changes than at least one or more, respectively, compared to those of the sows on the "inorganic" diet. Morphometrically, the density and vertical and horizontal diameters of the horn tubules was significantly higher and smaller, respectively, in the hoof horn of sows which received the "organic" compared to those which received the "inorganic" source diet. Partial substitution of the inorganic zinc, copper and manganese in sows' diet with their chelated complexes, provided a comparative advantage against a conventional, inorganic mineral source diet, at least under the conditions examined in the current study, in terms of macroscopic

  12. Crosstalk between Zinc Status and Giardia Infection: A New Approach

    Humberto Astiazarán-García


    Full Text Available Zinc supplementation has been shown to reduce the incidence and prevalence of diarrhea; however, its anti-diarrheal effect remains only partially understood. There is now growing evidence that zinc can have pathogen-specific protective effects. Giardiasis is a common yet neglected cause of acute-chronic diarrheal illness worldwide which causes disturbances in zinc metabolism of infected children, representing a risk factor for zinc deficiency. How zinc metabolism is compromised by Giardia is not well understood; zinc status could be altered by intestinal malabsorption, organ redistribution or host-pathogen competition. The potential metal-binding properties of Giardia suggest unusual ways that the parasite may interact with its host. Zinc supplementation was recently found to reduce the rate of diarrhea caused by Giardia in children and to upregulate humoral immune response in Giardia-infected mice; in vitro and in vivo, zinc-salts enhanced the activity of bacitracin in a zinc-dose-dependent way, and this was not due to zinc toxicity. These findings reflect biological effect of zinc that may impact significantly public health in endemic areas of infection. In this paper, we shall explore one direction of this complex interaction, discussing recent information regarding zinc status and its possible contribution to the outcome of the encounter between the host and Giardia.

  13. Prediction of DNA-binding specificity in zinc finger proteins

    Sumedha Roy; Shayoni Dutta; Kanika Khanna; Shruti Singla; Durai Sundar


    Zinc finger proteins interact via their individual fingers to three base pair subsites on the target DNA. The four key residue positions −1, 2, 3 and 6 on the alpha-helix of the zinc fingers have hydrogen bond interactions with the DNA. Mutating these key residues enables generation of a plethora of combinatorial possibilities that can bind to any DNA stretch of interest. Exploiting the binding specificity and affinity of the interaction between the zinc fingers and the respective DNA can help to generate engineered zinc fingers for therapeutic purposes involving genome targeting. Exploring the structure–function relationships of the existing zinc finger–DNA complexes can aid in predicting the probable zinc fingers that could bind to any target DNA. Computational tools ease the prediction of such engineered zinc fingers by effectively utilizing information from the available experimental data. A study of literature reveals many approaches for predicting DNA-binding specificity in zinc finger proteins. However, an alternative approach that looks into the physico-chemical properties of these complexes would do away with the difficulties of designing unbiased zinc fingers with the desired affinity and specificity. We present a physico-chemical approach that exploits the relative strengths of hydrogen bonding between the target DNA and all combinatorially possible zinc fingers to select the most optimum zinc finger protein candidate.

  14. Synthesis, crystal structure and investigation of mononuclear copper(II) and zinc(II) complexes of a new carboxylate rich tripodal ligand and their interaction with carbohydrates in alkaline aqueous solution.

    Stewart, Christopher D; Pedraza, Mayra; Arman, Hadi; Fan, Hua-Jun; Schilling, Eduardo Luiz; Szpoganicz, Bruno; Musie, Ghezai T


    A new carboxylate rich asymmetric tripodal ligand, N-[2-carboxybenzomethyl]-N-[carboxymethyl]-β-alanine (H3camb), and its di-copper(II), (NH4)2[1]2, and di-zinc(II), ((CH3)4N)2[2]2, complexes have been synthesized as carbohydrate binding models in aqueous solutions. The ligand and complexes have been fully characterized using several techniques, including single crystal X-ray diffraction. The interactions of (NH4)2[1]2 and ((CH3)4N)2[2]2 with D-glucose, D-mannose, D-xylose and xylitol in aqueous alkaline media were investigated using UV-Vis and (13)C-NMR spectroscopic techniques, respectively. The molar conductance, NMR and ESI-MS studies indicate that the complexes dissociate in solution to produce the respective complex anions, 1(-) and 2(-). Complexes 1(-) and 2(-) showed chelating ability towards the naturally abundant and biologically relevant sugars, D-glucose, D-mannose, D-xylose, and xylitol. The complex ions bind to one molar equivalent of the sugars, even in the presence of stoichiometric excess of the substrates, in solution. Experimentally obtained spectroscopic data and computational results suggest that the substrates bind to the metal center in a bidentate fashion. Apparent binding constant values, pK(app), between the complexes and the substrates were determined and a specific mode of substrate binding is proposed. The pK(app) and relativistic density functional theory (DFT) calculated Gibbs free energy values indicate that D-mannose displayed the strongest interaction with the complexes. Syntheses, characterizations, detailed substrate binding studies using spectroscopic techniques, single crystal X-ray diffraction and geometry optimizations of the complex-substrates with DFT calculations are also reported.

  15. Zinc oxide overdose

    Zinc oxide is an ingredient in many products. Some of these are certain creams and ointments used ... prevent or treat minor skin burns and irritation. Zinc oxide overdose occurs when someone eats one of ...


    Marek Pająk


    Full Text Available The research was carried out in the Świerklaniec Forest District, the Brynica sub-district, which is located in the immediate vicinity of a metallurgical plant, a zinc mine named Huta Cynku "Miasteczko Śląskie" (HCMŚ. In autumn 2008, in the area in question, 31 permanent trial plots were established, aligned within a regular net of squares, with dimensions of 1500×1500 m. The trial plots were located to the north-east and to the east of the emitter (the HCMŚ zinc mine, accordingly with the direction of prevailing winds. In September 2013, and September and October 2014, sporocarps of bay bolete (Xerocomus badius (Fr. E. were collected from the trial plots. The analyses performed for the material gathered covered a determination of heavy metal content in mushrooms (Zn, Pb and Cd, using a method of inductively coupled plasma atomic emission spectroscopy ICP-AES. This paper aimed to establish the accumulation levels of selected heavy metals (Zn, Pb and Cd in bay bolete growing in forests of the Brynica sub-district, in the Świerklaniec Forest District, and the correlation between their content in soil and in the mushrooms under scrutiny. The analyses revealed that the contamination degree in the investigated species was extremely high. The content of toxic elements in bay bolete significantly exceeded the acceptable standards referring to the maximum content of heavy metals in mushrooms, which was particularly true for cadmium.

  17. Influence of structural factors on the thermal stability of zinc{sup (II)} and boron{sup (III)} complexes with iodo- and bromosubstituted 2,2′-dipyrrines

    Guseva, G.B., E-mail:; Antina, E.V.; Nuraneeva, E.N.


    Highlights: • Halogenated zinc{sup (II)} and boron{sup (III)} dipyrrinates are thermal stable up to 179–266 °C in argon. • Intramolecular red-ox-reactions are the main cause of the lowering of stability complexes. • Stability of complexes is increased when passing from I- to Br-substituted dipyrrinates. • The obtained results are interest in the development of laser dyes and sensors for PDT. - Abstract: The results of the analysis of thermal stability for zinc {sup (II)} and boron {sup (III)} complexes with 3,3′,5,5′-tetramethyl-4-ethyl-4′-iodo-2,2-dipyrrin [HL{sup 1}], 3,3′-diamyl-4,4′-dimethyl-5,5′-dibromo-2,2′-dipyrrin [HL{sup 2}] and 3,3′,5,5′-tetramethyl-4,4′-dibromo-2,2′-dipyrrin [HL{sup 3}] of the composition [Zn(L{sup 1}){sub 2}]–[Zn(L{sup 3}){sub 2}] and [BF{sub 2}L{sup 1}]–[BF{sub 2}L{sup 3}] are presented. The influence of halogenation of dipyrrin ligand is manifested in decreasing thermal stability of [Zn(L){sub 2}] and [BF{sub 2}L] when replacing 4,4′-dibromosubstituted dipyrrin on 5,5′-dibromo- or 4-monoiodosubstituted ligand. Intramolecular red-ox-reactions with participation of halogen atoms are the main cause of thermal stability lowering of dipyrrinates [Zn(L){sub 2}] and [BF{sub 2}L] compared with alkylsubstituted analogs. The obtained results are interesting for the development of laser dyes and sensors for PDT.

  18. Complexation and toxicity of copper in higher plants. II. Different mechanisms for copper versus cadmium detoxification in the copper-sensitive cadmium/zinc hyperaccumulator Thlaspi caerulescens (Ganges Ecotype).

    Mijovilovich, Ana; Leitenmaier, Barbara; Meyer-Klaucke, Wolfram; Kroneck, Peter M H; Götz, Birgit; Küpper, Hendrik


    The cadmium/zinc hyperaccumulator Thlaspi caerulescens is sensitive toward copper (Cu) toxicity, which is a problem for phytoremediation of soils with mixed contamination. Cu levels in T. caerulescens grown with 10 microm Cu(2+) remained in the nonaccumulator range (hyperaccumulation and metal resistance are highly metal specific. Cu-induced inhibition of photosynthesis followed the "sun reaction" type of damage, with inhibition of the photosystem II reaction center charge separation and the water-splitting complex. A few individuals of T. caerulescens were more Cu resistant. Compared with Cu-sensitive individuals, they recovered faster from inhibition, at least partially by enhanced repair of chlorophyll-protein complexes but not by exclusion, since the content of Cu in their shoots was increased by about 25%. Extended x-ray absorption fine structure (EXAFS) measurements on frozen-hydrated leaf samples revealed that a large proportion of Cu in T. caerulescens is bound by sulfur ligands. This is in contrast to the known binding environment of cadmium and zinc in the same species, which is dominated by oxygen ligands. Clearly, hyperaccumulators detoxify hyperaccumulated metals differently compared with nonaccumulated metals. Furthermore, strong features in the Cu-EXAFS spectra ascribed to metal-metal contributions were found, in particular in the Cu-resistant specimens. Some of these features may be due to Cu binding to metallothioneins, but a larger proportion seems to result from biomineralization, most likely Cu(II) oxalate and Cu(II) oxides. Additional contributions in the EXAFS spectra indicate complexation of Cu(II) by the nonproteogenic amino acid nicotianamine, which has a very high affinity for Cu(II) as further characterized here.

  19. 微波固相法合成邻苯二甲酸锌、铜配合物%Synthesis of Zinc( Ⅱ ) and Copper( Ⅱ ) Complexes with Phthalic Acid Ligand by Microwave Solid-State Method

    张艳; 钟国清; 熊鑫; 蒋琪英


    以邻苯二甲酸( H2phth)、乙酸锌或乙酸铜为原料,通过微波固相法合成了邻苯二甲酸锌、铜配合物Zn(phth)·2H2O和Cu (phth)·H2O,用化学分析、元素分析、傅里叶变换红外光谱、X射线粉末衍射、热分析对配合物的组成和结构进行了表征.结果表明,邻苯二甲酸配体中的羧基以双齿桥式与Zn(Ⅱ)或Cu(Ⅱ)结合形成配合物,其热分解包括失水、配体的氧化分解过程,最后完全分解为金属氧化物.%Zinc ( II ) and copper ( II ) complexes of o-phthalic acid (H2phth) were synthesized by microwave solid-state method with o-phthalic acid, zinc acetate or copper acetate as raw materials. Chemical and elemental analysis, fourier transformed infrared spectra (FTIR) , X-ray powder diffraction (XRD) and thermogravimetry-derivative thermogravimetry(TG-DTG) were applied to characterize the composition and structure of the compounds. The results show that the compositions of the complexes are Zn(phth) ? 2H2O and Cu(phth) ? H2O,and the ligand is coordinated simultaneously with Zn (II) or Cu ( II ) via the carboxyl group of o-phthalic acid to form bidentate chelates. Thermal decomposition processes of the complexes include dehydration, oxidation and pyrolysis of the ligand, and finally as metallic oxide.

  20. Synthesis and characterization of zinc(II, palladium(II and platinum(II complex with 2’-[1-(2-pyridinylethylidene] oxamohydrazide. The crystal structure of bis{2’-[1-(2-pyridinylethylidene]oxamohydrazido}zinc(II trihydrate



    Full Text Available Complexes of Zn(II, Pd(II and Pt(II with 2’-[1-(2-pyridinylethylidene]oxamohydrazide (Hapsox were synthesized and their structures were determined. All the complexes are of a neutral type with two apsox ligands coordinated to Zn(II and one apsox ligand coordinated to Pd(II or Pt(II. In each case, the polydentate was coordinated via pyridine and hydrazone nitrogens and a-oxyazine oxygen, forming an octahedral geometry around Zn(II, and a square planar one around Pd(II and Pt(II. The structure determination was performed by IR, 1H-NMR and 13C-NMR spectroscopy, and for the Zn(II complex by X-ray structure analysis.

  1. Horse Liver Alcohol Dehydrogenase: Zinc Coordination and Catalysis

    Plapp, Bryce V.; Savarimuthu, Baskar Raj; Ferraro, Daniel J.; Rubach, Jon K.; Brown, Eric N.; Ramaswamy, S. (Iowa)


    During catalysis by liver alcohol dehydrogenase (ADH), a water bound to the catalytic zinc is replaced by the oxygen of the substrates. The mechanism might involve a pentacoordinated zinc or a double-displacement reaction with participation by a nearby glutamate residue, as suggested by studies of human ADH3, yeast ADH1, and some other tetrameric ADHs. Zinc coordination and participation of water in the enzyme mechanism were investigated by X-ray crystallography. The apoenzyme and its complex with adenosine 5'-diphosphoribose have an open protein conformation with the catalytic zinc in one position, tetracoordinated by Cys-46, His-67, Cys-174, and a water molecule. The bidentate chelators 2,2'-bipyridine and 1,10-phenanthroline displace the water and form a pentacoordinated zinc. The enzyme–NADH complex has a closed conformation similar to that of ternary complexes with coenzyme and substrate analogues; the coordination of the catalytic zinc is similar to that found in the apoenzyme, except that a minor, alternative position for the catalytic zinc is ~1.3 Å from the major position and closer to Glu-68, which could form the alternative coordination to the catalytic zinc. Complexes with NADH and N-1-methylhexylformamide or N-benzylformamide (or with NAD+ and fluoro alcohols) have the classical tetracoordinated zinc, and no water is bound to the zinc or the nicotinamide rings. The major forms of the enzyme in the mechanism have a tetracoordinated zinc, where the carboxylate group of Glu-68 could participate in the exchange of water and substrates on the zinc. Hydride transfer in the Michaelis complexes does not involve a nearby water.

  2. Horse Liver Alcohol Dehydrogenase: Zinc Coordination and Catalysis.

    Plapp, Bryce V; Savarimuthu, Baskar Raj; Ferraro, Daniel J; Rubach, Jon K; Brown, Eric N; Ramaswamy, S


    During catalysis by liver alcohol dehydrogenase (ADH), a water bound to the catalytic zinc is replaced by the oxygen of the substrates. The mechanism might involve a pentacoordinated zinc or a double-displacement reaction with participation by a nearby glutamate residue, as suggested by studies of human ADH3, yeast ADH1, and some other tetrameric ADHs. Zinc coordination and participation of water in the enzyme mechanism were investigated by X-ray crystallography. The apoenzyme and its complex with adenosine 5'-diphosphoribose have an open protein conformation with the catalytic zinc in one position, tetracoordinated by Cys-46, His-67, Cys-174, and a water molecule. The bidentate chelators 2,2'-bipyridine and 1,10-phenanthroline displace the water and form a pentacoordinated zinc. The enzyme-NADH complex has a closed conformation similar to that of ternary complexes with coenzyme and substrate analogues; the coordination of the catalytic zinc is similar to that found in the apoenzyme, except that a minor, alternative position for the catalytic zinc is ∼1.3 Å from the major position and closer to Glu-68, which could form the alternative coordination to the catalytic zinc. Complexes with NADH and N-1-methylhexylformamide or N-benzylformamide (or with NAD(+) and fluoro alcohols) have the classical tetracoordinated zinc, and no water is bound to the zinc or the nicotinamide rings. The major forms of the enzyme in the mechanism have a tetracoordinated zinc, where the carboxylate group of Glu-68 could participate in the exchange of water and substrates on the zinc. Hydride transfer in the Michaelis complexes does not involve a nearby water.

  3. Zinc(II and copper(II complexes with pheophytin and mesoporphyrin and their stability to UV-B irradiation: Vis spectroscopy studies

    Zvezdanović Jelena B.


    Full Text Available Stability of Zn(II and Cu(II complexes of porphyrin derivatives (pheophytin and mesoporphyrin to UV-B -irradiation has been studied by absorbance spectroscopy in 95% ethanol. The chosen porphyrins as well as their heavy metal complexes undergo photochemical decomposition obeying first-order kinetics. In general, pheophytin is more stable than mesoporphyrin to UV-B irradiation. On the other hand, stability of Zn(II-complex is smaller than Cu(II-complex both for pheophytin and mesoporphyrin; however while Cu(II-complex with pheophytin is more stable than the one with mesoporphyrin, with Zn(II-complex the situation is vice versa.

  4. Zinc and cadmium monosalicylates

    Kharitonov, Yu.Ya.; Tujebakhova, Z.K. (Moskovskij Khimiko-Tekhnologicheskij Inst. (USSR))


    Zinc and cadmium monosalicylates of the composition MSal, where M-Zn or Cd, Sal - twice deprotonated residue of salicylic acid O-HOC/sub 6/H/sub 4/COOH (H/sub 2/Sal), are singled out and characterized. When studying thermograms, thermogravigrams, IR absorption spectra, roentgenograms of cadmium salicylate compounds (Cd(OC/sub 6/H/sub 4/COO) and products of their thermal transformations, the processes of thermal decomposition of the compounds have been characterized. The process of cadmium monosalicylate decomposition takes place in one stage. Complete loss of salicylate acido group occurs in the range of 320-460 deg. At this decomposition stage cadmium oxide is formed. A supposition is made that cadmium complex has tetrahedral configuration, at that, each salicylate group plays the role of tetradentate-bridge ligand. The compound evidently has a polymer structure.

  5. On the Lewis acidic character of bis(salicylaldiminato)zinc(ii) Schiff-base complexes: a computational and experimental investigation on a series of compounds varying the bridging diimine.

    Forte, Giuseppe; Oliveri, Ivan Pietro; Consiglio, Giuseppe; Failla, Salvatore; Di Bella, Santo


    This contribution explores the effect of the 1,2-diimine bridge upon the Lewis acidic character of a series of bis(salicylaldiminato)zinc(ii), ZnL, Schiff-base complexes. The structure of the monomeric and dimeric ZnL complexes, and of the 1 : 1 adducts with pyridine, ZnL·py, is fully optimized by means of DFT calculations. The Gibbs free energy for the dimerization of ZnL complexes and for the formation of ZnL·py adducts is evaluated by accurate composite calculations. It accounts for their spontaneous dimerization and for the greater stability of the ZnL·py adducts with respect to the dimers. Calculated binding constants for the formation ZnL·py adducts are in excellent agreement with experimentally derived values, thus allowing establishing a relative Lewis acidity scale within this series. While the complex derived from the non-conjugated ethylenediamine reveals the lowest Lewis acidity, the complex derived from the diaminomaleonitrile represents the stronger Lewis acidic species. These findings are in good agreement with the greater catalytic activity observed for ZnL Schiff-base complexes derived from conjugated 1,2-diamines in comparison to the non-conjugated analogues. Both in ZnL dimers as well as in ZnL·py adducts the geometry of the coordination sphere seems to be a relevant feature to assess their relative stability. Thus, while the quasi-planarity of ZnL monomers of the conjugated diimines is an unfavourable feature in the dimerization process, it represents an important aspect in stabilizing ZnL·py adducts in a nearly perfect square-pyramidal coordination. These features are relevant for the sensing and catalytic properties of these complexes.

  6. Cadmium and zinc relationships

    Elinder, C.; Piscator, M.


    Higher mammals, such as homo sapiens, accumulate zinc in kidney cortex almost equimolarly with cadmium. A different pattern seems to be present in liverthere is a limited increase of zinc in two species of large farm animals compared with a marked increase in the laboratory. In large farm animals, an equimolar increase of zinc with cadmium in renal cortex seems to indicate that the form of metallothionein that binds equal amounts of cadmium and zinc in present. Differences in cadmium and zinc relationships in large animals and humans compared with laboratory animals must be carefully considered. (4 graphs, 26 references)

  7. Influencia de la identidad grupal en la cohesion estudio piloto

    Bohórquez, M. Rocío; Lorenzo, Macarena


    La cohesión grupal es uno de los procesos dinámicos más estudiados en los equipos deportivos, su relación con procesos como el clima grupal o la eficacia colectiva ha sido ampliamente abordada. Sin embargo, el estudio de la influencia que la identidad grupal pudiera tener sobre la cohesión está aún por emprender. Así, el objetivo de este estudio fue determinar la influencia que la identidad grupal pudiera tener sobre la cohesión de los equipos deportivos. En el experimento p...

  8. Flotation Experiment Study on a Copper-Lead-Zinc Complex Polymetallic Ore in Inner Mongolia%内蒙古某铜铅锌复杂多金属矿的浮选试验研究

    宋涛; 洪家薇; 刘宸婷


    试验矿样取自内蒙古某地的铜铅锌复杂多金属矿,原矿含Cu 0.25%、Pb 2.53%、Zn 4.47%,并且伴生Ag 92.5 g/t、In 42.5 g/t,研究了该矿石的浮选工艺以及在浮选过程中各种药剂的用量,最终得到铜精矿中含Cu 17.62%、回收率达到58.26%;铅精矿含Pb 66.55%、回收率高达90.39%;锌精矿含Zn 48.12%,回收率90.29%;与此同时,铅精矿含Ag达到1 642.0 g/t、回收率60.3%,锌精矿含In达到248.7 g/t、回收率达到53.5%.结果表明,此浮选工艺可有效处理该复杂多金属矿.%The experiment sample is taken from a copper-lead-zinc complex polymetallic deposit in Inner Mongolia, there are 0. 25 % Cu, 2. 53 % Pb, 4.47% Zn in the raw ore, and it also associated with 92. 5 g/t Ag and 42. 5 g/t In, the flotation process of this ore and also the dosage of agents which used in the flotation process is researched, the copper concentrate contents Cu 17.6% , and the recovery can be reached to 58. 26% ; the lead concentrate contents Pb 66. 55% , the recovery reach up to 90. 39% ; the zinc concentrate contents Ag 1 642.0 g/t, the recovery is 60. 3% ; the zinc concentrate contents In 248. 7 g/t, the recovery is 53.5%. The results showed that this flotation process can treat this complex polymetallic ore effectively.

  9. Zinc Binding by Lactic Acid Bacteria

    Jasna Mrvčić


    Full Text Available Zinc is an essential trace element in all organisms. A common method for the prevention of zinc deficiency is pharmacological supplementation, especially in a highly available form of a metalloprotein complex. The potential of different microbes to bind essential and toxic heavy metals has recently been recognized. In this work, biosorption of zinc by lactic acid bacteria (LAB has been investigated. Specific LAB were assessed for their ability to bind zinc from a water solution. Significant amount of zinc ions was bound, and this binding was found to be LAB species-specific. Differences among the species in binding performance at a concentration range between 10–90 mg/L were evaluated with Langmuir model for biosorption. Binding of zinc was a fast process, strongly influenced by ionic strength, pH, biomass concentration, and temperature. The most effective metal-binding LAB species was Leuconostoc mesenteroides (27.10 mg of Zn2+ per gram of dry mass bound at pH=5 and 32 °C, during 24 h. FT-IR spectroscopy analysis and electron microscopy demonstrated that passive adsorption and active uptake of the zinc ions were involved.

  10. Zinc and skin biology.

    Ogawa, Youichi; Kawamura, Tatsuyoshi; Shimada, Shinji


    Of all tissues, the skin has the third highest abundance of zinc in the body. In the skin, the zinc concentration is higher in the epidermis than in the dermis, owing to a zinc requirement for the active proliferation and differentiation of epidermal keratinocytes. Here we review the dynamics and functions of zinc in the skin as well as skin disorders associated with zinc deficiency, zinc finger domain-containing proteins, and zinc transporters. Among skin disorders associated with zinc deficiency, acrodermatitis enteropathica is a disorder caused by mutations in the ZIP4 transporter and subsequent zinc deficiency. The triad acrodermatitis enteropathica is characterized by alopecia, diarrhea, and skin lesions in acral, periorificial, and anogenital areas. We highlight the underlying mechanism of the development of acrodermatitis because of zinc deficiency by describing our new findings. We also discuss the accumulating evidence on zinc deficiency in alopecia and necrolytic migratory erythema, which is typically associated with glucagonomas. Copyright © 2016 Elsevier Inc. All rights reserved.

  11. Cadmium and zinc relationships.

    Elinder, C G; Piscator, M


    Cadmium and zinc concentrations in kidney and liver have been measured under different exposure situations in different species including man. The results show that zinc increases almost equimolarly with cadmium in kidney after long-term low-level exposure to cadmium, e.g., in man, horse, pig, and lamb. In contrast, the increase of zinc follows that of cadmium to only a limited extent, e.g., in guinea pig, rabbit, rat, mouse, and chicks. In liver, the cadmium--zinc relationship seems to be reversed in such a way that zinc increases with cadmium more markedly in laboratory animals than in higher mammals. These differences between cadmium and zinc relationships in humans and large farm animals and those in commonly used laboratory animals must be considered carefully before experimental data on cadmium and zinc relationships in laboratory animals can be extrapolated to humans.

  12. DFT/TD-DFT study on spectroscopic properties of zinc(II, nickel(II, and palladium(II metal complexes with a thiourea derivative

    Wang Xin


    Full Text Available The geometries, electronic structures, and spectral properties of three metal complexes Zn(C10H12N3OS2 (1, Ni(C10H12N3OS2 (2, and Pd(C10H12N3OS2 (3 with N-(2-pyridinylmorpholine-4-carbothioamide as a ligand are investigated by means of DFT (density functional theory and TD-DFT (time-dependent density functional theory methods. Complex 1 is a distorted tetrahedral geometry, while complexes 2 and 3 present a distorted square-planar coordination environment. In the simulated range, the spectrum of complex 1 has five obvious absorption peaks and one of them has the strongest intensity. The latter two complexes have one more absorption peak and shoulder peak with the similar intensity. Moreover, the strongest peaks of complexes 2.

  13. [Zinc and type 2 diabetes].

    Fukunaka, Ayako; Fujitani, Yoshio


    Pancreatic β cells contain the highest amount of zinc among cells within the human body, and hence, the relationship between zinc and diabetes has been a topic of great interest. While many studies demonstrating possible involvement of zinc deficiency in diabetes have been reported, precise mechanisms how zinc regulates glucose metabolism are still far from understood. Recent studies revealed that zinc can transmit signals that are driven by a variety of zinc transporters in a tissue and cell-type specific manner and deficiency in some zinc transporters may cause human diseases. Here, we review the role of zinc in metabolism particularly focusing on the emerging role of zinc transporters in diabetes.

  14. Root-secreted nicotianamine from Arabidopsis halleri facilitates zinc hypertolerance by regulating zinc bioavailability.

    Tsednee, Munkhtsetseg; Yang, Shun-Chung; Lee, Der-Chuen; Yeh, Kuo-Chen


    Hyperaccumulators tolerate and accumulate extraordinarily high concentrations of heavy metals. Content of the metal chelator nicotianamine (NA) in the root of zinc hyperaccumulator Arabidopsis halleri is elevated compared with nonhyperaccumulators, a trait that is considered to be one of the markers of a hyperaccumulator. Using metabolite-profiling analysis of root secretions, we found that excess zinc treatment induced secretion of NA in A. halleri roots compared with the nonhyperaccumulator Arabidopsis thaliana. Metal speciation analysis further revealed that the secreted NA forms a stable complex with Zn(II). Supplying NA to a nonhyperaccumulator species markedly increased plant zinc tolerance by decreasing zinc uptake. Therefore, NA secretion from A. halleri roots facilitates zinc hypertolerance through forming a Zn(II)-NA complex outside the roots to achieve a coordinated zinc uptake rate into roots. Secretion of NA was also found to be responsible for the maintenance of iron homeostasis under excess zinc. Together our results reveal root-secretion mechanisms associated with hypertolerance and hyperaccumulation. © 2014 American Society of Plant Biologists. All Rights Reserved.

  15. La influencia cristiana en la filosofía latinoamericana

    Mora, Arnoldo


    El presente estudio muestra la influencia de la religión cristiana en los orígenes y posterior desarrollo de la filosofía latinoamericana. This essay is a historical overhaul of the influence of the christian faith in the birth and ulterior development of the latinamerican philosophy.

  16. Factores humanos y su influencia en la productividad

    Mirza Cequea


    Full Text Available La productividad es un concepto de naturaleza multidimensional en la que influyen ciertas características y comportamientos del individuo, dicha influencia implica procesos psicológicos y psicosociales complejos de cuantificar que constituyen los factores humanos. El objetivo general de la investigación, es analizar los factores humanos y su influencia en la productividad, vista desde la perspectiva de tres unidades diferentes; individuo, grupo y organización. Para tal fin, se plantearon tres modelos diseñados con relaciones causales diferentes, a objeto de determinar el modelo que mejor explica esta influencia. La metodología utilizada fue explicativa de tipo experimental. El método aplicado fue el hipotético deductivo. Se compararon tres modelos utilizando la técnica de modelos rivales de la metodología de Ecuaciones Estructurales. Este criterio permite contrastar modelos a fin de determinar el de mejor ajuste. El resultado determinó que los tres modelos presentan ajustes razonables de aceptación y explican las relaciones causales planteadas y su influencia en la productividad. Del análisis de los ajustes de los tres modelos se concluye que el Modelo B es el que mejor explica la relación de los factores humanos y la productividad

  17. Complexity

    Gershenson, Carlos


    The term complexity derives etymologically from the Latin plexus, which means interwoven. Intuitively, this implies that something complex is composed by elements that are difficult to separate. This difficulty arises from the relevant interactions that take place between components. This lack of separability is at odds with the classical scientific method - which has been used since the times of Galileo, Newton, Descartes, and Laplace - and has also influenced philosophy and engineering. In recent decades, the scientific study of complexity and complex systems has proposed a paradigm shift in science and philosophy, proposing novel methods that take into account relevant interactions.

  18. Synthesis, structural, optical band gap and biological studies on iron (III), nickel (II), zinc (II) and mercury (II) complexes of benzyl α-monoxime pyridyl thiosemicarbazone

    Bedier, R. A.; Yousef, T. A.; Abu El-Reash, G. M.; El-Gammal, O. A.


    New ligand, (E)-2-((E)-2-(hydroxyimino)-1,2-diphenylethylidene)-N-(pyridin-2 yl) hydrazinecarbothioamide (H2DPPT) and its complexes [Fe(DPPT)Cl(H2O)], [Ni(H2DPPT)2Cl2], [Zn(HDPPT)(OAc)] and [Hg(HDPPT)Cl](H2O)4 were isolated and characterized by various of physico-chemical techniques. IR spectra show that H2DPPT coordinates to the metal ions as neutral NN bidentate, mononegative NNS tridentate and binegative NNSN tetradentate, respectively. From the modeling studies, the bond length, bond angle, HOMO, LUMO and dipole moment had been calculated to confirm the geometry of the ligands and their investigated complexes. The thermal studies showed the type of water molecules involved in metal complexes Furthermore, the kinetic and thermodynamic parameters for the different decomposition steps were calculated using the Coats-Redfern and Horowitz-Metzger methods. Also, the optical band gap (Eg) has been calculated to elucidate the conductivity of the isolated complexes. The optical transition energy (Eg) is direct and equals 3.34 and 3.44 ev for Ni and Fe complexes, respectively. The ligand and their metal complexes were screened for antibacterial activity against the following bacterial species, Bacillus thuringiensis, Staphylococcus aureus, Pseudomonas aeuroginosa and Escherichia coli. The results revealed that the metal complexes have more potent antibacterial compared with the ligand. Also, the degradation effect of the investigated compounds was tested showing that, Ni complex exhibited powerful and complete degradation effect on DNA.


    Jing-shu Wu; Min Xiao; Hu He; Shuan-jin Wang; Dong-mei Han; Yue-zhong Meng


    Using supported multi-component zinc dicarboxylate catalyst,poly(1,2-propylene carbonate-co-l,2-cyclohexylene carbonate) (PPCHC) was successfully synthesized from carbon dioxide (CO2) with propylene oxide (PO) and cyclohexene oxide (CHO).The conversion of epoxides dramatically increased up to 89.7% (yield:384.2 g of polymer per g of Zn) with increasing reaction temperature from 60℃ to 80℃.The optimized reaction temperature is 80℃.The chemical structure,the molecular weight,as well as thermal and mechanical properties of the resulting terpolymers were investigated extensively.When CHO feed content (mol%) is lower than 10%,the PPCHC terpolymers have number average molecular weight (Mn)ranging from 102 × 103 to 202 × 103 and molecular weight distribution (MWD) values ranging from 2.8 to 3.5.In contrast to poly(propylene carbonate) (PPC),the introduction of small amount of CHO leads to increase in the glass transition temperature from 38.0℃ to 42.6℃.Similarly,the mechanical strength of the synthesized terpolymer is greatly enhanced due to the incorporation of CHO.These improvements in mechanical and thermal properties are of importance for the practical application of PPC.

  20. Effect of Complex Ion Concentration on the Particle Size of Nano Zinc Aluminium Oxide(ZAO)%络离子浓度对掺铝氧化锌(ZAO)纳米粉体粒径的影响

    颜东亮; 陈林; 宋杰光


    Zinc aluminium oxide (ZAO) nanoparticles were prepared by complex salt method. A new complex salt crystal, ( NH4 ) 1.95 ( Zn0.95 Al0.05 ) ( SO4 ) 2·6H2O, was synthesized in the experiment, which proved the formation of complex ion in the initial reaction solution. The influence of complex ion concentration on the particle size of ZAO powder was researched by adjusting the addition of (NH4 )2SO4. ZAO powders were characterized by XRD, SEM and laser particle size analyzer. The results indicated that the existing of complex ion decreased the concentration of dissociative metal ion and increased the controllability of primary particle size, which was in favor of the preparation of ZAO nanometer powder.%采用络盐法制备了掺铝氧化锌(ZAO)纳米粉体.通过新复合络盐晶体-(NH4)1.95(Zn0.95Al0.05)(SO4)2·6H2O的合成证实了反应初始溶液中形成了络离子.通过改变(NH4)2SO4的加入量研究了络离子浓度对ZAO粒径的影响.通过XRD、SEM和激光粒度仪对ZAO粉体进行了表征.结果表明:络离子的存在,降低了反应初始溶液中游离金属离子的浓度,使得产物的一次粒径的可调控性增强,有利于纳米级ZAO粉体的制备.

  1. 三元络合碱性电沉积锌镍合金的抗腐蚀性能研究%Research on Corrosion Resistance of Ternary Complexation Alkaline Electrodeposition Zinc-nickel Alloy

    张秀; 王少龙; 龙晋明; 裴和中; 由劲博


    The zinc-nickel alloy coating of electrodeposition preparation was made by the alkaline zinc-nickel alloy plating bath which is composed of tetraethylenepentamine (TEPA),potassium sodium tartrate and triethanolamine (TEA) ternary mixture as nickel ions complexing agent on low carbon steel substrate.The effect of different electrodeposition parameters (the current density and the relative content of nickel ions) on the corrosion electrochemical behavior of zinc-nickel alloy coating in 3.5 % NaCl solutions was investigated by polarization curve and electrochemical impedance spectroscopy.The results indicate that the coating on the substrate has an optimal protective effect when nickel content of the bath within a broad range (n (Ni2 +)/n (Ni2 + + Zn2 +) =15 %-30 %) changes.The coating corrosion resistance is the strongest when the current density within 2-3 A/dm2.However,the current density is too low and too high will decrease the corrosion resistance of the coating.%采用四乙烯五胺(TEPA)、酒石酸钾钠和三乙醇胺(TEA)三元混合物作为镍离子络合剂配制碱性锌镍合金镀液,在低碳钢基材上电沉积制备锌镍合金镀层.利用电化学工作站测试了镀层在3.5% NaCl溶液中的极化曲线和电化学阻抗谱,考察不同电沉积条件参数(电流密度和镍离子相对含量)对锌镍合金镀层的腐蚀电化学行为的影响.结果表明:当镀液的镍含量在较宽范围内(n(Ni2+)/n(Ni2+ +Zn2+) =15%~30%)变化时,所得镀层对基体都有很好的防护作用;当电流密度为2~3 A/dm2时得到的镀层抗腐蚀能力最强,而当电流密度过低和过高时都会使镀层的耐蚀性有所降低.

  2. Improved zinc electrode and rechargeable zinc-air battery

    Ross, P.N. Jr.


    The invention comprises an improved rechargeable zinc-air cell/battery having recirculating alkaline electrolyte and a zinc electrode comprising a porous foam support material which carries the active zinc electrode material. 5 figs.

  3. Zinc stannate nanostructures: hydrothermal synthesis

    Sunandan Baruah and Joydeep Dutta


    Full Text Available Nanostructured binary semiconducting metal oxides have received much attention in the last decade owing to their unique properties rendering them suitable for a wide range of applications. In the quest to further improve the physical and chemical properties, an interest in ternary complex oxides has become noticeable in recent times. Zinc stannate or zinc tin oxide (ZTO is a class of ternary oxides that are known for their stable properties under extreme conditions, higher electron mobility compared to its binary counterparts and other interesting optical properties. The material is thus ideal for applications from solar cells and sensors to photocatalysts. Among the different methods of synthesizing ZTO nanostructures, the hydrothermal method is an attractive green process that is carried out at low temperatures. In this review, we summarize the conditions leading to the growth of different ZTO nanostructures using the hydrothermal method and delve into a few of its applications reported in the literature.

  4. Preparation of zinc oxide coatings by using newly designed metal–organic complexes of Zn: Effect of molecular structure of the precursor and surfactant over the crystallization, growth and luminescence

    Brahma, Sanjaya, E-mail: [Materials Research Centre, Indian Institute of Science, Bangalore 560012 (India); Department of Materials Science and Engineering, National Cheng Kung University, Tainan 701, Taiwan (China); Shivashankar, S.A. [Materials Research Centre, Indian Institute of Science, Bangalore 560012 (India); Centre for Nano Science and Engineering, Indian Institute of Science, Bangalore 560012 (India)


    Graphical abstract: ZnO coating comprised of tapered ZnO nanorods using Zn(acac){sub 2} bipy as the precursor. Highlights: • Newly designed precursors were used for the fabrication of ZnO coating. • ZnO coatings (1.5–2 μm) were achieved quickly (1–5 min) by a simple microwave process. • The coatings are uniform having high density of nucleation and excellent growth rate. • Luminescence could be tuned by varying molecular structure of the precursor. • Possible growth mechanism is described in detail. -- Abstract: We report large scale deposition of tapered zinc oxide (ZnO) nanorods on Si(1 0 0) substrate by using newly designed metal–organic complex of zinc (Zn) as the precursor, and microwave irradiation assisted chemical synthesis as a process. The coatings are uniform and high density ZnO nanorods (∼1.5 μm length) grow over the entire area (625 mm{sup 2}) of the substrate within 1–5 min of microwave irradiation. ZnO coatings obtained by solution phase deposition yield strong UV emission. Variation of the molecular structure/molecular weight of the precursors and surfactants influence the crystallinity, morphology, and optical properties of ZnO coatings. The precursors in addition with the surfactant and the solvent are widely used to obtain desired coating on any substrate. The growth mechanism and the schematics of the growth process of ZnO coatings on Si(1 0 0) are discussed.

  5. Zinc composite anode for batteries with solid electrolyte

    Tedjar, F.; Melki, T.; Zerroual, L.

    A new negative composite anode for batteries with a solid electrolyte is studied. Using a complex of zinc ammonium chloride mixed with zinc metal powder, the advantage of the Zn/Zn 2+ electrode ( e = -760 mV) is kept while the energy density and the shelf-life of the battery are increased.

  6. Zinc composite anode for batteries with solid electrolyte

    Tedjar, F.; Melki, T.; Zerroual, L. (Setif Univ. (Algeria). Unite de Recherche Electrochimie)


    A new negative composite anode for batteries with a solid electrolyte is studied. Using a complex of zinc ammonium chloride mixed with zinc metal powder, the advantage of the Zn/Zn[sup 2+] electrode (e = -760 mV) is kept while the energy density and the shelf-life of the battery are increased. (orig.).

  7. Novel zinc complexes of a non-steroidal anti-inflammatory drug, niflumic acid: Structural characterization, human-DNA and albumin binding properties.

    Smolková, Romana; Zeleňák, Vladimír; Smolko, Lukáš; Kuchár, Juraj; Rabajdová, Miroslava; Ferenčáková, Michaela; Mareková, Mária


    Three novel Zn(II) complexes of NSAID niflumic acid (Hnif) were prepared and studied, namely; [Zn(MeOH)4(nif)2] (1), [Zn(cyclam)(nif)2] (2) and [Zn(nif)2(tmen)] (3), where nif is deprotonated niflumic acid, cyclam is 1,4,8,11-Tetraazacyclotetradecane and tmen is N,N,N',N'-Tetramethylethylenediamine. The complexes have been characterized by infrared spectroscopy, elemental and thermal analysis and single-crystal X-ray structure analysis. All three complexes contain two deprotonated niflumato anions monodentately coordinated via carboxylato groups. Furthermore, fluorescence binding studies of the prepared compounds with human genomic DNA-EB (ethidium bromide) were carried out, which suggest that all complexes are able to bind to DNA via intercalation. Moreover, from the obtained results it followed that complexes 2 and 3 bind to DNA from the tissue with aortic aneurysm (aDNA) and control (cDNA) with a different strength. Additionally, complexes 1-3 exhibit good binding affinity to human serum albumin with high binding constant. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  8. Analgesic and Anti-Inflammatory Activities of Salicylaldehyde 2-Chlorobenzoyl Hydrazone (H2LASSBio-466, Salicylaldehyde 4-Chlorobenzoyl Hydrazone (H2LASSBio-1064 and Their Zinc(II Complexes

    Eliezer J. Barreiro


    Full Text Available Salicylaldehyde 2-chlorobenzoyl hydrazone (H2LASSBio-466, salicylaldehyde 4-chlorobenzoyl hydrazone (H2LASSBio-1064 and their complexes [Zn(LASSBio-466H2O]2 (1 and [Zn(HLASSBio-1064Cl]2 (2 were evaluated in animal models of peripheral and central nociception, and acute inflammation. All studied compounds significantly inhibited acetic acid-induced writhing response. Upon coordination the anti-nociceptive activity was favored in the complex 1. H2LASSBio-466 inhibited only the first phase of the formalin test, while 1 was active in the second phase, like indomethacin, indicating its ability to inhibit nociception associated with the inflammatory response. Hence coordination to zinc(II altered the pharmacological profile of H2LASSBio-466. H2LASSBio-1064 inhibited both phases but this effect was not improved by coordination. The studied compounds did not increase the latency of response in the hot plate model, indicating their lack of central anti-nociceptive activity. All compounds showed levels of inhibition of zymosan-induced peritonitis comparable or superior to indomethacin, indicating an expressive anti-inflammatory profile.

  9. Complex


    Schiff bases and their complex compounds have been studied for their .... establishing coordination of the N–(2 – hydroxybenzyl) - L - α - valine Schiff base ..... (1967); “Spectrophotometric Identification of Organic Compounds”, Willey, New.

  10. Chelators for investigating zinc metalloneurochemistry.

    Radford, Robert J; Lippard, Stephen J


    The physiology and pathology of mobile zinc signaling has become an important topic in metalloneurochemistry. To study the action of mobile zinc effectively, specialized tools are required that probe the temporal and positional changes of zinc ions within live tissue and cells. In the present article we describe the design and implementation of selective zinc chelators as antagonists to interrogate the function of mobile zinc, with an emphasis on the pools of vesicular zinc in the terminals of hippocampal mossy fiber buttons.

  11. Zinc coordination spheres in protein structures.

    Laitaoja, Mikko; Valjakka, Jarkko; Jänis, Janne


    Zinc metalloproteins are one of the most abundant and structurally diverse proteins in nature. In these proteins, the Zn(II) ion possesses a multifunctional role as it stabilizes the fold of small zinc fingers, catalyzes essential reactions in enzymes of all six classes, or assists in the formation of biological oligomers. Previously, a number of database surveys have been conducted on zinc proteins to gain broader insights into their rich coordination chemistry. However, many of these surveys suffer from severe flaws and misinterpretations or are otherwise limited. To provide a more comprehensive, up-to-date picture on zinc coordination environments in proteins, zinc containing protein structures deposited in the Protein Data Bank (PDB) were analyzed in detail. A statistical analysis in terms of zinc coordinating amino acids, metal-to-ligand bond lengths, coordination number, and structural classification was performed, revealing coordination spheres from classical tetrahedral cysteine/histidine binding sites to more complex binuclear sites with carboxylated lysine residues. According to the results, coordination spheres of hundreds of crystal structures in the PDB could be misinterpreted due to symmetry-related molecules or missing electron densities for ligands. The analysis also revealed increasing average metal-to-ligand bond length as a function of crystallographic resolution, which should be taken into account when interrogating metal ion binding sites. Moreover, one-third of the zinc ions present in crystal structures are artifacts, merely aiding crystal formation and packing with no biological significance. Our analysis provides solid evidence that a minimal stable zinc coordination sphere is made up by four ligands and adopts a tetrahedral coordination geometry.

  12. Determination of Constant-Volume Combustion Energy for the Complexes of Zinc Nitrate with Four Amino Acids%硝酸锌与四种α-氨基酸配合物的恒容燃烧能测定

    谢钢; 杨旭武; 陈三平; 高胜利; 史启祯


    Ten solid complexes of zinc nitrate with L-α-leucine(Leu), L-α-valine(Val), L-α-tryptophan(Try) andL-α-threonine(Thr) were prepared in water. The compositions of these complexes are determined by chemicalanalysis and elemental analysis, which are identified as Zn (Leu) (NO3) 2 @ 2H2O (A), Zn (Leu)2 (NO3)2 @ H2O (B),Zn(Val) (NO3)2 @ 2H2O(C), Zn(Val) 2(NO3)2 @ H2O(D), Zn(Val) 3(NO3) 2 @ H2O(E), Zn(Try) (NO3)2 @ 2H2O(F), Zn(Try)2(NO3)2 @ H2O(G), Zn(Thr) (NO3)2 @ 2H2O(H), Zn(Thr) 2(NO3)2 @ H2O(I) and Zn(Thr) 3(NO3)@ H2O(J) . The constant-volume combustion energies of the complexes, Δc U(complex), were determined by aprecise rotating bomb calorimeter at 298.15K. Standard enthalpies of combustion, ΔcH-m(complex, s, 298. 15K),and standard enthalpies of formation, ΔfH-m (complex, s, 298. 15K) for these complexes were calculated as(4523.22 ± 2.08), (7208.86 ± 4.28), (3442.21 ± 1.85), (5971.21 ±3.32), (9007.26 ± 4.24),(5802.35±2.14), (10891.58±3.01), (2147.40±1.28), (4120.83±0.99), (6444.68±3.85)kJ@mol-1and (615.67±2.27), (1863.16±4.60), (1017.34±2.00), (1742.93±3.61), (2245.70±4.73),(1161.18±2.61), (1829.71±4.20), (1632.82±1.43), (1885.55±1.50), (2770. 25 ± 4. 21) kJ @ mol-1,respectively.

  13. Synthesis, spectroscopic and thermal characterization of sulpiride complexes of iron, manganese, copper, cobalt, nickel, and zinc salts. Antibacterial and antifungal activity

    Mohamed, Gehad G.; Soliman, Madiha H.


    Sulpiride (SPR; L) is a substituted benzamide antipsychotic which is reported to be a selective antagonist of central dopamine receptors and claimed to have mood-elevating properties. The ligation behaviour of SPR drug is studied in order to give an idea about its potentiality towards some transition metals in vitro systems. Metal complexes of SPR have been synthesized by reaction with different metal chlorides. The metal complexes of SPR with the formula [MCl 2(L) 2(H 2O) 2]· nH 2O [M = Mn(II), Co(II), Ni(II), Cu(II) and Zn(II); n = 0-2] and [FeCl 2(HL)(H 2O) 3]Cl·H 2O have been synthesized and characterized using elemental analysis (CHN), electronic (infrared, solid reflectance and 1H NMR spectra) and thermal analyses (TG and DTA). The molar conductance data reveal that the bivalent metal chelates are non-electrolytes while Fe(III) complex is 1:1 electrolyte. IR spectra show that SPR is coordinated to the metal ions in a neutral monodentate manner with the amide O. From the magnetic and solid reflectance spectra, octahedral geometry is suggested. The thermal decomposition processes of these complexes were discussed. The correlation coefficient, the activation energies, E*, the pre-exponential factor, A, and the entropies, Δ S*, enthalpies, Δ H*, Gibbs free energies, Δ G*, of the thermal decomposition reactions have been derived from thermogravimetric (TG) and differential thermogravimetric (DTG) curves. The synthesized ligand and its metal complexes were also screened for their antibacterial and antifungal activity against bacterial species ( Escherichia coli and Staphylococcus aureus) and fungi ( Aspergillus flavus and Candida albicans). The activity data show that the metal complexes are found to have antibacterial and antifungal activity than the parent drug and less than the standard.

  14. Synthesis, spectroscopic and thermal characterization of sulpiride complexes of iron, manganese, copper, cobalt, nickel, and zinc salts. Antibacterial and antifungal activity.

    Mohamed, Gehad G; Soliman, Madiha H


    Sulpiride (SPR; L) is a substituted benzamide antipsychotic which is reported to be a selective antagonist of central dopamine receptors and claimed to have mood-elevating properties. The ligation behaviour of SPR drug is studied in order to give an idea about its potentiality towards some transition metals in vitro systems. Metal complexes of SPR have been synthesized by reaction with different metal chlorides. The metal complexes of SPR with the formula [MCl(2)(L)(2)(H(2)O)(2)].nH(2)O [M=Mn(II), Co(II), Ni(II), Cu(II) and Zn(II); n=0-2] and [FeCl(2)(HL)(H(2)O)(3)]Cl.H(2)O have been synthesized and characterized using elemental analysis (CHN), electronic (infrared, solid reflectance and (1)H NMR spectra) and thermal analyses (TG and DTA). The molar conductance data reveal that the bivalent metal chelates are non-electrolytes while Fe(III) complex is 1:1 electrolyte. IR spectra show that SPR is coordinated to the metal ions in a neutral monodentate manner with the amide O. From the magnetic and solid reflectance spectra, octahedral geometry is suggested. The thermal decomposition processes of these complexes were discussed. The correlation coefficient, the activation energies, E*, the pre-exponential factor, A, and the entropies, DeltaS*, enthalpies, DeltaH*, Gibbs free energies, DeltaG*, of the thermal decomposition reactions have been derived from thermogravimetric (TG) and differential thermogravimetric (DTG) curves. The synthesized ligand and its metal complexes were also screened for their antibacterial and antifungal activity against bacterial species (Escherichia coli and Staphylococcus aureus) and fungi (Aspergillus flavus and Candida albicans). The activity data show that the metal complexes are found to have antibacterial and antifungal activity than the parent drug and less than the standard.

  15. Examination of nanoformulated crosslinked polymers complexed with copper/zinc superoxide dismutase as a therapeutic strategy for angiotensin II-mediated hypertension

    Savalia, Krupa

    Excessive generation of superoxide (O2·-) has been extensively implicated as a signaling molecule in cardiovascular pathologies, including hypertension. As a major risk factor for myocardial infarction, stroke, and heart failure, the morbidity and mortality associated with hypertension is a worldwide epidemic. Although there are several standard therapies that effectively lower blood pressure, many hypertensive patients have uncontrolled blood pressure despite taking available medications. Thus, there is a necessity to develop new pharmacotherapies that target novel molecular effectors (e.g. O2·-) that have been implicated to be integral in the pathogenesis of hypertension. To overcome the failed therapeutic impact of currently available antioxidants in cardiovascular disease, we developed a nanomedicine-based delivery system for the O2 ·- scavenging enzyme, copper/zinc superoxide dismutase (CuZnSOD), in which CuZnSOD protein is electrostatically bound to poly-L-lysine (PLL 50)-polyethylene glycol (PEG) block co-polymer to form CuZnSOD nanozyme. Different formulations of CuZnSOD nanozyme are covalently stabilized by either reducible or non-reducible crosslinked bonds between the PLL50-PEG polymers. Herein, we tested the overall hypothesis that PLL50-PEG CuZnSOD nanozyme delivers active CuZnSOD protein to neurons and decreases blood pressure in a model of Angll-dependent hypertension. As determined by electron paramagnetic resonance (EPR) spectroscopy, nanozymes retain full SOD enzymatic activity. Furthermore, non-reducible crosslinked nanozyme delivers active CuZnSOD protein to central neurons in culture (CATH.a neurons) without inducing significant neuronal toxicity. In vivo studies conducted in Angll-mediated hypertensive adult male C57BL/6 mice demonstrate that the non-reducible crosslinked nanozyme significantly attenuates blood pressure when given directly into the brain and prevents the further increase in hypertension when intravenously (IV) administered

  16. Binding of free and protein-associated zinc to rat spermatozoa.

    Sansone, G; Martino, M; Abrescia, P


    1. The zinc content of rat spermatozoa increases, upon ejaculation, from 0.035 to 1.055 micrograms/10(6) cells. 2. The rat seminal plasma holds zinc both as free ion and as protein-bound forms. 3. Zinc-free ions bind in vitro to rat epididymal spermatozoa. 4. Zinc-protein complexes can be isolated, by a chromatographic procedure, from the dorsolateral lobe of rat prostate. 5. The isolated zinc-protein complexes bind in vitro to rat epididymal spermatozoa.

  17. 席夫碱大环双核锌配合物的合成与表征%Synthesis and crystal structure of macrocyclic Schiff base binuclear zinc( Ⅱ )complex

    康海霞; 马宁; 傅玉琴; 李森兰


    A tetraaza macrocyclic Schiff base was synthesized through the reaction of acetone and ethylenediamine by the catalysis of perchloric acid. The Schiff base reacted with ZnO and NaN3 to form a binuclear zinc ( Ⅱ ) macrocyclic complex. The complex was characterized by infrared spectrum and X-Ray single crystal diffraction. It belongs to monoclinic system with space groupC2/c,α = 2.4914(2)nm,b = 1.4 9748(13)nm,c=1.26800(11)nm;β=l02. 1900( 10)°;v=4. 6240(7)nm3 ,Z=4,Dc = 1.482 Mg/m\\Mr = 1032.03 ,F(000)= 2160,final R=0.0506,wR = 0. 1434. The Zinc atom is five-coordinated by five nitrogen atoms(four nitrogen atoms come from the Schiff base and one nitrogen atom comes from the azido anion). As a result, a slightly distorted triangle double-cone geometry forms.%本文用丙酮和乙二胺在高氯酸催化下合成了四氮杂十四环席夫碱(1),并用此化合物(1)与氧化锌和叠氮化钠反应,生成锌的双核大环配合物.通过X-射线单晶衍射和红外光谱对其进行了结构表征.该配合物属单斜晶系,C2/c空间群,晶胞参数为a=2.4914 (2) nm,b=1.4 9748 (13) nm,c=1.26800( 11 )nm;β=102.1900(10)°;v=4.6240(7) nm3,Z=4,Dc=1.482Mg/m3,Mr=1032.03,F(000)=2160,最终R=0.0506,wR=0.1434.该配合物中锌原子是五配位,它们分别和大环配体上的4个氮原子及叠氮根负离子两端的氮原子配位形成畸变的三角双锥构型.

  18. Influencia de la Medicina Francesa en Colombia

    Ernesto Andrade Valderrama


    Full Text Available

    Me da autoridad para hablar ante ustedes, quienes por segunda vez en nuestra Historia y ahora en una seria Asociación reviven los lazos de la Medicina Colombiana con la gran Escuela Francesa, el haber pertenecido a una de las últimas generaciones, formadas en la Universidad Nacional, que estudiaron toda la carrera en los textos provenientes de ese país y recibieron de maestros, casi todos formados bajo esa notable influencia, todos los principios y normas del ejercicio profesional. Disminuída casi al mínimo, tras la ruptura de comunicación y situación originada por la Segunda Guerra Mundial y tras los cambios, que en el orden social y tecnológico han ocurrido en estos últimos cincuenta años, hoy buscan todas las entidades que tienen a su cargo la Educación Médica, revivir la imagen de un médico general, familiar o comunitario, que pueda restituir la perdida relación Médico-Paciente, base de la antigua Escuela Francesa y que correctamente orientado y utilizando la esplendorosa tecnología de este final de siglo, pueda ser la salvación para el cuidado integral del paciente del próximo milenio que se avecina.

    A través de la Historia, se ha visto cómo el cetro de la Medicina ha rotado por diversas culturas y países. España, por razones políticas, alejada de Francia, recibió, en el campo médico el influjo de Alemania e Inglaterra. A sus colonias de América, fué muy poco lo que de ellas llegó. Sólo hasta finales del siglo XVIII, vino un hombre genial, naturalista y médico, quien pasara a la Historia Universal con la célebre Expedición Botánica y que fué el padre de la medicina colombiana: José Celestino Mutis. El puso en marcha la primera Escuela de Medicina, en 1802 y allí estudiaron los primeros médicos que pasada la Guerra de la Independencia, encabezados por José Félix Merizalde, habrían de recibir la primera Misión Francesa, en 1823.

    Médicos franceses conocidos antes en el país fueron

  19. Deletion of the zupT gene for a zinc importer influences zinc pools in Cupriavidus metallidurans CH34.

    Herzberg, M; Bauer, L; Nies, D H


    complex, and to the loss of metal resistance. This phenomenon occurred only if the ΔzupT cells had been cultivated for several transfers in solid culture medium, which generated severe zinc starvation. Thus, two zinc pools appear to exist in C. metallidurans: one pool of at least 20,000 tightly bound Zn(II) ions, in addition to a second pool of up to 200,000 cations bound loosely and with low substrate specificity.

  20. Synthesis and crystal structure of nickel(II) and zinc(II) complexes with 2,4-bis(3,5-dimethylpyrazol-1-yl)-6-methoxyl- 1,3,5-triazine

    YANG; Chi


    synthesis, crystal and molecular structure of terpy and bis(terpy)nickel(II) chloride decahydrate, Inorg. Chim. Acta, 1990, 178: 47.[10]Bhattacharyya, S., Kumar, S. B., Dutta, S. K. Et al., Zinc(II) and copper (II) complexes of pentacoordinating ligands with pyrazolyl arms: synthesis, structure, redox and spectroscopic properties, Inorg. Chem., 1996, 35: 1967.

  1. Interaction of zinc and cobalt with dipeptides and their DNA binding studies

    P Rabindra Reddy; M Radhika; K Srinivas Rao


    Interactions of zinc and cobalt with peptides cysteinylglycine and histidylglycine have been studied. The binding modes were identified and geometry assigned. Stabilities of these complexes and their ability to bind DNA have been investigated. It is demonstrated that only zinc complexes bind DNA as compared to cobalt complexes.

  2. Copper(II), cobalt(II), nickel(II) and zinc(II) complexes of Schiff base derived from benzil-2,4-dinitrophenylhydrazone with aniline

    N Raman; S Ravichandran; C Thangaraja


    New Schiff base chelates of Cu(II), Co(II), Ni(II) and Zn(II) derived from benzil-2,4-dinitrophenylhydrazone with aniline have been synthesised. Microanalytical data, molar conductance, and magnetic susceptibility values have been obtained, and IR, 1H NMR, 13C NMR, UV-Vis, CV and EPR spectral studies have been carried out to suggest tentative structures for the complexes.

  3. Relaciones intergubernamentales, actores emergentes y mecanismos de influencia

    Obdulia Vega


    Full Text Available Las ONG ejercen influencia sobre los gobiernos, misma que ha sido estudiada con poca sistematicidad. En este trabajo, se examina el elusivo concepto de influencia y se establece un recorte teórico y analítico para el estudio de la influencia de las ONG ambientalistas sobre las relaciones entre diferentes niveles de gobierno en México. Se analiza el caso de la construcción de un confinamiento de residuos peligrosos en Guadalcázar (cerca de la ciudad de San Luis Potosí. En dicho caso, las relaciones entre gobierno federal, gobierno estatal y gobierno municipal en México se vieron afectadas por la presión externa del gobierno de los Estados Unidos de Norteamérica. Más aún, la influencia de la sociedad civil potosina, a través de ONGA cuya esfera de atención se concentraba en el área geográfica de San Luis Potosí, ejerció un impacto decisivo sobre la forma en la cual se desarrollaron los eventos que culminaron en una disputa formal en los tribunales a la luz del Tratado de Libre Comercio de América del Norte (TLCAN En este trabajo examinamos el caso de Metalclad a la luz de un marco teórico interdisciplinario, y definimos hasta qué punto las ONGA lograron influir sobre las relaciones intergubernamentales entre gobiernos federal, estatal y municipal.

  4. Palladium(II) and zinc(II) complexes of neutral [N2O2] donor Schiff bases derived from furfuraldehyde: Synthesis, characterization, fluorescence and corrosion inhibitors of ligands

    Ali, Omyma A. M.


    Metal complexes of Schiff bases derived from furfuraldehyde and 4,5-dimethyl-1,2-phenylendiamine (L1) or 4,5-dichloro-1,2-phenylendiamine (L2) have been reported and characterized based on elemental analyses, IR, 1H NMR, UV-Vis, magnetic moment, molar conductance and thermal analysis. The complexes are found to have the formulae [PdL1-2]Cl2 and [ZnL1-2](AcO)2·H2O. The molar conductance data reveal that Pd(II) and Zn(II) chelates are ionic in nature and are of the type 2:1 electrolytes. The spectral data are consistent with a square planar and tetrahedral geometry around Pd(II) and Zn(II), respectively, in which the ligands act as tetradentate ligands. The thermal behavior of some chelates is studied and the activation thermodynamic parameters are calculated using Coats-Redfern method. The corrosion inhibition of stainless steel types 410 and 304 in 1 M HCl using the synthesized Schiff bases as inhibitors have been studied by weight loss method. The obtained data considered these ligands as efficient corrosion inhibitors. The ligands and their metal complexes exhibited considerable antibacterial activity against Staphylococcusaureus, and Escherichiacoli and antifungal activity against Candida albicans.

  5. Potentiometric and spectrometric study: Copper(II), nickel(II) and zinc(II) complexes with potentially tridentate and monodentate ligands

    R N Patel; Nripendra Singh; R P Shrivastava; K K Shukla; P K Singh


    Equilibrium and solution structural study of mixed-metal-mixed-ligand complexes of Cu(II), Ni(II) and Zn(II) with L-cysteine, L-threonine and imidazole are conducted in aqueous solution by potentiometry and spectrophotometry. Stability constants of the binary, ternary and quaternary complexes are determined at 25 ± 1 ° C and in = 0.1 M NaClO4. The results of these two methods are made selfconsistent, then rationalized assuming an equilibrium model including the species H3A, H2A, A, BH, B, M(OH), M(OH)2, M(A), MA(OH), M(B), M(A)(B), M2(A)2(B), M2(A)2(B-H), M1M2(A)2(B) and M1M2(A)2(B-H) (where the charges of the species have been ignored for the sake of simplicity) (A = L-cysteine, L-threonine, salicylglycine, salicylvaline and BH = imidazole). Evidence of the deprotonation of BH ligand is available at alkaline H. N1H deprotonation of the bidentate coordinated imidazole ligand in the binuclear species at H > 7.0 is evident from spectral measurements. Stability constants of binary M(A), M(B) and ternary M(A)(B), complexes follow the Irving-Williams order.

  6. Metalloantibiotics: synthesis, characterization and in-vitro antibacterial studies on cobalt (II), copper (II), nickel (II) and zinc (II) complexes with cloxacillin.

    Chohan, Zahid H; Supuran, Claudiu T


    The synthesis and characterization of cloxacillin (clox) complexes with divalent metal ions [Co (II), Cu (II), Ni (II) and Zn (II)] is described. The nature of bonding of the chelated cloxacillin and the structures of the metal complexes have been elucidated on the basis of their physical and spectroscopic data. In all the complexes, the cloxacillin acts as a uninegatively charged bidentate ligand with coordination involving the carboxylate-O and endocyclic-N of the beta-lactam ring. The new compounds have been screened for in-vitro antibacterial activity against Escherichia coli (a), Klebsiella pneumonae (b), Proteus mirabilis (c), Pseudomonas aeruginosa (d), Salmonella typhi (e), Shigella dysentriae (f), Bacillus cereus (g), Corynebacterium diphtheriae (h), Staphylococcus aureus (j) and Streptococcus pyogenes (k) bacterial strains. The brine shrimp bioassay was also carried out to study their in-vitro cytotoxic properties. All compounds, respectively, showed a promising activity (90%) against five bacterial species at 10 microg/ml concentration and a significant activity (52%) against the same test bacteria at 25 microg/ml concentration.

  7. Palladium(II) and zinc(II) complexes of neutral [N2O2] donor Schiff bases derived from furfuraldehyde: synthesis, characterization, fluorescence and corrosion inhibitors of ligands.

    Ali, Omyma A M


    Metal complexes of Schiff bases derived from furfuraldehyde and 4,5-dimethyl-1,2-phenylendiamine (L1) or 4,5-dichloro-1,2-phenylendiamine (L2) have been reported and characterized based on elemental analyses, IR, 1H NMR, UV-Vis, magnetic moment, molar conductance and thermal analysis. The complexes are found to have the formulae [PdL1-2]Cl2 and [ZnL1-2](AcO)2·H2O. The molar conductance data reveal that Pd(II) and Zn(II) chelates are ionic in nature and are of the type 2:1 electrolytes. The spectral data are consistent with a square planar and tetrahedral geometry around Pd(II) and Zn(II), respectively, in which the ligands act as tetradentate ligands. The thermal behavior of some chelates is studied and the activation thermodynamic parameters are calculated using Coats-Redfern method. The corrosion inhibition of stainless steel types 410 and 304 in 1 M HCl using the synthesized Schiff bases as inhibitors have been studied by weight loss method. The obtained data considered these ligands as efficient corrosion inhibitors. The ligands and their metal complexes exhibited considerable antibacterial activity against Staphylococcusaureus, and Escherichiacoli and antifungal activity against Candida albicans.

  8. Chiroptical properties, binding affinity, and photostability of a conjugated zinc porphyrin dimer complexed with left-handed Z-DNA and right-handed B-DNA.

    Choi, Jung Kyu; Reed, Aisha; Balaz, Milan


    We have studied the UV-vis absorption and chiroptical properties, binding affinity and photostability of a conjugated positively charged butadiyne-linked Zn(ii) porphyrin dimer bound to DNA sequence poly(dG-dC)2. Right-handed B-DNA, spermine-induced Z-DNA and Co(iii)-induced Z-DNA have been explored. Resonance light scattering (RLS) spectra showed formation of porphyrin aggregates in the presence of all DNA forms with the largest aggregates formed with B-DNA. The porphyrin dimer gave rise to induced bisignate circular dichroism (CD) signals in the presence of the left-handed Z-DNA conformations. On the other hand, the dimer stayed nearly chiroptically silent when complexed with the B-form of poly(dG-dC)2. Our results indicated that the conjugated Zn(ii) porphyrin dimer can be used as a sensor for the chiroptical detection of Z-DNA in the visible (400-500 nm) and near-infrared region of the electromagnetic spectrum (700-800 nm). The helicity of DNA had little effect on the dimer binding affinities. The photostability of the porphyrin dimer complexed with any form of DNA was higher than that of the free molecule. The porphyrin dimer bound to Z-DNA exhibited slower photobleaching than the B-DNA dimer complex.

  9. Rapid growth of nanotubes and nanorods of würtzite ZnO through microwave-irradiation of a metalorganic complex of zinc and a surfactant in solution

    Sanjaya Brahma; Kalya Jagannatha Rao; Srinivasarao Shivashankar


    Large quantities of single-crystalline ZnO nanorods and nanotubes have been prepared by the microwave irradiation of a metalorganic complex of zinc, in the presence of a surfactant. The method is simple, fast, and inexpensive (as it uses a domestic microwave oven), and yields pure nanostructures of the hexagonal würtzite phase of ZnO in min, and requires no conventional templating. The ZnO nanotubes formed have a hollow core with inner diameter varying from 140–160 nm and a wall of thickness, 40–50 nm. The length of nanorods and nanotubes varies in the narrow range of 500–600 nm. These nanostructures have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). The ZnO nanorods and nanotubes are found by SAED to be single-crystalline. The growth process of ZnO nanorods and nanotubes has been investigated by varying the surfactant concentration and microwave irradiation time. Based on the various results obtained, a tentative and plausible mechanism for the formation of ZnO nanostructures is proposed.

  10. Hydrothermal Synthesis and Crystal Structure of a Zinc Complex: [Zn2.5(phen)(BDC)2(OH)](phen = 1,10-Phenanthroline, BDC= Benzene-1,4-dicarboxylic Acid)

    WANG Qing-Wei; LI Xiu-Mei; SHI Lin-Fang


    A metal-organic coordination polymer [Zn2.5(phen)(BDC)2(OH)]2 (phen = 1,10-phenanthroline, BDC = benzene-1,4-dicarboxylic acid)1 has been hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction, elemental analyses and IR spectro-scopy. The complex crystallizes in the triclinic system, space group P1 with a = 11.199(2), b =11.593(2), c = 11.865(3) A, α= 99.330(1), β=111.506(1),γ = 104.804(1)°, V= 1328.4(5) A3, Dc=1.722 g/cm3, Z = 1, Mr = 1377.82, F(000) = 692, μ(MoKa) = 2.306 mm-1, S = 1.093, R = 0.0281 and wR= 0.0756 for 4179 observed reflections (Ⅰ 20(Ⅰ)). The coordination polyhedron around Zn(Ⅱ)can be described as a tetrahedron, trigonal bipyramid and octahedron. It is worth noting that the crystal structure of 1 is composed of tetranuclear zinc clusters linked by {ZnO6} units.

  11. Determination of total polyphenols in the zinc complex of polyphenol by Folin-Ciocalteu colorimetry%Folin-Ciocalteu分光光度法测定茶多酚锌配合物中多酚的含量

    王彦兵; 胥艳; 魏永春; 刘小强; 刘绣华


    A quantitative determination method for total polyphenols content in the Zinc complex of polyphenol was developed by using Folin-Ciocalteu colorimetry with gallic acid as reference compound. The results showed that the linear range of calibration curve was 0 - 8. 54 mg ·L-1. The RSD (relative standard deviation) of stability, precision, repeatability and recovery rate were in the range of 0. 39% -1. 23%. Therefore, FC method is a convenient, fast and accurate method to determine the total polyphenols of tea products.%以没食子酸为对照品,采用Folin-Ciocalteu比色法测定了茶多酚锌配合物(TP-Zn)中多酚的含量.结果表明,多酚质量浓度在0~8.54 mg ·L-1范围内与吸光度呈良好的线性关系;稳定性、精密度、重现性和回收率实验的相对标准偏差在0.39%~1.23%范围内.该法是一种简便、快速、准确测定茶叶制品中多酚含量的可靠方法.

  12. Low-cost chemiresistive sensor for volatile amines based on a 2D network of a zinc(II) Schiff-base complex

    Mirabella, S.; Oliveri, I. P.; Ruffino, F.; Maccarrone, G.; Di Bella, S.


    A marked chemiresistive behavior is revealed in a nanostructured material obtained by spin-coating a solution of a bis(salycilaldiminato)Zn(II) Schiff-base (ZnSB) complex. The resulting submicron 2D network exhibits reversible changes in absorbance and resistance under the cycles of absorption and desorption of a volatile amine. These results are explained in terms of a Lewis donor-acceptor interaction between the ZnSB (acceptor) and the chemisorbed amine (donor). The 2D network of ZnSB was employed as a sensing element to fabricate a low-cost device for the volatile amines detection, showing promising results for food spoilage detection.

  13. 铜、铁、锌-氟尿嘧啶配合物合成及其对肿瘤细胞增殖的抑制%Copper, iron, zinc-fluorouracil complexes synthesized in vitro inhibit tumor cell proliferation

    周轶平; 陈元晓; 周云; 石中正; 罗敏; 钟文远; 陈英杰


    背景:有机抗癌药与金属盐形成配合物后会形成新的结构或改变离子浓度,因此改变二者的毒性与活性而产生协同作用。目的:寻求高效低毒的新型金属-氟尿嘧啶配合物抗肿瘤药物。方法:以铜、铁、锌盐和氟尿嘧啶为原料,合成了4种配合物,分别为[Cu(5-Fu)2Cl2],[Cu(5-Fu)2(NO3)2],[Fe(5-Fu)3]SO4和[Zn(5-Fu)2Cl2]。用元素分析和质谱法分析配合物的化学结构。分别以4种配合物溶液、4种盐溶液、顺铂、氟尿嘧啶培养人白血病细胞株K562与人结肠癌细胞株HCT-116,改良MTT法测试细胞增殖。结果与结论:配合物的元素分析及摩尔电导数据初步确定了配合物的化学式,质谱结果进一步证明氟尿嘧啶确实与金属离子Cu2+、Fe2+、Zn2+配位。在0.1-100 mg/L质量浓度范围内,4种配合物对K562和HCT-116细胞增殖均有不同程度的抑制作用,4种配合物对K562和HCT-116细胞增殖的IC50值均低于氟尿嘧啶组,其细胞毒活性是氟尿嘧啶的1.5-7.8倍。表明铜盐、锌盐、铁盐与氟尿嘧啶形成配合物后有协同抑制肿瘤组织细胞增殖的作用。%BACKGROUND:Anticancer drug and organic metal complexes wil form a new structure or a change in ion concentration, thus changing both the activity and toxicity to produce a synergistic effect. OBJECTIVE:To synthesize new high-efficient and low-toxic metal-fluorouracil complexes as anticancer drugs. METHODS:Copper, zinc and iron salts and fluorouracil were used to synthesize four copper, zinc and iron-fluorouracil complexes that were [Cu(5-Fu)2Cl2], [Cu(5-Fu)2(NO3)2], [Fe(5-Fu)3]SO4 and [Zn(5-Fu)2Cl2]. Preliminary chemical structures of the four complexes were confirmed by elemental analysis and mass spectrometry. Their inhibitory activity on human cancer cells, human leukemia cellline K562 and human colon cancer cellline HCT-116, was measured by MTT colorimetric assay. RESULTS AND CONCLUSION:[Cu(5-Fu)2Cl2], [Cu

  14. Design and synthesis of a new terbium complex-based luminescent probe for time-resolved luminescence sensing of zinc ions.

    Ye, Zhiqiang; Xiao, Yunna; Song, Bo; Yuan, Jingli


    Luminescent probes/chemosensors based on lanthanide complexes have shown great potentials in various bioassays due to their unique long-lived luminescence property for eliminating short-lived autofluorescence with time-resolved detection mode. In this work, we designed and synthesized a new dual-chelating ligand {4'-[N,N-bis(2-picolyl)amino]methylene-2,2':6',2'-terpyridine-6,6'-diyl} bis(methylenenitrilo) tetrakis(acetic acid) (BPTTA), and investigated the performance of its Tb(3+) complex (BPTTA-Tb(3+)) for the time-resolved luminescence sensing of Zn(2+) ions in aqueous media. Weakly luminescent BPTTA-Tb(3+) can rapidly react with Zn(2+) ions to display remarkable luminescence enhancement with high sensitivity and selectivity, and such luminescence response can be realized repeatedly. Laudably, the dose-dependent luminescence enhancement shows a good linear response to the concentration of Zn(2+) ions with a detection limit of 4.1 nM. To examine the utility of the new probe for detecting intracellular Zn(2+) ions, the performance of BPTTA-Tb(3+) in the time-resolved luminescence imaging of Zn(2+) ions in living HeLa cells was investigated. The results demonstrated the applicability of BPTTA-Tb(3+) as a probe for the time-resolved luminescence sensing of intracellular Zn(2+) ions.

  15. Slow relaxation of the magnetization in an Isostructural series of Zinc-lanthanide complexes: an integrated EPR and AC susceptibility study

    Amjad, Asma; Madalan, Augustin; Andruh, Marius; Caneschi, Andrea; Sorace, Lorenzo; University of Bucharest, Faculty of Chemistry, Inorganic Chemistry Laboratory, Bucharest, Romania Collaboration


    Lanthanide based molecular complexes have shown potential to behave as single molecule magnets proficient to function above cryogenic temperatures. In this work we explore the dynamics of one such family, [Zn(LH)2Ln](NO3)3 .6H2O - (Ln = Nd3+, Dy3+, Tb3+, Ho3+, Er3+, Yb3+) . The series has a single lanthanide ion as a magnetic center in a low symmetry environment; the dynamics and energy landscape of the series is explored using X-band EPR, AC and DC susceptibility over a range of temperature, field and frequency. DC magnetic data show χT value consistent with expected behavior. EPR spectra for Er3+ and Yb3+ complexes shows EPR spectra typical for easy-plane and quasi-isotropic systems respectively, thus explaining the lack of out of phase susceptibility even in an external applied filed. However, Dy3+ derivative show slow relaxation of the magnetization in zero field up to 15 K and is, accordingly EPR silent.

  16. Synthesis and Crystal Structure of a Tetranuclear Carboxylate-bridged Lanthanum(III)-Zinc(II) Complex [La2Zn2(m-CNC6H4COO)10(Py)2(C2H5OH)2


    The title complex was prepared from self-assembly reaction of La(NO3)3×6H2O, Zn(NO3)2×6H2O, m-cyanobenzoic acid (m-CNC6H4COOH) and pyridine (Py) in refluxing ethanol and its structure was determined by single-crystal X-ray diffraction. Crystallographic data: C94H62N12La2O22Zn2, Mr = 2120.12, triclinic space group P _ 1, a = 13.2219(5), b = 13.2713(5), c = 14.1987(6) ?, a = 69.156(1), b = 84.034(1), g = 89.400(1) °, V = 2314.9(2) ?3, Z = 1, Dc = 1.521 g/cm3, F(000) = 1060, m (MoKa) = 14.94 cm-1, the final R = 0.043 and wR = 0.117 for 6381 unique reflections with I > 2s(I). Crystal structure determination shows that the neighboring lanthanum(III) and zinc(II) ions are bridged by three bidentate m-cyanobenzonate ligands in the syn-syn fashion to form a pair of dinuclear [LaZn(m-CNC6H4COO)3(Py)(C2H5OH)] subunits, being linked together by two bidentate and two tridentate m-cyanobenzonate groups in the syn-syn and syn-anti modes, respectively, to construct a tetranuclear La-Zn complex [La2Zn2(m-CNC6H4COO)10(Py)2(C2H5OH)2].

  17. Low serum zinc level in dpression

    SA Mousavi


    Full Text Available BACKGROUND: Major Depressive Disorder (MDD is a common disorder, with a lifetime prevalence of about 15 percent, perhaps as high as 25 percent for women. The etiology of MDD is too complex to be explained totally by a single social, developmental, or biological theory. A variety of factors appear to work together to cause or precipitate depressive disorders. Various functions have been reported for trace elements such as zink in recovery or exacerbation of depression. METHODS: In this experimental study, we studied 46 patients with MDD based on DSM IV criteria, among the patients referred to mental disorders clininc of Noor Hospital. Twenty Patients were men and 26 were women. Thirty two volunteers of general population were evaluated for depression with Beck depression test who did not show any depressive symptoms with this test. A blood sample of 5cc was obtained from each person and the serum zinc concentration was measured. Data gathered and analyzed with SPSS, logistic regression and chi-squar tests. RESULTS: Serum zinc concentrations were 74 to 130 mg/dl in men and 60 to 128 mg/dl in women of control group. Serum zinc concentration was 30 to 60 mg/dl in depressive patients that it was lower in women than men. The difference between serum zinc concentrations of normal and depressive persons was meaningful (P = 0.02. CONCLUSION: In our study, the serum concentration of zinc was about half of normal value. This study replicates previous findings that major depressed subjects show significantly lowered serum zinc concentration. KEYWORDS: Depression, zinc.


    S.B. Strashnova


    Full Text Available The complexes of general formula MCl2∙L1-4∙nH2O (where L1 - N-(2,4,7-trinitrofluorenilidene-9-p-dimethyl-aminoanilin, L2 - N-(2,4,5,7-tetranitrofluorenilidene-9-p-dimethylaminoaniline, L3 - N-(2,4,7-trinitrofluorenilidene-N-(p-dimethylaminophenylhydroxylamine, L4 - N-(2,4,5,7-tetranitrofluorenilidene-9-N-(p-dimethylaminophenyl-hydroxylamine; M=Cu, Co, Ni, Zn; n= 1-3 have been synthesized and investigated by different methods. Spectral criteria of co-ordination of the molecules L1 –L4 in electronic adsorption spectra were detected.

  19. Zinc electrode and rechargeable zinc-air battery

    Ross, Jr., Philip N.


    An improved zinc electrode is disclosed for a rechargeable zinc-air battery comprising an outer frame and a porous foam electrode support within the frame which is treated prior to the deposition of zinc thereon to inhibit the formation of zinc dendrites on the external surface thereof. The outer frame is provided with passageways for circulating an alkaline electrolyte through the treated zinc-coated porous foam. A novel rechargeable zinc-air battery system is also disclosed which utilizes the improved zinc electrode and further includes an alkaline electrolyte within said battery circulating through the passageways in the zinc electrode and an external electrolyte circulation means which has an electrolyte reservoir external to the battery case including filter means to filter solids out of the electrolyte as it circulates to the external reservoir and pump means for recirculating electrolyte from the external reservoir to the zinc electrode.

  20. Zinc in diet

    ... Zinc is also needed for the senses of smell and taste. During pregnancy, infancy, and childhood the ... sense of taste Problems with the sense of smell Skin sores Slow growth Trouble seeing in the ...

  1. Zinc level and obesity

    Doaa S.E. Zaky


    Conclusion Plasma zinc concentration in obese individuals showed an inverse relationship with the waist circumference and BMI as well as serum low-density lipoprotein-cholesterol and correlated positively with high-density lipoprotein.

  2. Zinc level and obesity

    Doaa S.E Zaky; Eman A Sultan; Mahmoud F Salim; Rana S Dawod


    Background Obesity is a chronic condition that is associated with disturbances in the metabolism of zinc. Therefore, the aim of this study was to investigate the relationship between serum zinc level and different clinical and biochemical parameters in obese individuals. Patients and methods Twenty-four individuals with BMI more than 30 kg/m 2 and 14 healthy controls (BMI < 24 kg/m 2 ) were assessed for BMI and waist circumference using anthropometric measurements. Colorimetric tes...

  3. Structures and properties of 1,8,15,22-tetrasubstituted phthalocyaninato zinc and nickel complexes: substitution and axially coordination effects study based on density functional theory calculations.

    Wan, Liang; Zhang, Yuexing; Qi, Dongdong; Jiang, Jianzhuang


    On the basis of the density functional theory (DFT) calculation of ZnPc (1), Zn[Pc(alpha-OC(5)H(11))(4)] (2), Ni[Pc(alpha-OC(5)H(11))(4)] (3), and Zn[Pc(alpha-OC(5)H(11))(4)]xH(2)O (4), the effects of non-peripheral substitution, different transition metals, and axial water coordination on the molecular structure, molecular orbital, atomic charge, infrared (IR) spectrum, and electronic absorption spectrum were investigated. The calculation results reveal that bulky 3-pentyloxy groups at the non-peripheral positions of the phthalocyanine ring evince great changes in structure and properties: they deflect the isoindole units, lift the frontier molecular orbitals, alter the atomic charge distribution, shift the bands of IR and electronic absorption spectra, etc. Though the central metal can shorten or lengthen the bond length, its effect on the electronic structure and properties of the phthalocyanine complex is very limited. Axial coordination significantly enhances the non-planarity of the phthalocyanine ring and, thus, alters the electronic structure, which is important for the formation of novel dimeric supramolecular structures through intermolecular hydrogen bonds. In addition, the calculated structures of 3 as well as the simulated IR and electronic absorption spectra of 4 were compared with the experimental data and showed good agreement.

  4. Analysis of reaction and transport processes in zinc air batteries

    Schröder, Daniel


    This book contains a novel combination of experimental and model-based investigations, elucidating the complex processes inside zinc air batteries. The work presented helps to answer which battery composition and which air-composition should be adjusted to maintain stable and efficient charge/discharge cycling. In detail, electrochemical investigations and X-ray transmission tomography are applied on button cell zinc air batteries and in-house set-ups. Moreover, model-based investigations of the battery anode and the impact of relative humidity, active operation, carbon dioxide and oxygen on zinc air battery operation are presented. The techniques used in this work complement each other well and yield an unprecedented understanding of zinc air batteries. The methods applied are adaptable and can potentially be applied to gain further understanding of other metal air batteries. Contents Introduction on Zinc Air Batteries Characterizing Reaction and Transport Processes Identifying Factors for Long-Term Stable O...

  5. Anti-inflammatory activity and gastric lesions induced by zinc-tenoxicam.

    Nascimento, Jorge Willian L; Santos, Luiz Henrique; Nothenberg, Michael S; Coelho, Márcio M; Oga, Seizi; Tagliati, Carlos A


    Oral administration of tenoxicam or zinc-tenoxicam complex inhibited to a similar extent carrageenin-induced paw oedema and granulomatous tissue formation in rats as well as the acetic acid induced writhing response in mice. Gastric lesions induced by oral administration of zinc-tenoxicam were reduced in number and severity when compared with those induced by tenoxicam or the co-administration of tenoxicam and zinc acetate. However, after intraperitoneal administration, both zinc-tenoxicam and tenoxicam plus zinc acetate induced a reduced number of gastric lesions as compared with tenoxicam.

  6. The bioavailability of four zinc oxide sources and zinc sulphate in broiler chickens

    Veldkamp, T.; Diepen, van, C.A.; Bikker, P.


    Zinc is an essential trace element for all farm animal species. It is commonly included in animal diets as zinc oxide, zinc sulphate or organically bound zinc. Umicore Zinc Chemicals developed zinc oxide products with different mean particle sizes. Umicore Zinc Chemicals requested Wageningen UR Livestock Research to determine the bioavailability of four zinc oxide sources and zinc sulphate in broiler chickens. A precise estimate of the bioavailability of zinc sources is required both for fulf...

  7. Treatment of zinc deficiency without zinc fortification

    Donald OBERLEAS; Barbara F. HARLAND


    Zinc (Zn) deficiency in animals became of interest until the 1950s. In this paper, progresses in researches on physi-ology of Zn deficiency in animals, phytate effect on bioavailability of Zn, and role of phytase in healing Zn deficiency of animals were reviewed. Several studies demonstrated that Zn is recycled via the pancreas; the problem of Zn deficiency was controlled by Zn homeostasis. The endogenous secretion of Zn is considered as an important factor influencing Zn deficiency, and the critical molar ratio is 10. Phytate (inositol hexaphosphate) constituted up to 90% of the organically bound phosphorus in seeds. Great improvement has been made in recent years on isolating and measuring phytate, and its structure is clear. Phytate is considered to reduce Zn bioavailability in animal. Phytase is the enzyme that hydrolyzes phytate and is present in yeast, rye bran, wheat bran, barley, triticale, and many bacteria and fungi. Zinc nutrition and bioavailability can be enhanced by addition of phytase to animal feeds. Therefore, using phytase as supplements, the most prevalent Zn deficiency in animals may be effectively corrected without the mining and smelting of several tons of zinc daily needed to correct this deficiency by fortification worldwide.

  8. Molecular dynamics of sialic acid analogues complex with cholera toxin and DFT optimization of ethylene glycol-mediated zinc nanocluster conjugation.

    Sharmila, D Jeya Sundara; Jino Blessy, J


    Cholera is an infectious disease caused by cholera toxin (CT) protein of bacterium Vibrio cholerae. A sequence of sialic acid (N-acetylneuraminic acid, NeuNAc or Neu5Ac) analogues modified in its C-5 position is modelled using molecular modelling techniques and docked against the CT followed by molecular dynamics simulations. Docking results suggest better binding affinity of NeuNAc analogue towards the binding site of CT. The NeuNAc analogues interact with the active site residues GLU:11, TYR:12, HIS:13, GLY:33, LYS:34, GLU:51, GLN:56, HIE:57, ILE:58, GLN:61, TRP:88, ASN:90 and LYS:91 through intermolecular hydrogen bonding. Analogues N-glycolyl-NeuNAc, N-Pentanoyl-NeuNAc and N-Propanoyl-NeuNAc show the least XPGscore (docking score) of -9.90, -9.16, and -8.91, respectively, and glide energy of -45.99, -42.14 and -41.66 kcal/mol, respectively. Stable nature of CT-N-glycolyl-NeuNAc, CT-N-Pentanoyl-NeuNAc and CT-N-Propanoyl-NeuNAc complexes was verified through molecular dynamics simulations, each for 40 ns using the software Desmond. All the nine NeuNAc analogues show better score for drug-like properties, so could be considered as suitable candidates for drug development for cholera infection. To improve the enhanced binding mode of NeuNAc analogues towards CT, the nine NeuNAc analogues are conjugated with Zn nanoclusters through ethylene glycol (EG) as carriers. The NeuNAc analogues conjugated with EG-Zn nanoclusters show better binding energy towards CT than the unconjugated nine NeuNAc analogues. The electronic structural optimization of EG-Zn nanoclusters was carried out for optimizing their performance as better delivery vehicles for NeuNAc analogues through density functional theory calculations. These sialic acid analogues may be considered as novel leads for the design of drug against cholera and the EG-Zn nanocluster may be a suitable carrier for sialic acid analogues.

  9. Morphology of ZnS Particles Produced from Various Zinc Salts by Homogeneous Precipitation


    acetato, sulfato , chloro and nitrato complexes of zinc corrected for the ionic strengths of the solutions that we used (9). Complex species involving...chloride system 8 Table I Concentration equilibrium constants for acetato, nitrato, sulfato and chloro complexes of Znz- ions found by interpolation...this conclusion. Although stability constants for acetato complexes of zinc (Table I) are very close to those for sulfato complexes, nucleation is

  10. The mouse nac1 gene, encoding a cocaine-regulated Bric-a-brac Tramtrac Broad complex/Pox virus and Zinc finger protein, is regulated by AP1.

    Mackler, S A; Homan, Y X; Korutla, L; Conti, A C; Blendy, J A


    NAC1 cDNA was identified as a novel transcript induced in the nucleus accumbens from rats chronically treated with cocaine. NAC1 is a member of the Bric-a-brac Tramtrac Broad complex/Pox virus and Zinc finger family of transcription factors and has been shown by overexpression studies to prevent the development of behavioral sensitization resulting from repeated cocaine treatment. This paper reports the cloning and characterization of the corresponding gene. The mouse Nac1 gene consist of six exons, with exon 2 containing an alternative splice donor, providing a molecular explanation of the splice variants observed in mouse and rat. Transcripts of Nac1 were ubiquitously detected in different mouse tissues with prominent expression in the brain. The mouse Nac1 gene was localized to chromosome 8, suggesting a highly plausible candidate gene to explain differences in cocaine-induced behaviors between C57BL6/J and DBA/2J mice that had previously been mapped to the area. In addition, a functional AP1 binding site has been identified in an intron 1 enhancer of the Nac1 gene that plays an essential role in the activation of the gene in differentiation of neuroblastoma cells. Co-transfection with c-jun and c-fos expression plasmids, which encode the two subunits of AP1, activated the wild type Nac1 intron 1 enhancer two-fold over basal, nearly at the level of NAC1 enhancer activity seen in differentiated N2A cells. Mutation of the AP1 site completely abrogated all activation of the NAC1 enhancer in differentiated N2A cells. Activation of immediate early genes such as c-fos and c-jun following chronic drug treatments has been well characterized. The present data describe one potential regulatory cascade involving these transcription factors and activation of NAC1. Identification of drug induced alterations in gene expression is key to understanding the types of molecular adaptations underlying addiction.

  11. Influencia del Capital Intelectual en la Competitividad de los Hoteles


    El objetivo de la presente investigación es conocer la influencia del capital intelectual en la competitividad de las empresas hoteleras de 1 a 5 estrellas de Aguascalientes, México. La medición del capital intelectual, que es el recurso intangible de las organizaciones contenido en el capital humano, capital estructural y capital relacional que genera competitividad y riqueza presente y futura, se realiza a través de un instrumento tipo Likert de 61 reactivos, cuyos resultados son comparados...

  12. Una retórica de la influencia

    Cecilia González


    Full Text Available Entre las últimas décadas del siglo XIX y las primeras del XX se publica en el Río de la Plata un número considerable de relatos anclados en los debates que recorren la cultura europea del momento y que giran en torno a fenómenos de influencia. Este denominador común se declina, según los textos, en una serie de temas privilegiados : hipnosis, sugestión, herencia, mimetismo, vampirismo, parasitismo, emanación de todo tipo de rayos, ondas y fluidos capaces de modificar el comportamiento de un ...

  13. Influencia de la microbiota intestinal en la obesidad



    La prevalencia de la obesidad es cada vez mayor y especialmente en niños y adolescentes. En el desarrollo de la obesidad interviene la dieta, factores genéticos, endócrinos, psicológicos y ambientales. El primer objetivo específico fue determinar la influencia de una intervención para el tratamiento de la obesidad sobre la microbiota intestinal de adolescentes obesos y con sobrepeso. Mediante las técnicas de la reacción en cadena de la polimerasa a tiempo real (q-PCR) y de hibridación...

  14. Controlled Growth of ZnSe Nanocrystals by Tuning Reactivity and Amount of Zinc Precursor

    Lai-Jun Zhang


    Full Text Available Zinc selenide (ZnSe nanocrystals were synthesized via a phosphine-free route using the highly reactive alkylamine-H2Se complex as selenium precursor and zinc precursors with different reactivity. The reactivity of zinc precursor was tuned by using three kinds of zinc carboxylates with different alkyl chain lengths, including zinc acetate, zinc nonanoate, and zinc stearate. The effect of the reactivity and the amount of zinc precursor on nucleation and growth of ZnSe nanocrystals were investigated by ultraviolet-visible absorption and photoluminescence spectra. Result indicates that the growth and optical property of the resulting ZnSe nanocrystals are strongly dependent on the alkyl chain length and the amount of the zinc carboxylates and both shorter alkyl chain length, and more amount of zinc carboxylate will lead to faster growth of ZnSe nanocrystals. This allows that the controlled growth and excellent optical property of high-quality ZnSe nanocrystals can be achieved by combining the different reactivity and the used amount of zinc precursor, such as by using stoichiometric and reactive Zn precursor and Se precursor or by using larger amount of more unreactive Zn precursor relative to the highly reactive alkylamine-H2Se complex precursor.

  15. Spectrophotometric determination of micro quantities of zinc in rocks

    Huffman, C.; Lipp, H.H.; Rader, L.F.


    A chemical method is presented for the determination of microgram amounts of zinc in rocks. Zinc is absorbed on anion-exchange resin from 1.2 M hydrochloric acid and eluted with 0.01 M hydrochloric acid. A diethyldithiocarbamate separation removes traces of interfering elements from the eluate. The zinc-diethyldithiocarbamate complex is extracted into chloroform at pH 8.5 and reextracted from other elements in the chloroform solution with 0.16 M hydrochloric acid and finally determined spectrophotometrically as the zincon complex at 621 m??. The coefficient of variation of the method determined from replicate determinations of zinc on 75 selected samples of basalt, ranging in zinc content from 0.004 to 0.018 per cent, was found to be 6.3 per cent and essentially constant in the range of zinc content studied. This method of analysis has been used extensively for a study of zinc in basalts reported by Rader, Swadley, Huffman and Lipp (companion paper, 1963). ?? 1963.

  16. Microstructure and Performances of Nanocrystalline Zinc-nickel Alloy Coatings

    LI Guang-yu; LIAN Jian-she; NIU Li-yuan; JIANG Zhong-hao


    Nanocrystalline zinc-nickel alloy coatings were deposited from an alkaline zincate bath contained an organic additive that can reduce polarization and a complexing agent. SEM and TEM observations and XRD analysis were performed to examine the microstructure and phase composition of the coatings. The nickel content in deposits is 12.0~14.7% and the coating is consisted of single nanocrystalline γ-phase structure (Ni5Zn21), with grain average grain size about 15nm. The nanocrystalline zinc-nickel alloy coatings have better corrosion resistance, less brittleness and higher microhardness than the conventional zinc coatings.

  17. Microstructure and Performances of Nanocrystalline Zinc-nickel Alloy Coatings

    LIGuang-yu; LIANJian-she; NIULi-yuan; JIANGZhong-hao


    Nanocrystalline zinc-nickel alloy coatings were deposited from an alkaline zincate bath contained an organic additive that can reduce polarization and a complexing agent. SEM and TEM observations and XRD analysis were performed to examine the microstructure and phase composition of the coatings. The nickel content in deposits is 12.0-14.7% and the coating is consisted of single nanectystalline γ-phase structure (Ni5Zn21), with grain average grain size about 15nm. The nanocrystalline zinc-nickel alloy coatings have better corrosion resistance, less brittleness and higher microhardness than the conventional zinc coatings.

  18. Root-Secreted Nicotianamine from Arabidopsis halleri Facilitates Zinc Hypertolerance by Regulating Zinc Bioavailability1[W][OPEN

    Tsednee, Munkhtsetseg; Yang, Shun-Chung; Lee, Der-Chuen; Yeh, Kuo-Chen


    Hyperaccumulators tolerate and accumulate extraordinarily high concentrations of heavy metals. Content of the metal chelator nicotianamine (NA) in the root of zinc hyperaccumulator Arabidopsis halleri is elevated compared with nonhyperaccumulators, a trait that is considered to be one of the markers of a hyperaccumulator. Using metabolite-profiling analysis of root secretions, we found that excess zinc treatment induced secretion of NA in A. halleri roots compared with the nonhyperaccumulator Arabidopsis thaliana. Metal speciation analysis further revealed that the secreted NA forms a stable complex with Zn(II). Supplying NA to a nonhyperaccumulator species markedly increased plant zinc tolerance by decreasing zinc uptake. Therefore, NA secretion from A. halleri roots facilitates zinc hypertolerance through forming a Zn(II)-NA complex outside the roots to achieve a coordinated zinc uptake rate into roots. Secretion of NA was also found to be responsible for the maintenance of iron homeostasis under excess zinc. Together our results reveal root-secretion mechanisms associated with hypertolerance and hyperaccumulation. PMID:25118254

  19. Light-Controlled Release and Uptake of Zinc Ions in Solution by a Photochromic Terthiazole-Based Ligand.

    Guérin, Juliette; Léaustic, Anne; Berthet, Jérôme; Métivier, Rémi; Guillot, Régis; Delbaere, Stéphanie; Nakatani, Keitaro; Yu, Pei


    We have synthesized and fully characterized a photochromic zinc complex with a terphenylthiazole-based ligand with a salen-like cavity. The solution stability of the complex was found to be greatly dependent on the state of the photochromic ligand and an interesting photo-triggered release and uptake of zinc ions was found as well as monitored by its fluorescence. The contrasting stability difference of the zinc complex between its two isomeric states was rationalized by DFT calculations.

  20. Zinc effects on growth and development of infant with low birth weight.

    Rafael Jiménez


    Full Text Available Antecedentes: El zinc es un elemento traza de gran importancia para el crecimiento intrauterino y postnatal de niños con retardo del crecimiento. Objetivos: Evaluar el efecto de la suplementación con sulfato de zinc en el crecimiento y desarrollo psicomotor en una cohorte de niños con bajo peso al nacer, durante el primer año de vida. Pacientes y métodos: Se realizó un estudio longitudinal doble ciego de una cohorte de 163 recién nacidos distribuidos al azar en dos grupos: el grupo de los suplementados correspondió a 87 lactantes a los que se le suministró una dosis de 10 mg/día de una solución de sulfato de zinc durante los primeros 6 meses de vida; el grupo de los no suplementados estuvo compuesto por 76 lactantes a los que se le suministró una solución de 10 ml de suero fisiológico ausente de zinc en igual período. Resultados: El incremento de peso se relaciona de forma positiva con la suplementación con zinc, lo cual se evidencia en la curva de ganancia de peso y el análisis de observaciones repetidas realizado para esta variable; sin embargo, la variable talla no sufre la influencia de la misma manera. En relación con el desarrollo psicomotor, el índice de desarrollo motor se ve positivamente influido por la suplementación con zinc, no así el índice de desarrollo mental. Conclusiones: La suplementación de 10 mg de sulfato de zinc en niños con bajo peso al nacer durante 6 meses es beneficiosa para el incremento del peso y el desarrollo motor de estos lactantes.

  1. Zinc Determination in Pleural Fluid

    Nazan DEMİR; DEMİR, Yaşar


    In this study, an enzymatic zinc determination method was applied to pleural fluid, the basis of which was the regaining of the activity of apo carbonic anhydrase by the zinc present in the sample. The method was used for pleural fluid zinc determination in order to show the application to body fluids other than serum. For this purpose, pleural fluids were obtained from 20 patients and zinc concentrations were determined. Carbonic anhydrase was purified by affinity chromatography from bovine ...

  2. The bioavailability of four zinc oxide sources and zinc sulphate in broiler chickens

    Veldkamp, T.; Diepen, van J.T.M.; Bikker, P.


    Zinc is an essential trace element for all farm animal species. It is commonly included in animal diets as zinc oxide, zinc sulphate or organically bound zinc. Umicore Zinc Chemicals developed zinc oxide products with different mean particle sizes. Umicore Zinc Chemicals requested Wageningen UR

  3. The bioavailability of four zinc oxide sources and zinc sulphate in broiler chickens

    Veldkamp, T.; Diepen, van J.T.M.; Bikker, P.


    Zinc is an essential trace element for all farm animal species. It is commonly included in animal diets as zinc oxide, zinc sulphate or organically bound zinc. Umicore Zinc Chemicals developed zinc oxide products with different mean particle sizes. Umicore Zinc Chemicals requested Wageningen UR Live

  4. Trace elements in human physiology and pathology: zinc and metallothioneins.

    Tapiero, Haim; Tew, Kenneth D


    Zinc is one of the most abundant nutritionally essential elements in the human body. It is found in all body tissues with 85% of the whole body zinc in muscle and bone, 11% in the skin and the liver and the remaining in all the other tissues. In multicellular organisms, virtually all zinc is intracellular, 30-40% is located in the nucleus, 50% in the cytoplasm, organelles and specialized vesicles (for digestive enzymes or hormone storage) and the remainder in the cell membrane. Zinc intake ranges from 107 to 231 micromol/d depending on the source, and human zinc requirement is estimated at 15 mg/d. Zinc has been shown to be essential to the structure and function of a large number of macromolecules and for over 300 enzymic reactions. It has both catalytic and structural roles in enzymes, while in zinc finger motifs, it provides a scaffold that organizes protein sub-domains for the interaction with either DNA or other proteins. It is critical for the function of a number of metalloproteins, inducing members of oxido-reductase, hydrolase ligase, lyase family and has co-activating functions with copper in superoxide dismutase or phospholipase C. The zinc ion (Zn(++)) does not participate in redox reactions, which makes it a stable ion in a biological medium whose potential is in constant flux. Zinc ions are hydrophilic and do not cross cell membranes by passive diffusion. In general, transport has been described as having both saturable and non-saturable components, depending on the Zn(II) concentrations involved. Zinc ions exist primarily in the form of complexes with proteins and nucleic acids and participate in all aspects of intermediary metabolism, transmission and regulation of the expression of genetic information, storage, synthesis and action of peptide hormones and structural maintenance of chromatin and biomembranes.

  5. Environmental risk limits for zinc

    Bodar CWM; SEC


    Environmental Riks Limits (ERLs) were derived for zinc. ERLs serve as advisory values to set environmental quality standards in the Netherlands. The ERLs for zinc closely follow the outcomes of earlier discussions on zinc within the Water Framework Directive and EC Regulation 793/93. The ERLs refer

  6. Environmental risk limits for zinc

    Bodar CWM; SEC


    Environmental Riks Limits (ERLs) were derived for zinc. ERLs serve as advisory values to set environmental quality standards in the Netherlands. The ERLs for zinc closely follow the outcomes of earlier discussions on zinc within the Water Framework Directive and EC Regulation 793/93. The ERLs ref

  7. Zinc Phosphide Poisoning

    Erdal Doğan


    Full Text Available Zinc phosphide has been used widely as a rodenticide. Upon ingestion, it gets converted to phosphine gas in the body, which is subsequently absorbed into the bloodstream through the stomach and the intestines and gets captured by the liver and the lungs. Phosphine gas produces various metabolic and nonmetabolic toxic effects. Clinical symptoms are circulatory collapse, hypotension, shock symptoms, myocarditis, pericarditis, acute pulmonary edema, and congestive heart failure. In this case presentation, we aim to present the intensive care process and treatment resistance of a patient who ingested zinc phosphide for suicide purposes.

  8. Preparation and the Standard Enthalpy of Formation on 2-Amino-4, 6-dimethyl-pyrimidine and the Related Complexes of Zinc%2-氨基-4,6-二甲基嘧啶与锌盐配合物的制备及生成焓测定

    陈三平; 魏青; 焦宝娟; 高胜利


    The complexes of zinc chloride and zinc nitrate with 2-amino-4, 6-dimethyl-pyrimidine (ADMP) were preparedthrough reflux in alcohol. The compositions of the complexes Zn(ADMP)2Cl2 (b) and Zn(ADMP)2(NO3)2 @ 4H2O(c) were determined by chemical and elemental analyses. The complexes were characterized by IR, XPS, 1H NMRand TG-DTG techniques. The constant-volume combustion energies of ADMP and the complexes, △cE, weredetermined by a precise rotating bomb calorimeter at 298. 15K. They were ( -3664. 53 + 1.18) kJ @ mol-1,( - 7130. 94 + 3.69) kJ @ mol-1, and ( - 7637. 87 + 5.71 ) kJ @ mol-1. Their standard enthalpies of combustion,△chΘm, and standard enthalpies of formation, △fHΘm, were calculated. They were ( -3666.39 + 1. 18)kJ @ mol-1,(-7129.70+3.69)kJ@ mol-1, (-7632.91 ±5.71)kJ@mol-1and (19.09±1.43)kJ@mol-1, (-411.96±4.03)kJ@mol-1, (-1153.28±6.02)kJ@mol-1.

  9. Growth mechanisms of zinc oxide and zinc sulfide films by mist chemical vapor deposition

    Uno, Kazuyuki; Yamasaki, Yuichiro; Tanaka, Ichiro


    The growth mechanisms of zinc oxide and zinc sulfide films by mist chemical vapor deposition (mist-CVD) were experimentally investigated from the viewpoint of mist behaviors and chemical reactions. The proper growth model, either vaporization or the Leidenfrost model, was studied by supplying two kinds of mists with different kinds of sources, such as H2 16O and H2 18O for ZnO growth and ZnCl2 and thiourea for ZnS growth. Moreover, the origin of the oxygen atoms of ZnO was investigated using a quantitative analysis. The role of chloro complex of zinc in the growth of ZnS from aqueous solutions was also examined by systematic studies.

  10. Zinc fate in animal husbandry systems.

    Romeo, A; Vacchina, V; Legros, S; Doelsch, E


    Zinc (Zn) is considered in animal production systems as both an essential nutrient and a possible pollutant. While it is generally supplemented at low levels in animal diets, with less than 200 mg kg(-1) in complete feeds, it is under scrutiny due to potential accumulation in the environment. This explains why international regulations limit maximum supplementation levels in animal feeds in a stricter way. This article gives an overview of the current knowledge on the fate of zinc in animal production systems, from animal diets to animal wastes. Some analytical methods can be used for the quantification and qualification of Zn chemical forms: X-ray crystallography, electrospray tandem mass spectrometry, separation techniques, hyphenated techniques… Analysis of chelated forms issued from complex matrices, like hydrolysed proteins, remains difficult, and the speciation of Zn in diluted carriers (premix and feed) is a challenge. Our understanding of Zn absorption has made progress with recent research on ZnT/Zip families and metallothioneins. However, fine-tuned approaches towards the nutritional and metabolic interactions for Zn supplementation in farm conditions still require further studies. The speciation of zinc in pig manure and poultry litter has been a priority as monogastric animals are usually raised under intensive conditions and fed with high quantities of trace minerals, leading to high animal density and elevated quantities of zinc from animal wastes.

  11. Doped zinc oxide microspheres

    Arnold, Jr., Wesley D.; Bond, Walter D.; Lauf, Robert J.


    A new composition and method of making same for a doped zinc oxide microsphere and articles made therefrom for use in an electrical surge arrestor which has increased solid content, uniform grain size and is in the form of a gel.

  12. Zinc in multiple sclerosis

    Bredholt, Mikkel; Fredriksen, Jette Lautrup


    In the last 35 years, zinc (Zn) has been examined for its potential role in the disease multiple sclerosis (MS). This review gives an overview of the possible role of Zn in the pathogenesis of MS as well as a meta-analysis of studies having measured Zn in serum or plasma in patients with MS...

  13. Creep Resistant Zinc Alloy

    Frank E. Goodwin


    This report covers the development of Hot Chamber Die Castable Zinc Alloys with High Creep Strengths. This project commenced in 2000, with the primary objective of developing a hot chamber zinc die-casting alloy, capable of satisfactory service at 140 C. The core objectives of the development program were to: (1) fill in missing alloy data areas and develop a more complete empirical model of the influence of alloy composition on creep strength and other selected properties, and (2) based on the results from this model, examine promising alloy composition areas, for further development and for meeting the property combination targets, with the view to designing an optimized alloy composition. The target properties identified by ILZRO for an improved creep resistant zinc die-casting alloy were identified as follows: (1) temperature capability of 1470 C; (2) creep stress of 31 MPa (4500 psi); (3) exposure time of 1000 hours; and (4) maximum creep elongation under these conditions of 1%. The project was broadly divided into three tasks: (1) Task 1--General and Modeling, covering Experimental design of a first batch of alloys, alloy preparation and characterization. (2) Task 2--Refinement and Optimization, covering Experimental design of a second batch of alloys. (3) Task 3--Creep Testing and Technology transfer, covering the finalization of testing and the transfer of technology to the Zinc industry should have at least one improved alloy result from this work.

  14. Creep Resistant Zinc Alloy

    Frank E. Goodwin


    This report covers the development of Hot Chamber Die Castable Zinc Alloys with High Creep Strengths. This project commenced in 2000, with the primary objective of developing a hot chamber zinc die-casting alloy, capable of satisfactory service at 140 C. The core objectives of the development program were to: (1) fill in missing alloy data areas and develop a more complete empirical model of the influence of alloy composition on creep strength and other selected properties, and (2) based on the results from this model, examine promising alloy composition areas, for further development and for meeting the property combination targets, with the view to designing an optimized alloy composition. The target properties identified by ILZRO for an improved creep resistant zinc die-casting alloy were identified as follows: (1) temperature capability of 1470 C; (2) creep stress of 31 MPa (4500 psi); (3) exposure time of 1000 hours; and (4) maximum creep elongation under these conditions of 1%. The project was broadly divided into three tasks: (1) Task 1--General and Modeling, covering Experimental design of a first batch of alloys, alloy preparation and characterization. (2) Task 2--Refinement and Optimization, covering Experimental design of a second batch of alloys. (3) Task 3--Creep Testing and Technology transfer, covering the finalization of testing and the transfer of technology to the Zinc industry should have at least one improved alloy result from this work.

  15. Zinc in Multiple Sclerosis

    Bredholt, Mikkel; Frederiksen, Jette Lautrup


    In the last 35 years, zinc (Zn) has been examined for its potential role in the disease multiple sclerosis (MS). This review gives an overview of the possible role of Zn in the pathogenesis of MS as well as a meta-analysis of studies having measured Zn in serum or plasma in patients with MS...

  16. Studies on nanocrystalline zinc coating

    H B Muralidhara; Y Arthoba Naik


    Nano zinc coatings were deposited on mild steel by electrodeposition. The effect of additive on the morphology of crystal size on zinc deposit surface and corrosion properties were investigated. Corrosion tests were performed for dull zinc deposits and bright zinc deposits in aqueous NaCl solution (3.5 wt.%) using electrochemical measurements. The results showed that addition of additive in the deposition process of zinc significantly increased the corrosion resistance. The surface morphology of the zinc deposits was studied by scanning electron microscopy (SEM). The preferred orientation and average size of the zinc electrodeposited particles were obtained by X-ray diffraction analysis. The particles size was also characterized by TEM analysis.

  17. Influencias e innovaciones en el piano jazz: Brad Mehldau

    Sevilla Llisterri, Jorge


    El presente artículo trata las tendencias actuales del piano jazz a través de la figura de Brad Mehldau, quien se diera a conocer en la década de los noventa. La importancia de Mehldau radica en que, mientras por un lado ha sabido asimilar la tradición del jazz, también ha sido capaz de incorporar nuevas estrategias a la hora de abordar los aspectos rítmico, melódico y armónico de la improvisación. El artículo realiza un análisis de las influencias en Mehldau, proviniendo éstas tanto de la mú...

  18. Synthesis and crystal structure of zinc(Ⅱ) complexe with N-[(1-methylimidazole-2-yl)methyl]-β-alanine%N-[(1-甲基-2-咪唑基)-1-亚甲基]-β-丙氨酸锌配合物的合成及晶体结构

    杨仕平; 刘文明; 张凡; 陈红梅; 余锡宾


    The dinuclear complexes [ Zn (MIMHA) ] 2 ( MIMHAH = N- [ (1-methylimidazole-2-yl) methyl ] -β-alanine ) was prepared and characterized by single-crystal X-ray analysis. Crystal data: monlclineic, space group P21/c, a =8.792(2), b = 9.267(2), c = 16.942(2)A°, β= 99.5(2), V = 1351.6(2)A°3, and Z = 2. The zinc( Ⅱ ) atom was co-ordinated in a tetrahedral geometry(N2Cl2),which positions were occupied by one nitrogen atom and one oxygen atom from the ligand and two chlorine atoms.

  19. Interaction Between Yeasts and Zinc

    Nicola, Raffaele De; Walker, Graeme

    Zinc is an essential trace element in biological systems. For example, it acts as a cellular membrane stabiliser, plays a critical role in gene expression and genome modification and activates nearly 300 enzymes, including alcohol dehydrogenase. The present chapter will be focused on the influence of zinc on cell physiology of industrial yeast strains of Saccharomyces cerevisiae, with special regard to the uptake and subsequent utilisation of this metal. Zinc uptake by yeast is metabolism-dependent, with most of the available zinc translocated very quickly into the vacuole. At cell division, zinc is distributed from mother to daughter cells and this effectively lowers the individual cellular zinc concentration, which may become zinc depleted at the onset of the fermentation. Zinc influences yeast fermentative performance and examples will be provided relating to brewing and wine fermentations. Industrial yeasts are subjected to several stresses that may impair fermentation performance. Such stresses may also impact on yeast cell zinc homeostasis. This chapter will discuss the practical implications for the correct management of zinc bioavailability for yeast-based biotechnologies aimed at improving yeast growth, viability, fermentation performance and resistance to environmental stresses

  20. Zinc homeostasis and neurodegenerative disorders

    Bernadeta eSzewczyk


    Full Text Available Zinc is an essential trace element, whose importance to the function of the central nervous system (CNS is increasingly being appreciated. Alterations in zinc dyshomeostasis has been suggested as a key factor in the development of several neuropsychiatric disorders. In the CNS, zinc occurs in two forms: the first being tightly bound to proteins and, secondly, the free, cytoplasmic or extracellular form found in presynaptic vesicles. Under normal conditions, zinc released from the synaptic vesicles modulates both ionotropic and metabotropic post-synaptic receptors. While under clinical conditions such as traumatic brain injury, stroke or epilepsy, the excess influx of zinc into neurons has been found to result in neurotoxicity and damage to postsynaptic neurons. On the other hand, a growing body of evidence suggests that a deficiency, rather than an excess, of zinc leads to an increased risk for the development of neurological disorders. Indeed, zinc deficiency has been shown to affect neurogenesis and increase neuronal apoptosis, which can lead to learning and memory deficits. Altered zinc homeostasis is also suggested as a risk factor for depression, Alzheimer’s disease, aging and other neurodegenerative disorders. Under normal CNS physiology, homeostatic controls are put in place to avoid the accumulation of excess zinc or its deficiency. This cellular zinc homeostasis results from the actions of a coordinated regulation effected by different proteins involved in the uptake, excretion and intracellular storage/trafficking of zinc. These proteins include membranous transporters (ZnT and Zip and metallothioneins (MT which control intracellular zinc levels. Interestingly, alterations in ZnT and MT have been recently reported in both aging and Alzheimer’s disease. This paper provides an overview of both clinical and experimental evidence that implicates a dysfunction in zinc homeostasis in the pathophysiology of depression, Alzheimer

  1. Dietary catechins and procyanidins modulate zinc homeostasis in human HepG2 cells.

    Quesada, Isabel M; Bustos, Mario; Blay, Mayte; Pujadas, Gerard; Ardèvol, Anna; Salvadó, M Josepa; Bladé, Cinta; Arola, Lluís; Fernández-Larrea, Juan


    Catechins and their polymers procyanidins are health-promoting flavonoids found in edible vegetables and fruits. They act as antioxidants by scavenging reactive oxygen species and by chelating the redox-active metals iron and copper. They also behave as signaling molecules, modulating multiple cell signalling pathways and gene expression, including that of antioxidant enzymes. This study aimed at determining whether catechins and procyanidins interact with the redox-inactive metal zinc and at assessing their effect on cellular zinc homeostasis. We found that a grape-seed procyanidin extract (GSPE) and the green tea flavonoid (-)-epigallocatechin-3-gallate (EGCG) bind zinc cations in solution with higher affinity than the zinc-specific chelator Zinquin, and dose-dependently prevent zinc-induced toxicity in the human hepatocarcinoma cell line HepG2, evaluated by the lactate dehydrogenase test. GSPE and EGCG hinder intracellular accumulation of total zinc, measured by atomic flame absorption spectrometry, concomitantly increasing the level of cytoplasmic labile zinc detectable by Zinquin fluorescence. Concurrently, GSPE and EGCG inhibit the expression, evaluated at the mRNA level by quantitative reverse transcriptase-polymerase chain reaction, of zinc-binding metallothioneins and of plasma membrane zinc exporter ZnT1 (SLC30A1), while enhancing the expression of cellular zinc importers ZIP1 (SLC39A1) and ZIP4 (SLC39A4). GSPE and EGCG also produce all these effects when HepG2 cells are stimulated to import zinc by treatment with supplemental zinc or the proinflammatory cytokine interleukin-6. We suggest that extracellular complexation of zinc cations and the elevation of cytoplasmic labile zinc may be relevant mechanisms underlying the modulation of diverse cell signaling and metabolic pathways by catechins and procyanidins.

  2. Pinacol Coupling Reactions Catalyzed by Active Zinc

    Hui ZHAO; Wei DENG; Qing Xiang GUO


    Pinacol coupling reactions catalyzed by active zinc revealed high activity and extensive suitability. The efficiency of the reaction was improved apparently owing to decreasing reductive potential of zinc. In addition, the results indicated that the zinc activity has a direct relation to the coupling reactivity compared to untreated zinc or other general active zinc.

  3. Zinc-Laccase Biofuel Cell

    Abdul Aziz Ahmad


    Full Text Available A zinc-laccase biofuel cell adapting the zinc-air cell design features is investigated. A simple cell design configuration is employed: a membraneless single chamber and a freely suspended laccase in a quasi-neutral buffer electrolyte. The cell is characterised according to its open-circuit voltage, polarization profile, power density plot and discharge capacity at constant current. The biocatalytic role of laccase is evident from the polarization profile and power output plot. Performance comparison between a single chamber and dual chamber cell design is also presented. The biofuel cell possessed an open-circuit voltage of 1.2 V and delivered a maximum power density of 0.9 mW/cm2 at current density of 2.5 mA/cm2. These characteristics are comparable to biofuel cell utilising a much more complex system design.KEY WORDS (keyword:  Biofuel cell, Bioelectrochemical cell, Zinc anode, Laccase and Oxidoreductase.ABSTRAK: Sel bio-bahan api zink-laccase dengan adaptasi daripada ciri-ciri rekabentuk sel zink-udara telah dikaji. Sel dengan konfigurasi rekabentuk yang mudah digunapakai: ruangan tunggal tanpa membran dan laccase diampaikan secara bebas di dalam elektrolit pemampan quasi-neutral. Sel dicirikan berdasarkan voltan litar terbuka, profil polarisasi, plot ketumpatan kuasa dan kapasiti discas pada arus malar. Peranan laccase sebagai bio-pemangkin adalah amat ketara daripada profil polarisasi dan plot ketumpatan kuasa. Perbandingan prestasi di antara sel dengan rekabentuk ruangan tunggal and dwi-ruangan turut diketengahkan. Seperti dijangkakan, sel dengan rekabentuk ruangan tunggal menunjukkan kuasa keluaran yang lebih rendah jika dibandingkan dengan rekabentuk dwi-ruangan kemungkinan disebabkan fenomena cas bocor. Sel bio-bahan api ini mempunyai voltan litar terbuka 1.2 V dan memberikan ketumpatan kuasa maksima 0.9 mW/cm2 pada ketumpatan arus 2.5 mA/cm2. Ciri-ciri ini adalah sebanding dengan sel bio-bahan api yang menggunapakai rekabentuk sel

  4. DMPD: Zinc in human health: effect of zinc on immune cells. [Dynamic Macrophage Pathway CSML Database

    Full Text Available 18385818 Zinc in human health: effect of zinc on immune cells. Prasad AS. Mol Med. ...2008 May-Jun;14(5-6):353-7. (.png) (.svg) (.html) (.csml) Show Zinc in human health: effect of zinc on immun...e cells. PubmedID 18385818 Title Zinc in human health: effect of zinc on immune cells. Authors Prasad AS. Pu

  5. Comparison of Hydrogen Elimination from Molecular Zinc and Magnesium Hydride Clusters

    Intemann, J.; Sirsch, Peter; Harder, Sjoerd


    In analogy to the previously reported tetranuclear magnesium hydride cluster with a bridged dianionic bis-beta-diketiminate ligand, a related zinc hydride cluster has been prepared. The crystal structures of these magnesium and zinc hydride complexes are similar: the metal atoms are situated at the

  6. The assembly of supramolecular boxes and coordination polymers based on bis-zinc-salphen building blocks

    Kuil, M.; Puijk, I.M.; Kleij, A.W.; Tooke, D.M.; Spek, A.L.; Reek, J.N.H.


    We report the assembly of supramolecular boxes and coordination polymers based on a rigid bis-zinc(II)-salphen complex and various ditopic nitrogen ligands. The use of the bis-zinc(II)-salphen building block in combination with small ditopic nitrogen ligands gave organic coordination polymers both

  7. Comparison of Hydrogen Elimination from Molecular Zinc and Magnesium Hydride Clusters

    Intemann, J.; Sirsch, Peter; Harder, Sjoerd


    In analogy to the previously reported tetranuclear magnesium hydride cluster with a bridged dianionic bis-beta-diketiminate ligand, a related zinc hydride cluster has been prepared. The crystal structures of these magnesium and zinc hydride complexes are similar: the metal atoms are situated at the

  8. Synthesis and characterization of iron(III), manganese(II), cobalt(II), nickel(II), copper(II) and zinc(II) complexes of salicylidene-N-anilinoacetohydrazone (H2L1) and 2-hydroxy-1-naphthylidene-N-anilinoacetohydrazone (H2L2).

    AbouEl-Enein, S A; El-Saied, F A; Kasher, T I; El-Wardany, A H


    Salicylidene-N-anilinoacetohydrazone (H(2)L(1)) and 2-hydroxy-1-naphthylidene-N-anilinoacetohydrazone (H(2)L(2)) and their iron(III), manganese(II), cobalt(II), nickel(II), copper(II) and zinc(II) complexes have been synthesized and characterized by IR, electronic spectra, molar conductivities, magnetic susceptibilities and ESR. Mononuclear complexes are formed with molar ratios of 1:1, 1:2 and 1:3 (M:L). The IR studies reveal various modes of chelation. The electronic absorption spectra and magnetic susceptibility measurements show that the iron(III), nickel(II) and cobalt(II) complexes of H(2)L(1) have octahedral geometry. While the cobalt(II) complexes of H(2)L(2) were separated as tetrahedral structure. The copper(II) complexes have square planar stereochemistry. The ESR parameters of the copper(II) complexes at room temperature were calculated. The g values for copper(II) complexes proved that the Cu-O and Cu-N bonds are of high covalency.

  9. Alkaline battery with low mercury content in zinc anode. Alkalisk batteri

    Kuemmel, K.


    An alkaline battery comprises a manganese dioxide mercury cathode, a zinc anode and an alkaline electrolyte. The battery has a low mercury content in the zinc anode which contains an inhibitor complex containing: (a) inhibitor tensides having a hydrophilic lepophilic balance number higher than 10 and less than 20; and (b) inhibitors of the naphthylamine-sulphonic acid type and radicals. The inhibitors are added to the anode gel and used in amount 25 to 100 ppm. The anode current collector is coated with a layer of pore-less zinc of same composition as the zinc anode. (au)

  10. Compartmentation of metals in foliage of Populus tremula grown on soils with mixed contamination. II. Zinc binding inside leaf cell organelles

    Vollenweider, Pierre, E-mail: pierre.vollenweider@wsl.c [Swiss Federal Institute for Forest, Snow and Landscape Research (WSL), Zuercherstrasse 111, 8903 Birmensdorf (Switzerland); Bernasconi, Petra [Swiss Federal Institute for Forest, Snow and Landscape Research (WSL), Zuercherstrasse 111, 8903 Birmensdorf (Switzerland); Environmental Protection Office (AfU), Aabachstrasse 5, 6300 Zug (Switzerland); Gautschi, Hans-Peter [Centre for Microscopy and Image Analysis (CMI), University of Zurich, Gloriastrasse 30, 8006 Zuerich (Switzerland); Menard, Terry; Frey, Beat; Guenthardt-Goerg, Madeleine S. [Swiss Federal Institute for Forest, Snow and Landscape Research (WSL), Zuercherstrasse 111, 8903 Birmensdorf (Switzerland)


    The phytoextraction potential of plants for removing heavy metals from polluted soils is determined by their capacity to store contaminants in aboveground organs and complex them safely. In this study, the metal compartmentation, elemental composition of zinc deposits and zinc complexation within leaves from poplars grown on soil with mixed metal contamination was analysed combining several histochemical and microanalytical approaches. Zinc was the only heavy metal detected and was stored in several organelles in the form of globoid deposits showing {beta}-metachromasy. It was associated to oxygen anions and different cations, noteworthy phosphorous. The deposit structure, elemental composition and element ratios indicated that zinc was chelated by phytic acid ligands. Maturation processes in vacuolar vs. cytoplasmic deposits were suggested by differences in size and amounts of complexed zinc. Hence, zinc complexation by phytate contributed to metal detoxification and accumulation in foliage but could not prevent toxicity reactions therein. - Zinc contaminants translocated to symplast of aged leaves were detoxified by phytic acid ligands.

  11. Depleted zinc: Properties, application, production.

    Borisevich, V D; Pavlov, A V; Okhotina, I A


    The addition of ZnO, depleted in the Zn-64 isotope, to the water of boiling water nuclear reactors lessens the accumulation of Co-60 on the reactor interior surfaces, reduces radioactive wastes and increases the reactor service-life because of the inhibitory action of zinc on inter-granular stress corrosion cracking. To the same effect depleted zinc in the form of acetate dihydrate is used in pressurized water reactors. Gas centrifuge isotope separation method is applied for production of depleted zinc on the industrial scale. More than 20 years of depleted zinc application history demonstrates its benefits for reduction of NPP personnel radiation exposure and combating construction materials corrosion.

  12. Chloroquine is a zinc ionophore.

    Jing Xue

    Full Text Available Chloroquine is an established antimalarial agent that has been recently tested in clinical trials for its anticancer activity. The favorable effect of chloroquine appears to be due to its ability to sensitize cancerous cells to chemotherapy, radiation therapy, and induce apoptosis. The present study investigated the interaction of zinc ions with chloroquine in a human ovarian cancer cell line (A2780. Chloroquine enhanced zinc uptake by A2780 cells in a concentration-dependent manner, as assayed using a fluorescent zinc probe. This enhancement was attenuated by TPEN, a high affinity metal-binding compound, indicating the specificity of the zinc uptake. Furthermore, addition of copper or iron ions had no effect on chloroquine-induced zinc uptake. Fluorescent microscopic examination of intracellular zinc distribution demonstrated that free zinc ions are more concentrated in the lysosomes after addition of chloroquine, which is consistent with previous reports showing that chloroquine inhibits lysosome function. The combination of chloroquine with zinc enhanced chloroquine's cytotoxicity and induced apoptosis in A2780 cells. Thus chloroquine is a zinc ionophore, a property that may contribute to chloroquine's anticancer activity.

  13. Zinc In CCl4 Toxicity


    Objective To investigate the protective effect of zinc in CCl4-induced hepatotoxicity. Methods Rats were treated with zinc acetate for four days. The zinc doses were 5 mg Zn/kg and 10 mg Zn/kg body weight respectively. Two groups of the zinc acetate-treated rats were later challenged with a single dose of CCl4 (1.5 mL/kg body weight). Results Compared to control animals, the plasma of rats treated with CCl4 showed hyperbilirubinaemia, hypoglycaemia, hypercreatinaemia and hypoproteinaemia. When the animals were however supplemented with zinc in form of zinc acetate before being dosed with CCl4, the 5 mg Zn/kg body weight of zinc acetate reversed the hypoproteinaemia induced by CCl4, whereas the 10mg Zn/kg body weight of zinc acetate reversed the hypoglycaemia, hyperbilimbinaemia and hypercreatinaemia induced by CCl4. Conclusion The 10mug Zn/kg body weight of zinc acetate is more consistent in protecting against CCl4 hepatotoxicity. The possible mechanisms of protection are highlighted.


    盛晓阳; 沈立松; 徐翀; 吴湘如; 陈宏新; 洪照毅


    Objective Observation of the effects of lower concentrations of zinc (20~400μmol/L), which is nearby the physiological concentration, on etoposide induced HL-60 cells apoptosis. Methods Using the flow cytometry , DNA extraction, electrophoresis , and fiuoresence microscopic observation. Results We demonstrated that the low concentrations of zinc also affect cells apoptosis. If zinc was added at early time, even 200μmol/L could inhibit VP16 induced HL-60 cell apoptosis completely in 4h. But at this concentration, zinc also seems to have cell toxicity, not prolong the time of protection effect. Conclusion Zinc plays multiple roles in cellular functions and in protecting cells from exogenous deleterious factors. Zinc plays a complex, dose- and time-dependent role in apoptosis.

  15. Application of zinc isotope tracer technology in tracing soil heavy metal pollution

    Norbu, Namkha; Wang, Shuguang; Xu, Yan; Yang, Jianqiang; Liu, Qiang


    Recent years the soil heavy metal pollution has become increasingly serious, especially the zinc pollution. Due to the complexity of this problem, in order to prevent and treat the soil pollution, it's crucial to accurately and quickly find out the pollution sources and control them. With the development of stable isotope tracer technology, it's able to determine the composition of zinc isotope. Based on the theory of zinc isotope tracer technique, and by means of doing some latest domestic and overseas literature research about the zinc isotope multi-receiving cups of inductively coupled plasma mass spectrometer (MC-ICP-MS) testing technology, this paper summarized the latest research results about the pollution tracer of zinc isotope, and according to the deficiencies and existing problems of previous research, made outlooks of zinc isotope fractionation mechanism, repository establishment and tracer multiple solutions.

  16. Synthesis and characterization of dinuclear macrocyclic cobalt(II), copper(II) and zinc(II) complexes derived from 2,2,2('),2(')-S,S[bis(bis-N,N-2-thiobenzimidazolyloxalato-1,2-ethane)]: DNA binding and cleavage studies.

    Arjmand, Farukh; Aziz, Mubashira


    New homodinuclear macrocyclic complexes of cobalt(II), copper(II) and zinc(II) were isolated from the newly synthesized ligand 2,2,2',2'-S,S[bis(bis-N,N-2-thiobenzimidazolyloxalato-1,2-ethane)]. The structures of the complexes were elucidated by elemental analysis, molar conductance measurements, IR, 1H NMR, 13C NMR, electronic and ESI-MS spectroscopic techniques. In complex 1, Co(II) ions possess a tetrahedral coordination environment composed of O2S2 donor atoms while its Cu(II) and Zn(II) counterparts 2 and 3, respectively, reveal a six coordinate octahedral structure, defined by the O2S2 donors from the macrocyclic ring and two chloride ions. Molar conductance and spectroscopic data also support the proposed geometry of the complexes. DNA binding properties of complexes 1-3 were investigated using electronic absorption spectroscopy, fluorescence spectroscopy, viscosity measurements and cyclic voltammetry. The absorption spectra of complexes 2 and 3 with calf thymus DNA showed hypochromism, while complex 1 showed hyperchromism attributed to a partial intercalation and electrostatic binding modes, respectively. The intrinsic binding constant K(b) of complexes 1-3 were determined as 16.6 x 10(4) M(-1), 4.25 x 10(4) M(-1) and 3.0 x 10(4) M(-1), respectively. The decrease in the relative specific viscosity of calf thymus DNA with increasing concentration of the complexes authenticates the partial intercalation binding mode. Gel electrophoresis of complex 2 with plasmid DNA demonstrated that complex exhibits excellent "artificial" nuclease activity.

  17. Zinc acetylacetonate hydrate adducted with nitrogen donor ligands: Synthesis, spectroscopic characterization, and thermal analysis

    Brahma, Sanjaya; Shivashankar, S. A.


    We report synthesis, spectroscopic characterization, and thermal analysis of zinc acetylacetonate complex adducted by nitrogen donor ligands, such as pyridine, bipyridine, and phenanthroline. The pyridine adducted complex crystallizes to monoclinic crystal structure, whereas other two adducted complexes have orthorhombic structure. Addition of nitrogen donor ligands enhances the thermal property of these complexes as that with parent metal-organic complex. Zinc acetylacetonate adducted with pyridine shows much higher volatility (106 °C), decomposition temperature (202 °C) as that with zinc acetylacetonate (136 °C, 220 °C), and other adducted complexes. All the adducted complexes are thermally stable, highly volatile and are considered to be suitable precursors for metal organic chemical vapor deposition. The formation of these complexes is confirmed by powder X-ray diffraction, Fourier transform infrared spectroscopy, mass spectroscopy, and elemental analysis. The complexes are widely used as starting precursor materials for the synthesis of ZnO nanostructures by microwave irradiation assisted coating process.

  18. Zinc supplementation for tinnitus.

    Person, Osmar C; Puga, Maria Es; da Silva, Edina Mk; Torloni, Maria R


    Tinnitus is the perception of sound without external acoustic stimuli. Patients with severe tinnitus may have physical and psychological complaints and their tinnitus can cause deterioration in their quality of life. At present no specific therapy for tinnitus has been found to be satisfactory in all patients. In recent decades, a number of reports have suggested that oral zinc supplementation may be effective in the management of tinnitus. Since zinc has a role in cochlear physiology and in the synapses of the auditory system, there is a plausible mechanism of action for this treatment. To evaluate the effectiveness and safety of oral zinc supplementation in the management of patients with tinnitus. The Cochrane ENT Information Specialist searched the ENT Trials Register; Central Register of Controlled Trials (CENTRAL 2016, Issue 6); PubMed; EMBASE; CINAHL; Web of Science;; ICTRP and additional sources for published and unpublished trials. The date of the search was 14 July 2016. Randomised controlled trials comparing zinc supplementation versus placebo in adults (18 years and over) with tinnitus. We used the standard methodological procedures recommended by Cochrane. Our primary outcome measures were improvement in tinnitus severity and disability, measured by a validated tinnitus-specific questionnaire, and adverse effects. Secondary outcomes were quality of life, change in socioeconomic impact associated with work, change in anxiety and depression disorders, change in psychoacoustic parameters, change in tinnitus loudness, change in overall severity of tinnitus and change in thresholds on pure tone audiometry. We used GRADE to assess the quality of the evidence for each outcome; this is indicated in italics. We included three trials involving a total of 209 participants. The studies were at moderate to high risk of bias. All included studies had differences in participant selection criteria, length of follow-up and outcome measurement

  19. Interaction between nanoparticles generated by zinc chloride treatment and oxidative responses in rat liver

    Azzouz I


    Full Text Available Inès Azzouz, Hamdi Trabelsi, Amel Hanini, Soumaya Ferchichi, Olfa Tebourbi, Mohsen Sakly, Hafedh AbdelmelekLaboratory of Integrative Physiology, Faculty of Sciences of Bizerte, Carthage University, TunisiaAbstract: The aim of the present study was to investigate the interaction of zinc chloride (3 mg/kg, intraperitoneally [ip] in rat liver in terms of the biosynthesis of nanoparticles. Zinc treatment increased zinc content in rat liver. Analysis of fluorescence revealed the presence of red fluorescence in the liver following zinc treatment. Interestingly, the co-exposure to zinc (3 mg/kg, ip and selenium (0.20 mg/L, per os [by mouth] led to a higher intensity of red fluorescence compared to zinc-treated rats. In addition, X-ray diffraction measurements carried out on liver fractions of zinc-treated rats point to the biosynthesis of zinc sulfide and/or selenide nanocomplexes at nearly 51.60 nm in size. Moreover, co-exposure led to nanocomplexes of about 72.60 nm in size. The interaction of zinc with other mineral elements (S, Se generates several nanocomplexes, such as ZnS and/or ZnSe. The nanocomplex ZnX could interact directly with enzyme activity or indirectly by the disruption of mineral elements' bioavailability in cells. Subacute zinc or selenium treatment decreased malondialdehyde levels, indicating a drop in lipid peroxidation. In addition, antioxidant enzyme assays showed that treatment with zinc or co-treatment with zinc and selenium increased the activities of glutathione peroxidase, catalase, and superoxide dismutase. Consequently, zinc complexation with sulfur and/or selenium at nanoscale level could enhance antioxidative responses, which is correlated to the ratio of number of ZnX nanoparticles (X=sulfur or X=selenium to malondialdehyde level in rat liver.Keywords: nanocomplexes biosynthesis, antioxidative responses, X-ray diffraction, fluorescence microscopy, liver

  20. Inhibitory zinc-enriched terminals in mouse spinal cord

    Danscher, G; Jo, S M; Varea, E;


    The ultrastructural localization of zinc transporter-3, glutamate decarboxylase and zinc ions in zinc-enriched terminals in the mouse spinal cord was studied by zinc transporter-3 and glutamate decarboxylase immunohistochemistry and zinc selenium autometallography, respectively.The distribution...

  1. Analisis de redes sociales y procesos de influencia en la toma de decision grupal

    Jorge Ricardo Vivas


    Full Text Available En el presente trabajo se analizan los procesos de influencia por medio del estudio de las relaciones entre medidas convencionales y estructurales en tareas de toma de decisión grupal. Se exploraron los componentes de conectividad y prestigio como facilitadores del proceso de influencia; la conectividad por medio del flujo global, la participación, la densidad de la red ego centrada y la cohesión o distancia reticular. El prestigio se analizó por medio del status sociométrico, medidas de influencia y centralidad (grado, prestigio y poder y medidas de equivalencia estructural para delimitar roles y posiciones. Se utilizó la prueba Supervivencia en la Luna y participaron 70 alumnos de tercer año de la Carrera de Psicología. Los resultados muestran que existe una asociación significativa entre el conocimiento previo a la tarea y la influencia social medida como contribución al producto grupal, que las medidas de centralidad tienen relación con aspectos de la dinámica grupal y no con la contribución al producto y que los roles varían dentro y fuera de la tarea. La influencia está significativamente asociada a la densidad de la red personal. La interpretación de los resultados sugiere que las redes personales de baja densidad favorecen la capacidad de influencia en la producción grupal y que la alta cohesión y conectividad subgrupal la deterioran. También sugieren que las medidas de centralidad se relacionan con influencia en el tráfico comunicacional pero no con la productividad. Y que el status previo y el obtenido durante la actividad, no se vinculan con la producción.

  2. Zinc absorption by young adults from supplemental zinc citrate is comparable with that from zinc gluconate and higher than from zinc oxide.

    Wegmüller, Rita; Tay, Fabian; Zeder, Christophe; Brnic, Marica; Hurrell, Richard F


    The water-soluble zinc salts gluconate, sulfate, and acetate are commonly used as supplements in tablet or syrup form to prevent zinc deficiency and to treat diarrhea in children in combination with oral rehydration. Zinc citrate is an alternative compound with high zinc content, slightly soluble in water, which has better sensory properties in syrups but no absorption data in humans. We used the double-isotope tracer method with (67)Zn and (70)Zn to measure zinc absorption from zinc citrate given as supplements containing 10 mg of zinc to 15 healthy adults without food and compared absorption with that from zinc gluconate and zinc oxide (insoluble in water) using a randomized, double-masked, 3-way crossover design. Median (IQR) fractional absorption of zinc from zinc citrate was 61.3% (56.6-71.0) and was not different from that from zinc gluconate with 60.9% (50.6-71.7). Absorption from zinc oxide at 49.9% (40.9-57.7) was significantly lower than from both other supplements (P zinc oxide. We conclude that zinc citrate, given as a supplement without food, is as well absorbed by healthy adults as zinc gluconate and may thus be a useful alternative for preventing zinc deficiency and treating diarrhea. The more insoluble zinc oxide is less well absorbed when given as a supplement without food and may be minimally absorbed by some individuals. This trial was registered at as NCT01576627.

  3. Testicular apoptosis after dietary zinc deficiency: ultrastructural and TUNEL studies.

    Kumari, Deepa; Nair, Neena; Bedwal, Ranveer Singh


    The present study was conducted in Wistar rats to determine whether prepubertal dietary zinc deficiency causes apoptotic changes in testes. Prepubertal male Wistar rats (40-50 gm) were divided into 3 groups: zinc control (ZC), pairfed (PF), and zinc deficient (ZD). Control and pairfed groups were given a 100 ppm zinc diet while the deficient groups received 1 ppm zinc diet for 2 and 4 weeks (w), respectively. Ultrastructural studies revealed several apoptotic features such as wavy basement membrane, displaced nuclei, chromatin condensation, plasma membrane blebbing, nuclear membrane dissolution, loss of inter-Sertoli cell junctional complexes, and intercellular bridges and deformed mitochondria. A variable spectrum of sperm defects had also been visualized e.g., acrosomal deformities such as decapitation and a ring of condensed chromatin around the nuclear periphery, deformed sperm heads with a condensed nucleus, tail-elements with superfluous cytoplasm, and damage to the mitochondrial sheath and aggregation of spermatozoa within the membrane. This was further supported by TUNEL studies. Apoptotic index, epididymal sperm concentration, motility, and fertility index also revealed a significant (P zinc deficient groups (2 and 4 w) when compared with their respective control and pairfed groups. All the above findings are indicative that changes observed in the testes after dietary zinc deficiency are due to the onset of apoptosis. Increased apoptotic degeneration in testes may cause irreversible changes in the germ cells associated with decreased epididymal sperm concentration, motility, and fertility index which contributes to the low efficiency of spermatogenesis thereby indicating a possible role of zinc in fertility.

  4. α-硫辛酸合锌对痴呆模型小鼠学习记忆能力的影响%Effects of Zinc α-lipoate Complex on the Learning and Memory Abilities of Scopolamine-induced Amnesia Mice

    张迪; 李燕; 罗瑛; 田卫群; 周青山


    Objective To investigate effects of zincα-lipoate complex on the learning and memory abilities as well as the oxidative stress in scopolamine-induced amnesia mice. Methods A total of 32 mice were randomly divided into the model control group, the group with α-lipoic acid, the group with zinc sulfate, the group with zincα-lipoate complex. rats in each group were administered corresponding drugs and trained with Y-maze five hours later. After 8 days,Rats in each group received the celiac injection of the scopolamine at a dose of 5mg/kg. After half an hour, the memory ability was tested, and then the mice were decapitated. The content of GSH and protein, the activity of SOD in the cerebral tissue were determined. Results Compared with the model control group and other groups, the zincα-li-poate complex can decrease the false times and the activity of SOD (P < 0. 01) in the cerebral tissue, while increase the content of GSH (P < 0. 01) and protein (P < 0. 05). Conclusion The zinc α-lipoate complex can improve the learning and memory abilities and de-crease the level of oxidative stress in the cerebral tissue of amnesia mice.%目的 观察α-硫辛酸合锌对东莨菪碱致痴呆模型小鼠学习记忆能力及氧化应激的影响. 方法 将32只昆明小鼠随机均分成模型对照组、硫辛酸组、硫酸锌组、α-硫辛酸合锌组. 每组每天分别给予生理盐水、硫辛酸、硫酸锌和α-硫辛酸合锌,每次给药5h后进行Y迷宫训练,连续8天后各组均给予5mg/kg东莨菪碱,半小时后进行记忆能力测试. 测定小鼠匀浆后脑组织内还原型谷胱甘肽和蛋白含量及超氧化物歧化酶的活力. 结果 与模型对照组及其他各组相比,α-硫辛酸合锌组小鼠错误次数明显减少,脑组织内还原型谷胱甘肽和蛋白质含量明显升高(P<0. 05),超氧化物歧化酶活力明显降低(P<0. 01). 结论α-硫辛酸合锌可以显著提高痴呆小鼠的学习记忆能力,降低脑组织内氧化应激水平.

  5. Efecto del zinc sobre el crecimiento y desarrollo del niño con bajo peso al nacer

    Rafael Jiménez


    Full Text Available Antecedentes: El zinc es un elemento traza de gran importancia para el crecimiento intrauterino y postnatal de niños con retardo del crecimiento.Objetivos: Evaluar el efecto de la suplementación con sulfato de zinc en el crecimiento y desarrollo psicomotor en una cohorte de niños con bajo peso al nacer, durante el primer año de vida. Pacientes y métodos: Se realizó un estudio longitudinal doble ciego de una cohorte de 163 recién nacidos distribuidos al azar en dos grupos: el grupo de los suplementados correspondió a 87 lactantes a los que se le suministró una dosis de 10 mg/día de una solución de sulfato de zinc durante los primeros 6 meses de vida; el grupo de los no suplementados estuvo compuesto por 76 lactantes a los que se le suministró una solución de 10 ml de suero fisiológico ausente de zinc en igual período. Resultados: El incremento de peso se relaciona de forma positiva con la suplementación con zinc, lo cual se evidencia en la curva de ganancia de peso y el análisis de observaciones repetidas realizado para esta variable; sin embargo, la variable talla no sufre la influencia de la misma manera. En relación con el desarrollo psicomotor, el índice de desarrollo motor se ve positivamente influido por la suplementación con zinc, no así el índice de desarrollo mental. Conclusiones: La suplementación de 10 mg de sulfato de zinc en niños con bajo peso al nacer durante 6 meses es beneficiosa para el incremento del peso y el desarrollo motor de estos lactantes.

  6. El zinc: oligoelemento esencial

    C. Rubio

    Full Text Available En este artículo se hace una revisión exhaustiva del zinc, elemento metálico esencial para el funcionamiento del organismo. Repasamos y reflejamos aspectos relacionados con la farmacocinética, con las fuentes dietéticas más importantes, así como las IDR (Ingestas Dietéticas Recomendadas del mismo. También se hace mención a los signos y síntomas relacionados tanto con una ingesta deficiente, como con posibles efectos tóxicos, derivados de ingestas excesivas.

  7. Zinc Base Die Castings


    183 B86- 33T SAE N.J .zn Co. B86-33T 1934 SAE N.J.Zn Cc,. Zamak 3N AllO;E Cl C2 Allo~ XXI 221 Zarnak 2 .A.llo;z XXIII .Allol XXIII 202 Zamak 2 O...2 Pb ,Fe, Cd, C:’. 3 special high gra1e ?:inc. • t • • ; -J TABLE II Chemical Composition for Zinc Alloy Nuuber Zam.ak 2 Zamak 3...was alco given regarding the aging of the alloys. The a1loy3 Aupplied were: Zamak 2, Zamak 3, Zamak 3-S (Stabilized to hasten contraction which

  8. Nanostructures of zinc oxide

    Zhong Lin Wang


    Full Text Available Zinc oxide (ZnO is a unique material that exhibits semiconducting, piezoelectric, and pyroelectric multiple properties. Using a solid-vapor phase thermal sublimation technique, nanocombs, nanorings, nanohelixes/nanosprings, nanobows, nanobelts, nanowires, and nanocages of ZnO have been synthesized under specific growth conditions. These unique nanostructures unambiguously demonstrate that ZnO is probably the richest family of nanostructures among all materials, both in structures and properties. The nanostructures could have novel applications in optoelectronics, sensors, transducers, and biomedical science because it is bio-safe.

  9. Influencia del Capital Intelectual en la Competitividad de los Hoteles

    Jorge Luis Heredia Heredia


    Full Text Available El objetivo de la presente investigación es conocer la influencia del capital intelectual en la competitividad de las empresas hoteleras de 1 a 5 estrellas de Aguascalientes, México. La medición del capital intelectual, que es el recurso intangible de las organizaciones contenido en el capital humano, capital estructural y capital relacional que genera competitividad y riqueza presente y futura, se realiza a través de un instrumento tipo Likert de 61 reactivos, cuyos resultados son comparados con la competitividad de los hoteles, medida a través de la rentabilidad por habitación disponible. Los resultados muestran la relación positiva entre el capital intelectual y la competitividad de los hoteles. La información podría ser útil en al menos tres dimensiones: primero, para diseñar los planes estratégicos de las empresas hoteleras; segundo, como apoyo para el diseño de las políticas del sector turismo y, tercero, como base académica para continuar en el desarrollo trabajos sobre el capital intelectual en otro tipo de organizaciones, con el interés de apoyar las decisiones empresariales y las políticas económicas.

  10. Danxia Zinc Smelter started construction


    <正>Zinc smelting project of Danxia Smelting Plant has a total investment of about RMB 4 billion, which is designed by Changsha Engineering & Research Institute of Nonferrous Metallurgy and planned to be implemented in three stages. The first stage 100,000 tons of electrolytic zinc improvement work is planned to be completed by the end of 2008. The second and third stages

  11. The use of bis (-2-ethylhexyl) phosphoric acid for the extraction of zinc from concentrated ammonium chloride solutions

    Amer, S.; Luis, A.; Cuadra, A. de la; Caravaca, C.


    The extraction of zinc from concentrated ammonium chloride solutions by means of the bis(-2-ethylhexyl) phosphoric acid is studied. Mass balances and chemical equilibria relating the different chemical species in both phases are presented in order to establish a model describing the behaviour of the different species. Good agreement between experimental data and theoretical curves is obtained. A comparison of the zinc extraction from a strong complexing medium as that of concentrated ammonium chloride solutions with an uncomplexing zinc perchlorate solution is made, in order to see the influence of the complexing effect of the aqueous phase on zinc extraction. (Author) 36 p.

  12. 锌铋复杂氧化物Bi2Zn5O8的合成及其晶体生长特性%Synthesis and Crystal Growth Characteristic of Zinc Bismuth Complex Oxide Bi2Zn5O8



    The zinc bismuth complex oxides were prepared from zinc sulfate, bismuth nitrate and sodium hydroxide under ultrasonic irradiation.The effects of feed order and feed molar ratio on the final product were studied.The properties of the product were characterized by TG-DTA, SEM and TEM.The chemical composition was defined by means of X-ray fluorescence and continuous titration.The TEM and SEM images showed the dendrite crystal was formed.%利用硫酸锌、硝酸铋、氢氧化钠为原料在超声体系中反应合成锌铋复杂氧化物,考察了反应物料比和加料顺序对产物组成的影响.经X射线荧光及化学滴定确定了产物的分子式为Bi2Zn5O8,并由TEM、SEM和TG-DTA等方法对所得产物进行表征.TEM和SEM结果显示晶体呈枝蔓晶生长.

  13. A simple liposome assay for the screening of zinc ionophore activity of polyphenols.

    Clergeaud, Gael; Dabbagh-Bazarbachi, Husam; Ortiz, Mayreli; Fernández-Larrea, Juan B; O'Sullivan, Ciara K


    An efficient liposomal system for screening the zinc ionophore activity of a selected library consisting of the most relevant dietary polyphenols is presented. The zinc ionophore activity was demonstrated by exploring the use of zinc-specific fluorophore FluoZin-3 loaded liposomes as simple membrane tools that mimic the cell membrane. The zinc ionophore activity was demonstrated as the capacity of polyphenols to transport zinc cations across the liposome membrane and increase the zinc-specific fluorescence of the encapsulated fluorophore FluoZin-3. In addition, the zinc chelation strength of the polyphenols was also tested in a competition assay based on the fluorescence quenching of zinc-dependent fluorescence emitted by zinc-FluoZin-3 complex. Finally, the correlation between the chelation capacity and ionophore activity is demonstrated, thus underlining the sequestering or ionophoric activity that the phenolic compounds can display, thus, providing better knowledge of the importance of the structural conformation versus their biological activity. Furthermore, the assays developed can be used as tools for rapid, high-throughput screening of families of polyphenols towards different biometals.

  14. Regulation of the Saccharomyces cerevisiae DPP1-encoded diacylglycerol pyrophosphate phosphatase by zinc.

    Han, G S; Johnston, C N; Chen, X; Athenstaedt, K; Daum, G; Carman, G M


    The DPP1 gene, encoding diacylglycerol pyrophosphate (DGPP) phosphatase from Saccharomyces cerevisiae, has recently been identified as a zinc-regulated gene, and it contains a putative zinc-responsive element (UAS(ZRE)) in its promoter. In this work we examined the hypothesis that expression of DGPP phosphatase was regulated by zinc availability. The deprivation of zinc from the growth medium resulted in a time- and dose-dependent induction of beta-galactosidase activity driven by a P(DPP1)-lacZ reporter gene. This regulation was dependent on the UAS(ZRE) in the DPP1 promoter and was mediated by the Zap1p transcriptional activator. Induction of the DGPP phosphatase protein and activity by zinc deprivation was demonstrated by immunoblot analysis and measurement of the dephosphorylation of DGPP. The regulation pattern of DGPP phosphatase in mutants defective in plasma membrane (Zrt1p and Zrt2p) and vacuolar membrane (Zrt3p) zinc transporters indicated that enzyme expression was sensitive to the cytoplasmic levels of zinc. DGPP phosphatase activity was inhibited by zinc by a mechanism that involved formation of DGPP-zinc complexes. Studies with well characterized subcellular fractions and by indirect immunofluorescence microscopy revealed that the DGPP phosphatase enzyme was localized to the vacuolar membrane.

  15. Differences in the nature of the interaction of insulin and proinsulin with zinc.

    Grant, P T; Coombs, T L; Frank, B H


    1. The reversible interaction of zinc with pig insulin and proinsulin has been studied at pH7 by equilibrium dialysis (ultrafiltration) and by sedimentation equilibrium and velocity measurements in the ultracentrifuge. Binding values calculated from equilibria, where the ratio of free to bound zinc was varied in the range 0.01:1-10:1, indicated that proinsulin and insulin each contained two main orders of zinc binding with very different affinities for the metal. 2. In equilibria containing low concentrations of free zinc (free: bound ratios of 0.01-0.1:1) both insulin and proinsulin aggregated to form soluble hexamers containing firmly bound zinc (up to 0.284g-atom/monomer) with an apparent intrinsic association constant of 1.9x10(6)m(-1). 3. Higher concentrations of zinc (free: bound ratios of 0.1-10.0:1) resulted in a progressive difference in the zinc binding, aggregation and solubility properties of the metal complexes of insulin and proinsulin. At the highest concentration of free zinc, proinsulin bound a total of more than 5.0g-atom/monomer and aggregated to form a mixture of soluble polymers (mainly 5.1S). In contrast, insulin bound a total of only 1.0g-atom/monomer and was almost completely precipitated from solution. 4. These results would indicate that the presence of the peptide segment connecting the insulin moiety in proinsulin does not prevent the firm binding of zinc to the insulin moiety and the formation of hexamers of zinc-proinsulin. At the same time although the connecting peptide contains additional sites of lower affinity for zinc, which should facilitate inter- and intra-molecular cross-linking, the general conformation of the zinc-proinsulin hexamer must preclude the formation of very large and close-packed aggregates that are insoluble in solutions at equilibrium.

  16. 21 CFR 73.1991 - Zinc oxide.


    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Zinc oxide. 73.1991 Section 73.1991 Food and Drugs... ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1991 Zinc oxide. (a) Identity. (1) The color additive zinc...). It is principally composed of Zn. (2) Color additive mixtures for drug use made with zinc oxide...

  17. Chronic zinc exposure decreases the surface expression of NR2A-containing NMDA receptors in cultured hippocampal neurons.

    Jia Zhu

    Full Text Available BACKGROUND: Zinc distributes widely in the central nervous system, especially in the hippocampus, amygdala and cortex. The dynamic balance of zinc is critical for neuronal functions. Zinc modulates the activity of N-methyl-D-aspartate receptors (NMDARs through the direct inhibition and various intracellular signaling pathways. Abnormal NMDAR activities have been implicated in the aetiology of many brain diseases. Sustained zinc accumulation in the extracellular fluid is known to link to pathological conditions. However, the mechanism linking this chronic zinc exposure and NMDAR dysfunction is poorly understood. METHODOLOGY/PRINCIPAL FINDINGS: We reported that chronic zinc exposure reduced the numbers of NR1 and NR2A clusters in cultured hippocampal pyramidal neurons. Whole-cell and synaptic NR2A-mediated currents also decreased. By contrast, zinc did not affect NR2B, suggesting that chronic zinc exposure specifically influences NR2A-containg NMDARs. Surface biotinylation indicated that zinc exposure attenuated the membrane expression of NR1 and NR2A, which might arise from to the dissociation of the NR2A-PSD-95-Src complex. CONCLUSIONS: Chronic zinc exposure perturbs the interaction of NR2A to PSD-95 and causes the disorder of NMDARs in hippocampal neurons, suggesting a novel action of zinc distinct from its acute effects on NMDAR activity.

  18. Influencia de las regiones de estabilidad del biorreactor

    Isabel Cristina Paz Astudillo


    Full Text Available Influence of bioreactor stability regions in the efficient production of fuel ethanol Título corto: Influencia de las regiones de estabilidad en la producción de alcohol carburanteResumen Colombia ha desarrollado un proyecto ambicioso en la producción de alcohol carburante, y actualmente es uno de los países líderes de América Latina en la producción de biocombustibles. No obstante, algunas de sus plantas industriales productoras de etanol presentan problemas durante el arranque y la operación de los fermentadores, que afectan adversamente la productividad del proceso global. Estudios teóricos y experimentales demuestran que el comportamiento dinámico del proceso depende de los fenómenos de estabilidad que exhibe el sistema. En este trabajo se muestra la influencia de las regiones de estabilidad sobre la eficiencia del proceso tomando como criterios de evaluación índices de impacto económico y ambiental. Para esto, se realizó un análisis de estabilidad donde se tomó como parámetro de operación principal la velocidad de dilución. Se empleó un programa propio desarrollado sobre Matlab® para generar diagramas de bifurcación y de fase. El algoritmo de reducción de residuos (WAR desarrollado por la Agencia de Protección Ambiental de los Estados Unidos, y el software SuperPro Designer®, fueron utilizados respectivamente para hacer la evaluación ambiental y económica del proceso. Como resultado, se evidenció que los procesos continuos de fermentación se pueden llevar a cabo en diferentes regiones de estabilidad, y que las variables de respuesta, tales como el rendimiento, dependen de la región de operación seleccionada. Finalmente, se llegó a la conclusión de que la evaluación de la estabilidad de los procesos de fermentación debe incluirse en las etapas de diseño de bioprocesos para garantizar su buen desempeño.  Palabras clave: bioetanol, fermentación, análisis de estabilidad, impacto económico, impacto

  19. Horizontal gene transfer of zinc and non-zinc forms of bacterial ribosomal protein S4

    Luthey-Schulten Zaida


    Full Text Available Abstract Background The universal ribosomal protein S4 is essential for the initiation of small subunit ribosomal assembly and translational accuracy. Being part of the information processing machinery of the cell, the gene for S4 is generally thought of as being inherited vertically and has been used in concatenated gene phylogenies. Here we report the evolution of ribosomal protein S4 in relation to a broad sharing of zinc/non-zinc forms of the gene and study the scope of horizontal gene transfer (HGT of S4 during bacterial evolution. Results In this study we present the complex evolutionary history of ribosomal protein S4 using 660 bacterial genomes from 16 major bacterial phyla. According to conserved characteristics in the sequences, S4 can be classified into C+ (zinc-binding and C- (zinc-free variants, with 26 genomes (mainly from the class Clostridia containing genes for both. A maximum likelihood phylogenetic tree of the S4 sequences was incongruent with the standard bacterial phylogeny, indicating a departure from strict vertical inheritance. Further analysis using the genome content near the S4 genes, which are usually located in a conserved gene cluster, showed not only that HGT of the C- gene had occurred at various stages of bacterial evolution, but also that both the C- and C+ genes were present before the individual phyla diverged. To explain the latter, we theorize that a gene pool existed early in bacterial evolution from which bacteria could sample S4 gene variants, according to environmental conditions. The distribution of the C+/- variants for seven other zinc-binding ribosomal proteins in these 660 bacterial genomes is consistent with that seen for S4 and may shed light on the evolutionary pressures involved. Conclusion The complex history presented for "core" protein S4 suggests the existence of a gene pool before the emergence of bacterial lineages and reflects the pervasive nature of HGT in subsequent bacterial evolution

  20. Cytotoxicity of zinc in vitro.

    Borovanský, J; Riley, P A


    The effect of zinc ions on B16 mouse melanoma lines, HeLa cells and I-221 epithelial cells was investigated in vitro in order to ascertain whether sensitivity to Zn2+ is a general feature of cells in vitro and in an attempt to elucidate the mechanism(s) of zinc cytotoxicity. The proliferation of B16, HeLa and I-221 cell lines was inhibited by 1.25 x 10(-4), 1.50 x 10(-4) and 1.50 x 10(-4) mol/l Zn2+, respectively. The free radical scavengers, methimazole and ethanol, did not suppress the toxicity of Zn2+, neither did superoxide dismutase or catalase. The addition of the chelating agent EDTA reduced the zinc cytotoxicity. It was possible to suppress the cytotoxicity of zinc by increasing the concentration of either Fe2+ or Ca2+ but not Mg2+, which suggests that a prerequisite for the toxic action of zinc is entry into cells using channels that are shared with iron or calcium. This view was supported by experiments in which transferrin intensified the cytotoxic action of zinc in serum-free medium. Another agent facilitating zinc transport, prostaglandin E2, inhibited the proliferation of the B16 melanoma cell line. There were no conspicuous differences in zinc toxicity to pigmented and unpigmented cells. The toxic effect of zinc in the cell systems studied exceeded that of iron, copper, manganese and cobalt in the same concentration range. In vitro, Zn2+ should be regarded as a dangerous cation.

  1. Lagrangian modeling of atmospheric dispersion of radionuclides and geographical information systems as tools to support emergency planning in area of influence of nuclear complex of Angra dos Reis, RJ, Brazil; Modelagem Lagrangeana da dispersao atmoferica de radionuclideos e sistemas de informacao geografica como ferramentas de suporte ao planejamento de emergencia na area de influencia do complexo nuclear de Angra dos Reis, RJ

    Silva, Corbiniano


    Industrial accidents generally endanger structures and the set of environmental influence area where the enterprises are located, especially when affected by atmospheric dispersion of their pollutants, whose concern with the evacuation of the population is the main goal in emergency situations. Considering the nuclear complex Angra dos Reis - RJ, based on computer modeling analysis of the mechanisms of pollutant dispersion in conjunction with geographic information systems were developed. Thus, information about the dispersion of radionuclides - from simulations performed on the HYSPLIT; meteorological data (direction, intensity and calm on the wind regime and analysis of the wind field in the region using WRF), occurrence of landslides and data on the environmental study area were integrated into a GIS database using ArcGIS platform. Aiming at the identification and definition of escape routes in case of evacuation from accidental events in CNAAA, the results point solutions for long-term planning, based on weather and landslides, and short-term, supported by simulations of the dispersion radionuclides, in order to support actions that assist local emergency planning. (author)

  2. Zinc Oxide Nanoparticle Photodetector

    Sheng-Po Chang


    Full Text Available A zinc oxide (ZnO nanoparticle photodetector was fabricated using a simple method. Under a 5 V applied bias, its dark current and photocurrent were 1.98×10-8 and 9.42×10-7 A, respectively. In other words, a photocurrent-to-dark-current contrast ratio of 48 was obtained. Under incident light at a wavelength of 375 nm and a 5 V applied bias, the detector’s measured responsivity was 3.75 A/W. The transient time constants measured during the turn-ON and turn-OFF states were τON=204 s and τOFF=486 s, respectively.

  3. Analisis de redes sociales y procesos de influencia en la toma de decision grupal

    Jorge Ricardo Vivas


    En el presente trabajo se analizan los procesos de influencia por medio del estudio de las relaciones entre medidas convencionales y estructurales en tareas de toma de decisión grupal. Se exploraron los componentes de conectividad y prestigio como facilitadores del proceso de influencia; la conectividad por medio del flujo global, la participación, la densidad de la red ego centrada y la cohesión o distancia reticular. El prestigio se analizó por medio del status sociométrico, medidas de infl...

  4. Los mecanismos de influencia en el liderazgo: dos estudios de caso

    Lancheros Guzman, David antonio; Zuluaga Lopez, Luis Felipe; Daza Rodriguez, Paola


    Este trabajo investigativo busca aportar a la literatura sobre las tácticas de influencia en el liderazgo. Surge como una aplicación, a dos casos específicos, del proyecto de investigación “Los mecanismos de influencia en la relación de liderazgo”, desarrollado por el profesor Juan Javier Saavedra Mayorga e inscrito en la línea de investigación en Estudios Organizacionales del Grupo de Investigación en Dirección y Gerencia. La investigación tiene como objetivo fundamental identificar las...

  5. Influencia del clima escolar y familiar en adolescentes, víctimas de ciberacoso

    Jessica Ortega Barón; Sofía Buelga Vasquez; María Jesús Cava Caballero


    El ciberacoso es un fenómeno de creciente preocupación social que afecta cada vez más a niños y adolescentes de todos los países desarrollados. A diferencia de la considerable literatura que hay sobre las relaciones entre el acoso escolar y el contexto familiar y escolar, todavía hay pocos trabajos sobre la influencia de estos entornos sociales en el problema del ciberacoso. Mediante una metodología cuantitativa, el objetivo principal del presente estudio fue analizar la influencia del contex...

  6. Influencia del clima escolar y familiar en adolescentes, víctimas de ciberacoso

    Ortega Barón, Jessica; Buelga, Sofía; Cava, María Jesús


    El ciberacoso es un fenómeno de creciente preocupación social que afecta cada vez más a niños y adolescentes de todos los paí- ses desarrollados. A diferencia de la considerable literatura que hay sobre las relaciones entre el acoso escolar y el contexto familiar y escolar, todavía hay pocos trabajos sobre la influencia de estos entornos sociales en el problema del ciberacoso. Mediante una metodología cuantitativa, el objetivo principal del presente estudio fue analizar la influencia...

  7. Influencia del clima escolar y familiar en adolescentes, víctimas de ciberacoso

    Jessica Ortega Barón; Sofía Buelga Vasquez; María Jesús Cava Caballero


    El ciberacoso es un fenómeno de creciente preocupación social que afecta cada vez más a niños y adolescentes de todos los países desarrollados. A diferencia de la considerable literatura que hay sobre las relaciones entre el acoso escolar y el contexto familiar y escolar, todavía hay pocos trabajos sobre la influencia de estos entornos sociales en el problema del ciberacoso. Mediante una metodología cuantitativa, el objetivo principal del presente estudio fue analizar la influencia del contex...

  8. Voy para la U: influencia de las relaciones materno y paterno filiales en la experiencia universitaria

    Berrocal Garcerant, Diana Margarita


    Voy para la U. Influencia de las relaciones materno y paterno filiales en la experiencia universitaria, el objeto de esta investigación fue comprender las relaciones de género y poder en el vínculo de universitarios y universitarias con sus padres y madres, y las influencias posibles de esto en sus experiencias relacionales, tomando como ejes de análisis las relaciones contemporáneas con la madre y el padre, o quien ejerce sus funciones; las identidades como jóvenes estudiantes de la universi...

  9. Use of serum zinc concentration as an indicator of population zinc status.

    Hess, Sonja Y; Peerson, Janet M; King, Janet C; Brown, Kenneth H


    Assessing the prevalence and severity of zinc deficiency in populations is critical to determine the need for and appropriate targeting of zinc intervention programs and to assess their effectiveness for improving the health and well-being of high-risk populations. However, there is very little information on the zinc status of populations worldwide due to the lack of consensus on appropriate biochemical indicators of zinc status. The objective of this review was to evaluate the use of serum zinc concentration as an indicator of population zinc status. We have reviewed the response of serum zinc concentration to dietary zinc restriction and zinc supplementation. In addition, we completed pooled analyses of nine zinc intervention trials in young children to assess the relations between serum zinc concentration of individuals before treatment and their responses to zinc supplementation. Also, in updated combined analyses of previously published data, we investigated the relation between the mean initial serum zinc concentration of a study population and their mean growth responses to zinc supplementation in randomized intervention trials among children. The results from depletion/repletion studies indicate that serum zinc concentrations respond appreciably to severe dietary zinc restriction, although there is considerable interindividual variation in these responses. There is also clear evidence that both individual and population mean serum zinc concentrations increase consistently during zinc supplementation, regardless of the initial level of serum zinc concentration. By contrast, an individual's serum zinc concentration does not reliably predict that person's response to zinc supplementation. Serum zinc concentration can be considered a useful biomarker of a population's risk of zinc deficiency and response to zinc interventions, although it may not be a reliable indicator of individual zinc status.

  10. Polyacrylate microspheres for tunable fluorimetric zinc ions sensor.

    Woźnica, Emilia; Maksymiuk, Krzysztof; Michalska, Agata


    A novel concept of optical fluorimetric sensing using polymeric microspheres is explored on example of zinc ions sensors. The novel approach proposed uses the advantage of concomitant presence in a microsphere of two compounds: a receptor, fluorescently silent complexing ligand and an optical transducer, fluorescent compound. Binding of the analyte by the ligand affects its absorption spectrum, leading to decrease of the free ligand absorption and increase of complex absorption band. The decrease of free ligand absorption exposes emission of the transducer, yielding increase in fluorescence intensity on analyte concentration increase. This approach was verified experimentally using Zn(2+) as a model analyte, the fluorimetric sensor obtained uses 1-(2-pyridylazo)-2-naphthol (PAN) as analyte sensitive receptor and pyrene as optical transducer. In the absence of zinc ions in the sample emission of pyrene embedded in the spheres was significantly quenched, whereas increase of Zn(2+) ions concentration in the sample resulted in dependence of fluorescence intensity on logarithm of zinc ions concentration in extraordinary wide range, from 10(-7) to 0.1 M. The response mechanism was explained by surface accumulation of zinc ion-PAN complex on the microsphere/sample solution interface. It was also shown that introduction of cation-exchanging sites to the microspheres significantly alters the responses pattern leading to high sensitivity over relatively limited concentration range (3-4 orders of magnitude). In the latter case the observed responses can be tuned to occur in chosen concentration range, simply by adjusting sample pH.

  11. Assessment of zinc finger orientations by residual dipolar coupling constants

    Tsui, Vickie; Zhu Leiming; Huang, T.-H.; Wright, Peter E.; Case, David A. [Scripps Research Institute, Department of Molecular Biology (United States)


    Residual dipolar coupling constants measured in anisotropic solution contain information on orientations between internuclear vectors and the magnetic field, providing long-range information that may help determine the relative orientations of distinct domains in biomolecules. Here we describe the measurement and use of residual dipolar coupling restraints in the refinement of the structure of the complex of DNA with three zinc fingers of transcription factor IIIA (TFIIIA), measured in a DMPC/DHPC bicelle solution. These dipolar restraints were applied on a variety of orientations of the zinc finger domains (derived from crystallography, previous NMR studies, and systematic modeling) in order to examine the validity and sensitivity of using residual dipolar splittings to study interdomain orientations. The spread in interdomain angles between zinc fingers is reduced from 24 deg. to 9 deg. upon incorporation of dipolar restraints. However, the results also show that the ability to determine relative orientations is strongly dependent on the structural accuracy of the local domain structures.

  12. Zinc tolerance and zinc removal ability of living and dried biomass of Desmodesmus communis.

    Novák, Zoltán; Jánószky, Mihály; B-Béres, Viktória; Nagy, Sándor Alex; Bácsi, István


    Effects of zinc on growth, cell morphology, oxidative stress, and zinc removal ability of the common phytoplankton species Desmodesmus communis were investigated at a concentration range of 0.25-160 mg L(-1) zinc. Cell densities and chlorophyll content decreased in treated cultures, changes in coenobia morphology and elevated lipid peroxidation levels appeared above 2.5 mg L(-1) zinc. The most effective zinc removal was observed at 5 mg L(-1) zinc concentration, while maximal amount of removed zinc appeared in 15 mg L(-1) zinc treated culture. Removed zinc is mainly bound on the cell surface. Dead biomass adsorbed more zinc than living biomass relative to unit of dry mass, but living biomass was more effective, relative to initial zinc content. This study comprehensively examines the zinc tolerance and removal ability of D. communis and demonstrates, in comparison with published literature, that these characteristics of different isolates of the same species can vary within a wide range.

  13. Zinc toxicology following particulate inhalation

    Cooper Ross


    Full Text Available The current mini-review describes the toxic effects of zinc inhalation principally in the workplace and associated complications with breathing and respiration. The International Classification of Functioning, Disability and Health Criteria were used to specifically select articles. Most of the commercial production of zinc involves the galvanizing of iron and the manufacture of brass. The recommended daily allowance for adults is 15 mg zinc/day. Metal fume fever associated with inhalation of fumes of ZnO is characterized by fatigue, chills, fever, myalgias, cough, dyspnea, leukocytosis, thirst, metallic taste and salivation. ZnCl 2 inhalation results in edema in the alveolar surface and the protein therein the lavage fluid is elevated. Particular pathological changes associated with zinc intoxication include: pale mucous membranes; jaundice; numerous Heinz bodies; and marked anemia. Adequate ambient air monitors for permissible exposure limits, excellent ventilation and extraction systems, and approved respirators are all important in providing adequate protection.

  14. Hydrothermal Synthesis, Crystal Structure and Fluorescence Properties of a Three-dimensional Triply-bridged Binuclear Zinc(Ⅱ) Complex [Zn2(Mba)3(Phen)2EtOH)]·ClO4%Hydrothermal Synthesis, Crystal Structure and Fluorescence Properties of a Three-dimensional Triply-bridged Binuclear Zinc(Ⅱ) Complex [Zn2(Mba)3(Phen)2EtOH)]·ClO4

    CHEN Zhi-Min; FENG Yong-Lan; YANG Ying-Qun; LI Wei; Zheng-Ji; CHEN Man-Sheng


    The novel complex [Zn2(Mba)3(Phen)2EtOH)]·ClO4 (Hrnba = methoxybenzoic acid, Phen = 1,10-phenanthroline, EtOH = ethanol) was synthesized by hydrothermal reactions, and its structure was determined by X-ray diffraction. The crystal belongs to the triclinic system, space group Pi with a = 1.15362(1), b = 1.3655(3), c = 1.61451(1) nm, α= 72.842(2), β = 83.259(3), y = 72.083(2)°, V = 2.3112(6) nm3, Z = 2,μ(MoKa) = 11.71 cm-1, F(000) = 1120, R = 0.0552 and wR = 0.1157 (I 〉 2σ(I)). The two centric zinc(H) ions in the complex locate in a distorted octahedral coordination geometry and a distorted trigonal bipyramid coordination geometry, respectively. Two bridging bidentate carboxyl groups and a μ2-O carboxyl group from three methoxybenzoic acids act as the bridge to link two Zn(Ⅱ) ions. The asymmetric units are connected by π-π packing interactions between aromatic rings to form a three-dimensional supramolecular network. The experimental results show a good fluorescence property for the complex.

  15. Prevalence of Zinc Deficiency by “ Zinc Taste Test” in Pre School Children in Yazd.

    Gh Maleki


    Full Text Available Introduction: Zinc deficiency is a health problem in many communities, especially among children because of growth spurt. Zinc deficiency can cause;growth limitation, delay in sexuel maturity, behavior disorders and abnormalities of immune system,susceptibility to respiratory and gasterointestinal infections and impairment of taste and smell perception. Material and Method: One of the methods of assessment the zinc defeciency is “ Zinc taste test” using zinc sulfate solution 0.1% , this test performed used to assess the zinc deficiency among preshool childeren in Yazd. The results were evaluated with measurments of weight,height and demographic data. 400 preschool children were selected by multi stage random sampling.Having good taste perception of zinc sulfate 0.1% was used as impaired taste test ( zinc deficiency and having bad taste perception as normal zinc level. Results: Regarding to zinc taste test 73.9% of study group had zinc deficiency (77.6%femal, 69.7% male There were no significant relation between zinc deficiency and measurment of weight and height,but there was higher prevalence of zinc deficiency in children who were below the 5th percentile in height and weight by age. Conclusion: 70% of preschool children in yazd had zinc deficiency assessed by “ zinc taste test”,31% of adolecents in Tehran have had zinc deficiency based on plasma , erythrocyte and hairindex. There is no significant relation between zinc deficiency and antropometric and demographic data, in this study and the study that had been done on adolescents in Tehran.Considering the prevalnce of zinc deficiency with “ Zinc taste test” ;it seems more accurate studies need to be done like zinc measurment in WBC,RBC and Platelets and zinc taste test at the same time,if correlation coefficients between zinc taste test and other tests were very strong , we can used zinc tase test in the different age for assessment of zinc body.

  16. Morphology study of electrodeposited zinc from zinc sulfate solutions as anode for zinc-air and zinc-carbon batteries

    Nurhaswani Alias; Ahmad Azmin Mohamad


    The morphology of Zinc (Zn) deposits was investigated as anode for aqueous batteries. The Zn was deposited from zinc sulfate solution in direct current conditions on a copper surface at different current densities. The morphology characterization of Zn deposits was performed via field emission scanning electron microscopy. The Zn deposits transformed from a dense and compact structure to dendritic form with increasing current density. The electrodeposition of Zn with a current density of 0.02...

  17. Laboratory Study on the Removal of Fluorine from High Fluorine Bearing Zinc Oxide Ore

    Yaozhong LAN; Liaoyuan YE; Rose W. Smith


    An ever increasing demand for zinc has resulted in worldwide efforts to exploit complex and lean grade reserves of zinc oxide ore. In this study experiments were done on zinc recovery from high-fluorine bearing zinc oxide ore. First the effect of different variables on fluorine removal was investigated. Optimum experimental conditions occurred when the temperature was 1173 K, roasting time was 90 min and air flow was at a velocity of 5 m/min, the fluorine removal from the samples reached over 93%. The results obtained indicate that fluorine removal is not enhanced by adding diluted sulfuric acid or water as a binder. Second the roasted materials were leached with a diluted sulfuric acid,neutralized, flocculated and filtrated. The residual fluorine content in the leached solutions was less than 38 mg/L,which satisfies the requirement of fluorine content in the leached solutions for the production of electrolytic zinc.

  18. [Role of zinc in type 2 diabetes].

    Tamaki, Motoyuki; Fujitani, Yoshio


    Pancreatic β cells contain the highest amount of zinc among cells within the human body, and hence, the relationship between zinc and diabetes has been of great interest. To date, many studies of zinc and diabetes have been reported, including studies demonstrating that diabetic patients and mice have a decreased amount of zinc in the pancreas. Zinc may counteract the deleterious effects of oxidative stress, which contributes to reduced insulin resistance, and may also protect pancreatic β cells from glucolipotoxicity. Recently, we have shown that SLC30A8/zinc transporter 8, which is a transporter expressed on the surface of insulin granules, plays a key role in zinc transport into insulin granules and in the regulation of hepatic insulin clearance. Here, we review the role of zinc in whole-body maintenance and the latest information on the relationship between zinc and diabetes.

  19. Leptin and zinc relation : In regulation of food intake and immunity

    Abdulkerim Kasim Baltaci


    Full Text Available Leptin is synthesized and released by the adipose tissue. Leptin, which carries the information about energy reserves of the body to the brain, controls food intake by acting on neuropeptide Y (NPY, which exercises a food-intake-increasing effect through relevant receptors in the hypothalamus. Zinc deficiency is claimed to result in anorexia, weight loss, poor food efficiency, and growth impairment. The fact that obese individuals have low zinc and high leptin levels suggests that there is a relation between zinc and nutrition, and consequently also between zinc and leptin. Leptin deficiency increases the predisposition to infections and this increase is associated with the impairments in the production of cytokines. Zinc has a key role in the sustenance of immune resistance against infections. Dietary zinc deficiency negatively affects CD +4 cells, Th functions, and consequently, cell-mediated immunity by causing a decrease in the production of IL-2, IF-γ, and TNF-α, which are Th1 products. The relation between zinc and the concerned cytokines in particular, and the fact that leptin has a part in the immune responses mediated by these cytokines demonstrate that an interaction among cellular immunity, leptin and zinc is inevitable. An overall evaluation of the information presented above suggests that there are complex relations among food intake, leptin and zinc on one hand and among cellular immunity, leptin and zinc on the other. The aim of the present review was to draw attention to the possible relation between zinc and leptin in dietary regulation and cellular immunity.

  20. Amidinate Ligands in Zinc coordination sphere: Synthesis and structural diversity



    A one-pot reaction involving neosilyllithium and three different carbodiimides (RN=C=NR, R =cyclohexyl, isopropyl and tert-butyl) in diethyl ether, followed by the addition of anhydrous $ZnCl_{2}$, afforded,in high yield, corresponding homoleptic zinc amidinate complexes having the molecular formulae$[Zn{CyN=C(CH_{2}SiMe_{3})NCy}_{2}]$ (1),$[Zn^{{i}PrN=C(CH_{2}SiMe_{3})N^{i}Pr}_{2}]$ (2) and [Zn$^{{t}BuN=C(CH_{2}SiMe_{3})N^{t}Bu}_{2}]$ (3), respectively, and amidinato moieties in the zinc coordination sphere. Solid state structures of complexes1-3 are reported thereafter - all the three complexes are isostructural, and each of them consists of twofour-membered metallacycles.

  1. Influencia de colorantes ftalocianinicos funcionales en el tamaño molecular del poliestireno

    J. Bernal Castillo


    Full Text Available Se examina la influencia de Silico ftalocianinas funcionales en cantidades pequeñas, pero suficientes para colorear el polímero, sobre el tamaño molecular del poliestireno. Los cálculos se basan en la determinación de peso molecular medioa partir de la viscosidad intrínseca.

  2. Estudio de la influencia del pretensado en la resistencia a cortante en vigas


    Se pretende estudiar la influencia del pretensado, en vigas continuas, en la resistencia a cortante de vigas de hormigón. Para ello se ensayarán seis vigas de siete metros con diferentes configuraciones en el Laboratorio de Tecnología de las Estructuras del Departamento.

  3. De la influencia al poder: elementos para una mirada foucaultiana al Liderazgo

    Juan Javier Saavedra Mayorga; Mauricio Sanabria; Ali Smida


    El artículo tiene como objetivo contribuir a la construcción de una mirada crítica al liderazgo. Examina la posibilidad de estudiar el problema central del liderazgo, el de la influencia, desde un punto de vista...

  4. De la influencia al poder: elementos para una mirada foucaultiana al Liderazgo

    Juan Javier Saavedra Mayorga; Mauricio Sanabria; Ali Smida


      El artículo tiene como objetivo contribuir a la construcción de una mirada crítica al liderazgo. Examina la posibilidad de estudiar el problema central del liderazgo, el de la influencia, desde un punto de vista...

  5. Synthesis, crystal structures and spectroscopy of meclofenamic acid and its metal complexes with manganese(II), copper(II), zinc(II) and cadmium(II). Antiproliferative and superoxide dismutase activity.

    Kovala-Demertzi, Dimitra; Staninska, Malgorzata; Garcia-Santos, Isabel; Castineiras, Alfonso; Demertzis, Mavroudis A


    Some new complexes of meclofenamic acid (N-(2,6-dichloro-m-tolyl)anthranilic acid), Hmeclo (1), with potentially interesting biological activities are described. Complexes [Mn(meclo)(2)] (2), [Cu(meclo)(2)(H(2)O)(2)] (3), [Zn(meclo)(2)(H(2)O)(2)] (4) and [Cd(meclo)(2)(H(2)O)(2)] (5) were prepared and structurally characterized by means of vibrational, electronic and (1)H and (13)C NMR spectroscopies. The crystal structure of complexes [Cu(4)(meclo)(6)(OH)(2)(DMSO)(2)]2DMSO (3a) and [Cd(meclo)(2)(DMSO)(3)] (5a) have been determined by X-ray crystallography. Complex (3a) is a centrosymmetric tetramer built up around the planar cyclic Cu(2)(OH)(2) unit. Complex 5a is mononuclear seven-coordinated complex with the meclofenamato ligand behaving as a bidentate deprotonated chelating ligand. Intra and intermolecular hydrogen bonds stabilize these two structures, while the crystal packing is determined by π-π and C-H--π interactions. Meclofenamic acid and its metal complexes have been evaluated for antiproliferative activity in vitro against the cells of three human cancer cell lines, MCF-7 (breast cancer cell line), T24 (bladder cancer cell line), and A-549 (non-small cell lung carcinoma), and a mouse fibroblast L-929 cell line. Complex 5 exhibits the highest selectivity against MCF-7 and 4 shows the highest selectivity against T-24. Complexes 2-5 were found to be more potent cytotoxic agents against T-24 and complex 5 against MCF-7 cancer cell lines than the prevalent benchmark metallodrug, cis-platin. The superoxide dismutase activity was measured by the Fridovich test which showed that complex [Cu(meclo)(2)(H(2)O)(2)] is a good superoxide scavenger.

  6. Syntheses, electronic structures and EPR/UV–vis–NIR spectroelectrochemistry of nickel(II), copper(II) and zinc(II) complexes with a tetradentate ligand based on S-methylisothiosemicarbazide

    Arion, Vladimir B.; Rapta, Peter; Telser, Joshua; Shova, Sergiu S.; Breza, Martin; Lušpai, Karol; Kožišek, Jozef


    Template condensation of 3,5-di-tert-butyl-2-hydroxybenzaldehyde S-methylisothiosemicarbazone with pentane-2,4-dione and triethyl orthoformate at elevated temperature resulted in metal complexes of the type MIIL, where M = Ni, Cu and H2L = novel tetradentate organic ligand. These complexes are relevant to the active site of the copper enzymes galactose oxid...

  7. Synthesis, physico-chemical studies of manganese(II), cobalt(II), nickel(II), copper(II) and zinc(II) complexes with some p-substituted acetophenone benzoylhydrazones and their antimicrobial activity.

    Singh, Vinod P; Singh, Shweta; Katiyar, Anshu


    Complexes of the type [M(pabh)(H2O)Cl], [M(pcbh)(H2O)Cl] and [M(Hpabh)(H2O)2 (SO4)] where, M = Mn(II), Co(II), Ni(II), Cu(II) and Zn(II); Hpabh = p-amino acetophenone benzoyl hydrazone and Hpcbh = p-chloro acetophenone benzoyl hydrazone have been synthesized and characterized with the help of elemental analyses, electrical conductance, magnetic susceptibility measurements, electronic, ESR and IR spectra, thermal (TGA & DTA) and X-ray diffraction studies. Co(II), Ni(II) and Cu(II) chloride complexes are square planar, whereas their sulfate complexes have spin-free octahedral geometry. ESR spectra of Cu(II) complexes with Hpabh are axial and suggest d(x(2)-y(2) as the ground state. The ligand is bidentate bonding through > C = N--and deprotonated enolate group in all the chloro complexes, whereas, >C = N and >C = O groups in all the sulfato complexes. Thermal studies (TGA & DTA) on [Cu(Hpabh)(H2O)2(SO4)] indicate a multistep decomposition pattern, which are both exothermic and endothermic in nature. X-ray powder diffraction parameters for [Co(pabh)(H2O)Cl] and [Ni(Hpabh)(H2O)2(SO4)] correspond to tetragonal and orthorhombic crystal lattices, respectively. The ligands as well as their complexes show a significant antifungal and antibacterial activity. The metal complexes are more active than the ligand.

  8. Actitudes hacia la influencia de la sociedad en la ciencia y la tecnología

    Manassero Mas, M.ª Antonia


    Full Text Available Not available.La filosofía tradicional de la ciencia presenta ésta como un conocimiento objetivo, aislado de influencias externas, mientras que la moderna sociología y epistemología de la ciencia sostienen la influencia de los factores contextuales. Este estudio analiza las actitudes de estudiantes y profesorado sobre la influencia de la sociedad en la ciencia y tecnología mediante una serie de cuestiones referidas a distintos factores sociales, como el gobierno, las empresas e industrias, el ejército, la cultura, los grupos de especial interés o la educación científica y tecnológica del público. Las actitudes obtenidas muestran diferente intensidad y se fundan en distintas razones justificativas, aunque se observa una tendencia a admitir mayoritariamente esta influencia sobre la ciencia cuando se refiere a un factor general, mientras que cuando la influencia de la sociedad se concreta en factores más concretos, las actitudes no concitan tanta unanimidad. Las diferencias entre estudiantes según el grado de exposición a la ciencia no son tan importantes como cabría esperar, y las diferencias de género, cuando se controla la variable anterior son escasas. El análisis comparativo entre profesorado y alumnado muestra más coincidencias que diferencias, y cuando se comparan los estudiantes canadienses con los españoles existen tantas diferencias como coincidencias. Finalmente, se discuten algunas implicaciones para la enseñanza de las ciencias desde una perspectiva de ciencia-tecnología-sociedad (CTS.

  9. Coordination study of recombinant human-like collagen and zinc (II)

    Yu, Yuan-Yuan; Fan, Dai-Di


    In the present investigation, the complex of recombinant human-like collagen (r-HLC) with zinc (II) has been synthesized in aqueous solution and was analyzed by UV-vis spectroscopy, FTIR spectroscopy, circular dichroism (CD) spectroscopy, thermo gravimetric (TG) and differential scanning calorimetry (DSC) analysis. It can be concluded from UV-vis spectra that there exists interaction between r-HLC and zinc, and the complex is a new chemical compound different from pure r-HLC. In the complex of Zn, recombinant human-like collagen acts as ligand, linking the zinc ion via both groups of C dbnd O and N-H. Besides, the results of TG and DSC confirm that the complex was significantly different from ligand, and the former is more thermally stable in comparison with the latter. The results obtained from the current investigation are of crucial importance to understand the r-HLC-Zn complex and provide theoretical evidence for the further study.

  10. Influence of DNA-methylation on zinc homeostasis in myeloid cells: Regulation of zinc transporters and zinc binding proteins.

    Kessels, Jana Elena; Wessels, Inga; Haase, Hajo; Rink, Lothar; Uciechowski, Peter


    The distribution of intracellular zinc, predominantly regulated through zinc transporters and zinc binding proteins, is required to support an efficient immune response. Epigenetic mechanisms such as DNA methylation are involved in the expression of these genes. In demethylation experiments using 5-Aza-2'-deoxycytidine (AZA) increased intracellular (after 24 and 48h) and total cellular zinc levels (after 48h) were observed in the myeloid cell line HL-60. To uncover the mechanisms that cause the disturbed zinc homeostasis after DNA demethylation, the expression of human zinc transporters and zinc binding proteins were investigated. Real time PCR analyses of 14 ZIP (solute-linked carrier (SLC) SLC39A; Zrt/IRT-like protein), and 9 ZnT (SLC30A) zinc transporters revealed significantly enhanced mRNA expression of the zinc importer ZIP1 after AZA treatment. Because ZIP1 protein was also enhanced after AZA treatment, ZIP1 up-regulation might be the mediator of enhanced intracellular zinc levels. The mRNA expression of ZIP14 was decreased, whereas zinc exporter ZnT3 mRNA was also significantly increased; which might be a cellular reaction to compensate elevated zinc levels. An enhanced but not significant chromatin accessibility of ZIP1 promoter region I was detected by chromatin accessibility by real-time PCR (CHART) assays after demethylation. Additionally, DNA demethylation resulted in increased mRNA accumulation of zinc binding proteins metallothionein (MT) and S100A8/S100A9 after 48h. MT mRNA was significantly enhanced after 24h of AZA treatment also suggesting a reaction of the cell to restore zinc homeostasis. These data indicate that DNA methylation is an important epigenetic mechanism affecting zinc binding proteins and transporters, and, therefore, regulating zinc homeostasis in myeloid cells.

  11. Cobalt (II, nickel (II, copper (II and zinc (II complexes of 1-(phenyl(phenylamino methylpyrrolidine-2,5-dione and 2-((phenylaminomethyl isoindoline-1,3-dione and their biological activity

    D. Tamil Vendan


    Full Text Available The new Mannich bases 1-(phenyl(phenylaminomethylpyrrolidine-2,5-dione (SBA was synthesized from the condensation of succinimide, benzaldehyde and aniline. 2-((phenylaminomethylisoindoline-1,3-dione (PFA was derived from pthalimide, formaldehyde and aniline. The general formula of the Co (II, Ni (II, Cu (II and Zn (II chloro complexes, ML2X2 are reported. The ligands and the complexes have been characterized by various physical-chemical techniques such as elemental analysis, molar conductance, magnetic susceptibility measurements, infrared and electronic spectra. The spectral analysis to ascertain mode of bonding and overall geometry of the complexes revealed octahedral geometries.

  12. Zinc Plating Industry Drives Zinc Consumption by Power Grids, Railways and Highways


    <正>On the afternoon of June 30, at the Chengdu Lead and Zinc Summit, more than 150 partici-pants voted for the product they felt drives zinc consumption the most. 48% went for zinc plat-ing products, 16% voted for zinc oxide,

  13. High dose zinc supplementation induces hippocampal zinc deficiency and memory impairment with inhibition of BDNF signaling.

    Yang Yang

    Full Text Available Zinc ions highly concentrate in hippocampus and play a key role in modulating spatial learning and memory. At a time when dietary fortification and supplementation of zinc have increased the zinc consuming level especially in the youth, the toxicity of zinc overdose on brain function was underestimated. In the present study, weaning ICR mice were given water supplemented with 15 ppm Zn (low dose, 60 ppm Zn (high dose or normal lab water for 3 months, the behavior and brain zinc homeostasis were tested. Mice fed high dose of zinc showed hippocampus-dependent memory impairment. Unexpectedly, zinc deficiency, but not zinc overload was observed in hippocampus, especially in the mossy fiber-CA3 pyramid synapse. The expression levels of learning and memory related receptors and synaptic proteins such as NMDA-NR2A, NR2B, AMPA-GluR1, PSD-93 and PSD-95 were significantly decreased in hippocampus, with significant loss of dendritic spines. In keeping with these findings, high dose intake of zinc resulted in decreased hippocampal BDNF level and TrkB neurotrophic signaling. At last, increasing the brain zinc level directly by brain zinc injection induced BDNF expression, which was reversed by zinc chelating in vivo. These results indicate that zinc plays an important role in hippocampus-dependent learning and memory and BDNF expression, high dose supplementation of zinc induces specific zinc deficiency in hippocampus, which further impair learning and memory due to decreased availability of synaptic zinc and BDNF deficit.

  14. High dose zinc supplementation induces hippocampal zinc deficiency and memory impairment with inhibition of BDNF signaling.

    Yang, Yang; Jing, Xiao-Peng; Zhang, Shou-Peng; Gu, Run-Xia; Tang, Fang-Xu; Wang, Xiu-Lian; Xiong, Yan; Qiu, Mei; Sun, Xu-Ying; Ke, Dan; Wang, Jian-Zhi; Liu, Rong


    Zinc ions highly concentrate in hippocampus and play a key role in modulating spatial learning and memory. At a time when dietary fortification and supplementation of zinc have increased the zinc consuming level especially in the youth, the toxicity of zinc overdose on brain function was underestimated. In the present study, weaning ICR mice were given water supplemented with 15 ppm Zn (low dose), 60 ppm Zn (high dose) or normal lab water for 3 months, the behavior and brain zinc homeostasis were tested. Mice fed high dose of zinc showed hippocampus-dependent memory impairment. Unexpectedly, zinc deficiency, but not zinc overload was observed in hippocampus, especially in the mossy fiber-CA3 pyramid synapse. The expression levels of learning and memory related receptors and synaptic proteins such as NMDA-NR2A, NR2B, AMPA-GluR1, PSD-93 and PSD-95 were significantly decreased in hippocampus, with significant loss of dendritic spines. In keeping with these findings, high dose intake of zinc resulted in decreased hippocampal BDNF level and TrkB neurotrophic signaling. At last, increasing the brain zinc level directly by brain zinc injection induced BDNF expression, which was reversed by zinc chelating in vivo. These results indicate that zinc plays an important role in hippocampus-dependent learning and memory and BDNF expression, high dose supplementation of zinc induces specific zinc deficiency in hippocampus, which further impair learning and memory due to decreased availability of synaptic zinc and BDNF deficit.

  15. Synthesis and Crystal Structure of an Azide Bridged Binuclear Zinc(II) Complex Including the Reduced Derivative of Nitronyl Nitroxide,[Zn(Him2Py)(N3)2]2

    王利亚; 张晨曦; 廖代正; 姜宗慧; 阎世平


    The title compound [Zn(Him2Py)(N3)2]2 (Zn2C26H38N18O2, Mr = 765.48) has been prepared and structurally characterized by X-ray diffraction methods. It crystallizes in monoclinic, space group P21/n with a = 10.989(3), b = 11.519(3), c = 13.812(4) A, β = 101.700(5)°,V = 1711.9(9) A3, Z = 2, Dc = 1.485 g/cm3,μ(MoKα) = 1.456 mm~1, F(000) = 792, the final R =0.0401 and wR = 0.0861 for 2054 observed reflections with I>2σ(I). The imino nitroxide 2-(3 ′-methyl-2′-pyridyl)-4,4,5,5-tetramethyl-4,5-dihydro-lH-imidazolyl-l-oxyl (im2Py) was reduced to obtain 2-(3′-methyl -2′-pyridyl)-4,4,5,5-tetramethyl-4,5-dihydro-lH-imidazole-1-ydroxy (Him2Py)coordinating to the zinc (Ⅱ) ion, around which the coordination geometry is a square-based pyramid with a terminal nitrogen atom located at the apical position. The four basal sites are occupied by two μ1,1 nitrogen atoms from two different bridging azide ions and two nitrogen atoms from Him2Py.The units of [Zn(Him2Py)(N3)2]2 were connected as two dimension planes by intermolecular hydrogen bonds.

  16. Synthesis, structure, photoluminescence and antitumour activity of zinc complex based on 2-(2-(1H-benzo-[d]imidazol-2-yl)benzyl)-1H-benzo-[d]imidazole

    Che, Zhijian; Wang, Shaoxiang; Liu, Shenggui; Li, Guobi; Wu, Qiting; Lin, Chunyu; Kong, Linglang; Wang, Sheng


    A new complex [Zn(bbb)Cl2]·DMF, where bbb is 2-(2-(1H-benzo[d]imidazol-2-yl)benzyl)-1H-benzo[d]imidazole, was synthesized and characterized by element analysis, 1H NMR and X-ray single crystal structure analyses. For complex: crystal system, triclinic, space group, P-1, a = 9.4661(13), b = 10.3534(14), c = 13.0025(18) Å, α = 73.477(2), β = 80.743(2), γ = 88.658(2)°, V = 1205.5(3) Å3, Z = 2. In this complex, the Zn2+ distorted tetrahedron geometry is coordinated by two nitrogen atoms from 2-(2-(1H-benzo[d]imidazol-2-yl)benzyl)-1H-benzo[d]imidazole and two Cl-. The complex emits yellow green luminescence with the maximal emission peak at 550 nm in DMF solution. The complex exhibits inhibition on the growth of Eca109 cancer cell with IC50 value of 8.9 ± 1.1 μM, which was lower than that of cisplatin (14.3 ± 1.4 μM). This complex has potential application in treatment of esophageal cancer.

  17. Two different zinc(II)-aqua complexes held up by a metal-oxide based support: Synthesis, crystal structure and catalytic activity of [HMTAH]2[{Zn(H2O)5}{Zn(H2O)4}{Mo7O24}].2H2O (HMTAH = protonated hexamethylenetetramine)

    T Arumuganathan; A Srinivasarao; T Vijay Kumar; Samar K Das


    An inorganic−organic hybrid material, [HMTAH]2[{Zn(H2O)5}{Zn(H2O)4}{Mo7O24}].2H2O (1) (where HMTAH = protonated hxamethylenetetramine) has been synthesized and structurally characterized. The compound 1 crystallizes in a monoclinic space group 2/. The crystal data of 1: = 43.12(3), = 12.399(10), = 16.285(13), = 111.131(11), = 8. Its crystal structure shows that two different Zn(II)-aqua complexes, [Zn(H2O)5]2+ and [Zn(H2O)4]2+ are covalently coordinated to a heptamolybdateanion [Mo7O24]6- resulting in an anionic species of polyoxometalate supported zinc-aqua complexes, [{Zn(H2O)}{Zn(H2O)4}{Mo7O24}]2-, that is stabilized with two protonated hexamethylenetetramine cations in the title compound 1. In the crystal structure, both lattice water molecules are found to interact with the heptamolybdate cluster anion and the protonated hexamethylenetetramine cation resulting in an intricate three-dimensional hydrogen bonding network. Interestingly, compound 1 exhibits catalytic activity towards oxidation of some primary alcohols.

  18. Conversion of nitrite to nitric oxide at zinc via S-nitrosothiols.

    Cardenas, Allan Jay P; Abelman, Rebecca; Warren, Timothy H


    Nitrite is an important reservoir of nitric oxide activity in the plasma and cells. Using a biomimetic model, we demonstrate the conversion of zinc-bound nitrite in the tris(pyrazolyl)borate complex (iPr2)TpZn(NO2) to the corresponding S-nitrosothiol RSNO and zinc thiolate (iPr2)TpZn-SR via reaction with thiols H-SR. Decomposition of the S-nitrosothiol formed releases nitric oxide gas.

  19. Entretenimiento, espiritualidad, familia y su relación con la influencia de pares en el consumo

    Rolando Salazar Sarmiento; Rocío Morales; Samuel Noh; Bruna Brands; Hayley Hamilton; Denise Gastaldo; Maria da Gloria Miotto Wright; Francisco Cumsille; Akwatu Khenti


    ... en Bogotá, Colombia y la influencia del grupo de pares, en torno al efecto moderador de factores socio-culturales como las relaciones familiares, el entretenimiento y la espiritualidad en dicho consumo...

  20. Zinc supplementation in children with cystic fibrosis

    Cystic fibrosis (CF) leads to malabsorption of macro- and micronutrients. Symptomatic zinc deficiency has been reported in CF but little is known about zinc homeostasis in children with CF. Zinc supplementation (Zn suppl) is increasingly common in children with CF but it is not without theoretcial r...

  1. 21 CFR 558.78 - Bacitracin zinc.


    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Bacitracin zinc. 558.78 Section 558.78 Food and... in Animal Feeds § 558.78 Bacitracin zinc. (a) Specifications. Type A medicated articles containing bacitracin zinc equivalent to 10, 25, 40, or 50 grams per pound bacitracin. (b) Approvals. See No. 046573...

  2. 21 CFR 582.5991 - Zinc oxide.


    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Zinc oxide. 582.5991 Section 582.5991 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... 1 § 582.5991 Zinc oxide. (a) Product. Zinc oxide. (b) Conditions of use. This substance is...

  3. 21 CFR 182.8991 - Zinc oxide.


    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Zinc oxide. 182.8991 Section 182.8991 Food and... CONSUMPTION (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients § 182.8991 Zinc oxide. (a) Product. Zinc oxide. (b) Conditions of use. This substance is generally recognized as safe when used...

  4. 21 CFR 73.2991 - Zinc oxide.


    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Zinc oxide. 73.2991 Section 73.2991 Food and Drugs... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2991 Zinc oxide. (a) Identity and specifications. The color additive zinc oxide shall conform in identity and specifications to the requirements of §...

  5. Zinc metalloproteins as medicinal targets.

    Anzellotti, A I; Farrell, N P


    Zinc bioinorganic chemistry has emphasized the role of the metal ion on the structure and function of the protein. There is, more recently, an increasing appreciation of the role of zinc proteins in a variety of human diseases. This critical review, aimed at both bioinorganic and medicinal chemists, shows how apparently widely-diverging diseases share the common mechanistic approaches of targeting the essential function of the metal ion to inhibit activity. Protein structure and function is briefly summarized in the context of its clinical relevance. The status of current and potential inhibitors is discussed along with the prospects for future developments (162 references).

  6. 粤北覆盖区复杂环境隐伏铅锌矿探测技术集成有效性研究%Effective research of detection technology integration in concealed lead-zinc mine under complex environment in covered area,north Guangdong

    陆一敢; 李学彪; 曾高福; 乔小芳; 敬荣中; 周奇明


    凡口铅锌矿是粤北地区超大型铅锌矿床,发育独特的覆盖区复杂地质环境。本文以凡口铅锌矿为例,在前人研究的基础上,应用高精度磁法、可控源音频大地电磁法、土壤电吸附、氡气、吸附烃-汞气体测量、及导电率等多种物化探勘查技术。通过对凡口矿床及外围进行对比分析和研究,建立凡口矿区有效探测技术集成,优选方法组合为高精度磁法、CSAMT、土壤吸附烃-汞气体及氡气测量,CSAMT中低阻异常、烃-汞正异常重叠区域、在构造有利部位是矿体的主要赋矿部位。结合矿区资料,预测在212剖面线(120~140)号间,宽度约700~800m,62剖面线(60~80)号间,宽度约800m 存在两处有利的赋矿异常,为凡口铅锌矿深部找矿预测研究提供切实可行的勘查技术与方法。%Fankou Pb-Zn ore deposit is a superscale lead-zinc deposit in northern area of Guangdong with cov-erage soil and unique complex geological environment.Taking Fankou Lead-zinc deposit for an example,it is based on the previous research for application of high precision magnetic method,controlled source audio fre-quency magnetotelluric method,soil electric adsorption,radon,adsorption hydrocarbon-mercury gas meas-urement,and the conductivity and other geophysical and geochemical exploration technology.The compara-tive analysis and research of Fankou lead-zinc ore deposit and its periphery area are carried out to establish ef-fective detection technology integration,optimization method for high precision magnetic method,CSAMT, soil adsorption hydrocarbon-mercury gas and radon measurement,CSAMT low resistance anomaly,hydro-carbon and mercury anomaly overlap region for that the construction site is the main advantage of orebody mine site.Based on these data,ore forecast along No.212 profile (120 ~ 140 dots)are carried out in the width of about 700~800 meters,while ore forecast along No.62 profile (60~80 dots)are also carried out in the width

  7. Anti-oxidant, in vitro, in vivo anti-inflammatory activity and antiproliferative activity of mefenamic acid and its metal complexes with manganese(II), cobalt(II), nickel(II), copper(II) and zinc(II).

    Kovala-Demertzi, Dimitra; Hadjipavlou-Litina, Dimitra; Staninska, Malgorzata; Primikiri, Alexandra; Kotoglou, Chronis; Demertzis, Mavroudis A


    Some new complexes of mefenamic acid with potentially interesting biological activity are described. The complexes of mefenamic acid [Mn(mef)(2)(H(2)O)(2)], 1, [Co(mef)(2)(H(2)O)(2)], 2, [Ni(mef)(2)(H(2)O)(2)], 3, [Cu(mef)(2)(H(2)O)](2), 4 and [Zn(mef)(2)], 5, were prepared by the reaction of mefenamic acid, a potent anti-inflammatory drug with metal salts. Optical and infrared spectral data of these new complexes are reported. Monomeric six-coordinated species were isolated in the solid state for Mn(II), Ni(II) and Co(II), dimeric five-coordinated for Cu(II) and monomeric four-coordinated for Zn(II). In DMF or CHCl(3) solution the coordination number is retained and the coordinated molecules of water are replaced by solvent molecules. The anti-oxidant properties of the complexes were evaluated using the 1,1-diphenyl-2-picrylhydrazyl, DPPH, free radical scavenging assay. The scavenging activities of the complexes were measured and compared with those of the free drug and vitamin C. We have explored their ability to inhibit soybean lipoxygenase, beta-glucuronidase and trypsin- induced proteolysis. The complex [Mn(mef)(2)(H(2)O)(2)] exhibits the highest antioxidant activity and the highest inhibitory effect against the soybean lipogygenase (LOX), properties that are not demonstrated by mefenamic acid. Their inhibitory effects on rat paw edema induced by Carrageenan was studied and compared with those of mefenamic acid. The complex [Zn(mef)(2)] exhibited a strong inhibitory effect at 0.1 mmol/Kg B.W. (81.5 +/- 1.3% inhibition), superior to the inhibition induced by mefenamic acid at the same dose (61.5 +/- 2.3% inhibition). Mefenamic acid and its metal complexes have been evaluated for antiproliferative activity in vitro against the cells of three human cancer cell lines: MCF-7 (human breast cancer cell line), T24 (bladder cancer cell line), A-549 (non-small cell lung carcinoma) and a mouse fibroblast L-929 cell line. The copper(II) complex displays against T24, MCF-7

  8. Effect of resveratrol and zinc on intracellular zinc status in normal human prostate epithelial cells

    To evaluate the influence of resveratrol on cellular zinc status, normal human prostate epithelial (NHPrE) cells were treated with 6 levels of resveratrol (0, 0.5, 1, 2.5, 5 and 10 microM) and 4 levels of zinc [0, 4, 16, and 32 microM for zinc-deficient (ZD), zinc-normal (ZN), zinc-adequate (ZA), an...

  9. Synthesis, characterization, X-ray crystal structures and antibacterial activities of Schiff base ligands derived from allylamine and their vanadium(IV), cobalt(III), nickel(II), copper(II), zinc(II) and palladium(II) complexes

    Amiri Rudbari, Hadi; Iravani, Mohammad Reza; Moazam, Vahid; Askari, Banafshe; Khorshidifard, Mahsa; Habibi, Neda; Bruno, Giuseppe


    A new Schiff base ligand, HL2, and four new Schiff base complexes, NiL12, PdL12, NiL22 and ZnL22, have been prepared and characterized by elemental analysis (CHN), FT-IR and UV-Vis spectroscopy. 1H and 13C NMR techniques were employed for characterization of the ligand (HL2) and the diamagnetic complexes (PdL12 and ZnL22). The molecular structures of PdL12, NiL22 and ZnL22 complexes were determined by the single crystal X-ray diffraction technique. The crystallographic data reveal that in these complexes the metal centers are four-coordinated by two phenolate oxygen and two imine nitrogen atoms of two Schiff base ligands. The geometry around the metal center in the PdL12 and NiL22 complexes is square-planar and for ZnL22 it is a distorted tetrahedral.In the end, five new (HL2, NiL12, PdL12, NiL22 and ZnL22) and six reported (HL1, VOL12, CoL13, CuL12, ZnL12 and Zn2L14) Schiff base compounds were tested for their in vitro antimicrobial activity against Staphylococcus aureus and Escherichia coli as examples of Gram-positive and Gram-negative bacterial strains, respectively, by disc diffusion method.

  10. Syntheses, electronic structures, and EPR/UV-vis-NIR spectroelectrochemistry of nickel(II), copper(II), and zinc(II) complexes with a tetradentate ligand based on S-methylisothiosemicarbazide.

    Arion, Vladimir B; Rapta, Peter; Telser, Joshua; Shova, Sergiu S; Breza, Martin; Luspai, Karol; Kozisek, Jozef


    Template condensation of 3,5-di-tert-butyl-2-hydroxybenzaldehyde S-methylisothiosemicarbazone with pentane-2,4-dione and triethyl orthoformate at elevated temperatures resulted in metal complexes of the type M(II)L, where M = Ni and Cu and H(2)L = a novel tetradentate ligand. These complexes are relevant to the active site of the copper enzymes galactose oxidase and glyoxal oxidase. Demetalation of Ni(II)L with gaseous hydrogen chloride in chloroform afforded the metal-free ligand H(2)L. Then by the reaction of H(2)L with Zn(CH(3)COO)(2)·2H(2)O in a 1:1 molar ratio in 1:2 chloroform/methanol, the complex Zn(II)L(CH(3)OH) was prepared. The three metal complexes and the prepared ligand were characterized by spectroscopic methods (IR, UV-vis, and NMR spectroscopy), X-ray crystallography, and DFT calculations. Electrochemically generated one-electron oxidized metal complexes [NiL](+), [CuL](+), and [ZnL(CH(3)OH)](+) and the metal-free ligand cation radical [H(2)L](+•) were studied by EPR/UV-vis-NIR and DFT calculations. These studies demonstrated the interaction between the metal ion and the phenoxyl radical.

  11. Spectroscopic characterization of copper(I) binding to apo and metal-reconstituted zinc finger peptides.

    Doku, Reginald T; Park, Grace; Wheeler, Korin E; Splan, Kathryn E


    Cu(I) exhibits high affinity for thiolate ligands, suggesting that thiol-rich zinc or iron binding sites may be subject to disruption during copper stress conditions. Zinc fingers constitute a large class of metalloproteins that use a combination of cysteine and histidine residues that bind Zn(II) as a structural element. Despite the shared preference of both copper and zinc for thiolate and amine coordination, the susceptibility of zinc finger domains toward copper substitution is not well studied. We report spectroscopic studies that characterize the Cu(I) binding properties of the zinc finger consensus peptides CP-CCHH, CP-CCHC, and CP-CCCC and the C-terminal zinc finger domain of HIV-1 nucleocapsid protein p7 (NCp7_C). Cu(I) binds to both the apopeptides and the Co(II)-substituted peptides, and the stoichiometry of Cu(I) binding is dependent on the number of cysteine thiols at the metal binding site. Fluorescence studies of the Zn(II)-NCp7_C complex indicate that Cu(I) also effectively competes with Zn(II) at the metal binding site, despite the high affinity of Zn(II) for the CCHC binding motif. Circular dichroism studies on both CP-CCHC and NCp7_C show that the conformations of the Cu(I)-bound complexes differ substantially from those of the Zn(II) species, implying that Cu(I) substitution is likely to impact zinc finger function. These results show that for the peptides studied here, Cu(I) is the thermodynamically favored metal despite the known high Zn(II) affinity of zinc finger domains, suggesting that Cu(I)-substituted zinc finger domains might be relevant in the context of both copper toxicity mechanisms and copper-responsive transcription factors.

  12. 热镀锌厂酸洗废水及锌灰中锌回收%Recovery of zinc from wastewater and zinc ash of zinc hot galvanizing plants

    许玉东; 孙燕如; 郑雪琴


    Steamed acid process, ammonia complexation process and sulphide precipitation process were conducted to investigate separation and recovery of zinc and iron from wastewater and zinc ash of zinc hot galvani- zing plants. Different HC1 evaporation characterization, zinc extracting effect with ammonia leaching process, and using the acidity of wastewater to leach out zinc ash and then separating zinc and iron from acid leaching so- lution by ammonia complexation were performed, respectively. Selective precipitation of zinc with Na2S from acid leaching solution based on product solubility was employed under different conditions of Na2S dosage, aeration time, pH value and reaction time. It is found that addition of sulphuric acid can slightly promote the evaporation of HC1. Ammonia complexation could hardly separate zinc from iron. On the contrary, sulphide precipitation can isolate zinc and iron effectively. Under the optimal conditions, the recovery rate of iron, the precipitation rate of zinc and the purity of ZnS can reach 97.12% , 99.99% and 68.51% , respectively.%分别采用蒸酸法、氨络合法和硫化沉淀法分离回收热镀锌厂酸洗废水及锌灰中锌铁。分别考察了酸洗废水中盐酸的逸出特性和氨浸法回收蒸馏渣中锌的效果;利用酸洗废水的酸度浸取锌灰中的锌并用氨络合法分离酸浸出液中锌铁;利用硫化物不同溶度积选择性沉淀酸浸出液中的锌,考察了Na2S加入量、曝气时间、反应溶液pH和反应时间的影响。研究结果表明硫酸的加入能提高盐酸的蒸发率但效果不明显,氨络合法难于有效分离锌铁,但硫化物沉淀法可较好地分离锌铁,铁回收率可达97.12%,锌沉淀率达到99.99%,所得沉淀物中ZnS纯度为68.51%。

  13. Cobalt(II), nickel(II), copper(II), and zinc(II) complexes with [3(5)]adamanzane, 1,5,9,13-tetraazabicyclo[7.7.3]nonadecane, and [(2.3)(2).2(1)] adamanzane, 1,5,9,12-tetraazabicyclo[7.5.2]hexadecane.

    Broge, L; Pretzmann, U; Jensen, N; Søtofte, I; Olsen, C E; Springborg, J


    Isolation of the free bicyclic tetraamine, [3(5)]adamanzane.H(2)O (1,5,9,13-tetraazabicyclo[7.7.3]nonadecane.H(2)O), is reported along with the synthesis and characterization of a copper(II) complex of the smaller macrocycle [(2.3)(2).2(1)]adamanzane (1,5,9,12-tetraazabicyclo[7.5.2]hexadecane) and of three cobalt(II), four nickel(II), one copper(II), and two zinc(II) complexes with [3(5)]adamanzane. For nine of these compounds (2-8, 10b, and 12) the single-crystal X-ray structures were determined. The coordination geometry around the metal ion is square pyramidal in [Cu([(2.3)(2).2(1)]adz)Br]ClO(4) (2) and trigonal bipyramidal in the isostructural structures [Cu([3(5)]adz)Br]Br (3), [Ni([3(5)]adz)Cl]Cl (5), [Ni([3(5)]adz)Br]Br (6), and [Co([3(5)]adz)Cl]Cl (8). In [Ni([3(5)]adz)(NO(3))]NO(3) (4) and [Ni([3(5)]adz)(ClO(4))]ClO(4) (7) the coordination geometry around nickel(II) is a distorted octahedron with the inorganic ligands at cis positions. The coordination polyhedron around the metal ion in [Co([3(5)]adz)][ZnCl(4)] (10b) and [Zn([3(5)]adz)][ZnCl(4)] (12) is a slightly distorted tetrahedron. Anation equilibrium constants were determined spectrophotometrically for complexes 2-6 at 25 and 40 degrees C and fall in the region 2-10 M(-1) for the halide complexes and 30-65 M(-1) for the nickel(II) nitrate complex (4). Rate constants for the dissociation of the macrocyclic ligand from the metal ions in 5 M HCl were determined for complexes 2, 3, 5, 8, 10, and 12. The reaction rates vary from half-lives at 40 degrees C of 14 min for the dissociation of the Zn([3(5)]adz)(2+) complex (12) to 14-15 months for the Ni([3(5)]adz)Cl(+) ion (5).

  14. Gamma-ray peak shapes from cadmium zinc telluride detectors

    Namboodiri, M.N.; Lavietes, A.D.; McQuaid, J.H.


    We report the results of a study of the peak shapes in the gamma spectra measured using several 5 x 5 x 5 mm{sup 3} cadmium zinc telluride (CZT) detectors. A simple parameterization involving a Gaussian and an exponential low energy tail describes the peak shapes sell. We present the variation of the parameters with gamma energy. This type of information is very useful in the analysis of complex gamma spectra consisting of many peaks.

  15. Zinc poisoning associated with separation anxiety in an Argentinean bulldog.

    Goicoa, A; Fidalgo, L E; Suárez, M L; Espino, L; Pérez-López, M; Santamarina, G


    Separation anxiety in dogs is a complex behavioral syndrome produced by many causes. A hunter 4y-old male Argentinean Bulldog had dental disturbances and gastrointestinal and cutaneous symptoms due to high plasma zinc and low copper and calcium plasma concentration. His behavior made him bite galvanized wire fences in his cage and bunk that contained his food, both of a Zn-containing material. Specific treatment resulted in complete recovery.

  16. Microwave Solid Phase Synthesis, Crystal Structure and Characterization of 3,5-Diiodosalicylaldehyde-Phenylamine-Zinc(Ⅱ) Complex%3,5-二碘水杨醛缩苯胺合锌(Ⅱ)配合物的微波固相合成、结构及表征

    徐锁平; 冯莉


    The title complex, 3 ,5-diiodosalicylaldehyde-phenylamine-zinc( Ⅱ ) has been designed and microwave solid phase synthesized by 3, 5-diiodosalicylaldehyde-phenylamine and zinc acetate. The structure was determined by IR spectra, elemental analysis and single X-ray crystallography. The title complex crystallizes in the monoclinic space group C2/c. Cell parameters; a = 2. 2287(2) nm, 6=1. 1699(4) nm, c=2.6065(3) nm, β =94. 579(3)°, V = 6.5667(12) nm3, Z=8, F(000) =3872, R [I> 2a (I) ] , R1, =0. 0547, wR2 = 0. 1316, S = 1. 024 The Zn( Ⅱ) adopts a distorted tetrahedral geometry, coordinated by two nitrogens and two oxygens from 3 ,5-diiodosalicylaldehyde-phenylamine.%采用微波固相法制备了3,5-二碘水杨醛缩苯胺合锌(Ⅱ)配合物,利用红外光谱、元素分析进行了表征,并利用单晶X射线衍射仪测定了该配合物的结构.结构解析表明,目标配合物为单斜晶系,C2/c空间群,晶胞参数a=2.2287(2) nm,b=1.1699(4) nm,c =2.6065(3) nm,β=94.579(3)°,V=6.5667(12) nm3,Z=8,F(000)=3872,最终偏差因子(对I>2σ(I)的衍射点),R1=0.0547,wR2 =0.1316,S=1.024.目标配合物结构中,中心Zn(Ⅱ)离子分别与来自两个3,5-二碘水杨醛缩苯胺的两个N原子和两个O原子配位,形成一个稍微扭曲的四面体.

  17. Dimerization of Human Growth Hormone by Zinc

    Cunningham, Brian C.; Mulkerrin, Michael G.; Wells, James A.


    Size-exclusion chromatography and sedimentation equilibrium studies demonstrated that zinc ion (Zn2+) induced the dimerization of human growth hormone (hGH). Scatchard analysis of 65Zn2+ binding to hGH showed that two Zn2+ ions associate per dimer of hGH in a cooperative fashion. Cobalt (II) can substitute for Zn2+ in the hormone dimer and gives a visible spectrum characteristic of cobalt coordinated in a tetrahedral fashion by oxygen- and nitrogen-containing ligands. Replacement of potential Zn2+ ligands (His18, His21, and Glu174) in hGH with alanine weakened both Zn2+ binding and hGH dimer formation. The Zn2+-hGH dimer was more stable than monomeric hGH to denaturation in guanidine-HCl. Formation of a Zn2+-hGH dimeric complex may be important for storage of hGH in secretory granules.

  18. Estudio de la influencia de la microestructura sobre la deformabilidad en caliente de un acero inoxidable dúplex

    Iza-Mendia, A.


    Full Text Available The complexity of the hot deformation behaviour of the ferrite and austenite in a duplex structure is increased as compared with that of single phase ferritic or austenitic steels. Important factors are: the spatial phase distribution with respect to the direction of the imposed deformation, the codeformation of both phases having considerably different mechanical properties, and the nature of the interface between austenite and ferrite. In the present study, the influence of these factors on the crack formation during the hot deformation is analyzed.

    El comportamiento frente al conformado en caliente de la ferrita y de la austenita, en una estructura dúplex, es muy diferente al que presentan ambas fases por separado en los aceros monofásicos austeníticos o ferríticos. A ello contribuyen, entre otros, la distribución espacial de las fases con respecto a la deformación impuesta, la codeformación de dos fases, con propiedades mecánicas muy diferentes, y la naturaleza de la intercara. En el presente trabajo se analiza la influencia de estos factores en la formación de daño bajo condiciones de deformación en caliente.

  19. Self-assembling chiral metallo-clefts; synthesis and molecular structure of N,N'-bis(12H-benzo[a]xanthen-12-ylidene)-1,2-ethanediamine zinc(II)-dichloride complex

    Barf, Tjeerd; Jansen, Johan F.G.A.; Bolhuis, Fré van; Spek, Anthony L.; Feringa, Bernard


    Bulky ligands for cleft-type metal complexes were synthesized from thio ketones and diamines in yields varying from 20–80%. A molecular structure determination of one ligand N,N'-bis(12H-benzo[a]-xanthen-12-ylidene)-1,2-propanediamine (19) was performed. A metallocleft was constructed by a self-asse




    Bulky ligands for cleft-type metal complexes were synthesized from thio ketones and diamines in yields varying from 20-80%. A molecular structure determination of one ligand N,N'-bis(12H-benzo[a]-xanthen-12-ylidene)-1,2-propanediamine (19) was performed. A metallo-cleft was constructed by a self-ass

  1. DNA binding and antiproliferative activity toward human carcinoma cells of copper(II) and zinc(II) complexes of a 2,5-diphenyl[1,3,4]oxadiazole derivative.

    Terenzi, Alessio; Fanelli, Mirco; Ambrosi, Gianluca; Amatori, Stefano; Fusi, Vieri; Giorgi, Luca; Turco Liveri, Vincenzo; Barone, Giampaolo


    The interaction of calf thymus DNA with [CuL(ClO(4))]ClO(4)·H(2)O (1) and [ZnLBr]Br·H(2)O (2) (L = 9,12,15,18,27,28-hexaaza-29-oxatetracyclo[,7).0(20,25)]enneicosa-2,4,6,20,22,24,26,28(1)-octaene) dicationic complexes in aqueous solution at neutral pH, was investigated by variable-temperature UV-vis absorption, circular dichroism and fluorescence spectroscopy. The values of the DNA-binding constants of these complexes, determined by competitive binding spectrofluorimetric titrations of ethidium bromide (EB)-DNA solutions, are (6.7 ± 0.5) × 10(6) M(-1) for CuL(2+) and (4.7 ± 0.5) × 10(5) M(-1) for ZnL(2+). These data together with a through analysis of the spectroscopic behaviour consistently suggest that both compounds are effective DNA binders. Interestingly, the DNA-binding strength of these complexes has been found to be correlated to their in vitro cytotoxic activity toward human breast carcinoma cells, although the complex with lower DNA-binding affinity is more active. In fact, biological studies showed that when the compounds are delivered through the cell membrane by a lipidic carrier, the cell survival is sensibly reduced, up to 58% with 1 and to 31% with 2.

  2. Zinc dyshomeostasis during polymicrobial sepsis in mice involves zinc transporter Zip14 and can be overcome by zinc supplementation.

    Wessels, Inga; Cousins, Robert J


    Integrity of the immune system is particularly dependent on the availability of zinc. Recent data suggest that zinc is involved in the development of sepsis, a life-threatening systemic inflammation with high death rates, but with limited therapeutic options. Altered cell zinc transport mechanisms could contribute to the inflammatory effects of sepsis. Zip14, a zinc importer induced by proinflammatory stimuli, could influence zinc metabolism during sepsis and serve as a target for therapy. Using cecal ligation-and-puncture (CLP) to model polymicrobial sepsis, we narrowed the function of ZIP14 to regulation of zinc homeostasis in hepatocytes, while hepatic leukocytes were mostly responsible for driving inflammation, as shown by higher expression of IL-1β, TNFα, S100A8, and matrix metalloproteinase-8. Using Zip14 knockout (KO) mice as a novel approach, we found that ablation of Zip14 produced a delay in development of leukocytosis, prevented zinc accumulation in the liver, altered the kinetics of hypozincemia, and drastically increased serum IL-6, TNFα, and IL-10 concentrations following CLP. Hence, this model revealed that the zinc transporter ZIP14 is a component of the pathway for zinc redistribution that contributes to zinc dyshomeostasis during polymicrobial sepsis. In contrast, using the identical CLP model, we found that supplemental dietary zinc reduced the severity of sepsis, as shown by amelioration of cytokines, calprotectins, and blood bacterial loads. We conclude that the zinc transporter ZIP14 influences aspects of the pathophysiology of nonlethal polymicrobial murine sepsis induced by CLP through zinc delivery. The results are promising for the use of zinc and its transporters as targets for future sepsis therapy.

  3. Pharmacokinetics of zinc tannate after intratesticular injection.

    Migally, N B; Fahim, M S


    Forty-eight sexually mature male rats were injected intratesticularly with either 1, 3, or 6 mg zinc tannate (Kastrin) or with saline (as control). Zinc localized only in low concentration in primary spermatocytes and could not be detected in spermatogonia, Sertoli cells, spermatids, or spermatozoa. Forty-eight hours after injection of 1 mg Kastrin, zinc was accumulated in the spermatogonia and primary spermatocytes while, after injection of 3 mg, zinc was preferentially localized in Sertoli cells and spermatids; however, zinc was observed in the spermatids and spermatozoa 48 h after injection with 6 mg, and germ cells lost their identity and were fragmented after 1 week.

  4. Non-Chromate Passivation of Zinc

    Tang, Peter Torben; Bech-Nielsen, G.


    . There is no known environmental or health risk involved using the treatments mentioned above. All components used in the baths are non toxic compared to Cr(VI). Alloy coatings such as zinc/nickel, zinc/cobalt, zinc/tin and all types of pure zinc coating (from cyanide, acidic or alkaline baths) have been treated...... minutes, in any one of the baths, at 60¢XC. Some movement of the submerged samples, or stirring with air-bubbles, should be applied, just as a thorough rinse of the zinc surface immediately before the pas-sivation is extremely important....

  5. Can N-acetyl-L-cysteine affect zinc metabolism when used as a paracetamol antidote?

    Brumas, V; Hacht, B; Filella, M; Berthon, G


    N-Acetyl-L-cysteine (NAC) has long been used in the treatment of chronic lung diseases. Inhalation and oral administration of the drug are both effective in reducing mucus viscosity. In addition, NAC oral therapy allows to restore normal mucoprotein secretion in the long term. Although displaying heavy metal-complexing potential, NAC exerts no detectable influence on the metabolism of essential trace metals when used in the above context (i.e. at doses near 600 mg day-1). However, this may no longer be the case when NAC is used as an oxygen radical scavenger, like in the treatment of paracetamol poisoning. In the latter case, intravenous doses as high as 20 g day-1 are administered, which may induce excessive zinc urinary excretion. In order to allow a better appreciation of the risk of zinc depletion during NAC therapy, the present work addresses the role of this drug towards zinc metabolism at the molecular level. First, formation constants for zinc-NAC complexes have been determined under physiological conditions. Then, computer simulations for blood plasma and gastrointestinal fluid have been run to assess the influence of NAC and its metabolites (e.g. cysteine and glutathione) on zinc excretion and absorption. Blood plasma simulations reveal that NAC can effectively mobilise an important fraction of zinc into urinary excretable complexes as from concentrations of 10(-3) mol dm-3 (which corresponds to a dose of about 800 mg). This effect can still be enhanced by the action of NAC metabolites, among which cysteine is the most powerful zinc sequestering agent. In contrast, simulations relative to gastrointestinal conditions suggest that NAC should tend to increase zinc absorption, regardless of its dose.

  6. Potential interaction between zinc ions and a cyclodextrin-based diclofenac formulation.

    Hamdan, Imad I; El-Sabawi, Dina; Abdel Jalil, Mariam


    Complexes of diclofenac sodium (DF-Na) with hydroxypropyl betacyclodextrin (HPβCD) were prepared by co-evaporation in a 1:1 ratio and characterized in light of previously reported data. Phase solubility diagrams were obtained for DF-Na with HPβCD in the presence and absence of zinc ions. Dissolution profiles were obtained for DF-Na and its HPβCD complex at acidic (pH 1.2) as well as in phosphate buffer (pH 6.8), in the presence and absence of zinc. HPβCD, as expected, was shown to improve the dissolution of DF-Na in acidic medium but not in phosphate buffer (pH 6.8). The presence of zinc ions decreased the in vitro dissolution of DF-HPβCD complex in acidic medium (pH 1.2) but not in phosphate buffer (pH 6.8). It was confirmed that the precipitate that was formed by zinc ions in the presence of HPβCD and DF-Na contained no cyclodextrin and most likely it was a mixture of the complexes: DF2-Zn and DF-Zn with some molecules of water. In vivo experiments on rats have shown that HPβCD has no statistically significant effect on absorption or bioavailability of DF-Na in spite of the observed improvement of its in vitro dissolution by HPβCD. Moreover, zinc ions were shown to decrease the absorption rate of DF-Na in rats model but did neither significantly alter the absorption nor bioavailability of DF-HPβCD complex. The zinc induced precipitates of DF were shown to have significantly different crystalline properties when HPβCD was present. Therefore, the pharmaceutical details of a DF-Na preparation should be considered when designing the formulation and predicting possible interaction between DF-Na (or other potential NSAIDs) and zinc metal.

  7. Formazanate Ligands as Structurally Versatile, Redox-Active Analogues of beta-Diketiminates in Zinc Chemistry

    Chang, Mu-Chieh; Roewen, Peter; Travieso-Puente, Raquel; Lutz, Martin; Otten, Edwin


    A range of tetrahedral bis(formazanate)zinc complexes with different steric and electronic properties of the formazanate ligands were synthesized. The solid-state structures for several of these were determined by X-ray crystallography, which showed that complexes with symmetrical, unhindered ligand

  8. Effect of calcium, copper, and zinc levels in a rapeseed meal diet on mineral and trace element utilization in the rat.

    Larsen, T; Sandström, B


    Mineral and trace element interactions were studied in a balance trial with rats. Calcium, copper, and zinc were supplied to a rapeseed meal diet in a factorial design. Animals were fed ad libitum, and absorption, excretion, and retention of the elements were evaluated either as fractions of total intake or in relation to nitrogen retention to account for differences in food intake and lean body mass increment. The intrinsic content of minerals and trace elements was sufficient to support growth at a rate that could be expected from the rapeseed protein quality. However, when calcium was included in the diet, the intrinsic dietary level of zinc appeared to be limiting, despite the fact that the zinc level was twice the recommended level. Additional zinc supply reversed growth impairment. This calcium-zinc interaction is believed to be owing to the formation of phytate complexes. Calcium addition influenced the calcium, phosphorus, magnesium, zinc, and iron--but not the copper--balances. The addition of calcium reduced the availability of the intrinsic zinc, whereas no effect was seen in the zinc-fortified groups. The availability of intrinsic copper was in a similar way significantly impaired by addition of dietary zinc, whereas copper-supplied groups were unaffected by zinc addition. Intrinsic iron availability was also dependent upon zinc addition, although in a more ambiguous way. Thus, addition of extrinsic minerals to a diet high in phytate can result in significant impairments of growth and mineral utilization.

  9. Binding of zinc and iron to wheat bread, wheat bran, and their components.

    Ismail-Beigi, F; Faraji, B; Reinhold, J G


    Wholemeal wheat bread decreases the availability and intestinal absorption of divalent metals. To define this action further, binding of zinc in vitro to a wheat wholemeal bread (Tanok), dephytinized Tanok, and cellulose was determined at pH 5.0 to 7.5. Zinc binding by each was highly pH-dependent and reached a maximum at pH 6.5 to 7.5. Removal of phytate from Tanok did not reduce its binding capability. Wheat bran at pH 6.5 and 6.8 bound 72% of iron (0.5 microgram/ml of solution) and 82.5% of zinc (1.43 microgram/ml solution), respectively. Lignin and two of the hemicellulose fractions of wheat bran and high binding capabilities for zinc (85.6, 87.1, and 82.1%, respectively) whereas a third had a lower zinc-binding capability (38.7%). Binding of zinc to various celluloses and dextrans is also demonstrated. Formation of complexes of these metals with wheat fiber can explain, at least in part, the decreased availability of dietary iron and zinc in wholemeal wheat bread.

  10. Palladium-Catalyzed α-Arylation of Zinc Enolates of Esters: Reaction Conditions and Substrate Scope

    Hama, Takuo; Ge, Shaozhong; Hartwig, John F.


    The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc enolates of esters is reported. Reactions of three different types of zinc enolates have been developed. α-Arylation of esters occurs in high yields with isolated Reformatsky reagents, with Reformatsky reagents generated from α-bromo esters and activated zinc, and with zinc enolates generated by quenching lithium enolates of esters with zinc chloride. The use of zinc enolates, instead of alkali metal enolates, greatly expands the scope of the arylation of esters. The reactions occur at room temperature or at 70 °C with bromoarenes containing cyano, nitro, ester, keto, fluoro, enolizable hydrogen, hydroxyl or amino functionality and with bromopyridines. The scope of esters encompasses acyclic acetates, propionates, and isobutyrates, α-alkoxyesters, and lactones. The arylation of zinc enolates of esters was conducted with catalysts bearing the hindered pentaphenylferrocenyl di-tert-butylphosphine (Q-phos) or the highly reactive dimeric Pd(I) complex {[P(t-Bu)3]PdBr}2. PMID:23931445

  11. Replacement of reserves zinc based on the recycling of technogenic raw materials

    Olga Sergeevna Bryantseva


    Full Text Available In the article, the perspective trends of the expansion of the mineral-ore base of the Russian producers of zinc by recycling of technogenic raw materials are considered. The important role of recycling of resources for sustainable development of society and improve the environmental safety is justified. The main structural and dynamic characteristics of the use of mineral resource base for the production of zinc in Russia are considered. Raw materials opportunities and constraints for the development of zinc production are analyzed. In the paper, the structure and dynamics of the use of recycled materials by the largest producer of zinc in Russia are investigated. The methodical approach to the estimation of effectiveness of the industrial processing of technogenic metallurgical raw materials with the strategic flexibility of the implementation of projects is proposed and approved. The estimation of the effectiveness of a complex industrial processing of metallurgical zinc-containing dusts in a real production is carried out. The value of the strategic flexibility of the project of the industrial processing of the zinc-containing technogenic raw material is determined on the basis of the developed systematic approach. The value of the processes of recycling for sustainable production of zinc in Russia is revealed.

  12. Zinc Status Affects Glucose Homeostasis and Insulin Secretion in Patients with Thalassemia

    Ellen B. Fung


    Full Text Available Up to 20% of adult patients with Thalassemia major (Thal live with diabetes, while 30% may be zinc deficient. The objective of this study was to explore the relationship between zinc status, impaired glucose tolerance and insulin sensitivity in Thal patients. Charts from thirty subjects (16 male, 27.8 ± 9.1 years with Thal were reviewed. Patients with low serum zinc had significantly lower fasting insulin, insulinogenic and oral disposition indexes (all p < 0.05 and elevated glucose response curve, following a standard 75 g oral load of glucose compared to those with normal serum zinc after controlling for baseline (group × time interaction p = 0.048. Longitudinal data in five patients with a decline in serum zinc over a two year follow up period (−19.0 ± 9.6 μg/dL, showed consistent increases in fasting glucose (3.6 ± 3.2 mg/dL and insulin to glucose ratios at 120 min post glucose dose (p = 0.05. Taken together, these data suggest that the frequently present zinc deficiency in Thal patients is associated with decreased insulin secretion and reduced glucose disposal. Future zinc trials will require modeling of oral glucose tolerance test data and not simply measurement of static indices in order to understand the complexities of pancreatic function in the Thal patient.

  13. Zinc Transfer Kinetics of Metallothioneins and Their Fragmentswith Apo-carbonic Anhydrase

    HUANG, Zhong-Xian; LIU, Fang; ZHENG, Qi; YU, Wen-Hao


    Tne zinc transfer reactions from Zn7-MT-I, Zn7-MT-Ⅱ, Zn4α fragment (MT-I) and Zn4-α fragment (MT-Ⅱ) to apo-carbonic anhydrase have been studied. In each reaction, no more than one zinc ion per molecule is involved in metal transfer.Zn7-MT-I and Zn7-MT-Ⅱ donate zinc to apo-carbonic anhydrase and de novo constitute it at a comparable efficiency,while Zn7-MT-Ⅱ exhibits a little faster rate. Surprisingiy,Zinc is released from Zn4-α fragment (MT-Ⅱ) with a much faster rate than from Zn4-α fragment (MT-I), whose rate is close to that of Zn7-MT-I. The reason for the difference is still unknown. Introducing complex compounds into this system may give rise to an effect on the reaction. The transfer from Zn7-MT-Ⅱ in the presence of reduced glutathione shows little difference compare to the control, suggesting that the reduced glutathione is not involved in zinc transfer process. However,glutathione disulfide does accelerate this zinc transfer reaction remarkably, indicating that the oxidative factors contribute to zinc rlease from metallothioneins.

  14. Palladium-catalyzed α-arylation of zinc enolates of esters: reaction conditions and substrate scope.

    Hama, Takuo; Ge, Shaozhong; Hartwig, John F


    The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides with zinc enolates of esters is reported. Reactions of three different types of zinc enolates have been developed. α-Arylation of esters occurs in high yields with isolated Reformatsky reagents, with Reformatsky reagents generated from α-bromo esters and activated zinc, and with zinc enolates generated by quenching alkali metal enolates of esters with zinc chloride. The use of zinc enolates, instead of alkali metal enolates, greatly expands the scope of the arylation of esters. The reactions occur at room temperature or at 70 °C with bromoarenes containing cyano, nitro, ester, keto, fluoro, enolizable hydrogen, hydroxyl, or amino functionality and with bromopyridines. The scope of esters encompasses acyclic acetates, propionates, and isobutyrates, α-alkoxyesters, and lactones. The arylation of zinc enolates of esters was conducted with catalysts bearing the hindered pentaphenylferrocenyl di-tert-butylphosphine (Q-phos) or the highly reactive dimeric Pd(I) complex {[P(t-Bu)3]PdBr}2.

  15. Zinc leaching from tire crumb rubber.

    Rhodes, Emily P; Ren, Zhiyong; Mays, David C


    Because tires contain approximately 1-2% zinc by weight, zinc leaching is an environmental concern associated with civil engineering applications of tire crumb rubber. An assessment of zinc leaching data from 14 studies in the published literature indicates that increasing zinc leaching is associated with lower pH and longer leaching times, but the data display a wide range of zinc concentrations, and do not address the effect of crumb rubber size or the dynamics of zinc leaching during flow through porous crumb rubber. The present study was undertaken to investigate the effect of crumb rubber size using the synthetic precipitation leaching procedure (SPLP), the effect of exposure time using quiescent batch leaching tests, and the dynamics of zinc leaching using column tests. Results indicate that zinc leaching from tire crumb rubber increases with smaller crumb rubber and longer exposure time. Results from SPLP and quiescent batch leaching tests are interpreted with a single-parameter leaching model that predicts a constant rate of zinc leaching up to 96 h. Breakthrough curves from column tests displayed an initial pulse of elevated zinc concentration (~3 mg/L) before settling down to a steady-state value (~0.2 mg/L), and were modeled with the software package HYDRUS-1D. Washing crumb rubber reduces this initial pulse but does not change the steady-state value. No leaching experiment significantly reduced the reservoir of zinc in the crumb rubber.

  16. Dinuclear complexes of copper and zinc with m-xylene/cyclohexane-linked bis-aspartic acids: synthesis, characterization, dioxygen activation, and catalytic oxidation of nitrobenzene in pure aqueous solution.

    Zhu, Shourong; Qiu, Zhixiang; Ni, Tianjun; Zhao, Xiujuan; Yan, Shikai; Xing, Feifei; Zhao, Yongmei; Bai, Yueling; Li, Mingxing


    Two new m-xylene/cyclohexane-linked bis-aspartic acid ligands, L(b) and L(c), were synthesized via Michael addition in basic aqueous solution. Their structures were characterized by elemental analysis, NMR and MS spectrometry. Both ligands react with Cu(II) and Zn(II) to form dinuclear complexes, with M2L(OH)(-) the major species in neutral/weak basic aqueous solution. To quantify the relative interaction strength between a Lewis acid and base, a new parameter σ = log K/14 was proposed which compares the stability constant with the binding constant between H(+) and OH(-). The dinuclear copper complexes (L(b)-2Cu and L(c)-2Cu) react with H2O2 in aqueous solution. The reaction in 0.020 M phosphate buffer at pH 7.5 is first-order for [L(c)-2Cu], but second-order for [L(b)-2Cu]. The oxidation products are oxygenated and/or dehydrogenated species. Radical trapping tests indicate that both complexes slightly scavenge the OH˙ radical, but generate the H˙ radical. L(c)-2Cu generates the H˙ radical much more effectively than that of L(b)-2Cu when reacted with H2O2. Both complexes are excellent catalysts for the oxidation of nitrobenzene in the presence of H2O2 in weakly basic aqueous solution. The oxidation follows the rate-law v = k[complex][nitrobenzene][H2O2]. The k values in pH 8.0 phosphate buffer at 25 °C are 211.2 ± 0.3 and 607.9 ± 1.7 mol(-2) L(2) s(-1) for L(b)-2Cu and L(c)-2Cu, respectively. The Arrhenius activation energies are 69.4 ± 2.2 and 70.0 ± 4.3 kJ mol(-1) for L(b)-2Cu and L(c)-2Cu, respectively, while the Arrhenius pre-exponential factors are 2.62 × 10(14) and 1.06 × 10(15), respectively. The larger pre-exponential factor makes L(c)-2Cu more catalytically active than L(b)-2Cu. These complexes are some of the most effective oxidation catalysts known for the oxidation of nitrobenzene.

  17. Non-Chromate Passivation of Zinc

    Tang, Peter Torben; Bech-Nielsen, G.


    . There is no known environmental or health risk involved using the treatments mentioned above. All components used in the baths are non toxic compared to Cr(VI). Alloy coatings such as zinc/nickel, zinc/cobalt, zinc/tin and all types of pure zinc coating (from cyanide, acidic or alkaline baths) have been treated...... successfully. The corrosion resistance against white rust on zinc and zinc alloys is just as good as that of yellow chromate, although the result de-pends on the corrosion test method as well as on the nature of the zinc substrate pas-sivated. The passivation procedure is simply a dip for approxi-mately 2...

  18. Zinc Therapy in Dermatology: A Review

    Mrinal Gupta


    Full Text Available Zinc, both in elemental or in its salt forms, has been used as a therapeutic modality for centuries. Topical preparations like zinc oxide, calamine, or zinc pyrithione have been in use as photoprotecting, soothing agents or as active ingredient of antidandruff shampoos. Its use has expanded manifold over the years for a number of dermatological conditions including infections (leishmaniasis, warts, inflammatory dermatoses (acne vulgaris, rosacea, pigmentary disorders (melasma, and neoplasias (basal cell carcinoma. Although the role of oral zinc is well-established in human zinc deficiency syndromes including acrodermatitis enteropathica, it is only in recent years that importance of zinc as a micronutrient essential for infant growth and development has been recognized. The paper reviews various dermatological uses of zinc.

  19. Zinc-The key to preventing corrosion

    Kropschot, S.J.; Doebrich, Jeff L.


    Centuries before it was identified as an element, zinc was used to make brass (an alloy of zinc and copper) and for medicinal purposes. Metallic zinc and zinc oxide were produced in India sometime between the 11th and 14th centuries and in China in the 17th century, although the discovery of pure metallic zinc is credited to the German chemist Andreas Marggraf, who isolated the element in 1746. Refined zinc metal is bluish-white when freshly cast; it is hard and brittle at most temperatures and has relatively low melting and boiling points. Zinc alloys readily with other metals and is chemically active. On exposure to air, it develops a thin gray oxide film (patina), which inhibits deeper oxidation (corrosion) of the metal. The metal's resistance to corrosion is an important characteristic in its use.


    Lemes, Igor José Mendes; Silva, Jessica Lorrany; Batelo, Everton A Pimentel; Silveira, Ricardo Azoubel da Mota


    Resumo. O resfriamento nao uniforme de perfis metalicos durante o processo de fabricação gera um estado de tensoes residuais na secao transversal. Codigos normativos descrevem a distribuicao dessas tensoes de formas diferentes. Este trabalho visa investigar numericamente a influencia desses modelos no comportamento de secoes transversais de aco I isoladas e mistas atraves das curvas: rigidez `a flexao-momento fletor, relacao momento-curvatura e curvas de interacao (in´ıcio de plastificacao e ...