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Sample records for monocarboxylate-functionalized cyanine dyes

  1. Optoelectronic properties of natural cyanin dyes.

    Science.gov (United States)

    Calzolari, A; Varsano, D; Ruini, A; Catellani, A; Tel-Vered, R; Yildiz, H B; Ovits, O; Willner, I

    2009-07-30

    An integrated theoretical/experimental study of the natural cyanin dye is presented in terms of its structural and optoelectronic properties for different gas-phase and prototypical device configurations. Our microscopic analysis reveals the impact of hydration and hydroxylation reactions, as well as of the attached sugar, on ground and optically excited states, and it illustrates the visible-light harvesting capability of the dye. Our optical experiments at different and controlled pH concentrations allow for a direct comparison with theoretical results. We analyze the many different contributions to photocurrent of the various portions of a prototypical device and, as a proof of principle, we propose the addition of specific ligands to control the increase of the photocurrent yield in the cyanin-based electrochemical device.

  2. Cyanine-like dyes with large bond-length alternation.

    Science.gov (United States)

    Thorley, Karl J; Hales, Joel M; Kim, Hyeongeu; Ohira, Shino; Brédas, Jean-Luc; Perry, Joseph W; Anderson, Harry L

    2013-07-29

    Herein, the synthesis and properties of alkyne-bridged carbocations, which are analogous in structure to cyanine dyes, are reported. An alkene-bridged dye, linked at the third position of the indole, was also synthesized as a reference compound. These new carbocations are stable under ambient conditions, allowing characterization by UV/Vis and NMR ((1)H and (13)C) spectroscopies. These techniques revealed a large degree of delocalization of the positive charge, similar to a previously reported porphyrin carbocation. The linear and nonlinear optical properties are compared with cyanine dyes and triarylmethyl cations, to investigate the effects of the bond-length alternation and the overall molecular geometry. The value of Re(γ), the real part of the third-order microscopic polarizability, of -1.3×10(-33)  esu for the alkyne-linked cation is comparable to that of a cyanine dye of similar length. Nondegenerate two-photon absorption spectra showed that the alkene-bridged dye exhibited characteristics of cyanines, whereas the alkyne-bridged dye is reminiscent of octupolar chromophores, such as the triarylmethyl carbocation brilliant green. Such attributes were confirmed and rationalized by quantum chemical calculations.

  3. On the nature of excited electronic states in cyanine dyes: implications for visual pigment spectra

    Science.gov (United States)

    Dinur, Uri; Honig, Barry; Schulten, Klaus

    1980-06-01

    CNDO/S CI calculations are carried out on polyenes and on cyanine dyes. In contrast to polyenes, doubly excited configurations have a strong effect on the first optically allowed excited state in cyanines. Protonated Schiff bases of retinal are closely related to cyanine dyes, with important consequences for models of visual pigment spectra and photochemistry.

  4. Cyanine dyes in solid state organic heterojunction solar cells

    Science.gov (United States)

    Heier, Jakob; Peng, Chuyao; Véron, Anna C.; Hany, Roland; Geiger, Thomas; Nüesch, Frank A.; Vismara, Marcus V. G.; Graeff, Carlos F. O.

    2014-10-01

    Today numerous cyanine dyes that are soluble in organic solvents are available, driven by more than a century of research and development of the photographic industry. Several properties specific to cyanine dyes suggest that this material class can be of interest for organic solar cell applications. The main absorption wavelength can be tuned from the ultra-violet to the near-infrared. The unparalleled high absorption coefficients allow using very thin films for harvesting the solar photons. Furthermore, cyanines are cationic polymethine dyes, offering the possibility to modify the materials by defining the counteranion. We here show specifically how counterions can be utilized to tune the bulk morphology when blended with fullerenes. We compare the performance of bilayer heterojunction and bulk heterojunction solar cells for two different dyes absorbing in the visible and the near-infrared. Light-induced Electron Spin Resonance (LESR) was used to study the charge transfers of light induced excitons between cyanine dyes and the archetype fullerene C60. LESR results show good correlation with the cell performance.

  5. Protein purification by aminosquarylium cyanine dye-affinity chromatography.

    Science.gov (United States)

    Silva, M S; Graça, V C; Reis, L V; Santos, P F; Almeida, P; Queiroz, J A; Sousa, F

    2013-12-01

    The most selective purification method for proteins and other biomolecules is affinity chromatography. This method is based on the unique biological-based specificity of the biomolecule-ligand interaction and commonly uses biological ligands. However, these ligands may present some drawbacks, mainly because of their cost and lability. Dye-affinity chromatography overcomes the limitations of biological ligands and is widely used owing to the low cost of synthetic dyes and to their resistance to biological and chemical degradation. In this work, immobilized aminosquarylium cyanine dyes are used in order to exploit affinity interactions with standard proteins such as lysozyme, α-chymotrypsin and trypsin. These studies evaluate the affinity interactions occurring between the immobilized ligand and the different proteins, as a reflection of the sum of several molecular interactions, namely ionic, hydrophobic and van der Waals, spread throughout the structure, in a defined spatial manner. The results show the possibility of using an aminosquarylium cyanine dye bearing a N-hexyl pendant chain, with a ligand density of 1.8 × 10(-2) mmol of dye/g of chromatographic support, to isolate lysozyme, α-chymotrypsin and trypsin from a mixture. The application of a decreasing ammonium sulfate gradient resulted in the recovery of lysozyme in the flowthrough. On the other hand, α-chymotrypsin and trypsin were retained, involving different interactions with the ligand. In conclusion, this study demonstrates the potential applicability of ligands such as aminosquarylium cyanine dyes for the separation and purification of proteins by affinity chromatography.

  6. Syntheses and absorption-structure relationships of some new photosensitizer cyanine dyes

    Indian Academy of Sciences (India)

    H A Shindy; A I M Koraiem

    2002-04-01

    New biheterocyclic compound was synthesized as starting material to prepare new photosensitizers mono-, tri-, substituted tri-, azadimethine and mixed cyanine dyes. Absorption-structure relationship of the synthesized cyanine dyes were determined by studying their electronic spectral behaviour in ethanol. The structure of the compounds were identified by elemental analysis, IR and 1H NMR spectral data.

  7. Two-photon excited photoconversion of cyanine-based dyes

    Science.gov (United States)

    Kwok, Sheldon J. J.; Choi, Myunghwan; Bhayana, Brijesh; Zhang, Xueli; Ran, Chongzhao; Yun, Seok-Hyun

    2016-03-01

    The advent of phototransformable fluorescent proteins has led to significant advances in optical imaging, including the unambiguous tracking of cells over large spatiotemporal scales. However, these proteins typically require activating light in the UV-blue spectrum, which limits their in vivo applicability due to poor light penetration and associated phototoxicity on cells and tissue. We report that cyanine-based, organic dyes can be efficiently photoconverted by nonlinear excitation at the near infrared (NIR) window. Photoconversion likely involves singlet-oxygen mediated photochemical cleavage, yielding blue-shifted fluorescent products. Using SYTO62, a biocompatible and cell-permeable dye, we demonstrate photoconversion in a variety of cell lines, including depth-resolved labeling of cells in 3D culture. Two-photon photoconversion of cyanine-based dyes offer several advantages over existing photoconvertible proteins, including use of minimally toxic NIR light, labeling without need for genetic intervention, rapid kinetics, remote subsurface targeting, and long persistence of photoconverted signal. These findings are expected to be useful for applications involving rapid labeling of cells deep in tissue.

  8. Cyanine dyes in biophysical research: the photophysics of polymethine fluorescent dyes in biomolecular environments.

    Science.gov (United States)

    Levitus, Marcia; Ranjit, Suman

    2011-02-01

    The breakthroughs in single molecule spectroscopy of the last decade and the recent advances in super resolution microscopy have boosted the popularity of cyanine dyes in biophysical research. These applications have motivated the investigation of the reactions and relaxation processes that cyanines undergo in their electronically excited states. Studies show that the triplet state is a key intermediate in the photochemical reactions that limit the photostability of cyanine dyes. The removal of oxygen greatly reduces photobleaching, but induces rapid intensity fluctuations (blinking). The existence of non-fluorescent states lasting from milliseconds to seconds was early identified as a limitation in single-molecule spectroscopy and a potential source of artifacts. Recent studies demonstrate that a combination of oxidizing and reducing agents is the most efficient way of guaranteeing that the ground state is recovered rapidly and efficiently. Thiol-containing reducing agents have been identified as the source of long-lived dark states in some cyanines that can be photochemically switched back to the emissive state. The mechanism of this process is the reversible addition of the thiol-containing compound to a double bond in the polymethine chain resulting in a non-fluorescent molecule. This process can be reverted by irradiation at shorter wavelengths. Another mechanism that leads to non-fluorescent states in cyanine dyes is cis-trans isomerization from the singlet-excited state. This process, which competes with fluorescence, involves the rotation of one-half of the molecule with respect to the other with an efficiency that depends strongly on steric effects. The efficiency of fluorescence of most cyanine dyes has been shown to depend dramatically on their molecular environment within the biomolecule. For example, the fluorescence quantum yield of Cy3 linked covalently to DNA depends on the type of linkage used for attachment, DNA sequence and secondary structure

  9. Enhanced Photostability of Genetically Encodable Fluoromodules Based on Fluorogenic Cyanine Dyes and a Promiscuous Protein Partner

    OpenAIRE

    Shank, Nathaniel I.; Zanotti, Kimberly J.; Lanni, Frederick; Berget, Peter B.; Armitage, Bruce A.

    2009-01-01

    Fluoromodules are discrete complexes of biomolecules and fluorogenic dyes. Binding of the dyes to their cognate biomolecule partners results in enhanced dye fluorescence. We exploited a previously reported promiscuous binding interaction between a single chain, variable fragment antibody protein and a family of cyanine dyes to create new protein-dye fluoromodules that exhibit enhanced photostability while retaining high affinity protein-dye binding. Modifications to the dye structure included...

  10. Sequence-dependent fluorescence of cyanine dyes on microarrays.

    Science.gov (United States)

    Agbavwe, Christy; Somoza, Mark M

    2011-01-01

    Cy3 and Cy5 are among the most commonly used oligonucleotide labeling molecules. Studies of nucleic acid structure and dynamics use these dyes, and they are ubiquitous in microarray experiments. They are sensitive to their environment and have higher quantum yield when bound to DNA. The fluorescent intensity of terminal cyanine dyes is also known to be significantly dependent on the base sequence of the oligonucleotide. We have developed a very precise and high-throughput method to evaluate the sequence dependence of oligonucleotide labeling dyes using microarrays and have applied the method to Cy3 and Cy5. We used light-directed in-situ synthesis of terminally-labeled microarrays to determine the fluorescence intensity of each dye on all 1024 possible 5'-labeled 5-mers. Their intensity is sensitive to all five bases. Their fluorescence is higher with 5' guanines, and adenines in subsequent positions. Cytosine suppresses fluorescence. Intensity falls by half over the range of all 5-mers for Cy3, and two-thirds for Cy5. Labeling with 5'-biotin-streptavidin-Cy3/-Cy5 gives a completely different sequence dependence and greatly reduces fluorescence compared with direct terminal labeling.

  11. Sequence-dependent fluorescence of cyanine dyes on microarrays.

    Directory of Open Access Journals (Sweden)

    Christy Agbavwe

    Full Text Available Cy3 and Cy5 are among the most commonly used oligonucleotide labeling molecules. Studies of nucleic acid structure and dynamics use these dyes, and they are ubiquitous in microarray experiments. They are sensitive to their environment and have higher quantum yield when bound to DNA. The fluorescent intensity of terminal cyanine dyes is also known to be significantly dependent on the base sequence of the oligonucleotide. We have developed a very precise and high-throughput method to evaluate the sequence dependence of oligonucleotide labeling dyes using microarrays and have applied the method to Cy3 and Cy5. We used light-directed in-situ synthesis of terminally-labeled microarrays to determine the fluorescence intensity of each dye on all 1024 possible 5'-labeled 5-mers. Their intensity is sensitive to all five bases. Their fluorescence is higher with 5' guanines, and adenines in subsequent positions. Cytosine suppresses fluorescence. Intensity falls by half over the range of all 5-mers for Cy3, and two-thirds for Cy5. Labeling with 5'-biotin-streptavidin-Cy3/-Cy5 gives a completely different sequence dependence and greatly reduces fluorescence compared with direct terminal labeling.

  12. Combination of Cyanine Behaviour and Giant Hyperpolarisability in Novel Merocyanine Dyes: Beyond the Bond Length Alternation (BLA) Paradigm.

    Science.gov (United States)

    Parthasarathy, Venkatakrishnan; Pandey, Ravindra; Stolte, Matthias; Ghosh, Sampa; Castet, Frédéric; Würthner, Frank; Das, Puspendu Kumar; Blanchard-Desce, Mireille

    2015-09-28

    Merocyanine dyes that exhibit antithetic cyanine-like behaviour and giant first-order hyperpolarisability (β) values have been designed. These cyanine-type dyes open up an intriguing route towards molecular-based electro-optic materials as well as new second-harmonic generation dyes for imaging.

  13. Doping Evolution and Junction Formation in Stacked Cyanine Dye Light-Emitting Electrochemical Cells.

    Science.gov (United States)

    Jenatsch, Sandra; Wang, Lei; Bulloni, Matia; Véron, Anna C; Ruhstaller, Beat; Altazin, Stéphane; Nüesch, Frank; Hany, Roland

    2016-03-01

    Cyanine dyes are fluorescent organic salts with intrinsic conductivity for ionic and electronic charges. Recently ( J. Am. Chem. Soc. 2013 , 135 , 18008 - 18011 ), these features have been exploited in cyanine light-emitting electrochemical cells (LECs). Here, we demonstrate that stacked, constant-voltage driven trimethine cyanine LECs with various counteranions develop a p-i-n junction that is composed of p- and n-doped zones and an intrinsic region where light-emission occurs. We introduce a method that combines spectral photocurrent response measurements with optical modeling and find that at maximum current the intrinsic region is centered at ∼37% away from the anode. Transient capacitance, photoluminescence and attenuance experiments indicate a device situation with a narrow p-doped region, an undoped region that occupies ∼72% of the dye layer thickness and an n-doped region with a maximum doping concentration of 0.08 dopant/cyanine molecule. Finally, we observe that during device relaxation the parent cyanines are not reformed. We ascribe this to irreversible reactions between doped cyanine radicals. For sterically conservative cyanine dyes, this suggests that undesired radical decomposition pathways limit the LEC long-term stability in general.

  14. Key Structural Elements of Unsymmetrical Cyanine Dyes for Highly Sensitive Fluorescence Turn-On DNA Probes.

    Science.gov (United States)

    Uno, Kakishi; Sasaki, Taeko; Sugimoto, Nagisa; Ito, Hideto; Nishihara, Taishi; Hagihara, Shinya; Higashiyama, Tetsuya; Sasaki, Narie; Sato, Yoshikatsu; Itami, Kenichiro

    2017-01-17

    Unsymmetrical cyanine dyes, such as thiazole orange, are useful for the detection of nucleic acids with fluorescence because they dramatically enhance the fluorescence upon binding to nucleic acids. Herein, we synthesized a series of unsymmetrical cyanine dyes and evaluated their fluorescence properties. A systematic structure-property relationship study has revealed that the dialkylamino group at the 2-position of quinoline in a series of unsymmetrical cyanine dyes plays a critical role in the fluorescence enhancement. Four newly designed unsymmetrical cyanine dyes showed negligible intrinsic fluorescence in the free state and strong fluorescence upon binding to double-stranded DNA (dsDNA) with a quantum yield of 0.53 to 0.90, which is 2 to 3 times higher than previous unsymmetrical cyanine dyes. A detailed analysis of the fluorescence lifetime revealed that the dialkylamino group at the 2-position of quinoline suppressed nonradiative decay in favor of increased fluorescence quantum yield. Moreover, these newly developed dyes were able to stain the nucleus specifically in fixed HeLa cells examined by using a confocal laser-scanning microscope.

  15. Symmetrical and asymmetrical cyanine dyes. Synthesis, spectral properties, and BSA association study.

    Science.gov (United States)

    Pisoni, Diego S; Todeschini, Letícia; Borges, Antonio César A; Petzhold, Cesar L; Rodembusch, Fabiano S; Campo, Leandra F

    2014-06-20

    New cyanines were prepared by an efficient and practical route with satisfactory overall yield from low-cost starting materials. The photophysical behavior of the cyanines was investigated using UV-vis and steady-state fluorescence in solution, as well as their association with bovine serum albumin (BSA) in phosphate buffer solution (PBS). No cyanine aggregation was observed in organic solvents or in phosphate buffer solution. The alkyl chain length in the quaternized nitrogen was shown to be fundamental for BSA detection in PBS in these dyes.

  16. Highly efficient cyanine dyes used for nanocrystalline TiO2 electrode sensitization

    Science.gov (United States)

    Meng, Fanshun; Ren, Yanjie; Gao, Enqin; Cai, Shengmin; Chen, Kongchang; Tian, He

    2002-02-01

    With the development made by Graetzel et al on solar cell, the studies on dye-sensitized nanocrystalline TiO2 solar cell have been widely investigated. Here we synthesized four cyanine dyes containing carboxyl group. The absorption spectra and fluorescent spectra of the dyes in solution and in adsorbed state on the surface semiconductor were measured. These dyes have high absorption coefficient (~10 5M-1 cm-1), which is a major factor that affects the conversion efficiency of the solar cell. These cyanine dyes were used to sensitize nanocrystalline TiO2, and the photoelectrochemical properties of the electrodes sensitized by these cyanine dyes were measured. From the absorption spectra of the electrode it can be seen that these dyes have been efficiently adsorbed on nanocrystalline TiO2. The maximum IPCE values of dye CY-1, CY-2, CY-3 and CY-4 were 42%, 51.8%, 75.9% and 22.2% respectively. The results show that cyanine dye derivatives are promising sensitizers for nanocrystalline solar cell.

  17. Benz[c,d]indolium-containing Monomethine Cyanine Dyes: Synthesis and Photophysical Properties

    OpenAIRE

    Eduardo Soriano; Cory Holder; Andrew Levitz; Maged Henary

    2015-01-01

    Asymmetric monomethine cyanines have been extensively used as probes for nucleic acids among other biological systems. Herein we report the synthesis of seven monomethine cyanine dyes that have been successfully prepared with various heterocyclic moieties such as quinoline, benzoxazole, benzothiazole, dimethyl indole, and benz[e]indole adjoining benz[c,d]indol-1-ium, which was found to directly influence their optical and energy profiles. In this study the optical properties vs. structural ch...

  18. Spectroscopic Investigation on the Interaction of a Cyanine Dye with Serum Albumins

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ya-Zhou; YANG Qian-Fan; DU Hong-Yan; TANG Ya-Lin; XU Guang-Zhi; YAN Wen-Peng

    2008-01-01

    The interactions of a cyanine dye with human serum albumin (HSA) and bovine serum albumin (BSA) have been investigated by using absorption and fluorescence spectra.Absorption spectral studies show that binding to the serum albumins leads to a bathochromic shift of the monomer band together with a notable intensity change.Furthermore, the number of binding sites (n) was identified by the absorption spectra.There is a constant enhancement of fluorescence quantum yield when the cyanine dye complexes with HSA or BSA.The apparent binding constant (Ka) and the free energy changes (△G) were obtained by analysis of fluorescence data of the cyanine dye in the absence and presence of HSA and BSA.Compared to BSA, HSA associates with the dye in a stronger way.

  19. Explorations of the application of cyanine dyes for quantitative alpha-synuclein detection

    NARCIS (Netherlands)

    Volkova, K.D.; Kovalska, V.B.; Segers-Nolten, Gezina M.J.; Veldhuis, G.; Veldhuis, G.J.; Subramaniam, Vinod; Yarmoluk, S.M.

    2009-01-01

    We examined the practical aspects of using fluorescent mono (T-284) and trimethinecyanine (SH-516) dyes for detecting and quantifying fibrillar α-synuclein (ASN). We studied the interaction of cyanine dyes with fibrillar proteins using fluorescence spectroscopy and atomic force microscopy. The comme

  20. Synthesis and physicochemical studies of some new quinolinoxazine pentamethine cyanine dyes

    Directory of Open Access Journals (Sweden)

    R.M. Abd El-Aal

    2017-01-01

    Full Text Available Polymethine cyanine dyes belong to a well-known class of organic compounds, which have been used in photography and as information storage in laser technology. A series of novel cyanine dyes were synthesized through the formylation of quinolinium[b,c]1,4-oxazine-chloride salt 1. Reaction of compound 2-chloro-3-formyl-quinolinium[b,c]1,4-oxazine-chloride salt 2 with different molar ratios of 2(4-methyl substituted heterocyclic in basic catalysis afforded the corresponding 2-chloroquinolinium[b,c]1,4-oxazine-chloride salt-3[2(4]-dimethine (3a–c, quinolinium[b,c]-1,4-oxazinechloride salt-2,3[2(4]-pentamethine (4a–c and quinolino[b,c]1,4-oxazine-6yl[2(4]-monomethine-/2,3[2(4]-pentamethine cyanine dyes (5a–c respectively. The structure of the dyes was characterized by elemental analysis, visible absorption, fluorescence emission, IR, 1H-NMR and mass spectroscopy. The correlations between the structure and properties of these dyes have been studied. A comparison of the visible absorption maxima between compounds 3b, 4b and 5b showed that asymmetrical mono-pentamethine cyanine dye 5b reveals a bathochromic shift than both dimethine 3b and pentamethine cyanine dyes 4b. This could be attributed to the more extensive π-conjugation and increasing number of methine groups in asymmetric pentamethine. All the observations and analytical spectra in this paper support the syntheses of new di-, penta- and mono-/pentamethine cyanine dyes. The absorption spectra of dyes were investigated in organic solvents. The results indicated that the excitation for their colour is a simple charge-transfer from oxygen atom of oxazine nucleus and/or nitrogen atom of pyridine (quinoline nucleus to N-quaternary salts in di-, penta- and mono-/pentamethine cyanine dyes respectively. These dyes showed positive solvatochromism with increased solvent polarity, which depends on the structure and the type of dye.

  1. A new class of cyanine-like dyes with large bond-length alternation.

    Science.gov (United States)

    Ohira, Shino; Hales, Joel M; Thorley, Karl J; Anderson, Harry L; Perry, Joseph W; Brédas, Jean-Luc

    2009-05-06

    Cyanines, which represent a class of charged chromophores with an odd number of pi-conjugated carbons, display unique electronic and optical properties attributed to the strong electronic delocalization and the absence of any significant carbon-carbon bond-length alternation (BLA) along their backbones. The flatness of the corresponding electronic potential makes cyanine dyes the compounds to which simple free-electron theory can be applied in the most relevant way. Recently, cations of porphyrin dimers linked by a pi-conjugated bridge with an odd number of carbons and presenting alternating single and triple bonds were shown to possess linear and nonlinear optical properties analogous to those of cyanines. Here, by using a joint theoretical and experimental approach, we demonstrate the correspondence between cyanines and the new class of alkyne carbocations, in spite of their marked difference in BLA.

  2. Optimization of Cyanine Dye Stability and Analysis of FRET Interaction on DNA Microarrays.

    Science.gov (United States)

    von der Haar, Marcel; Heuer, Christopher; Pähler, Martin; von der Haar, Kathrin; Lindner, Patrick; Scheper, Thomas; Stahl, Frank

    2016-11-30

    The application of DNA microarrays for high throughput analysis of genetic regulation is often limited by the fluorophores used as markers. The implementation of multi-scan techniques is limited by the fluorophores' susceptibility to photobleaching when exposed to the scanner laser light. This paper presents combined mechanical and chemical strategies which enhance the photostability of cyanine 3 and cyanine 5 as part of solid state DNA microarrays. These strategies are based on scanning the microarrays while the hybridized DNA is still in an aqueous solution with the presence of a reductive/oxidative system (ROXS). Furthermore, the experimental setup allows for the analysis and eventual normalization of Förster-resonance-energy-transfer (FRET) interaction of cyanine-3/cyanine-5 dye combinations on the microarray. These findings constitute a step towards standardization of microarray experiments and analysis and may help to increase the comparability of microarray experiment results between labs.

  3. Optimization of Cyanine Dye Stability and Analysis of FRET Interaction on DNA Microarrays

    Directory of Open Access Journals (Sweden)

    Marcel von der Haar

    2016-11-01

    Full Text Available The application of DNA microarrays for high throughput analysis of genetic regulation is often limited by the fluorophores used as markers. The implementation of multi-scan techniques is limited by the fluorophores’ susceptibility to photobleaching when exposed to the scanner laser light. This paper presents combined mechanical and chemical strategies which enhance the photostability of cyanine 3 and cyanine 5 as part of solid state DNA microarrays. These strategies are based on scanning the microarrays while the hybridized DNA is still in an aqueous solution with the presence of a reductive/oxidative system (ROXS. Furthermore, the experimental setup allows for the analysis and eventual normalization of Förster-resonance-energy-transfer (FRET interaction of cyanine-3/cyanine-5 dye combinations on the microarray. These findings constitute a step towards standardization of microarray experiments and analysis and may help to increase the comparability of microarray experiment results between labs.

  4. A comparative study of the photosensitizing characteristics of some cyanine dyes.

    Science.gov (United States)

    Delaey, E; van Laar, F; De Vos, D; Kamuhabwa, A; Jacobs, P; de Witte, P

    2000-03-01

    The present work has been carried out to explore the potential application of cyanines in photodynamic therapy. After photosensitization, the in vitro cytotoxic and antiproliferative activity on HeLa cells of a total of 35 cyanines belonging to several chemical subgroups is explored. Most of these cyanines have never been used before in similar experimental work. From a first set of experiments, it is found that none of the krypto-, oxa- and imidacyanines is photobiologically active on HeLa cells. Conversely, five thiacyanines (Thiacl-5), one rhodacyanine (Rhodac) and four indocyanines (Indoc2, Indoc4, Indoc5, Indoc7) show photodependent cytotoxicity or antiproliferative effects. A more detailed study shows that out of the ten selected compounds, eight cyanines feature significant photodependent cytotoxic and antiproliferative effects. All possess maximum absorption ranges between 545 and 824 nm. In particular, Rhodac, a tetramethinemeromonomethine rhodacyanine dye with an absorption maximum of 655 nm (ethanol) and a molar absorption coefficient epsilon = 108000 shows very promising photo-dependent biological activity. In general, the measured singlet oxygen quantum yield of the selected cyanines is low (cyanines with a partition coefficient close to 1.5 accumulate to the highest extent in HeLa cells, while the more hydrophobic compounds (e.g., indocyanines) concentrate less intracellularly.

  5. Cationic cyanine dyes: impact of symmetry-breaking on optical absorption and third-order polarizabilities.

    Science.gov (United States)

    Yesudas, Kada

    2013-11-28

    A systematic study is carried out to find the exact crossover point from symmetric to asymmetric configurations (symmetry-breaking) in a series of cationic cyanine dyes. Hybrid density functional with varying exact-exchange admixture has been used to understand the impact of HF exchange both in the gas phase and in the presence of dielectric medium. This approach provides a basis for understanding the electronic structure and photophysical properties of cyanine dyes. The crossover points predicted using this method are in good agreement with the experiment. The SAC-CI method is used to evaluate the lowest S0 → S1 transition energies in the gas phase. These transitions are preferably dominated by the promotion of an electron from HOMO → LUMO. The average static third-order polarizabilities, [γ], are obtained within the three-state model approximation. The analysis showed that for symmetric cyanines, the calculated [γ] values are large and negative, mainly originated from the large S0 → S1 transition moments and small S0 → S1 transition energies. For asymmetric cyanines, the [γ] values are positive and mainly originate from the large change in the ground and first excited state dipole moments. However, both configurations do not include contributions from the two-photon absorption. Further, the localization of charge densities in the HOMO and LUMO indicates that the symmetric and asymmetric cyanines act as promising materials for molecular wires and molecular switches which are fundamental building blocks for molecular electronic devices.

  6. Specific fluorescent detection of fibrillar alpha-synuclein using mono- and trimethine cyanine dyes.

    Science.gov (United States)

    Volkova, K D; Kovalska, V B; Balanda, A O; Losytskyy, M Yu; Golub, A G; Vermeij, R J; Subramaniam, V; Tolmachev, O I; Yarmoluk, S M

    2008-02-01

    With the aim of searching of novel amyloid-specific fluorescent probes the ability of series of mono- and trimethine cyanines based on benzothiazole, pyridine and quinoline heterocycle end groups to recognize fibrillar formations of alpha-synuclein (ASN) was studied. For the first time it was revealed that monomethine cyanines can specifically increase their fluorescence in aggregated ASN presence. Dialkylamino-substituted monomethine cyanine T-284 and meso-ethyl-substituted trimethine cyanine SH-516 demonstrated the higher emission intensity and selectivity to aggregated ASN than classic amyloid stain Thioflavin T, and could be proposed as novel efficient fluorescent probes for fibrillar ASN detection. Studies of structure-function dependences have shown that incorporation of amino- or diethylamino- substituents into the 6-position of the benzothiazole heterocycle yields in a appearance of a selective fluorescent response to fibrillar alpha-synuclein presence. Performed calculations of molecular dimensions of studied cyanine dyes gave us the possibility to presume, that dyes bind with their long axes parallel to the fibril axis via insertion into the neat rows (so called 'channels') running along fibril.

  7. Linear Dichroism of Cyanine Dyes in Stretched Polyvinyl Alcohol Films: A Physical Chemistry Laboratory Experiment.

    Science.gov (United States)

    Natarajan, L. V.; And Others

    1983-01-01

    Provides background information, procedures, and results of an undergraduate physical chemistry experiment on the polarization of absorption spectra of cyanine dyes in stretched polyvinyl alcohol films. The experiment gives a simple demonstration of the concept of linear dichromism and the validity of the TEM method used in the analyses. (JN)

  8. Fast Optical Switching Using Oriented Cyanine Dye-Doped Nematic Liquid Crystal

    Institute of Scientific and Technical Information of China (English)

    JIN Zhao-Hui; LI Zhong-Yu; KASATANI Kazuo; OKAMOTO Hiroaki

    2006-01-01

    @@ A cyanine dye, 2-[7-(1,3-dihydro-1,3,3-trimethyl-2H-indol-2-ylidene)-1,3,5-heptatrienyl]-1,3,3-trimethy1-3H-indolium iodide (NK-125), is doped in 4-cyano-4'-pentylbiphenyl (5 CB), and the mixture is sandwiched between two pieces of rubbed glass plates.

  9. Linear Dichroism of Cyanine Dyes in Stretched Polyvinyl Alcohol Films: A Physical Chemistry Laboratory Experiment.

    Science.gov (United States)

    Natarajan, L. V.; And Others

    1983-01-01

    Provides background information, procedures, and results of an undergraduate physical chemistry experiment on the polarization of absorption spectra of cyanine dyes in stretched polyvinyl alcohol films. The experiment gives a simple demonstration of the concept of linear dichromism and the validity of the TEM method used in the analyses. (JN)

  10. 6,6 '-Disubstituted benzothiazole trimethine cyanines - new fluorescent dyes for DNA detection

    Science.gov (United States)

    Kovalska, Vladyslava B.; Volkova, Kateryna D.; Losytskyy, Mykhaylo Yu.; Tolmachev, Olexiy I.; Balanda, Anatoliy O.; Yarmoluk, Sergiy M.

    2006-10-01

    The influence of methyl-, 2-hydroxyethyl-, dimethyl-, diethyl- and benzoyl-amino substituents in the 6,6'-positions of benzothiazole heterocycle of trimethine cyanines on their spectral-luminescent properties and behavior in presence of DNA, RNA and BSA was studied. It was shown that incorporation of 6,6'-substituents generally leads to the increase in dyes tendency to aggregation, resulting in the considerable decrease in the emission intensity of the disubstituted dyes as compared to the unsubstituted ones. Emission of the studied 6,6'-disubstited dyes in DNA presence is considerably more intensive than in presence of RNA, that points on the existing of DNA binding preference for the mentioned dyes. Insertion of benzoyl-amino groups into the 6,6'-positions permitted us to design the DNA-sensitive dyes on the basis of symmetric trimethine cyanines with unsubstituted polymethine chain, while typically such dyes slightly respond on the presence of biopolymers. 6,6'-Benzoyl-amino-disubstituted trimethine cyanines are proposed as efficient dyes for DNA detection.

  11. 6,6'-Disubstituted benzothiazole trimethine cyanines--new fluorescent dyes for DNA detection.

    Science.gov (United States)

    Kovalska, Vladyslava B; Volkova, Kateryna D; Losytskyy, Mykhaylo Yu; Tolmachev, Olexiy I; Balanda, Anatoliy O; Yarmoluk, Sergiy M

    2006-10-01

    The influence of methyl-, 2-hydroxyethyl-, dimethyl-, diethyl- and benzoyl-amino substituents in the 6,6'-positions of benzothiazole heterocycle of trimethine cyanines on their spectral-luminescent properties and behavior in presence of DNA, RNA and BSA was studied. It was shown that incorporation of 6,6'-substituents generally leads to the increase in dyes tendency to aggregation, resulting in the considerable decrease in the emission intensity of the disubstituted dyes as compared to the unsubstituted ones. Emission of the studied 6,6'-disubstited dyes in DNA presence is considerably more intensive than in presence of RNA, that points on the existing of DNA binding preference for the mentioned dyes. Insertion of benzoyl-amino groups into the 6,6'-positions permitted us to design the DNA-sensitive dyes on the basis of symmetric trimethine cyanines with unsubstituted polymethine chain, while typically such dyes slightly respond on the presence of biopolymers. 6,6'-Benzoyl-amino-disubstituted trimethine cyanines are proposed as efficient dyes for DNA detection.

  12. Accessing Structurally Diverse Near-Infrared Cyanine Dyes for Folate Receptor-Targeted Cancer Cell Staining.

    Science.gov (United States)

    König, Sandra G; Krämer, Roland

    2017-03-24

    Folate receptor (FR) targeting is one of the most promising strategies for the development of small-molecule based cancer imaging agents since the FR is highly overexpressed on the surface of many cancer cell types. FR-targeted conjugates of NIR emissive cyanine dyes are in advanced clinical trials for fluorescence-guided surgery and are valuable research tools for optical molecular imaging in animal models. Only a small number of promising conjugates has been evaluated so far. Analysis of structure-performance relations to identify critical factors modulating the performance of targeted conjugates is essential for successful further optimization. This contribution addresses the need for convenient synthetic access to structurally diverse NIR-emissive cyanine dyes for conjugation with folic acid. Structural variations were introduced to readily available cyanine precursors in particular via C-C-coupling reactions including Suzuki- and (for the first time with these types of dyes) Sonogashira cross couplings. Photophysical properties such as absorbance maxima, brightness, and photostability are highly dependent on the molecular structure. Selected modified cyanines were conjugated to folic acid for cancer cell targeting. Several conjugates display a favorable combination of high fluorescence brightness and photostability with high affinity to FR positive cancer cells, and enable the selective imaging of these cells with low background.

  13. Dynamics of the higher lying excited states of cyanine dyes. An ultrafast fluorescence study.

    Science.gov (United States)

    Guarin, Cesar A; Villabona-Monsalve, Juan P; López-Arteaga, Rafael; Peon, Jorge

    2013-06-20

    The electronic relaxation dynamics of the second singlet excited states of several cyanine dyes was studied through the femtosecond fluorescence up-conversion technique. Our interest in these molecules comes from the potential applications of systems with upper excited singlet states with a long lifetime, which can include electron and energy transfer from the higher lying singlets after one- or two-photon absorption. We studied three series of cyanines with 4-quinolyl, 2-quinolyl, or benzothiazolyl type end groups, each with varying sp(2) carbon conjugation lengths in the methinic bridge. The dynamics after electronic excitation to singlet states above the fluorescent state vary significantly as a function of cyanine structure and conjugation length. In particular, for the 4-quinolyl series the cyanine with an intermediate conjugation length (three methinic carbons) has the slowest S2 decays with lifetimes of 5.4 ps in ethanol and 6.6 ps in ethylene glycol. On the other hand, we observed that the 2-quinolyl family has S2 decay times in the subpicosecond range independent of the conjugation length between the end groups. The slowest internal conversion was observed for the benzothiazolyl type cyanine with five methinic carbons, with an S2 lifetime of 17.3 ps in ethanol. For the planar cyanines of this study we observed for the first time a clear systematic trend in the S2 decay times which closely follow the energy gap law. It was also demonstrated that a slow S2 decay is as well observed upon excitation through degenerate two-photon absorption with near-IR pulses. The present study isolates the most important variables for the design of cyanines with long S2 lifetimes.

  14. Benz[c,d]indolium-containing Monomethine Cyanine Dyes: Synthesis and Photophysical Properties.

    Science.gov (United States)

    Soriano, Eduardo; Holder, Cory; Levitz, Andrew; Henary, Maged

    2015-12-24

    Asymmetric monomethine cyanines have been extensively used as probes for nucleic acids among other biological systems. Herein we report the synthesis of seven monomethine cyanine dyes that have been successfully prepared with various heterocyclic moieties such as quinoline, benzoxazole, benzothiazole, dimethyl indole, and benz[e]indole adjoining benz[c,d]indol-1-ium, which was found to directly influence their optical and energy profiles. In this study the optical properties vs. structural changes were investigated using nuclear magnetic resonance and computational approaches. The twisted conformation unique to monomethine cyanines was exploited in DNA binding studies where the newly designed sensor displayed an increase in fluorescence when bound in the DNA grooves compared to the unbound form.

  15. Benz[c,d]indolium-containing Monomethine Cyanine Dyes: Synthesis and Photophysical Properties

    Directory of Open Access Journals (Sweden)

    Eduardo Soriano

    2015-12-01

    Full Text Available Asymmetric monomethine cyanines have been extensively used as probes for nucleic acids among other biological systems. Herein we report the synthesis of seven monomethine cyanine dyes that have been successfully prepared with various heterocyclic moieties such as quinoline, benzoxazole, benzothiazole, dimethyl indole, and benz[e]indole adjoining benz[c,d]indol-1-ium, which was found to directly influence their optical and energy profiles. In this study the optical properties vs. structural changes were investigated using nuclear magnetic resonance and computational approaches. The twisted conformation unique to monomethine cyanines was exploited in DNA binding studies where the newly designed sensor displayed an increase in fluorescence when bound in the DNA grooves compared to the unbound form.

  16. Halogenated pentamethine cyanine dyes exhibiting high fidelity for G-quadruplex DNA.

    Science.gov (United States)

    Nanjunda, Rupesh; Owens, Eric A; Mickelson, Leah; Alyabyev, Sergey; Kilpatrick, Nancy; Wang, Siming; Henary, Maged; Wilson, W David

    2012-12-15

    Design and optimization of quadruplex-specific small molecules is developing into an attractive strategy for anti-cancer therapeutics with some promising candidates in clinical trials. A number of therapeutically favorable features of cyanine molecules can be effectively exploited to develop them as promising quadruplex-targeting agents. Herein, the design, synthesis and evaluation of a series of dimethylindolenine cyanine dyes with varying halogen substitutions are reported. Their interactions with telomeric and c-myc quadruplexes as well as a reference duplex sequence have been evaluated using thermal melting, biosensor-surface plasmon resonance, circular dichroism, isothermal titration calorimetry and mass spectrometry. Thermal melting analysis indicates that these ligands exhibit significant quadruplex stabilization and a very low duplex binding, with the dimethyl incorporation of paramount importance for decreased duplex affinity. Circular dichroism studies showed that the interaction of cyanines with quadruplex structures are primarily through stacking at one or both ends of the terminal tetrads with the two (trimethylammonium)propyl groups interacting in the accessible quadruplex grooves. Surface plasmon resonance and mass spectral studies shows the formation of an initial strong 1:1 complex followed by a significantly weaker secondary binding. Isothermal calorimetry studies show that the interaction of cyanines is predominantly entropy driven. In line with the design principles, this work provides new insights for further developing potent, highly selective cyanines as promising quadruplex-specific agents.

  17. Trimethine cyanine dyes as fluorescent probes for amyloid fibrils: The effect of N,N'-substituents.

    Science.gov (United States)

    Kuperman, Marina V; Chernii, Svitlana V; Losytskyy, Mykhaylo Yu; Kryvorotenko, Dmytro V; Derevyanko, Nadiya O; Slominskii, Yurii L; Kovalska, Vladyslava B; Yarmoluk, Sergiy M

    2015-09-01

    The effect of various N,N'-substituents in the molecule of benzothiazole trimethine cyanine dye on its ability to sense the amyloid aggregates of protein was studied. The dyes are low fluorescent when free and in the presence of monomeric proteins, but their emission intensity sharply increases in complexes with aggregated insulin and lysozyme, with the fluorescence quantum yield reaching up to 0.42. The dyes carrying butyl, hydroxyalkyl, and phenylalkyl groups as N,N'-substituents possess the increased fluorescent sensitivity to fibrillar lysozyme, whereas the ones carrying quaternary amino groups are preferably sensitive to fibrillar insulin. This fluorescent sensitivity preference provided by the N,N'-functional groups could be explained by the interaction between these groups and protein side chains. The strongest fluorescent response (up to 70times) and the same sensitivity to aggregates of both proteins were exhibited by the dye D-51 carrying N-sulfoalkyl group. The studied cyanines allow the detection of fibrillar aggregates in the wide range up to 0.8 to 300μg/ml and permit monitoring the protein aggregation kinetics with high reproducibility. The modification of trimethine cyanine dyes by functional substituents in N,N'-positions is suggested as a tool for the design of fluorescent molecules with the enhanced fluorescent sensitivity to the fibrillar aggregates of proteins.

  18. Photophysical investigations of squaraine and cyanine dyes and their interaction with bovine serum albumin

    Science.gov (United States)

    Saikiran, M.; Sato, D.; Pandey, S. S.; Kato, T.

    2016-04-01

    A model far-red sensitive symmetrical squaraine dye (SQ-3) and unsymmetrical near infra-red sensitive cyanine dye (UCD-1) bearing direct-COOH functionalized indole ring were synthesized, characterized and subjected to photophysical investigations including their interaction with bovine serum albumin (BSA) as a model protein in phosphate buffer solution (PBS). Both of the dyes exhibit strong interaction with BSA in phosphate buffer with high apparent binding constant. A judicious tuning of hydrophobic main backbone with reactive functionality for associative interaction with active site of BSA has been found to be necessary for BSA detection in PBS.

  19. Spectroscopic studies of thiatri-, penta- and heptamethine cyanine dyes II. Infrared and resonance Raman spectra of thiatri-, penta- and heptamethine cyanine dyes

    Science.gov (United States)

    Fujimoto, Yasuhiko; Katayama, Norihisa; Ozaki, Yukihiro; Yasui, Shigeo; Iriyama, Keiji

    1992-11-01

    Infrared (IR) and resonance Raman (RR) spectra of thiatri-, penta- and heptamethine cyanine dyes in the solid state and in solution have been measured. Most of the intense bands observed in the 1600-1100 cm -1 region of the RR spectra may be assigned to totally symmetric stretching modes of the central conjugated system of the cyanines, while most of the strong IR bands in the 1600-1300 cm -1 region are probably due to antisymmetric stretching modes. The intense RR bands do not have their counterparts in the IR spectra and vice versa. A pseudo-mutual exclusion rule seems to be operative for the cyanine vibrational spectra in the 1600-1300 cm -1 region, indicating that the central conjugated systems of the cyanines have nearly symmetrical structure, i.e. the extended all-trans forms of the methine chains and the bond orders of 1.5 of the CC and CN bonds in both the solution and solid states. The IR spectra of 3-ethyl-2-[3-(3-ethyl-2-benzothiazolinylidene)-1-propenyl]benzothiazolium iodide (NK-76) and 3-ethyl-2-[7-(3-ethyl-2-benzothiazolinylidene)-1,3,5-heptatrienyl]benzothiazolium iodide (NK-126) change little between the solid and solution states while those of 3-octadecyl-2-[3-(3-octadecyl-2-benzothiazolinylidene)-1-propenyl]benzothiazolium iodide (NK-2560) and 3-octadecyl-2-[7-(3-octadecyl-2-benzothiazolinylidene)-1,3,5-heptatrienyl]benzothiazolium perchlorate (NK-2861) alter significantly between the two states in the frequencies of bands due to the stretching modes of their central conjugated systems. The results suggest that the electronic states of the central conjugated systems of NK-2560 and NK-2861 undergo appreciable changes on going from the solid to the solution states.

  20. Study on the Synthesis and Spectra of a Novel Kind of Carbozole Benzothiazole Indole Styryl Cyanine Dye with a Carbazole Bridged Chain.

    Science.gov (United States)

    Fei, Xuening; Hao, Yachao; Gu, Yingchun; Li, Chao; Yu, Lu

    2014-03-01

    Based on the frequently-used cyanine dye probe thiazole orange (TO) and Cy3, a novel kind of styryl cyanine dye was designed and synthesized. Carbazole was inserted into the structures of two cyanine dyes, TO and Cy3, to act as a bridge to link the benzothiazole and indole. This modification resulted in a novel kind of carbozole benzothiazole indole cyanine dye with a carbazole-bridged chain. The dyes were characterized by HNMR and MS. The spectra of the novel dyes were also studied and the results showed that the fluorescence wavelength of novel carbazole benzothiazole indole cyanine dye shifted red, the Stokes shift and Fluorescence quantum yields increased and the fluorescence intensity was enhanced compared to that of TO. These results indicated that the novel dye could be used as an excellent fluorescent probe in biological labeling.

  1. Single molecule fluorescence fluctuations of the cyanine dyes linked covalently to DNA

    Institute of Scientific and Technical Information of China (English)

    AUMILER; Damir

    2009-01-01

    The intersystem crossing and isomerization dynamics of free-Cy3,Cy3-ssDNA,free-Cy5 and Cy5-ssDNA are obtained through simple analysis of rapid on/off blinking from single molecule fluorescence intensity time-traces and the fluorescence correlation spectroscopy(FCS).The on-and off-times observed in fluorescence time traces of single cyanine dyes are due to the formation of the triplet state and isomerization,where both the interaction with DNA and long central polymethine chain of cyanine dyes increase the barriers of isomerization,leading to long off-time.The results indicate that the single molecule fluorescence fluctuation together with the resulting second autocorrelation analysis are powerful methods for determining the triplet state and isomerization dynamics,which could be the simple techniques and complementary to other spectroscopic techniques,such as fluorescence decay measurement and laser flash photolysis to study the photophysical processes of complex molecules.

  2. Spectral Fine Tuning of Cyanine Dyes: Electron Donor-Acceptor Substituted Analogues of Thiazole Orange†

    Science.gov (United States)

    Rastede, Elizabeth E.; Tanha, Matteus; Yaron, David; Watkins, Simon C.; Waggoner, Alan S.; Armitage, Bruce A.

    2015-01-01

    The introduction of electron donor and acceptor groups at strategic locations on a fluorogenic cyanine dye allows fine-tuning of the absorption and emission spectra while preserving the ability of the dye to bind to biomolecular hosts such as double-stranded DNA and a single-chain antibody fragment originally selected for binding to the parent unsubstituted dye, thiazole orange (TO). The observed spectral shifts are consistent with calculated HOMO-LUMO energy gaps and reflect electron density localization on the quinoline half of TO in the LUMO. A dye bearing donating methoxy and withdrawing trifluoromethyl groups on the benzothiazole and quinoline rings, respectively, shifts the absorption spectrum to sufficiently longer wavelengths to allow excitation at green wavelengths as opposed to the parent dye, which is optimally excited in the blue. PMID:26171668

  3. Modulation of Mitochondriotropic Properties of Cyanine Dyes by in Organello Copper-Free Click Reaction.

    Science.gov (United States)

    Negwer, Inka; Hirsch, Markus; Kaloyanova, Stefka; Brown, Tom; Peneva, Kalina; Butt, Hans-Jürgen; Koynov, Kaloian; Helm, Mark

    2017-09-19

    Cyanine (Cy) dyes show a general propensity to localize in polarized mitochondria. This mitochondriotropism was used to perform a copper-free click reaction in the mitochondria of living cells. The in organello reaction of dyes Cy3 and Cy5 led to a product that was easily traceable by Förster resonance energy transfer (FRET). As determined by confocal laser scanning microscopy, the Cy3-Cy5 conjugate showed enhanced retention in mitochondria, relative to that of the starting compounds. This enhancement of a favorable property can be achieved by synthesis in organello, but not outside mitochondria. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Aggregation behavior of novel heptamethine cyanine dyes upon their binding to native and fibrillar lysozyme.

    Science.gov (United States)

    Vus, Kateryna; Tarabara, Ulyana; Kurutos, Atanas; Ryzhova, Olga; Gorbenko, Galyna; Trusova, Valeriya; Gadjev, Nikolai; Deligeorgiev, Todor

    2017-04-05

    Two newly synthesized symmetrical heptamethine cyanine dyes, AK7-5 and AK7-6, absorbing in the region of low autofluorescence of biological samples, have been tested for their ability to detect proteins aggregated into amyloid fibrils. In aqueous solution these probes possess three absorption bands corresponding to the monomer, dimer and H-aggregate species. The association of the dye with fibrillar lysozyme was followed by the enhancement of the monomer band and the reduction of the H-band. The absorption spectra measured at various fibril concentrations were analyzed in terms of the model allowing for the shift of equilibria between various dye species due to the binding of monomers and dimers of AK7-5 and AK7-6 to amyloid fibrils. The association constants and stoichiometries of the dye-fibril complexation have been evaluated. In contrast to fibrillar lysozyme, the native protein brought about strong J-aggregate formation accompanied by a marked drop in the absorbance of the dye monomer species. Quantum chemical calculations and simple docking studies showed that AK7-5 and AK7-6 monomers can bind to the grooves, running parallel to the fibril axis. Due to their ability to distinguish between the native and fibrillar protein states, the novel cyanines are recommended as complementary to existing amyloid markers.

  5. Synthesis and application of water-soluble, photoswitchable cyanine dyes for bioorthogonal labeling of cell-surface carbohydrates.

    Science.gov (United States)

    Mertsch, Alexander; Letschert, Sebastian; Memmel, Elisabeth; Sauer, Markus; Seibel, Jürgen

    2016-09-01

    The synthesis of cyanine dyes addressing absorption wavelengths at 550 and 648 nm is reported. Alkyne functionalized dyes were used for bioorthogonal click reactions by labeling of metabolically incorporated sugar-azides on the surface of living neuroblastoma cells, which were applied to direct stochastic optical reconstruction microscopy (dSTORM) for the visualization of cell-surface glycans in the nm-range.

  6. A Valence-Bond Nonequilibrium Solvation Model for a Twisting Cyanine Dye

    CERN Document Server

    McConnell, Sean; Olsen, Seth

    2014-01-01

    We study a two-state valence-bond electronic Hamiltonian model of non-equilibrium solvation during the excited-state twisting reaction of monomethine cyanines. These dyes are of interest because of the strong environment-dependent enhancement of their fluorescence quantum yield that results from suppression of competing non-radiative decay via twisted internal charge-transfer (TICT) states. For monomethine cyanines, where the ground state is a superposition of structures with different bond and charge localization, there are two twisting pathways with different charge localization in the excited state. The Hamiltonian designed to be as simple as possible consistent with a few well-enumerated assumptions. It is defined by three parameters and is a function of two $\\pi$-bond twisting angle coordinates and a single solvation coordinate. For parameters corresponding to symmetric monomethines, there are two low-energy twisting channels on the excited-state surface that lead to a manifold of twisted intramolecular ...

  7. Synthesis and Absorption Characteristics of Two Infrared Cyanine Dyes

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Two infrared dyes, 1,3,3,1', 3', 3'-hexamethylindotricarbocyanine iodide (A) and 1,3,3,1',3',3'-hexamethyl-11-chloro-10,12-propylenetricarbocyanine iodide (B), were synthesized and characterized by melting point, elemental analysis, IR, and 1H-NMR. Their electron absorption spectra, laser absorption characteristics and solubility were investigated. The results showed that A and B have maximum absorption peaks at around 748 nm and 774 nm, respectivey, which match well with the wavelength output of the near infrared laser diode. The dyes were found to have photoinduced fading during irradiation with the infrared laser, especially in the presence of oxygen. However, this procession can be greatly slowed by using a layer of poly(vinyl alcohol) to barricade the dyes from oxygen. The experiments also showed that the dyes were thermally stable but decayed under strong sunlight. Furthermore, they are easily dissolved in some common solvents.

  8. Synthesis and spectra of a kind of novel longer-wavelength benzoxazole indole styryl cyanine dye with a carbazole-bridged chain.

    Science.gov (United States)

    Fei, Xuening; Gu, Yingchun; Li, Chao; Liu, Yuru; Yu, Lu

    2013-01-01

    Based on cyanine dye probe oxazole yellow (YO) and Cy(3), a series of novel styryl cyanine dyes were designed and synthesized. Carbazole was inserted into the structures of YO and Cy(3) to act as a bridge to link the benzoxazole and indole group. This modification resulted in a novel kind of benzoxazole indole styryl cyanine dye with a carbazole-bridged chain. The dyes were characterized by (1)HNMR and MS. The spectra of the novel dyes were also performed and the results showed that the maximum emission wavelength of the carbazole styryl cyanine dye was shifted red, the Stokes shift increased and the fluorescence intensity enhanced compared with those of YO and Cy(3). These results indicated that the novel dye could be used as an excellent fluorescent probe in biological labeling.

  9. Highly Efficient Photosensitization of Mesoporous TiO2 Electrode with a Cyanine Dye

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A low cost cyanine dye,1,1-dimethyl-3-ethyl-2-[3-(1,3-dihydro-3,3-dimethyl-1-ethyl-5-carboxyl-2H-indol-2-ylidene)-1-propenyl]-1H-benz[e] indolium iodide (1) was synthesized and applied to sensitize mesoporous TiO2 electrode.Photoresponse of the electrode was extended to the visible and remarkably high incident photon-to-current conversion efficiency (IPCE) over 70% was achieved from 500 nm to 600 nm.

  10. Self-assembled structure of cyanine dyes: J-aggregates characteristicson optical information storing microcrystals

    Institute of Scientific and Technical Information of China (English)

    JIANG Xiaoli; LI Xiaowei; LAI Weidong; MENG Tao; FENG Xiaomin; ZHANG Jixian

    2006-01-01

    Dye sensitization is a fundamental function for solar cell and silver halide (AgX) microcrystal to increase the optoelectronic conversion efficiency. In this paper, the spectral properties and self-assembled structure of three types of cyanine dyes, adsorbed both on (100) surface of 0.4 μm AgBr cubic crystal and (111) surface of 1.8 μm AgBr tabular crystal, were studied with combination ofspectroscopy and atomic force microscopy (AFM) technique. Rectangular aggregation structure is formed on the crystal faces of (100) and (111) for both anionic and cationic dyes, while herringbone-stacking structure is formed by anionic-cationic dye, and a J-band spectrum is correspondingly detected. The photoelectron property of dye-sensitized samples was also investigated with microwave absorption and dielectric spectrum detection technology. After excited by a 355 nm fast-pulse laser, the photoelectron decay process of anionic-cationic dye sensitized sample is the fastest. This indicates that the affection of anionic-cationic dye aggregates to the photoelectron decay is the biggest, and the sensitization is more efficient.

  11. A Cyanine Dye Encapsulated Porous Fibrous Mat for Naked-Eye Ammonia Sensing.

    Science.gov (United States)

    Ji, Chendong; Ma, Lijing; Yin, Meizhen; Yang, Wantai; Pan, Kai

    2016-08-19

    Electrospun ultrathin fiber-based sensors are desirable because of their practicality and sensitivity. Ammonia-detection systems are in high demand in different areas, including the industrial and agricultural fields. However, current technologies rely on large and complex instruments that restrict their actual utilization. Herein, we report a flexible naked-eye ammonia sensor, the polylactic acid-cyanine (PLA-Cy) fibrous mat, which was fabricated by blending a carboxyl-functionalized cyanine dye (D1) into electospun PLA porous fibers. The sensing mat was shown to undergo a naked-eye-detectable color change from white to blue upon exposure to ammonia vapor. The mat showed high selectivity to ammonia gas with a detection limit of 3.3 ppm. Aggregated D1 was first encapsulated by PLA and was then ionized by NH3 . These mechanisms were examined by photophysical studies and scanning electron microscopy. The aggregation-deaggregation process of D1 in the PLA-Cy fibrous mat led to the color change. This work provides a facile method for the naked-eye detection of ammonia and a novel strategy for the use of organic dyes in ammonia sensing.

  12. Single molecule fluorescence fluctuations of the cyanine dyes linked covalently to DNA

    Institute of Scientific and Technical Information of China (English)

    LV Wei; CHEN XuDong; AUMILER Damir; XIA AnDong

    2009-01-01

    The intersystem crossing and isomerization dynamics of free-Cy3,Cy3-ssDNA,free-Cy5 and Cy5-ssDNA are obtained through simple analysis of rapid on/off blinking from single molecule fluo rescence intensity time-traces and the fluorescence correlation spectroscopy(FCS).The on-and off-times observed in fluorescence time traces of single cyanine dyes are due to the formation of the triplet state and isomerization,where both the interaction with DNA and long central polymethine chain of cyanine dyes increase the barriers of isomerization,leading to long off-time.The results indicate that the single molecule fluorescence fluctuation together with the resulting second autocorrelation analysis are powerful methods for determining the triplet state and isomerization dynamics,which could be the simple techniques and complementary to other spectroscopic techniques,such as fluorescence decay measurement and laser flash photolysis to study the photophysical processes of complex molecules.

  13. Exciton transport in thin-film cyanine dye J-aggregates

    CERN Document Server

    Valleau, Stéphanie; Yung, Man-Hong; Aspuru-Guzik, Alán

    2012-01-01

    We present a theoretical model for the study of exciton dynamics in J-aggregated monolayers of fluorescent dyes. The excitonic evolution is described by a Monte-Carlo wave function approach which allows for a unified description of the quantum (ballistic) and classical (diffusive) propagation of an exciton on a lattice in different parameter regimes. The transition between the ballistic and diffusive regime is controlled by static and dynamic disorder. As an example, the model is applied to three cyanine dye J-aggregates: TC, TDBC, and U3. Each of the molecule-specific structure and excitation parameters are estimated using time-dependent density functional theory. The exciton diffusion coefficients are calculated and analyzed for different degrees of film disorder and are correlated to the physical properties and the structural arrangement of molecules in the aggregates. Further, exciton transport is anisotropic and dependent on the initial exciton energy. The upper-bound estimation of the exciton diffusion ...

  14. Synthesis and systematic evaluation of symmetric sulfonated centrally C-C bonded cyanine near-infrared dyes for protein labelling

    NARCIS (Netherlands)

    Wal, Van Der Steffen; Kuil, Joeri; Valentijn, A.R.P.M.; Leeuwen, Van Fijs W.B.

    2016-01-01

    The most commonly used near-infrared cyanine dyes contain an aryl ether that is not fully stable towards nucleophiles. Replacement of the aryl ether by a more stable carbon-carbon bond can improve the stability. In this work we have synthesized a series of four negatively-charged symmetrical C-C

  15. Synthesis and systematic evaluation of symmetric sulfonated centrally C-C bonded cyanine near-infrared dyes for protein labelling

    NARCIS (Netherlands)

    Wal, Van Der Steffen; Kuil, Joeri; Valentijn, A.R.P.M.; Leeuwen, Van Fijs W.B.

    2016-01-01

    The most commonly used near-infrared cyanine dyes contain an aryl ether that is not fully stable towards nucleophiles. Replacement of the aryl ether by a more stable carbon-carbon bond can improve the stability. In this work we have synthesized a series of four negatively-charged symmetrical C-C

  16. Why the Particle-in-a-Box Model Works Well for Cyanine Dyes but Not for Conjugated Polyenes

    Science.gov (United States)

    Autschbach, Jochen

    2007-01-01

    We investigate why the particle-in-a-box (PB) model works well for calculating the absorption wavelengths of cyanine dyes and why it does not work for conjugated polyenes. The PB model is immensely useful in the classroom, but owing to its highly approximate character there is little reason to expect that it can yield quantitative agreement with…

  17. Spectroscopy of cyanine dyes in fluid solution at atmospheric and high pressure: The effect of viscosity on nonradiative processes

    Energy Technology Data Exchange (ETDEWEB)

    Murphy, S.; Sauerwein, B.; Drickamer, H.G.; Schuster, G.B. (Univ. of Illinois, Urbana, IL (United States))

    1994-12-22

    The spectroscopy of cyanine dyes was examined at atmospheric pressure and at high pressure in a series of alcohols and other solvents. Variation of external pressure provides the means to control viscosity over a wide range in one solvent at constant temperature. The findings reveal that the nonradiative relaxation of cyanines in fluid solution can occur when the motion leading to the formation of the cis isomer is stopped completely. Analysis of the viscosity dependence of the nonradiative relaxation rate constant reveals consistent deviation from the Kramers-DSE relation. 33 refs., 5 figs., 2 tabs.

  18. Behaviour of fluorescence emission of cyanine dyes, cyanine based fluorescent nanoparticles and CdSe/ZnS quantum dots in water solution upon specific thermal treatments.

    Science.gov (United States)

    Mortati, Leonardo; Miletto, Ivana; Alberto, Gabriele; Caputo, Giuseppe; Sassi, Maria Paola

    2011-05-01

    Fluorescence techniques are widely used as detection methods in a wide range of biological imaging and analytical applications. The purpose of this work is to determine a measurement method which leads to a comparison between different classes of fluorophores in term of stability of the fluorescence signal upon thermal treatment cycles. This kind of investigation can determine whether the fluorophore performance is affected by heating/cooling cycles and to what extent. The fluorophores considered in this work were organic fluorophores belonging to the family of indocyanine dyes (IRIS3 by Cyanine Technologies S.p.A.) in their molecular form or encapsulated within silica nanoparticles, and CdSe/ZnS carboxyl quantum dots (Qdots 565 ITK by Invitrogen). The NIST Standard Reference Material® SRM 1932 fluorescein solution was used in the certified concentration as reference material in order to evaluate the repeatability of the used spectrofluorimeter. The proposed measurement protocol allows to characterize all kind of fluorophores upon thermal treatments. This allows direct comparison of their performance under temperature changes, giving useful guidelines for the selection of the most suitable fluorophore for the envisaged application. Moreover the method appears to be a promising tool for the characterisation of reference fluorescent materials. The experimental results demonstrate that each fluorophore class shows a specific behaviour. The experimental data analysis points out an important hysteresis effect for quantum dots that was not detected for cyanine molecules and was only slightly detected for cyanine doped silica nanoparticles.

  19. Novel cyanine dyes and homodimeric styryl dyes as fluorescent probes for assessment of lactic acid bacteria cell viability.

    Science.gov (United States)

    Tropcheva, Rositsa; Lesev, Nedyalko; Danova, Svetla; Stoitsova, Stoyanka; Kaloyanova, Stefka

    2015-02-01

    Innovations in labeling techniques and in the design and synthesis of dye structures are closely related to the development of service equipment such as light sources and detection methods. Novel styryl homodimers and monomethine cyanine dyes were synthesized and their staining abilities for discrimination between live and dead lactic acid bacterial cells were investigated. The dyes were combined in pairs based on their excitation and emission maxima and the capacity to penetrate through cell membranes of viable bacterial cells. The absorption maxima in the same region and the large Stocks shifts of the styryl derivatives allowed viability analysis to be done with epifluorescent microscope with a very basic configuration - one light source about 480nm and one filter for the fluorescent emissions. A staining protocol was developed and applied for live/dead analysis of Bulgarian yoghurt starters. The live cells quantification by the fluorescence dyes coincided well with the results of the much more time-consuming tests by plate counting. Thus, the proposed dye combinations are appropriate for rapid viability estimation in small laboratories that may have conventional equipment. Copyright © 2015 Elsevier B.V. All rights reserved.

  20. Rational Molecular Design and Synthesis of Highly Thermo- and Photostable Near-Infrared-Absorbing Heptamethine Cyanine Dyes with the Use of Fluorine Atoms.

    Science.gov (United States)

    Funabiki, Kazumasa; Yagi, Kazutaka; Ueta, Masato; Nakajima, Mitsuru; Horiuchi, Masako; Kubota, Yasuhiro; Mastui, Masaki

    2016-08-22

    Highly thermo- and photostable, near-infrared-absorbing heptamethine cyanine dyes were achieved with the use of fluorine-containing components. In particular, one prepared heptamethine cyanine dye, bearing a tetrakis(pentafluorophenyl)borate as a counter anion and an N-ethyl-2,2,2-trifluoroacetamido group at the meso position, showed not only a high decomposition temperature (Tdt ), but also very high photostability toward white LED irradiation.

  1. Controlled Modulation of Serum Protein Binding and Biodistribution of Asymmetric Cyanine Dyes by Variation of the Number of Sulfonate Groups

    Directory of Open Access Journals (Sweden)

    Franziska M. Hamann

    2011-07-01

    Full Text Available To assess the suitability of asymmetric cyanine dyes for in vivo fluoro-optical molecular imaging, a comprehensive study on the influence of the number of negatively charged sulfonate groups governing the hydrophilicity of the DY-67x family of asymmetric cyanines was performed. Special attention was devoted to the plasma protein binding capacity and related pharmacokinetic properties. Four members of the DY-67x cyanine family composed of the same main chromophore, but substituted with a sequentially increasing number of sulfonate groups (n = 1−4; DY-675, DY-676, DY-677, DY-678, respectively, were incubated with plasma proteins dissolved in phosphate-buffered saline. Protein binding was assessed by absorption spectroscopy, gel electrophoresis, ultrafiltration, and dialysis. Distribution of dye in organs was studied by intraveneous injection of 62 nmol dye/kg body weight into mice (n = 12; up to 180 minutes postinjection using whole-body near-infrared fluorescence imaging. Spectroscopic studies, gel electrophoresis, and dialysis demonstrated reduced protein binding with increasing number of sulfonate groups. The bovine serum albumin binding constant of the most hydrophobic dye, DY-675, is 18 times higher than that of the most hydrophilic fluorophore, DY-678. In vivo biodistribution analysis underlined a considerable influence of dye hydrophilicity on biodistribution and excretion pathways, with the more hydrophobic dyes, DY-675 and DY-676, accumulating in the liver, followed by strong fluorescence signals in bile and gut owing to accumulation in feces and comparatively hydrophilic DY-678-COOH accumulating in the bladder. Our results demonstrate the possibility of selectively controlling dye-protein interactions and, thus, biodistribution and excretion pathways via proper choice of the fluorophore's substitution pattern. This underlines the importance of structure-property relationships for fluorescent labels. Moreover, our data could provide the

  2. J-aggregates of amphiphilic cyanine dyes: Self-organization of artificial light harvesting complexes

    Directory of Open Access Journals (Sweden)

    Stefan Kirstein

    2006-01-01

    Full Text Available The simultaneous chemical linkage of cyanine dye chromophores with both hydrophobic and hydrophilic substituents leads to a new type of amphiphilic molecules with the ability of spontaneous self-organization into highly ordered aggregates of various structures and morphologies. These aggregates carry the outstanding optical properties of J-aggregates, namely, efficient exciton coupling and fast exciton energy migration, which are essential for the build up of artificial light harvesting systems. The morphology of the aggregates depends sensitively on the molecular structure of the chemical substituents of the dye chromophore. Accordingly, lamellar ribbon-like structures, vesicles , tubes, and bundles of tubes are found depending on the dyes and the structure can further be altered by addition of surfactants, alcohols, or other additives. Altogether the tubular structure is the most noticeable structural motif of these types of J-aggregates. The optical spectra are characterized in general by a complex exciton spectrum which is composed of several electronic transitions. The spectrum is red-shifted as a total with respect to the monomer absorption and exhibits resonance fluorescence from the lowest energy transition. For the tubular structures, the optical spectra can be related to a structural model. Although the molecules itself are strictly achiral, a pronounced circular dichroism (CD is observed for the tubular aggregates and explained by unequal distribution of left- and right-handed helicity of the tubes. Photo-induced electron transfer (PET reactions from the dye aggregates to electron acceptor molecules lead to superquenching which proves the delocalization of the excitation. This property is used to synthesize metal nanoparticles on the aggregate surface by photo-induced reduction of metal ions.

  3. Preclinical evaluation of a novel cyanine dye for tumor imaging with in vivo photoacoustic imaging

    Science.gov (United States)

    Temma, Takashi; Onoe, Satoru; Kanazaki, Kengo; Ono, Masahiro; Saji, Hideo

    2014-09-01

    Photoacoustic imaging (PA imaging or PAI) has shown great promise in the detection and monitoring of cancer. Although nanocarrier-based contrast agents have been studied for use in PAI, small molecule contrast agents are required due to their ease of preparation, cost-effectiveness, and low toxicity. Here, we evaluated the usefulness of a novel cyanine dye IC7-1-Bu as a PAI contrast agent without conjugated targeting moieties for in vivo tumor imaging in a mice model. Basic PA characteristics of IC7-1-Bu were compared with indocyanine green (ICG), a Food and Drug Administration approved dye, in an aqueous solution. We evaluated the tumor accumulation profile of IC7-1-Bu and ICG by in vivo fluorescence imaging. In vivo PAI was then performed with a photoacoustic tomography system 24 and 48 h after intravenous injection of IC7-1-Bu into tumor bearing mice. IC7-1-Bu showed about a 2.3-fold higher PA signal in aqueous solution compared with that of ICG. Unlike ICG, IC7-1-Bu showed high tumor fluorescence after intravenous injection. In vivo PAI provided a tumor to background PA signal ratio of approximately 2.5 after intravenous injection of IC7-1-Bu. These results indicate that IC7-1-Bu is a promising PAI contrast agent for cancer imaging without conjugation of targeting moieties.

  4. Interfacing click chemistry with automated oligonucleotide synthesis for the preparation of fluorescent DNA probes containing internal xanthene and cyanine dyes.

    Science.gov (United States)

    Astakhova, I Kira; Wengel, Jesper

    2013-01-14

    Double-labeled oligonucleotide probes containing fluorophores interacting by energy-transfer mechanisms are essential for modern bioanalysis, molecular diagnostics, and in vivo imaging techniques. Although bright xanthene and cyanine dyes are gaining increased prominence within these fields, little attention has thus far been paid to probes containing these dyes internally attached, a fact which is mainly due to the quite challenging synthesis of such oligonucleotide probes. Herein, by using 2'-O-propargyl uridine phosphoramidite and a series of xanthenes and cyanine azide derivatives, we have for the first time performed solid-phase copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) click labeling during the automated phosphoramidite oligonucleotide synthesis followed by postsynthetic click reactions in solution. We demonstrate that our novel strategy is rapid and efficient for the preparation of novel oligonucleotide probes containing internally positioned xanthene and cyanine dye pairs and thus represents a significant step forward for the preparation of advanced fluorescent oligonucleotide probes. Furthermore, we demonstrate that the novel xanthene and cyanine labeled probes display unusual and very promising photophysical properties resulting from energy-transfer interactions between the fluorophores controlled by nucleic acid assembly. Potential benefits of using these novel fluorescent probes within, for example, molecular diagnostics and fluorescence microscopy include: Considerable Stokes shifts (40-110 nm), quenched fluorescence of single-stranded probes accompanied by up to 7.7-fold light-up effect of emission upon target DNA/RNA binding, remarkable sensitivity to single-nucleotide mismatches, generally high fluorescence brightness values (FB up to 26), and hence low limit of target detection values (LOD down to <5 nM).

  5. Mixtures of achiral amphiphilic cyanine dyes form helical tubular J-aggregates

    Energy Technology Data Exchange (ETDEWEB)

    Berlepsch, Hans v., E-mail: h.v.berlepsch@fzem.fu-berlin.de [Forschungszentrum fuer Elektronenmikroskopie, Institut fuer Chemie und Biochemie, Freie Universitaet Berlin, Fabeckstrasse 36a, D-14195 Berlin (Germany); Ludwig, Kai [Forschungszentrum fuer Elektronenmikroskopie, Institut fuer Chemie und Biochemie, Freie Universitaet Berlin, Fabeckstrasse 36a, D-14195 Berlin (Germany); Kirstein, Stefan [Institut fuer Physik, Humboldt Universitaet zu Berlin, Newtonstrasse 15, D-12489 Berlin (Germany); Boettcher, Christoph, E-mail: christoph.boettcher@fzem.fu-berlin.de [Forschungszentrum fuer Elektronenmikroskopie, Institut fuer Chemie und Biochemie, Freie Universitaet Berlin, Fabeckstrasse 36a, D-14195 Berlin (Germany)

    2011-06-23

    Graphical abstract: Two amphiphilic carbocyanine dye molecules that have very similar molecular structure and form J-aggregates of different morphology are mixed in an aqueous solution. The aggregates of the mixture are of the same morphology as the aggregates of one of the dyes but exhibit a different absorption spectrum. The details of the morphology are analysed by using 3D-reconstruction techniques of cryo-TEM images and are discussed in the context of their optical behaviour. Highlights: {yields} Two sulfonate-substituted amphiphilic cyanines form mixed J-aggregates in water. {yields} Absorption spectrum is not a superposition of pure component spectra. {yields} Cryo-TEM reveals 13 nm thin bilayered nanotubes with helical ultrastructure. {yields} The spatial structure of aggregates is determined by 3D-reconstruction techniques. - Abstract: The amphiphilic 3,3'-bis(2-sulfoethyl) and 3,3'-bis(2-sulfopropyl) substituted 5,5',6,6'-tetrachlorobenzimidacarbocyanine dyes (C8S2 and C8S3) self-aggregate in aqueous solution to form mixed J-aggregates. The individual dyes form planar (C8S2) or tubular (C8S3) aggregates, while the mixed solution forms tubular aggregates that are morphologically identical to those obtained from the pure C8S3. The optical spectra however differ significantly indicating a different structure on the molecular length scale. The structure and morphology is independent of the mixing ratio if the content of C8S2 is above 10%. The structure of the mixed C8S3/C8S2 aggregates is investigated in detail by means of cryogenic transmission electron microscopy (cryo-TEM) in combination with a 3D-image reconstruction technique, which yields a structure with a spatial resolution of {approx}2 nm. A comparison with the 3D structure of the tubular aggregates of C8S3 could not resolve any differences. Any structural difference that could describe the spectroscopic difference of the two types of tubular aggregates must be below this

  6. Twisted cyanines: a non-planar fluorogenic dye with superior photostability and its use in a protein-based fluoromodule.

    Science.gov (United States)

    Shank, Nathaniel I; Pham, Ha H; Waggoner, Alan S; Armitage, Bruce A

    2013-01-09

    The cyanine dye thiazole orange (TO) is a well-known fluorogenic stain for DNA and RNA, but this property precludes its use as an intracellular fluorescent probe for non-nucleic acid biomolecules. Further, as is the case with many cyanines, the dye suffers from low photostability. Here, we report the synthesis of a bridge-substituted version of TO named α-CN-TO, where the central methine hydrogen of TO is replaced by an electron withdrawing cyano group, which was expected to decrease the susceptibility of the dye toward singlet oxygen-mediated degradation. An X-ray crystal structure shows that α-CN-TO is twisted drastically out of plane, in contrast to TO, which crystallizes in the planar conformation. α-CN-TO retains the fluorogenic behavior of the parent dye TO in viscous glycerol/water solvent, but direct irradiation and indirect bleaching studies showed that α-CN-TO is essentially inert to visible light and singlet oxygen. In addition, the twisted conformation of α-CN-TO mitigates nonspecific binding and fluorescence activation by DNA and a previously selected TO-binding protein and exhibits low background fluorescence in HeLa cell culture. α-CN-TO was then used to select a new protein that binds and activates fluorescence from the dye. The new α-CN-TO/protein fluoromodule exhibits superior photostability to an analogous TO/protein fluoromodule. These properties indicate that α-CN-TO will be a useful fluorogenic dye in combination with specific RNA and protein binding partners for both in vitro and cell-based applications. More broadly, structural features that promote nonplanar conformations can provide an effective method for reducing nonspecific binding of cationic dyes to nucleic acids and other biomolecules.

  7. Ultrafast twisting motions and intramolecular charge-transfer reaction in a cyanine dye trapped in molecular nanocavities

    Science.gov (United States)

    Fayed, T. A.; Organero, J. A.; Garcia-Ochoa, I.; Tormo, L.; Douhal, A.

    2002-09-01

    Emission properties of the cyanine dye, 1-(2-naphthyl)-2-ethenyl-(2-benzothiazolium) iodide, in aqueous nanocavities offered by cyclodextrins and in a film of a polymeric matrix were studied by means of steady-state and picosecond time-resolved emission spectroscopy. The results show the occurrence of a fast twisting motion and a subsequent intramolecular charge-transfer reaction. The initial step can be prevented by the size of the nanocavity which governs the spectral position of the fluorescence band and lifetime of the excited encapsulated host.

  8. New peripherally-substituted naphthalo-cyanines: synthesis, characterisation and evaluation in dye-sensitized photoelectrochemical solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Xiyou, Li; Long, N.J.; Clifford, J.N.; Compbell, C.J.; Durrant, J.R. [Imperial College of Science, Technology and Medicine, Dept. of Chemstry, London (United Kingdom)

    2002-08-01

    A series of novel tetra-substituted naphthalo-cyanines featuring hydroxy and carboxylate substituents in peripheral positions have been synthesised in reasonable yields and characterised by spectroscopic techniques. The photochemical properties of the tetra-acid derivative 7 were examined following immobilisation on a nanocrystalline TiO{sub 2} surface and photoinduced dye cations were observed following optical excitation. 7 has a redox potential of 0.25 V (vs. Ag/AgCl), which is lower than is required for an efficient regeneration reaction and, therefore, results in limited photocurrent flow when 7 is used in photoelectrochemical solar cells. (authors)

  9. Photo-induced interaction of thioglycolic acid (TGA)-capped CdTe quantum dots with cyanine dyes

    Science.gov (United States)

    Abdelbar, Mostafa F.; Fayed, Tarek A.; Meaz, Talaat M.; Ebeid, El-Zeiny M.

    2016-11-01

    The photo-induced interaction of three different sizes of thioglycolic acid (TGA)-capped CdTe quantum dots (CdTe QDs) with two monomethine cyanine dyes belonging to the thiazole orange (TO) family has been studied. Positively charged cyanines interact with QDs surface which is negatively charged due to capping agent carboxylate ions. The energy transfer parameters including Stern-Volmer constant, Ksv, number of binding sites, n, quenching sphere radius, r, the critical energy transfer distance, R0, and energy transfer efficiencies, E have been calculated. The effect of structure and the number of aggregating molecules have been studied as a function of CdTe QDs particle size. Combining organic and inorganic semiconductors leads to increase of the effective absorption cross section of the QDs which can be utilized in novel nanoscale designs for light-emitting, photovoltaic and sensor applications. A synthesized triplet emission of the studied dyes was observed using CdTe QDs as donors and this is expected to play a potential role in molecular oxygen sensitization and in photodynamic therapy (PDT) applications.

  10. Use of a cyanine dye probe to estimate the composition of the vitreous body after enzymatic treatment

    Science.gov (United States)

    Panova, Ina G.; Tatikolov, Alexander S.; Sharova, Natalia P.

    2010-02-01

    The aim of this work was to study the effect of enzymes such as proteinase K, trypsin, collagenase with hyaluronidase, as well as a mixture of all these enzymes, on albumin and collagens incorporated in the vitreous body, using a cyanine dye as a spectral-fluorescent probe. We studied the vitreous body of the eyes of 19/20-week human fetuses, in which, as we showed earlier, the concentration of albumin in the vitreous body is sufficiently high. Proteinase K steeply decreased the albumin content in the vitreous body, whereas trypsin and hyaluronidase with collagenase had no effect on the albumin content. Collagen was not subjected to proteinase K. Enzymatic digestion of collagen occurred under the action of collagenase with hyaluronidase. The content of albumin and collagen sharply decreased in the system after treatment of the vitreous body with mixture of all enzymes. Hence, the results obtained showed that, even being in the mixture, these enzymes have a selective effect on albumin and collagens. The possibility to study the dose-dependent character of enzymatic vitreolysis using a cyanine dye probe has been shown. The spectral-fluorescent probe for albumin and collagens proved to be useful for experimental approaches at screening the enzymatic mixtures possessing the selective action. The study performed is considered as a preclinical trial, and the method presented as promising for the further research in this field. The effect of the enzymes used for therapeutic purposes on the functional conditions of the vitreous body should be studied.

  11. Dielectric and thermal effects on the optical properties of natural dyes: a case study on solvated cyanin.

    Science.gov (United States)

    Malcıoğlu, Osman Bariş; Calzolari, Arrigo; Gebauer, Ralph; Varsano, Daniele; Baroni, Stefano

    2011-10-05

    The optical properties of the flavylium state of the cyanin dye are simulated numerically by combining Car-Parrinello molecular dynamics and linear-response time-dependent density functional theory calculations. The spectrum of the dye calculated in the gas phase is characterized by two peaks in the yellow and in the blue (green and violet), using a GGA-PBE (hybrid-B3LYP) DFT functional, which would bring about a greenish (bright orange) color incompatible with the dark purple hue observed in nature. Describing the effect of the water solvent through a polarizable continuum model does not modify qualitatively the resulting picture. An explicit simulation of both solvent and thermal effects using ab initio molecular dynamics results instead in a spectrum that is compatible with the observed coloration. This result is analyzed in terms of the spectroscopic effects of the molecular distortions induced by thermal fluctuations.

  12. Review on near-infrared heptamethine cyanine dyes as theranostic agents for tumor imaging, targeting, and photodynamic therapy

    Science.gov (United States)

    Shi, Changhong; Wu, Jason Boyang; Pan, Dongfeng

    2016-05-01

    A class of near-infrared fluorescence (NIRF) heptamethine cyanine dyes that are taken up and accumulated specifically in cancer cells without chemical conjugation have recently emerged as promising tools for tumor imaging and targeting. In addition to their fluorescence and nuclear imaging-based tumor-imaging properties, these dyes can be developed as drug carriers to safely deliver chemotherapy drugs to tumors. They can also be used as effective agents for photodynamic therapy with remarkable tumoricidal activity via photodependent cytotoxic activity. The preferential uptake of dyes into cancer but not normal cells is co-operatively mediated by the prevailing activation of a group of organic anion-transporting polypeptides on cancer cell membranes, as well as tumor hypoxia and increased mitochondrial membrane potential in cancer cells. Such mechanistic explorations have greatly advanced the current application and future development of NIRF dyes and their derivatives as anticancer theranostic agents. This review summarizes current knowledge and emerging advances in NIRF dyes, including molecular characterization, photophysical properties, multimodal development and uptake mechanisms, and their growing potential for preclinical and clinical use.

  13. Characterization of the vitreous body of the human eye using a cyanine dye as a spectral and fluorescent probe

    Science.gov (United States)

    Panova, Ina G.; Tatikolov, Alexander S.

    2009-02-01

    We used one of cyanine dyes as a spectral and fluorescent probe in the study of the composition of the extracellular matrix of the human eye (its vitreous body). Owing to the unique ability of the dye to bind to collagens and human serum albumin, we revealed the simultaneous presence of both types of biomacromolecules in the vitreous body. The formation of the dye complex with human serum albumin leads to appearance of a long-wavelength absorption band (~612 nm) and a steep rise of fluorescence, whereas in the presence of collagens the dye forms J-aggregates with a longer-wavelength absorption band (640-660 nm) and moderate fluorescence. In this work we studied the composition of the human fetus vitreous body and its dynamics from 9 to 31 gestation weeks. On the basis of the data obtained by this method, we may assume that albumin, being a carrier protein, probably provides the vitreous body and surrounding tissues with necessary growth factors, hormones, lipids, vitamins, and some other biomolecules. The data show that the dye is promising not only for study of albumin functions in eye development, but also for characterization of some eye diseases and for analysis of other extracellular media.

  14. Specific fluorescent detection of fibrillar α-synuclein using mono- and trimethine cyanine dyes

    NARCIS (Netherlands)

    Volkova, K.D.; Kovalska, V.B.; Balanda, A.O.; Losytskyy, M.Yu; Golub, A.G.; Vermeij, R.J.; Subramaniam, V.; Tolmachev, O.I.; Yarmoluk, S.M.

    2008-01-01

    With the aim of searching of novel amyloid-specific fluorescent probes the ability of series of mono- and trimethine cyanines based on benzothiazole, pyridine and quinoline heterocycle end groups to recognize fibrillar formations of α-synuclein (ASN) was studied. For the first time it was revealed t

  15. J-Aggregates of Amphiphilic Cyanine Dyes for Dye-Sensitized Solar Cells: A Combination between Computational Chemistry and Experimental Device Physics

    Directory of Open Access Journals (Sweden)

    M. S. A. Abdel-Mottaleb

    2014-01-01

    Full Text Available We report on the design and structure principles of 5,5′-6,6′-tetrachloro-1,1′-dioctyl-3,3′-bis-(3-carboxypropyl-benzimidacarbocyanine (Dye 1. Such metal-free amphiphilic cyanine dyes have many applications in dye-sensitized solar cells. AFM surface topographic investigation of amphiphilic molecules of Dye 1 adsorbed on TiO2 anode reveals the ability of spontaneous self-organization into highly ordered aggregates of fiber-like structure. These aggregates are known to exhibit outstanding optical properties of J-aggregates, namely, efficient exciton coupling and fast exciton energy migration, which are essential for building up artificial light harvesting to the photovoltaic device. A light-to-electricity conversion efficiency of DSSC based on the metal free amphiphilic Dye 1 is η=3.75, which is about 50% of that based on metal-based N719 Ru-dye (Di-tetrabutylammoniumcis-bis(isothiocyanatobis(2,2′-bipyridyl-4,4′-dicarboxylatoruthenium(II. DFT and TD-DFT studies show that large intramolecular charge transfer takes place from the HOMO to LUMO. HOMO is localized on a part of the molecule with almost no contribution from the carboxylic moiety. This clearly indicates that the anchoring carboxylic group plays a minor role.

  16. Near IR two photon absorption of cyanines dyes: application to optical power limiting at telecommunication wavelengths

    Science.gov (United States)

    Bouit, Pierre-Antoine; Wetzel, Guillaume; Feneyrou, Patrick; Bretonnière, Yann; Kamada, Kenji; Maury, Olivier; Andraud, Chantal

    2008-02-01

    The design and synthesis of symmetrical and unsymmetrical heptamethine cyanines is reported. These chromophores present significant two-photon cross section in the 1400-1600 nm spectral range. In addition, they display optical power limiting (OPL) properties. OPL curves were interpreted on the basis of two-photon absorption (2PA) followed by excited state absorption (ESA). Finally, these molecules present several relevant properties (nonlinear absorption properties, two-step gram scale synthesis, high solubility, good thermal stability), which could lead to numerous practical applications in material science (solid state optical limiting, signal processing) or in biology (imaging).

  17. Kinetic competition in liquid electrolyte and solid-state cyanine dye sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Tatay, S.; Gavina, P. [ICMol-UV, Poligono Industrial La Coma s/n, Paterna (Spain); Haque, S.A.; O' Regan, B.C.; Durrant, J.R. [Centre for Electronic Materials and Devices, Chemistry Department, Imperial College, South Kensington, London SW7 2AZ (United Kingdom); Vidal-Ferran, A. [Catalan Institution for Research and Advanced Studies ICREA, Barcelona (Spain); Palomares, E. [Institute of Chemical Research of Catalonia ICIQ, Avgda, Paysos Catalans 16, 43007 Tarragona (Spain); Verhees, W.J.H.; Kroon, J.M. [ECN Solar Energy, Petten (Netherlands)

    2007-08-15

    The photovoltaic performance of liquid electrolyte and solid-state dye sensitized solar cells, employing a squarilium methoxy cyanide dye, are evaluated in terms of interfacial electron transfer kinetics. Dye adsorption to the metal oxide film resulted in a mixed population of aggregated and monomeric sensitizer dyes. Emission quenching data, coupled with transient absorption studies, indicate that efficient electron injection was only achieved by the monomeric dyes, with the aggregated dye population having an injection yield an order of magnitude lower. In liquid electrolyte devices, transient absorption studies indicate that photocurrent generation is further limited by slow kinetics of the regeneration of monomeric dye cations by the iodide/iodine redox couple. The regeneration dynamics are observed to be too slow ( 100 {mu}s) to compete effectively with the recombination of injected electrons with dye cations. In contrast, for solid-state devices employing the organic hole conductor spiro-OMeTAD, the regeneration dynamics are fast enough (1{mu}s) to compete effectively with this recombination reaction, resulting in enhanced photocurrent generation.

  18. Cyanine dyes as intercalating agents: kinetic and thermodynamic studies on the DNA/Cyan40 and DNA/CCyan2 systems.

    Science.gov (United States)

    Biver, Tarita; De Biasi, Angela; Secco, Fernando; Venturini, Marcella; Yarmoluk, Sergiy

    2005-07-01

    The interaction of cyanines with nucleic acids is accompanied by intense changes of their optical properties. Consequently these molecules find numerous applications in biology and medicine. Since no detailed information on the binding mechanism of DNA/cyanine systems is available, a T-jump investigation of the kinetics and equilibria of binding of the cyanines Cyan40 [3-methyl-2-(1,2,6-trimethyl-4(1H)pyridinylidenmethyl)-benzothiazolium ion] and CCyan2 [3-methyl-2-[2-methyl-3-(3-methyl-2(3H)-benzothiazolylidene)-1-propenyl]-benzothiazolium ion] with CT-DNA is performed at 25 degrees C, pH 7 and various ionic strengths. Bathochromic shifts of the dye absorption band upon DNA addition, polymer melting point displacement (DeltaT = 8-10 degrees C), site size determination (n = 2), and stepwise kinetics concur in suggesting that the investigated cyanines bind to CT-DNA primary by intercalation. Measurements with poly(dA-dT).poly(dA-dT) and poly(dG-dC).poly(dG-dC) reveal fair selectivity of CCyan2 toward G-C basepairs. T-jump experiments show two kinetic effects for both systems. The binding process is discussed in terms of the sequence D + S left arrow over right arrow D,S left arrow over right arrow DS(I) left arrow over right arrow DS(II), which leads first to fast formation of an external complex D,S and then to a partially intercalated complex DS(I) which, in turn, converts to DS(II), a more stable intercalate. Absorption spectra reveal that both dyes tend to self-aggregate; the kinetics of CCyan2 self-aggregation is studied by T-jump relaxation and the results are interpreted in terms of dimer formation.

  19. Photostabilizing effects of singlet oxygen quenchers on long chain cyanine dyes

    Institute of Scientific and Technical Information of China (English)

    曾万学; 陈萍; 郑德水; Tsuneki Okazaki; Masaaki Hayami

    1995-01-01

    The total rate constants of the reaction of six antioxidants with singlet oxygen were measuredby fluorospectroscopy,and the effects of these antioxidants on the photostability of the dyes were alsoinvestigated kinetically.The results reveal that the six antioxidants are the effective quenchers of singlet oxygen(1O2)and can increase the photostability of the dyes.The power of metal chelates to quench 1O2 is thestrongest,and the chelates show the most effects on the photostability of the dyes.The photostability of thedyes has something to do with the relative amount of the antioxidant used.

  20. Study on time-resolved fluorescence dynamics of cyanine dye sensitizing AgBr

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The fluorescence spectra of three different dyes adsorbed on the tabular and cubic AgBr microcrystals are obtained by the picosecond time-resolved streak camera technique. The dependence of the ultrafast electron transferring from dye-aggre-gates to the conduction band of AgBr and the efficiency of spectral sensitization on different kinds of dyes with different concentrations is analyzed. Further more,the microcosmic mechanism of the sensitization process is discussed. It is found that the fluorescence decay curves are fitted very well by the double exponential func-tion,consisting of a slow component and a fast one with large amplitude. We con-sider this fast one mainly attributable to the electron transfer from dye J-aggre-gates to the conduction band of AgBr.

  1. 三甲川花菁染料合成工艺优化研究%Study on the Optimization of Synthesis Technique of Trimethine Cyanine Dyes

    Institute of Scientific and Technical Information of China (English)

    李海波; 郭建莹

    2015-01-01

    Based on the traditional production technique of trimethine cyanine dyes, which takes naphthalene hydrazine hydrochloride as raw material and involves processes of reduction, alkylation and condensation, this paper improves the tra-ditional production control conditions and the proportion of raw materials to reduce the variety and quantity of by-products and increase the yield of target products. After the process optimization, the production rate of dyes has increased by 20%. This improvement offers reference to the industrial production of other kinds of cyanine dyes.%以β-萘肼盐酸盐为原料,通过还原、烷基化、缩合生产三甲川花菁染料的工艺,改进传统生产控制条件以及原料比例,降低副产物种类和数量,提高目标产物产率.工艺优化后,染料生产率提高 20%,以上,为工业生产其他种类的花菁染料提供了借鉴.

  2. First-Principles Calculation of the Optical Properties of an Amphiphilic Cyanine Dye Aggregate

    NARCIS (Netherlands)

    Haverkort, Frank; Stradomska, Anna; Vries, Alex H. de; Knoester, Jasper

    2014-01-01

    Using a first-principles approach, we calculate electronic and optical properties of molecular aggregates of the dye amphi-pseudoisocyanine, whose structures we obtained from molecular dynamics (MD) simulations of the self-aggregation process. Using quantum chemistry methods, we translate the struct

  3. Tri- and Pentamethine Cyanine Dyes for Fluorescent Detection of alpha-Synuclein Oligomeric Aggregates

    NARCIS (Netherlands)

    Kovalska, V.B.; Losytskyy, M.Y.; Tolmachev, O.I.; Slominskii, Y.L.; Segers-Nolten, G.M.; Subramaniam, V.; Yarmoluk, S.M.

    2012-01-01

    The pathogenesis of Parkinson's disease that is the second most common neurodegenerative disease is associated with formation of different aggregates of alpha-synuclein (ASN), namely oligomers and amyloid fibrils. Current research is aimed on the design of fluorescent dyes for the detection of oligo

  4. A dioxaborine cyanine dye as a photoluminescence probe for sensing carbon nanotubes

    Science.gov (United States)

    Lutsyk, Petro; Verbitsky, Anatoly; Piryatinski, Yuri; Shandura, Mykola

    2016-01-01

    The unique properties of carbon nanotubes have made them the material of choice for many current and future industrial applications. As a consequence of the increasing development of nanotechnology, carbon nanotubes show potential threat to health and environment. Therefore, development of efficient method for detection of carbon nanotubes is required. In this work, we have studied the interaction of indopentamethinedioxaborine dye (DOB-719) and single-walled carbon nanotubes (SWNTs) using absorption and photoluminescence (PL) spectroscopy. In the mixture of the dye and the SWNTs we have revealed new optical features in the spectral range of the intrinsic excitation of the dye due to resonance energy transfer from DOB-719 to SWNTs. Specifically, we have observed an emergence of new PL peaks at the excitation wavelength of 735 nm and a redshift of the intrinsic PL peaks of SWNT emission (up to 40 nm) in the near-infrared range. The possible mechanism of the interaction between DOB-719 and SWNTs has been proposed. Thus, it can be concluded that DOB-719 dye has promising applications for designing efficient and tailorable optical probes for the detection of SWNTs. PMID:28144547

  5. Tri- and pentamethine cyanine dyes for fluorescent detection of alpha-synuclein oligomeric aggregates

    NARCIS (Netherlands)

    Kovalska, V.B.; Yu Losytskyy, M.; Tolmachev, O.I.; Slominskii, Yu.L.; Segers-Nolten, G.M.J.; Subramaniam, V.; Yarmoluk, S.M.

    2012-01-01

    The pathogenesis of Parkinson’s disease that is the second most common neurodegenerative disease is associated with formation of different aggregates of α-synuclein (ASN), namely oligomers and amyloid fibrils. Current research is aimed on the design of fluorescent dyes for the detection of oligomeri

  6. Polymorphism of Two-Dimensional Cyanine Dye J-Aggregates and Its Genesis: Fluorescence Microscopy and Atomic Force Microscopy Study.

    Science.gov (United States)

    Prokhorov, Valery V; Perelygina, Olga M; Pozin, Sergey I; Mal'tsev, Eugene I; Vannikov, Anatoly V

    2015-12-01

    Polymorphic J-aggregates of monomethine cyanine dye 3,3'-di(γ-sulfopropyl)-5,5'-dichlorotiamonomethinecyanine (TC) have been studied by fluorescence optical microscopy (FOM) and by atomic force microscopy (AFM). The in situ FOM observations in a solution drop distinguish two J-aggregate morphology classes: flexible strips and rigid rods. The AFM imaging of dried samples reveals a strong J-aggregate structural rearrangement under adsorption on a mica surface with the strips self-folding and the rods squashing into rectangular bilayers and much deeper destruction. In the present work, the following structural conclusions have been drawn on the basis of careful consideration of strip crystal habits and various structural features of squashed/destructed rods: (1) the tubular morphology of TC rods is directly proved by FOM measurements in the solution bulk; (2) the staircase model of molecular arrangement in strips is proposed explaining the characteristic ∼44° skew angle in strip vertices; (3) a model of tube formation by a close-packed helical winding of flexible monolayer strips is proposed and justified which explains the observed J-aggregate polymorphism and strip-to-rod polymorphic transformations in a wide spatiotemporal scale; (4) at a nanoscale, an unexpectedly complex quasi-one-dimensional organization in J-aggregate two-dimensional monolayers is observed by high-resolution AFM imaging of constituent nanostrips separated by a characteristic distance in the range of 6-10 nm. The obtained results indicate that the underlying monolayer structure is the same for all J-aggregate polymorphs.

  7. Effect of solvents on the barrierless reaction in the excited state of cyanine dye

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    UV-Vis, fluorescence spectroscopy and time resolved spectroscopic technique on picosecond and femto- second scales have been utilized to investigate the effect of steric hindrance and multiple hydroxyl groups of solvents on the barrierless isomerization in excited state of 3, 3′- di(3-sulfopropyl)thiacyanine triethylaminium salt. The results show that the factors mentioned above may be responsible for a different "short-time behavior" of the bleaching signal on the ground state and nonlinear viscosity dependence of the excited-state lifetime in isopropanol and glycol. These phenomena are distinguished from the situation reported in the long-chained monohydroxyl alcohol solvents. However, the dye molecule still exhibits the analyzing- wavelength dependence of the observed fluorescence lifetime, that is, the fluorescence lifetime increases with the increasing of analyzing-wavelength. The conclusions are in agreement with those drawn from femtosecond upconversion fluorescence experiments and further exemplify the barrierless isomerization model in the excited state.

  8. Radiation chemistry of cyanine dyes: Oxidation and reduction of merocyanine 540. [Accelerated electrons

    Energy Technology Data Exchange (ETDEWEB)

    Harriman, A. (Univ. of Texas, Austin (United States)); Shoute, L.C.T.; Neta, P. (National Inst. of Standards and Technology, Gaithersburg, MD (United States))

    1991-03-21

    Merocyanine 540 (MC) shows promise as a treatment for certain types of leukemia. It is shown that MC readily undergoes one-electron reduction under pulse radiolytic conditions. The {pi}-radical anion, produced by reduction with hydrated electrons and 2-hydroxypropyl radicals, disproportionates rapidly (k = 1.9 {times} 10{sup 9} M{sup {minus}1}s{sup {minus}1}) under anaerobic conditions but reduces O{sub 2} to superoxide ions (k = 1.6 {times} 10{sup 9} M{sup {minus}1}s{sup {minus}1}) in aerated solution. The dye reacts with trichloromethylperoxyl radicals (k = 9 {times} 10{sup 8} M{sup {minus}1}s{sup {minus}1}) to form several products, one of which is believed to be an adduct formed by addition of CCl{sub 3}OO{sup {sm bullet}} to the bridgehead carbon atom of the benzoxazole subunit. This species decays via first-order kinetics (k = 4.0 {times} 10{sup 3} s{sup {minus}1}) under pulse radiolytic conditions to form cleavage products. A second primary product is believed to arise from addition of CCl{sub 3}O{sub 2}{sup {sm bullet}} to the polymethine chain to form an {alpha}-amino carbon-centered radical capable of reducing O{sub 2} to superoxide ions. Preliminary studies indicate that the breakdown products are cytotoxic and could be important intermediates for the known antiviral activity of MC.

  9. Hierarchial coassembly of a cyanine dye in poly(vinyl alcohol) fibrous films by electrospinning.

    Science.gov (United States)

    Demir, Mustafa M; Horzum, Nesrin; Özen, Bengisu; Özçelik, Serdar

    2013-09-19

    We report molecular aggregate formation of TTBC (1,1',3,3'-tetraethyl-5,5',6,6'-tetrachlorobenzimidazolocarbocyanine) in submicrometer-sized PVA (poly(vinyl alcohol)) fibers by electrospinning. The formation of the molecular aggregate is examined by solution and instrumental parameters of electrospinning. The precursor solution of PVA/TTBC, in the range of 0.016-0.065 wt % is subjected to electrospinning under an electrical field ranging from 0.95 to 1.81 kV cm(-1). Both randomly deposited and uniaxially aligned fibers are achieved by using two parallel-positioned metal strips as counter electrode. Photoluminescence and polarized Fourier transform infrared spectroscopies are employed to determine spectral properties of the fibers. H-aggregates are formed within the electrospun fibers, regardless of their alignment, and H- and J-type aggregates coexist in the alternative spin-coated and the cast films. A strongly polarized photoluminescence emission is observed in the direction of uniaxially aligned fibers as a result of the orientation of the H-aggregates along the fiber axis. We demonstrate that electrospinning is a process capable of forming and orienting TTBC aggregates during the structural development of the polymer/dye nanofibers. These fibrous films may potentially find applications in optics and electronics.

  10. A Long-Wavelength Fluorescent Squarylium Cyanine Dye Possessing Boronic Acid for Sensing Monosaccharides and Glycoproteins with High Enhancement in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Hiroyuki Nakazumi

    2012-04-01

    Full Text Available Fluorescence sensing of saccharides and glycoproteins using a boronic acid functionalized squarylium cyanine dye (“SQ-BA” is characterized in terms of synthetic, fluorometric, thermodynamic and kinetic parameters. In our previous work, this newly synthesized dye was successfully applied to the separation and quantification of Gram-positive bacteria by capillary electrophoresis with laser-induced fluorescence detection (CE-LIF; however, the fundamental properties of the dye and its saccharide complexes still required elucidation, as presented in this paper. The dye itself forms nonemissive, soluble aggregates in aqueous solution. With the addition of a monosaccharide, the dye aggregate dissociates to form an emissive monomer accompanied by the formation of a cyclic cis-diol ester with long-wavelength emission (lex = 630 nm, lem = 660 nm. A very large fluorescence enhancement factor of 18× was observed for the sensing dye as a fructose complex at pH 10, yielding a limit of detection of 10 mM fructose. The relative order of fluorescence enhancement of SQ-BA with other monosaccharides was found to be: fructose > ribose > arabinose ≈ galactose > xylose > mannose > rhamnose > fucose ≈ glucose; and apparent affinity constants of 102.80, 102.08 and 100.86 M−1 were determined for fructose, ribose and glucose, respectively. Formation of the emissive complexes occurred within minutes, proving the kinetics of the sugar-dye interactions to be suitable for on-column labeling methods in CE-LIF. Furthermore, the sensing dye was successfully applied to glycoproteins, mucin type I–S and type III, which were detected with high sensitivity in batch aqueous solution as a result of the sugar-selective boronic acid-diol esterification as well as hydrophobic interactions.

  11. Supramolecular Assembly of Complementary Cyanine Salt J-Aggregates

    KAUST Repository

    Li, Zhong’an

    2015-09-09

    An understanding of structure–property relationships in cyanine dyes is critical for their design and application. Anionic and cationic cyanines can be organized into complementary cyanine salts, offering potential building blocks to modulate their intra/intermolecular interactions in the solid state. Here, we demonstrate how the structures of these complementary salts can be tuned to achieve highly ordered J-type supramolecular aggregate structures of heptamethine dyes in crystalline solids.

  12. Supramolecular Assembly of Complementary Cyanine Salt J-Aggregates.

    Science.gov (United States)

    Li, Zhong'an; Mukhopadhyay, Sukrit; Jang, Sei-Hum; Brédas, Jean-Luc; Jen, Alex K-Y

    2015-09-23

    An understanding of structure-property relationships in cyanine dyes is critical for their design and application. Anionic and cationic cyanines can be organized into complementary cyanine salts, offering potential building blocks to modulate their intra/intermolecular interactions in the solid state. Here, we demonstrate how the structures of these complementary salts can be tuned to achieve highly ordered J-type supramolecular aggregate structures of heptamethine dyes in crystalline solids.

  13. Photosensitizer (PS)-cyanine dye (CD) conjugates: Impact of the linkers joining the PS and CD moieties and their orientation in tumor-uptake and photodynamic therapy (PDT).

    Science.gov (United States)

    James, Nadine S; Joshi, Penny; Ohulchanskyy, Tymish Y; Chen, Yihui; Tabaczynski, Walter; Durrani, Farukh; Shibata, Masayuki; Pandey, Ravindra K

    2016-10-21

    To investigate the impact of linker(s) joining the photosensitizer HPPH [3-(1'-hexyloxy) ethyl-3-devinylpyropheophorbide-a] and the cyanine dye (CD) in tumor-imaging and photodynamic therapy (dual-function agents), a series of HPPH-CD conjugates were synthesized. The modifications were done in an attempt to minimize Forster Resonance Energy Transfer (FRET) between the two chromophores and maximize singlet oxygen production. Among the conjugates containing variable length of linkers, the HPPH-CD conjugate, in which the photosensitizer (PS) and the CD was joined by four Carbon [(CH2)4] units showed higher tumor uptake, improved tumor contrast and limited skin uptake in mice bearing Colon-26 (BALB/c) or U87 tumors in Nude mice. The bi-functional agents in which the HPPH was linked at the meta-position of phenyl-substituted CD 5, 6 and 7 showed longer tumor response (cure) than the corresponding para-substituted analogs 2, 3, and 4, which suggests that the orientation of the PS and CD moieties within the conjugate also makes a substantial difference in tumor-specificity. Compared to HPPH, the singlet oxygen yields of all the HPPH-CD conjugates were significantly low, and required a higher therapeutic dose to achieve the same in vivo response obtained by HPPH-PDT alone. However, conjugate 6 produced a higher singlet oxygen yield with reduced FRET and exhibited enhanced long-term PDT efficacy in mice bearing Colon-26 (BALB/c) and U87 tumors (nude) than its counterparts, including our lead compound (HPPH-CD), making it the most efficacious of the series. Thus, these conjugates bearing cyanine dye moiety (CD) provide an opportunity of imaging deeply seated tumors for fluorescence-guided surgery with an option of PDT.

  14. Water-soluble pyrrolopyrrole cyanine (PPCy) NIR fluorophores.

    Science.gov (United States)

    Wiktorowski, Simon; Rosazza, Christelle; Winterhalder, Martin J; Daltrozzo, Ewald; Zumbusch, Andreas

    2014-05-11

    Water-soluble derivatives of pyrrolopyrrole cyanines (PPCys) have been synthesized by a post-synthetic modification route. In highly polar media, these dyes are excellent NIR fluorophores. Labeling experiments show how these novel dyes are internalized into mammalian cells.

  15. Relation of molecular structure to Franck-Condon bands in the visible-light absorption spectra of symmetric cationic cyanine dyes.

    Science.gov (United States)

    Lin, Katrina Tao Hua; Silzel, John W

    2015-05-05

    A Franck-Condon (FC) model is used to study the solution-phase absorbance spectra of a series of seven symmetric cyanine dyes having between 22 and 77 atoms. Electronic transition energies were obtained from routine visible-light absorbance and fluorescence emission spectra. Harmonic normal modes were computed using density functional theory (DFT) and a polarizable continuum solvent model (PCM), with frequencies corrected using measured mid-infrared spectra. The model predicts the relative energies of the two major vibronic bands to within 5% and 11%, respectively, and also reproduces structure-specific differences in vibronic band shapes. The bands themselves result from excitation of two distinct subsets of normal modes, one with frequencies between 150 and 625cm(-1), and the other between 850 and 1480cm(-1). Vibronic transitions excite symmetric in-plane bending of the polymethine chain, in-plane bends of the polymethine and aromatic C-H bonds, torsions and deformations of N-alkyl substituents, and in the case of the indocyanines, in-plane deformations of the indole rings. For two dyes, the model predicts vibronic coupling into symmetry-breaking torsions associated with trans-cis photoisomerization.

  16. Investigation on the Cyanine Dyes Supramolecular Assembly and Chiral Inducement by Fulvic Acid%黄腐酸对菁染料超分子组装及手性调控研究

    Institute of Scientific and Technical Information of China (English)

    张秀凤; 陈蕾; 杨千帆; 孙晓然; 陈宏博; 杨光; 唐亚林

    2014-01-01

    Using cyanine dyes supramolecular as molecular probes to mark FA has important significance in life sciences and pharmaceutical chemistry ,w hich can detect FA as drug efficacy mechanism and the change in physiological activity .In the pres-ent paper ,we investigated supramolecular assembly and chiral inducement of cyanine dyes template by FA with absorption and circular dichroism (CD) spectra .The result suggests that FA can induce cyanine dyes from J-aggregation to monomer along with different colors change and has strong affinity with cyanine dye monomer .The template of FA not only can translate the chirality of MTC H-aggregation to other two states ,but also induce ETC J-aggregation to molecular rearrangement and form left-handed helix of J-aggregates .Besides ,the association of PTC with FA ,i .e .binding to FA gave rise to the J-aggregation CD signals . Meanwhile ,it was inferred that the meso substituent of cyanine dyes play an important role in the interaction between FA and the J-aggregation:the smaller the meso substituent ,the higher the affinity interacted with FA .Clearly ,the binding abilities be-tween cyanine dyes and FA follow the order of MTC> ETC> PTC .These results support that the cyanine dyes supramolecular aggregates can be used as a kind of excellent molecular probes for specific recognition of FA and achieve the effect of visual in-spection .%利用菁染料超分子作为分子探针对黄腐酸进行标记,检测黄腐酸和药效机制,对于生命科学和药物化学领域的发展具有重要意义。采用紫外-可见吸收光谱和圆二色谱研究黄腐酸作为模板对不同结构菁染料超分子的组装及手性调控。结果表明:黄腐酸能诱导三种菁染料 J-聚集体解聚为单体并伴有体系表观颜色的变化,并与菁染料单体之间具有很高亲和力。黄腐酸作为模板不仅可以诱导M TC形成具有一定手性的H-聚集体,而且能使M TC的 H-聚集体的手性出现两次反

  17. Photophysics of cyanine dyes adsorbed onto surfaces. Sub-nanosecond fluorescence lifetime measurements of 3,3'-diethyloxadicarbocyanine iodide and photoisomer

    Energy Technology Data Exchange (ETDEWEB)

    Vieira Ferreira, L.; Oliveira, A.; Henbest, K. [and others

    1998-01-01

    This report describes the experiment entitled 'Photophysics of Cyanine dyes on Surfaces'; carried out at the Central Laser Facility (CLF) from the 6th to the 20th January 1997. The experiment, funded by the Framework IV Large-Scale Facilities Access Scheme, was proposed by Prof. L.F. Vieira Ferreira, Centro de Quimica-Fisica Molecular, Complexo 1, IST, 1096 Lisboa Codex, Portugal, and carried out by visiting researchers from the Institute. They were supported by researchers from the Central Laser Facility, Rutherford Appleton Laboratory. Experimental results: The photo physics of 3,3'-Diethyloxadicarbocyanine iodide (DODCI) adsorbed onto swollen microcrystalline cellulose was investigated. Two fluorescence emissions band have been observed and assigned. One was due to singlet excited momers and a second new emission, seen at high laser fluences, was due to the formation of a photoisomer. The DODCI stays entrapped between the polymer chains and nonradiative pathways for deactivation are reduced, the lifetimes of the excited states were measured using time resolved fluorescence lifetimes techniques. The fluorescence lifetimes of the excited states are longer lived in a swollen cellulose matrix. The photoisomer emission especially lives an order of magnitude longer than in homogeneous media.

  18. Exploring the dynamics of fluorescence staining of bacteria with cyanine dyes for the development of kinetic assays

    Science.gov (United States)

    Thomas, Marlon Sheldon

    Bacterial infections continue to be one of the major health risks in the United States. The common occurrence of such infection is one of the major contributors to the high cost of health care and significant patient mortality. The work presented in this thesis describes spectroscopic studies that will contribute to the development of a fluorescent assay that may allow the rapid identification of bacterial species. Herein, the optical interactions between six bacterial species and a series of thiacyanine dyes are investigated. The interactions between the dyes and the bacterial species are hypothesized to be species-specific. For this thesis, two Gram-negative strains, Escherichia coli (E. coli) TOP10 and Enterobacter aerogenes; two Gram-positive bacterial strains, Bacillus sphaericus and Bacillus subtilis; and two Bacillus endospores, B. globigii and B. thuringiensis, were used to test the proposed hypothesis. A series of three thiacyanine dyes---3,3'-diethylthiacyanine iodide (THIA), 3,3'-diethylthiacarbocyanine iodide (THC) and thiazole orange (THO)---were used as fluorescent probes. The basis of our spectroscopic study was to explore the bacterium-induced interactions of the bacterial cells with the individual thiacyanine dyes or with a mixture of the three dyes. Steady-state absorption spectroscopy revealed that the different bacterial species altered the absorption properties of the dyes. Mixed-dye solutions gave unique absorption patterns for each bacteria tested, with competitive binding observed between the bacteria and spectrophotometric probes (thiacyanine dyes). Emission spectroscopy recorded changes in the emission spectra of THIA following the introduction of bacterial cells. Experimental results revealed that the emission enhancement of the dyes resulted from increases in the emission quantum yield of the thiacyanine dyes upon binding to the bacteria cellular components. The recorded emission enhancement data were fitted to an exponential (mono

  19. Comparison of the sequence-dependent fluorescence of the cyanine dyes Cy3, Cy5, DyLight DY547 and DyLight DY647 on single-stranded DNA.

    Science.gov (United States)

    Kretschy, Nicole; Somoza, Mark M

    2014-01-01

    Cyanine dyes are commonly used for fluorescent labeling of DNA and RNA oligonucleotides in applications including qPCR, sequencing, fluorescence in situ hybridization, Förster resonance energy transfer, and labeling for microarray hybridization. Previous research has shown that the fluorescence efficiency of Cy3 and Cy5, covalently attached to the 5' end of single-stranded DNA, is strongly sequence dependent. Here, we show that DY547 and DY647, two alternative cyanine dyes that are becoming widely used for nucleic acid labeling, have a similar pattern of sequence-dependence, with adjacent purines resulting in higher intensity and adjacent cytosines resulting in lower intensity. Investigated over the range of all 1024 possible DNA 5mers, the intensities of Cy3 and Cy5 drop by ∼ 50% and ∼ 65% with respect to their maxima, respectively, whereas the intensities of DY547 and DY647 fall by ∼ 45% and ∼ 40%, respectively. The reduced magnitude of change of the fluorescence intensity of the DyLight dyes, particularly of DY647 in comparison with Cy5, suggests that these dyes are less likely to introduce sequence-dependent bias into experiments based on fluorescent labeling of nucleic acids.

  20. Comparison of the sequence-dependent fluorescence of the cyanine dyes Cy3, Cy5, DyLight DY547 and DyLight DY647 on single-stranded DNA.

    Directory of Open Access Journals (Sweden)

    Nicole Kretschy

    Full Text Available Cyanine dyes are commonly used for fluorescent labeling of DNA and RNA oligonucleotides in applications including qPCR, sequencing, fluorescence in situ hybridization, Förster resonance energy transfer, and labeling for microarray hybridization. Previous research has shown that the fluorescence efficiency of Cy3 and Cy5, covalently attached to the 5' end of single-stranded DNA, is strongly sequence dependent. Here, we show that DY547 and DY647, two alternative cyanine dyes that are becoming widely used for nucleic acid labeling, have a similar pattern of sequence-dependence, with adjacent purines resulting in higher intensity and adjacent cytosines resulting in lower intensity. Investigated over the range of all 1024 possible DNA 5mers, the intensities of Cy3 and Cy5 drop by ∼ 50% and ∼ 65% with respect to their maxima, respectively, whereas the intensities of DY547 and DY647 fall by ∼ 45% and ∼ 40%, respectively. The reduced magnitude of change of the fluorescence intensity of the DyLight dyes, particularly of DY647 in comparison with Cy5, suggests that these dyes are less likely to introduce sequence-dependent bias into experiments based on fluorescent labeling of nucleic acids.

  1. On-column labeling of gram-positive bacteria with a boronic acid functionalized squarylium cyanine dye for analysis by polymer-enhanced capillary transient isotachophoresis.

    Science.gov (United States)

    Saito, Shingo; Massie, Tara L; Maeda, Takeshi; Nakazumi, Hiroyuki; Colyer, Christa L

    2012-03-06

    A new asymmetric, squarylium cyanine dye functionalized by boronic acid ("SQ-BA") was designed and synthesized for on-capillary labeling of gram-positive bacteria to provide for high sensitivity detection by way of a modified form of capillary electrophoresis with laser induced fluorescence detection (CE-LIF). The CE-based separation employed a polymer-enhanced buffer with capillary transient isotachophoresis in a new hybrid method dubbed "PectI." It was found that the addition of various monosaccharides to SQ-BA in a batch aqueous solution greatly enhanced the emission of the boronic acid functionalized dye by a factor of up to 18.3 at a long wavelength (λ(ex) = 630 nm, λ(em) = 660 nm) with a high affinity constant (K = ~10(2.80) M(-1)) superior to other sugar probes. Semiempirical quantum mechanics calculations suggest that the mechanism for this high enhancement may involve the dissociation of initially nonemissive dye associates (stabilized by an intramolecular hydrogen bond) upon complex formation with sugars. The fluorescence emission of SQ-BA was also significantly enhanced in the presence of a gram-positive bacterial spore, Bacillus globigii (Bg), which serves as a simulant of B. anthracis (or anthrax) and which possesses a peptidoglycan (sugar)-rich spore coat to provide ample sites for interaction with the dye. Several peaks were observed for a pure Bg sample even with polyethyleneoxide (PEO) present in the CE separation buffer, despite the polymer's previously demonstrated ability to focus microoorganisms to a single peak during migration. Likewise, several peaks were observed for a Bg sample when capillary transient isotachophoresis (ctITP) alone was employed. However, the new combination of these techniques as "PectI" dramatically and reproducibly focused the bacteria to a single peak with no staining procedure. Using PectI, the trace detection of Bg spores (corresponding to approximately three cells per injection) along with separation efficiency

  2. Isolation Mechanism of Supersensitization of Cyanine Dyes J-Aggregates%J-聚集态染料超增感作用隔离机理

    Institute of Scientific and Technical Information of China (English)

    勃·依·沙比罗; 石钟豪

    2001-01-01

    An isolation mechanism of supersensitization of cyanine dyesJ-aggregates is considered.It consists of decrease of electron-hole recombination due to space separation of the J-aggregates and the products of chemical sensitization .It is concluded that the basis for the isolation mechanism of supersensitization is a specific adsorption of organic compounds on (Ag,Au)S-centers.This adsorption is determined by conformity of distance between charges in 1, 3-dipoles of supersensitizer to distance between Ag+ (Au+ )and S2-ions in (Ag,Au)S cluster.The fundamental differences of the isolation mechanism from well known Gilman′ s reduction mechanism allows to realize superadditive supersensitization effect by the use of compositions of organic substances with a various structures.%根据“隔离”机理,超增感作用是由于J-聚集态染料与化学增感产物之间的空间分离而减少电子与空穴的复合。“隔离”是基于有机物在(Ag,Au)S中心上的独特吸附。这种独特吸附取决于超增感剂1,3偶极矩上的电荷距离是否与(Ag,Au)S斑中Ag+(Au+)和S-2离子之间的距离相符合。“隔离”机理不同于熟知的Gilman“还原”机理,根据本机理可通过不同结构有机物的组合应用使超增感作用获得超加和效应。

  3. Nucleation, growth, and dissolution of Ag nanostructures formed in nanotubular J-aggregates of amphiphilic cyanine dyes

    CERN Document Server

    Polzer, Egon Steeg Frank; Qiao, Yan; Rabe, Jürgen P; Kirstein, Stefan

    2015-01-01

    The nucleation, growth, and dissolution of silver nanowires within tubular aggregates of the dye C8S3 are investigated. The tubular aggregates are formed in aqueous solution from amphiphilic dyes and the silver wires are grown from silver salt. Samples were investigated systematically and in detail using cryo-TEM and TEM at different time steps after addition of silver salt (AgNO3) and short illumination with blue light (420 nm) for production of nuclei. The enhanced concentration of silver ions in proximity of the aggregates surface leads to favoured growth of seeds at or within the aggregates. The early stage of the seed growth is observable by cryo-TEM and shows to be well separated and isolated. There are no indications that nuclei are formed at preferred defect sites at the aggregates which is interpreted as homogeneous nucleation. The spatial position of the majority of initially formed seeds discriminates between growth of particles at the outer surface of the aggregate or wires at the inner space. The...

  4. Absorption Band Shapes of a Push-Pull Dye Approaching the Cyanine Limit: A Challenging Case for First Principle Calculations.

    Science.gov (United States)

    Capobianco, Amedeo; Borrelli, Raffaele; Landi, Alessandro; Velardo, Amalia; Peluso, Andrea

    2016-07-21

    The absorption band shapes of a solvent tunable donor-acceptor dye have been theoretically investigated by using Kubo's generating function approach, with minimum energy geometries and normal coordinates computed at the DFT level of theory. The adopted computational procedure allows us to include in the computation of Franck-Condon factors the whole set of normal modes, without any limitation on excitation quanta, allowing for an almost quantitative reproduction of the absorption band shape when the equilibrium geometries of the ground and the excited states are well predicted by electronic computations. Noteworthy, the functionals that yield more accurate band shapes also provide good prediction of the moment variations upon excitation; because the latter quantities are rarely available, theoretical simulation of band shapes could be a powerful tool for choosing the most appropriate computational method for predictive purposes.

  5. Characterization of the apoptotic response induced by the cyanine dye D112: a potentially selective anti-cancer compound.

    Directory of Open Access Journals (Sweden)

    Ning Yang

    Full Text Available Chemotherapeutic drugs that are used in anti-cancer treatments often cause the death of both cancerous and noncancerous cells. This non-selective toxicity is the root cause of untoward side effects that limits the effectiveness of therapy. In order to improve chemotherapeutic options for cancer patients, there is a need to identify novel compounds with higher discrimination for cancer cells. In the past, methine dyes that increase the sensitivity of photographic emulsions have been investigated for anti-cancer properties. In the 1970's, Kodak Laboratories initiated a screen of approximately 7000 dye structural variants for selective toxicity. Among these, D112 was identified as a promising compound with elevated toxicity against a colon cancer cell line in comparison to a non-transformed cell line. Despite these results changing industry priorities led to a halt in further studies on D112. We decided to revive investigations on D112 and have further characterized D112-induced cellular toxicity. We identified that in response to D112 treatment, the T-cell leukemia cell line Jurkat showed caspase activation, mitochondrial depolarization, and phosphatidylserine externalization, all of which are hallmarks of apoptosis. Chemical inhibition of caspase enzymatic activity and blockade of the mitochondrial pathway through Bcl-2 expression inhibited D112-induced apoptosis. At lower concentrations, D112 induced growth arrest. To gain insight into the molecular mechanism of D112 induced mitochondrial dysfunction, we analyzed the intracellular localization of D112, and found that D112 associated with mitochondria. Interestingly, in the cell lines that we tested, D112 showed increased toxicity toward transformed versus non-transformed cells. Results from this work identify D112 as a potentially interesting molecule warranting further investigation.

  6. INTERACTION OF LASER RADIATION WITH MATTER. LASER PLASMA: Limitation of high-power optical radiation by organic molecules: I. Substituted pyranes and cyanine dyes

    Science.gov (United States)

    Kopylova, T. N.; Svetlichnyi, Valerii A.; Mayer, G. V.; Reznichenko, A. V.; Podgaetskii, Vitalii M.; Ponomareva, O. V.; Samsonova, L. G.; Filinov, D. N.; Pomogaev, V. A.; Tel'minov, E. N.; Lapin, I. N.; Svetlichnaya, N. N.; Sinchenko, E. I.

    2003-11-01

    Photophysical processes proceeding in polyatomic organic molecules (pyran derivatives and cyanines) excited by high-power laser radiation at 532 nm are studied. Some properties of their changes depending on the structure, solvent, and excitation conditions are determined. The effect of limitation of high-power exciting radiation by the organic molecules is found. The maximum limitation (Kmax = 15.0 at the initial transmission equal to 70%) was observed for the cyanine derivative and is comparable to this effect for fullerenes C60, which are widely used as radiation limiters.

  7. Cyanines Bearing Quaternary Azaaromatic Moieties

    OpenAIRE

    Sbliwa, Wanda; Matusiak, Grazyna; Bachowska, Barbara

    2006-01-01

    Selected cyanines bearing quaternary azaaromatic moieties are presented, showing their monomers, dimers and polymers, as well as their possible applications. Cyanines having NLO properties are also briefly described.

  8. High sensitivity analysis of water-soluble, cyanine dye labeled proteins by high-performance liquid chromatography with fluorescence detection

    Energy Technology Data Exchange (ETDEWEB)

    Qiao Xiaoqiang [CAS Key Laboratory of Separation Science for Analytical Chemistry, National Chromatographic Research and Analysis Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100039 (China); Wang Li [State Key Laboratory of Fine Chemicals, Dalian University of Technology, 158 Zhongshan Road, Dalian 116012 (China); Ma Junfeng [CAS Key Laboratory of Separation Science for Analytical Chemistry, National Chromatographic Research and Analysis Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100039 (China); Deng Qiliang; Liang Zhen [CAS Key Laboratory of Separation Science for Analytical Chemistry, National Chromatographic Research and Analysis Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China); Zhang Lihua, E-mail: lihuazhang@dicp.ac.cn [CAS Key Laboratory of Separation Science for Analytical Chemistry, National Chromatographic Research and Analysis Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China); Peng Xiaojun [State Key Laboratory of Fine Chemicals, Dalian University of Technology, 158 Zhongshan Road, Dalian 116012 (China); Zhang Yukui [CAS Key Laboratory of Separation Science for Analytical Chemistry, National Chromatographic Research and Analysis Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China)

    2009-04-27

    A water-soluble sulfo-3H-indocyanine dye, the active N-hydroxysuccinimide ester of 3H-Indolium,1-[(4-carboxyphenyl)methyl]-2-[3-[1-[(4-carboxyphenyl)methyl] -1,3-dihydro-3,3-dimethyl-5-sulfo-2H-indol-2-ylidene]-1-propenyl] -3,3-dimethyl-5-sulfo-(9CI) (sb-cy3-NHS), containing two p-carboxybenzyl groups on nitrogen atoms, previously developed by our laboratory, was for the first time used for protein derivatization, followed by HPLC separation and fluorescence detection. With bovine serum albumin (BSA) as a model protein, effects of various experimental conditions, including denaturant concentration, reaction time and temperature, the pH value of buffer, and the molar ratio of fluorescence reagent to protein, on protein derivatization efficiency were systematically investigated. Under the optimal conditions, the limit of detection (LOD) for derivatized BSA was decreased to 12.8 nM, about 100-fold lower than that by UV and fluorescence detection with commercial fluorescein isothiocyanate (FITC) as labeling reagent. For HPLC analysis, an on-column excess fluorescence reagent depletion technique was developed based on the hydrophilicity of sb-cy3-NHS, which could avoid the interference on the analysis of target compounds. In addition, sb-cy3-NHS was applied for the derivatization of a three-protein mixture and egg white proteins. Compared to the results labeled by FITC, more proteins with low concentrations could be labeled by sb-cy3-NHS, resulting in improved detection sensitivity for protein analysis. All these results demonstrated that sb-cy3-NHS might be promising in detecting low abundance proteins, especially in the quantitative analysis of proteins.

  9. An OFF–ON–OFF type of pH fluorescent sensor: Benzo[c,d]indole-based dimethine cyanine dye-synthesis, spectral properties and density functional theory studies

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Qi [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi’an 710069 (China); Hong Su, Xiao [College of Life Sciences, Northwest University, Xi’an 710069 (China); Ying Wang, Lan, E-mail: wanglany@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi’an 710069 (China); Sun, Wei; Bo Lei, Yi [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi’an 710069 (China); Yi Wen, Zhen [Institute of Modern Physics, Northwest University, Xi’an 710069 (China)

    2014-10-15

    We synthesized a novel OFF–ON–OFF type of pH-dependent fluorescent sensor: benzo[c,d]indole-based dimethine cyanine dye D1, with donor-π-acceptor (D-π-A) structure based on intramolecular charge transfer system (ICT), which employed dimethine cyanine dye as a fluorophore and pentavalent nitrogen NH{sup +} group as a pH modulator, respectively. The product was identified by {sup 1}H NMR, {sup 13}C NMR, IR, UV–vis and HRMS. The investigation of spectral properties found that dye D1 showed excellent spectroscopic properties and its absorption maxima and fluorescence quantum yield were basically larger in protic solvent than in aprotic solvent. Meanwhile, the absorption spectra of D1 were revealed to hypochromatic-shift and the absorption intensity was gradually decreased along with the increase of pH value. Interestingly, dye D1 showed remarkable fluorescence when pH value was in the range of 6.00–9.80 with the peak at 8.21, which was defined as an OFF–ON–OFF type of pH-dependent fluorescent sensors based on ICT. In addition, dye D1 exhibited a high selectivity for H{sup +} over other common ions, such as Cl{sup −}, K{sup +}, Fe{sup 2+} etc. Theoretical calculations based on density functional theory (DFT) were employed to provide a better understanding of this particular dye sensor. These results indicated that D1 would be able to act as an efficient pH-sensor and had a potential to play an important role in biological and medical study. - Highlights: • A new benzo[c,d]indole-based pH fluorescent sensor was synthesized without adding catalyst. • The absorption spectra of dye D1 were associated with the solvents’ pK{sub a} value. • The sensor showed OFF–ON–OFF fluorescence in pH buffer, with the peak at 8.21. • The sensor had high sensitivity and selectivity.

  10. Design, synthesis and biological evaluation of trimethine cyanine dyes as fluorescent probes for the detection of tau fibrils in Alzheimer's disease brain and olfactory epithelium.

    Science.gov (United States)

    Gu, Jiamin; Anumala, Upendra Rao; Heyny-von Haußen, Roland; Hölzer, Jana; Goetschy-Meyer, Valérie; Mall, Gerhard; Hilger, Ingrid; Czech, Christian; Schmidt, Boris

    2013-06-01

    Shedding light on grey matter: Fluorescent trimethine cyanines were evaluated as imaging probes for neurofibrillary tangles in post-mortem brain sections of Alzheimer's disease patients. These probes bind to neurofibrillary tangles with high contrast and selectivity over amyloid β plaques. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Tailoring cyanine dark states for improved optically modulated fluorescence recovery.

    Science.gov (United States)

    Mahoney, Daniel P; Owens, Eric A; Fan, Chaoyang; Hsiang, Jung-Cheng; Henary, Maged M; Dickson, Robert M

    2015-04-02

    Cyanine dyes are well-known for their bright fluorescence and utility in biological imaging. However, cyanines also readily photoisomerize to produce nonemissive dark states. Co-illumination with a secondary, red-shifted light source on-resonance with the longer wavelength absorbing dark state reverses the photoisomerization and returns the cyanine dye to the fluorescent manifold, increasing steady-state fluorescence intensity. Modulation of this secondary light source dynamically alters emission intensity, drastically improving detection sensitivity and facilitating fluorescence signals to be recovered from an otherwise overwhelming background. Red and near-IR emitting cyanine derivatives have been synthesized with varying alkyl chain lengths and halogen substituents to alter dual-laser fluorescence enhancement. Photophysical properties and enhancement with dual laser modulation were coupled with density functional calculations to characterize substituent effects on dark state photophysics, potentially improving detection in high background biological environments.

  12. Cyanine dye used for recordable DVDR production Dye process of Organica Dye 967%用于可记录DVDR生产的花菁染料--Organica Dye 967花菁染料的调配

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    @@ 一、综述 1.染料信息 0rganica Dye 967是一种新型独特的花菁染料. 出厂时Dye 967染料处于随时可以调配的粉末状态,在包装中包括染料粉末和稳定剂;只溶于一种溶剂(TFP);在没有调配的状态下,如果保存得当,该染料可以保证超过1年的保存期限;如果采用比较稳定的溶剂,该染料可以被循环使用10次以上;适用于目前的所有DVDR生产设备.

  13. 甲苄基不对称三甲川菁染料的合成及光谱性能%Synthesis and Properties of N-4-methylbenzyl Trimethine Cyanine Dye

    Institute of Scientific and Technical Information of China (English)

    宋波; 房正薇; 郭晶丽; 姜婷婷

    2012-01-01

    2,3,3-Trimethyl-3H-indole-5-sulfonic acid was synthesized using 4-hydrazinylbenzenesulfonic acid and 3-methyl-2-butanone in acidic medium. 2,3,3 Trimethyl-3H-indoleninium-5-sulfonate and N-4-methylbenzyl-2,3,3-trimethyl-3H-indoleninium-5-sulfonates were synthesized. The title water soluble trimethine cyanine dye was synthesized by one step and purified by C18 reverse phase column chromatograph. The structure of the title dye was confirmed by 1HNMR. The spectral properties of the title dye were detected.%以对肼基苯磺酸和3-甲基-2-丁酮为原料经催化合成2,3,3.三甲基-3H-吲哚-5.磺酸,进一步制得钾盐。经钾盐合成Ⅳ-甲苄基取代吲哚季铵盐。采用一步法将钾盐与吲哚季铵盐缩合为一种不对称三甲川菁染料,并考查其光谱性能。所合成染料经C-18反相柱分离提纯,利用核磁共振氢谱进行了结构表征。

  14. Synthesis and Spectra of Functional Unsymmetrial Trimethine Cyanine Dyes%不对称功能性吲哚三甲川菁染料的合成及光谱

    Institute of Scientific and Technical Information of China (English)

    谷迎春; 费学宁; 刘玉茹; 王义启

    2012-01-01

    以苯肼盐酸盐为原料,将其与甲基异丙基酮通过闭环反应,生成2,3,3-三甲基吲哚的衍生物,再经过与溴乙烷、六溴己酸反应成吲哚盐,然后和二甲脒反应得到吲哚乙烯基苯胺,最后合成了两种不同取代基团的水溶性的不对称三甲川吲哚菁染料,并通过核磁、质谱等测试手段对其结构进行表征.研究了该染料的紫外吸收光谱和荧光光谱.%The 2,3,3-trimethyl indole derivatives were synthesized by closed-loop reaction from phenylhydrazine derivatives and methyl isopropyl ketone.Then the 2,3,3-trimethyl indole derivatives were alkylated by ethyl bromide,6-bromhexine acid to afford indole salts,which then were reacted with N,N'-diphenylformamidine to get indole ethylene aniline.At last,the unsymmetrical water soluble cyanine dyes with two different functional groups were synthesized.The structures of the dyes were characterized by 1HNMR,MS.The UV absorption and fluorescence spectra of the dyes were also studied.

  15. Photophysics of aminophenyl substituted pyrrolopyrrole cyanines

    OpenAIRE

    Wiktorowski, Simon; Fischer, Georg; Winterhalder, Martin; Daltrozzo, Ewald; Zumbusch, Andreas

    2012-01-01

    A series of novel pyrrolopyrrole cyanines (PPCys) bearing various aminophenyl substituents at the diketopyrrolopyrrole (DPP) core are presented. Compared to their alkoxyphenyl substituted analogues, these dyes feature additional intense electronic transitions of charge-transfer character which give detailed insight into the optical properties of PPCys. The energetic mixing of the involved orbitals has pronounced effects on the absorption and fluorescence behavior. Protonation of the amino fun...

  16. 新型中位取代七甲川菁染料的合成及光稳定性研究%Synthesis, Characterization and Spectral Properties of Novel Meso-Substituted Heptamethine Cyanine Dye

    Institute of Scientific and Technical Information of China (English)

    陈秀英; 郭琳; 贾显林; 高海燕; 郑昌戈

    2012-01-01

    Two novel meso-substituted heptamethine cyanine dyes were prepared and characterized by ' HNMR and HRMS spectra. The absorption and emission spectral properties in different solvents were studied. The maxima of the absorption and fluorescent spectra of the dyes 3b and 3c were at 677/790 nm and 647/786 run in methanol respectively with larger stokes shifts of 113 nm and 139 nm. The photo-degradation reaction showed that the rate constants for the three dyes 3a-3c were 1. 21× l0-3mol/min, 1. 81× l0-3mol/min and 2. 14× l0-3mol/ min respectively. Cyclic voltammetry showed that the oxidative potentials for 3a-3c were 0. 729 V, 0. 624 V and 0. 598 V respectively. The experiment of photodegradation showed that electron-withdrawing group on methine chain of heptamethine cyanine dye enhanced the photostability and electron-donating group on methine chain decreased the photostability of the dyes. The ability of donating and withdrawing affected the photostability of the dyes. The hydrogen bond on substituted atom on methine chain was favor for enhancing the photostability of the dyes. And hydrogen bond of chlorine atom on methine chain was in favor of enhancing the photostability of the dyes. But nitrogen atom on methine chain can not form hydrogen bond and not helpful for the photostability of the dyes.%本文合成了两种新型中位取代近红外七甲川菁染料,采用核磁1 HN-MR和HRMS质谱对其结构进行了表征,并测试了染料在不同溶剂中的吸收光谱和荧光发射光谱性质.染料3b、3c在甲醇中的最大吸收波长和最大荧光发射波长分别为677/790 nm和647/786 nm,斯托克斯位移分别为113 nm、139 nm,经过光降解实验测试得到3种染料3a—3c在乙醇中的光降解速率常数分别为1.21×10-3 mol/min、1.81×l0-3mol/min和2.14×103mol/min.循环伏安法测得染料3a—3c的氧化电位分别在0.729 V、0.624V和0.598V.光降解实验表明:七甲川菁染料中位亚甲基链上吸电基取代增强染

  17. Color in Bridge-Substituted Cyanines.

    Science.gov (United States)

    Olsen, Seth

    2016-12-29

    Theories of color in cyanine dyes have evolved around the idea of a "resonance" of structures with distinct bonding and charge localization. Understanding the emergence of resonance models from the underlying many-electron problem remains a central issue for these systems. Here, the issue is addressed using a maximum-entropy approach to valence-bond representations of state-averaged complete-active space self-consistent field models. The approach allows calculation of energies and couplings of high-energy valence-bond structures that mediate superexchange couplings and chemical bonding. A series of valence-bond Hamiltonians for a series of bridge-substituted derivatives of Michler's hydrol blue (a monomethine cyanine) is presented. The Hamiltonians are approximated with a simple linear model parametrized by the Brown-Okamoto σp(+) parameter of the bridge substituent. A quantitative lower bound on σp(+), beyond which a resonant cyanine-like ground state will not exist, is presented. The large effective coupling in two-state resonance models emerges from superexchange associated with either covalent bonding or charge-carrier delocalization, with the former contribution significantly the stronger. The results provide ab initio justification for empirical diabatic-state models of methine optical response. They are of general interest for understanding the optoelectronic response in cyanines.

  18. 苯并噻唑类核酸分子荧光探针的合成及光谱性质%Synthesis and Spectral Properties of Benzothiazole Cyanine Dyes for Nucleic Acid Fluorescence Probe

    Institute of Scientific and Technical Information of China (English)

    陈秀英; 郭琳; 郑昌戈; 高海燕; 安文

    2012-01-01

    设计合成了3种两端杂环氮原子上具有不同取代基的苯并噻唑类不对称三甲川菁染料,并对染料的结构进行了表征.测试了染料在乙醇中的吸收和荧光发射光谱,染料的最大吸收值和荧光发射值分别在629 ~635 nm和656 ~672nm之间.染料8、9和10的斯托克斯位移分别为23、37和27nm.染料在溶剂中基本无荧光,荧光量子产率小于0.021,可以极大的降低染料自身的荧光背景干扰.染料的光降解实验表明,两端杂环氮原子苄基取代后可以明显增强染料的光稳定性.测试循环伏安曲线得到染料的氧化电位分别为0.535、0.456和0.399 V,氧化电位越大,光降解速率常数越小,与光降解实验得到的降解速率常数结果一致.%Three novel asymmetric trimethine benzothiazole cyanine dyes with different iV-substituents were designed and synthesized. The structures of the dyes were characterized, and the maximums of the spectral absorption and emission of the dyes in ethanol were found in the range of 629 ~ 635 nm and 656 ~ 672 nm. The Stokes shift values for dyes 8, 9 and 10 were 23, 37 and 27 nm, respectively. The dyes were almost non-fluorescent in solvents with a low fluorescent quantum yield of less than 0. 021 in ethanol, which could reduce the background interference greatly. The photodegradation experiment showed that the introduction of benzyl group on the heteroaromatic rings improved the photostabilites of the dyes obviously.' The oxidizing potentials for the dyes 8, 9 and 10 were at 0. 535, 0.456 and 0. 399 V ts SCE, which was consistent with the data of photodegradation experiment.

  19. 一种菁染料-β-环糊精的合成及其对水溶液中Cu2+的定量识别研究%Synthesis of a cyanine dye-β-cyclodextrin and its inclusion with bluestone

    Institute of Scientific and Technical Information of China (English)

    任海晶; 王军; 皇甫惠君; 刘世川

    2011-01-01

    A cyanine dyeβ-cyclodextrin (Dye-β-CD) was synthesized. The Dye-β-CD as host compounds with fluorescent probes was studied in supramolecular inclusion complexes by UV-vis spectral titration. The results showed that Dye-β-CD could be determind, Dye-β-CD and bluestone could form inclusion complexes with a ratio of 1:1 under pH value of 7. 2. The corresponding inclusion constant was 5.47 × 104 L/mol according to the Benesi-Hildebrand equation. It was indicated that the Dye-β-CD was an excellent host compound with a fluorescent probe.%合成了一种菁染料-β-环糊精化合物(Dye-β-CD),采用紫外-可见光谱法探讨了以Dye-β-CD作为带有荧光探针的主体化合物在水质分析中的应用.结果表明,Dye-β-CD能够在pH =7.2的缓冲溶液介质中对Cu2进行定量识别,根据Benesi-Hildebrand方程确定Dye-β-CD与硫酸铜包结比为1,其包合常数为5.47×104 L/mol,表明Dye-β-CD是一种优良的带有荧光探针的主体化合物.

  20. Investigation on Synthesis and Photostabilities of Novel Asymmetric Benzothiazole Trimethine Cyanine Dyes%新型不对称苯并噻唑三次甲基菁染料的合成及光稳定性研究

    Institute of Scientific and Technical Information of China (English)

    陈秀英; 郭琳; 郑昌戈; 高海燕; 王海军; 张丹

    2012-01-01

    合成了系列杂环氮原子具有不同取代基的不对称苯并噻唑三次甲基菁染料,染料结构经过质谱、1H NMR表征,测试了染料在乙醇中的吸收和荧光发射光谱,染料的最大吸收值和荧光发射值分别在628~631和662~666 nm之间.染料在溶剂中几乎无荧光,可以极大的降低染料自身的荧光背景干扰.染料的光降解实验表明:喹啉环 上辛烷基取代和噻唑环上苄基取代时,染料的光稳定性最强.染料8a~8d的光降解速率常数分别为6.38×10-4,12.5×10-4,2.68×10-4和6.30×10-4 mol·min-1.循环伏安实验法测试了染料的氧化电位.%Novel asymmetric trimethine benzothiazole cyanine dyes with different N-substituents were synthesized and characterized by MS and 'H NMR techniques. The maximums of absorption and emission spectra of the dyes in ethanol were in the range of 628~631 and 662~666 nm, respectively. The dyes were almost non-fluorescent in solvents, which can reduce the background interference greatly. The photodegradation experiment showed that the octyl group on quinoline ring and benzyl group on benzothiazole ring improved the photostabilites of the dyes obviously. The rate constants of photoreaction of the dyes 8a~8d were 6.38× 10-4, 12.5× 10-4, 2.68×10-4 and 6.30×10 4 mol·min-1, respectively. Oxidation potentials were determined by cyclic voltammetry.

  1. On the excited-state multi-dimensionality in cyanines

    Science.gov (United States)

    Dietzek, Benjamin; Brüggemann, Ben; Persson, Petter; Yartsev, Arkady

    2008-03-01

    Vibrational coherences in a photoexcited cyanine dye are preserved for the time-scale of diffusive torsional motion to the bottom of the excited-state potential. The coherently excited modes are virtually unaffected by solvent friction and thus distinct from the bond-twisting motion, which is strongly coupled to the surrounding solvent. We correlate the modes apparent in the resonance Raman and the four-wave mixing signal of 1,1'-diethyl-2,2'-cyanine with the understanding of optimal control of isomerization. In turn, the experimental results illustrate that optimal control might be used to obtain vibrational information complementary to conventional spectroscopic data.

  2. Taking up the cyanine challenge with quantum tools.

    Science.gov (United States)

    Le Guennic, Boris; Jacquemin, Denis

    2015-03-17

    Cyanine derivatives, named from the Greek word kyanos meaning dark-blue, were discovered more than 150 years ago and remain one of the most widely used classes of organic dyes with contemporary applications in photography (panchromatic emulsions), information storage (CD-R and DVD-R media) and biochemistry (DNA and protein labeling) fields. Cyanine chromogens consist of a charged π-conjugated segment containing an odd number of sp(2) carbon atoms with the chain capped at the extremities by two electronegative centers, typically nitrogen or oxygen atoms. Cyanines are characterized by a vanishing bond length alternation indicating nearly equal carbon-carbon bond lengths, as well as a very intense and sharp absorption band presenting a shoulder. This hallmark band undergoes a strong red shift when the chain is extended. This so-called vinyl shift is extremely large (ca. 100 nm for each pair of carbon atoms added in the π-conjugated path), making cyanines ideal building blocks for the design of devices with near-infrared applications. Numerous cyanines also exhibit emission bands with large quantum yields. These exceptional optical properties explain why both canonical cyanines and the corresponding fluoroborates (e.g., boron-dipyrromethene, BODIPY) remain the focus of an ever-growing body of experimental work. In turn, this popularity has stimulated quantum mechanical investigations aiming, on the one hand, at probing the specific electronic nature of cyanine dyes and, on the other hand, at helping to design new dyes. However, the adiabatic approximation to time-dependent density functional theory, the most widespread ab initio model for electronically excited states, fails to accurately reproduce the absorption spectra of cyanine derivatives: it yields a systematic and large underestimation of the experimental wavelengths irrespective of the details of the computational protocol. In contrast, highly correlated wave function approaches provide accurate transition

  3. β-环糊精与几种菁染料包合物的动态结构 及包合平衡的NMR研究%STUDY OF THE DYNAMIC STRUCTURES AND EQUILIBRIA OF β-CYCLODEXTRIN WITH CYANINE DYES

    Institute of Scientific and Technical Information of China (English)

    唐亚林; 冯娟; 徐广智; 向俊峰; 陈次平; 阎文鹏

    2001-01-01

    The results of 1H NMR investigation of β-Cyclodextrin inclusion complexes with three cyanine dyes in D\\-2O and DMSO solution are reported in this paper, It was found that there is difference in chemical shift of some protons both of β-Cyclodextrin cavity and of cyanine dyes between after and before complexing,the position of which is dependent upon the inclusive degree. Fluorescence spectroscopy of cyanine dyes showed that the fluorescence intensity of these dyes is obviously quenched due to the forming of inclusions with β-Cyclodextrin, calculation results based on fluorescence spectroscopy indicated that β-Cyclodextrin formed 1∶1 inclusion with three cyanine dyes respectively. Information about hydrogen bond was induced from the study of temperature dependence of chemical shift of hydroxyl protons in β-Cyclodextrin cavity, OH-3 and OH-6. Their equilibrium constants of inclusion complexes were obtained from NMR chemical shift titration. The structure model of three inclusion complexes and dynamic process entering β-Cyclodextrin cavity has been described in this paper.%用核磁共振方法研究了β-CD与三种菁染料3,3′-二(3-磺丙基)噻菁三乙胺盐(dyeA)、3,3′-二(3-磺丙基)-5-氯-噻菁三乙胺盐(dyeB)和3,3′-二(3-磺丙基)-5,5′-二苯基-9-乙基恶碳菁(dyeC)在溶液中的包合现象和包合物的动态结构,实验发现β-CD环糊精疏水腔中的H-3和H-5以及三种菁染料的芳环上质子的化学位移由于形成包合物而发生明显变化,而且峰的位置随包合程度的不同而不同. 实验中发现包合物的荧光强度随β-CD浓度增加而减弱,相应计算表明β-CD与三种菁染料形成了1∶1的包合物.本文研究了三种包合物中主体部分OH-3和OH-6的化学位移随温度变化的情况,获得了包合物中氢键强弱的信息,通过NMR化学位移滴定法计算得到了三种包合物在水溶液中的稳定常数,在上述工作的基础上,本文提出了

  4. Verdict: Time-Dependent Density Functional Theory "Not Guilty" of Large Errors for Cyanines.

    Science.gov (United States)

    Jacquemin, Denis; Zhao, Yan; Valero, Rosendo; Adamo, Carlo; Ciofini, Ilaria; Truhlar, Donald G

    2012-04-10

    We assess the accuracy of eight Minnesota density functionals (M05 through M08-SO) and two others (PBE and PBE0) for the prediction of electronic excitation energies of a family of four cyanine dyes. We find that time-dependent density functional theory (TDDFT) with the five most recent of these functionals (from M06-HF through M08-SO) is able to predict excitation energies for cyanine dyes within 0.10-0.36 eV accuracy with respect to the most accurate available Quantum Monte Carlo calculations, providing a comparable accuracy to the latest generation of CASPT2 calculations, which have errors of 0.16-0.34 eV. Therefore previous conclusions that TDDFT cannot treat cyanine dyes reasonably accurately must be revised.

  5. Cyanines as efficient photosensitizers in photodynamic reaction: photophysical properties and in vitro photodynamic activity.

    Science.gov (United States)

    Kulbacka, J; Pola, A; Mosiadz, D; Choromanska, A; Nowak, P; Kotulska, M; Majkowski, M; Hryniewicz-Jankowska, A; Purzyc, L; Saczko, J

    2011-04-01

    The purpose of the present study was to explore the potential application of cyanines in photodynamic treatment. The photophysical features of four cyanines (KF570, HM118, FBF-749, and ER-139) were investigated by elemental and spectral analyses. Two malignant cell lines (MCF-7/WT and MCF-7/DOX) were used to test the potential for use in the photodynamic therapy. The cytotoxic effects of these dyes were determined by the MTT assay after 4 and 24 h of incubation with the cyanine. KF570 and HM118 were irradiated with red light (630-nm filter) and FBF-749 and ER-139 with green light (435-nm filter). The results showed that the cyanine HM118 demonstrated a major phototoxic effect. It was also noted that the efficiency of photodynamic therapy was higher in the doxorubicin-resistant cell line (MCF-7/DOX).

  6. 菁类染料敏化的固态纳米TiO2光电化学电池%A Solid-state Unsymmetrical Cyanine Dye Sensitized Nanoporous TiO2 Photoelectrochemical Cell

    Institute of Scientific and Technical Information of China (English)

    张莉; 任焱杰; 张正诚; 方世碧; 田禾; 蔡生民

    2001-01-01

    染料敏化TiO2光电化学电池具有较高的能量转换效率,价格仅为传统单晶硅太阳能电池的1/10,成为半导体光电化学领域的研究热点[1-4]。但该类电池内的电解液可流动,造成电池密封困难,限制其实用化。针对这一问题,采用无机p-型半导体材料[5,6]和高分子导体等电解液替代物组装固态光电化学电池成为该领域的新的研究方向[7-9]。我们[10]用凝胶网络高分子电解质组装成固态电池,取得了令人满意的结果。电池中原使用的敏化剂是顺二硫氰根-双(2,2′-联吡啶-4,4′-二羧酸)合钌(Ⅱ)(cis-bis)(thiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylate)ruthenium(Ⅱ),其价格昂贵,合成路线复杂。本文用自合成的、价格低廉的纯有机不对称菁类染料(Cyanine dye,以下简称为CD)敏化TiO2电极和基于聚氧乙烯(PEO)的凝胶网络高分子电解质组装成固态电池,并研究了所得固态电池的光电转换性能。

  7. Contribution to the development of the dye laser emitting in the near infrared: application to the investigation of the laser characteristics of a series of cyanines. [Thesis

    Energy Technology Data Exchange (ETDEWEB)

    Hirth, A.

    1974-08-07

    Laser emission achieved by means of fluorescent substances is reviewed. Qualitative results were obtained with a diagram of the molecule energy level, and quantitative results were obtained with the aid of formulas for the gain and critical inversion as a function of both the spectroscopic and kinetic parameters of the molecule. For flash light devices, the development of rapid discharge circuits and coaxial flash tube light sources allowed a certain number of arrangements to be designed. Laser emission of a series of tricarbocyanine molecules could be obtained via direct excitation by means of flash tube light sources. The emission wavelengths were compared with the emitted luminous efficiency. The influence of the physico-chemical parameters on the emission characteristics is detailed. Methods applied to dye lasers for the visible area were extended to those for the near infrared. Results were obtained either by tuning the emission wavelength or by generation of ultra-short infrared light pulses by mode locking in a cavity applied to three lasers emitting at 800, 870, and 950 nm.

  8. Synthesis and spectral properties of near-infrared aminophenyl-, hydroxyphenyl-, and phenyl-substituted heptamethine cyanines.

    Science.gov (United States)

    Lee, Hyeran; Mason, J Christian; Achilefu, Samuel

    2008-01-18

    Diverse meso-aminophenyl-, hydroxyphenyl-, and phenyl-substituted heptamethine cyanine dyes were prepared by a modified Suzuki--Miyaura method in good yields. In addition, direct Suzuki coupling of Vilsmeier--Haack reagent extends the procedure to the synthesis of otherwise difficult cyanine dyes containing multiple heteroatoms in the indolium ring. The new compounds possess excellent spectral properties and can be used to label bioactive molecules and nanoparticles. The one-pot synthesis procedure eliminates the cumbersome steps of protecting/deprotecting amino or hydroxy groups.

  9. Mode coupling in organic dye lasers

    Energy Technology Data Exchange (ETDEWEB)

    Hirth, A.

    1973-10-25

    Saturable dye triggering is discussed together with relaxation time and pulse duration. The influence of stimulated emission is detailed. Experimental results of mode coupling with cyanines and xanthines, flash excited and not, are reported.

  10. Solvent effects on cyanine derivatives: a PCM investigation.

    Science.gov (United States)

    Jacquemin, Denis; Chibani, Siwar; Le Guennic, Boris; Mennucci, Benedetta

    2014-07-17

    In this work, we present time-dependent density functional theory calculations of the excited-state geometries and electronic properties of both model cyanines and BODIPY derivatives, which are particularly challenging dyes for theoretical chemistry. In particular, we focus on environmental effects, using a panel of approaches derived from the polarizable continuum model, including full corrected linear response (cLR) values determined through a very recently developed approach. It turns out that in idealized quasi-linear cyanines, all approaches provide very similar excited-state geometries though linear response (LR), and cLR models yield very different transition energies. For the fluoroborate derivatives, LR apparently overestimates the planarity of the excited-state geometries, and cLR optimizations yield slightly smaller fluorescence energies than LR, making these values closer to experimental references. The computed corrections are however too small to explain (taken alone) the significant theory/experiment discrepancies.

  11. Cyanine dye–protein interactions: Looking for fluorescent probes for amyloid structures

    NARCIS (Netherlands)

    Volkova, K.D.; Kovalska, V.B.; Balanda, A.O.; Vermeij, R.J.; Subramaniam, V.; Slominskii, Yu.L.; Yarmoluk, S.M.

    2007-01-01

    We ascertained the ability to detect fibrillar β-lactoglobulin (BLG) of a series of mono-, tri-, penta-, and heptamethinecyanines based on benzothiazole and benzimidazole heterocycles, and of benzothiazole squaraine. Fluorescence properties of these cyanine dyes were measured in the unbound state an

  12. Pre-clinical Evaluation of a Cyanine-Based SPECT Probe for Multimodal Tumor Necrosis Imaging

    NARCIS (Netherlands)

    M.A. Stammes (Marieke A.); Knol-Blankevoort, V.T. (Vicky T.); Cruz, L.J. (Luis J.); Feitsma, H.R.I.J. (Hans R. I. J.); L. Mezzanotte (Laura); Cordfunke, R.A. (Robert A.); Sinisi, R. (Riccardo); Dubikovskaya, E.A. (Elena A.); Maeda, A. (Azusa); DaCosta, R.S. (Ralph S.); Bierau, K. (Katja); Chan, A. (Alan); E.L. Kaijzel (Eric); T.J.A. Snoeks (thomas); E.R. van Beek (Ermond); C.W.G.M. Löwik (Clemens)

    2016-01-01

    textabstractPurpose: Recently we showed that a number of carboxylated near-infrared fluorescent (NIRF) cyanine dyes possess strong necrosis avid properties in vitro as well as in different mouse models of spontaneous and therapy-induced tumor necrosis, indicating their potential use for cancer diagn

  13. Synthesis and Spectroscopic Characterisation of N-Alkyl Quaternary Ammonium Salts Typical Precursors of Cyanines

    OpenAIRE

    Almeida, P; Reis, L. V.; SANTOS, P.F.; Ramos, S. S.; Pardal, A. C.

    2002-01-01

    The synthesis and spectroscopic characterisation of some representative N-alkylsubstituted quaternary ammonium salts derived from benzothiazole, benzoxazole, benzoselenazole, indole and quinoline are described. These heterocyclic salts, bearing an activated methyl group in the 2-position in relation to the nitrogen atom and N-methyl, -pentyl, -hexyl and -decyl chains, are typical precursors of cyanine dyes.

  14. Synthesis and Spectroscopic Characterisation of N-Alkyl Quaternary Ammonium Salts Typical Precursors of Cyanines

    Directory of Open Access Journals (Sweden)

    P. Almeida

    2002-03-01

    Full Text Available The synthesis and spectroscopic characterisation of some representative N-alkylsubstituted quaternary ammonium salts derived from benzothiazole, benzoxazole, benzoselenazole, indole and quinoline are described. These heterocyclic salts, bearing an activated methyl group in the 2-position in relation to the nitrogen atom and N-methyl, -pentyl, -hexyl and -decyl chains, are typical precursors of cyanine dyes.

  15. Blue to near-IR energy transfer cascade within a dye-doped polymer matrix, mediated by a photochromic molecular switch.

    Science.gov (United States)

    Dryza, Viktoras; Smith, Trevor A; Bieske, Evan J

    2016-02-21

    The spectroscopic properties of a poly(methyl methacrylate) matrix doped with a coumarin dye, a cyanine dye, and a photochromic spiropyran dye have been investigated. Before UV irradiation of the matrix, excitation of the coumarin dye results in minimal energy transfer to the cyanine dye. The energy transfer is substantially enhanced following UV irradiation of the matrix, which converts the colourless spiropyran isomer to the coloured merocyanine isomer, which then acts as an intermediate bridge by accepting energy from the coumarin dye and then donating energy to the cyanine dye. This demonstration of a switchable energy transfer cascade should help initiate new research directions in molecular photonics.

  16. A naked-eye and ratiometric near-infrared probe for palladium via modulation of a π-conjugated system of cyanines.

    Science.gov (United States)

    Wang, Xiaohang; Guo, Zhiqian; Zhu, Shiqin; Tian, He; Zhu, Weihong

    2014-11-14

    A ratiometric and colorimetric cyanine-based palladium sensor with an excellent selectivity and sensitivity has been designed. Notably, the modulation of π-conjugated electrons in cyanine dyes can result in a ratiometric fluorescence change with a large Stokes shift (270 nm), especially for realizing palladium detection in aqueous samples using indicator paper and in living cells by ratiometric mode. The limit of detection is as low as 0.3 ppb.

  17. Extraction of catechol violet, chrome azurol S and eriochrome cyanine R with chloroform solutions of liquid anion-exchangers.

    Science.gov (United States)

    Przeszlakowski, S; Wydra, H

    1984-06-01

    The extraction of Catechol Violet, Chrome Azurol S and Eriochrome Cyanine R with chloroform solutions of tri-n-octylamine (TOA), TOA hydrochloride and Aliquat 336 has been investigated. From the extraction isotherms, absorption spectra of the organic phases and dependence of the extraction coefficients on extractant concentration, it was found that the singly-charged anions HL(-) are extracted preferentially, but acidic groups other than sulphonate can also form ion-pairs with alkylammonium cations at higher pH values of the aqueous phase, and at high acidity these dyes can be extracted other than by an anion-exchange reaction. The three dyes (especially Eriochrome Cyanine R and Chrome Azurol S) were strongly extracted with the liquid anion-exchanger used and Aliquat 336 was a better extractant than TOA or TOA hydrochloride. The absorption spectra for the organic phases containing Chrome Azurol S and Eriochrome Cyanine R depended on the extractant used.

  18. Cyanine polyene reactivity: scope and biomedical applications.

    Science.gov (United States)

    Gorka, Alexander P; Nani, Roger R; Schnermann, Martin J

    2015-07-28

    Cyanines are indispensable fluorophores that form the chemical basis of many fluorescence-based applications. A feature that distinguishes cyanines from other common fluorophores is an exposed polyene linker that is both crucial to absorption and emission and subject to covalent reactions that dramatically alter these optical properties. Over the past decade, reactions involving the cyanine polyene have been used as foundational elements for a range of biomedical techniques. These include the optical sensing of biological analytes, super-resolution imaging, and near-IR light-initiated uncaging. This review surveys the chemical reactivity of the cyanine polyene and the biomedical methods enabled by these reactions. The overarching goal is to highlight the multifaceted nature of cyanine chemistry and biology, as well as to point out the key role of reactivity-based insights in this promising area.

  19. Photobleaching of asymmetric cyanines used for fluorescence imaging of single DNA molecules.

    Science.gov (United States)

    Kanony, C; Akerman, B; Tuite, E

    2001-08-22

    The photobleaching of the cyanine dyes YO and YOYO has been investigated for both free and DNA-bound dyes, using absorption and fluorescence spectroscopy coupled with fluorescence microscopy. For the free dyes, the nature of the reactive species involved in the photodegradation process is different for the monomer and the dimer, as shown by scavenger studies. For DNA-bound dyes, photoinduced fading of the visible absorption band occurs by different pathways depending on the drug binding mode and can be attenuated by appropriate scavengers. However, none of these scavengers were found to have any significant effect on the photobleaching of dye fluorescence. It appears that the reduction of fluorescence intensity comes from a quenching of the dye fluorescence by modified DNA bases, possibly 8-oxo-7,8-dihydro-2'-deoxyguanosine.

  20. Conformational Switching of π-Conjugated Junctions from Merocyanine to Cyanine States by Solvent Polarity.

    Science.gov (United States)

    Arjona-Esteban, Alhama; Stolte, Matthias; Würthner, Frank

    2016-02-12

    Directed by the solvent polarity, the prevalent conformation of a polymethine dye bearing a branched π-conjugated junction can be switched from a heptamethine donor-acceptor (DA) merocyanine-type π-conjugated system to a nonamethine DAD cyanine-type π-conjugated scaffold. Concomitantly the absorption maximum shifts from 585 nm in dichloromethane to 748 nm in methanol solution.

  1. Photophysical and photosensitizing properties of selected cyanines.

    Science.gov (United States)

    Kassab, Kawser

    2002-08-01

    The present work has been carried out to obtain detailed information about the photophysical and photobiological properties of selected cyanines, in view of their possible use as photosensitizing agents. All the cyanines studied by us except CY-IV (3,3'-diethyl-4,4'-oxacarbocyanine), expressed an accelerated photobleaching in aqueous medium, a poor generation of singlet oxygen, and a relative weak photosensitizing activity towards albumin. On the cellular level, all cyanines exhibited a significant phototoxicity towards Balb/c 3T3 cells, upon irradiation with a total fluence of 30 J/cm(2). CY-III (3,3'-diethylcarbothiocayanine iodide) and CY-II (1,1'-diethyl-4,4'-carbocyanine iodide) appear to be promising photosensitizers, in spite of previous reports on the inefficiency of the former cyanine, and the rapid photobleaching of the latter compound.

  2. Cyanine Conformational Restraint in the Far-Red Range.

    Science.gov (United States)

    Michie, Megan S; Götz, Ralph; Franke, Christian; Bowler, Matthew; Kumari, Nikita; Magidson, Valentin; Levitus, Marcia; Loncarek, Jadranka; Sauer, Markus; Schnermann, Martin J

    2017-09-13

    Far-red cyanine fluorophores find extensive use in modern microscopy despite modest quantum yields. To improve the photon output of these molecules, we report a synthetic strategy that blocks the major deactivation pathway: excited-state trans-to-cis polyene rotation. In the key transformation, a protected dialdehyde precursor undergoes a cascade reaction to install the requisite tetracyclic ring system. The resulting molecules exhibit the characteristic features of conformational restraint, including improved fluorescence quantum yield and extended lifetime. Moreover, these compounds recover from hydride reduction with dramatically improved efficiency. These observations enable efficient single-molecule localization microscopy in oxygenated buffer without addition of thiols. Enabled by modern organic synthesis, these studies provide a new class of far-red dyes with promising spectroscopic and chemical properties.

  3. Syntheses and properties of photostable near-infrared cyanines and their cyclodextrin conjugates

    Institute of Scientific and Technical Information of China (English)

    Li Qiu Wang; Lin Zhao; Wei Wei Nie; Li Hui Zheng; Ji Dong Wang; Qiu Rong Li; Jing Zhai; Zhi Wei Liu; Xiao Jun Peng

    2008-01-01

    Three fluorescent indocyanines containing p-carboxybenzyl groups on N atoms in the heterocyclic rings were synthesized under supersonic. The maxima wavelength of the absorption and emission of the dyes were 550-800 nm in water. Compared with those in aqueous solutions, the fluorescence intensity of the dyes in the α/β-cyclodextrin, Al3+, Zn2+, Sn2+ or the α/β-cyclodextrin in the aqueous solutions of the cations became stronger. The crystal shapes of the dyes and their cyclodextrin inclusions were mostly acicular or polygon. The NHS-carboxyl squarylium indocyanine was prepared and used to conjugate with taurine or benzylamine, the results indicated that the dyes could couple covalently to biomass containing free NH2 group. Structure and some thermal parameters of the molecule of the trimethine cyanine were obtained by DFT method of Gaussian 03.

  4. Valence-bond non-equilibrium solvation model for a twisting monomethine cyanine

    Science.gov (United States)

    McConnell, Sean; McKenzie, Ross H.; Olsen, Seth

    2015-02-01

    We propose and analyze a two-state valence-bond model of non-equilibrium solvation effects on the excited-state twisting reaction of monomethine cyanines. Suppression of this reaction is thought responsible for environment-dependent fluorescence yield enhancement in these dyes. Fluorescence is quenched because twisting is accompanied via the formation of dark twisted intramolecular charge-transfer (TICT) states. For monomethine cyanines, where the ground state is a superposition of structures with different bond and charge localizations, there are two possible twisting pathways with different charge localizations in the excited state. For parameters corresponding to symmetric monomethines, the model predicts two low-energy twisting channels on the excited-state surface, which leads to a manifold of TICT states. For typical monomethines, twisting on the excited state surface will occur with a small barrier or no barrier. Changes in the solvation configuration can differentially stabilize TICT states in channels corresponding to different bonds, and that the position of a conical intersection between adiabatic states moves in response to solvation to stabilize either one channel or the other. There is a conical intersection seam that grows along the bottom of the excited-state potential with increasing solvent polarity. For monomethine cyanines with modest-sized terminal groups in moderately polar solution, the bottom of the excited-state potential surface is completely spanned by a conical intersection seam.

  5. Electronic spectra and trans—cis isomerism of streptopolymethine cyanines. A CS INDO CI study

    Science.gov (United States)

    Momicchioli, Fabio; Baraldi, Ivan; Ponterini, Glauco; Berthier, Gaston

    The understanding of the role played by cyanine dyes in various fields of application calls for a thorough knowledge of the excited state properties of their parent chromophores, i.e. cationic streptopolymethyne cyanines. For this aim we performed a detailed CS INDO CI investigation on the electronic spectra of tri-, penta- and heptamethine cyanines, both unsubstituted (TC, PC, HC) and terminally substituted by methyl groups (BMTC, BMPC, BMHC). The study comprised S0 Sn, and S0 Tn transitions of the trans and all mono- cis isomers. CI expansions involved solely π orbitals of the polymethine chains and pseudo-π orbitals of the substituents and included all singly-excited and the most important doubly- and triply-excited configurations. The spectroscopic effects of methyl substitution are fairly well described and are shown to be especially important in the upper excited states. The identification of the photochemically formed stereoisomers is attempted in terms of mono- cis isomers. For BMPC, in particular, we report the absorption spectrum of the phototropic form and show that the photoisomer is identifiable as the 3-4 cis form.

  6. Symmetry loss of heptamethine cyanines: an example of dipole generation by ion-pairing effect

    Science.gov (United States)

    Pascal, Simon; Bouit, Pierre-Antoine; Le Guennic, Boris; Parola, Stéphane; Maury, Olivier; Andraud, Chantal

    2013-03-01

    The development of near-infrared dyes for third order nonlinear optical applications and particularly for optical power limiting at telecommunications wavelengths triggered the revival of old dyes like polymethine dyes featuring an odd number of carbon atoms. Currently numerous research endeavor is focused on the understanding of their spectroscopy in solution and in the solid state in close relationship with their electronic structure. In this context, the dramatic effect of the counter ion on the heptamethine optical properties was highlighted depending on the dissociating character of the media. The unusual consideration of this parameter allows us to explore the so-called "cyanine limit" and to finely tune the heptamethine absorption in view of future use as dopant in a material for optical limiting applications.

  7. Influence of chemically p-type doped active organic semiconductor on the film thickness versus performance trend in cyanine/C60 bilayer solar cells

    Science.gov (United States)

    Jenatsch, Sandra; Geiger, Thomas; Heier, Jakob; Kirsch, Christoph; Nüesch, Frank; Paracchino, Adriana; Rentsch, Daniel; Ruhstaller, Beat; C Véron, Anna; Hany, Roland

    2015-01-01

    Simple bilayer organic solar cells rely on very thin coated films that allow for effective light absorption and charge carrier transport away from the heterojunction at the same time. However, thin films are difficult to coat on rough substrates or over large areas, resulting in adverse shorting and low device fabrication yield. Chemical p-type doping of organic semiconductors can reduce Ohmic losses in thicker transport layers through increased conductivity. By using a Co(III) complex as chemical dopant, we studied doped cyanine dye/C60 bilayer solar cell performance for increasing dye film thickness. For films thicker than 50 nm, doping increased the power conversion efficiency by more than 30%. At the same time, the yield of working cells increased to 80%. We addressed the fate of the doped cyanine dye, and found no influence of doping on solar cell long term stability. PMID:27877804

  8. Influence of chemically p-type doped active organic semiconductor on the film thickness versus performance trend in cyanine/C60 bilayer solar cells.

    Science.gov (United States)

    Jenatsch, Sandra; Geiger, Thomas; Heier, Jakob; Kirsch, Christoph; Nüesch, Frank; Paracchino, Adriana; Rentsch, Daniel; Ruhstaller, Beat; C Véron, Anna; Hany, Roland

    2015-06-01

    Simple bilayer organic solar cells rely on very thin coated films that allow for effective light absorption and charge carrier transport away from the heterojunction at the same time. However, thin films are difficult to coat on rough substrates or over large areas, resulting in adverse shorting and low device fabrication yield. Chemical p-type doping of organic semiconductors can reduce Ohmic losses in thicker transport layers through increased conductivity. By using a Co(III) complex as chemical dopant, we studied doped cyanine dye/C60 bilayer solar cell performance for increasing dye film thickness. For films thicker than 50 nm, doping increased the power conversion efficiency by more than 30%. At the same time, the yield of working cells increased to 80%. We addressed the fate of the doped cyanine dye, and found no influence of doping on solar cell long term stability.

  9. NMR screening of new carbocyanine dyes as ligands for affinity chromatography.

    Science.gov (United States)

    Cruz, Carla; Boto, Renato E F; Drzazga, Anna K; Almeida, Paulo; Queiroz, João A

    2014-04-01

    Four new carbocyanines containing symmetric and asymmetric heterocyclic moieties and N-carboxyalkyl groups have been synthesized and characterized. The binding mechanism established between these cyanines and several proteins was evaluated using saturation transfer difference (STD) NMR. The results obtained for the different dyes revealed a specific interaction to the standard proteins lysozyme, α-chymotrypsin, ribonuclease (RNase), bovine serum albumin (BSA), and gamma globulin. For instance, the two un-substituted symmetrical dyes (cyanines 1 and 3) interacted preferentially through its benzopyrrole and dibenzopyrrole units with lysozyme, α-chymotrypsin, and RNase, whereas the symmetric disulfocyanine dye (cyanine 2) bound BSA and gamma globulin through its carboxyalkyl chains. On the other hand, the asymmetric dye (cyanine 4) interacts with lysozyme and α-chymotrypsin through benzothiazole moiety and with RNase through dibenzopyrrole unit. Thus, STD-NMR technique was successfully used to screen cyanine-protein interactions and determine potential binding sites of the cyanines for posterior use as ligands in affinity chromatography.

  10. [Synthesis of functionalized cyanines. Fluorescence properties following complexation of cations].

    Science.gov (United States)

    Mazières, M R; Duprat, C; Sutra, E; Lamandé, L; Bergon, M; Bellan, J; Wolf, J G; Roques, C

    2003-01-01

    The ionophoric properties of podands containing dioxazaphosphocane moieties linked by inactive spacers were studied. To increase the detection sensibility of these compounds we introduced a cyanine as spacer. Fluorescence analysis demonstrated the interest of cyanines as active spacers since the complexation by cations as Ca2+ and Mg2+ gives an enhancement of the emission intensity.

  11. Nontemplated Approach to Tuning the Spectral Propertiesof Cyanine-Based Fluorescent NanoGUMBOS

    Energy Technology Data Exchange (ETDEWEB)

    Das, Susmita [Louisiana State University; Bwambok, David [Louisiana State University; El-Zahab, Bilal [Lousianna State University; Monk, Joshua [Louisiana State University; De Rooy, Sergio [Louisiana State University; Challa, Santhosh [Louisiana State University; Li, Min [Lousianna State University; Hung, Francisco [Louisiana State University; Baker, Gary A [ORNL; Warner, Isiah M [ORNL

    2010-01-01

    Template-free controlled aggregation and spectral properties in fluorescent organic nanoparticles (FONs) is highly desirable for various applications.Herein, we report a nontemplated method for controlling the aggregation in near-infrared (NIR) cyanine-based nanoparticles derived from a group of uniformmaterials based on organic salts (GUMBOS). Cationic heptamethine cyanine dye 1,10,3,3,30,30-hexamethylindotricarbocyanine (HMT) was coupled with five different anions, viz., [NTf2 -], [BETI-], [TFPB-], [AOT-], and [TFP4B-], by an ion-exchange method to obtain the respective GUMBOS. The nanoGUMBOS obtained via a reprecipitation method were primarily amorphous and spherical (30-100 nm) as suggested by selected area electron diffraction (SAED) and transmission electron microscopy (TEM). The formation of tunable self-assemblies within the nanoGUMBOS was characterized using absorption and fluorescence spectroscopy in conjunction with molecular dynamics simulations. Counterion-controlled spectral properties observed in the nanoGUMBOS were attributed to variations in J/H ratios with different anions. Association with the [AOT-] anion afforded predominant J aggregation enabling the highest fluorescence intensity, whereas [TFP4B-] disabled the fluorescence due to predominantHaggregation in the nanoparticles. Analyses of the stacking angle of the cations based on molecular dynamic simulation results in [HMT][NTf2], [HMT][BETI], and [HMT][AOT] dispersed in water and a visual analysis of the representative simulation snapshots also imply that the type of aggregation was controlled through the counterion associated with the dye cation.

  12. Theoretical study of trans-cis photoisomerism in polymethine cyanines

    Science.gov (United States)

    Momicchioli, Fabio; Baraldi, Ivan; Berthier, Gaston

    1988-06-01

    The trans-cis photoisomerism of polymethine dyes has been interpreted so far using different and rather inconsistent models of the potential energy surfaces. In order to search for a unified electronic model, we tackled the problem again from an intramolecular point of view. Our study consisted in qualitative MO considerations followed by explicit (CS INDO) calculations of the S 0, T 1 and S 1 potential energy curves for a proper model system: pentamethine cyanine isomerizing around the 2-3 and 3-4 bonds. Torsional energy levels for the calculated potential curves were also obtained. The main conclusions are: (i) the photoreaction proceeds through a "non-spectroscopic" (perp) S 1 minimum which exists also in the isolated molecule, (ii) this twisted excited species has charge transfer character (TICT), as opposed to the biradicaloid character of the "non-spectroscopic" S 1 minimum involved in the trans→cis photoisomerization of olefines (e.g., stilbene). The possible consequences on the dynamics of the excited state relaxation in non-polar solvents are envisaged.

  13. Advancing with pyrrolopyrrole cyanines: a next generation class of near-infrared fluorophores

    Science.gov (United States)

    Wiktorowski, S.; Fischer, G. M.; Daltrozzo, E.; Zumbusch, A.

    2012-03-01

    Fluorescent dyes are the basis for a broad range of modern techniques in life and material sciences. Consequently, there is a pressing need for the development of new classes of NIR fluorophores in recent years. Pyrrolopyrrole Cyanines (PPCys) are a novel class of NIR chromophores that were first presented in 2007 by Fischer and coworkers.[1] Their optical properties are marked by strong and narrowband NIR absorptions, strong NIR fluorescence and hardly any absorption in the visible range. The absorption maxima can be tuned over a broad range while high fluorescence quantum yields are maintained. PPCys are attractive candidates for labelling applications or as selective NIR absorbers. Moreover, PPCys exhibit very high photostability. Due to these outstanding photophysical properties, PPCys are heading into a promising future as NIR dyes.

  14. PHOTOPOLYMERIZATION OF MMA INITIATED BY CYANINE DYE AND HEXAARYLBIIMIDAZOLE

    Institute of Scientific and Technical Information of China (English)

    1998-01-01

    The photoinitiating system composed of 1-ethyl-3'-methyl thiacyanine bromide (C-I), 2-chlorohexaarylbiimidazole (o-Cl-HABI) and 3-mercapto-4-methyl-4H-1, 2, 4-triazole (MTA), which act as sensitizer, initiator and hydrogen-donor respectively, can be used to initiate the polymerization of methyl methacrylate (MMA). The kinetic study was carried out in trichloromathane solution at 30℃ by using dilatometry. The relation between the polymerization rate and the concentrations of C-I, o-Cl-HABI, MTA and MMA was studied.

  15. Reactive Species Involved in the Regioselective Photooxidation of Heptamethine Cyanines.

    Science.gov (United States)

    Nani, Roger R; Kelley, James A; Ivanic, Joseph; Schnermann, Martin J

    2015-11-01

    Heptamethine cyanines are important near-IR fluorophores used in many fluorescence applications. Despite this utility, these molecules are susceptible to light-promoted reactions (photobleaching) involving photochemically generated reactive oxygen species (ROS). Here, we have sought to define key chemical aspects of this nearly inescapable process. Near-IR photolysis of a model heptamethine cyanine leads to the regioselective oxidative cleavage of the cyanine polyene. We report the first quantitative analysis of the major reaction pathway following either photolysis or exposure to candidate ROS. These studies clearly indicate that only singlet oxygen ((1)O2), and not other feasible ROS, recapitulates the direct photolysis pathway. Computational studies were employed to investigate the regioselectivity of the oxidative cleavage process, and the theoretical ratio is comparable to observed experimental values. These results provide a more complete picture of heptamethine cyanine photooxidation, and provide insight for design of improved compounds for future applications.

  16. Fluorescent cyanine probe for DNA detection and cellular imaging

    Science.gov (United States)

    Zheng, Yong-Chao; Zheng, Mei-Ling; Zhao, Zhen-Sheng; Duan, Xuan-Ming

    2014-03-01

    In our study, two carbazole-based cyanines, 3,6-bis[2-(1-methylpyridinium)vinyl]-9-methyl carbazole diiodide (A) and 6,6'-bis[2-(1-methylpyridinium)vinyl]-bis(9-methyl-carbazol-3yl)methane diiodide (B) were synthesized and employed as light-up probes for DNA and cell imaging. Both of the cyanine probes possess a symmetric structure and bis-cationic center. The obvious induced circular dichroism signals in circular dichroism spectra reveal that the molecules can specifically interact with DNA. Strong fluorescence enhancement is observed when these two cyanines are bound to DNA. These cyanine probes show high binding affinity to oligonucleotides but different binding preferences to various secondary structures. Confocal microscopy images of fixed cell stained by the probes exhibit strong brightness and high contrast in nucleus with a very low cytoplasmic background.

  17. Fast and Accurate Electronic Excitations in Cyanines with the Many-Body Bethe-Salpeter Approach.

    Science.gov (United States)

    Boulanger, Paul; Jacquemin, Denis; Duchemin, Ivan; Blase, Xavier

    2014-03-11

    The accurate prediction of the optical signatures of cyanine derivatives remains an important challenge in theoretical chemistry. Indeed, up to now, only the most expensive quantum chemical methods (CAS-PT2, CC, DMC, etc.) yield consistent and accurate data, impeding the applications on real-life molecules. Here, we investigate the lowest lying singlet excitation energies of increasingly long cyanine dyes within the GW and Bethe-Salpeter Green's function many-body perturbation theory. Our results are in remarkable agreement with available coupled-cluster (exCC3) data, bringing these two single-reference perturbation techniques within a 0.05 eV maximum discrepancy. By comparison, available TD-DFT calculations with various semilocal, global, or range-separated hybrid functionals, overshoot the transition energies by a typical error of 0.3-0.6 eV. The obtained accuracy is achieved with a parameter-free formalism that offers similar accuracy for metallic or insulating, finite size or extended systems.

  18. Cyanine-loaded lipid nanoparticles for improved in vivo fluorescence imaging

    Science.gov (United States)

    Texier, Isabelle; Goutayer, Mathieu; da Silva, Anabela; Guyon, Laurent; Djaker, Nadia; Josserand, Véronique; Neumann, Emmanuelle; Bibette, Jérôme; Vinet, Françoise

    2009-09-01

    Fluorescence is a very promising radioactive-free technique for functional imaging in small animals and, in the future, in humans. However, most commercial near-infrared dyes display poor optical properties, such as low fluorescence quantum yields and short fluorescence lifetimes. In this paper, we explore whether the encapsulation of infrared cyanine dyes within the core of lipid nanoparticles (LNPs) could improve their optical properties. Lipophilic dialkylcarbocyanines DiD and DiR are loaded very efficiently in 30-35-nm-diam lipid droplets stabilized in water by surfactants. No significant fluorescence autoquenching is observed up to 53 dyes per particle. Encapsulated in LNP, which are stable for more than one year at room temperature in HBS buffer (HEPES 0.02 M, EDTA 0.01 M, pH 5.5), DiD and DiR display far improved fluorescence quantum yields Φ (respectively, 0.38 and 0.25) and longer fluorescence lifetimes τ (respectively, 1.8 and 1.1 ns) in comparison to their hydrophilic counterparts Cy5 (φ=0.28, τ=1.0 ns) and Cy7 (φ=0.13, τ=0.57 ns). Moreover, dye-loaded LNPs are able to accumulate passively in various subcutaneous tumors in mice, thanks to the enhanced permeability and retention effect. These new fluorescent nanoparticles therefore appear as very promising labels for in vivo fluorescence imaging.

  19. Laser dye toxicity, hazards, and recommended controls

    Energy Technology Data Exchange (ETDEWEB)

    Mosovsky, J.A.

    1983-05-06

    Laser dyes are complex fluorescent organic compounds which, when in solution with organic solvents, form a lasing medium. The wavelength of a dye laser's output beam can vary with different dyes, concentrations, and solvents, giving it a tunable feature capable of emitting ultraviolet, visible, or infrared radiation. Toxicity information on the approximately 100 commercially available laser dyes is very scarce. Limited animal experimentation has been performed with only a few dyes. This paper summarizes what is known about laser dye toxicity, and offers recommendations for controlling dye hazards. The laser dyes investigated have been categorized according to their central chemical structures. These include the xanthenes (rhodamines and fluoresceins), polymethines (cyanines and carbocyanines), coumarins, and stilbenes. A few other miscellaneous dyes that do not fall into one of these categories have also been investigated. Prepared laser dye solutions usually contain very small quantities of dye--typical dye concentrations are 10/sup -2/ to 10/sup -5/ molar. For this reason, the solvent in which the dye is dissolved plays an important role when defining potential hazards. Practically all the solvents used are flammable and toxic by inhalation and skin absorption, and therefore must be controlled properly.

  20. STUDY OF DYE-SENSITIZED SYSTEMS FOR PHOTOIMAGING

    Institute of Scientific and Technical Information of China (English)

    Fang Gao; Chun-ying Zhao; Yong-yuan Yang; Li-dong Li

    2001-01-01

    o-Chloro-hexaarylbiimidazole (o-C1-HABI) can be sensitized efficiently by cyanine dyes, the cyclopentanone and cyclohexanone dyes, when exposed to xenon lamp (use filter cut λ _< 400 nm). The photoreaction between the photoinitiator and the dyes was completed through an electron transfer process. Excellent results have been obtained in photoimaging studies, e.g. the resolution of the image can reach 7 μm. The influence of the content of the dyes and the heat after the exposure on the resolution of the image was investigated.

  1. Nonlinear optical properties of a self-organized dye thin film

    Institute of Scientific and Technical Information of China (English)

    Haifeng Kang; Yizhong Yuan; Zhenrong Sun; Zugeng Wang

    2007-01-01

    @@ A self-organized thin film of a cyanine dye is fabricated by the spin-coating technique and is characterized by ultraviolet-visible spectroscopy, infrared (IR) spectroscopy, small-angle X-ray diffraction, ellipsometer,and atomic force microscopy (AFM). The nonlinear optical properties of the thin films are investigated by degenerate four wave mixing (DFWM) technique. The cyanine dye thin film sample exhibits high optical nonlinearities (χ(3) = 2.55 × 10-12 esu), and the mechanism is analyzed by the exciton coupling theory.

  2. Resonance light scattering spectral study of the interaction of cyanine dye with nucleic acids and its analytical applications%花菁-脱氧核糖核酸的共振光散射光谱及其分析应用

    Institute of Scientific and Technical Information of China (English)

    方芳; 张志涛; 朱昌青

    2012-01-01

    研究了一种苯并噻唑阳离子花菁与脱氧核糖核酸(DNA)作用的共振光散射光谱,在pH 6.0的六次甲基四胺-HCl缓冲介质中,痕量DNA的加入使花菁在590nm的共振光散射强度显著增强.在最佳实验条件下,增强的共振光散射强度与DNA浓度具有良好的线性关系,据此建立了一种测定DNA的共振光散射光谱法.方法的线性范围为:小牛胸腺DNA(CT DNA),0~20μg/mL,鱼精子DNA(FS DNA),0~ 15μg/mL;检出限分别为0.005 μg/mL和0.008μg/mL.该方法已用于合成样品中DNA的测定.%The resonance light scattering (RLS) spectra of benzothiazole cationic cyanine with deoxyribonucleic acid (DNA) have been studied. The RLS intensity of cyanine at 590nm is greatly enhanced by the addition of trace amounts of DNA in pH 6.0 hexamethylene tetramine-HCl media. Under the optical experimental conditions, the enhanced RLS intensity was proportional to the concentration of DNA. The RLS method for the determination of DNA was established. The linear ranges of the method are 0 ~20μg/mL for CT DNA and 0 ~ 15(μg/mL for FS DNA,and the detection limits are 0. 005μg/mL and 0. 008μg/mL respectively. The method has been applied to the determination of DNA in synthetic samples.

  3. Tracking of the nuclear wavepacket motion in cyanine photoisomerization by ultrafast pump-dump-probe spectroscopy.

    Science.gov (United States)

    Wei, Zhengrong; Nakamura, Takumi; Takeuchi, Satoshi; Tahara, Tahei

    2011-06-01

    Understanding ultrafast reactions, which proceed on a time scale of nuclear motions, requires a quantitative characterization of the structural dynamics. To track such structural changes with time, we studied a nuclear wavepacket motion in photoisomerization of a prototype cyanine dye, 1,1'-diethyl-4,4'-cyanine, by ultrafast pump-dump-probe measurements in solution. The temporal evolution of wavepacket motion was examined by monitoring the efficiency of stimulated emission dumping, which was obtained from the recovery of a ground-state bleaching signal. The dump efficiency versus pump-dump delay exhibited a finite rise time, and it became longer (97 fs → 330 fs → 390 fs) as the dump pulse was tuned to longer wavelengths (690 nm → 950 nm → 1200 nm). This result demonstrates a continuous migration of the leading edge of the wavepacket on the excited-state potential from the Franck-Condon region toward the potential minimum. A slowly decaying feature of the dump efficiency indicated a considerable broadening of the wavepacket over a wide range of the potential, which results in the spread of a population distribution on the flat S(1) potential energy surface. The rapid migration as well as broadening of the wavepacket manifests a continuous nature of the structural dynamics and provides an intuitive visualization of this ultrafast reaction. We also discussed experimental strategies to evaluate reliable dump efficiencies separately from other ultrafast processes and showed a high capability and possibility of the pump-dump-probe method for spectroscopic investigation of unexplored potential regions such as conical intersections.

  4. Dimerization of green sensitizing cyanines in solution. A spectroscopic and theoretical study of the bonding nature

    Science.gov (United States)

    Baraldi, I.; Caselli, M.; Momicchioli, F.; Ponterini, G.; Vanossi, D.

    2002-01-01

    The bonding nature in cyanine-dye aggregates has been investigated by studying dimerization in solution of 3,3 '-disulfopropyl-4,5,4 ',5 '-dibenzo-9-ethyloxacarbocyanine (D) and three other oxacarbocyanine analogues (E, F, G) used as photographic sensitizers in the green spectral region. Quantitative information on the monomer-dimer equilibrium of dye D in different solvents and of its analogues (E, F, G) in water was obtained by measurement of the absorption spectrum as a function of dye concentration and of temperature. Dimerization was found to be generally driven by enthalpic factors traceable to strong attractive van der Waals interactions between the two large and highly polarizable dye molecules. Entropic contributions to ΔG0 usually favour dissociation but are smaller than the enthalpic ones. The visible absorption spectrum of the dimer consists in a classic two-branched exciton band with a marked splitting ( 1600 cm-1 in water). The experimental observations were the subject of a theoretical study including classical molecular dynamics (MD) and Monte Carlo (MC) calculations of the dimer structure and comparative analysis of monomer and dimer spectra by the CS INDO CI method. Computer simulations led to three similar H-type structures, the most stable of which is characterized by a distance of 4.7 Å between the planes of the chromophores and an endo-endo configuration of the sulfopropyl substituents. The calculated dimer spectrum was clearly interpreted in terms of exciton model but a quantitative agreement with the two-maximum exciton band could be obtained only by assuming substantial deviation of the long molecular axes from parallelism. On the basis of normal coordinate calculations it is suggested that such configurations may occur with a high probability in virtue of twisting vibrational motions of extremely low frequency.

  5. Longest-Wavelength Electronic Excitations of Linear Cyanines: The Role of Electron Delocalization and of Approximations in Time-Dependent Density Functional Theory.

    Science.gov (United States)

    Ii, Barry Moore; Autschbach, Jochen

    2013-11-12

    The lowest-energy/longest-wavelength electronic singlet excitation energies of linear cyanine dyes are examined, using time-dependent density functional theory (TDDFT) and selected wave function methods in comparison with literature data. Variations of the bond-length alternation obtained with different optimized structures produce small differences of the excitation energy in the limit of an infinite chain. Hybrid functionals with range-separated exchange are optimally 'tuned', which is shown to minimize the delocalization error (DE) in the cyanine π systems. Much unlike the case of charge-transfer excitations, small DEs are not strongly correlated with better performance. A representative cyanine is analyzed in detail. Compared with accurate benchmark data, TDDFT with 'pure' local functionals gives too high singlet excitation energies for all systems, but DFT-based ΔSCF calculations with a local functional severely underestimates the energies. TDDFT strongly overestimates the difference between singlet and triplet excitation energies. An analysis points to systematically much too small magnitudes of integrals from the DFT components of the exchange-correlation response kernel as the likely culprit. The findings support previous suggestions that the differential correlation energy between the ground and excited state is not correctly produced by TDDFT with most functionals.

  6. Progress in modifications and applications of fluorescent dye probe

    Institute of Scientific and Technical Information of China (English)

    Xuening Fei; Yingchun Gu

    2009-01-01

    This review summarizes the labeling technology and applications of fluorescent dye probe in biology,especially the characteristics,modifications and applications of cyanine dyes.Based on the currently available modification methods of fluorescent dye probe,we discuss the studies of enhancing the water-solubility,improving the degree of biocompatibility and target-labeling,increasing the sensitivity and decreasing the toxicity of fluorescent dye.We also give a brief introduction on the modification method,that the fluorescent dye is directly introduced onto the cell surfaces by amine derivatives or azides to intensify the transferring information of aberrant cells.We suggest that fluorescent dye modified with chitosan oligosaccharide can obviously increase the degree of biocompatibility and targetlabeling,and decrease the degree of toxicity.

  7. Selective G-Quadruplex DNA Recognition by a New Class of Designed Cyanines

    OpenAIRE

    Germann, Markus W.; David Wilson, W.; Henary, Maged M.; Huynh, Hang T.; Stroeva, Ekaterina M.; Dost, Tyler L.; Rupesh Nanjunda; Leah Mickelson; Owens, Eric A.

    2013-01-01

    A variety of cyanines provide versatile and sensitive agents acting as DNA stains and sensors and have been structurally modified to bind in the DNA minor groove in a sequence dependent manner. Similarly, we are developing a new set of cyanines that have been designed to achieve highly selective binding to DNA G-quadruplexes with much weaker binding to DNA duplexes. A systematic set of structurally analogous trimethine cyanines has been synthesized and evaluated for quadruplex targeting. The ...

  8. Modified zirconium-eriochrome cyanine R determination of fluoride

    Science.gov (United States)

    Thatcher, L.L.

    1957-01-01

    The Eriochrome Cyanine R method for determining fluoride in natural water has been modified to provide a single, stable reagent solution, eliminate interference from oxidizing agents, extend the concentration range to 3 p.p.m., and extend the phosphate tolerance. Temperature effect was minimized; sulfate error was eliminated by precipitation. The procedure is sufficiently tolerant to interferences found in natural and polluted waters to permit the elimination of prior distillation for most samples. The method has been applied to 500 samples.

  9. Noncovalent Labeling of Biomolecules with Red and Near- Infrared Dyes

    Directory of Open Access Journals (Sweden)

    Lucjan Strekowski

    2004-02-01

    Full Text Available Biopolymers such as proteins and nucleic acids can be labeled with a fluorescent marker to allow for their detection. Covalent labeling is achieved by the reaction of an appropriately functionalized dye marker with a reactive group on a biomolecule. The recent trend, however, is the use of noncovalent labeling that results from strong hydrophobic and/or ionic interactions between the marker and biomolecule of interest. The main advantage of noncovalent labeling is that it affects the functional activity of the biomolecule to a lesser extent. The applications of luminescent cyanine and squarylium dyes are reviewed.

  10. Necrosis avid near infrared fluorescent cyanines for imaging cell death and their use to monitor therapeutic efficacy in mouse tumor models.

    Science.gov (United States)

    Xie, Bangwen; Stammes, Marieke A; van Driel, Pieter B A A; Cruz, Luis J; Knol-Blankevoort, Vicky T; Löwik, Martijn A M; Mezzanotte, Laura; Que, Ivo; Chan, Alan; van den Wijngaard, Jeroen P H M; Siebes, Maria; Gottschalk, Sven; Razansky, Daniel; Ntziachristos, Vasilis; Keereweer, Stijn; Horobin, Richard W; Hoehn, Mathias; Kaijzel, Eric L; van Beek, Ermond R; Snoeks, Thomas J A; Löwik, Clemens W G M

    2015-11-17

    Quantification of tumor necrosis in cancer patients is of diagnostic value as the amount of necrosis is correlated with disease prognosis and it could also be used to predict early efficacy of anti-cancer treatments. In the present study, we identified two near infrared fluorescent (NIRF) carboxylated cyanines, HQ5 and IRDye 800CW (800CW), which possess strong necrosis avidity. In vitro studies showed that both dyes selectively bind to cytoplasmic proteins of dead cells that have lost membrane integrity. Affinity for cytoplasmic proteins was confirmed using quantitative structure activity relations modeling. In vivo results, using NIRF and optoacoustic imaging, confirmed the necrosis avid properties of HQ5 and 800CW in a mouse 4T1 breast cancer tumor model of spontaneous necrosis. Finally, in a mouse EL4 lymphoma tumor model, already 24 h post chemotherapy, a significant increase in 800CW fluorescence intensity was observed in treated compared to untreated tumors. In conclusion, we show, for the first time, that the NIRF carboxylated cyanines HQ5 and 800CW possess strong necrosis avid properties in vitro and in vivo. When translated to the clinic, these dyes may be used for diagnostic or prognostic purposes and for monitoring in vivo tumor response early after the start of treatment.

  11. New iodo-acetamido cyanines for labeling cysteine thiol residues. A strategy for evaluating plasma proteins and their oxido-redox status.

    Science.gov (United States)

    Bruschi, Maurizio; Grilli, Stefano; Candiano, Giovanni; Fabbroni, Serena; Della Ciana, Leopoldo; Petretto, Andrea; Santucci, Laura; Urbani, Andrea; Gusmano, Rosanna; Scolari, Francesco; Ghiggeri, Gian Marco

    2009-01-01

    Two new iodoacetamide-substituted cyanines, C3NIASO3 and C5NIASO3, were synthesized starting from hemicyanine and were utilized for labeling plasma proteins. Specificity, sensitivity and feasibility for SH residues was tested utilizing an equimolar mixture of standard proteins and with normal plasma. Oxidized plasma proteins following H(2)O(2 )exposure and plasma from patients with focal glomerulosclerosis were analyzed as models of altered protein oxido-redox status. Following optimization of the assay (dye/protein ratio, pH), C3NIASO3 and C5NIASO3 gave a sensitivity slightly better than N-hydroxysuccinimidyl dyes for plasma proteins and were successfully employed for differential display electrophoresis (DIGE). Twenty-nine proteins were detected in normal plasma after 2-DE while less proteins were detected in plasma of patients with glomerulosclerosis. Following massive 'in vitro' oxidation with H(2)O(2), C3NIASO3 and C5NIASO3 failed to detect any residual SH, implicating massive oxidation. In conclusion, this study describes the synthesis of two new iodoacetamide cyanines that can be utilized for the analysis of plasma proteins with 2-DE and DIGE. They are also indicated for the definition of the oxido-redox status of proteins and were successfully utilized to extend the analysis of oxidation damage in patients with glomerulosclerosis.

  12. Targeted Imaging of Tumor-Associated Macrophages by Cyanine 7-Labeled Mannose in Xenograft Tumors

    Directory of Open Access Journals (Sweden)

    Chong Jiang MD

    2017-01-01

    Full Text Available Mannose receptor is considered as a hallmark of M2-oriented tumor-associated macrophages (TAMs, but its utility in TAMs was rarely reported. Therefore, deoxymannose (DM, a high-affinity ligand of mannose receptor, was labeled with near-infrared dye cyanine 7 (Cy7, and its feasibility of targeted imaging on TAMs was evaluated in vitro and in vivo. The Cy7-DM was synthesized, and its binding affinity with induced TAMs in vitro, whole-body imaging in xenograft tumor mouse model in vivo, and the cellular localization in dissected tissues were evaluated. We demonstrated a high uptake of Cy7-DM by induced M2 macrophages and TAMs in tumor tissues. In vivo near-infrared live imaging visualized abundant TAMs in tumor lesions instead of inflammatory sites by Cy7-DM imaging, and the quantity of Cy7-DM signals in tumors was significantly higher than that shown in inflammatory sites from 1 to 8 hours of imaging. Our results suggest that mannose could rapidly and specifically target TAMs and is a promising candidate for targeted diagnosis of tumor with rich TAMs.

  13. Near-infrared dyes for molecular probes and imaging

    Science.gov (United States)

    Patonay, Gabor; Beckford, Garfield; Strekowski, Lucjan; Henary, Maged; Kim, Jun Seok; Crow, Sidney

    2009-02-01

    Near-Infrared (NIR) fluorescence has been used both as an analytical tool as molecular probes and in in vitro or in vivo imaging of individual cells and organs. The NIR region (700-1100 nm) is ideal with regard to these applications due to the inherently lower background interference and the high molar absorptivities of NIR chromophores. NIR dyes are also useful in studying binding characteristics of large biomolecules, such as proteins. Throughout these studies, different NIR dyes have been evaluated to determine factors that control binding to biomolecules, including serum albumins. Hydrophobic character of NIR dyes were increased by introducing alkyl and aryl groups, and hydrophilic moieties e.g., polyethylene glycols (PEG) were used to increase aqueous solubility. Recently, our research group introduced bis-cyanines as innovative NIR probes. Depending on their microenvironment, bis-cyanines can exist as an intramolecular dimer with the two cyanines either in a stacked form, or in a linear conformation in which the two subunits do not interact with each other. In this intramolecular H-aggregate, the chromophore has a low extinction coefficient and low fluorescence quantum yield. Upon addition of biomolecules, the H-and D- bands are decreased and the monomeric band is increased, with concomitant increase in fluorescence intensity. Introduction of specific moieties into the NIR dye molecules allows for the development of physiological molecular probes to detect pH, metal ions and other parameters. Examples of these applications include imaging and biomolecule characterizations. Water soluble dyes are expected to be excellent candidates for both in vitro and in vivo imaging of cells and organs.

  14. Theoretical analysis of the third-order nonlinear optical properties of linear cyanines and polyenes

    Science.gov (United States)

    Pierce, Brian M.

    1991-12-01

    The nonresonant (pi) -electronic component of (gamma) (- 3(omega) ;(omega) ,(omega) ,(omega) ), (gamma) (pi) , is calculated for all-trans, linear symmetric cyanine, and streptocyanine cations with no double-single bond-length alternation, and for cyanine cations with asymmetric geometries resulting from the artificial imposition of double-single bond-length alternation. These (gamma) (pi) are compared with those previously calculated for all-trans linear polyenes with double-single bond-length alternation, and for a new set calculated with geometries resulting from the artificial imposition of no double-single bond-length alternation. Bond-length alternation is found to dramatically affect (gamma) (pi) for the linear cyanines: the (gamma) (pi) for the symmetric cyanines are calculated to be negative; the (gamma) (pi) for the asymmetric cyanines change from negative to positive with increasing chain length. The (gamma) (pi) for the linear polyenes are always positive regardless of the extent of bond-length alternation; the (gamma) (pi) for the linear polyenes increase with decreasing bond-length alternation. The (gamma) (pi) for the symmetric linear cyanines increase more rapidly with the number of (pi) -electrons than the (gamma) (pi) for the linear polyenes: (gamma) (pi) (symmetric cyanines) varies as N(pi -e)8 and (gamma) (pi) (linear polyenes) varies as N(pi -e)4, where Npi-e equals 4, 6, 8, 10, 12. The (gamma xxxx component along the chain axis is the most dominant one of (gamma) (pi) for all linear molecules studied. The salient 1(pi) (pi) * states and the important terms in the sum-over-states expression that define (gamma) xxxx, and hence (gamma) (pi) , are identified for the molecules. The dependence of (gamma) (pi) and (beta) (pi) on the geometric asymmetry of a pentamethine cyanine cation is investigated. The polymethines in general, and the cyanines in particular, comprise a very interesting class of nonlinear optical, (pi) -electron molecules that

  15. Synthesis of A Cyanine Dye-β-Cyclodextrin and Its Inclusion with Chromium%一种菁染料-β-环糊精的合成及其对水溶液中Cr3+的定量识别研究

    Institute of Scientific and Technical Information of China (English)

    任海晶; 吉跃英; 陈强; 马兰; 任颖

    2014-01-01

    合成了一种菁染料-β-环糊精化合物(Dye-β-CD),采用紫外-可见光谱法探讨了以这种菁染料-β-环糊精作为带有荧光探针的主体化合物在水质分析中的应用.结果表明:该菁染料-β-环糊精能够在pH=7.2的缓冲溶液介质对Cr3+进行定量识别,根据Benesi-Hildebrand方程确定该菁染料-β-环糊精与硝酸铬包结比为1,其包合常数为5.47×104 L/mol,合成的菁染料-β-环糊精化合物是一种优良的带有荧光探针的主体化合物.

  16. Mechanism of intramolecular photostabilization in self-healing cyanine fluorophores.

    Science.gov (United States)

    van der Velde, Jasper H M; Ploetz, Evelyn; Hiermaier, Matthias; Oelerich, Jens; de Vries, Jan Willem; Roelfes, Gerard; Cordes, Thorben

    2013-12-16

    Organic fluorophores, which are popular labels for microscopy applications, intrinsically suffer from transient and irreversible excursions to dark-states. An alternative to adding photostabilizers at high concentrations to the imaging buffer relies on the direct linkage to the fluorophore. However, the working principles of this approach are not yet fully understood. In this contribution, we investigate the mechanism of intramolecular photostabilization in self-healing cyanines, in which photodamage is automatically repaired. Experimental evidence is provided to demonstrate that a single photostabilizer, that is, the vitamin E derivative Trolox, efficiently heals the cyanine fluorophore Cy5 in the absence of any photostabilizers in solution. A plausible mechanism is that Trolox interacts with the fluorophore through intramolecular quenching of triplet-related dark-states, which is a mechanism that appears to be common for both triplet-state quenchers (cyclooctatetraene) and redox-active compounds (Trolox, ascorbic acid, methylviologen). Additionally, the influence of solution-additives, such as cysteamine and procatechuic acid, on the self-healing process are studied. The results suggest the potential applicability of self-healing fluorophores in stochastic optical reconstruction microscopy (STORM) with optical super-resolution. The presented data contributes to an improved understanding of the mechanism involved in intramolecular photostabilization and has high relevance for the future development of self-healing fluorophores, including their applications in various research fields.

  17. A near-IR uncaging strategy based on cyanine photochemistry.

    Science.gov (United States)

    Gorka, Alexander P; Nani, Roger R; Zhu, Jianjian; Mackem, Susan; Schnermann, Martin J

    2014-10-08

    The development of photocaging groups activated by near-IR light would enable new approaches for basic research and allow for spatial and temporal control of drug delivery. Here we report a near-IR light-initiated uncaging reaction sequence based on readily synthesized C4'-dialkylamine-substituted heptamethine cyanines. Phenol-containing small molecules are uncaged through sequential release of the C4'-amine and intramolecular cyclization. The release sequence is initiated by a previously unexploited photochemical reaction of the cyanine fluorophore scaffold. The uncaging process is compatible with biological milieu and is initiated with low intensity 690 nm light. We show that cell viability can be inhibited through light-dependent release of the estrogen receptor antagonist, 4-hydroxycyclofen. In addition, through uncaging of the same compound, gene expression is controlled with near-IR light in a ligand-dependent CreER(T)/LoxP-reporter cell line derived from transgenic mice. These studies provide a chemical foundation that we expect will enable specific delivery of small molecules using cytocompatible, tissue penetrant near-IR light.

  18. Silver and Cyanine Staining of Oligonucleotides in Polyacrylamide Gel.

    Directory of Open Access Journals (Sweden)

    Weizhong Tang

    Full Text Available To explore why some oligonucleotides in denaturing polyacrylamide gel could not be silver-stained, 134 different oligonucleotides were analyzed using denaturing polyacrylamide gel electrophoresis stained with silver and asymmetric cyanine. As a result, we found that the sensitivity of oligos (dA, (dC, (dG and (dT to silver staining could be ranged as (dA > (dG > (dC > (dT from high to low. It was unexpected that oligo (dT was hard to be silver-stained. Moreover, the silver staining of an oligonucleotide containing base T could be partially or completely inhibited by base T. The inhibition of silver staining by base T was a competitive inhibition which could be affected by the amounts of the argyrophil nucleobase and base T, the cis-distance between the argyrophil nucleobase and base T, and the gel concentration. The changes of the intensity of an oligonucleotide band caused by the changes of DNA base composition were diverse and interesting. The intensity of some oligonucleotide bands would significantly change when the changes of DNA base composition accumulated to a certain extent (usually ≥ 4 nt. The sensitivity of cyanine staining of ≤ 11-nt long oligonucleotides could be enhanced about 250-fold by fixing the gels with methanol fixing solution.

  19. Solvation and thermal effects on the optical properties of naturaldyes: a case study on the flavylium cyanin

    Science.gov (United States)

    Calzolari, Arrigo; Malcioglu, Baris; Gebauer, Ralph; Varsano, Daniele; Baroni, Stefano

    2011-03-01

    We present a first-principles study of the effects of both hydration and thermal dynamics on the optical properties of a natural anthocyanin dye, namely, cyanin (Cya), in aqueous solution. We combine Car-Parrinello molecular dynamics and time-dependent density functional theory (TDDFT) approaches to simulate the time evolution of UV-vis spectrum of the hydrated Cya molecule at room temperature [2,3]. The spectrum of the dye calculated in the gas phase is characterized by two peaks in the red and in the blue, which would bring about a greenish hue incompatible with the dark purple coloration observed in nature. Describing the effect of the water solvent through a polarizable continuum model does not modify qualitatively the resulting picture. An explicit simulation of both solvent and thermal effects using ab-initio molecular dynamics results instead in a spectrum that is compatible with the observed coloration. This result is analyzed in terms of the spectroscopic effects of molecular distortions, induced by thermal fluctuations.

  20. Left-handed DNA: intercalation of the cyanine thiazole orange and structural changes. A kinetic and thermodynamic approach.

    Science.gov (United States)

    Biver, Tarita; García, Begoña; Leal, José M; Secco, Fernando; Turriani, Elisa

    2010-10-28

    The conditions under which different structures of left-handed DNA (poly(dG-me(5)dC)·poly(dG-me(5)dC)) can exist are investigated by spectrofluorometric, spectrophotometric, circular dichroism and calorimetric measurements and the kinetics of the transformations are analysed. The effects of temperature, salt and ethanol content on the transitions are also studied. The left-handed structure obtained by addition of either Mg(2+) ions or EtOH corresponds to Z-DNA, whereas the structure obtained using the mixture Mg(2+)/EtOH corresponds to the aggregate Z*-DNA. Upon addition of the fluorescent cyanine Thiazole Orange (TO), the transition Z → B immediately starts, whereas Z*-DNA retains its left-handed configuration in the presence of TO provided that the ratio [dye]/[polymer] ≤ 0.1. The equilibria and kinetics of the TO binding to Z*-DNA are investigated under the above conditions using the T-jump technique. The reaction mechanism consists of two series steps, the first one being characterized by the formation of an external electrostatic complex and the second corresponding to the dye penetration between the base pairs. A comparison with the B-DNA/TO system is drawn.

  1. A two-state model of twisted intramolecular chargetransfer in monomethine dyes

    CERN Document Server

    Olsen, Seth

    2012-01-01

    We describe a two-state model Hamiltonian that can describes the development of twisted intramolecular charge-transfer behavior in monomethine dyes, both near and far from the cyanine limit. Monomethine dyes are useful as biological probes due to their binding-dependent fluorescence turn-on behavior. The model is a generalized Mulliken-Hush diabatic Hamiltonian wherein the diabatic energies and couplings are coupled to twisting about distinct bonds of the monomethine bridge. We parameterize the Hamiltonian against multireference perturbation theory calculations of the ground and excited states of four distinct oxonol protonation states of a green fluorescent protein chromophore model. The four chromophores illustrate different regimes of detuning from the cyanine limit. The model describes correctly the distinct relationships between twisting and charge-transfer behavior in each case. We expose a deep connection between the existence of twist-dependent polarization and the existence of twisted conical interse...

  2. Mono and trimethine cyanines Cyan 40 and Cyan 2 as probes for highly selective fluorescent detection of non-canonical DNA structures.

    Science.gov (United States)

    Kovalska, Vladyslava B; Losytskyy, Mykhaylo Yu; Yarmoluk, Sergiy M; Lubitz, Irit; Kotlyar, Alexander B

    2011-01-01

    Two of earlier reported dsDNA sensitive cyanine dyes-monomethine Cyan 40 and meso-substituted trimethine Cyan 2 were studied for their ability to interact with non-canonical DNA conformations. These dyes were characterized by spectral-luminescent methods in the presence of G-quadruplex, triplex and dsDNA motifs. We have demonstrated that Cyan 2 binds strongly and preferentially to triple- and quadruple-stranded DNA forms that results in a strong enhancement of the dye fluorescence, as compared to dsDNA, while Cyan 40 form fluorescent complexes preferentially only with the triplex form. Highly fluorescent complexes of Cyan 2 with DNA triplexes and G-quadruplexes and Cyan 40 with DNA triplexes are very stable and do not dissociate during gel electrophoresis, leading to preferential staining of the above DNA forms in gels. The data presented point to the intercalation mechanism of the Cyan 2 binding to G4-DNA, while the complexes of Cyan 40 and Cyan 2 with triplex DNA are believed to be formed via groove binding mode. The Cyan dyes can provide a highly sensitive method for detection and quantification of non-canonical structures in genome.

  3. Spectrophotometric determination of catecholamine using vanadium and eriochrome cyanine r

    Energy Technology Data Exchange (ETDEWEB)

    Nagaraja, Padmarajaiah; Shrestha, Ashwinee Kumar; Shivakumar, Anantharaman; Al-Tayar, Naef Ghallab Saeed; Gowda, Avinask K., E-mail: profpn58@yahoo.co [University of Mysore, Manasagangotri (India). Dept. of Studies in Chemistry

    2011-07-01

    highly sensitive spectrophotometric method for the analysis of catecholamine drugs; L-dopa and methyldopa, is described. The analysis is based on the reaction of drug molecules with vanadium (V) which is reduced to vanadium (IV) and form complex with eriochrome cyanine R to give products having maximum absorbance ({lambda}{sub max}) at 565 nm. Beer's law is obeyed in the range 0.028-0.84 and 0.099-0.996 {mu}g mL{sup -1} for L-dopa and methyldopa, respectively. The statistical analysis as well as comparison with reported methods demonstrated high precision and accuracy of the proposed method. The method was successfully applied in the analysis of pharmaceutical preparations. (author)

  4. Conformational analysis of polymethine dyes derived from the 2-azaazulene

    Science.gov (United States)

    Ryabitskii, Aleksey B.; Bricks, Julia L.; Kachkovskii, Aleksey D.; Kurdyukov, Vladimir V.

    2012-01-01

    A systematic investigation of the conformational structure was performed for the series of symmetrical and unsymmetrical mono-, tri-, pentamethine cyanines, and styryl dyes bearing 2-azaazulenium terminal group. The rotation energy barriers of terminal groups were determined via the dynamic variable temperature NMR experiments. The conformational transformation energy was calculated by quantum chemical methods (B3LYP and M05-2X) both for the cases of considering the solvent influence and not tacking it into account. Based on the comparison of theoretical and experimental data, relative electron-donating abilities and geometrical features of the heterocyclic terminal groups in 2-azaazulenium dyes were estimated. The arrangement of certain heterocyclic nuclei in order of basicity by considering the results of the dynamic NMR investigations was proposed. Influence of the conjugated chain length and the solvent nature on the conformational lability of the investigated dye molecules was discussed.

  5. Dye Sensitizers for Photodynamic Therapy

    Directory of Open Access Journals (Sweden)

    Harold S. Freeman

    2013-03-01

    Full Text Available Photofrin® was first approved in the 1990s as a sensitizer for use in treating cancer via photodynamic therapy (PDT. Since then a wide variety of dye sensitizers have been developed and a few have been approved for PDT treatment of skin and organ cancers and skin diseases such as acne vulgaris. Porphyrinoid derivatives and precursors have been the most successful in producing requisite singlet oxygen, with Photofrin® still remaining the most efficient sensitizer (quantum yield = 0.89 and having broad food and drug administration (FDA approval for treatment of multiple cancer types. Other porphyrinoid compounds that have received approval from US FDA and regulatory authorities in other countries include benzoporphyrin derivative monoacid ring A (BPD-MA, meta-tetra(hydroxyphenylchlorin (m-THPC, N-aspartyl chlorin e6 (NPe6, and precursors to endogenous protoporphyrin IX (PpIX: 1,5-aminolevulinic acid (ALA, methyl aminolevulinate (MAL, hexaminolevulinate (HAL. Although no non-porphyrin sensitizer has been approved for PDT applications, a small number of anthraquinone, phenothiazine, xanthene, cyanine, and curcuminoid sensitizers are under consideration and some are being evaluated in clinical trials. This review focuses on the nature of PDT, dye sensitizers that have been approved for use in PDT, and compounds that have entered or completed clinical trials as PDT sensitizers.

  6. [Tattooing dyes].

    Science.gov (United States)

    Lehmann, G; Pierchalla, P

    1988-01-01

    Nine different tattoo dyes were analysed by various tests. Mixtures of organic dyes and inorganic filler were found; the inorganic filler consisted mainly of titanium dioxide (TiO2). Heavy metals, e.g. mercury, cadmium, or chrome as the common components of the traditional tattoo dyes, are capable of evoking unwanted skin reactions, but were not detected. Tattoo dyes are not officially controlled, and thus it is not known which substances-in addition to those identified by us-are presently used to produce ornamental tattoos. However, our results suggest that classic dyes have been superceded by newer, mainly synthetic dyes.

  7. 新型菁类化合物溶液的皮秒非线性光学性质%Optical nonlinearity of novel cyanine compound solution at picosecond timescale

    Institute of Scientific and Technical Information of China (English)

    李中国; 葛剑锋; 易传祥; 宋瑛林

    2012-01-01

    利用带相位物体的非简并泵浦探测方法测量了一种新型菁类化合物溶液在皮秒时域的非线性光学性质.在接近材料线性吸收峰值的532 nm皮秒激光脉冲泵浦下,利用600 nm的皮秒激光脉冲作为探测光,测量了菁染料分子在近共振区的非线性折射动力学响应.结合相关理论,通过数值模拟最终确定了菁染料分子在600 nm波段的光物理参数.实验结果表明:该溶液的非线性光学效应来自于溶质菁染料分子的激发态非线性机制,该材料具备了较大的激发态折射体积,且单重激发态的寿命较短.该化合物具备非线性光学应用潜力.%The nonlinear refraction dynamics of a novel cyanine dye/DMF solution was investigated using time-resolved nondegenerate pump-probe system with phase object at pico-second timescale. The 532 nm laser pulse with 21-ps duration was used as the excitation and the laser pulse of 600 nm with 10-ps duration was used for probing. The experimental results show that the nonlinear optical response of cyanine solution originates from solute molecule' s excited-state nonlinear mechanism. The experiment curve is interpreted by numerical simulations based on a five-energy-level model and all of nonlinear optical parameters of cyanine dye at 600 nm are determined. This cyanine dye exhibits large change of refraction index per unit density for excited-state as well as short lifetime, indicating this compound can be a good candidate for future photonic applications.

  8. Dye Painting!

    Science.gov (United States)

    Johnston, Ann

    This resource provides practical instructions for applying color and design directly to fabric. Basic information about the dye painting process is given. The guide addresses the technical aspects of fabric dye and color use and offers suggestions for fabric manipulation and dye application in order to achieve various design effects. This…

  9. Dye Painting!

    Science.gov (United States)

    Johnston, Ann

    This resource provides practical instructions for applying color and design directly to fabric. Basic information about the dye painting process is given. The guide addresses the technical aspects of fabric dye and color use and offers suggestions for fabric manipulation and dye application in order to achieve various design effects. This…

  10. Impact of C4'-O-Alkyl Linker on in Vivo Pharmacokinetics of Near-Infrared Cyanine/Monoclonal Antibody Conjugates.

    Science.gov (United States)

    Sato, Kazuhide; Nagaya, Tadanobu; Nakamura, Yuko; Harada, Toshiko; Nani, Roger R; Shaum, James B; Gorka, Alexander P; Kim, Insook; Paik, Chang H; Choyke, Peter L; Schnermann, Martin J; Kobayashi, Hisataka

    2015-09-08

    Near-infrared (NIR) fluorophores have several advantages over visible-light fluorophores, including superior tissue penetration and lower autofluorescence. We recently accessed a new class of readily synthesized NIR cyanines containing a novel C4'-O-alkyl linker, which provides both high chemical stability and excellent optical properties. In this study, we provide the first in vivo analysis of this new class of compounds, represented by the tetrasulfonate FNIR-774 (Frederick NIR 774). Monoclonal antibody (mAb) conjugates of FNIR-774 were compared to conjugates of the commercially available dye (IRDye800CW (IR800)), one of the most widely used NIR fluorophores for clinical translation. Both dyes were conjugated to panitumumab (pan) or cetuximab (cet) with ratios of 1:2 or 1:5. Conjugates of both dyes demonstrated similar quenching capacity, stability, and brightness in target cells in vitro. In contrast, in vivo imaging in mice showed different pharmacokinetics between pan-FNIR-774 (1:5) and pan-IR800 (1:5), or cet-FNIR-774 (1:5) and cet-IR800 (1:5). Particularly at the higher labeling density, mAb-FNIR-774 conjugates showed superior specific accumulation in tumors compared with mAb-IR800 conjugates. Thus, FNIR-774 conjugates showed superior in vivo pharmacokinetics compared with IR800 conjugates, independent of the mAb. These results suggest that FNIR-774 is a promising fluorescent probe for NIR optical imaging.

  11. Kinetics study of ultrafast electron transfer from sensitized dyes to silver halide microcrystals

    Institute of Scientific and Technical Information of China (English)

    Yang Shao-Peng; Fan Guo-Zhi; Fan Shan-Shan; Cao Ning; Li Xiao-Wei; Jiang Xiao-Li; Fu Guang-Sheng

    2006-01-01

    Spectral sensitization micromechanism of cyanine dyes J-aggregate adsorbed on the tabular and cubic AgBr microcrystals with different dye concentrations is studied by using picosecond time-resolved fluorescence spectroscopy,and the dependences of electron transfer and spectral efficiency sensitization on different conditions are analysed in detail. With the steady spectroscopy, the wavelengths of absorption and fluorescence of J-aggregate adsorbed on AgBr microcrystals are found to shift to red relative to dye monomer. The spectrum of fluorescence has a red shift relative to the absorption peak. With the time-resolved fluorescence spectroscopy, the fluorescence decay curves of cyanine dyes J-aggregate adsorbed on the tabular and cubic AgBr grains are found to be fitted well by a double-exponential decay function. The fitting curves consist of a fast and a slow component. Because of the large amplitude of the fast component, this fast decay should be attributable mainly to the electron transfer from J-aggregate of dye to a conduction band of AgBr.

  12. Transparent organic photodetector using a near-infrared absorbing cyanine dye.

    Science.gov (United States)

    Zhang, Hui; Jenatsch, Sandra; De Jonghe, Jelissa; Nüesch, Frank; Steim, Roland; Véron, Anna C; Hany, Roland

    2015-03-24

    Organic photodetectors are interesting for low cost, large area optical sensing applications. Combining organic semiconductors with discrete absorption bands outside the visible wavelength range with transparent and conductive electrodes allows for the fabrication of visibly transparent photodetectors. Visibly transparent photodetectors can have far reaching impact in a number of areas including smart displays, window-integrated electronic circuits and sensors. Here, we demonstrate a near-infrared sensitive, visibly transparent organic photodetector with a very high average visible transmittance of 68.9%. The transmitted light of the photodetector under solar irradiation exhibits excellent transparency colour perception and rendering capabilities. At a wavelength of 850 nm and at -1 V bias, the photoconversion efficiency is 17% and the specific detectivity is 10(12) Jones. Large area photodetectors with an area of 1.6 cm(2) are demonstrated.

  13. “Turn-On” Protein Fluorescence: In Situ Formation of Cyanine Dyes

    Science.gov (United States)

    2015-01-01

    Protein reengineering of cellular retinoic acid binding protein II (CRABPII) has yielded a genetically addressable system, capable of binding a profluorophoric chromophore that results in fluorescent protein/chromophore complexes. These complexes exhibit far-red emission, with high quantum efficiencies and brightness and also exhibit excellent pH stability spanning the range of 2–11. In the course of this study, it became evident that single mutations of L121E and R59W were most effective in improving the fluorescent characteristics of CRABPII mutants as well as the kinetics of complex formation. The readily crystallizable nature of these proteins was invaluable to provide clues for the observed spectroscopic behavior that results from single mutation of key residues. PMID:25534273

  14. Research Progress on Cyanine Dye%菁染料的研究进展

    Institute of Scientific and Technical Information of China (English)

    王继东; 王丽秋

    2007-01-01

    菁染料以其特有的结构,已成为在光谱增感、光盘存储、生物分析、太阳能电池、无机离子和的测量等方面应用广泛的功能材料之一.本文综述了近几年的研究情况,简单介绍了菁染料的相关知识,和它在合成方面的进展,以及在以上几个方面的应用情况.

  15. Modelling of the cis-trans partitioning in the photoisomerizations of cyanines and stilbene derivatives

    Science.gov (United States)

    Caselli, M.; Momicchioli, F.; Ponterini, G.

    1993-12-01

    In the course of photoisomerization, polymethine cyanines as well as stilbene and its derivates decay from the S 1 potential energy minimum, corresponding to the perpendicular geometry, to yield either cis or trans ground-state molecules. The fraction of cis isomers obtained, α, spans a larger range of values for symmetric cyanines than for stilbene derivatives. It is argued that such different behaviour for the two classes of compounds should be traceable to the electronically different nature of their S 1 perp species. Making use of radiationless transition theory results, it is shown the relative location of the S 1 minimum and S 0 maximum along the internal rotation coordinate is crucial to the evaluation of α: even small differences between these critical twisting angles, which are more reasonably expected for polymethine cyanines than for stilbene-like compounds, may cause strong deviations from equipartitioning (α=0.5).

  16. Bond Alternation, Polarizability and Resonance Detuning in Methine Dyes

    CERN Document Server

    Olsen, Seth

    2010-01-01

    Many organic molecules with a high nonlinear polarizability have a "Brooker dye" structure, featuring electron accepting or donating groups separated by an unsaturated (methine or polyene) hydrocarbon bridge. These systems have been the topic of much discussion with regard to their structure-property relationships - particularly relationships linking nonlinear response to bond-length alternation. Here, we show that these relationships can be subsumed within the conceptual framework of a Brooker dye color proposed by Platt [J.R. Platt, J. Chem. Phys. 25 80 (1956)]. The key quantities of Platt's model are the Brooker basicity difference and the isoexcitation energy. These concepts provide a spectroscopic definition of the resonant (cyanine) limit, which is independent of other descriptors commonly used (e.g. bond length alternation). We establish a relation ship between the bond length and the Brooker basicity difference, with which we establish a natural origin for bond length alternation coordinates in asymme...

  17. Selective G-Quadruplex DNA Recognition by a New Class of Designed Cyanines

    Directory of Open Access Journals (Sweden)

    Markus W. Germann

    2013-11-01

    Full Text Available A variety of cyanines provide versatile and sensitive agents acting as DNA stains and sensors and have been structurally modified to bind in the DNA minor groove in a sequence dependent manner. Similarly, we are developing a new set of cyanines that have been designed to achieve highly selective binding to DNA G-quadruplexes with much weaker binding to DNA duplexes. A systematic set of structurally analogous trimethine cyanines has been synthesized and evaluated for quadruplex targeting. The results reveal that elevated quadruplex binding and specificity are highly sensitive to the polymethine chain length, heterocyclic structure and intrinsic charge of the compound. Biophysical experiments show that the compounds display significant selectivity for quadruplex binding with a higher preference for parallel stranded quadruplexes, such as cMYC. NMR studies revealed the primary binding through an end-stacking mode and SPR studies showed the strongest compounds have primary KD values below 100 nM that are nearly 100-fold weaker for duplexes. The high selectivity of these newly designed trimethine cyanines for quadruplexes as well as their ability to discriminate between different quadruplexes are extremely promising features to develop them as novel probes for targeting quadruplexes in vivo.

  18. Selective G-quadruplex DNA recognition by a new class of designed cyanines.

    Science.gov (United States)

    Nanjunda, Rupesh; Owens, Eric A; Mickelson, Leah; Dost, Tyler L; Stroeva, Ekaterina M; Huynh, Hang T; Germann, Markus W; Henary, Maged M; Wilson, W David

    2013-11-04

    A variety of cyanines provide versatile and sensitive agents acting as DNA stains and sensors and have been structurally modified to bind in the DNA minor groove in a sequence dependent manner. Similarly, we are developing a new set of cyanines that have been designed to achieve highly selective binding to DNA G-quadruplexes with much weaker binding to DNA duplexes. A systematic set of structurally analogous trimethine cyanines has been synthesized and evaluated for quadruplex targeting. The results reveal that elevated quadruplex binding and specificity are highly sensitive to the polymethine chain length, heterocyclic structure and intrinsic charge of the compound. Biophysical experiments show that the compounds display significant selectivity for quadruplex binding with a higher preference for parallel stranded quadruplexes, such as cMYC. NMR studies revealed the primary binding through an end-stacking mode and SPR studies showed the strongest compounds have primary KD values below 100 nM that are nearly 100-fold weaker for duplexes. The high selectivity of these newly designed trimethine cyanines for quadruplexes as well as their ability to discriminate between different quadruplexes are extremely promising features to develop them as novel probes for targeting quadruplexes in vivo.

  19. Design and synthesis of polymer-functionalized NIR fluorescent dyes--magnetic nanoparticles for bioimaging.

    Science.gov (United States)

    Yen, Swee Kuan; Jańczewski, Dominik; Lakshmi, Jeeva Lavanya; Dolmanan, Surani Bin; Tripathy, Sudhiranjan; Ho, Vincent H B; Vijayaragavan, Vimalan; Hariharan, Anushya; Padmanabhan, Parasuraman; Bhakoo, Kishore K; Sudhaharan, Thankiah; Ahmed, Sohail; Zhang, Yong; Tamil Selvan, Subramanian

    2013-08-27

    The fluorescent probes having complete spectral separation between absorption and emission spectra (large Stokes shift) are highly useful for solar concentrators and bioimaging. In bioimaging application, NIR fluorescent dyes have a greater advantage in tissue penetration depth compared to visible-emitting organic dyes or inorganic quantum dots. Here we report the design, synthesis, and characterization of an amphiphilic polymer, poly(isobutylene-alt-maleic anhyride)-functionalized near-infrared (NIR) IR-820 dye and its conjugates with iron oxide (Fe3O4) magnetic nanoparticles (MNPs) for optical and magnetic resonance (MR) imaging. Our results demonstrate that the Stokes shift of unmodified dye can be tuned (from ~106 to 208 nm) by the functionalization of the dye with polymer and MNPs. The fabrication of bimodal probes involves (i) the synthesis of NIR fluorescent dye (IR-820 cyanine) functionalized with ethylenediamine linker in high yield, >90%, (ii) polymer conjugation to the functionalized NIR fluorescent dye, and (iii) grafting the polymer-conjugated dyes on iron oxide MNPs. The resulting uniform, small-sized (ca. 6 nm) NIR fluorescent dye-magnetic hybrid nanoparticles (NPs) exhibit a wider emissive range (800-1000 nm) and minimal cytotoxicity. Our preliminary studies demonstrate the potential utility of these NPs in bioimaging by means of direct labeling of cancerous HeLa cells via NIR fluorescence microscopy and good negative contrast enhancement in T2-weighted MR imaging of a murine model.

  20. Conformational structure of the unsymmetrical monomethine cyanine bearing 2-azaazulene and 2-benzothiazole residues as terminal groups: Experimental and quantum-chemical investigation

    Science.gov (United States)

    Ryabitskii, Aleksey B.; Bricks, Julia L.; Kachkovskii, Aleksey D.; Chernega, Alexander N.; Vlasenko, Yurii G.

    2010-10-01

    Conformational features of unsymmetrical monomethine cyanine dye 2-[(2-butyl-1,3-dimethylcyclohepta[ c]pyrrol-6(2 H)-ylidene)methyl]-3-ethyl-1,3-benzothiazol-3-ium iodide-perchlorate have been investigated in solution by means of NMR spectroscopy and in the solid state by X-ray diffraction. The possibility of molecule conformational transformations was proved by scanning of potential energy surface along torsion angels. The corresponding energy barriers values have been calculated by means of DFT (B3LYP and M05-2X) methods. A comparison of structural parameters obtained by means of both methods was reported. The isomerization process was investigated by dynamic NMR spectroscopy. A comparison of 1H NMR spectra recorded in different solvents was performed. It was shown that in solution, intramolecular rotation around the bond С(6) аzaazulene-С methyne decelerated in NMR time scale took place. The data on dynamic behavior of dye molecules have been compared with the experimental X-ray data. Quantum-chemical calculation results are in agreement with the experimental data.

  1. CD-R, DVD-R. Function and coating technique of organic dye film; CD-R, DVD-R. Yuki shikisomaku no yakuwari to tofu gijutsu

    Energy Technology Data Exchange (ETDEWEB)

    Otsuki, S. [TDK Corp., Tokyo (Japan)

    1998-11-05

    This paper describes the function and coating technique of recording layer (organic dye film) of CD-R and DVD-R. The organic dye film is between the substrate and reflective film. When laser with an intensity in response to the information signal is irradiated to the organic dye film, the dye is decomposed and its reflectance is changed, to record the information. The recording characteristics are affected mainly by the composition of dye and thickness of the film. For the organic dye, safety and solubility in solvent are required from the viewpoint of the process, and optical constants, thermal properties, high-temperature/high-humidity resistance properties and optical resistance properties are required from the viewpoint of recording characteristics. The organic dye is classified into the cyanine dye, phthalocyanine dye and azo dye. The process of disk production consists of the substrate forming, due spin coating, reflective film spattering, UV protective layer coating, and disk pasting. For the spin coating, the dye solution is dropped on the substrate rotating at the low speed, and is uniformly coated by accelerating the rotation to remove the excess dye solution from the disk. Thickness of the film can be controlled by the rotating speed and its acceleration. Control of the dye film thickness is a significant control item of characteristics. 2 refs., 8 figs.

  2. Glycerol-based contrast agents: a novel series of dendronized pentamethine dyes.

    Science.gov (United States)

    Wycisk, Virginia; Pauli, Jutta; Welker, Pia; Justies, Aileen; Resch-Genger, Ute; Haag, Rainer; Licha, Kai

    2015-04-15

    The synthesis of water-soluble dyes, which absorb and emit in the range between 650 and 950 nm and display high extinction coefficients (ε) as well as high fluorescence quantum yields (Φf), is still a demand for optical imaging. We now present a synthetic route for the preparation of a new group of glycerol-substituted cyanine dyes from dendronized indole precursors that have been functionalized as N-hydroxysuccinimide (NHS) esters. High Φf values of up to 0.15 and extinction coefficients of up to 189 000 L mol(-1) cm(-1) were obtained for the pure dyes. Furthermore, conjugates of the new dendronized dyes with the antibody cetuximab (ctx) that were directed against the epidermal growth factor receptor (EGFR) of tumor cells could be prepared with dye to protein ratios between 0.3 and 2.2 to assess their potential as imaging probes. For the first time, ctx conjugates could be achieved without showing a decrease in Φf and with an increasing labeling degree that exceeded the value of the pure dye even at a labeling degree above 2. The incorporation of hydrophilically and sterically demanding dendrimers into cyanines prevented dimer formation after covalent conjugation to the antibody. The binding functionality of the resulting ctx conjugates to the EGFR was successfully demonstrated by cell microscopy studies using EGFR expressing cell lines. In summary, the combination of hydrophilic glycerol dendrons with reactive dye labels has been established for the first time and is a promising approach toward more powerful fluorescent labels with less dimerization.

  3. Absorption spectrum analysis based on singular value decomposition for photoisomerization and photodegradation in organic dyes

    Science.gov (United States)

    Kawabe, Yutaka; Yoshikawa, Toshio; Chida, Toshifumi; Tada, Kazuhiro; Kawamoto, Masuki; Fujihara, Takashi; Sassa, Takafumi; Tsutsumi, Naoto

    2015-10-01

    In order to analyze the spectra of inseparable chemical mixtures, many mathematical methods have been developed to decompose them into the components relevant to species from series of spectral data obtained under different conditions. We formulated a method based on singular value decomposition (SVD) of linear algebra, and applied it to two example systems of organic dyes, being successful in reproducing absorption spectra assignable to cis/trans azocarbazole dyes from the spectral data after photoisomerization and to monomer/dimer of cyanine dyes from those during photodegaradation process. For the example of photoisomerization, polymer films containing the azocarbazole dyes were prepared, which have showed updatable holographic stereogram for real images with high performance. We made continuous monitoring of absorption spectrum after optical excitation and found that their spectral shapes varied slightly after the excitation and during recovery process, of which fact suggested the contribution from a generated photoisomer. Application of the method was successful to identify two spectral components due to trans and cis forms of azocarbazoles. Temporal evolution of their weight factors suggested important roles of long lifetimed cis states in azocarbazole derivatives. We also applied the method to the photodegradation of cyanine dyes doped in DNA-lipid complexes which have shown efficient and durable optical amplification and/or lasing under optical pumping. The same SVD method was successful in the extraction of two spectral components presumably due to monomer and H-type dimer. During the photodegradation process, absorption magnitude gradually decreased due to decomposition of molecules and their decaying rates strongly depended on the spectral components, suggesting that the long persistency of the dyes in DNA-complex related to weak tendency of aggregate formation.

  4. Cyanine Photocages Enable the Near-IR Light Activation of Antibody-Drug Conjugates

    Science.gov (United States)

    Nani, Roger R.; Gorka, Alexander P.; Nagaya, Tadanobu; Kobayashi, Hisataka

    2016-01-01

    Despite significant progress in the clinical application of antibody drug conjugates (ADCs), novel cleavage strategies that provide improved selectivity are still needed. Near-IR light could provide a targetable, biocompatible external stimulus to initiate drug release. Here we report the first approach using near-IR light to cleave a small molecule from a biomacromolecule, which we apply to the problem of ADC linkage. Our method uses a recently developed near-IR uncaging reaction that exploits the photochemical reactivity of C4’-N-dialkylamine heptamethine cyanines. This communication describes the synthesis of bioconjugatable cyanine-small molecule photocages, bioconjugation and 690 nm light-mediated cleavage from the anti-EGFR antibody panitumumab, and initial in vitro and in vivo evaluation. These studies provide the critical chemical underpinning from which to develop this near-IR cleavable linker strategy. PMID:26403799

  5. Electrophile-integrating Smiles rearrangement provides previously inaccessible C4'-O-alkyl heptamethine cyanine fluorophores.

    Science.gov (United States)

    Nani, Roger R; Shaum, James B; Gorka, Alexander P; Schnermann, Martin J

    2015-01-16

    New synthetic methods to rapidly access useful fluorophores are needed to advance modern molecular imaging techniques. A new variant of the classical Smiles rearrangement is reported that enables the efficient synthesis of previously inaccessible C4'-O-alkyl heptamethine cyanines. The key reaction involves N- to O-transposition with selective electrophile incorporation on nitrogen. A representative fluorophore exhibits excellent resistance to thiol nucleophiles, undergoes productive bioconjugation, and can be used in near-IR fluorescence imaging applications.

  6. Enhancing sensitivity of SERRS nanoprobes by modifying heptamethine cyanine-based reporter molecules

    Directory of Open Access Journals (Sweden)

    Yunfei Zhang

    2016-07-01

    Full Text Available Surface enhanced resonance Raman scattering (SERRS is a physical phenomenon that occurs when the energy of incident light is close to that of electronic excitation of reporter molecules (RMs attached on substrates. SERRS has showed great promise in healthcare applications such as tumor diagnosis, image-guided tumor surgery and real-time evaluation of therapeutic response due to its ultra-sensitivity, manipulating convenience and easy accessibility. As the most widely used organic near-infrared (NIR fluorophore, heptamethine cyanines possess the electronic excitation energy that is close to the plasmon absorption energy of the gold nano-scaffolds, which results in the extraordinary enhancement of the SERRS signal. However, the effect of heptamethine cyanine structure and the gold nanoparticle morphology to the SERRS intensity are barely investigated. This work developed a series of SERRS nanoprobes in which two heptamethine cyanine derivatives (IR783 and IR780 were used as the RM and three gold nanoparticles (nanorod, nanosphere and nanostar were used as the substrates. Interestingly, even though IR780 and IR783 possess very similar chemical structure, SERRS signal produced by IR780 was determined as 14 times higher than that of IR783 when the RM concentration was 6.5 × 10−6M. In contrast, less than 4.0 fold SERRS signal intensity increase was measured by changing the substrate morphologies. Above experimental results indicate that finely tuning the chemical structure of the heptamethine cyanine could be a feasible way to develop robust SERRS probes to visualize tumor or guide tumor resection with high sensitivity and target to background ratio.

  7. Plasmonic fluorescent nanocomposites of cyanines self-assembled upon gold nanoparticle scaffolds.

    Science.gov (United States)

    Achyuthan, Komandoor E; Achyuthan, Ann M; Brozik, Susan M; Dirk, Shawn M; Lujan, Tracy R; Romero, Janet M; Harper, Jason C

    2012-01-01

    Plasmonic fluorescent nanocomposites are difficult to prepare due to strong quenching effects on fluorophores in the vicinity of noble metal nanoparticles such as gold (AuNPs). We successfully prepared plasmonic fluorescent nanocomposites of two cyanines (1 and 2) aggregating upon 2 - 40 nm AuNPs or streptavidin-conjugated 10 nm AuNPs. We used high throughput screening (HTS) for the first time to characterize the spectral properties, aggregation kinetics, aggregation density and photostability of the nanocomposites. Fluorescence from nanocomposites declined inversely with AuNPs size: 40 nm ≥ 20 nm > 10 nm > 5 nm > 2 nm. Sensitivity (limit of detection, LOD, 10(5) - 10(11) AuNPs/mL), brightness of the nanocomposites and surface coverage of AuNPs by cyanine aggregates were all influenced by five factors: 1) AuNPs size; 2) cyanine type (1 or 2); 3) aggregate density; 4) distance between aggregates and AuNPs surface; and 5) streptavidin protein conjugation to AuNPs. We propose a model for plasmonic fluorescent nanocomposites based on these observations. Our plasmonic fluorescent nanocomposites have applications in chemical and biological assays.

  8. Protein-Sized Bright Fluorogenic Nanoparticles Based on Cross-Linked Calixarene Micelles with Cyanine Corona.

    Science.gov (United States)

    Shulov, Ievgen; Rodik, Roman V; Arntz, Youri; Reisch, Andreas; Kalchenko, Vitaly I; Klymchenko, Andrey S

    2016-12-19

    The key challenge in the field of fluorescent nanoparticles (NPs) for biological applications is to achieve superior brightness for sizes equivalent to single proteins (3-7 nm). We propose a concept of shell-cross-linked fluorescent micelles, in which PEGylated cyanine 3 and 5 bis-azides form a covalently attached corona on micelles of amphiphilic calixarene bearing four alkyne groups. The fluorescence quantum yield of the obtained monodisperse NPs, with a size of 7 nm, is a function of viscosity and reached up to 15 % in glycerol. In the on-state they are circa 2-fold brighter than quantum dots (QD-585), which makes them the smallest PEGylated organic NPs of this high brightness. FRET between cyanine 3 and 5 cross-linkers at the surface of NPs suggests their integrity in physiological media, organic solvents, and living cells, in which the NPs rapidly internalize, showing excellent imaging contrast. Calixarene micelles with a cyanine corona constitute a new platform for the development of protein-sized ultrabright fluorescent NPs.

  9. Spectroscopic analyses of the noncovalent self-assembly of cyanines upon various nucleic acid scaffolds.

    Science.gov (United States)

    Achyuthan, Komandoor E; McClain, Jaime L; Zhou, Zhijun; Whitten, David G; Branch, Darren W

    2009-04-01

    We utilized self-assembly of cyanine chromophores to study the conformational changes in various types of nucleic acid scaffolds: single and double stranded DNA, linear or circular DNA and RNA. We identified a chromophore that became highly fluorescent after aggregating upon nucleic acids. Fluorescence from the aggregate was instantaneous after self-assembly. Temporal emission profiles displayed a biphasic trend demonstrating kinetic dependence for assembly and disassembly. Absorption spectra of the aggregate showed a red-shifted "shoulder" peak indicative of J-aggregate. Fluorescence from J-aggregates was also red-shifted. We utilized cyanine self-assembly to quantize various nucleic acids. The limits of detection and quantization for psiX174 DNA were 3 and 9 fmol, respectively. We similarly determined the sensitivity for various nucleic acids and established the optimum conditions for self-assembly. Collectively, the effects of methanol, salt, and full width at half maximum for cyanine fluorescence on DNA or carboxymethylamylose scaffolds, all suggested noncovalent, electrostatic, and hydrophobic forces were involved in supramolecular self-assembly. Our results facilitate a better understanding of supramolecular self-assembly.

  10. Spectrophotometric Study of Ternary Complex Forming Systems of Some Lanthanide Metal Ions with Eriochrome Cyanine R in Presence of Cetylpyridinium Bromide for Microdetermination

    Directory of Open Access Journals (Sweden)

    A. S. Dhepe

    2011-01-01

    Full Text Available Study of coordination compounds of lanthanide elements has received a great attention due to growing applications in science and technology. Number of chromogenic reagents form water soluble colored complexes with lanthanides. Eriochrome cyanine R (ECR a member of triphenylmethane type of dye has been reported to form green colored complexes with lanthanides and has been used for microdetermination of these metal ions. Addition of cationic surfactant, Cetylpyridinium bromide (CPB, a cationic surfactant sensitizes the color reactions of Gd(III, Tb(III, Dy(III, Ho(III and Lu(III with ECR. Formation of water soluble, highly colored ternary complexes with a considerable bathochromic shift of about 50 nm in presence of surfactant has been observed. Optimum reaction conditions and other analytical parameters were also evaluated. Stoichiometric ratio 1:3:3 of Ln: ECR: CPB are responsible for the observed rise in molar absorptivity and sensitivity. Beer’s law was obeyed between 0.50 to 13.00 ppm. Effective photometric range and molar absorptivity of these ternary complexes have been calculated. Effect of some common interfering ions on determination of these lanthanide metal ions was studied. A simple, rapid and highly sensitive spectrophotometeric method has been proposed for the determination of metal ions understudy.

  11. Waterless Textile Dyeing

    OpenAIRE

    Odabaşoğlu, Hakkı Yasin; AVİNÇ, Osman Ozan; Arzu YAVAŞ

    2013-01-01

    Supercritical carbon dioxide (scCO), having liquid-like densities, hereby provides hydrophobic dyes an advantage on dissolving. Their gas-like low viscosities and diffusion properties can lead to shorter dyeing durations compared to conventional water dyeing process. Supercritical carbon dioxide dyeing, a novel dyeing process, is an anhydrous dyeing and this process involves the use of less energy and chemicals than conventional water dyeing processes resulting in a potential of up to 50% low...

  12. Trichocyanines: a Red-Hair-Inspired Modular Platform for Dye-Based One-Time-Pad Molecular Cryptography.

    Science.gov (United States)

    Leone, Loredana; Pezzella, Alessandro; Crescenzi, Orlando; Napolitano, Alessandra; Barone, Vincenzo; d'Ischia, Marco

    2015-06-01

    Current molecular cryptography (MoCryp) systems are almost exclusively based on DNA chemistry and reports of cryptography technologies based on other less complex chemical systems are lacking. We describe herein, as proof of concept, the prototype of the first asymmetric MoCryp system, based on an 8-compound set of a novel bioinspired class of cyanine-type dyes called trichocyanines. These novel acidichromic cyanine-type dyes inspired by red hair pigments were synthesized and characterized with the aid of density functional theory (DFT) calculations. Trichocyanines consist of a modular scaffold easily accessible via an expedient condensation of 3-phenyl- or 3-methyl-2H-1,4-benzothiazines with N-dimethyl- or o-methoxyhydroxy-substituted benzaldehyde or cinnamaldehyde derivatives. The eight representative members synthesized herein can be classified as belonging to two three-state systems tunable through four different control points. This versatile dye platform can generate an expandable palette of colors and appears to be specifically suited to implement an unprecedented single-use asymmetric molecular cryptography system. With this system, we intend to pioneer the translation of digital public-key cryptography into a chemical-coding one-time-pad-like system.

  13. Cyanines as new fluorescent probes for DNA detection and two-photon excited bioimaging.

    Science.gov (United States)

    Feng, Xin Jiang; Wu, Po Lam; Bolze, Frédéric; Leung, Heidi W C; Li, King Fai; Mak, Nai Ki; Kwong, Daniel W J; Nicoud, Jean-François; Cheah, Kok Wai; Wong, Man Shing

    2010-05-21

    A series of cyanine fluorophores based on fused aromatics as an electron donor for DNA sensing and two-photon bioimaging were synthesized, among which the carbazole-based biscyanine exhibits high sensitivity and efficiency as a fluorescent light-up probe for dsDNA, which shows selective binding toward the AT-rich regions. The synergetic effect of the bischromophoric skeleton gives a several-fold enhancement in a two-photon absorption cross-section as well as a 25- to 100-fold enhancement in two-photon excited fluorescence upon dsDNA binding.

  14. Near-IR Light-Mediated Cleavage of Antibody-Drug Conjugates Using Cyanine Photocages.

    Science.gov (United States)

    Nani, Roger R; Gorka, Alexander P; Nagaya, Tadanobu; Kobayashi, Hisataka; Schnermann, Martin J

    2015-11-09

    Despite significant progress in the clinical application of antibody drug conjugates (ADCs), novel cleavage strategies that provide improved selectivity are still needed. Herein is reported the first approach that uses near-IR light to cleave a small molecule from a biomacromolecule, and its application to the problem of ADC linkage. The preparation of cyanine antibody conjugates, drug cleavage mediated by 690 nm light, and initial in vitro and in vivo evaluation is described. These studies provide the critical chemical underpinning from which to develop this near-IR light cleavable linker strategy.

  15. Hair dye poisoning

    Science.gov (United States)

    Hair tint poisoning ... Different types of hair dye contain different harmful ingredients. The harmful ingredients in permanent dyes are: Naphthylamine Other aromatic amino compounds Phenylenediamines Toluene ...

  16. DNA Microarrays for Aptamer Identification and Structural Characterization

    Science.gov (United States)

    2012-09-01

    serum albumin Cy3 Cyanine dye3 Cy5 Cyanine dye5 Cy3-BSA Cyanine dye3 conjugated to bovine serum albumin Cy3-Estradiol Cyanine dye3 conjugated to...estradiol antibody Cy3-IgE Cyanine dye3 conjugated to Immunoglobulin E Cy3-NPYsc Cyanine dye3 conjugated to scrambled neuropeptide Y sequence Cy3-SA... Cyanine dye3 conjugated to streptavidin Cy3-thrombin Cyanine dye3 conjugated to thrombin DNA deoxyribonucleic acid D/P dye-to-protein ratio

  17. SERS Characterization of the Indocyanine-Type Dye IR-820 on Gold and Silver Nanoparticles in the Near Infrared

    Directory of Open Access Journals (Sweden)

    Tatiana B. V. Neves

    2015-01-01

    Full Text Available The Raman spectrum of the indocyanine-type dye IR-820 has been assigned for both solid and solution. SERS spectra of IR-820 on both silver and gold nanoparticles suspensions excited at 1064 nm were obtained. AgNPs allowed the detection of the dye through SERS down to 0.1 micromoles per liter; for the AuNPs the lowest concentration of the dye detectable was 10 micromoles per liter. Changes in the SERS relative intensities compared to the Raman spectrum in solution are subtle, mostly due to the preresonance effect of the dye. However, a perpendicular orientation relative to the metallic surface was inferred for the dye on both AgNPs and AuNPs. The easily distinguishable SERS spectra of the dye excited at 1064 nm, together with the high biological compatibility of cyanine dyes, are both indicative that IR-820 could be used as a high-performance probe molecule for SERS.

  18. Exploration of Cyanine Compounds as Selective Inhibitors of Protein Arginine Methyltransferases: Synthesis and Biological Evaluation

    Science.gov (United States)

    2016-01-01

    Protein arginine methyltransferase 1 (PRMT1) is involved in many biological activities, such as gene transcription, signal transduction, and RNA processing. Overexpression of PRMT1 is related to cardiovascular diseases, kidney diseases, and cancers; therefore, selective PRMT1 inhibitors serve as chemical probes to investigate the biological function of PRMT1 and drug candidates for disease treatment. Our previous work found trimethine cyanine compounds that effectively inhibit PRMT1 activity. In our present study, we systematically investigated the structure–activity relationship of cyanine structures. A pentamethine compound, E-84 (compound 50), showed inhibition on PRMT1 at the micromolar level and 6- to 25-fold selectivity over CARM1, PRMT5, and PRMT8. The cellular activity suggests that compound 50 permeated the cellular membrane, inhibited cellular PRMT1 activity, and blocked leukemia cell proliferation. Additionally, our molecular docking study suggested compound 50 might act by occupying the cofactor binding site, which provided a roadmap to guide further optimization of this lead compound. PMID:25559100

  19. Floatation-spectrophotometric Determination of Thorium, Using Complex Formation with Eriochrome Cyanine R.

    Science.gov (United States)

    Shiri, Sabah; Delpisheh, Ali; Haeri, Ali; Poornajaf, Abdolhossein; Khezeli, Tahereh; Badkiu, Nadie

    2011-01-23

    A novel and sensitive floatation-spectrophotometric method is presented for determination of trace amounts of thorium in water samples. The method is based on the ion-associated formation between thorium, Eriochrome cyanine R and Brij-35 at pH = 4 media. The complex was floated in the interface of the aqueous phase and n-hexane by vigorous shaking. After removing the aqueous phase the floated particles were dissolved in methanol and the absorbance was measured at 607 nm. The influence of different important parameters such as Eriochrome cyanine R and surfactants concentration, pH, volume of n-hexane, standing time and interfering ions were evaluated. Under optimized conditions the calibration graph was linear in the range of 6-230 ng mL(-1) of thorium with a correlation coefficient of 0.9985. The limit of detections (LOD), based on signal to noise ratio (S/N) of 3 was 1.7 ng mL(-1). The relative standard deviations for determination of 150 and 30 ng ml(-1) of thorium were 3.26 and 4.41%, respectively (n = 10). The method showed a good linearity, recoveries, as well as some advantages such as sensitivity, simplicity, affordability and a high feasibility. The method was successfully applied to determine thorium in different water and urine samples.

  20. Pump-shaped dump optimal control reveals the nuclear reaction pathway of isomerization of a photoexcited cyanine dye.

    Science.gov (United States)

    Dietzek, Benjamin; Brüggemann, Ben; Pascher, Torbjörn; Yartsev, Arkady

    2007-10-31

    Using optimal control as a spectroscopic tool we decipher the details of the molecular dynamics of the essential multidimensional excited-state photoisomerization - a fundamental chemical reaction of key importance in biology. Two distinct nuclear motions are identified in addition to the overall bond-twisting motion: Initially, the reaction is dominated by motion perpendicular to the torsion coordinate. At later times, a second optically active vibration drives the system along the reaction path to the bottom of the excited-state potential. The time scales of the wavepacket motion on a different part of the excited-state potential are detailed by pump-shaped dump optimal control. This technique offers new means to control a chemical reaction far from the Franck-Condon point of absorption and to map details of excited-state reaction pathways revealing unique insights into the underlying reaction mechanism.

  1. Effect of Metal–Liquid Interface Composition on the Adsorption of a Cyanine Dye onto Gold Nanoparticles

    NARCIS (Netherlands)

    Guerrini, L.; Jurasekova, Z.; del Puerto, E.; Hartsuiker, Liesbeth; Domingo, C.; Garcia-Ramos, J.V.; Otto, Cornelis; Sanchez-Cortes, S.

    2013-01-01

    Synthesis of asymmetric nanoparticles, such as gold nanorods, with tunable optical properties providing metal structures with improved SERS performance is playing a critical role in expanding the use of SERS to imaging and sensing applications. However, the synthetic methods usually require

  2. Effect of Metal–Liquid Interface Composition on the Adsorption of a Cyanine Dye onto Gold Nanoparticles

    NARCIS (Netherlands)

    Guerrini, L.; Jurasekova, Z.; Puerto, del E.; Hartsuiker, L.; Domingo, C.; Garcia-Ramos, J.V.; Otto, C.; Sanchez-Cortes, S.

    2013-01-01

    Synthesis of asymmetric nanoparticles, such as gold nanorods, with tunable optical properties providing metal structures with improved SERS performance is playing a critical role in expanding the use of SERS to imaging and sensing applications. However, the synthetic methods usually require surfacta

  3. 菁染料的应用研究进展%Research Advances in the Application of Cyanine Dyes

    Institute of Scientific and Technical Information of China (English)

    蒋林玲; 李宝林

    2009-01-01

    菁染料具有光谱范围广、摩尔消光系数高、荧光量子产率较高以及灵敏度高等良好的特性,近年来,其作为功能性染料正在不断拓展应用范围.简单介绍了菁染料的结构,并就其在生物分析、化学分析、光谱增感、太阳能电池等方面的应用进行综述.

  4. Interfacing click chemistry with automated oligonucleotide synthesis for the preparation of fluorescent DNA probes containing internal xanthene and cyanine dyes

    DEFF Research Database (Denmark)

    Astakhova, I Kira; Wengel, Jesper

    2013-01-01

    for the first time performed solid-phase copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) click labeling during the automated phosphoramidite oligonucleotide synthesis followed by postsynthetic click reactions in solution. We demonstrate that our novel strategy is rapid and efficient for the preparation...

  5. Cyanine fluorochrome-labeled antibodies in vivo: assessment of tumor imaging using Cy3, Cy5, Cy5.5, and Cy7.

    Science.gov (United States)

    Ballou, B; Fisher, G W; Deng, J S; Hakala, T R; Srivastava, M; Farkas, D L

    1998-01-01

    Monoclonal antibodies to two different targetable antigens were conjugated to each of four commercially available cyanine fluorochromes. Equal amounts of all four antibodies were coinjected into tumor-bearing animals and imaged. Small, superficial tumors were adequately labeled using all four fluorochromes. Large tumors were labeled well only by Cy7, probably due to self-masking and dilution effects. Cy7 was superior to other cyanine fluorochromes for visualizing structures located deep within the animal.

  6. Cyanine 5.5 conjugated nanobubbles as a tumor selective contrast agent for dual ultrasound-fluorescence imaging in a mouse model.

    Directory of Open Access Journals (Sweden)

    Liyi Mai

    Full Text Available Nanobubbles and microbubbles are non-invasive ultrasound imaging contrast agents that may potentially enhance diagnosis of tumors. However, to date, both nanobubbles and microbubbles display poor in vivo tumor-selectivity over non-targeted organs such as liver. We report here cyanine 5.5 conjugated nanobubbles (cy5.5-nanobubbles of a biocompatible chitosan-vitamin C lipid system as a dual ultrasound-fluorescence contrast agent that achieved tumor-selective imaging in a mouse tumor model. Cy5.5-nanobubble suspension contained single bubble spheres and clusters of bubble spheres with the size ranging between 400-800 nm. In the in vivo mouse study, enhancement of ultrasound signals at tumor site was found to persist over 2 h while tumor-selective fluorescence emission was persistently observed over 24 h with intravenous injection of cy5.5-nanobubbles. In vitro cell study indicated that cy5.5-flurescence dye was able to accumulate in cancer cells due to the unique conjugated nanobubble structure. Further in vivo fluorescence study suggested that cy5.5-nanobubbles were mainly located at tumor site and in the bladder of mice. Subsequent analysis confirmed that accumulation of high fluorescence was present at the intact subcutaneous tumor site and in isolated tumor tissue but not in liver tissue post intravenous injection of cy5.5-nanobubbles. All these results led to the conclusion that cy5.5-nanobubbles with unique crosslinked chitosan-vitamin C lipid system have achieved tumor-selective imaging in vivo.

  7. BOXTO as a real-time thermal cycling reporter dye

    Indian Academy of Sciences (India)

    Ashraf I Ahmad

    2007-03-01

    The unsymmetrical cyanine dyes BOXTO (4-[6-(benzoxazole-2-yl-(3-methyl-)-2,3-dihydro-(benzo-1,3-thiazole)-2-methylidene)]-1-methyl-quinolinium chloride) and its positive divalent derivative BOXTO-PRO (4-[(3-methyl-6-(benzoxazole-2-yl)-2,3-dihydro-(benzo-1,3-thiazole)-2-methylidene)]-1-(3-trimethylammonium-propyl)-quinolinium dibromide) were studied as real-time PCR reporting fluorescent dyes and compared to SYBR GREEN I (SG) (2-[N-(3-dimethylaminopropyl)-N-propylamino]-4-[2,3-dihydro-3-methyl-(benzo-1,3-thiazol-2-yl)-methylidene]-1-phenyl-quinolinium). Unmodified BOXTO showed no inhibitory effects on real-time PCR, while BOXTO-PRO showed complete inhibition. Sufficient fluorescent signal was acquired when 0.5–1.0 M BOXTO was used with RotorGene and iCycler platforms. Statistical analysis showed that there is no significant difference between the efficiency and dynamic range of BOXTO and SG. BOXTO stock solution (1.5 mM) was stable at –20°C for more than one year and 40 M BOXTO solution was more stable than 5x SG when both were stored at 4°C for 45 days.

  8. Tunable Microfluidic Dye Laser

    DEFF Research Database (Denmark)

    Olsen, Brian Bilenberg; Helbo, Bjarne; Kutter, Jörg Peter

    2003-01-01

    We present a tunable microfluidic dye laser fabricated in SU-8. The tunability is enabled by integrating a microfluidic diffusion mixer with an existing microfluidic dye laser design by Helbo et al. By controlling the relative flows in the mixer between a dye solution and a solvent......, the concentration of dye in the laser cavity can be adjusted, allowing the wavelength to be tuned. Wavelength tuning controlled by the dye concentration was demonstrated with macroscopic dye lasers already in 1971, but this principle only becomes practically applicable by the use of microfluidic mixing...

  9. Structurally Rigid 9-Amino-benzo[c]cinnoliniums Make Up a Class of Compact and Large Stokes-Shift Fluorescent Dyes for Cell-Based Imaging Applications.

    Science.gov (United States)

    Shen, Yanming; Shang, Zhihao; Yang, Yanhong; Zhu, Shaojia; Qian, Xuhong; Shi, Ping; Zheng, Jing; Yang, Youjun

    2015-06-05

    Classic fluorescent dyes, such as coumarin, naphthalimide, fluorescein, BODIPY, rhodamine, and cyanines, are cornerstones of various spectroscopic and microscopic methods, which hold a prominent position in biological studies. We recently found that 9-amino-benzo[c]cinnoliniums make up a novel group of fluorophores that can be used in biological studies. They are featured with a succinct conjugative push-pull backbone, a broad absorption band, and a large Stokes shift. They are potentially useful as a small-molecule alternative to R-phycoerythrin to pair with fluorescein in multiplexing applications.

  10. Cyanine-based probe\\tag-peptide pair fluorescence protein imaging and fluorescence protein imaging methods

    Science.gov (United States)

    Mayer-Cumblidge, M. Uljana; Cao, Haishi

    2013-01-15

    A molecular probe comprises two arsenic atoms and at least one cyanine based moiety. A method of producing a molecular probe includes providing a molecule having a first formula, treating the molecule with HgOAc, and subsequently transmetallizing with AsCl.sub.3. The As is liganded to ethanedithiol to produce a probe having a second formula. A method of labeling a peptide includes providing a peptide comprising a tag sequence and contacting the peptide with a biarsenical molecular probe. A complex is formed comprising the tag sequence and the molecular probe. A method of studying a peptide includes providing a mixture containing a peptide comprising a peptide tag sequence, adding a biarsenical probe to the mixture, and monitoring the fluorescence of the mixture.

  11. A simple route to phosphamethine cyanines from S,N-heterocyclic carbenes.

    Science.gov (United States)

    Binder, Justin F; Corrente, Andrea M; Macdonald, Charles L B

    2016-02-07

    Although salts of thiazolium cations are known, many readily prepared iodide salts have eluded spectroscopic and structural characterization; herein, data for a variety of such salts are reported. It has been demonstrated that thiazolium cations can be deprotonated to generate S,N-heterocyclic carbenes and their "electron rich olefin" dimers, but use of the former has been largely overshadowed by that of the more common N-heterocyclic carbenes. We report herein that the deprotonation of thiazolium iodides and their subsequent reaction with a conveniently prepared triphosphenium precursor grants phosphamethine cyanine cations with solid-state geometry and electronic structure unlike those of NHC-stabilized cations. Protection of the phosphorus atom in such ions with elemental sulfur provides an air- and moisture-stable dithiophosphinium salt.

  12. Optimizing the second-order optical nonlinearities of organic molecules: asymmetric cyanines and highly polarized polyenes

    Science.gov (United States)

    Marder, Seth R.; Gorman, Christopher B.; Cheng, Lap-Tak A.; Tiemann, Bruce G.

    1993-02-01

    We recently reported that there is an optimal combination of donor and acceptor strengths for a given molecular length and bridge structure that maximizes (beta) . For this combination, there is the correct degree of bond length alternation and asymmetry in the molecule. Our recent findings suggest that molecules that can be viewed as asymmetric cyanines with relatively small amounts of bond length alternation are nearly optimal. In this manner, we have identified molecules with nonlinearities many times that of conventional chromophores for a given length. In this paper, we will present a new computational analysis that allows the correlation of bond length alternation with hyperpolarizabilities and will present EFISH data on simple donor-acceptor polyene chromophores.

  13. Preventing Radiobleaching of Cyanine Fluorophores Enhances Stability of Nuclear/NIRF Multimodality Imaging Agents

    Science.gov (United States)

    Hernandez, Reinier; Heskamp, Sandra; Rijpkema, Mark; Bos, Desirée L.; Goldenberg, David M.; McBride, William J.; Morgenstern, Alfred; Bruchertseifer, Frank; Cai, Weibo; Boerman, Otto C.

    2017-01-01

    Despite the large interest in nuclear/optical multimodality imaging, the effect of radiation on the fluorescence of fluorophores remains largely unexplored. Herein, we report on the radiobleaching of cyanine fluorophores and describe conditions to provide robust radioprotection under practical (pre)clinical settings. We determined the radiosensitivity of several cyanine fluorescent compounds, including IRDye 800CW (800CW) and a dual modality imaging tetrapeptide containing DOTA as chelator and Dylight 800 as fluorophore, exposed to increasing activities of 111In, 68Ga, or 213Bi (γ, EC/β, and α emitter, respectively). An activity and type of radiation-dependent radiation-induced loss of fluorescence, radiobleaching, of 800CW was observed upon incubation with escalating activities of 111In, 68Ga, or 213Bi. 68Ga showed the largest radiolytic effect, followed by 111In and 213Bi. The addition of oxygen radical scavengers including ethanol, gentisic acid, and ascorbic acid (AA), provided a concentration dependent radioprotective effect. These results supported the hypothesis of a free radical-mediated radiobleaching mechanism. AA provided the most robust radioprotection over a wide range of concentrations and preserved fluorescence at much higher radioactivity levels. Overall, both near-infrared fluorescent compounds displayed similar sensitivity, except for 213Bi-irradiated solutions, where the dual modality construct exhibited enhanced radiolysis, presumably due to direct radiation damage from α particles. Concurrently, AA was not able to preserve fluorescence of the dual-modality molecule labeled with 213Bi. Our findings have important consequences for several research areas including ROS sensing, radiation-mediated drug release (uncaging), fluorescent dosimetry, and in the preparation of dual-modality radiopharmaceuticals. PMID:28042311

  14. Toxicity of imine-iminium dyes and pigments: electron transfer, radicals, oxidative stress and other physiological effects.

    Science.gov (United States)

    Kovacic, Peter; Somanathan, Ratnasamy

    2014-08-01

    Although conjugation is well known as an important contributor to color, there is scant recognition concerning involvement of imine and iminium functions in the physiological effects of this class of dyes and pigments. The group includes the dyes methylene blue, rhodamine, malachite green, fuchsin, crystal violet, auramine and cyanins, in addition to the pigments consisting of pyocyanine, phthalocyanine and pheophytin. The physiological effects consist of both toxicity and beneficial aspects. The unifying theme of electron transfer-reactive oxygen species-oxidative stress is used as the rationale in both cases. Toxicity is frequently prevented or alleviated by antioxidants. The apparent dichotomy of methylene blue action as both oxidant and antioxidant is rationalized based on similar previous cases. This mechanistic approach may have practical benefit. This review is important in conveying, for the first time, a unifying mechanism for toxicity based on electron transfer-reactive oxygen species-oxidative stress arising from imine-iminium.

  15. A Novel Carbazole-based Cyanine as a Fluorescent Probe for Viscosity Detection%一种新型咔唑类菁染料黏度荧光探针

    Institute of Scientific and Technical Information of China (English)

    刘飞; 吴彤; 胡明明; 彭孝军; 樊江莉

    2012-01-01

    KQ, a carbazole-based cyanine dye with aldehyde, was synthesized. Dye KQ showed lower fluorescence quantum yield and no obvious fluorescence responses to the polarity of solvents and bio-macromole-cules such as nucleic acids. Dye KQ was very sensitive to the environmental viscosity and gave strong fluorescence enhancement with the increase of the viscosity. Notably, there is a linear relationship between them. The live cell imaging experiments manifested that KQ could penetrate the cell membrane easily, detect the viscosity of the cellular micro-environment and gave bright and explicit staining image of the inner membrane system of live cells.%合成了一种带有醛基的咔唑类菁染料KQ,其自身的荧光量子产率较低,对极性的敏感性小,且荧光信号不受核酸等生物分子的干扰.KQ对环境黏度有很好的荧光响应,相对荧光强度随着环境黏度的增大而增强,并且在1×10-3 ~1.3216 Pa·s黏度范围内,染料的荧光强度与溶液的黏度呈良好的线性关系.活细胞荧光成像实验结果表明,染料KQ具有良好的细胞膜通透性,并可对细胞内不同位置的黏度检测成像.

  16. Dyeing Properties of Basofil Fiber

    Institute of Scientific and Technical Information of China (English)

    JIANG Hong; DAI Jin-jin

    2002-01-01

    The structures and properties of Basofil fiber were studied using X- rays small angle diffraction analysis,differential- scanuing calorimeter and scanning electron microscopy. Disperse dyes, acid dyes and reactive dyes had been tried for dyeing Basefil fiber. It was shown disperse dyes were superior to other ones. The two series of high temperature dyes and low temperature dyes were compared for their suitability for Basofil fiber, and their dyeing behaviors were determined.

  17. Benzidine Dyes Action Plan

    Science.gov (United States)

    This Action Plan addresses the use of benzidine-based dyes and benzidine congener-based dyes, both metalized and non-metalized, in products that would result in consumer exposure, such as for use to color textiles.

  18. Early detection of breast cancer: a molecular optical imaging approach using novel estrogen conjugate fluorescent dye

    Science.gov (United States)

    Bhattacharjee, Shubhadeep; Jose, Iven

    2011-02-01

    Estrogen induced proliferation of mutant cells is widely understood to be the one of major risk determining factor in the development of breast cancer. Hence determination of the Estrogen Receptor[ER] status is of paramount importance if cancer pathogenesis is to be detected and rectified at an early stage. Near Infrared Fluorescence [NIRf] Molecular Optical Imaging is emerging as a powerful tool to monitor bio-molecular changes in living subjects. We discuss pre-clinical results in our efforts to develop an optical imaging diagnostic modality for the early detection of breast cancer. We have successfully carried out the synthesis and characterization of a novel target-specific NIRf dye conjugate aimed at measuring Estrogen Receptor[ER] status. The conjugate was synthesized by ester formation between 17-β estradiol and a hydrophilic derivative of Indocyanine Green (ICG) cyanine dye, bis-1,1-(4-sulfobutyl) indotricarbocyanine-5-carboxylic acid, sodium salt. In-vitro studies regarding specific binding and endocytocis of the dye performed on ER+ve [MCF-7] and control [MDA-MB-231] adenocarcinoma breast cancer cell lines clearly indicated nuclear localization of the dye for MCF-7 as compared to plasma level staining for MDA-MB-231. Furthermore, MCF-7 cells showed ~4.5-fold increase in fluorescence signal intensity compared to MDA-MB-231. A 3-D mesh model mimicking the human breast placed in a parallel-plate DOT Scanner is created to examine the in-vivo efficacy of the dye before proceeding with clinical trials. Photon migration and florescence flux intensity is modeled using the finite-element method with the coefficients (quantum yield, molar extinction co-efficient etc.) pertaining to the dye as obtained from photo-physical and in-vitro studies. We conclude by stating that this lipophilic dye can be potentially used as a target specific exogenous contrast agent in molecular optical imaging for early detection of breast cancer.

  19. Covalently deposited dyes: a new chromogen paradigm that facilitates analysis of multiple biomarkers in situ.

    Science.gov (United States)

    Day, William A; Lefever, Mark R; Ochs, Robert L; Pedata, Anne; Behman, Lauren J; Ashworth-Sharpe, Julia; Johnson, Donald D; May, Eric J; Grille, James G; Roberts, Esteban A; Kosmeder, Jerry W; Morrison, Larry E

    2017-01-01

    Multiplexed analysis of multiple biomarkers in a tissue sample requires use of reporter dyes with specific spectral properties that enable discrimination of signals. Conventional chromogens with broad absorbance spectra, widely used in immunohistochemistry (IHC), offer limited utility for multiplexed detection. Many dyes with narrow absorbance spectra, eg rhodamines, fluoresceins, and cyanines, potentially useful for multiplexed detection are well-characterized; however, generation of a chromogenic reagent useful for IHC analysis has not been demonstrated. Studies reported herein demonstrate utility of tyramine-chemistry for synthesis of a wide variety of new chromogenic dye conjugates useful for multiplexed in situ analysis using conventional light microscopes. The dyes, useful individually or in blends to generate new colors, provide signal sensitivity and dynamic range similar to conventional DAB chromogen, while enabling analysis of co-localized biomarkers. It is anticipated that this new paradigm will enable generation of a wide variety of new chromogens, useful for both research and clinical biomarker analysis that will benefit clinicians and patients.

  20. Restricted open-shell Kohn-Sham theory for π-π* transitions. I. Polyenes, cyanines, and protonated imines

    Science.gov (United States)

    Grimm, Stephan; Nonnenberg, Christel; Frank, Irmgard

    2003-12-01

    We present a self-consistent field algorithm for the restricted open-shell Kohn-Sham method which can be used to calculate excited states that have the same spatial symmetry as the corresponding ground states. The method is applied to π-π* transitions in polyenes, cyanines, and protonated imines. Excitation energies obtained with gradient corrected functionals are found to be significantly redshifted; the shift is constant within a homologous series. Planar excited state geometries have been optimized for all systems.

  1. Electrophile-Integrating Smiles Rearrangement Provides Previously Inaccessible C4′-O-Alkyl Heptamethine Cyanine Fluorophores

    Science.gov (United States)

    2016-01-01

    New synthetic methods to rapidly access useful fluorophores are needed to advance modern molecular imaging techniques. A new variant of the classical Smiles rearrangement is reported that enables the efficient synthesis of previously inaccessible C4′-O-alkyl heptamethine cyanines. The key reaction involves N- to O- transposition with selective electrophile incorporation on nitrogen. A representative fluorophore exhibits excellent resistance to thiol nucleophiles, undergoes productive bioconjugation, and can be used in near-IR fluorescence imaging applications. PMID:25562683

  2. Dyeing of Polypropylene Fibers with Vat Dyes

    Institute of Scientific and Technical Information of China (English)

    LIU Hang; ETTERS J. Nolan; LEONAS Karen K

    2006-01-01

    Polypropylene fibers have been extensively used in a variety of products, including carpets and upholstery, due to their non-absorbency, good weather resistance, good resistance to microorganisms and so on. Because of their hydrophobic and highly crystalline nature, those well-established conventional dyeing processes are difficult to apply to unmodified polypropylene. Colors of polypropylene fibers are primarily obtained by mass coloration which has the disadvantages of limited number of colors available and difficulties in inventory control due to the rapidly changing color needs of the market. In this paper, the use of vat dyes to dye polypropylene fabrics is investigated. Seventeen vat dyes were screened and factors influencing uptake of dyes by polypropylene fabrics were studied.

  3. Lipophilic Cationic Cyanines Are Potent Complex I Inhibitors and Specific in Vitro Dopaminergic Toxins with Mechanistic Similarities to Both Rotenone and MPP(.).

    Science.gov (United States)

    Kadigamuwa, Chamila C; Mapa, Mapa S T; Wimalasena, Kandatege

    2016-09-19

    We have recently reported that simple lipophilic cationic cyanines are specific and potent dopaminergic toxins with a mechanism of toxicity similar to that of the Parkinsonian toxin MPP(+). In the present study, a group of fluorescent lipophilic cyanines have been used to further exploit the structure-activity relationship of the specific dopaminergic toxicity of cyanines. Here, we report that all cyanines tested were highly toxic to dopaminergic MN9D cells with IC50s in the range of 60-100 nM and not toxic to non-neuronal HepG2 cells parallel to that previously reported for 2,2'- and 4,4'-cyanines. All cyanines nonspecifically accumulate in the mitochondria of both MN9D and HepG2 cells at high concentrations, inhibit the mitochondrial complex I with the inhibition potencies similar to the potent complex I inhibitor, rotenone. They increase the reactive oxygen species (ROS) production specifically in dopaminergic cells causing apoptotic cell death. These and other findings suggest that the complex I inhibition, the expression of low levels of antioxidant enzymes, and presence of high levels of oxidatively labile radical propagator, dopamine, could be responsible for the specific increase in ROS production in dopaminergic cells. Thus, the predisposition of dopaminergic cells to produce high levels of ROS in response to mitochondrial toxins together with their inherent greater demand for energy may contribute to their specific vulnerability toward these toxins. The novel findings that cyanines are an unusual class of potent mitochondrial toxins with specific dopaminergic toxicity suggest that their presence in the environment could contribute to the etiology of PD similar to that of MPP(+) and rotenone.

  4. Hair dye contact allergy

    DEFF Research Database (Denmark)

    Søsted, Heidi; Rastogi, Suresh Chandra; Andersen, Klaus Ejner

    2004-01-01

    Colouring of hair can cause severe allergic contact dermatitis. The most frequently reported hair dye allergens are p-phenylenediamine (PPD) and toluene-2,5-diamine, which are included in, respectively, the patch test standard series and the hairdressers series. The aim of the present study...... was to identify dye precursors and couplers in hair dyeing products causing clinical hair dye dermatitis and to compare the data with the contents of these compounds in a randomly selected set of similar products. The patient material comprised 9 cases of characteristic clinical allergic hair dye reaction, where...... exposure history and patch testing had identified a specific hair dye product as the cause of the reaction. The 9 products used by the patients were subjected to chemical analysis. 8 hair dye products contained toluene-2,5-diamine (0.18 to 0.98%). PPD (0.27%) was found in 1 product, and m-aminophenol (0...

  5. Ultrasonic dyeing of cellulose nanofibers.

    Science.gov (United States)

    Khatri, Muzamil; Ahmed, Farooq; Jatoi, Abdul Wahab; Mahar, Rasool Bux; Khatri, Zeeshan; Kim, Ick Soo

    2016-07-01

    Textile dyeing assisted by ultrasonic energy has attained a greater interest in recent years. We report ultrasonic dyeing of nanofibers for the very first time. We chose cellulose nanofibers and dyed with two reactive dyes, CI reactive black 5 and CI reactive red 195. The cellulose nanofibers were prepared by electrospinning of cellulose acetate (CA) followed by deacetylation. The FTIR results confirmed complete conversion of CA into cellulose nanofibers. Dyeing parameters optimized were dyeing temperature, dyeing time and dye concentrations for each class of the dye used. Results revealed that the ultrasonic dyeing produced higher color yield (K/S values) than the conventional dyeing. The color fastness test results depicted good dye fixation. SEM analysis evidenced that ultrasonic energy during dyeing do not affect surface morphology of nanofibers. The results conclude successful dyeing of cellulose nanofibers using ultrasonic energy with better color yield and color fastness results than conventional dyeing.

  6. Photophysical Studies of a New Water Soluble Indocarbocyanine Dye Adsorbed onto Microcrystalline Cellulose and b-Cyclodextrin

    Directory of Open Access Journals (Sweden)

    Luis F. Vieira Ferreira

    2013-05-01

    Full Text Available A water-soluble indocarbocyanine dye was synthesized and its photophysics were studied for the first time on two solid hosts, microcrystalline cellulose and b-cyclodextrin, as well as in homogeneous media. The inclusion of the indocarbocyanine moiety onto microcrystalline cellulose increased the dye aggregation with both H and J aggregates being formed. Adsorption on b-cyclodextrin enhanced aggregation in a similar way. The fluorescence quantum yields were determined for the powdered samples of the cyanine dye on the two hosts and a significant increase was observed relative to homogeneous solution. A remarkable concentration dependence was also detected in both cases. A lifetime distribution analysis has shown that the indocarbocyanine dye mainly occupies the amorphous part of cellulose and is not entrapped in the crystalline part of this host. In the b-CD case, the adsorption occurs outside the host cavity. In both hosts a strong concentration quenching effect is observed and only monomers emit. Both adsorptions may be explained by stereochemical constraints imposed by the two long sulphoethyl tails linked to nitrogen atoms of the indocarbocyanine dye.

  7. Elucidating the structure of merocyanine dyes with the ASEC-FEG method. Phenol blue in solution

    Science.gov (United States)

    Franco, Leandro R.; Brandão, Idney; Fonseca, Tertius L.; Georg, Herbert C.

    2016-11-01

    The electronic structure of phenol blue (PB) was investigated in several protic and aprotic solvents, in a wide range of dielectric constants, using atomistic simulations. We employed the sequential QM/MM and the free energy gradient methods to optimize the geometry of PB in each solvent at the MP2/aug-cc-pVTZ level. The ASEC mean field is used to include the ensemble average of the solute-solvent interaction into the molecular hamiltonian, both for the geometry optimization and for the calculations of the electronic properties. We found that the geometry of PB changes considerably, from a polyene-like structure in nonpolar solvents to a cyanine-like in water. Moreover, and quite interestingly, in protic solvents with higher dielectric constant than water, the structure of the molecule is less affected and lies in an intermediate state. The results illustrate the important role played by hydrogen bonds in the conformation of merocyanine dyes.

  8. Chirality generated by flows in pseudocyanine dye J-aggregates: revisiting 40 years old reports.

    Science.gov (United States)

    El-Hachemi, Zoubir; Arteaga, Oriol; Canillas, Adolf; Crusats, Joaquim; Llorens, Joan; Ribo, Josep M

    2011-09-01

    Spontaneous symmetry breaking in J-aggregates of cyanine dyes has a long history in chemical literature. In 1976, Honda and Hada claimed that they had achieved chiral induction (CD) by stirring J-aggregates of pseudocyanine. However, this report is controversial, as the combinations of linear dichroism and birefringence can lead to artifactual circular dichroic signals that are unrelated to molecular chirality. A Mueller matrix spectroscopy study, with an approach for the application of a gradient of the shear rate (solution layer between a rotating and a fixed disk) that differs from the simple vortex stirring used in the original report, shows that true CD can be induced in the sample. The phenomenon is discussed, taking into account the flow dynamics that allows the alignment of the aggregate particles and the gradient of shear rates that determines their folding/torsion, which leads to a chiral excitonic transition.

  9. Lepidine Orange derivative as a new dye for sensitive fluorescent detection of DNA

    Directory of Open Access Journals (Sweden)

    Didan Yu. V.

    2013-11-01

    Full Text Available Aim. To study new cyanine dye LO-7 as a reagent for dsDNA visualization in electrophoretic gels. Methods. Gel electrophoresis, restriction, fluorescence detection, mobility shift assay. Results. LO-7 binds to DNA to form stable highly fluorescent complexes. As little as 80 pg DNA can be detected in LO-7-stained agarose gel using a laser scanner, and 0.3 ng with UV-transilluminator. This sensitivity is several times higher than can be achieved with ethidium bromide, and close to that of SYBR Green I. Conclusions. LO-7 belongs to the most efficient stains for dsDNA visualization and thus can be used in bioanalytical applications where high sensitivity is required.

  10. Structures of an apo and a binary complex of an evolved archeal B family DNA polymerase capable of synthesising highly cy-dye labelled DNA.

    Directory of Open Access Journals (Sweden)

    Samantha A Wynne

    Full Text Available Thermophilic DNA polymerases of the polB family are of great importance in biotechnological applications including high-fidelity PCR. Of particular interest is the relative promiscuity of engineered versions of the exo- form of polymerases from the Thermo- and Pyrococcales families towards non-canonical substrates, which enables key advances in Next-generation sequencing. Despite this there is a paucity of structural information to guide further engineering of this group of polymerases. Here we report two structures, of the apo form and of a binary complex of a previously described variant (E10 of Pyrococcus furiosus (Pfu polymerase with an ability to fully replace dCTP with Cyanine dye-labeled dCTP (Cy3-dCTP or Cy5-dCTP in PCR and synthesise highly fluorescent "CyDNA" densely decorated with cyanine dye heterocycles. The apo form of Pfu-E10 closely matches reported apo form structures of wild-type Pfu. In contrast, the binary complex (in the replicative state with a duplex DNA oligonucleotide reveals a closing movement of the thumb domain, increasing the contact surface with the nascent DNA duplex strand. Modelling based on the binary complex suggests how bulky fluorophores may be accommodated during processive synthesis and has aided the identification of residues important for the synthesis of unnatural nucleic acid polymers.

  11. Synthesis and characterization of a Noble metal Enhanced Optical Nanohybrid (NEON): a high brightness detection platform based on a dye-doped silica nanoparticle.

    Science.gov (United States)

    Roy, Shibsekhar; Dixit, Chandra K; Woolley, Robert; O'Kennedy, Richard; McDonagh, Colette

    2012-05-29

    A highly bright and photostable, fluorescent nanohybrid particle is presented which consists of gold nanoparticles (GNPs) embedded in dye-doped silica in a core-shell configuration. The dye used is the near-infrared emitting 4,5-benzo-5'-(iodoacetaminomethyl)-1',3,3,3',3'-pentamethyl-1-(4-sulfobutyl) indodicarbo cyanine. The nanohybrid architecture comprises a GNP core which is separated from a layer of dye molecules by a 15 nm buffer layer and has an outer protective, undoped silica shell. Using this architecture, a brightness factor of 550 has been achieved compared to the free dye. This hybrid system, referred to as Noble metal Enhanced Optical Nanohybrid (NEON) in this paper, is the first nanohybrid construct to our knowledge which demonstrates such tunable fluorescence property. NEON has enhanced photostability compared to the free dye and compared to a control particle without GNPs. Furthermore, the NEON particle, when used as a fluorescent label in a model bioassay, shows improved performance over assays using a conventional single dye molecule label.

  12. Dyes as teratogens.

    Science.gov (United States)

    Sandor, S

    1992-01-01

    The main fats and problems of the role of dyes in prenatal pathology are reviewed. The first section deals with the practical aspects related to teratological screening of industrial dyes (including also the results obtained in this laboratory). In the second section, various aspects of azo-dye teratogenesis are largely discussed, including also the experimental contributions of this laboratory. Concluding remarks are made with respect to the importance and to the perspectives of this field of research.

  13. WATERLESS DYEING [REVIEW

    Directory of Open Access Journals (Sweden)

    DEVRENT Nalan

    2015-05-01

    Full Text Available The textile industry is believed to be one of the biggest consumers of water. Water consumption and exhaustion in dyeing textile materials in conventional methods is an important environmental problem. The cost of waste water treatment will cause a prominent problem in the future as it does today. Increasing consideration of ecologic consequences of industrial processes as well as legislation enforcing the avoidance of environmental problems have caused a reorientation of thinking and promoted projects for replacement of conventional technologies. One of these new technologies is dyeing in supercritical fluids. Dyeing with supercritical carbon dioxide is a favourable concept considering the value of water as a natural resource and the cost of waste water treatment. This dyeing method offers many advantages over conventional aqueous dyeing: During this dyeing process no water is used, therefore there is no waste water problem, no other chemicals are required; the carbon dioxide can be recycled; the dystuff which is not adsorbed on the substrate can be collected and reused; The necessary energy consumption in this process is relatively lower than is needed to heat water in conventional methods of dyeing. Due to unnecessary of drying process, it helps to save both energy and time; and dyeing cycle is shorter compared with traditional methods. In addition carbon dioxide is non-toxic and non-flammable. Supercritical fluid, supercritical dyeing, disperse dyestuffs, solid-fluid equilibrium

  14. Red Sicilian orange and purple eggplant fruits as natural sensitizers for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Calogero, Giuseppe; Marco, Gaetano Di [CNR, Istituto per i Processi Chimico-Fisici (Sede di Messina) Salita Sperone, C. da Papardo, I-98158 Faro Superiore Messina (Italy)

    2008-11-15

    Dye-sensitized solar cells (DSSCs) were assembled by using red Sicilian orange juice (Citrus Sinensis) and the purple extract of eggplant peels (Solanum melongena, L.) as natural sensitizers of TiO{sub 2} films. Conversion of solar light into electricity was successfully accomplished with both fruit-based solar cells. The best solar energy conversion efficiency ({eta}=0.66%) was obtained by red orange juice dye that, under AM 1.5 illumination, achieved up to J{sub sc}=3.84 mA/cm{sup 2}, V{sub oc}=0.340 V and fill factor=0.50. In the case of the extract of eggplant peels, the values determined were up to J{sub sc}=3.40 mA/cm{sup 2}, V{sub oc}=0.350 V and fill factor=0.40. Cyanidine-3-glucoside (cyanine) and delphinidin 3-[4-(p-coumaroyl)-L-rhamnosyl(1-6)-glucopyranoside]-5-glucopyranoside (nasunin) are the main pigments of cocktail dyes for red orange and eggplant, respectively. Actually, their application is far below the industrial requirements. Nevertheless, their study is an interesting multidisciplinary exercise useful for dissemination of knowledge and to educate people on renewable energy sources. Here, we report and discuss the role of the structure, the absorption spectra and the sensitization activity of the mentioned compounds. (author)

  15. Photo-oxidative action in MCF-7 cancer cells induced by hydrophobic cyanines loaded in biodegradable microemulsion-templated nanocapsules.

    Science.gov (United States)

    Wilk, Kazimiera A; Zielińska, Katarzyna; Pietkiewicz, Jadwiga; Skołucka, Nina; Choromańska, Anna; Rossowska, Joanna; Garbiec, Arnold; Saczko, Jolanta

    2012-07-01

    Searching for photodynamic therapy-effective nanocarriers which enable a photosensitizer to be selectively delivered to tumor cells with enhanced bioavailability and diminished dark cytotoxicity is of current interest. We have employed a polymer-based nanoparticle approach to encapsulate the cyanine-type photosensitizer IR-780 in poly(n-butyl cyanoacrylate) (PBCA) nanocapsules. The latter were fabricated by interfacial polymerization in oil-in-water (o/w) microemulsions formed by dicephalic and gemini saccharide-derived surfactants. Nanocarriers were characterized by SEM, AFM and DLS. The efficiency of PBCA nanocapsules as a potential system of photosensitizer delivery to human breast cancer cells was established by dark and photocytotoxicity as the function of the cellular mitochondria. The photodynamic effect of cyanine IR-780 was determined by investigation of oxidative stress markers. The nanocapsules were the main focus of our studies to examine their cellular uptake and dark and photocytotoxicity as the function of the cellular mitochondria as well as oxidative stress markers (i.e., lipid peroxidation and protein damage) in MCF-7/WT cancer cells. The effects of encapsulated IR-780 were compared with those of native photosensitizer. The penetration of the nanocapsules into cancer cells was visualized by CLSM and their uptake was estimated by FACS analysis. Cyanine IR-780 delivered in PBCA nanocapsules to MCF-7/WT cells retains its sensitivity upon photoirradiation and it is regularly distributed in the cell cytoplasm. The intensity of the photosensitizer-generated oxidative stress depends on IR-780 release from the effective uptake of polymeric nanocapsules and seems to remain dependent upon the surfactant structure in o/w microemulsion-based templates applied to nanocapsule fabrication.

  16. Linear and third-order nonlinear optical properties for the heptamethine cyanine chromophore H-aggregates thin film

    Institute of Scientific and Technical Information of China (English)

    YUAN YiZhong; KANG HaiFeng; SUN ZhenRong; WANG ZuGeng

    2007-01-01

    The thin film of a heptamethine cyanine chromophore HC was prepared by spin-coating technique. Its surface morphology and linear optical property were characterized by atomic force microscopy (AFM) and UV-visible absorption spectroscopy. The results show that HC molecules are arranged in a well-ordered H-aggregate type. The third-order nonlinear optical properties of the spin-coating film were also measured by degenerate four-wave mixing (DFWM) measurement. Enhanced third-order nonlinear susceptibility can be attributed to molecular aggregation effects, and the corresponding mechanism was dealt with by collective electronic oscillator (CEO) approach.

  17. Anaerobic azo dye reduction

    NARCIS (Netherlands)

    Zee, van der F.P.

    2002-01-01

    Azo dyes, aromatic moieties linked together by azo (-N=N-) chromophores, represent the largest class of dyes used in textile-processing and other industries. The release of these compounds into the environment is undesirable, not only because of their colour, but also because many azo

  18. Anaerobic azo dye reduction

    NARCIS (Netherlands)

    Zee, van der F.P.

    2002-01-01

    Azo dyes, aromatic moieties linked together by azo (-N=N-) chromophores, represent the largest class of dyes used in textile-processing and other industries. The release of these compounds into the environment is undesirable, not only because of their colour, but also b

  19. Coherent Plasmon-Exciton Coupling in Silver Platelet-J-aggregate Nanocomposites

    Science.gov (United States)

    2015-02-27

    suspensions containing silver nanoplatelets and a cyanine dye, 1,1?-diethyl-2,2?- cyanine iodide (PIC). PIC was electrostati- cally adsorbed onto the...visible spectra of colloidal suspensions containing silver nanoplatelets and a cyanine dye, 1,1?-diethyl-2,2?- cyanine iodide (PIC). PIC was...visible spectra of colloidal suspensions containing silver nanoplatelets and a cyanine dye, 1,1′-diethyl-2,2′- cyanine iodide (PIC). PIC was electrostati

  20. Determining Compatibilities of Reactive Dyes in Pad Dyeing

    Institute of Scientific and Technical Information of China (English)

    屠天民

    2001-01-01

    Compatibilities of reactive dyes were conventionally shown by exhausting curves. But the change of proportion of dyes in padding dyebath was difficult for pad dyeing to be described by these curves. In this paper, a kind of simulation of pad dyeing process was used to determine dyestuff compatibility in pad dyeing for ramie and linen fabrics. Seven reactive dyes were divided into three groups and tested., The group with Cibacron Yellow C - 2R, Red C - R, and Blue C - R showed very good compatibility both for ramie and linen,and the other two groups of dyes gave out correspondingly low compatibilities in the pad dyeing tests. The results of the method for determining the compatibility of dyes displayed good consistency with the actul pad dyeing process.

  1. Unsymmetrical Heptamethine Dyes for NIR Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Thomas Geiger

    2014-01-01

    Full Text Available Seven unsymmetrical heptamethine dyes with carboxylic acid functionality were synthesized and characterized. These near-infrared dyes exhibit outstanding photophysical properties depending on their heterocyclic moieties and molecular structure. As proof of principle, the dyes were used as photosensitizers in dye-sensitized solar cells. Using the most promising dye, an overall conversion efficiency of 1.22% and an almost colorless solar cell were achieved.

  2. Indole-based cyanine as a nuclear RNA-selective two-photon fluorescent probe for live cell imaging.

    Science.gov (United States)

    Guo, Lei; Chan, Miu Shan; Xu, Di; Tam, Dick Yan; Bolze, Frédéric; Lo, Pik Kwan; Wong, Man Shing

    2015-05-15

    We have demonstrated that the subcellular targeting properties of the indole-based cyanines can be tuned by the functional substituent attached onto the indole moiety in which the first example of a highly RNA-selective and two-photon active fluorescent light-up probe for high contrast and brightness TPEF images of rRNA in the nucleolus of live cells has been developed. It is important to find that this cyanine binds much stronger toward RNA than DNA in a buffer solution as well as selectively stains and targets to rRNA in the nucleolus. Remarkably, the TPEF brightness (Φσmax) is dramatically increased with 11-fold enhancement in the presence of rRNA, leading to the record high Φσmax of 228 GM for RNA. This probe not only shows good biocompatibility and superior photostability but also offers general applicability to various live cell lines including HeLa, HepG2, MCF-7, and KB cells and excellent counterstaining compatibility with commercially available DNA or protein trackers.

  3. Dyeing of Polyester with Disperse Dyes: Part 2. Synthesis and Dyeing Characteristics of Some Azo Disperse Dyes for Polyester Fabrics

    Directory of Open Access Journals (Sweden)

    Alya M. Al-Etaibi

    2016-06-01

    Full Text Available The goal of this study was to utilize carrier for accelerating the rate of dyeing not only to enhance dyeing of polyester fabrics dyed with disperse dyes 3a,b, but also to save energy. Both the color strength expressed as dye uptake and the fastness properties of the dyed fabrics were evaluated.

  4. Fong's: Saving Water in Dyeing

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    @@ In an effort to save the precious water resource and reduce the environmental impact, Fong's Industries Group along with its member companies, namely "Fong's National", "THEN", "Goller" and "Fong's Water Technology" provide an ecological dyeing solution to reduce the water consumption drastically through their innovative technologies covering the processes from yarn dyeing to piece dyeing and recycling of discharge after dyeing and finishing.

  5. Diode-pumped dye laser

    Science.gov (United States)

    Burdukova, O. A.; Gorbunkov, M. V.; Petukhov, V. A.; Semenov, M. A.

    2016-10-01

    This letter reports diode pumping for dye lasers. We offer a pulsed dye laser with an astigmatism-compensated three-mirror cavity and side pumping by blue laser diodes with 200 ns pulse duration. Eight dyes were tested. Four dyes provided a slope efficiency of more than 10% and the highest slope efficiency (18%) was obtained for laser dye Coumarin 540A in benzyl alcohol.

  6. Photophysical Study of a Series of Cyanines Part III. The Direct Photooxidation Reaction

    Science.gov (United States)

    Lepaja, Shukri; Strub, Henry; Lougnot, Daniel-Joseph

    1983-01-01

    The main degradative pathway of tricarbocyanine dyes in aerated solutions is demonstrated to be a photooxidation; using sensitization techniques and specific quenchers, this reaction is established to proceed via singlet oxygen for a part, and the site at which this species attacks the polymethinic skeleton is unambiguously determined. The major photoproduct is identified as being 1,3,3-trimethyl-2-indolinone.

  7. Extraction of dye

    African Journals Online (AJOL)

    ... Uganda is a home of thousands of largely unknown and undocumented plants. ... Dyes of natural origins are great for color appreciation as any variation in the ... Asteraceae characterized by bitter leaves, traditionally used for treating fever.

  8. Dye Application, Manufacture of Dye Intermediates and Dyes

    Science.gov (United States)

    Freeman, H. S.; Mock, G. N.

    It is difficult if not impossible to determine when mankind first systematically applied color to a textile substrate. The first colored fabrics were probably nonwoven felts painted in imitation of animal skins. The first dyeings were probably actually little more than stains from the juice of berries. Ancient Greek writers described painted fabrics worn by the tribes of Asia Minor. But just where did the ancient craft have its origins? Was there one original birthplace or were there a number of simultaneous beginnings around the world?

  9. Near‑infrared fluorescence imaging of prostate cancer using heptamethine carbocyanine dyes.

    Science.gov (United States)

    Yuan, Jianlin; Yi, Xiaomin; Yan, Fei; Wang, Fuli; Qin, Weijun; Wu, Guojun; Yang, Xiaojian; Shao, Chen; Chung, Leland W K

    2015-02-01

    Near‑infrared fluorescence (NIRF) imaging is an attractive novel modality for the detection of cancer. A previous study defined two organic polymethine cyanine dyes as ideal NIRF probes, IR‑783 and its derivative MHI‑148, which have excellent optical characteristics, superior biocompatibility and cancer targeting abilities. To investigate the feasibility of NIRF dye‑mediated prostate cancer imaging, dye uptake and subcellular co‑localization were investigated in PC‑3, DU‑145 and LNCaP human prostate cancer cells and RWPE‑1 normal prostate epithelial cells. Different organic anion transporting peptide (OATP) inhibitors were utilized to explore the potential role of the OATP subtype, including the nonspecific OATP inhibitor bromosulfophthalein, the OATP1 inhibitor 17β‑estradiol, the selective OATP1B1 inhibitor rifampicin and the selective OATP1B3 inhibitor cholecystokinin octapeptide. NIRF dyes were also used for the simulated detection of circulating tumor cells and the rapid detection of prostate cancer in human prostate cancer tissues and prostate cancer xenografts in mouse models. The results revealed that the cancer‑specific uptake of these organic dyes in prostate cancer cells occurred primarily via OATP1B3. A strong NIRF signal was detected in prostate cancer tissues, but not in normal tissues that were stained with IR‑783. Prostate cancer cells were recognized with particular NIR fluorescence in isolated mononuclear cell mixtures. The results of the present study demonstrated that NIRF dye‑mediated imaging is a feasible and practicable method for prostate cancer detection, although further investigative studies are required before clinical translation.

  10. Increase and saturation of the third order hyperpolarizabilities in homologous series of symmetric cyanines

    Science.gov (United States)

    Werncke, W.; Pfeiffer, M.; Johr, T.; Lau, A.; Grahn, W.; Johannes, H.-H.; Dähne, L.

    1997-04-01

    The chain length dependencies of the static third order hyperpolarizabilities γSTAT for the homologous series of benzthiacyanine dyes and of simple bis(dimethylamino)methine dyes were extrapolated from nondegenerate four wave mixing dispersion measurements and compared with theoretical values. Up to the heptamethine the π-electron contributions γSTATπ of both homologous series show a similar increase with the growing number of π-electrons ( N) of the chain ( γSTATπ ˜ - N8 ± 2). However, the absolute values of the benzthiacyanines are considerable higher than of the corresponding bis(dimethylamino)methines. Negative valued hyperpolarizabilities γSTATπ in the homologous series increasing up to γSTATπ = - 850 × 10 -36 esu were determined. For the first time a saturation of the nonlinearity could be observed experimentally in the series of benzthiacyanines for the longest chain (benzthicyanine nonamethine).

  11. Third-order nonlinear polarizabilities of a homologous series of symmetric cyanines

    Science.gov (United States)

    Johr, T.; Werncke, W.; Pfeiffer, M.; Lau, A.; Dähne, L.

    1995-12-01

    Third-order nonlinear polarizabilities of the homologous series of bis(dimethylamino)methine dyes (mono-, tri-, penta-, hepta- and non-amethine) were derived in the static frequency limit from dispersion curves measured by four-wave mixing techniques. Positive signs of the hyperpolarizabilities are obtained for mono- and trimethine: They are caused by positive contributions from δ electrons dominating the negative π electron contributions in the short chains. In the longer chains the hyperpolarizabilities exhibit negative signs and a strong enhancement (≈ - N11) with increasing chain lengths due to the growing number ( N) of contributing π electrons. A static hyperpolarizability of ≈ -1 × 10 -33 esu which is obtained for the nonamethine, is the largest off-resonant experimental value reported for a polymethine dye.

  12. Cyanine-based probe\\tag-peptide pair for fluorescence protein imaging and fluorescence protein imaging methods

    Science.gov (United States)

    Mayer-Cumblidge, M. Uljana; Cao, Haishi

    2010-08-17

    A molecular probe comprises two arsenic atoms and at least one cyanine based moiety. A method of producing a molecular probe includes providing a molecule having a first formula, treating the molecule with HgOAc, and subsequently transmetallizing with AsCl.sub.3. The As is liganded to ethanedithiol to produce a probe having a second formula. A method of labeling a peptide includes providing a peptide comprising a tag sequence and contacting the peptide with a biarsenical molecular probe. A complex is formed comprising the tag sequence and the molecular probe. A method of studying a peptide includes providing a mixture containing a peptide comprising a peptide tag sequence, adding a biarsenical probe to the mixture, and monitoring the fluorescence of the mixture.

  13. A theoretical study on the structural dependences of third-order optical nonlinearities of heterocycle-substituted polymethine cyanine chromophores

    Science.gov (United States)

    Wang, Chao; Yuan, Yizhong; Tian, Xiaohui; Sun, Jinyu; Shao, Hongjuan; Sun, Zhenrong

    2013-09-01

    The linear and third-order nonlinear optical properties of four polymethine cyanines (PC-1-PC-4) were investigated by UV-visible absorption spectroscopy and degenerate four-wave mixing (DFWM) technique. The second-order hyperpolarizabilities γ of the four chromophores achieve 10-31 esu. The dependence of their third-order optical nonlinearities on the molecular structure was discussed based on density functional theory (DFT) and time-dependent density functional theory (TDDFT) calculations. The calculated second-order hyperpolarizabilities γ well-reproduce the experimental trends. The results show that the third-order optical nonlinearities of the chromophores can be drastically enhanced by bulky heteroatom (such as selenium) with low electro-negativity, or extended π-conjugated terminal group.

  14. Electroporation and lipid nanoparticles with cyanine IR-780 and flavonoids as efficient vectors to enhanced drug delivery in colon cancer.

    Science.gov (United States)

    Kulbacka, Julita; Pucek, Agata; Kotulska, Małgorzata; Dubińska-Magiera, Magda; Rossowska, Joanna; Rols, Marie-Pierre; Wilk, Kazimiera Anna

    2016-08-01

    Nanocarriers and electroporation (also named electropermeabilization) are convenient methods to increase drug transport. In the current study, we present an effective support of drug delivery into cancer cells, utilizing these methods. We compare the efficiency of each of them and their combination. Multifunctional solid lipid nanoparticles (SLNs) loaded with a cyanine-type IR-780 - acting as a diagnostic agent and a photosensitizer, and a flavonoid derivative - baicalein (BAI) or fisetin (FIS) as a therapeutic cargo - were fabricated via solvent-diffusion method. A therapy supplemented with flavonoids may provide a more precise method to apply desirable lower drug doses and is more likely to result in lower toxicity and a decrease in tumor growth. The SLNs were stabilized with Phospholipon 90G at various concentrations; cetyl palmitate (CP) was applied as a solid matrix. The obtained nanosystems were characterized by dynamic light scattering (size along with size distribution), UV-vis (cargos encapsulation efficiency) and atomic force microscopy (morphology and shape). The obtained SLNs were used as drug carriers alone and in combination with electropermeabilization induced by millisecond pulsed electric fields of high intensity. Two cell lines were selected for the study: LoVo and CHO-K1. The viability was assessed after electroporation alone, the use of electroporation and nanoparticles, and nanoparticles or drugs alone. The intracellular accumulation of cyanine IR-780 and the impact on intracellular structure organization of cytoskeleton was visualized with confocal microscopy method with alpha-actin and beta-tubulin. In this study, the efficacy of nanoparticles with mixed cargo, additionally enhanced by electroporation, is demonstrated to act as an anticancer modality to eliminate cancer cells.

  15. Croatian Traditional Herbal Dyes For Textile Dyeing

    OpenAIRE

    Sutrlović, Ana

    2011-01-01

    Textiles, namely protein fibers, in continental part of central Europe have been traditionally dyed by natural dyes. In the process textile materials were pre or after treated by metal salts – mordants (usually: KAl(SO4)2•12H2O, SnCl2•2H2O, FeSO4•7H2O, CuSO4•5H2O). Most represented active substances in herbal extracts are flavonoid derivatives, which by complexing with metal ions constitute colored complexes. Depending on herb species and mordant applied, a wide palette of colors is available...

  16. Laser dye technology

    Energy Technology Data Exchange (ETDEWEB)

    Hammond, P R

    1999-09-01

    The author has worked with laser dyes for a number of years. A first interest was in the Navy blue-green program where a flashlamp pumped dye laser was used as an underwater communication and detection device. It made use of the optical window of sea-water--blue for deep ocean, green for coastal water. A major activity however has been with the Atomic Vapor Laser Isotope Separation Program (AVLIS) at the Lawrence Livermore National Laboratory. The aim here has been enriching isotopes for the nuclear fuel cycle. The tunability of the dye laser is utilized to selectively excite one isotope in uranium vapor, and this isotope is collected electrostatically as shown in Figure 1. The interests in the AVLIS program have been in the near ultra-violet, violet, red and deep-red.

  17. Hair cosmetics: dyes.

    Science.gov (United States)

    Guerra-Tapia, A; Gonzalez-Guerra, E

    2014-11-01

    Hair plays a significant role in body image, and its appearance can be changed relatively easily without resort to surgical procedures. Cosmetics and techniques have therefore been used to change hair appearance since time immemorial. The cosmetics industry has developed efficient products that can be used on healthy hair or act on concomitant diseases of the hair and scalp. Dyes embellish the hair by bleaching or coloring it briefly, for temporary periods of longer duration, or permanently, depending on the composition of a dye (oxidative or nonoxidative) and its degree of penetration of the hair shaft. The dermatologist's knowledge of dyes, their use, and their possible side effects (contact eczema, cancer, increased porosity, brittleness) can extend to an understanding of cosmetic resources that also treat hair and scalp conditions. Copyright © 2013 Elsevier España, S.L.U. and AEDV. All rights reserved.

  18. Hair Dye and Hair Relaxers

    Science.gov (United States)

    ... For Consumers Consumer Information by Audience For Women Hair Dye and Hair Relaxers Share Tweet Linkedin Pin it More sharing ... products. If you have a bad reaction to hair dyes and relaxers, you should: Stop using the ...

  19. Dyes with high affinity for polylactide

    Institute of Scientific and Technical Information of China (English)

    Liang He; Shu Fen Zhang; Bing Tao Tang; Li Li Wang; Jin Zong Yang

    2007-01-01

    Attempts were made to develop dyes with high affinity for polylactide as an alternative to the existent commercial disperse dyes.The dyes synthesized according to the affinity concept of dye to polylactide exhibited excellent dyeing properties on polylactide compared with the commercial disperse dyes.

  20. Azaquinolone dye lasers

    Energy Technology Data Exchange (ETDEWEB)

    Hammond, P.R.; Atkins, R.L.; Henry, R.A.; Fletcher, A.N.

    1978-07-25

    The invention provides a dye laser comprising a lasing solution of a 7-substituted azaquinolone-2 in which the aza nitrogen occupies at least one of the 5, 6 and 8 ring positions. The 7-substituent is hydroxy, alkoxy, amino or substituted amino. Substituents may be attached to other ring positions. The present lasing compounds are aza analogs of corresponding quinolone compounds and, hence, are named ''azaquinolone'' compounds. The dye lasers lase in the blue to near ultraviolet region.

  1. Hair care and dyeing.

    Science.gov (United States)

    Draelos, Zoe Diana

    2015-01-01

    Alopecia can be effectively camouflaged or worsened through the use of hair care techniques and dyeing. Proper hair care, involving hair styling and the use of mild shampoos and body-building conditioners, can amplify thinning scalp hair; however, chemical processing, including hair dyeing, permanent waving, and hair straightening, can encourage further hair loss through breakage. Many patients suffering from alopecia attempt to improve their hair through extensive manipulation, which only increases problems. Frequent haircuts to minimize split ends, accompanied by gentle handling of the fragile fibers, is best. This chapter offers the dermatologist insight into hair care recommendations for the alopecia patient.

  2. Dye solar cell research

    CSIR Research Space (South Africa)

    Cummings, F

    2009-11-01

    Full Text Available stream_source_info Cummings_2009.pdf.txt stream_content_type text/plain stream_size 3362 Content-Encoding UTF-8 stream_name Cummings_2009.pdf.txt Content-Type text/plain; charset=UTF-8 DYE SOLAR CELL RESEARCH Franscious... Cummings Energy and Processes Materials Science and Manufacturing Council for Scientific and Industrial Research P.O. Box 395 Pretoria 0001, South Africa 27 November 2009 CONTENT head2rightBackground head2rightCSIR Dye Solar Cell Research head2...

  3. Textile dye decolorization using cyanobacteria.

    Science.gov (United States)

    Parikh, Amit; Madamwar, Datta

    2005-03-01

    Cyanobacterial cultures isolated from sites polluted by industrial textile effluents were screened for their ability to decolorize cyclic azo dyes. Gloeocapsa pleurocapsoides and Phormidium ceylanicum decolorized Acid Red 97 and FF Sky Blue dyes by more than 80% after 26 days. Chroococcus minutus was the only culture which decolorized Amido Black 10B (55%). Chlorophyll a synthesis in all cultures was strongly inhibited by the dyes. Visible spectroscopy and TLC confirmed that color removal was due to degradation of the dyes.

  4. REUSE OF DECOLORIZED DYEING EFFLUENTS IN REPEATED DYEINGS

    Directory of Open Access Journals (Sweden)

    ÖNER Erhan

    2016-05-01

    Full Text Available In this experimental work, the effluents of the reactive and disperse dyeings were reused in the next dyeing after the decolourization by ozone gas. Accordingly, the polyester woven samples were dyed with C.I. Disperse Yellow 160, C.I. Disperse Red 77 and C.I. Disperse Blue 79:1, and the cotton woven samples were dyed with C.I. Reactive Yellow 176, C.I. Reactive Red 239 and C.I. Reactive Blue 221. The effluents of the dyeings with these dyes and also with their mixtures were decolorized by ozone gas. The colours of the samples dyed with the decolorized effluents were compared with the original dyeings (standards and the colour differences were calculated. Under the experimental conditions of this investigation, the many of the dyeing effluents were decolorized successfully, except the effluent of C.I. Disperse Red 77. In the case that this red disperse dye present in the dyebath, the decolorized effluent had a slight reddish colour. The colour differences between the original dyeing (standard and the samples dyed with the decolorized effluent are mostly below the tolerance (DE<1 or slightly above the tolerance. The solid colours and uniform dyeings were achieved in the dyeings. The method seems promising in decreasing the amount of water used in textile dyeings.

  5. OPTIMIZATION OF DYEING PARAMETERS TO DYE COTTON WITH CARROT EXTRACTION

    Directory of Open Access Journals (Sweden)

    MIRALLES Verónica

    2017-05-01

    Full Text Available Natural dyes derived from flora and fauna are believed to be safe because of non-toxic, non-carcinogenic and biodegradable nature. Furthermore, natural dyes do not cause pollution and waste water problems. Natural dyes as well as synthetic dyes need the optimum parameters to get a good dyeing. On some occasions, It is necessary the use of mordants to increase the affinity between cellulose fiber and natural dye, but there are other conditions to optimize in the dyeing process, like time, temperature, auxiliary porducts, etc. In addition, the optimum conditions are different depends on the type of dye and the fiber nature. The aim of this work is the use of carrot extract to dye cotton fabric by exhaustion at diverse dyeing conditions. Diffferent dyeing processes were carried out to study the effect of pH condition and the temperature, using 7, 6 and 4 pH values and 95 ºC and 130ºC for an hour. As a result some images of dyed samples are shown. Moreover, to evaluate the colour of each sample CIELAB parameters are analysed obtained by reflexion spectrophotometre. The results showed that the temperature used has an important influence on the colour of the dyed sample.

  6. 2, 2′- and 4, 4′-Cyanines are Transporter Independent in vitro Dopaminergic Toxins with the Specificity and Mechanism of Toxicity similar to MPP+

    OpenAIRE

    Kadigamuwa, Chamila C.; Le Viet, Q.; Wimalasena, Kandatege

    2015-01-01

    Specific uptake through dopamine transporter (DAT) followed by the inhibition of the mitochondrial complex-I have been accepted as the cause of the specific dopaminergic toxicity of MPP+. However, MPP+ is taken up into many cell types through other transporters suggesting that in addition to the efficient uptake, intrinsic vulnerability of dopaminergic cells may also contribute to their high sensitivity to MPP+ and similar toxins. To test this possibility, two simple cyanines were employed in...

  7. Levitated droplet dye laser

    DEFF Research Database (Denmark)

    Azzouz, H.; Alkafadiji, L.; Balslev, Søren

    2006-01-01

    a high quality optical resonator. Our 750 nL lasing droplets consist of Rhodamine 6G dissolved in ethylene glycol, at a concentration of 0.02 M. The droplets are optically pumped at 532 nm light from a pulsed, frequency doubled Nd:YAG laser, and the dye laser emission is analyzed by a fixed grating...

  8. Microfluidic Dye Lasers

    DEFF Research Database (Denmark)

    Kristensen, Anders; Balslev, Søren; Gersborg-Hansen, Morten

    2006-01-01

    A technology for miniaturized, polymer based lasers, suitable for integration with planar waveguides and microfluidic networks is presented. The microfluidic dye laser device consists of a microfluidic channel with an embedded optical resonator. The devices are fabricated in a thin polymer film...

  9. Alzheimer's Dye Test?

    Science.gov (United States)

    Science Teacher, 2005

    2005-01-01

    Massachusetts Institute of Technology (MIT) scientists have developed a new dye that could offer noninvasive early diagnosis of Alzheimer's disease, a discovery that could aid in monitoring the progression of the disease and in studying the efficacy of new treatments to stop it. The work is published in Angewandte Chemie. Today, doctors can only…

  10. Alzheimer's Dye Test?

    Science.gov (United States)

    Science Teacher, 2005

    2005-01-01

    Massachusetts Institute of Technology (MIT) scientists have developed a new dye that could offer noninvasive early diagnosis of Alzheimer's disease, a discovery that could aid in monitoring the progression of the disease and in studying the efficacy of new treatments to stop it. The work is published in Angewandte Chemie. Today, doctors can only…

  11. Dye laser principles with applications

    CERN Document Server

    Duarte, Frank J; Liao, Peter F; Kelley, Paul

    1990-01-01

    A tutorial introduction to the field of dye lasers, Dye Laser Principles also serves as an up-to-date overview for those using dye lasers as research and industrial tools. A number of the issues discussed in this book are pertinent not only to dye lasers but also to lasers in general. Most of the chapters in the book contain problem sets that expand on the material covered in the chapter.Key Features* Dye lasers are among the most versatile and successful laser sources currently available in use Offering both pulsed and continuous-wave operation and tunable from the near ultraviole

  12. Synthesis of azo pyridone dyes

    OpenAIRE

    Mijin Dušan Ž.; Ušćumlić Gordana S.; Valentić Nataša V.; Marinković Aleksandar D.

    2011-01-01

    Over 50% of all colorants which are used nowdays are azo dyes and pigments, and among them arylazo pyridone dyes (and pigments) have became of interest in last several decades due to the high molar extinction coefficient, and the medium to high light and wet fastness properties. They find application generally as disperse dyes. The importance of disperse dyes increased in the 1970s and 1980s due to the use of polyester and nylon as the main synthetic fibers. Also, disperse dyes were use...

  13. TEXTILE DYEING AND FINISHING JOURNAL

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    Abstract: Optim is dyed with Lanasol CE series dyes by micro-suspension technology, and the dyeing result is compared with that by traditional process. The optimal micro-suspension dyeing process is determined as follows: formic acid 1.5% (owl), micro-suspension promoter WR1.0% (owf), micro-suspension promoter TS 0.5 % (owl), dyestuff 5% (owf). The results show that micro-suspension dyeing increases the dye uptake percentage and colour fixation rate significantly; improves the handle and bulkiness without damaging the colour fastness of the dyed fabric.

  14. Multi-dye theranostic nanoparticle platform for bioimaging and cancer therapy

    Directory of Open Access Journals (Sweden)

    Singh AK

    2012-06-01

    Full Text Available Amit K Singh,1,2 Megan A Hahn,2 Luke G Gutwein,3 Michael C Rule,4 Jacquelyn A Knapik,5 Brij M Moudgil,1,2 Stephen R Grobmyer,3 Scott C Brown,2,61Department of Materials Science and Engineering, College of Engineering, 2Particle Engineering Research Center, College of Engineering, 3Division of Surgical Oncology, Department of Surgery, College of Medicine, 4Cell and Tissue Analysis Core, McKnight Brain Institute, 5Department of Pathology, College of Medicine, University of Florida, Gainesville, FL, USA; 6DuPont Central Research and Development, Corporate Center for Analytical Science, Wilmington, DE, USABackground: Theranostic nanomaterials composed of fluorescent and photothermal agents can both image and provide a method of disease treatment in clinical oncology. For in vivo use, the near-infrared (NIR window has been the focus of the majority of studies, because of greater light penetration due to lower absorption and scatter of biological components. Therefore, having both fluorescent and photothermal agents with optical properties in the NIR provides the best chance of improved theranostic capabilities utilizing nanotechnology.Methods: We developed nonplasmonic multi-dye theranostic silica nanoparticles (MDT-NPs, combining NIR fluorescence visualization and photothermal therapy within a single nanoconstruct comprised of molecular components. A modified NIR fluorescent heptamethine cyanine dye was covalently incorporated into a mesoporous silica matrix and a hydrophobic metallo-naphthalocyanine dye with large molar absorptivity was loaded into the pores of these fluorescent particles. The imaging and therapeutic capabilities of these nanoparticles were demonstrated in vivo using a direct tumor injection model.Results: The fluorescent nanoparticles are bright probes (300-fold enhancement in quantum yield versus free dye that have a large Stokes shift (>110 nm. Incorporation of the naphthalocyanine dye and exposure to NIR laser excitation

  15. Dye Aggregation in Ink Jet

    Institute of Scientific and Technical Information of China (English)

    Thomas Paul; Sarfraz Hussain

    2004-01-01

    Dye aggregation has long been recognised as a key factor in performance, and this is no less so in ink jet applications. The aggregation state was shown to be important in many different areas ranging from the use of dyes in photodynamic therapies all the way to colorants for dying of fabrics. Therefore different methods to investigate dye association qualitatively and quantitatively were developed. A simple procedure to study aggregation could be a useful tool to characterise dyes for ink jet printing. It is critically reviewed the methods used to study dye aggregation, and discussed some of the main conclusions. This will be illustrated by examples of ink jet dye aggregation and its study in aqueous and ink systems. The results are used to correlate the solution behaviour of dyes with their print performance.

  16. Optical Properties of Fluorescent Dyes

    Institute of Scientific and Technical Information of China (English)

    李戎; 陈东辉

    2001-01-01

    Fluorescent dyes have been widely used these years.Because of the special optical performance, conventional CCM systems seem to be unable to predict the recipes of fabrics dyed with fluorescent dyes. In order to enhance the functions of CCM systems, the optical properties of fluorescent dyes in their absorption region were investigated. It has been found that there was a fixed maximum absorption wavelength for each fluorescent dyes whatever its concentration is. Both absorption region and maximum absorption wavelength of the dyes in solution are the same to those in fabric, and that the absorption is directly proportional to the concentration of the dye. So the optical properties obtained in solutions cna be applied for describing the optics performance of fluorescent dyes in fabrics.

  17. Are allergenic disperse dyes used for dyeing textiles?

    Science.gov (United States)

    Malinauskiene, Laura; Zimerson, Erik; Bruze, Magnus; Ryberg, Kristina; Isaksson, Marléne

    2012-09-01

    There are no data showing that disperse dyes, used to patch test patients, are currently being used for dyeing synthetic garments. It is unknown whether disperse dyes, which are currently routinely patch tested, are in fact present in synthetic textiles on the market. To determine whether eight disperse dyes, hitherto most widely cited as allergenic, are still used in textiles that are sold in various countries. Textiles from 13 countries in Europe, Asia and the United States were analysed. The procedure used for dye identification was thin-layer chromatography. When there were matching spots from the textile extract and reference dye, high-performance liquid chromatography was performed. Of 121 analysed items, three showed positive results for some of the investigated disperse dyes. Four dyes in these items could be detected and confirmed by the use of high-performance liquid chromatography. A pair of light brown ladies' tights manufactured and purchased in Italy contained Disperse Yellow 3, Disperse Blue 124, and Disperse Blue 106, and a set of black bra and panties purchased in India contained Disperse Orange 1. The eight disperse dyes that are most frequently incriminated in textile dye dermatitis are very rarely used in textiles nowadays. © 2012 John Wiley & Sons A/S.

  18. FY 1980 Report on Dye Laser Materials

    Science.gov (United States)

    1981-02-01

    by block number) Dye Lasers Laser Dyes Tunable Lasers Photodegradation Rhodamine Dyes 20. ABSTRACT (Continue n resld* it necesiry and Identify by block...limited usefulness as a portable military device because of the photodegradation of the dye solution. Although there have been state-of-the-art reviews...on laser dyes , 1𔃼 the photodegradation of laser dyes ,3 and dye lasers, 4- 6 only authors from, or funded by, military organizations have given strict

  19. Plantas Tintureiras Dye Plants

    Directory of Open Access Journals (Sweden)

    Maria do Carmo Serrano

    2008-12-01

    Full Text Available Existe uma vasta bibliografia, até ao séc. XVIII, sobre plantas produtoras de corantes naturais, sendo que apenas um número limitado foi utilizado no tingimento de têxteis antigos, devido à capacidade de resistência à lavagem e ao desvanecimento. O cultivo de plantas ou a sua existência no mundo silvestre tiveram uma enorme importância sócio-económica para muitas comunidades espalhadas pelo mundo e pelas intensas trocas comerciais que geraram. A extracção dos corantes era feita a partir de diferentes partes de plantas ou árvores. Nalgumas plantas eram utilizadas as folhas, enquanto noutras se aproveitavam as flores, as raízes, os frutos, troncos ou sementes. Os corantes podiam ser extraídos através de processos complexos que envolviam diversas operações como maceração, destilação, fermentação, decantação, precipitação, filtração, etc. Neste âmbito, são apresentadas algumas das plantas cultivadas em Portugal e em muitos outros países europeus e que foram usadas em tinturaria. Este trabalho pretende ser um contributo para obstar à perda de conhecimentos das condições de cultivo e da forma como se maximizava a produção de corantes.A vast bibliography exists, until the 18th cen-tury, on natural dyes obtained from plants, but only one limited number was used in the dyeing of old textiles, due to capacity of resistance to wash and light fading. The culture of plants or its existence in the wild world had an enormous economical importance for many communities spread for the world, and the intense commercial exchanges that had generated. The extraction of dyes was done from different parts of plants or trees. In some plants was used the leaves, others, only the roots, the fruits, trunks or seeds. The dyes could be extracted through complex processes that involved various operations as maceration, distillation, fermentation, decantation, precipitation, filtration, etc. In this scope, some of the plants cultivated in

  20. Synthesis of azo pyridone dyes

    Directory of Open Access Journals (Sweden)

    Mijin Dušan Ž.

    2011-01-01

    Full Text Available Over 50% of all colorants which are used nowdays are azo dyes and pigments, and among them arylazo pyridone dyes (and pigments have became of interest in last several decades due to the high molar extinction coefficient, and the medium to high light and wet fastness properties. They find application generally as disperse dyes. The importance of disperse dyes increased in the 1970s and 1980s due to the use of polyester and nylon as the main synthetic fibers. Also, disperse dyes were used rapidly since 1970 in inks for the heat-transfer printing of polyester. The main synthetic route for the preparation of azo dyes is coupling reaction between an aromatic diazo compound and a coupling component. Of all dyes manufactured, about 60% are produced by this reaction. Arylazo pyridone dyes can be prepared from pyridone moiety as a coupling component, where substituent can be on nitrogen, and diazonim salts which can be derived from different substituted anilines or other heterocyclic derivatives. In addition, arylazo dyes containing pyridone ring can be prepared from arylazo diketones or arylazo ketoesters (obtained by coupling β-diketones or β-ketoesters with diazonim salts by condensation with cyanoacetamide. Disazo dyes can be prepared by tetrazotizing a dianiline and coupling it with a pyridone or by diazotizing aniline and coupling it with a dipyridone. Trisazo dyes can be also prepared by diazotizing of aniline and coupling it with a tripyridone or by hexazotizing a trianiline and coupling it with a pyridone. The main goal of this paper is to give a brief review on the synthesis of arylazo pyridone dyes due to the lack of such reviews. In addition, some properties of arylazo pyridone dyes as light fastness and azo-hydrazon tautomerism are disccused.

  1. 菁染料光解机理的前线分子轨道研究%Frontier molecular orbital study on photodegradation mechanism of cyanine dyes

    Institute of Scientific and Technical Information of China (English)

    尚兴宏; 贡雪东; 肖鹤鸣; 田禾

    2001-01-01

    通过SCF PM3和AM1 MO计算研究,揭示了正离子型菁染料与相应中性化合物在分子几何、电荷分布、前线分子轨道能级和组成等方面的不同特点.特别是根据前线轨道理论和成键三原则,通过比较氧的激发单态(1O*2)或超氧负离子自由基(O.-2)与标题物之间的前线轨道相互作用,阐明了标题物的光解机理和正离子较中性化合物光稳定的根由.结论与实验事实良好相符.

  2. 苯乙烯菁染料的合成及光谱性质%Syntheses and characterization of styryl cyanine dyes

    Institute of Scientific and Technical Information of China (English)

    胡志彪; 王兰英; 董发昕

    2002-01-01

    合成了3种未见文献报道的苯乙烯菁染料,用元素分析、红外光谱、紫外可见光谱和核磁共振谱对其结构进行了表征.根据紫外可见光谱和荧光光谱的数据,分析了不同取代基对其光谱性质的影响.

  3. Synthesis of Cyanine-style IR-absorbing Dye%菁型红外吸收染料的合成

    Institute of Scientific and Technical Information of China (English)

    邓继勇; 龙有前; 易斌

    2003-01-01

    以1,3,3,5-四甲基-2-亚甲基吲哚啉与2-氯-1-甲酰基-3-羟亚甲基环己烯为主要原料合成了1,3,3,5,1',3',3',5'-八甲基-11-氯-10,12-亚丙基吲哚三碳菁红外吸收染料.经熔点测定、元素分析、IR分析验证了产品的结构.该染料的电子吸收光谱表明其最大吸收波长为780nm.由高效液相色谱仪测定其纯度大于96.8%.

  4. 反胶束微环境对菁染料光谱性质的影响%Spectra of Cyanine Dye in Reversed Micelle

    Institute of Scientific and Technical Information of China (English)

    张志颖; 刘春艳

    2001-01-01

    通过对不同体系中菁染料吸收光谱及荧光光谱的研究,考察了微环境对菁染料存在状态的影响.主要研究了反胶束中菁染料的光谱性质,确定了反胶束中菁染料的存在状态,以及反胶束ω值,水团微组份及温度等对菁染料吸收及荧光光谱性质的影响.

  5. The Advance of Study on the Near-infrared Absorbing Cyanine Dyes%近红外吸收功能菁染料的研究进展

    Institute of Scientific and Technical Information of China (English)

    孙成才; 霍冀川; 雷永林; 吴瑞荣

    2006-01-01

    主要综述了在近红外吸收功能菁染料的合成过程中所使用的缩合剂及其特点、典型合成反应,并且综合分析了菁染料最大吸收波长、稳定性与其结构的关系,简述了近红外吸收功能菁染料的应用途径,从中归纳出了近红外吸收功能菁染料的发展方向.

  6. Dyeing fabrics with metals

    Science.gov (United States)

    Kalivas, Georgia

    2002-06-01

    Traditionally, in textile dyeing, metals have been used as mordants or to improve the color produced by a natural or synthetic dye. In biomedical research and clinical diagnostics gold colloids are used as sensitive signals to detect the presence of pathogens. It has been observed that when metals are finely divided, a distinct color may result that is different from the color of the metal in bulk. For example, when gold is finely divided it may appear black, ruby or purple. This can be seen in biomedical research when gold colloids are reduced to micro-particles. Bright color signals are produced by few nanometer-sized particles. Dr. William Todd, a researcher in the Department of Veterinary Science at the Louisiana State University, developed a method of dyeing fabrics with metals. By using a reagent to bond the metal particles deep into the textile fibers and actually making the metal a part of the chemistry of the fiber. The chemicals of the fabric influence the resulting color. The combination of the element itself, the size of the particle, the chemical nature of the particle and the interaction of the metal with the chemistry of the fabric determine the actual hue. By using different elements, reagents, textiles and solvents a broad range of reproducible colors and tones can be created. Metals can also be combined into alloys, which will produce a variety of colors. The students of the ISCC chapter at the Fashion Institute of Technology dyed fabric using Dr. Todd's method and created a presentation of the results. They also did a demonstration of dyeing fabrics with metals.

  7. Laser dye stability. Pt. 3. Bicyclic dyes in ethanol

    Energy Technology Data Exchange (ETDEWEB)

    Fletcher, A.N. (Naval Weapons Center, China Lake, Calif. (USA). Research Dept.)

    1977-11-01

    A commercial coaxial xenon flashlamp has been used to evaluate the stability of a variety of coumarin and quinolone laser dyes. The lasing characteristics of over 30 dyes have been quantitatively evaluated as a function of the total excitation energy to which recirculating dye solution has been exposed. Degradation constants were determined an an evaluation was made of the effects of functional group variation upon the stability of the dyes. Comparison with the data of other workers revealed that exclusion of excitation energy below 220 nm does not change the stability of 4-methyl coumarins, but can increase the stability of other coumarins as much as 50 fold.

  8. Near-infrared-emitting squaraine dyes with high 2PA cross-sections for multiphoton fluorescence imaging.

    Science.gov (United States)

    Ahn, Hyo-Yang; Yao, Sheng; Wang, Xuhua; Belfield, Kevin D

    2012-06-27

    Designed to achieve high two-photon absorptivity, new near-infrared (NIR) emitting squaraine dyes, (E)-2-(1-(2-(2-methoxyethoxy)ethyl)-5-(3,4,5-trimethoxystyryl)-1H-pyrrol-2-yl)-4-(1-(2-(2-methoxyethoxy)ethyl)-5-(3,4,5-trimethoxystyryl)-2H-pyrrolium-2-ylidene)-3-oxocyclobut-1-enolate (1) and (Z)-2-(4-(dibutylamino)-2-hydroxyphenyl)-4-(4-(dibutyliminio)-2-hydroxycyclohexa-2,5-dienylidene)-3-oxocyclobut-1-enolate (2), were synthesized and characterized. Their linear photophysical properties were investigated via UV-visible absorption spectroscopy and fluorescence spectroscopy in various solvents, while their nonlinear photophysical properties were investigated using a combination of two-photon induced fluorescence and open aperture z-scan methods. Squaraine 1 exhibited a high two-photon absorption (2PA) cross-section (δ2PA), ∼20 000 GM at 800 nm, and high photostability with the photochemical decomposition quantum yield one order of magnitude lower than Cy 5, a commercially available pentamethine cyanine NIR dye. The cytotoxicity of the squaraine dyes were evaluated in HCT 116 and COS 7 cell lines to assess the potential of these probes for biomedical imaging. The viability of both cell lines was maintained above 80% at dye concentrations up to 30 μM, indicating good biocompatibility of the probes. Finally, one-photon fluorescence microscopy (1PFM) and two-photon fluorescence microscopy (2PFM) imaging was accomplished after incubation of micelle-encapsulated squaraine probes with HCT 116 and COS 7 cells, demonstrating their potential in 2PFM bioimaging.

  9. Cold Pad-Batch dyeing method for cotton fabric dyeing with reactive dyes using ultrasonic energy.

    Science.gov (United States)

    Khatri, Zeeshan; Memon, Muhammad Hanif; Khatri, Awais; Tanwari, Anwaruddin

    2011-11-01

    Reactive dyes are vastly used in dyeing and printing of cotton fibre. These dyes have a distinctive reactive nature due to active groups which form covalent bonds with -OH groups of cotton through substitution and/or addition mechanism. Among many methods used for dyeing cotton with reactive dyes, the Cold Pad Batch (CPB) method is relatively more environment friendly due to high dye fixation and non requirement of thermal energy. The dyed fabric production rate is low due to requirement of at least twelve hours batching time for dye fixation. The proposed CPB method for dyeing cotton involves ultrasonic energy resulting into a one third decrease in batching time. The dyeing of cotton fibre was carried out with CI reactive red 195 and CI reactive black 5 by conventional and ultrasonic (US) method. The study showed that the use of ultrasonic energy not only shortens the batching time but the alkalis concentrations can considerably be reduced. In this case, the colour strength (K/S) and dye fixation (%F) also enhances without any adverse effect on colour fastness of the dyed fabric. The appearance of dyed fibre surface using scanning electron microscope (SEM) showed relative straightening of fibre convolutions and significant swelling of the fibre upon ultrasonic application. The total colour difference values ΔE (CMC) for the proposed method, were found within close proximity to the conventionally dyed sample.

  10. The Application of Electrochemical Impedance Techniques in Analyzing the AC Response of Some Two-electron Transfer Dye Systems

    Directory of Open Access Journals (Sweden)

    Farouk Rashwan

    2005-01-01

    Full Text Available The Electrochemical Impedance Spectroscopic techniques (EIS were used to investigate the behavior of some dye compounds (quinoid systems characterized with 2e-transfer processes. For this purpose, Alizarin Red S (ARS, Alizarin Cyanine (AC, Alizarin Viridin (AV and carminic acid were chosen for the measurements. The EIS experiments were performed using a small AC amplitude (10 mV p-p in addition to a relatively wide frequency range (0.01 Hz ≤ f ≤ 105 Hz. The investigations were carried out at room temperature in aqueous media (HClO4, NaClO4 and KNO3 on the Hanging Mercury Drop Electrode (HMDE and for comparison one experiment only was measured in aprotic solvent (DMF on the Pt-disc electrode. The EIS diagrams of these systems were characterized in the complex plane by two fundamental observations, the first of which is a straight line crossing the real axis at an angle of 45° (or at least nearly so and the second one is two semicircles beside each other corresponding to high-frequency and low-frequency regions, which are implying the presence of well-separated time constants. The EIS characteristic parameters for these dye systems were calculated and discussed.

  11. NMR spin-spin coupling constants in polymethine dyes as polarity indicators.

    Science.gov (United States)

    Murugan, N Arul; Aidas, Kestutis; Kongsted, Jacob; Rinkevicius, Zilvinas; Ågren, Hans

    2012-09-10

    Herein, we explore the use of spin-spin coupling constants (SSCCs) in merocyanine (MCYNE) dyes as indicators of polarity. For this purpose, we use Car-Parrinello hybrid quantum mechanics/molecular mechanics (QM/MM) to determine the structures of MCYNE in solvents of different polarity, followed by computations of the SSCCs by using QM/MM linear-response theory. The molecular geometry of MCYNE switches between neutral, cyanine-like, and zwitterionic depending on the polarity of the solvent. This structural variation is clearly reflected in the proton SSCCs in the polymethine backbone, which are highly sensitive to the dielectric nature of the environment; this mechanism can be used as a "polarity indicator" for different microenvironments. This result is highlighted by computing the SSCCs of the MCYNE probe in the cavity of the beta-lactoglobulin protein. The computed SSCCs clearly indicate a non-polar hydrophobic dielectric nature of this cavity. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Dye sensitized solar cells.

    Science.gov (United States)

    Wei, Di

    2010-03-16

    Dye sensitized solar cell (DSSC) is the only solar cell that can offer both the flexibility and transparency. Its efficiency is comparable to amorphous silicon solar cells but with a much lower cost. This review not only covers the fundamentals of DSSC but also the related cutting-edge research and its development for industrial applications. Most recent research topics on DSSC, for example, applications of nanostructured TiO(2), ZnO electrodes, ionic liquid electrolytes, carbon nanotubes, graphene and solid state DSSC have all been included and discussed.

  13. Dye Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Di Wei

    2010-03-01

    Full Text Available Dye sensitized solar cell (DSSC is the only solar cell that can offer both the flexibility and transparency. Its efficiency is comparable to amorphous silicon solar cells but with a much lower cost. This review not only covers the fundamentals of DSSC but also the related cutting-edge research and its development for industrial applications. Most recent research topics on DSSC, for example, applications of nanostructured TiO2, ZnO electrodes, ionic liquid electrolytes, carbon nanotubes, graphene and solid state DSSC have all been included and discussed.

  14. Carcinogenicity of hair dye components.

    Science.gov (United States)

    Van Duuren, B L

    1980-03-01

    The available animal carcinogenicity data on hair dye components was reviewed. From this review it became clear that certain hair dye components, some of which are still in hair dye formulations now on the market, are animal carcinogens. The compounds of concern that are still in use are: 3-amino-4-methoxyaniline, 2-nitro-4-aminoaniline and 3-nitro-4-hydroxyaniline. Certain azo dyes formerly used, and related compounds still in use, contain the benzidine moiety. Two of these compounds, Direct Blue 6 and Direct Black 38, have been shown to be metabolized in animals to the human carcinogen benzidine. Furthermore, skin absorption studies carried out with radiolabeled hair dye components applied to animal or human skin have conclusively shown that these compounds are systemically absorbed and excreted. Known cocarcinogens such as catechol and pyrogallol, which enhance benzo(a)pyrene carcinogenicity on mouse skin, are used as hair dye components. It is not known whether such compounds will enhance the carcinogenicity of substituted aniline hair dye chemicals. The available epidemiologic data are not sufficient to link hair dye use with an increased incidence in human cancer.

  15. Robust Colloidal Nanoparticles of Pyrrolopyrrole Cyanine J-Aggregates with Bright Near-Infrared Fluorescence in Aqueous Media: From Spectral Tailoring to Bioimaging Applications.

    Science.gov (United States)

    Yang, Cangjie; Wang, Xiaochen; Wang, Mingfeng; Xu, Keming; Xu, Chenjie

    2017-03-28

    Colloidal nanoparticles (NPs) containing near-infrared-fluorescent J-aggregates (JAGGs) of pyrrolopyrrole cyanines (PPcys) stabilized by amphiphilic block co-polymers were prepared in aqueous medium. JAGG formation can be tuned by means of the chemical structure of PPcys, the concentration of chromophores inside the polymeric NPs, and ultrasonication. The JAGG NPs exhibit a narrow emission band at 773 nm, a fluorescence quantum yield comparable to that of indocyanine green, and significantly enhanced photostability, which is ideal for long-term bioimaging.

  16. 2, 2'- and 4, 4'-Cyanines are transporter-independent in vitro dopaminergic toxins with the specificity and mechanism of toxicity similar to MPP⁺.

    Science.gov (United States)

    Kadigamuwa, Chamila C; Le, Viet Q; Wimalasena, Kandatege

    2015-11-01

    Specific uptake through dopamine transporter followed by the inhibition of the mitochondrial complex-I have been accepted as the cause of the specific dopaminergic toxicity of 1-methyl-4-phenylpyridinium (MPP(+) ). However, MPP(+) is taken up into many cell types through other transporters, suggesting that, in addition to the efficient uptake, intrinsic vulnerability of dopaminergic cells may also contribute to their high sensitivity to MPP(+) and similar toxins. To test this possibility, two simple cyanines were employed in a comparative study based on their unique characteristics and structural similarity to MPP(+) . Here, we show that they freely accumulate in dopaminergic (MN9D and SH-SY5Y) as well as in liver (HepG2) cells, but are specifically and highly toxic to dopaminergic cells with IC50s in the range of 50-100 nM, demonstrating that they are about 1000-fold more toxic than MPP(+) under similar experimental conditions. They cause mitochondrial depolarization non-specifically, but increase the reactive oxygen species specifically in dopaminergic cells leading to the apoptotic cell death parallel to MPP(+) . These and other findings suggest that the specific dopaminergic toxicity of these cyanines is due to the inherent vulnerability of dopaminergic cells toward mitochondrial toxins that lead to the excessive production of reactive oxygen species. Therefore, the specific dopaminergic toxicity of MPP(+) must also be, at least partly, due to the specific vulnerability of dopaminergic neurons. Thus, these cyanines could be stronger in vivo dopaminergic toxins than MPP(+) and their in vivo toxicities must be evaluated. Here, we show that cationic lipophilic cyanines with structural similarity to 1-methyl-4-phenylpyridinium (MPP(+) ) freely accumulate non-specifically, but only toxic to dopaminergic cells. They are 1000-fold more toxic than MPP(+) under similar conditions. They cause mitochondrial depolarization non-specifically, but increase the ROS

  17. Quantitative comparison of long-wavelength Alexa Fluor dyes to Cy dyes: fluorescence of the dyes and their bioconjugates.

    Science.gov (United States)

    Berlier, Judith E; Rothe, Anca; Buller, Gayle; Bradford, Jolene; Gray, Diane R; Filanoski, Brian J; Telford, William G; Yue, Stephen; Liu, Jixiang; Cheung, Ching-Ying; Chang, Wesley; Hirsch, James D; Beechem, Joseph M; Haugland, Rosaria P; Haugland, Richard P

    2003-12-01

    Amine-reactive N-hydroxysuccinimidyl esters of Alexa Fluor fluorescent dyes with principal absorption maxima at about 555 nm, 633 nm, 647 nm, 660 nm, 680 nm, 700 nm, and 750 nm were conjugated to antibodies and other selected proteins. These conjugates were compared with spectrally similar protein conjugates of the Cy3, Cy5, Cy5.5, Cy7, DY-630, DY-635, DY-680, and Atto 565 dyes. As N-hydroxysuccinimidyl ester dyes, the Alexa Fluor 555 dye was similar to the Cy3 dye, and the Alexa Fluor 647 dye was similar to the Cy5 dye with respect to absorption maxima, emission maxima, Stokes shifts, and extinction coefficients. However, both Alexa Fluor dyes were significantly more resistant to photobleaching than were their Cy dye counterparts. Absorption spectra of protein conjugates prepared from these dyes showed prominent blue-shifted shoulder peaks for conjugates of the Cy dyes but only minor shoulder peaks for conjugates of the Alexa Fluor dyes. The anomalous peaks, previously observed for protein conjugates of the Cy5 dye, are presumably due to the formation of dye aggregates. Absorption of light by the dye aggregates does not result in fluorescence, thereby diminishing the fluorescence of the conjugates. The Alexa Fluor 555 and the Alexa Fluor 647 dyes in protein conjugates exhibited significantly less of this self-quenching, and therefore the protein conjugates of Alexa Fluor dyes were significantly more fluorescent than those of the Cy dyes, especially at high degrees of labeling. The results from our flow cytometry, immunocytochemistry, and immunohistochemistry experiments demonstrate that protein-conjugated, long-wavelength Alexa Fluor dyes have advantages compared to the Cy dyes and other long-wavelength dyes in typical fluorescence-based cell labeling applications.

  18. LIQUID DYES'CHARACTERISTICS IN DYEING WASTE PAPER PULP AND THEIR APPLICATION

    Institute of Scientific and Technical Information of China (English)

    Xiaoping Wang; gang Chen; Aimin Tang; Hongwei Zhang

    2004-01-01

    In this paper, some liquid dyes were used to dye the waste paper pulp (OCC pulp and waste cement sack paper pulp), and their dyeing characteristics were analyzed, The liquid dyes include liquid basic yellow, liquid basic blue, liquid basic red, liquid basic orange, liquid basic brown and liquid direct black. We found that, each dye had its own dyeing characteristic while dyeing the waste paper pulp.Generally different types of liquid dyes were combined to dye the waste paper pulp, which the adding process must be noticed. We also observed that a black pigment could be applied together with said liquid dyes to dye or adjust the color of the bottom sheet for the fireproof board. We could also achieve the same dyeing result through different combinations of different dyes.

  19. The Application of Tea Dyeing to Silk

    Institute of Scientific and Technical Information of China (English)

    金成嬉

    2001-01-01

    Vegetable dyes are eco-friendly throughout the full production process. A study is conducted with the purpose of assessing the properties of dye extracted from green tea, black tea and the tea tree cultivated and used in Jiang Nan area of China. The extracted dyes are applied with and without mordants on silk fabric and the dyeing properties are evaluated.

  20. Effect of ferromagnetic nanoparticle on dyes biodegradation

    OpenAIRE

    Apostol, Laura; Pereira, Luciana; Pereira, Raquel; Alves, M.M.; Gavrilescu, M.

    2011-01-01

    In this study the biodecolourisation of two dyes, a xanthene dye, Erythrosine B (Ery B) and an azo dye, Reactive Red 51 (RR120), was investigated colourdecolourisationunder batch anaerobic conditions by using non - acclimated anaerobic granular sludge. The effect of ferromagnetic nanoparticle (FN) (as adsorbent or mediator) on dyes removal was experienced.

  1. Dyeing Properties of Natural Dye Syzygium cuminii on Silk

    Science.gov (United States)

    Narayana Swamy, V.; Ninge Gowda, K. N.; Sudhakar, R.

    2014-04-01

    Dyeing behavior of natural dye extracted from the bark of Syzygium cuminii L has been studied on silk fabric. Colour values and colour co-ordinates were examined in terms of K/S and L* a* b* C and h. A range of shades were obtained by using various mordants and mordanting techniques. Dye was tested for some of the eco-parameters using atomic absorption spectrophotometry and GC/MS. The test results were compared with the set standards to determine the eco-friendliness of natural dye. Their concentrations were much below the stipulated limits. Dyed samples were tested for antimicrobial activity against Gram-positive and Gram-negative bacteria and were found to possess antibacterial activity.

  2. Contact Allergy to Hair Dyes

    Directory of Open Access Journals (Sweden)

    Marie-Louise Anna Schuttelaar

    2016-06-01

    Full Text Available Many strong and extreme sensitizing chemicals, such as para-phenylenediamine (PPD, toluene-2,5-diamine (TDA and other aromatic amines or cross-reacting substances, are ingredients in hair dye products. The chemistry of hair dyeing and the immunological reactions to the potent sensitizing hair dye components are complex and have not been fully clarified up until now. Recently 2-methoxymethyl-p-phenylenediamine (ME-PPD, a PPD derivate with moderate skin-sensitizing properties, was developed. Although developed for the prevention of sensitization, ME-PPD appears to be tolerated in some PPD/TDA-allergic individuals.

  3. Spectrophotometric determination of aluminium in presence of iron with eriochrome cyanine R. Essays with a decolorated reagent; Determinacion espectrofotometrica de aluminio en presencia de hierro con eriocromocianina R. Ensayos con un reactivo decolorado

    Energy Technology Data Exchange (ETDEWEB)

    Barrachina Gomez, M.; Gasco Sanchez, L.; Fernandez Cellini, R.

    1962-07-01

    The behaviour of the extinction coefficient of aqueous solutions of Eriochrome Cyanine R is studied. It is found that at pH 5-6 the diluted acid solutions decolorate rapidly according to an exponential law (538 m{mu}). The fact that the decoloree solutions go on still reacting with the aluminium has. (Author) 12 refs.

  4. The reduction mechanism at the mercury electrode in a 0.9 M NaClO4+0.1 M HClO4 supporting electrolyte of an hydroxytriphenylmethane: Eriochrome Cyanine R

    NARCIS (Netherlands)

    Boodts, J.F.C.; Sluyters-Rehbach, M.; Sluyters, J.H.

    1979-01-01

    The reduction mechanism at a mercury electrode of Eriochrome Cyanine R, in a 0.9 M NaClO4+0.1 M HClO4 supporting electrolyte, has been investigated by several electrochemical techniques. By means of coulometry at constant potential and cyclic voltammetry it was demonstrated that a radical is formed,

  5. Spectrophotometric determination of aluminium in presence of iron with eriochrome cyanine R. Essays with a decolorated reagent; Determinacion espectrofotometrica de aluminio en presencia de hierro con eriocromocianina R. Ensayos con un reactivo decolorado

    Energy Technology Data Exchange (ETDEWEB)

    Barrachina Gomez, M.; Gasco Sanchez, L.; Fernandez Cellini, R.

    1962-07-01

    The behaviour of the extinction coefficient of aqueous solutions of Eriochrome Cyanine R is studied. It is found that at pH 5-6 the diluted acid solutions decolorate rapidly according to an exponential law (538 m{mu}). The fact that the decoloree solutions go on still reacting with the aluminium has. (Author) 12 refs.

  6. Survery on Actual Conditions of Food Dyes

    OpenAIRE

    佐藤,ひろみ

    1981-01-01

    Many food dyes are widely used as food additives in Japan, and many investigations have been pointed the problems of safety of these food dyes used in Japanese food. There are two types of commercial food dyes, one is synthetic dyes and the other is natural dyes.Recently Japanese food is not stained so colourfully, but it is stained faintly in colour near to natural food by using of mixed synthetic dyes. On their hand, many consumers have a tendency to prefer natural food dyes because they ha...

  7. Dye purity and dye standardization for biological staining

    DEFF Research Database (Denmark)

    Lyon, H O

    2002-01-01

    for separating, identifying and assaying dye components. In the second part of the review, descriptions are given of the standardized staining method approach using standard staining methods for assessing stains, and practical responses to stain impurity including commercial quality control, third-party quality...... control and standardization of reagents, protocols and documentation. Finally, reference is made to the current state of affairs in the dye field....

  8. Triplet losses in dye lasers

    Energy Technology Data Exchange (ETDEWEB)

    Baczynski, A.; Kossakowski, A.; Marszalek, T. (Uniwersytet Mikolaja Kopernika, Torun (Poland). Instytut Fizyki)

    1977-01-01

    The expression for losses due to triplet states in dye laser considered as a six-level system is given. It is shown that triplet losses depend on pumping parameters and photon number. Depending on molecular and cavity parameters two differe types of behavior of dye lasers are expected. Physical conditions are discussed in which triplet losses as well as photon number undergo a jump at the threshold.

  9. 菁染料和份菁染料溶液的光降解机理的研究%STUDY ON THE PHOTODEGRADATION MECHANISM OF CYANINE DYES AND MEROCYANINE DYES SOLUTION

    Institute of Scientific and Technical Information of China (English)

    杨松杰; 孟凡顺; 田禾; 姚思德

    2001-01-01

    利用UV-Vis吸收光谱仪和光化学反应器,研究了菁染料和份 菁染料溶液的光降解动力学,认为染料在乙腈溶液中的光褪色反应服从假一级或零级动力学 .利用GC/MS光谱仪检测了染料的光降解产物.与相应的份菁染料相比,携带正电荷的菁染料 具 有相对较好的光稳定性.研究结果表明,菁染料光降解反应的中间体可能是染料的半氧化态D ye+,并利用纳秒级闪光光解技术研究了Dye+的瞬态吸收光谱.

  10. Natural dyes as photosensitizers for dye-sensitized solar cell

    Energy Technology Data Exchange (ETDEWEB)

    Hao, Sancun; Wu, Jihuai; Huang, Yunfang; Lin, Jianming [Institute of Materials Physical Chemistry, Huaqiao University, Quanzhou, Fujian 362021 (China)

    2006-02-15

    The dye-sensitized solar cells (DSC) were assembled by using natural dyes extracted from black rice, capsicum, erythrina variegata flower, rosa xanthina, and kelp as sensitizers. The I{sub SC} from 1.142mA to 0.225mA, the V{sub OC} from 0.551V to 0.412V, the fill factor from 0.52 to 0.63, and P{sub max} from 58{mu}W to 327{mu}W were obtained from the DSC sensitized with natural dye extracts. In the extracts of natural fruit, leaves and flower chosen, the black rice extract performed the best photosensitized effect, which was due to the better interaction between the carbonyl and hydroxyl groups of anthocyanin molecule on black rice extract and the surface of TiO{sub 2} porous film. The blue-shift of absorption wavelength of the black rice extract in ethanol solution on TiO{sub 2} film and the blue-shift phenomenon from absorption spectrum to photoaction spectrum of DSC sensitized with black rice extract are discussed in the paper. Because of the simple preparation technique, widely available and low cheap cost natural dye as an alternative sensitizer for dye-sensitized solar cell is promising. (author)

  11. Discovery of Black Dye Crystal Structure Polymorphs: Implications for Dye Conformational Variation in Dye-Sensitized Solar Cells.

    Science.gov (United States)

    Cole, Jacqueline M; Low, Kian Sing; Gong, Yun

    2015-12-23

    We present the discovery of a new crystal structure polymorph (1) and pseudopolymorph (2) of the Black Dye, one of the world's leading dyes for dye-sensitized solar cells, DSSCs (10.4% device performance efficiency). This reveals that Black Dye molecules can adopt multiple low-energy conformers. This is significant since it challenges existing models of the Black Dye···TiO2 adsorption process that renders a DSSC working electrode; these have assumed a single molecular conformation that refers to the previously reported Black Dye crystal structure (3). The marked structural differences observed between 1, 2, and 3 make the need for modeling multiple conformations more acute. Additionally, the ordered form of the Black Dye (1) provides a more appropriate depiction of its anionic structure, especially regarding its anchoring group and NCS bonding descriptions. The tendency toward NCS ligand isomerism, evidenced via the disordered form 2, has consequences for electron injection and electron recombination in Black Dye embedded DSSC devices. Dyes 2 and 3 differ primarily by the absence or presence of a solvent of crystallization, respectively; solvent environment effects on the dye are thereby elucidated. This discovery of multiple Black Dye conformers from diffraction, with atomic-level definition, complements recently reported nanoscopic evidence for multiple dye conformations existing at a dye···TiO2 interface, for a chemically similar DSSC dye; those results emanated from imaging and spectroscopy, but were unresolved at the submolecular level. Taken together, these findings lead to the general notion that multiple dye conformations should be explicitly considered when modeling dye···TiO2 interfaces in DSSCs, at least for ruthenium-based dye complexes.

  12. Development of a novel ozone- and photo-stable HyPer5 red fluorescent dye for array CGH and microarray gene expression analysis with consistent performance irrespective of environmental conditions

    Directory of Open Access Journals (Sweden)

    Kille Peter

    2008-11-01

    Full Text Available Abstract Background Array-based comparative genomic hybridization (CGH and gene expression profiling have become vital techniques for identifying molecular defects underlying genetic diseases. Regardless of the microarray platform, cyanine dyes (Cy3 and Cy5 are one of the most widely used fluorescent dye pairs for microarray analysis owing to their brightness and ease of incorporation, enabling high level of assay sensitivity. However, combining both dyes on arrays can become problematic during summer months when ozone levels rise to near 25 parts per billion (ppb. Under such conditions, Cy5 is known to rapidly degrade leading to loss of signal from either "homebrew" or commercial arrays. Cy5 can also suffer disproportionately from dye photobleaching resulting in distortion of (Cy5/Cy3 ratios used in copy number analysis. Our laboratory has been active in fluorescent dye research to find a suitable alternative to Cy5 that is stable to ozone and resistant to photo-bleaching. Here, we report on the development of such a dye, called HyPer5, and describe its' exceptional ozone and photostable properties on microarrays. Results Our results show HyPer5 signal to be stable to high ozone levels. Repeated exposure of mouse arrays hybridized with HyPer5-labeled cDNA to 300 ppb ozone at 5, 10 and 15 minute intervals resulted in no signal loss from the dye. In comparison, Cy5 arrays showed a dramatic 80% decrease in total signal during the same interval. Photobleaching experiments show HyPer5 to be resistant to light induced damage with 3- fold improvement in dye stability over Cy5. In high resolution array CGH experiments, HyPer5 is demonstrated to detect chromosomal aberrations at loci 2p21-16.3 and 15q26.3-26.2 from three patient sample using bacterial artificial chromosome (BAC arrays. The photostability of HyPer5 is further documented by repeat array scanning without loss of detection. Additionally, HyPer5 arrays are shown to preserve sensitivity and

  13. Diffusion dynamics in microfluidic dye lasers

    DEFF Research Database (Denmark)

    Gersborg-Hansen, Morten; Balslev, Søren; Mortensen, Niels Asger

    2007-01-01

    We have investigated the bleaching dynamics that occur in opto-fluidic dye lasers, where the liquid laser dye in a channel is locally bleached due to optical pumping. Our studies suggest that for micro-fluidic devices, the dye bleaching may be compensated through diffusion of dye molecules alone....... By relying on diffusion rather than convection to generate the necessary dye replenishment, our observation potentially allows for a significant simplification of opto-fluidic dye laser device layouts, omitting the need for cumbersome and costly external fluidic handling or on-chip micro-fluidic pumping...

  14. Simultaneous dyeing and antibacterial finishing for cotton cellulose using a new reactive dye.

    Science.gov (United States)

    Farouk, R; Gaffer, H E

    2013-08-14

    Simultaneous dyeing and antibacterial finishing for cotton fabric using a new antibacterial reactive dye having a modified chemical structure to the commercial reactive dye CI Reactive Red 198 were studied. This modification was carried out by replacing metanilic acid in the commercial dye with 4-amino-N-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide (sulfadimidine). Optimum exhaustion and fixation values were achieved at 60 g/l sodium sulphate and 20 g/l sodium carbonate for both dyes. The modified dye exhibited higher substantivity, exhaustion and fixation efficiency compared to the commercial dye. Antibacterial activities of the dyed samples at different concentrations of both dyes were studied against gram positive (Staphylococcus aureus) and gram negative (Escherichia coli) bacteria. The cotton dyed with the modified dye shows higher antibacterial efficacy compared to the dyed cotton fabric using the commercial dye, especially on gram negative (E. coli) bacteria. All the reactive dyeings also exhibited high fastness properties.

  15. Natural Dyes as Photosensitizers for Dye-sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Hatem S. El-Ghamri

    2015-10-01

    Full Text Available Dye-sensitized solar cells (DSSCs were assembled using Zinc oxide (ZnO nanoparticles as a photoelectrode and natural dyes extracted from eight natural plants as photosensitizers. The structural properties of the synthesized ZnO nanoparticles were studied using XRD, SEM and TEM characterizations. Photovoltaic parameters such as short circuit current density Jsc, open circuit voltage Voc, fill factor FF, and overall conversion efficiency η for the fabricated cells were determined under 100 mW/cm2 illumination. It was found that the DSSC fabricated with the extracted safflower dye as a sensitizer showed the best performance. Also, its performance increased with increasing the sintering temperature of the semiconductor electrode with highest performance at 400 °C. Moreover, it was found that a semiconductor electrode of 7.5 μm thickness yielded the highest response.

  16. Fruit based Dye Sensitized Solar Cells

    Science.gov (United States)

    Ung, M. C.; Sipaut, C. S.; Dayou, J.; Liow, K. S.; Kulip, J.; Mansa, R. F.

    2017-07-01

    Dye Sensitized Solar Cell (DSSC) was first discovered in 1991 by O’regan and Gratzel. This new type of solar cell was reported to have lower production cost with efficiency as high as 12% which is comparable to conventional silicon solar cell. Initially, it uses ruthenium dye as light sensitizer for the operation. However, DSSC with ruthenium dyes are facing environment friendly issues due to the toxic chemicals and costly purification in processing ruthenium dye. Regardless of the poor performance in DSSC, natural dyes which are easy to prepare, cheap and environmental friendly still appear to be an alternative as dye sensitizer. In this study, dye sensitized solar cells (DSSCs) were fabricated using anthocyanin source dyes extracted from several local fruits. All the extracts absorb a wide range of the visible light and ultraviolet spectrum. Therefore, all of the natural dyes show light absorption properties which is important for a dye sensitizer. A DSSC is comprised of conductive substrate, nanoporous semiconductor TiO2 layer, dye sensitizer, electrolyte with redox couple and a counter electrode with catalyst. In this study, the effect of different light source and different counter electrode are been investigated. However, it is vital to know that further research need to do more on the locally Borneo sourced dyes to evaluate and enhance their performance in Dye Sensitized Solar Cell.

  17. 8-AminoBODIPYs: cyanines or hemicyanines? The effect of the coplanarity of the amino group on their optical properties.

    Science.gov (United States)

    Osorio-Martínez, Carlos A; Urías-Benavides, Arlette; Gómez-Durán, C F Azael; Bañuelos, Jorge; Esnal, Ixone; López Arbeloa, Iñigo; Peña-Cabrera, Eduardo

    2012-06-15

    The role of the amino group twisting ability in the BODIPY photophysics for nonsterically hindered and constrained molecular structures was studied. When a coplanar disposition of the amino and the BODIPY core is feasible, a hemicyanine-like delocalized π-system gives rise to novel blue and efficient BODIPY laser dyes. The key role of such rotamer is confirmed by newly synthesized derivatives where the amino and the BODIPY core are electronically decoupled by steric repulsions.

  18. Ion pairs of indobenzimidazolo cyanines: a structural study based on conductivity, absorption, fluorescence and 1H-NMR

    Science.gov (United States)

    Tatikolov, Aleksandr S.; Ishchenko, Aleksandr A.; Ghelli, Stefano; Ponterini, Glauco

    1998-11-01

    Asymmetric benzimidazolo carbo, di- and tricarbocyanines form ion pairs of the solvent-separated and contact types with different counterions in tetrahydrofuran, toluene and toluene-nitrile mixtures. The dissociation constants of the ion pairs in tetrahydrofuran, evaluated from conductivity data, do not depend on the length of the polymethine chain and show only a small decrease with decreasing counterion size. The absorption and fluorescence excitation spectra of the contact ion pairs exhibit a pronounced hypsochromic shift with respect to the solvated ions and the solvent-separated ion pairs. 1H-NMR experiments have provided information about the electronic structures of the ions of both the asymmetric dyes and the corresponding symmetric carbocyanines. They have also revealed different preferred anion locations in the contact ion pairs of the symmetric indocarbocyanine on one hand, and of the benzimidazolo carbocyanine and the asymmetric dyes on the other. This structural difference is suggested to be a cause of the observed opposite effects of ion pairing on the isomerization kinetics of the two groups of dyes.

  19. Dye Sysentized Solar Cell (Dyssc

    Directory of Open Access Journals (Sweden)

    A. Dileep,

    2015-11-01

    Full Text Available This paper presents a Dye sensitized solar cell (DYSSC, which is called as future generation solar cell. It is a new class of green photovoltaic cell based on photosynthesis principle in nature. DYSSCs are fabricated using two different natural dyes as sensitizers, which extracted from the materials existing in nature and our life, such as flowers, leaves, fruits, traditional Chinese medicines, and beverages. The use of sensitizers having a broad absorption band in conjunction with oxide films of nanocrystalline morphology permits to harvest a large fraction of sunlight. There are good prospects to produce these cells at lower cost and much better efficiency than conventional semiconductor devices by introducing various chemical and natural dyes. DYSSC are implemented with simple and new technique to overcome the energy crisis and excess cost of semiconductor solar cells.

  20. Dye Sensitized Tandem Photovoltaic Cells

    Energy Technology Data Exchange (ETDEWEB)

    Barber, Greg D.

    2009-12-21

    This work provided a new way to look at photoelectrochemical cells and their performance. Although thought of as low efficiency, a the internal efficiency of a 9% global efficiency dye sensitized solar cell is approximately equal to an 18% efficient silicon cell when each is compared to their useful spectral range. Other work undertaken with this contract also reported the first growth oriented titania and perovskite columns on a transparent conducting oxide. Other work has shown than significant performance enhancement in the performance of dye sensitized solar cells can be obtained through the use of coupling inverse opal photonic crystals to the nanocrystalline dye sensitized solar cell. Lastly, a quick efficient method was developed to bond titanium foils to transparent conducting oxide substrates for anodization.

  1. and dyes metabolized to benzidine were

    African Journals Online (AJOL)

    LAB

    2012-07-17

    Jul 17, 2012 ... intermediate in the production of various dyes, color salts and naphthols. In the past ... liver, kidney, nervous system, and various other organs of human's body ..... dye reduction: status review with emphasis on direct UV.

  2. Textile dyeing by dyestuffs of natural origin

    Directory of Open Access Journals (Sweden)

    Šmelcerović Miodrag

    2006-01-01

    Full Text Available The textile industry is one of the biggest industrial consumers of water especially dye houses which utilize synthetic dyes and other chemicals. Natural dyes are generally environmental friendly and have many advantages over synthetic dyes with respect to production and application. In recent years, there has been an interest in the application of these dyes due to their bio-degradability and higher compatibility with the environment. A review of previous work in the field of applying dyestuffs of natural source as possible textile dyes is given. From an ecological viewpoint, the substitution of chemical dyes by 'natural products' in textile dyeing may be feasible and may represent not only a strategy to reduce risks and pollutants, but also an opportunity for new markets and new businesses which can develop from the inclusion of ecology in trade policy.

  3. Triarylmethane Dyes for Artificial Repellent Cotton Fibers.

    Science.gov (United States)

    Montagut, Ana Maria; Gálvez, Erik; Shafir, Alexandr; Sebastián, Rosa María; Vallribera, Adelina

    2017-03-17

    Families of new hydrophobic and/or oleophobic triarylmethane dyes possessing long hydrocarbon or polyfluorinated chains have been prepared. When covalently grafted on to cotton fabric, these dyes give rise to a new type of colored superhydrophobic fibers.

  4. Synthesis of a highly Zn(2+)-selective cyanine-based probe and its use for tracing endogenous zinc ions in cells and organisms.

    Science.gov (United States)

    Guo, Zhiqian; Kim, Gun-Hee; Yoon, Juyoung; Shin, Injae

    2014-01-01

    The zinc ion has a key role in a variety of physiological and pathological processes. As a consequence, the development of sensitive and reliable methods to monitor the presence of zinc ions in cells and organisms is of great importance to biological research and biomedical applications. This protocol describes detailed procedures for the five-stage synthesis of a zinc ion-selective, cyanine-based fluorescent probe, CTMPA, from 2,6-bis(hydroxymethyl)pyridine. In addition, we describe its applications in the detection of Zn(2+) released during apoptosis in cells and endogenous Zn(2+) in living zebrafish. Notably, the use of CTMPA enabled our research group to monitor for the first time the presence of zinc ions in neuromasts of zebrafish via fluorescence. The approximate time frame for the synthesis of CTMPA is 4-5 d, and for its use in bioimaging is 8-10 h for cells and 2 h for zebrafish.

  5. Dye solubility in supercritical carbon dioxide fluid

    Directory of Open Access Journals (Sweden)

    Yan Jun

    2015-01-01

    Full Text Available Supercritical carbon dioxide fluid is an alternative solvent for the water of the traditional dyeing. The solubility of dyestuff affects greatly the dyeing process. A theoretical model for predicting the dye solubility is proposed and verified experimentally. The paper concludes that the pressure has a greater impact on the dyestuff solubility than temperature, and an optimal dyeing condition is suggested for the highest distribution coefficient of dyestuff.

  6. Water in supercritical carbon dioxide dyeing

    Directory of Open Access Journals (Sweden)

    Zheng Lai-Jiu

    2015-01-01

    Full Text Available This paper investigates the effect of water serving as entrainer on the dyeing of wool fabrics in supercritical carbon dioxide. Compared with previous supercritical dyeing methods, addition of water makes the dyeing process more effective under low temperature and low pressure. During dyeing process, dyestuff can be uniformly distributed on fabrics’s surface due to water interaction, as a result coloration is enhanced while color difference is decreased.

  7. Fong’s: Saving Water in Dyeing

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    In an effort to save the precious water resource and reduce the environmental impact, Fong’s Industries Group along with its member companies, namely "Fong’s National", "THEN", "Goller" and "Fong’s Water Technology" provide an ecological dyeing solution to reduce the water consumption drastically through their innovative technologies covering the processes from yarn dyeing to piece dyeing and recycling of discharge after dyeing and finishing.

  8. One-bath Dyeing of Polyester/Wool Blend with Disperse Dyes

    Institute of Scientific and Technical Information of China (English)

    蔡翔; 宋心远

    2001-01-01

    The role of auxiliary LAB as vehicle in dyeing polyester/wool blends with disperse dyes is described. Dye exhaustion and bonding on polyester/wool samples are studied under different experimental conditions - the LAB amount, the temperature and pH value- to achieve optimum conditions. The results are compared with those obtained with and without conventional dyeing auxiliary products. Although dye exhaustion is higher in the presence of commercial carriers, the dye bonded increases markedly in the presence of auxiliary LAB in both fibers. The role played by auxiliary LAB in polyester/wool blend dyeing can provide a new method for this process.

  9. Effect of dye structure and redox mediators on anaerobic azo and anthraquinone dye reduction

    Directory of Open Access Journals (Sweden)

    Mayara Carantino Costa

    2012-01-01

    Full Text Available We investigated the biological decolourisation of dyes with different molecular structures. The kinetic constant values (k1 achieved with azo dye Reactive Red 120 were 7.6 and 10.1 times higher in the presence of RM (redox mediators AQDS and riboflavin, respectively, than the assays lacking RM. The kinetic constant achieved with the azo dye Congo Red was 42 times higher than that obtained with the anthraquinone dye Reactive Blue 4. The effect of RM on dye reduction was more evident for azo dyes resistant to reductive processes, and ineffective for anthraquinone dyes because of the structural stability of the latter.

  10. Natural dyes versus lysochrome dyes in cheiloscopy: A comparative evaluation

    Directory of Open Access Journals (Sweden)

    Narendra Nath Singh

    2010-01-01

    Full Text Available Cheiloscopy is the study of lip prints. Lip prints are genotypically determined and are unique, and stable. At the site of crime, lip prints can be either visible or latent. To develop lip prints for study purpose various chemicals such as lysochrome dyes, fluorescent dyes, etc. are available which are very expensive. Vermilion (Sindoor used by married Indian women and indigo dye (fabric whitener are readily available, naturally derived, and cost-effective reagents available in India. Objective: To compare the efficacy of sudan black, vermilion, and indigo in developing visible and latent lip prints made on bone china cup, satin fabric, and cotton fabric. Materials and Methods: Out of 45 Volunteers 15 lip prints were made on bone China cup 15 lip prints on Satin fabric and 15 on Cotton fabric. Sudan black, vermilion and indigo were applied on visible and latent lip prints and graded as good (+,+, fair (+, and poor (- and statistically evaluated. Results: The vermilion and indigo dye gives comparable results to that of sudan black for developing visible and latent lip prints.

  11. Synthesis and dyeing performance of a novel polycarboxylic acid azo dye

    Institute of Scientific and Technical Information of China (English)

    Hua Xu; Bing Tao Tang; Shu Fen Zhang

    2011-01-01

    A novel reactive polycarboxylic acid dye was synthesized by the reaction of polymaleic anhydride (PMA) with 3-methyl-l-(4-sulfonylphenyl)-4-(4-aminophenylazo)-2-pyrazoline-5-one. The structure of the novel dye was characterized by FTIR, UV-vis and 13C NMR spectra. The dyeing properties of dye on cotton were tested, and the novel dye possessed high fixation and good fastness.

  12. Descoloration of industrial dyes and simulated textile effluents dyes by turnip peroxidase

    OpenAIRE

    Silva,Maria Cristina; Angelita D Corrêa; Torres, Juliana A.; Amorim, M. T. Pessoa de

    2012-01-01

    The removal of important textile dyes by turnip peroxidase (TNP) was evaluated. The textile effluents besides the residual dyes contain also chemical auxiliaries such as salts, dispersing and wetting agents. The effect of these was evaluated in the removal of the dyes reactive blue 21 and reactive blue 19 by TNP in synthetic effluents. A decrease of the efficency decolorization was observed. The action of the enzyme on colour removal of dye mixture was equivalent to the dyes alone. The chemic...

  13. Optimizing the Dyeing Process of Alkali-Treated Polyester Fabric with Dolu Natural Dye

    Directory of Open Access Journals (Sweden)

    M.F. Shahin

    2014-06-01

    Full Text Available An attempt has been made to optimize the process of dyeing polyester (PET fabric with natural dyes. Polyester has been first treated with NaOH solution in order to study its impact on the dyeability to the natural dye. The required and used colour component was extracted from a natural plant, namely: Rhubarb; Rheum officinale. The chemical structure of the used colouring matter is observed to have all the characteristics of a typical disperse dye. The colour strength of PET fabric was noticed to increase as a result of alkali treatment which may be attributed to the alteration in the hydrophobicity of polyester fibre. The most effective parameters that may affect the dye uptake of the natural dye on alkali-treated PET fabric and the final dyeing properties including dye bath pH, dyeing temperature and time were studied in details. The behaviour of the selected and used natural dye was found to be similar to that of disperse dyes. Addition of salicylic acid to the dye bath accelerated the rate of dyeing and subsequently higher colour strength was attained. Non- ionic dispersing agent was also used to ensure better dyeing uniformity and higher dispersion stability of dye liquor.

  14. Preparation of a Novel Chitosan Based Biopolymer Dye and Application in Wood Dyeing

    Directory of Open Access Journals (Sweden)

    Xiaoqian Wang

    2016-09-01

    Full Text Available A novel chitosan-based biopolymer dye possessing antibacterial properties was synthesized by reaction of O-carboxymethyl chitosan and Acid Red GR. The synthesized materials were characterized by Fourier transform infrared spectroscopy (FTIR, degree of substitution (DS, X-ray photoelectron spectroscopy (XPS, thermogravimetric analysis (TG, X-ray diffraction (XRD, water solubility test, antibacterial property test, and dyeing performance, including dye uptake, color difference, and fastness. Results showed that the synthesized dye was combined by –NH3+ of O-carboxymethyl chitosan and the sulfonic group of Acid Red GR. According to the comprehensive analysis of XRD and water solubility, the introduction of the carboxymethyl group and acid dye molecule changed the structure of the chitosan from compact to loose, which improved the synthesized dye’s water solubility. However, the thermal stability of the synthesized dye was decreased. The antibacterial property of the poplar wood dyed with the synthesized dye was enhanced and its antibacterial rate, specifically against Staphylococcus aureus and Escherichia coli, also increased to a rate of more than 99%. However, the dye uptake of the synthesized dye was lower than that of the original dye. Despite this, though, the dyeing effect of the synthesized dye demonstrated better water-fastness, and light-fastness than the original dye. Therefore, the novel chitosan-based biopolymer dye can be a promising product for wood dyeing.

  15. Hair Dyes and Cancer Risk

    Science.gov (United States)

    ... dye use and bladder cancer: a meta-analysis. Annals of Epidemiology 2014; 24(2),151–159. [PubMed ... in a prospective cohort of Chinese women. Cancer Science 2009; 100(6):1088-1091. [PubMed Abstract] Related ...

  16. Anthraquinone dyes for superhydrophobic cotton.

    Science.gov (United States)

    Salabert, J; Sebastián, R M; Vallribera, A

    2015-09-28

    Water-repellent, self-cleaning and stain resistant textiles are of interest for industrial applications. Anthraquinone reactive dyes were covalently grafted onto cotton fabric surfaces obtaining bright colors with good wash-fastness properties and giving rise to breathable superhydrophobic textiles with self-cleaning properties.

  17. Waste Water Treatment of Dye Contamination

    OpenAIRE

    Pattana Boonyaprapa

    2009-01-01

    The objectives of this research were to study tie-dye process data and wastewater characteristics from 60 entrepreneurs, and to study the colour density treatment in pilot scale by using upflow anaerobic filters. From 60 filled-out questionnaires, it was found that all tie-dye entrepreneurs used reactive dyes by a hot method. Ninety-eight percent of the tie-dye enterpreneurs produced wastewater at the rate of not more than 1500 liters per day. All of them lacked tie-dye wastewater treatment s...

  18. [Leather azo dyes: mutagenic and carcinogenic risks].

    Science.gov (United States)

    Clonfero, E; Venier, P; Granella, M; Levis, A G

    1990-01-01

    The paper reviews the carcinogenicity and mutagenicity data on azo dyes used in the leather industry. Two water soluble benzidine-based dyes were classified as "probably carcinogenic to humans" by the International Agency for Research on Cancer (IARC). No other dyes have been evaluated by the IARC. Of the 48 azo dyes assayed in the Salmonella/microsome test, 20 gave positive results. Attention is drawn to the important role of the in vivo metabolism of azo compounds, which includes a preliminary reduction of the azo bonds and subsequent release of the aromatic amines of the dye. A useful assay (Prival test) for evaluating the mutagenic properties of azo dyes involves a reductive step that permits the release of any genotoxic agents present in the compounds. A list of leather azo dyes is furnished that are considered as potentially harmful due to the presence of a carcinogenic aromatic amine (benzidine, p-aminobenzene and derivatives) in their formulae.

  19. Evaluation of bimetal doped TiO2 in dye fragmentation and its comparison to mono-metal doped and bare catalysts

    Science.gov (United States)

    Malika, Manjakuppam; Rao, Ch. Venkatanarasimha; Das, Raj Kumar; Giri, Ardhendu Sekhar; Golder, Animes Kumar

    2016-04-01

    There are instances that bimetal doped semiconductor materials impart superior photocatalytic activity than bare and mono-metal doping. In this study, visible light responsive mono- (Cu/TiO2 and Ni/TiO2) and bi-metal doped (Cu-Ni/TiO2) TiO2 photocatalysts with wide band gap energy were synthesized via co-precipitation method with an equal mass ratio of Cu and Ni. The catalyst characterization was performed using Diffuse Reflectance UV-visible (DR-UV-vis) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, X-ray Diffraction (XRD), zeta-potential and Transmission Electron Microscopy (TEM) analyzes. The charge balancing effect of Cu and Ni caused a notable reduction in the optical band gap of TiO2 to 2.91 eV with Cu-Ni/TiO2. The synthesis method increased the anatase phase significantly along with the crystallite size. Cu-Ni/TiO2 displayed a lesser destabilization tendency, and the absolute value of zeta-potentials increased much at pH > pHzpc resulted from the higher oxygen vacancies. The activity of Ni/TiO2, Cu/TiO2, and Cu-Ni/TiO2 was tested for the degradation dynamics and kinetics of Eriochrome Cyanine Red (ECR), an anionic dye. Cu doping exhibited a better dye decomposition because of the low recombination rate of electron/hole pair as a full 3d sub-level of Cu is energetically more favorable than a full 4s sub-level of Ni. The mechanism of dye decomposition releasing inorganic ions is also proposed and validated from the mass spectra.

  20. Dyeing of Jute with Reactive Dyes: Optimisation of the Process Variables and Assessment of Colourfastness Characteristics

    Science.gov (United States)

    Samanta, A. K.; Chakraborty, Sharmistha; Guha Roy, T. K.

    2012-08-01

    This paper deals with the studies on the effect of dye concentration, electrolyte (common salt) concentration, dyeing time, dyeing temperature, soda ash concentration, pH of the dye solution and material to liquor ratio (MLR) on colour strength and other colour parameters after being dyed of jute fabrics with reactive dyes, namely, Turquoise blue, Lemon Yellow, Red CN colours. The dye absorption increases with increase in electrolyte (common salt) concentration, dyeing time, dyeing temperature, soda ash concentration, pH and decreases with increase of MLR. Colour fastness to wash, light and rubbing for the dyed samples has been studied and reported. It is observed that reactive dye gives overall good colour fastness to both washing and rubbing. But the light fastness has been found to be moderate only, due to the UV-light initiated fading of jute fibre itself change of the colour substrate, ie, undyed material. This colour fastness has been significantly resolved by post treatment with 1 % benzotriazole.

  1. Dyeing of Polyester Woven Fabric with Disperse Dye Using Conventional and Microwave Technique

    Directory of Open Access Journals (Sweden)

    Uzma Syed

    2014-07-01

    Full Text Available Polyester fabric is generally dyed using high temperature dyeing technique and carrier. Both techniques require high energy consumption while few carriers are toxic in nature. In this study, 100% polyester woven fabric was dyed by microwave and conventional dyeing technique with disperse dye; Foron Blue RD GLN by an exhaust method for short dyeing cycle (15 and 30 min. The fabric samples were dyed using conventional high temperature dyeing technique using recommended recipe. Moreover, samples were also dyed using microwave technique with recommended recipe and by the addition of salt and urea, pre-treatment with caustic and organic solvent for improving the dye uptake value and fastness properties. The dyeing assessment; (K/S?max value by Datacolor spectrophotometer, dye uniformity by optical microscope and washing fastness by grey scale were measured. It has been observed that over conventional dyeing method, microwave irradiation dyed sample gives almost 70% high (K/S?max value and uniform dye penetration and good to very good washing fastness property. In addition, microwave dyeing gives excellent dyeing behavior at short dyeing cycle; 15 min; hence saves energy and sustainable dyeing process

  2. COMPARATIVE STUDY OF TWO DYEING METHODS USING REACTIVE DYE

    OpenAIRE

    HINOJOSA Belén; MONTAVA Ignacio; BOU-BELDA Eva; Díaz, Pablo

    2016-01-01

    Environment preservation is a common worry not only for people but for companies as well. Industry is more and more concern about the necessity of developing new and more respectful processes. Dye is one of the most important processes in the textile industry but it is also considered as no too safe regarding environment issues. This process uses large amounts of water and generates big volumes of wastewater. Following this issue, new regulations and laws emerge to control the waste generate...

  3. COMPARATIVE STUDY OF TWO DYEING METHODS USING REACTIVE DYE

    Directory of Open Access Journals (Sweden)

    HINOJOSA Belén

    2016-05-01

    Full Text Available Environment preservation is a common worry not only for people but for companies as well. Industry is more and more concern about the necessity of developing new and more respectful processes. Dye is one of the most important processes in the textile industry but it is also considered as no too safe regarding environment issues. This process uses large amounts of water and generates big volumes of wastewater. Following this issue, new regulations and laws emerge to control the waste generated. This leads to the companies and increased costs in terms of wastewater treatments and high water consumption. In this research we compare two systems on garment finishing application, the conventional bath process and the new Ecofinish system that is able to save water and product. To compare these processes, we carried out a reactive dyeing using both systems in order to determine the quality differences in the final product. For this purpose, the samples have been tested to washing and rubbing fastness, according to UNE EN ISO 105 C10 and UNE- EN ISO 105 X12 standards, respectively. This study confirms that this system achieves water savings and reduces the wastewater produced, getting a good dyeing. This process can be considered as an alternative to the conventional one.

  4. Artificial evolution of coumarin dyes for dye sensitized solar cells.

    Science.gov (United States)

    Venkatraman, Vishwesh; Abburu, Sailesh; Alsberg, Bjørn Kåre

    2015-11-07

    The design and discovery of novel molecular structures with optimal properties has been an ongoing effort for materials scientists. This field has in general been dominated by experiment driven trial-and-error approaches that are often expensive and time-consuming. Here, we investigate if a de novo computational design methodology can be applied to the design of coumarin-based dye sensitizers with improved properties for use in Grätzel solar cells. To address the issue of synthetic accessibility of the designed compounds, a fragment-based assembly is employed, wherein the combination of chemical motifs (derived from the existing databases of structures) is carried out with respect to user-adaptable set of rules. Rather than using computationally intensive density functional theory (DFT)/ab initio methods to screen candidate dyes, we employ quantitative structure-property relationship (QSPR) models (calibrated from empirical data) for rapid estimation of the property of interest, which in this case is the product of short circuit current (Jsc) and open circuit voltage (Voc). Since QSPR models have limited validity, pre-determined applicability domain criteria are used to prevent unacceptable extrapolation. DFT analysis of the top-ranked structures provides supporting evidence of their potential for dye sensitized solar cell applications.

  5. [Benzidine dyes and risk of bladder cancer].

    Science.gov (United States)

    Miyakawa, M; Yoshida, O

    1989-12-01

    Until the early 1970's there was little concern about dyes which contain benzidine as an integral part of their chemical structure. Furthermore, use of the finished dyes was not considered dangerous. To ascertain whether azo dyes are associated with risk of development of bladder tumors in workers who handpaint Yuzen-type silk kimonos in Kyoto, we investigated the disintegration of dyes to benzidine. In these studies, we found that in rats and mice benzidine-based dyes are metabolized to benzidine and that the azo linkage of benzidine dyes is reduced by Escherichia coli and soil bacteria. These experimental findings were reported previously. In this report, we outline an approach to these studies. Many of the dyes used to color paper, textiles, lipstick, bait used by fishermen, as well as hair dyes, and dyes used in research, for pharmaceutical products, and by defence personnel for the detection of liquid chemical warfare agents, have been shown to be potentially mutagenic or carcinogenic. We review the literature on these dyes.

  6. Zeolite-dye micro lasers

    CERN Document Server

    Vietze, U; Laeri, F; Ihlein, G; Schüth, F; Limburg, B; Abraham, M

    1998-01-01

    We present a new class of micro lasers based on nanoporous molecular sieve host-guest systems. Organic dye guest molecules of 1-Ethyl-4-(4-(p-Dimethylaminophenyl)-1,3-butadienyl)-pyridinium Perchlorat were inserted into the 0.73-nm-wide channel pores of a zeolite AlPO$_4$-5 host. The zeolitic micro crystal compounds where hydrothermally synthesized according to a particular host-guest chemical process. The dye molecules are found not only to be aligned along the host channel axis, but to be oriented as well. Single mode laser emission at 687 nm was obtained from a whispering gallery mode oscillating in a 8-$\\mu$m-diameter monolithic micro resonator, in which the field is confined by total internal reflection at the natural hexagonal boundaries inside the zeolitic microcrystals.

  7. Synthesis, characterization and dyeing behavior of heterocyclic acid dyes and mordent acid dyes on wool and silk fabrics

    Directory of Open Access Journals (Sweden)

    Patel Hitendra M.

    2012-01-01

    Full Text Available Novel heterocyclic acid and mordent acid dyes were synthesized by the coupling of diazonium salt solution of different aromatic amines with 2- butyl-3-(4-hydroxybenzoylbenzofuran. The resulting heterocyclic acid dyes were characterized by spectral techniques, i.e., elemental analysis, IR, 1HNMR, 13C-NMR spectral studies and UV- visible spectroscopy. The dyeing performance of all the heterocyclic acid dyes was evaluated on wool and silk fabrics. The dyeing of chrome pre treated wool and silk fabrics showed better hues on mordented fabrics. Dyeing of wool and silk fabrics resulted in pinkish blue to red shades with very good depth and levelness. The dyed fabrics showed excellent to very good light, washing, perspiration, sublimation and rubbing fastness.

  8. Batchwise dyeing of bamboo cellulose fabric with reactive dye using ultrasonic energy.

    Science.gov (United States)

    Larik, Safdar Ali; Khatri, Awais; Ali, Shamshad; Kim, Seong Hun

    2015-05-01

    Bamboo is a regenerated cellulose fiber usually dyed with reactive dyes. This paper presents results of the batchwise dyeing of bamboo fabric with reactive dyes by ultrasonic (US) and conventional (CN) dyeing methods. The study was focused at comparing the two methods for dyeing results, chemicals, temperature and time, and effluent quality. Two widely used dyes, CI Reactive Black 5 (bis-sulphatoethylsulphone) and CI Reactive Red 147 (difluorochloropyrimidine) were used in the study. The US dyeing method produced around 5-6% higher color yield (K/S) in comparison to the CN dyeing method. A significant savings in terms of fixation temperature (10°C) and time (15 min), and amounts of salt (10 g/L) and alkali (0.5-1% on mass of fiber) was realized. Moreover, the dyeing effluent showed considerable reductions in the total dissolved solids content (minimum around 29%) and in the chemical oxygen demand (minimum around 13%) for the US dyebath in comparison to the CN dyebath. The analysis of colorfastness tests demonstrated similar results by US and CN dyeing methods. A microscopic examination on the field emission scanning electron microscope revealed that the US energy did not alter the surface morphology of the bamboo fibers. It was concluded that the US dyeing of bamboo fabric produces better dyeing results and is a more economical and environmentally sustainable method as compared to CN dyeing method.

  9. Dye Photodestruction in a Solid-State Dye Laser with a Polymeric Gain Medium

    Science.gov (United States)

    Popov, Sergei

    1998-09-01

    The process of dye photodestruction in a solid-state dye laser is studied, and implemented is a polymeric gain medium doped with a strongly concentrated dye. The behavior of the conversion efficiency in the polymeric gain medium pumped with different laser-pulse repetition rates and the process of dye photobleaching are analyzed. The contribution of the heating of the host material into the dye molecules deactivation is discussed. The negative effect of high dye concentration on the dye stability under a high pump repetition rate is reported and analyzed for the first time to my knowledge. A comparison of the present results with recently published data demonstrates the major role of photodestruction, rather than direct thermodestruction, in the dye stability of the solid-state gain medium. The role of additives with low molecular weights in the polymeric matrix, for increasing the stability of the gain material, is discussed.

  10. Laser dye stability. Pt. 4. Photodegradation relationships for bicyclic dyes in alcohol solutions

    Energy Technology Data Exchange (ETDEWEB)

    Fletcher, A.N. (Naval Weapons Center, China Lake, Calif. (USA). Research Dept.)

    1978-05-01

    Changes in the absorption of a dye laser solution are examined after excitation with a xenon flashlamp. It is found that the rate of bleaching as a function of the total input energy of coumarin or quinolone dyes in ethanol increases in direct proportion to the dye concentration. This relationship suggests that the dye reacts with a photoproduct of the solvent rather than being directly decomposed by the xenon flash. We have measured the conversion of the dye to form products, P, absorbing at the lasing wavelength. Results correspond to the dye reacting with a precursor of P to form either insoluble products or ones not absorbing at the lasing wavelength. Thus larger total amounts of bleached dye do not proportionately increase P, and hence do not proportionately inhibit lasing. Furthermore, we find that P increases with the total input energy fairly independent of the rate of bleaching for a given bicyclic dye in an alcohol solution.

  11. Increased light harvesting in dye-sensitized solar cells with energy relay dyes

    KAUST Repository

    Hardin, Brian E.

    2009-06-21

    Conventional dye-sensitized solar cells have excellent charge collection efficiencies, high open-circuit voltages and good fill factors. However, dye-sensitized solar cells do not completely absorb all of the photons from the visible and near-infrared domain and consequently have lower short-circuit photocurrent densities than inorganic photovoltaic devices. Here, we present a new design where high-energy photons are absorbed by highly photoluminescent chromophores unattached to the titania and undergo Förster resonant energy transfer to the sensitizing dye. This novel architecture allows for broader spectral absorption, an increase in dye loading, and relaxes the design requirements for the sensitizing dye. We demonstrate a 26% increase in power conversion efficiency when using an energy relay dye (PTCDI) with an organic sensitizing dye (TT1). We estimate the average excitation transfer efficiency in this system to be at least 47%. This system offers a viable pathway to develop more efficient dye-sensitized solar cells.

  12. Environmentally Friendly Techniques for Wool Dyeing Process

    Directory of Open Access Journals (Sweden)

    Antighin Simona

    2015-11-01

    Full Text Available The aim of this research was to evaluate the influence of dyeing process on the quality of surface waters contaminated with heavy metals and organic compounds, resulted after the wool dyeing process. In order to mark out this aspects an environment friendly method was proposed which involves dyeing wool fiber with new complex combinations derived from a new acid dyes which were complexed, using copper, iron, nickel and zinc salts at 2:1 combination ratio. In order to point out the environmental point of view of wastewaters an experimental protocol was tested by dyeing wool fiber at different pH. Evaluation of complexed combinations impact on the environment involve the following indicators: consumption degree of dyeing solution from the process bath, treatment degree related to the organic content expressed by COD indicator and treatment degree related to the heavy metal concentration respectively.

  13. Biological wastewater treatment of azo dyes

    Energy Technology Data Exchange (ETDEWEB)

    Shaul, G.M.; Dempsey, C.R.; Dostal, K.A. (Environmental Protection Agency, Cincinnati, OH (USA))

    1988-09-01

    EPA Water Engineering Research Laboratory, Office of Research and Development, undertook a study to determine the fate of specific water soluble azo dye compounds in the activated sludge process (ASP). The study was approached by dosing the feed to the pilot ASP systems with various water soluble azo dyes and by monitoring each dye compound through the system, analyzing both liquid and sludge samples. The fate of the parent dye compound was assessed via mass balance calculations. These data could determine if the compound was removed by adsorption, apparent biodegradation, or not removed at all. The paper presents results for 18 dye compounds tested from June 1985 through August 1987. The study was conducted at EPAs Test and Evaluation Facility in Cincinnati, Ohio. The objective of this study was to determine the partitioning of water soluble azo dyes in the ASP.

  14. Adsorptive Properties of Dyes to Cellulosic Sheet and Discoloration of Dye Solution by UV-ray Irradiation

    Institute of Scientific and Technical Information of China (English)

    Zhou Yu; Iida Ikuho; Minato Kazuya; Kurosu Hiroshi

    2005-01-01

    The adsorptive properties and selectivity of dyes and water molecules to cellulosic sheet, dependence of adsorptive properties of dyes on the concentration of dye solution, and discoloration of the dye solution due to the UV-ray irradiation were determined for 18 kinds of commercial dyes. The results are as follows: 1) the adsorptive properties of dyes to cellulose sheet differed greatly, but did not depend on the dye types such as acidic, basic and so on; 2) adsorptive properties of dyes to cellulosic sheet depended on the concentration of dye solution and were classified into 4 types: concentration-independent, increasing or decreasing with dye concentration, and having a maximum. This classification was irrelevant to the dye types; 3) the irradiation of UV-ray did not cause significant discoloration of dye solution itself, which suggested that wood components as well as dye molecules influence the discoloration of wood.

  15. Hair dye poisoning and the developing world

    Directory of Open Access Journals (Sweden)

    Sampathkumar Krishnaswamy

    2009-01-01

    Full Text Available Hair dye poisoning has been emerging as one of the important causes of intentional self harm in the developing world. Hair dyes contain paraphenylene-diamine and a host of other chemicals that can cause rhabdomyolysis, laryngeal edema, severe metabolic acidosis and acute renal failure. Intervention at the right time has been shown to improve the outcome. In this article, we review the various manifestations, clinical features and treatment modalities for hair dye poisoning.

  16. 1983 Annual Report on Laser Dyes.

    Science.gov (United States)

    1984-04-01

    absorption at the lasing wavelength due to the accumula- tion of reaction products from the photodegradation of a laser dye is analyzed thioretically...Laser Dyes O by A. N. Fletcher Research DopetMrnt APRIL 1984 NAVAL WEAPONS CENTER CHINA LAKE, CALIFORNIA 93555 Appoved for ftc qesege dt"" ba n ftsd...work presented in seven open literature publications on laser dyes . This work originated within the Chemistry Division and was performed and/or

  17. Stability and efficiency of dye-sensitized solar cells based on papaya-leaf dye

    Science.gov (United States)

    Suyitno, Suyitno; Saputra, Trisma Jaya; Supriyanto, Agus; Arifin, Zainal

    2015-09-01

    The present article reports on the enhancement of the performance and stability of natural dye-based dye-sensitized solar cells (DSSCs). Natural dyes extracted from papaya leaves (PL) were investigated as sensitizers in TiO2-based DSSCs and evaluated in comparison with N719 dye. The acidity of the papaya-leaf extract dyes was tuned by adding benzoic acid. The TiO2 film-coated fluorine-doped tin oxide glass substrates were prepared using the doctor-blade method, followed by sintering at 450 °C. The counter electrode was coated by chemically deposited catalytic platinum. The working electrodes were immersed in N719 dye and papaya dye solutions with concentrations of 8 g/100 mL. The absorbance spectra of the dyes were obtained by ultra-violet-visible spectroscopy. The energy levels of the dyes were measured by the method of cyclic voltammetry. In addition, Fourier transform infrared spectroscopy was used to determine the characteristic functionalities of the dye molecules. The DSSC based on the N719 dye displayed a highest efficiency of 0.87% whereas those based on papaya-leaf dye achieved 0.28% at pH 3.5. The observed improved efficiency of the latter was attributed to the increased current density value. Furthermore, the DSSCs based on papaya-leaf dye with pH 3.5-4 exhibited better stability than those based on N719 dye. However, further studies are required to improve the current density and stability of natural dye-based DSSCs, including the investigation of alternative dye extraction routes, such as isolating the pure chlorophyll from papaya leaves and stabilizing it.

  18. Isolation and screening of azo dye decolorizing bacterial isolates from dye-contaminated textile wastewater

    OpenAIRE

    Shahid Mahmood; Muhammad Arshad; Azeem Khalid; Zilli Huma Nazli; Tariq Mahmood

    2011-01-01

    Azo dyes are released into wastewater streams without any pretreatment and pollute water and soilenvironments. To prevent contamination of our vulnerable resources, removal of these dye pollutants is of greatimportance. For this purpose, wastewater samples were collected from dye-contaminated sites of Faisalabad. About200 bacterial isolates were isolated through enrichment and then tested for their potential to remove RemazolBlack-B azo dye in liquid medium. Five bacterial isolates capable of...

  19. Optimizing the Dyeing Process of Alkali-Treated Polyester Fabric with Dolu Natural Dye

    OpenAIRE

    M. F. Shahin; Ahmed, R. M.

    2014-01-01

    An attempt has been made to optimize the process of dyeing polyester (PET) fabric with natural dyes. Polyester has been first treated with NaOH solution in order to study its impact on the dyeability to the natural dye. The required and used colour component was extracted from a natural plant, namely: Rhubarb; Rheum officinale. The chemical structure of the used colouring matter is observed to have all the characteristics of a typical disperse dye. The colour strength of PE...

  20. Solvent-free fluidic organic dye lasers.

    Science.gov (United States)

    Choi, Eun Young; Mager, Loic; Cham, Tran Thi; Dorkenoo, Kokou D; Fort, Alain; Wu, Jeong Weon; Barsella, Alberto; Ribierre, Jean-Charles

    2013-05-06

    We report on the demonstration of liquid organic dye lasers based on 9-(2-ethylhexyl)carbazole (EHCz), so-called liquid carbazole, doped with green- and red-emitting laser dyes. Both waveguide and Fabry-Perot type microcavity fluidic organic dye lasers were prepared by capillary action under solvent-free conditions. Cascade Förster-type energy transfer processes from liquid carbazole to laser dyes were employed to achieve color-variable amplified spontaneous emission and lasing. Overall, this study provides the first step towards the development of solvent-free fluidic organic semiconducting lasers and demonstrates a new kind of optoelectronic applications for liquid organic semiconductors.

  1. Accurate simulation of optical properties in dyes.

    Science.gov (United States)

    Jacquemin, Denis; Perpète, Eric A; Ciofini, Ilaria; Adamo, Carlo

    2009-02-17

    Since Antiquity, humans have produced and commercialized dyes. To this day, extraction of natural dyes often requires lengthy and costly procedures. In the 19th century, global markets and new industrial products drove a significant effort to synthesize artificial dyes, characterized by low production costs, huge quantities, and new optical properties (colors). Dyes that encompass classes of molecules absorbing in the UV-visible part of the electromagnetic spectrum now have a wider range of applications, including coloring (textiles, food, paintings), energy production (photovoltaic cells, OLEDs), or pharmaceuticals (diagnostics, drugs). Parallel to the growth in dye applications, researchers have increased their efforts to design and synthesize new dyes to customize absorption and emission properties. In particular, dyes containing one or more metallic centers allow for the construction of fairly sophisticated systems capable of selectively reacting to light of a given wavelength and behaving as molecular devices (photochemical molecular devices, PMDs).Theoretical tools able to predict and interpret the excited-state properties of organic and inorganic dyes allow for an efficient screening of photochemical centers. In this Account, we report recent developments defining a quantitative ab initio protocol (based on time-dependent density functional theory) for modeling dye spectral properties. In particular, we discuss the importance of several parameters, such as the methods used for electronic structure calculations, solvent effects, and statistical treatments. In addition, we illustrate the performance of such simulation tools through case studies. We also comment on current weak points of these methods and ways to improve them.

  2. Tunable Optofluidic Third Order DFB Dye Laser

    DEFF Research Database (Denmark)

    Gersborg-Hansen, Morten; Kristensen, Anders

    2007-01-01

    We present a low-threshold polymer-based nanofluidic dye laser. By employing a third order DFB laser resonator, we demonstrate a threshold fluence of ~7 muJ/mm2 and a tunability of 45 nm using a single laser dye......We present a low-threshold polymer-based nanofluidic dye laser. By employing a third order DFB laser resonator, we demonstrate a threshold fluence of ~7 muJ/mm2 and a tunability of 45 nm using a single laser dye...

  3. Solubilization of Hydrophobic Dyes in Surfactant Solutions

    Directory of Open Access Journals (Sweden)

    Ali Reza Tehrani-Bagha

    2013-02-01

    Full Text Available In this paper, the use of surfactants for solubilization of hydrophobic organic dyes (mainly solvent and disperse dyes has been reviewed. The effect of parameters such as the chemical structures of the surfactant and the dye, addition of salt and of polyelectrolytes, pH, and temperature on dye solubilization has been discussed. Surfactant self-assemble into micelles in aqueous solution and below the concentration where this occurs—the critical micelle concentration (CMC—there is no solubilization. Above the CMC, the amount of solubilized dye increases linearly with the increase in surfactant concentration. It is demonstrated that different surfactants work best for different dyes. In general, nonionic surfactants have higher solubilization power than anionic and cationic surfactants. It is likely that the reason for the good performance of nonionic surfactants is that they allow dyes to be accommodated not only in the inner, hydrocarbon part of the micelle but also in the headgroup shell. It is demonstrated that the location of a dye in a surfactant micelle can be assessed from the absorption spectrum of the dye-containing micellar solution.

  4. Release Control of Dye from Agar Ball

    OpenAIRE

    板屋, 智之; 山村, 俊貴; 唐澤, 有太朗

    2013-01-01

    Agar is a special product of Nagano prefecture. To utilize agar gel as adsorbing or releasing material of dyes or drugs, spherical agar gel “agar ball” was prepared by dropping aqueous agar solution into salad oil. And releasing behavior of a dye (rhodamine B) from agar ball was studied. The dye is released easily from agar ball, but the release can be controlled by hybiridazation of agar and galatin. In addition, it was found that agar ball could extract the dye from oil phase containing the...

  5. The microbial degradation of azo dyes: minireview.

    Science.gov (United States)

    Chengalroyen, M D; Dabbs, E R

    2013-03-01

    The removal of dyes in wastewater treatment plants still involves physical or chemical processes. Yet numerous studies currently exist on degradation based on the use of microbes-which is a well-studied field. However progress in the use of biological methods to deal with this environmentally noxious waste is currently lacking. This review focuses on the largest dye class, that is azo dyes and their biodegradation. We summarize the bacteria identified thus far which have been implicated in dye decolorization and discuss the enzymes involved and mechanisms by which these colorants are broken down.

  6. Photostability of low cost dye-sensitized solar cells based on natural and synthetic dyes

    Science.gov (United States)

    Abdou, E. M.; Hafez, H. S.; Bakir, E.; Abdel-Mottaleb, M. S. A.

    2013-11-01

    This paper deals with the use of some natural pigments as well as synthetic dyes to act as sensitizers in dye-sensitized solar cells (DSSCs). Anthocyanin dye extracted from rosella (Hibiscus sabdariffa L.) flowers, the commercially available textile dye Remazole Red RB-133 (RR) and merocyanin-like dye based on 7-methyl coumarin are tested. The photostability of the three dyes is investigated under UV-Vis light exposure. The results show a relatively high stability of the three dyes. Moreover, the photostability of the solid dyes is studied over the TiO2 film electrodes. A very low decolorization rates are recorded as; rate constants k = 1.6, 2.1 and 1.9 × 10-3 min-1 for anthocyanin, RR and coumarin dyes, respectively. The stability results favor selecting anthocyanin as a promising sensitizer candidate in DSSCs based on natural products. Dyes-sensitized solar cells are fabricated and their conversion efficiency (η) is 0.27%, 0.14% and 0.001% for the anthocyanin, RR and coumarin dyes, respectively. Moreover, stability tests of the sealed cells based on anthocyanin and RR dyes are done under continuous light exposure of 100 mW cm-2, reveals highly stable DSSCs.

  7. Photostability of low cost dye-sensitized solar cells based on natural and synthetic dyes.

    Science.gov (United States)

    Abdou, E M; Hafez, H S; Bakir, E; Abdel-Mottaleb, M S A

    2013-11-01

    This paper deals with the use of some natural pigments as well as synthetic dyes to act as sensitizers in dye-sensitized solar cells (DSSCs). Anthocyanin dye extracted from rosella (Hibiscus sabdariffa L.) flowers, the commercially available textile dye Remazole Red RB-133 (RR) and merocyanin-like dye based on 7-methyl coumarin are tested. The photostability of the three dyes is investigated under UV-Vis light exposure. The results show a relatively high stability of the three dyes. Moreover, the photostability of the solid dyes is studied over the TiO2 film electrodes. A very low decolorization rates are recorded as; rate constants k=1.6, 2.1 and 1.9×10(-3)min(-1) for anthocyanin, RR and coumarin dyes, respectively. The stability results favor selecting anthocyanin as a promising sensitizer candidate in DSSCs based on natural products. Dyes-sensitized solar cells are fabricated and their conversion efficiency (η) is 0.27%, 0.14% and 0.001% for the anthocyanin, RR and coumarin dyes, respectively. Moreover, stability tests of the sealed cells based on anthocyanin and RR dyes are done under continuous light exposure of 100mWcm(-2), reveals highly stable DSSCs.

  8. COMPARATIVE STUDY OF DYEING EFFICIENCY AND RETENTION CAPACITY OF HERBAL HAIR DYES

    Directory of Open Access Journals (Sweden)

    Pingle R.P

    2013-04-01

    Full Text Available In the present investigation, attempts were made to make a powder herbal hair dye that gives dark brown to black colour to hair, resembling natural hair colour with better dyeing effect and greater retention capacity on comparison with marketed herbal hair dye formulation. Most of the marketed herbal hair dye formulations contain para-phenylenediamine at 20-25% concentrations which is the main ingredient of commercial synthetic dyes. It is known to trigger allergic skin reactions in many people. Ayurvedic powder hair dye devoid of any synthetic agent was prepared in present research work and evaluated for dyeing efficiency. Different combinations of powdered leaves, fruits of plants like Madayantika, Bhringraj, Amla and Nilini were evaluated as hair dyes. The polyherbal hair dye compositions containing large proportion of Nili, Mehendi and 5% Bhringraj and Amla, blended with 5% loha bhasma were prepared and evaluated for physicochemical parameters like particle size, colour, pH, angle of repose and bulk density. Ayurvedic polyherbal powder hair dye of present investigation is semi-permanent in nature and exhibit better dyeing efficiency than marketed herbal hair dye.

  9. Estimation of Fluorescent Dye Amount in Tracer Dye Test

    Science.gov (United States)

    Pekkan, Emrah; Balkan, Erman; Balkan, Emir

    2015-04-01

    Karstic groundwater is more influenced by human than the groundwater that disperse in pores. On the other hand karstic groundwater resources, in addition to providing agricultural needs, livestock breeding, drinking and domestic water in most of the months of the year, they also supply drinking water to the wild life at high altitudes. Therefore sustainability and hydrogeological investigation of karstic resources is critical. Tracing techniques are widely used in hydrologic and hydrogeologic studies to determine water storage, flow rate, direction and protection area of groundwater resources. Karanfil Mountain (2800 m), located in Adana, Turkey, is one of the karstic recharge areas of the natural springs spread around its periphery. During explorations of the caves of Karanfil mountain, a 600 m deep cave was found by the Turkish and Polish cavers. At the bottom of the cave there is an underground river with a flow rate of approximately 0.5 m3/s during August 2014. The main spring is located 8 km far from the cave's entrance and its mean flow rate changes between 3.4 m3/s and 0.21 m3/s in March and September respectively according to a flowrate observation station of Directorate of Water Works of Turkey. As such frequent storms, snowmelt and normal seasonal variations in rainfall have a significant and rapid effect on the volume of this main spring resource. The objective of our research is to determine and estimate dye amount before its application on the field inspired from the previously literature on the subject. This estimation is intended to provide a preliminary application of a tracer test of a karstic system. In this study dye injection, inlet point will be an underground river located inside the cave and the observation station will be the spring that is approximately 8 km far from the cave entrance. On the other hand there is 600 meter elevation difference between cave entrance and outlet spring. In this test Rodamin-WT will be used as tracer and the

  10. Dye lasers. Citations from the NTIS data base

    Science.gov (United States)

    Cavagnaro, D. M.

    1980-08-01

    Studies on dye laser theory, design, components, optical systems, and frequency range are presented in approximately 96 citations. Abstracts on lasing dyes, pumping, tuning, excitation, molecular structure, and modulation are included. Studies on dye laser use in spectroscopy are covered.

  11. Studies of 2-azaazulenium derivatives - 3: The nature of electron transitions and spectral properties of styryl dyes containing terminal groups of different types

    Science.gov (United States)

    Bricks, Julia L.; Stanova, Alona V.; Ryabitsky, Aleksey B.; Yashchuk, Valeriy M.; Kachkovsky, Aleksey D.

    2013-02-01

    This paper presents the results of a quantum-chemical study of the molecular geometry and electron structure as well as spectral measurements of absorption and 13C NMR spectra of dimethylaminostyryls, methoxystyryls, and methylstyryls bearing 2-azaazlenium (AA) moiety in comparison with analogous dyes containing 2-benzimidazolim and 4-pyrylium residues. Based on the analysis of both calculations and experimental data, it was concluded that these types of extremely unsymmetrical cyanines differ between each other only slightly in the ground state with respect to the charge distribution and molecular geometry while their spectral properties reveal a considerable difference between dimethylaminostyryls and methoxystyryls due to the lowest disposition of the lone electron pair level of the oxygen atom and hence, limiting basicity of the p-methoxyphenylene residue. It was shown that appearance of a high-positioned local level generated by AA terminal group caused the inversion of the delocalized and quasi-local electron transitions in AA-methoxystyryl and hence drastic changes in its absorption spectrum.

  12. Preparation and Dyeing Performance of a Novel Crosslinking Polymeric Dye Containing Flavone Moiety

    Institute of Scientific and Technical Information of China (English)

    TANG Lijun; TANG Bingtao; ZHANG Shufen

    2011-01-01

    A yellow crosslinking polymeric dye was prepared by grafting the flavone moiety containing azo chromophore onto polyvinylamine backbone.The λ max of this polymeric dye in water is 382 nm.The polymeric dye is fixed to silk and cotton with a crosslinking agent,2-chloro-4,6-di(aminobenzene-4'-β-sulphatoethylsulphone)-1,3,5-s-triazine,which acts as a bridge between the fiber and dye molecules.The fixation of this polymeric dye reaches 99% and the dyed samples exhibit excellent rubbing and washing fastness.

  13. Synthesis of monoazo disperse dyes based on 2-aminoheterocycles and their dyeing performance on nylon fabrics

    Directory of Open Access Journals (Sweden)

    VITHAL SOMA PATEL

    2000-11-01

    Full Text Available Novel monoazo disperse dyes based on various 2-aminoheterocycles were prepared using N-methyl-N-(2-hydroxyethylaniline as the coupling component. All the dyes were applied as disperse dyes on nylon fabric. These dyes have been found to give a wide range of colour shades with very good depth, brightness and levelness on nylon fabric. The visible absorption spectra, elemental analysis and Rf values were investigated. The percentage dye bath exhaustion on fabric was found to be very good. The dyed fabric showed very good to excellent fastness to light, washing, rubbing and perspiration. The sublimation fastness was found to be excellent.

  14. Incorporating Multiple Energy Relay Dyes in Liquid Dye-Sensitized Solar Cells

    KAUST Repository

    Yum, Jun-Ho

    2011-01-05

    Panchromatic response is essential to increase the light-harvesting efficiency in solar conversion systems. Herein we show increased light harvesting from using multiple energy relay dyes inside dye-sensitized solar cells. Additional photoresponse from 400-590 nm matching the optical window of the zinc phthalocyanine sensitizer was observed due to Förster resonance energy transfer (FRET) from the two energy relay dyes to the sensitizing dye. The complementary absorption spectra of the energy relay dyes and high excitation transfer efficiencies result in a 35% increase in photovoltaic performance. © 2011 Wiley-VCH Verlag GmbH& Co. KGaA.

  15. Dye Sensitized Solar Cell, DSSC

    Directory of Open Access Journals (Sweden)

    Pongsatorn Amornpitoksuk

    2003-07-01

    Full Text Available A dye sensitized solar cell is a new type of solar cell. The operating system of this solar cell type is similar to plant’s photosynthesis process. The sensitizer is available for absorption light and transfer electrons to nanocrystalline metal oxide semiconductor. The ruthenium(II complexes with polypyridyl ligands are usually used as the sensitizers in solar cell. At the present time, the complex of [Ru(2,2',2'’-(COOH3- terpy(NCS3] is the most efficient sensitizer. The total photon to current conversion efficiency was approximately 10% at AM = 1.5.

  16. Low Temperature Dyeing of Cashmere Fibers and Products

    Institute of Scientific and Technical Information of China (English)

    SUI Shu-ying; ZHU Ping; CHEN Guo-hua; LI Ru-qin

    2005-01-01

    A special designed multi-functional dyeing auxiliary, SFR503, is adopted in mordant dyeing process for cashmere fibers, sliver and fabric. The results of decreasing dyeing temperature, shortening the dyeing period, reducing the fiber damage and improved quality of the cashmere have been obtained. The percentage of dyeing exhaustion and color fastness of final products were further improved in this regards. A suggested technique, bath ratio, dyeing process curve and dye recipe were raised in the paper. SFR-503s swelling, wetting, leveling, brightening effect for cashmere during dyeing process were discussed.

  17. Characteristics of dye Rhoeo spathacea in dye sensitizer solar cell (DSSC)

    Science.gov (United States)

    Sumardiasih, Sri; Obina, Wilfrida M.; Cari; Supriyanto, Agus; Septiawan, Trio Y.; Khairuddin

    2017-01-01

    Dye-sensitized solar cell (DSSC) is a device that converts solar energy into electrical energy. The magnitude of the efficiency of DSSC is mainly based on the amount of dye absorbed by the surface of TiO2. In this work, used natural dye extracted from leaves Rhoeo spathacea. The dye partially used to immerse of TiO2 as working electrodes, and the rest are directly mixed TiO2 paste to obtain dye titanium dioxide.The paste TiO2 and dye titanium dioxide coated onto the fluorine-doped tin oxide (FTO) glass plate by spin coating method. The absorbance spectra of the dye, dye titanium dioxide and TiO2 were obtained by UV-Vis spectroscopy. The conductivity of the dye, dye titanium dioxide, and TiO2 was measured by two point probe El-Kahfi 100. The DSSC based on dye titanium dioxide that stirring for 5 hours the highest efficiency of 0,0520 % whereas those based on TiO2 immersed for 36 hours showed achieved 0,0501 % obtained from I-V characterization.

  18. The Influence of Cationization on the Dyeing Performance of Cotton Fabrics with Direct Dyes

    Directory of Open Access Journals (Sweden)

    M. F. Shahin

    2015-08-01

    Full Text Available The effect of cationic modification of cotton fabrics, using cationic agent (Chromatech 9414 on direct dyeing characteristics was studied in this work. Cationization of cotton fabric at different conditions (pH, cationic agent concentration, temperature and time was investigated and the optimum conditions were determined . Nitrogen content of cotton samples pretreated with cationic agent was indicated. The results showed that increasing cationic agent concentration lead to higher nitrogen content on cotton fabric . The cationized cotton fabrics were dyed with two direct dyes (C.I. Direct Yellow 142 - C.I. Direct red 224 and the results were compared to untreated cotton fabrics. The parameters which may affect the dyeing process such as dye concn., addition of salt, time and temperature of dyeing were studied. The dyeing results illustrate that cationization improves the fabric dyeability compared to the uncationized cotton and the magnitude of increase in colour depth depends on the nitrogen content of the cationized cotton fabric .The results also refer to possibility of dyeing cationized cotton fabric with direct dyes without addition of electrolytes to give colour strength higher than that achieved on uncationized cotton using conventional dyeing method .Another important advantage of cationic treatment is in the saving of dye concn., energy ,dyeing time , rinse water and subsequently saving of waste water treatment , and finally minimizes the environmental pollution . The changes in surface morphology of fibres after cationization were identified by various methods such as wettability and scanning with the electron microscope. Different fastness properties were evaluated.

  19. Steric and Solvent Effect in Dye-Sensitized Solar Cells Utilizing Phenothiazine-Based Dyes

    Directory of Open Access Journals (Sweden)

    Hany Kafafy

    2014-01-01

    Full Text Available Three phenothiazine-based dyes have been prepared and utilized as dye-sensitized solar cells (DSSCs. The effects of dye-adsorption solvent on the performances of dye-sensitized solar cells based on phenothiazine dyes were investigated in this study. The highest conversion efficiency of 3.78% was obtained using ethanol (EtOH and 2.53% for tetrahydrofuran (THF, respectively, as dye-adsorption solvents. Cell performance using EtOH as a dye-adsorption solvent showed relatively higher performance than that using THF. Electrochemical and photochemical tests of phenothiazine dyes in solution and adsorbed on the TiO2 surface showed less dye loading and coverage on the TiO2 surface during adsorption in the case of THF, which decreased the solar cell performance of the DSSC using THF as adsorption solvent compared with using EtOH as adsorption solvent. Meanwhile, the steric effect of phenothiazine-based (PT1–3 dyes was also investigated. Dye with longer and branched aliphatic chain in the order of PT1, PT2, and PT3 showed an increased resistance of the recombination reaction and electron lifetime, thereby increasing Voc and enhancing the overall cell performance because of the sterically hindered conformation of the phenothiazines.

  20. Characterization of Natural Dye Extracted from Wormwood and Purple Cabbage for Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Ho Chang

    2013-01-01

    Full Text Available This study used natural dyes as sensitizers of dye-sensitized solar cells (DSSCs to replace expensive chemical synthetic dyes. We prepared two natural dyes, chlorophyll dye and anthocyanin dye, by extracting them from wormwood and purple cabbage, respectively. Moreover, we mixed the prepared chlorophyll dye and anthocyanin dye at 5 different volume ratios to form cocktail dyes. For preparation of photoelectrode, P25 TiO2 nanoparticles were used to prepare paste, which was coated on fluorine-doped tin oxide (FTO conductive glass by the spin coating method at different spin coating speeds in order to form TiO2 thin films with different thicknesses. The DSSC prepared by the cocktail dye achieves photoelectric conversion efficiency (η of 1.95%, open-circuit voltage (VOC of 0.765 V, and short-circuit current density (JSC of 5.83 mA/cm2. Moreover, the prepared DSSC sensitized solely by chlorophyll extract of wormwood achieved a photoelectric conversion efficiency (η of 0.9%, whereas the DSSC sensitized solely by anthocyanin extract of purple cabbage achieved a photoelectric conversion efficiency of 1.47%, achieving the longest lifetime of electrons amongst these three dyes.

  1. Hairdressers' skin exposure to hair dyes during different hair dyeing tasks.

    Science.gov (United States)

    Lind, Marie-Louise; Johnsson, Stina; Lidén, Carola; Meding, Birgitta; Boman, Anders

    2017-08-09

    The high risk of occupational skin disease among hairdressers, caused by skin exposure to irritants and sensitizers, such as hair dye substances, is of great concern. The aim of the present study was to assess how the various tasks involved in hair dyeing contribute to hairdressers' exposure to hair dye, in order to enable the formulation of well-founded recommendations on working routines that will reduce exposure and prevent occupational disease. Skin exposure to hair dye was measured for 20 hairdressers applying highlights and all-over hair colour with the hand rinsing technique. Resorcinol was used as a proxy for hair dye exposure. Applying hair dye and cutting the newly dyed hair were the tasks that contributed most to exposure in treatments for highlights. After cutting all-over-coloured hair, all hairdressers had measurable amounts of hair dyes on both hands. Hairdressers are exposed to hair dye ingredients during all steps of the hair dyeing procedure. Cutting newly dyed hair contributes significantly to exposure. As initial steps for the prevention of occupational disease resulting from hair dye exposure, we suggest cutting hair before dyeing it, and wearing gloves during all other work tasks. © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

  2. High Excitation Transfer Efficiency from Energy Relay Dyes in Dye-Sensitized Solar Cells

    KAUST Repository

    Hardin, Brian E.

    2010-08-11

    The energy relay dye, 4-(Dicyanomethylene)-2-methyl-6-(4- dimethylaminostyryl)-4H-pyran (DCM), was used with a near-infrared sensitizing dye, TT1, to increase the overall power conversion efficiency of a dye-sensitized solar cell (DSC) from 3.5% to 4.5%. The unattached DCM dyes exhibit an average excitation transfer efficiency (EÌ?TE) of 96% inside TT1-covered, mesostructured TiO2 films. Further performance increases were limited by the solubility of DCM in an acetonitrile based electrolyte. This demonstration shows that energy relay dyes can be efficiently implemented in optimized dye-sensitized solar cells, but also highlights the need to design highly soluble energy relay dyes with high molar extinction coefficients. © 2010 American Chemical Society.

  3. Study on Application of Natural Plant Dye Gardenia on Cotton Coloration and the Dyeing Mechanism

    Institute of Scientific and Technical Information of China (English)

    ZHOU Lan; SHAO Jian-zhong

    2006-01-01

    Based on the analysis of the structure and properties of gardenia, the gardenia was extracted in neutral bath. The mordant dyeing of cotton, including pre-mordant, one-bath and post-mordant were studied, and the dyeing properties such as dye K/S value and color fastness were investigated.According to the structure and property of mordants including alum, copper sulfate, iron sulfate and rare earth,the interaction mechanisms among gardenia, mordant and cotton fibers were analyzed and the processing factors affecting the mordant dyeing were discussed. As a result,gardenia showed favorable dyeing performance on cotton.The soaping color fastness and crocking fastness were improved by 0.5 - 1 grade after fixation process with the selected dye-fixing agent and optimized process conditions.The dyeing process and fixation process were optimized.

  4. Eco-Friendly Dyeing of Cotton with Indigo Dye By Electrochemical Method

    Science.gov (United States)

    Prabu, H. Gurumallesh; Sarala, K.; Babu, S. Ananda; Savitha, K. U.

    2011-07-01

    Eco-friendly dyeing of cotton was performed in two step process; (i) enzymatic pre-treatment of grey cotton fabric and (ii) Electrochemical dyeing of the pre-treated cotton fabric with indigo. The enzymatic pre-treatment was done in three methods; (i) amylase treatment only, (ii) amylase and hydrogen peroxide treatment and (iii) single bath method. The dyeing was carried out with the pre-treated cotton fabric. The reduction of indigo dye by electrochemical method was initiated by applying potential. Then the dyeing was carried out different concentrations of dye, glucose and NaOH. Conventional method of dyeing was also carried out and compared with the electrochemical method. Dyeability was measured by computer colour matching (CCM) GretagMacbeth colour eye 2180UV instrument.

  5. Dyeing of UV irradiated cotton and polyester fabrics with multifunctional reactive and disperse dyes

    Directory of Open Access Journals (Sweden)

    Ijaz Ahmad Bhatti

    2016-03-01

    Full Text Available The dyeing behaviour of UV irradiated cotton and polyester fabrics using multifunctional reactive and disperse dyes has been investigated. The plain, woven, mercerized, bleached, cotton and polyester fabrics were exposed to UV radiation (180 w, 254 nm for 30, 60, 90 and 120 min. Dyeing was performed using irradiated fabric with a dye solution of un-irradiated reactive and disperse/azo dyes. The dyeing parameters such as, temperature, time, pH and salt concentration have been optimized. The colour strength values of dyed fabrics were evaluated by comparing irradiated and un-irradiated cotton and polyester fabrics in CIE Lab systems using spectra flash SF600. Finally ISO standard methods were employed to observe the effect of UV radiation on fastness properties. It was found that UV radiation has a potential to improve the colour strength values of cotton and polyester fabrics by using reactive and disperse dyes.

  6. Dyeing behaviour of gamma irradiated cotton fabric using Lawson dye extracted from henna leaves (Lawsonia inermis)

    Science.gov (United States)

    Rehman, Fazal-ur; Adeel, Shahid; Qaiser, Summia; Ahmad Bhatti, Ijaz; Shahid, Muhammad; Zuber, Mohammad

    2012-11-01

    Dyeing behavior of gamma irradiated cotton fabric using Lawson dye extracted from henna leaves has been investigated. Cotton and dye powder are irradiated to different absorbed doses of 2, 4, 6, 8 and 10 kGy using Cs-137 gamma irradiator. The dyeing parameters such as dyeing time, electrolyte (salt) concentration and mordant concentrations using copper and iron as mordants are optimized. Dyeing is performed using un-irradiated and irradiated cotton with dye solutions and their color strength values are evaluated in CIE Lab system using Spectraflash -SF650. Methods suggested by International Standard Organization (ISO) have been employed to investigate the colourfastness properties such as colourfastness to light, washing and rubbing of irradiated dyed fabric. It is found that gamma ray treatment of cotton dyed with extracts of henna leaves has significantly improved the color strength as well as enhanced the rating of fastness properties.

  7. Adsorption of dyes on Sahara desert sand.

    Science.gov (United States)

    Varlikli, Canan; Bekiari, Vlasoula; Kus, Mahmut; Boduroglu, Numan; Oner, Ilker; Lianos, Panagiotis; Lyberatos, Gerasimos; Icli, Siddik

    2009-10-15

    Sahara desert sand (SaDeS) was employed as a mineral sorbent for retaining organic dyes from aqueous solutions. Natural sand has demonstrated a strong affinity for organic dyes but significantly lost its adsorption capacity when it was washed with water. Therefore, characterization of both natural and water washed sand was performed by XRD, BET, SEM and FTIR techniques. It was found that water-soluble kyanite, which is detected in natural sand, is the dominant factor affecting adsorbance of cationic dyes. The sand adsorbs over 75% of cationic dyes but less than 21% for anionic ones. Among the dyes studied, Methylene Blue (MB) demonstrated the strongest affinity for Sahara desert sand (Q(e)=11.98 mg/g, for initial dye solution concentration 3.5 x 10(-5)mol/L). The effects of initial dye concentration, the amount of the adsorbent, the temperature and the pH of the solution on adsorption capacity were tested by using Methylene Blue as model dye. Pseudo-first-order, pseudo-second-order and intraparticle diffusion models were applied. It was concluded that adsorption of Methylene Blue on Sahara desert sand followed pseudo-second order kinetics. Gibbs free energy, enthalpy change and entropy change were calculated and found -6411 J/mol, -30360 J/mol and -76.58 J/mol K, respectively. These values indicate that the adsorption is an exothermic process and has a spontaneous nature at low temperatures.

  8. Hair Dye Poisoning in a Paediatric Patient

    Directory of Open Access Journals (Sweden)

    Jolly Chandran

    2012-01-01

    Full Text Available Hair dye ingestion with suicidal intention has increased among rural Indian population and is associated with significant mortality. We report a teenager who presented with cervicofacial edema, respiratory distress, rhabdomyolysis, and myocarditis after ingesting the hair dye Super Vasmol 33. Early and supportive treatment can prevent morbidity and mortality.

  9. Supramolecular assemblies based on glycoconjugated dyes

    NARCIS (Netherlands)

    Schmidt, Bettina

    2016-01-01

    Supramolecular assemblies of glycoconjugated dyes can be tailored with properties that make them attractive for use in biomedical applications. For example, when assemblies of glycoconjugated dyes are displaying carbohydrates on their periphery in a polyvalent manner, these assemblies can be used to

  10. Use of slag for dye removal

    Energy Technology Data Exchange (ETDEWEB)

    Ramakrishna, K.R.; Viraraghavan, T. [Univ. of Regina, Saskatchewan (Canada). Faculty of Engineering

    1998-09-01

    Adsorption techniques employing activated carbon have been found to be reasonably effective in the removal of some of the ionic impurities in water. However, economic considerations may require the use of inexpensive sorbents which are either naturally available or available as waste products from manufacturing processes. Slag is one such waste product obtained during the manufacture of steel, and the present study investigates dye removal characteristics of slag from colored waters. Aqueous solutions prepared from commercial grade acid, basic, and disperse dyes were used in this study, and batch pH, kinetic, and isotherm studies were undertaken on a laboratory scale. The data were evaluated for applicability to the Langmuir, Freundlich, and BET isotherm models, and the removal capacity of slag was compared with that of granular activated carbon. Results indicated approximately 94% removal of the disperse dye by slag, compared with a removal of approximately 49% achieved by activated carbon. Removal of acid dyes (dyes containing anionic groups) was reasonably good (approximately 47 and 74%), though not as good as obtained using activated carbon (approximately 100%). Column studies were conducted with a disperse dye (nonionic, slightly soluble in water), and analysis of data showed a sorption capacity of 1.3 mg of disperse dye per gram of slag. However, effluent dye concentrations were found to be higher than the permissible levels for discharge to receiving waters.

  11. Degradation of anthraquinone dyes by ozone

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The decolorization of three kinds of anthraquinone dyes by ozone was investigated and the residues in the degradation solution were analyzed. The results indicate that the decolorizing effects are obvious with the decolorization efficiency of dyes all above 96% in 40 min. The pH value and TOC concentration decline while the conductivity increases with the lapse of reaction time.The complicated dye molecules are decomposed to simple compounds with -SO3H, -Cl in the dye molecules transformed into SO4 2-, Cl-, and nitrogen partially degrades into NO3- according to the bases of different groups. The organic acids are found in the degradation solutions and dyes with larger relative molecular mass are decomposed into substances with larger relative molecular mass.

  12. Molecular engineering of simple phenothiazine-based dyes to modulate dye aggregation, charge recombination, and dye regeneration in highly efficient dye-sensitized solar cells.

    Science.gov (United States)

    Hua, Yong; Chang, Shuai; He, Jian; Zhang, Caishun; Zhao, Jianzhang; Chen, Tao; Wong, Wai-Yeung; Wong, Wai-Kwok; Zhu, Xunjin

    2014-05-19

    A series of simple phenothiazine-based dyes, namely, TP, EP, TTP, ETP, and EEP have been developed, in which the thiophene (T), ethylenedioxythiophene (E), their dimers, and mixtures are present to modulate dye aggregation, charge recombination, and dye regeneration for highly efficient dye-sensitized solar cell (DSSC) applications. Devices sensitized by the dyes TP and TTP display high power conversion efficiencies (PCEs) of 8.07 (Jsc = 15.2 mA cm(-2), Voc =0.783 V, fill factor (FF) = 0.679) and 7.87 % (Jsc = 16.1 mA cm(-2), Voc = 0.717 V, FF = 0.681), respectively; these were measured under simulated AM 1.5 sunlight in conjunction with the I(-)/I3(-) redox couple. By replacing the T group with the E unit, EP-based DSSCs had a slightly lower PCE of 7.98 % with a higher short-circuit photocurrent (Jsc) of 16.7 mA cm(-2). The dye ETP, with a mixture of E and T, had an even lower PCE of 5.62 %. Specifically, the cell based on the dye EEP, with a dimer of E, had inferior Jsc and Voc values and corresponded to the lowest PCE of 2.24 %. The results indicate that the photovoltaic performance can be finely modulated through structural engineering of the dyes. The selection of T analogues as donors can not only modulate light absorption and energy levels, but also have an impact on dye aggregation and interfacial charge recombination of electrons at the interface of titania, electrolytes, and/or oxidized dye molecules; this was demonstrated through DFT calculations, electrochemical impedance analysis, and transient photovoltage studies.

  13. Detection of live circulating tumor cells by a class of near-infrared heptamethine carbocyanine dyes in patients with localized and metastatic prostate cancer.

    Science.gov (United States)

    Shao, Chen; Liao, Chun-Peng; Hu, Peizhen; Chu, Chia-Yi; Zhang, Lei; Bui, Matthew H T; Ng, Christopher S; Josephson, David Y; Knudsen, Beatrice; Tighiouart, Mourad; Kim, Hyung L; Zhau, Haiyen E; Chung, Leland W K; Wang, Ruoxiang; Posadas, Edwin M

    2014-01-01

    Tumor cells are inherently heterogeneous and often exhibit diminished adhesion, resulting in the shedding of tumor cells into the circulation to form circulating tumor cells (CTCs). A fraction of these are live CTCs with potential of metastatic colonization whereas others are at various stages of apoptosis making them likely to be less relevant to understanding the disease. Isolation and characterization of live CTCs may augment information yielded by standard enumeration to help physicians to more accurately establish diagnosis, choose therapy, monitor response, and provide prognosis. We previously reported on a group of near-infrared (NIR) heptamethine carbocyanine dyes that are specifically and actively transported into live cancer cells. In this study, this viable tumor cell-specific behavior was utilized to detect live CTCs in prostate cancer patients. Peripheral blood mononuclear cells (PBMCs) from 40 patients with localized prostate cancer together with 5 patients with metastatic disease were stained with IR-783, the prototype heptamethine cyanine dye. Stained cells were subjected to flow cytometric analysis to identify live (NIR(+)) CTCs from the pool of total CTCs, which were identified by EpCAM staining. In patients with localized tumor, live CTC counts corresponded with total CTC numbers. Higher live CTC counts were seen in patients with larger tumors and those with more aggressive pathologic features including positive margins and/or lymph node invasion. Even higher CTC numbers (live and total) were detected in patients with metastatic disease. Live CTC counts declined when patients were receiving effective treatments, and conversely the counts tended to rise at the time of disease progression. Our study demonstrates the feasibility of applying of this staining technique to identify live CTCs, creating an opportunity for further molecular interrogation of a more biologically relevant CTC population.

  14. Detection of live circulating tumor cells by a class of near-infrared heptamethine carbocyanine dyes in patients with localized and metastatic prostate cancer.

    Directory of Open Access Journals (Sweden)

    Chen Shao

    Full Text Available Tumor cells are inherently heterogeneous and often exhibit diminished adhesion, resulting in the shedding of tumor cells into the circulation to form circulating tumor cells (CTCs. A fraction of these are live CTCs with potential of metastatic colonization whereas others are at various stages of apoptosis making them likely to be less relevant to understanding the disease. Isolation and characterization of live CTCs may augment information yielded by standard enumeration to help physicians to more accurately establish diagnosis, choose therapy, monitor response, and provide prognosis. We previously reported on a group of near-infrared (NIR heptamethine carbocyanine dyes that are specifically and actively transported into live cancer cells. In this study, this viable tumor cell-specific behavior was utilized to detect live CTCs in prostate cancer patients. Peripheral blood mononuclear cells (PBMCs from 40 patients with localized prostate cancer together with 5 patients with metastatic disease were stained with IR-783, the prototype heptamethine cyanine dye. Stained cells were subjected to flow cytometric analysis to identify live (NIR(+ CTCs from the pool of total CTCs, which were identified by EpCAM staining. In patients with localized tumor, live CTC counts corresponded with total CTC numbers. Higher live CTC counts were seen in patients with larger tumors and those with more aggressive pathologic features including positive margins and/or lymph node invasion. Even higher CTC numbers (live and total were detected in patients with metastatic disease. Live CTC counts declined when patients were receiving effective treatments, and conversely the counts tended to rise at the time of disease progression. Our study demonstrates the feasibility of applying of this staining technique to identify live CTCs, creating an opportunity for further molecular interrogation of a more biologically relevant CTC population.

  15. Photophysical and electrochemical properties, and molecular structures of organic dyes for dye-sensitized solar cells.

    Science.gov (United States)

    Ooyama, Yousuke; Harima, Yutaka

    2012-12-21

    Dye-sensitized solar cells (DSSCs) based on organic dyes adsorbed on oxide semiconductor electrodes, such as TiO(2), ZnO, or NiO, which have emerged as a new generation of sustainable photovoltaic devices, have attracted much attention from chemists, physicists, and engineers because of enormous scientific interest in not only their construction and operational principles, but also in their high incident-solar-light-to-electricity conversion efficiency and low cost of production. To develop high-performance DSSCs, it is important to create efficient organic dye sensitizers, which should be optimized for the photophysical and electrochemical properties of the dyes themselves, with molecular structures that provide good light-harvesting features, good electron communication between the dye and semiconductor electrode and between the dye and electrolyte, and to control the molecular orientation and arrangement of the dyes on a semiconductor surface. The aim of this Review is not to make a list of a number of organic dye sensitizers developed so far, but to provide a new direction in the epoch-making molecular design of organic dyes for high photovoltaic performance and long-term stability of DSSCs, based on the accumulated knowledge of their photophysical and electrochemical properties, and molecular structures of the organic dye sensitizers developed so far.

  16. Molecularly imprinted polymers for some reactive dyes.

    Science.gov (United States)

    Okutucu, Burcu; Akkaya, Alper; Pazarlioglu, Nurdan Kasikara

    2010-01-01

    Depending upon their structure, azo- and anthraquinonic dyes are the two major classes and together represent 90% of all organic colorants. Adsorption of dye molecules onto a sorbent can be an effective, low-cost method of color removal. Most of the techniques used for removal of dyes are of high production cost, and the regeneration also makes them uneconomical. There is much interest in the development of cheaper and effective newer materials for use as adsorbents. Molecular imprinting is a new kind of materials that can be alternative adsorbents. In this study, molecularly imprinted polymers of three textile dyes (Cibacron Orange P-4R, Cibacron Red P-4B, Cibacron Black PSG) were prepared. Methacrylic acid was used as a monomer for red and orange dyes and acrylamide was used for black dye. Methanol:acetonitrile was used as a porogen. The selective recognition ability of the molecularly imprinted polymers was studied by an equilibrium-adsorption batch method. The adsorption data are for Cibacron Black PSG 65% and nonimprinted polymer (NIP) 25%; Cibacron Red P-4B 72% and NIP 18%; and Cibacron Orange P-4R 45% and NIP 10%, respectively. Dye-imprinted polymers were used as a solid-phase extraction material for selective adsorption from wastewater of textile factory.

  17. Dye sequestration using agricultural wastes as adsorbents

    Directory of Open Access Journals (Sweden)

    Kayode Adesina Adegoke

    2015-12-01

    Full Text Available Color is a visible pollutant and the presence of even minute amounts of coloring substance makes it undesirable due to its appearance. The removal of color from dye-bearing effluents is a major problem due to the difficulty in treating such wastewaters by conventional treatment methods. The most commonly used methods for color removal are biological oxidation and chemical precipitation. However, these processes are effective and economic only in the case where the solute concentrations are relatively high. Most industries use dyes and pigments to color their products. The presence of dyes in effluents is a major concern due to its adverse effect on various forms of life. The discharge of dyes in the environment is a matter of concern for both toxicological and esthetical reasons. It is evident from a literature survey of about 283 recently published papers that low-cost adsorbents have demonstrated outstanding removal capabilities for dye removal and the optimal equilibrium time of various dyes with different charcoal adsorbents from agricultural residues is between 4 and 5 h. Maximum adsorptions of acidic dyes were obtained from the solutions with pH 8–10. The challenges and future prospects are discussed to provide a better framework for a safer and cleaner environment.

  18. Advanced oxidation of acid and reactive dyes

    DEFF Research Database (Denmark)

    Arslan-Alaton, I.; Gursoy, B.H.; Schmidt, Jens Ejbye

    2008-01-01

    M) for 10:hsp sp="0.25" min Fenton treatment at pH 3, resulting in reduced chemical oxygen demand and dissolved organic carbon removal efficiencies; only acetate was detected as a stable dye oxidation end product. During anaerobic digestion, 100, 29% and no inhibition in methane production was observed...... for the untreated blue, red and orange dyes, respectively. The inhibitory effect of the blue reactive dye on methane production was ∼21% after Fenton treatment. Neither untreated nor treated dyes exhibited an inhibitory effect on denitrification. Aerobic glucose degradation was inhibited by 23-29% by untreated dyes......The effect of untreated and Fenton-treated acid dyes (C.I. Acid Red 183 and C.I. Acid Orange 51) and a reactive dye (C.I. Reactive Blue 4) on aerobic, anoxic and anaerobic processes was investigated. The optimum Fe2+:H2O2 molar ratio was selected as 1:5 (4:hsp sp="0.25" mM:20:hsp sp="0.25"m...

  19. Evaluation of bimetal doped TiO{sub 2} in dye fragmentation and its comparison to mono-metal doped and bare catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Malika, Manjakuppam; Rao, Ch. Venkatanarasimha; Das, Raj Kumar [Department of Chemical Engineering, Indian Institute of Technology Guwahati, Assam 781 039 (India); Giri, Ardhendu Sekhar [Department of Chemical Engineering, National Institute of Technology Jalandhar, Punjab 144 011 (India); Golder, Animes Kumar, E-mail: animes@iitg.ernet.in [Department of Chemical Engineering, Indian Institute of Technology Guwahati, Assam 781 039 (India)

    2016-04-15

    Graphical abstract: - Highlights: • Bimetal doped TiO{sub 2} showed a higher reduction in band gap than mono-metal doping. • Lower zeta-potential for bimetal doped TiO{sub 2} improved its stability in the aqueous media. • Metal doping increased crystallite sizes and also the anatase phase of doped TiO{sub 2}. • Dye degradation even up to 99% through decarboxylation and sulphonation reactions. - Abstract: There are instances that bimetal doped semiconductor materials impart superior photocatalytic activity than bare and mono-metal doping. In this study, visible light responsive mono- (Cu/TiO{sub 2} and Ni/TiO{sub 2}) and bi-metal doped (Cu–Ni/TiO{sub 2}) TiO{sub 2} photocatalysts with wide band gap energy were synthesized via co-precipitation method with an equal mass ratio of Cu and Ni. The catalyst characterization was performed using Diffuse Reflectance UV–visible (DR-UV–vis) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, X-ray Diffraction (XRD), zeta-potential and Transmission Electron Microscopy (TEM) analyzes. The charge balancing effect of Cu and Ni caused a notable reduction in the optical band gap of TiO{sub 2} to 2.91 eV with Cu–Ni/TiO{sub 2}. The synthesis method increased the anatase phase significantly along with the crystallite size. Cu–Ni/TiO{sub 2} displayed a lesser destabilization tendency, and the absolute value of zeta-potentials increased much at pH > pH{sub zpc} resulted from the higher oxygen vacancies. The activity of Ni/TiO{sub 2}, Cu/TiO{sub 2}, and Cu–Ni/TiO{sub 2} was tested for the degradation dynamics and kinetics of Eriochrome Cyanine Red (ECR), an anionic dye. Cu doping exhibited a better dye decomposition because of the low recombination rate of electron/hole pair as a full 3d sub-level of Cu is energetically more favorable than a full 4s sub-level of Ni. The mechanism of dye decomposition releasing inorganic ions is also proposed and validated from the mass spectra.

  20. Ultrasound energy to accelerate dye uptake and dye-fiber interaction of reactive dye on knitted cotton fabric at low temperatures.

    Science.gov (United States)

    Tissera, Nadeeka D; Wijesena, Ruchira N; de Silva, K M Nalin

    2016-03-01

    Acoustic cavitation formed due to propagation of ultrasound wave inside a dye bath was successfully used to dye cotton fabric with a reactive dye at lower temperatures. The energy input to the system during sonication was 0.7 W/cm(2). This was within the energy range that contributes towards forming cavitation during ultra-sonication. The influence of ultrasound treatment on dye particle size and fiber morphology is discussed. Particle size analysis of the dye bath revealed ultra-sonication energy was capable of de-agglomeration of hydrolyzed dye molecules during dyeing. SEM micrograph and AFM topographical image of the fiber surface revealed fiber morphology remains unchanged after the sonication. The study was extended in understanding the contribution of ultrasound method of dyeing towards achieving good color strength on the fabric, compared to the normal heating method of dyeing. Study showed color strength obtained using ultra sound method of dyeing is higher compared to normal heating dyeing. Ultrasound energy was able to achieve the good color strength on cotton fabric at very low temperature such as 30 °C, which was approximately 230% more than the color strength achieved in normal heating method of dyeing. This indicates that energy input to the system using ultrasound was capable of acting as an effective alternative method of dyeing knitted cotton fabrics with reactive dye.

  1. Dyeing Performance of Soybean Fiber Treated with Low Temperature Plasma

    Institute of Scientific and Technical Information of China (English)

    WANG Li-ming; SHEN Yong; DING Ying; ZHANG Hui-fang

    2006-01-01

    The soybean fiber was treated with low temperature plasma and the dyeing performance of the treated soybean fiber was also researched. The results show that the speed of dyeing and the percentages of balance dyeing have a sharp increase after being treated. So the dyeing temperature and the dosage of acid can be reduced without damaging the bulk fiber structure.

  2. Bleaching and diffusion dynamics in optofluidic dye lasers

    DEFF Research Database (Denmark)

    Gersborg-Hansen, Morten; Balslev, Søren; Mortensen, Asger

    2007-01-01

    The authors have investigated the bleaching dynamics that occur in optofluidic dye lasers where the liquid laser dye in a microfluidic channel is locally bleached due to optical pumping. They find that for microfluidic devices, the dye bleaching may be compensated through diffusion of dye molecules...... pumping devices. ©2007 American Institute of Physics....

  3. Supramolecular hair dyes: a new application of cocrystallization

    DEFF Research Database (Denmark)

    Delori, Amit; Urquhart, Andrew; Oswald, Iain D. H.

    2016-01-01

    The manuscript presents the first report of hair dyes of various colors formed by cocrystallization. Unlike the most popular oxidative hair dye (OHD) products, these dyes are NH3 free and do not require H2O2 as a color developer. The importance of these new hair dyes products is further enhanced...

  4. Contact allergy to common ingredients in hair dyes

    DEFF Research Database (Denmark)

    Søsted, Heidi; Rustemeyer, Thomas; Gonçalo, Margarida

    2013-01-01

    p-Phenylenediamine (PPD) is the primary patch test screening agent for hair dye contact allergy, and approximately 100 different hair dye chemicals are allowed.......p-Phenylenediamine (PPD) is the primary patch test screening agent for hair dye contact allergy, and approximately 100 different hair dye chemicals are allowed....

  5. Production of Textile Reddish Brown Dyes by Fungi

    Directory of Open Access Journals (Sweden)

    Atalla, M. Mabrouk

    2011-01-01

    Full Text Available Eleven fungal strains were tested for their ability to produce brown and reddish brown textile dyes using H-acid (1-naphthol-8-amino-3, 6-disulfonic acid as a dye precursor in the fermentation medium. All tested fungal strains exhibited high ability to produce dyes varying in both dye color (brown to reddish brown and fastness properties to washing, perspiration and UV light. The produced dyes were subjected to further analysis for quantitative determination of dye components for investigation of their inter-relations as well as their role in dye color and stability.

  6. Decolourisation of Red 5 MB dye by microbes isolated from textile dye effluent.

    Science.gov (United States)

    Subashini, P; Hiranmaiyadav, R; Premalatha, M S

    2010-07-01

    One of the major environmental problems is the presence of dye materials in textile wastewater, which need to be removed before releasing into the environment. Some dyes are toxic and carcinogenic in nature. The discharge of the textile effluent into rivers and lakes leads to higher BOD causing threat to aquatic life. Development of efficient dye degradation requires suitable strain and its use under favorable condition to realize the degradation potential. In this study, three microorganisms were isolated from the Red 5 MB dye containing textile wastewater. They were identified and tested for the dye decolourisation provided with different sugars as carbon source. The percentage of dye decolorized by Bacillus subtilis, Aspergillus flavus and Aspergillus fumigatus were found to be about 40%, 75% and 53.8% respectively.

  7. Molecular design of organic dyes based on vinylene hexylthiophene bridge for dye-sensitized solar cells

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Three donor-(π-spacer)-acceptor(D-π-A) organic dyes,containing different groups(triphenylamine,di(p-tolyl)phenylamine,and 9-octylcarbazole moieties) as electron donors,were designed and synthesized.Nanocrystalline TiO2 dye-sensitized solar cells were fabricated by using these dyes.It was found that the variation of electron donors in the D-π-A dyes played an important role in modifying and tuning photophysical properties of organic dyes.Under standard global AM 1.5 solar condition,the DSSC based on the dye D2 showed the best photovoltaic performance:a short-circuit photocurrent density(Jsc) of 13.93 mA/cm2,an open-circuit photovoltage(Voc) of 0.71 V,and a fill factor(FF) of 0.679,corresponding to solar-to-electric power conversion efficiency(η) of 6.72%.

  8. Molecular design of organic dyes based on vinylene hexylthiophene bridge for dye-sensitized solar cells

    Institute of Scientific and Technical Information of China (English)

    LIU DaXi; ZHAO Bin; SHEN Ping; HUANG Hui; LIU LiMing; TAN SongTing

    2009-01-01

    Three donor-(TT-spacer)-acceptor (D-tt-A) organic dyes,containing different groups (triphenylamine,di(p-tolyl)phenylamine,and 9-octylcarbazole moieties) as electron donors,were designed and synthesized. Nanocrystalline TiO2 dye-sensitized solar cells were fabricated by using these dyes. It was found that the variation of electron donors in the D-tt-A dyes played an important role in modifying and tuning photophysical properties of organic dyes. Under standard global AM 1.5 solar condition,the DSSC based on the dye D2 showed the best photovoltaic performance: a short-circuit photocurrent density (Jsc) of 13.93 mA/cm2,an open-circuit photovoltage (Voc) of 0.71 V,and a fill factor (FF) of 0.679,corresponding to solar-to-electric power conversion efficiency (77) of 6.72%.

  9. Dye ingredients and energy conversion efficiency at natural dye sensitized solar cells

    Science.gov (United States)

    Özbay Karakuş, Mücella; Koca, İrfan; Er, Orhan; Çetin, Hidayet

    2017-04-01

    In this work, natural dyes extracted from the same genus but different species flowers were used as sensitizer in Dye Sensitized Solar Cell (DSSC). To clearly show dye ingredients effect on electrical characteristics, the same genus flowers were selected. The dye ingredients were analyzed by Gas Chromatography Mass Spectrometer (GC-MS). The dyes were modified by a procedure that includes refluxing in acetone. All results indicate a relationship between gallic acid quantity in dyes and solar cell efficiency. To gain further insight, the solar cell parameters were obtained by using the single-diode and double-diode models and they were compared to each other. It was observed that the applied process causes a decrease in series resistance. How the modification process and gallic acid affect energy conversion efficiency were argued in detail in the frame of results that were obtained from solar cell models.

  10. Design of NIR Chromenylium-Cyanine Fluorophore Library for "Switch-ON" and Ratiometric Detection of Bio-Active Species In Vivo.

    Science.gov (United States)

    Wei, Yanfen; Cheng, Dan; Ren, Tianbing; Li, Yinhui; Zeng, Zebing; Yuan, Lin

    2016-02-02

    The real-time monitoring of key biospecies in the living systems has received thrusting attention during the past decades. Specifically, fluorescent detection based on near-infrared (NIR) fluorescent probes is highly favorable for live cells, live tissues, and even animal imaging, owing to the substantial merits of the NIR window, such as minimal phototoxicity, deep penetration into tissues, and low autofluorescence background. Nevertheless, developing potent NIR fluorescent probes still poses serious challenges to the chemists because traditional NIR fluorophores are less tunable than visible-wavelength fluorophores. To address this issue, here we report a set of novel NIR hybrid fluorophores, namely, the hybrid chromenylium-cyanine fluorophore (CC-Fluor), in which both the fluorescence intensity and the emission wavelength can be easily adjusted by the conformational changes and substitution groups. Compared to known NIR fluorophores, the new CC-Fluors are substantially advantageous for NIR probe development: (1) CC-Fluors display tunable and moderate Stokes shifts and quantum yields; (2) the fluorophores are stable at physiological conditions after long-term incubation; (3) the absorption maxima of CC-Fluors coincide with the common laser spectral lines in mainstream in vivo imaging systems; (4) most importantly, CC-Fluors can be easily modified to prepare NIR probes targeting various biospecies. To fully demonstrate the practical utility of CC-Fluors, we report two innovative NIR probes, a ratiometric pH probe and a turn-on Hg(2+) probe, both are successfully employed in live animal imaging. Hence, the detailed studies allow us to confirm that CC-Fluors can work as an excellent platform for developing NIR probes for the detection of species in living systems.

  11. Ultrasonic assisted dispersive solid-phase microextraction of Eriochrome Cyanine R from water sample on ultrasonically synthesized lead (II) dioxide nanoparticles loaded on activated carbon: Experimental design methodology.

    Science.gov (United States)

    Bahrani, Sonia; Ghaedi, Mehrorang; Mansoorkhani, Mohammad Javad Khoshnood; Asfaram, Arash; Bazrafshan, Ali Akbar; Purkait, Mihir Kumar

    2017-01-01

    The present research focus on designing an appropriate dispersive solid-phase microextraction (UA-DSPME) for preconcentration and determination of Eriochrome Cyanine R (ECR) in aqueous solutions with aid of sonication using lead (II) dioxide nanoparticles loaded on activated carbon (PbO-NPs-AC). This material was fully identified with XRD and SEM. Influence of pH, amounts of sorbent, type and volume of eluent, and sonication time on response properties were investigated and optimized by central composite design (CCD) combined with surface response methodology using STATISTICA. Among different solvents, dimethyl sulfoxide (DMSO) was selected as an efficient eluent, which its combination by present nanoparticles and application of ultrasound waves led to enhancement in mass transfer. The predicted maximum extraction (100%) under the optimum conditions of the process variables viz. pH 4.5, eluent 200μL, adsorbent dosage 2.5mg and 5min sonication was close to the experimental value (99.50%). at optimum conditions some experimental features like wide 5-2000ngmL(-1) ECR, low detection limit (0.43ngmL(-1), S/N=3:1) and good repeatability and reproducibility (relative standard deviation, <5.5%, n=12) indicate versatility in successful applicability of present method for real sample analysis. Investigation of accuracy by spiking known concentration of ECR over 200-600ngmL(-1) gave mean recoveries from 94.850% to 101.42% under optimal conditions. The procedure was also applied for the pre-concentration and subsequent determination of ECR in tap and waste waters.

  12. Natural Dye Extracted from Vitex negundo as a Potential Alternative to Synthetic Dyes for Dyeing of Silk

    Science.gov (United States)

    Narayana Swamy, Venkataramanappa; Gowda, Kurikempanadoddi Ninge; Sudhakar, Rajagopal

    2016-04-01

    Since the last decade, the application of natural dyes on textile material has been gaining popularity all over the world, possibly because of the increasing awareness of issues concerning the environment, ecology and pollution control. The present paper investigates extraction of natural dye from leaves of the plant Vitex negundo, which is an abundant, cheap, and readily available agricultural by-product. Water extracts from V. negundo was used to dye silk fabrics. Optimum extraction conditions included pH 9, duration 120 min, and temperature 90 °C. Optimum dyeing conditions included dyeing pH 5 and duration of 60 min. Potash alum, tannic and tartaric acid were used as mordants, all of which are benign to human health and the environment. Color strength and color coordinates in terms of L*, a*, b*, C, and h were examined. A range of shades were obtained when fabrics were dyed with different mordants and mordanting techniques. The extracted dye was tested for some of the eco-parameters using atomic absorption spectrophotometry and GC/MS. The test results were compared with set standards to determine the eco-friendliness of natural dye. Their concentrations were found to be lower than the stipulated limits. Dyed samples were tested for antimicrobial activity against gram-positive and gram-negative bacteria. The dyed silk fabrics showed acceptable fastness properties and were also found to possess antibacterial activity. It can be concluded that the abundantly available agricultural by-product V. negundo has great potential to be effectively utilized as a natural dye for silk.

  13. EFFECT OF TEMPERATURE ON THE DYEING OF COTTON FABRIC WITH MONASCUS PURPUREUS DYE

    OpenAIRE

    Tripti Basant*, Shahnaz Jahan

    2016-01-01

    Textile industry is one of the most significant contributor to world economy and a major consumer of dyes. The nature provides rich and diverse source of dyes all the while being environmentally safe,   Nowadays, with the increasing awareness about health, wellness as well as environment among the general populace, there has been a renewed interest in natural sources of pigments for dyes. This is because naturally produced colors are not toxic nor carcinogenic to humans and are more e...

  14. The Removal of Composite Reactive Dye from Dyeing Unit Effluent Using Sewage Sludge Derived Activated Carbon

    OpenAIRE

    REDDY, Sajjala SREEDHAR

    2006-01-01

    Activated carbon was prepared from dried municipal sewage sludge and batch mode adsorption experiments were conducted to study its potential to remove composite reactive dye from dyeing unit effluent. Adsorption parameters for the Langmuir and Freundlich isotherms were determined and the effects of effluent pH, adsorbent dosage, contact time and initial dye concentration were studied. The toxicity characteristic leaching protocol (TCLP) was used to assess the acceptability of sewage ...

  15. Estrogen receptor-targeted optical imaging of breast cancer cells with near-infrared fluorescent dye

    Science.gov (United States)

    Jose, Iven; Deodhar, Kodand; Chiplunkar, Shuba V.; Patkar, Meena

    2010-02-01

    Molecular imaging provides the in vivo characterization of cellular molecular events involved in normal and pathologic processes. With the advent of optical molecular imaging, specific molecules, proteins and genes may be tagged with a luminescent reporter and visualized in small animals. This powerful new tool has pushed in vivo optical imaging to the forefront as it allows for direct determination of drug bio-distribution and uptake kinetics as well as an indicator of biochemical activity and drug efficacy. Although optical imaging encompasses diverse techniques and makes use of various wavelengths of light, a great deal of excitement in molecular research lies in the use of tomographic and fluorescence techniques to image living tissues with near-infrared (NIR) light. Nonionizing, noninvasive near-infrared optical imaging has great potential to become promising alternative for breast cancer detection. Fluorescence spectroscopy studies of human tissue suggest that a variety of lesions show distinct fluorescence spectra compared to those of normal tissue. It has also been shown that exogenous dyes exhibit selective uptake in neoplastic lesions and may offer the best contrast for optical imaging. Use of exogenous agents would provide fluorescent markers, which could serve to detect embedded tumors in the breast. In particular, the ability to monitor the fluorescent yield and lifetime may also enable biochemical specificity if the fluorophore is sensitive to a specific metabolite, such as oxygen. As a first step, we have synthesized and characterized one such NIR fluorescent dye conjugate, which could potentially be used to detect estrogen receptors (ER)[2] . The conjugate was synthesized by ester formation between 17-β estradiol and a hydrophilic derivative of indocyanine green (ICG) cyanine dye, bis-1, 1-(4-sulfobutyl) indotricarbocyanine-5- carboxylic acid, sodium salt. The ester formed was found to have an extra binding ability with the receptor cites as

  16. Data mining with molecular design rules identifies new class of dyes for dye-sensitised solar cells

    NARCIS (Netherlands)

    Cole, Jacqueline M.; Low, Kian Sing; Ozoe, Hiroaki; Stathi, Panagiota; Kitamura, Chitoshi; Kurata, Hiroyuki; Rudolf, Petra; Kawase, Takeshi

    2014-01-01

    A major deficit in suitable dyes is stifling progress in the dye-sensitised solar cell (DSC) industry. Materials discovery strategies have afforded numerous new dyes; yet, corresponding solution-based DSC device performance has little improved upon 11% efficiency, achieved using the N719 dye over tw

  17. Effect of Solvent, Dye-Loading Time, and Dye Choice on the Performance of Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Fahd M. Rajab

    2016-01-01

    Full Text Available Anatase titania films with a thickness of up to 20 μm and deposited over a fluorine-doped tin-oxide substrate are impregnated with ruthenium dyes N-719 and N-749 using Dip and supercritical-fluid methods for the purpose of fabricating dye-sensitized solar cell devices. The dyes are dissolved in different solvent mixtures, including supercritical carbon dioxide, as well as combinations of more traditional solvents including mixtures of acetonitrile, and t-butanol. Analytical studies included thin-film analyzing and scanning electron microscopy to measure titania film thickness and porosity, UV-Vis spectroscopy to quantify dye concentration, and current-voltage device characterizations to assess energy conversion efficiency, as well as open-circuit voltage decay measurements and quantum efficiency to examine electron collection efficiency. A significant result is that using the dye N-749 in a solvent that includes supercritical carbon dioxide leads to energy conversion efficiencies that are higher for devices with a thick 20 μm semiconductor film than for the case of devices with thinner films, including the 10 μm film thickness that is traditionally considered an upper threshold. The supercritical-fluid method for the N-719 dye also enabled shorter impregnation duration than more conventional classical Dip Methods.

  18. Simulation of Na channel inactivation by thiazine dyes

    OpenAIRE

    1982-01-01

    Some dyes of the methylene blue family serve as artificial inactivators of the sodium channels when present inside squid axons at a concentration of approximately 0.1 mM. The dyes restore a semblance of inactivation after normal inactivation has been destroyed by pronase. In fibers that inactivate normally, the dyes hasten the decay of sodium current. Many dye-blocked channels conduct transiently on exit of the dye molecule after repolarization to the holding potential. In contrast, normally ...

  19. USE OF A NATURAL DYE FROM SERRATIA MARCESCENS SUBSPECIES MARCESCENS IN DYEING OF TEXTILE FABRICS

    Directory of Open Access Journals (Sweden)

    Ravindra Adivarekar

    2013-06-01

    Full Text Available A strain of Serratia marcescens subspecies marcescens capable of producing a novel rose red pigment with a mass of 112 Da has been isolated from Mahim Mangroove soil. Studies regarding the growth conditions of bacteria, partial characterization of the produced pigment and use of this rose red pigment to dye natural fabrics has been studied and described. Dyeing of wool, cotton and silk fabrics with this rose red microbial pigment as natural dye indicated that the colour strength values and the dye uptake were high with satisfactory fastness properties of the dyed fabric.

  20. Bioremediation of dyes by fungi isolated from contaminated dye effluent sites for bio-usability.

    Science.gov (United States)

    Rani, Babita; Kumar, Vivek; Singh, Jagvijay; Bisht, Sandeep; Teotia, Priyanku; Sharma, Shivesh; Kela, Ritu

    2014-01-01

    Biodegradation and detoxification of dyes, Malachite green, Nigrosin and Basic fuchsin have been carried out using two fungal isolates Aspergillus niger, and Phanerochaete chrysosporium, isolated from dye effluent soil. Three methods were selected for biodegradation, viz. agar overlay and liquid media methods; stationary and shaking conditions at 25 °C. Aspergillus niger recorded maximum decolorization of the dye Basic fuchsin (81.85%) followed by Nigrosin (77.47%), Malachite green (72.77%) and dye mixture (33.08%) under shaking condition. Whereas, P. chrysosporium recorded decolorization to the maximum with the Nigrosin (90.15%) followed by Basic fuchsin (89.8%), Malachite green (83.25%) and mixture (78.4%). The selected fungal strains performed better under shaking conditions compared to stationary method; moreover the inoculation of fungus also brought the pH of the dye solutions to neutral from acidic. Seed germination bioassay study exhibited that when inoculated dye solutions were used, seed showed germination while uninoculated dyes inhibited germination even after four days of observation. Similarly, microbial growth was also inhibited by uninoculated dyes. The excellent performance of A. niger and P. chrysporium in the biodegradation of textile dyes of different chemical structures suggests and reinforces the potential of these fungi for environmental decontamination.

  1. Synthesis of Plant Phenol-derived Polymeric Dyes for Direct or Mordant-based Hair Dyeing.

    Science.gov (United States)

    Im, Kyung Min; Jeon, Jong-Rok

    2016-12-01

    Effective hair dyeing through in situ incubation of keratin hair with the products of fungal laccase-catalyzed polymerization of plant phenols has been previously demonstrated. However, the dyeing process takes a long time to complete compared to commercial hair-dyeing products. To overcome this bottleneck, pre-synthesized polymeric products of the oxidative reaction of Trametes versicolor laccase on catechin and catechol, either with or without mordant agents (e.g., FeSO4), were here employed to achieve permanent keratin hair dyeing in various colors and shades. The laccase action in acidic sodium acetate buffer led to a deep black coloration after coupling reactions between the plant phenols. The colored dye products were then desalted and concentrated with ultrafiltration. The dyes, with or without mordant agents, caused a significant increase in ΔE values (i.e., color difference value) in gray human hair within 2.5 hours. In addition, different keratin colors and shades were induced depending upon the mordanting and pH changes. The dyed hair also exhibited a strong resistance to detergent treatments, indicating that our methods can give rise to permanent hair dyeing. Overall, our work has provided novel insight into developing eco-friendly hair-dyeing methods as alternatives to commercial toxic diamine-based dyes.

  2. Industrial scale salt-free reactive dyeing of cationized cotton fabric with different reactive dye chemistry.

    Science.gov (United States)

    Nallathambi, Arivithamani; Venkateshwarapuram Rengaswami, Giri Dev

    2017-10-15

    Dyeing of knitted cotton goods in the industry has been mostly with reactive dyes. Handling of salt laden coloured effluent arising out of dyeing process is one of the prime concerns of the industry. Cationization of cotton is one of the effective alternative to overcome the above problem. But for cationization to be successful at industrial scale it has to be carried out by exhaust process and should be adoptable for the various dye chemistries currently practiced in the industry. Hence, in the present work, industrial level exhaust method of cationization process was carried out with concentration of 40g/L and 80g/L. The fabrics were dyed with dyes of three different dye chemistry and assessed for its dyeing performance without the addition of salt. Dye shades ranging from medium to extra dark shades were produced without the addition of salt. This study will provide industries the recipe that can be adopted for cationized cotton fabric for the widely used reactive dyes at industrial level. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Dyeing of Organic Cotton Fabric using Conventional and Ultrasonic Exhaust Dyeing Method

    Directory of Open Access Journals (Sweden)

    Uzma Syed

    2013-04-01

    Full Text Available In this research dyeing behavior of organic cotton woven fabric using ultrasonic technique and conventional dyeing method has been compared. The fabric samples were dyed with reactive dyes Drimarene Red Cl-5B and Drimarene Blue Cl-BR (0.5% owf using exhaust dyeing method. The samples were ultrasonically dyed at varied temperature (60, 50 and 40oC for 60, 50, 40 and 30 minutes and for conventional method at varied temperature but at recommended time, 60 minutes. For optimizing the dyeing behavior, the samples were causticized by pad-batch method and then dyed with ultrasonic technique at varied temperature and time. It has been observed organic cotton fabric dyed using ultrasonic exhaust method at 60oC for 50 minutes gives highest (K/S?max value, excellent fastness property, deeper dye diffusion and less surface deterioration compared to the conventional dyeing method. Moreover, causticized and dyed sample with ultrasonic technique at 60oC for 30 minutes gives colour strength value almost equal to the conventional recommended dyeing method. Hence, dyeing of organic material using ultrasonic exhaust method saves energy and time

  4. Bioremediation of dyes by fungi isolated from contaminated dye effluent sites for bio-usability

    Directory of Open Access Journals (Sweden)

    Babita Rani

    2014-09-01

    Full Text Available Biodegradation and detoxification of dyes, Malachite green, Nigrosin and Basic fuchsin have been carried out using two fungal isolates Aspergillus niger, and Phanerochaete chrysosporium, isolated from dye effluent soil. Three methods were selected for biodegradation, viz. agar overlay and liquid media methods; stationary and shaking conditions at 25 °C. Aspergillus niger recorded maximum decolorization of the dye Basic fuchsin (81.85% followed by Nigrosin (77.47%, Malachite green (72.77% and dye mixture (33.08% under shaking condition. Whereas, P. chrysosporium recorded decolorization to the maximum with the Nigrosin (90.15% followed by Basic fuchsin (89.8%, Malachite green (83.25% and mixture (78.4%. The selected fungal strains performed better under shaking conditions compared to stationary method; moreover the inoculation of fungus also brought the pH of the dye solutions to neutral from acidic. Seed germination bioassay study exhibited that when inoculated dye solutions were used, seed showed germination while uninoculated dyes inhibited germination even after four days of observation. Similarly, microbial growth was also inhibited by uninoculated dyes. The excellent performance of A. niger and P. chrysporium in the biodegradation of textile dyes of different chemical structures suggests and reinforces the potential of these fungi for environmental decontamination.

  5. Bioremediation of dyes by fungi isolated from contaminated dye effluent sites for bio-usability

    Science.gov (United States)

    Rani, Babita; Kumar, Vivek; Singh, Jagvijay; Bisht, Sandeep; Teotia, Priyanku; Sharma, Shivesh; Kela, Ritu

    2014-01-01

    Biodegradation and detoxification of dyes, Malachite green, Nigrosin and Basic fuchsin have been carried out using two fungal isolates Aspergillus niger, and Phanerochaete chrysosporium, isolated from dye effluent soil. Three methods were selected for biodegradation, viz. agar overlay and liquid media methods; stationary and shaking conditions at 25 °C. Aspergillus niger recorded maximum decolorization of the dye Basic fuchsin (81.85%) followed by Nigrosin (77.47%), Malachite green (72.77%) and dye mixture (33.08%) under shaking condition. Whereas, P. chrysosporium recorded decolorization to the maximum with the Nigrosin (90.15%) followed by Basic fuchsin (89.8%), Malachite green (83.25%) and mixture (78.4%). The selected fungal strains performed better under shaking conditions compared to stationary method; moreover the inoculation of fungus also brought the pH of the dye solutions to neutral from acidic. Seed germination bioassay study exhibited that when inoculated dye solutions were used, seed showed germination while uninoculated dyes inhibited germination even after four days of observation. Similarly, microbial growth was also inhibited by uninoculated dyes. The excellent performance of A. niger and P. chrysporium in the biodegradation of textile dyes of different chemical structures suggests and reinforces the potential of these fungi for environmental decontamination. PMID:25477943

  6. Dyeing regions of oxidative hair dyes in human hair investigated by nanoscale secondary ion mass spectrometry.

    Science.gov (United States)

    Kojima, Toru; Yamada, Hiromi; Yamamoto, Toshihiko; Matsushita, Yasuyuki; Fukushima, Kazuhiko

    2013-06-01

    To develop more effective oxidative hair coloring products, it is important to understand the localization of colored chromophores, which are formed from oxidative dyes, in the fine structure of hair. However, the dyeing regions of oxidative hair dyes in the fine structure of hair have not been extensively examined. In this study, we investigated the distribution and localization of colored chromophores formed by an oxidative hair coloring product in the fine structure of human hair by using a stable isotope-labeled oxidative dye with nanoscale secondary ion mass spectrometry (NanoSIMS). First, formation of the colored chromophore from a deuterium-labeled oxidative dye was examined by visible spectra similarly to a study of its formation using nonlabeled oxidative dye. Furthermore, the formation of binuclear indo dye containing deuterium in its chemical structure was confirmed using time-of-flight secondary ion mass spectrometry (TOF-SIMS) analysis. As a result of the NanoSIMS image on a cross-sectional dyed hair, although deuterium ions were detected in whole hair cross-section, quite a few of them were detected at particulate regions. These particulate regions of the dyed black hair in which deuterium ions were intensely detected were identified as melanin granules, by comparing the dyeing behaviors of black and white hair. NanoSIMS analysis revealed that melanin granules of black human hair are important dyeing regions in oxidative hair coloring. Copyright © 2013 Elsevier B.V. All rights reserved.

  7. Efficient synthesis of triarylamine-based dyes for p-type dye-sensitized solar cells

    Science.gov (United States)

    Wild, Martin; Griebel, Jan; Hajduk, Anna; Friedrich, Dirk; Stark, Annegret; Abel, Bernd; Siefermann, Katrin R.

    2016-05-01

    The class of triarylamine-based dyes has proven great potential as efficient light absorbers in inverse (p-type) dye sensitized solar cells (DSSCs). However, detailed investigation and further improvement of p-type DSSCs is strongly hindered by the fact that available synthesis routes of triarylamine-based dyes are inefficient and particularly demanding with regard to time and costs. Here, we report on an efficient synthesis strategy for triarylamine-based dyes for p-type DSSCs. A protocol for the synthesis of the dye-precursor (4-(bis(4-bromophenyl)amino)benzoic acid) is presented along with its X-ray crystal structure. The dye precursor is obtained from the commercially available 4(diphenylamino)benzaldehyde in a yield of 87% and serves as a starting point for the synthesis of various triarylamine-based dyes. Starting from the precursor we further describe a synthesis protocol for the dye 4-{bis[4‧-(2,2-dicyanovinyl)-[1,1‧-biphenyl]-4-yl]amino}benzoic acid (also known as dye P4) in a yield of 74%. All synthesis steps are characterized by high yields and high purities without the need for laborious purification steps and thus fulfill essential requirements for scale-up.

  8. Modeling the efficiency of Förster resonant energy transfer from energy relay dyes in dye-sensitized solar cells

    KAUST Repository

    Hoke, Eric T.

    2010-02-11

    Förster resonant energy transfer can improve the spectral breadth, absorption and energy conversion efficiency of dye sensitized solar cells. In this design, unattached relay dyes absorb the high energy photons and transfer the excitation to sensitizing dye molecules by Förster resonant energy transfer. We use an analytic theory to calculate the excitation transfer efficiency from the relay dye to the sensitizing dye accounting for dynamic quenching and relay dye diffusion. We present calculations for pores of cylindrical and spherical geometry and examine the effects of the Förster radius, the pore size, sensitizing dye surface concentration, collisional quenching rate, and relay dye lifetime. We find that the excitation transfer efficiency can easily exceed 90% for appropriately chosen dyes and propose two different strategies for selecting dyes to achieve record power conversion efficiencies. © 2010 Optical Society of America.

  9. Preparation and Application of Microencapsulated Disperse Dyes

    Institute of Scientific and Technical Information of China (English)

    罗艳; 陈水林

    2001-01-01

    Microcapsules containing disperse dyes were prepared by means of in-situ polymerization. Polyester fabrics were multiple-transfer printed and color-mix printed using those microencapsulated dyes under different process conditions. By color measurement instrument, it can be seen that the times of multiple-transfer printing are up to ten while under appropriate conditions, especially when the transfer printing time is 50 seconds and the transfer printing temperature is 180°C. On the other hand, the K/S value of each transfer printing can keep almost constant. Meanwhile, the visual effect of color- mix printing with microencapsulated disperse dyes is special in the varicolored exhibiting if compared with conventional disperse dyes.

  10. Thermal treatment of dyes from military munitions

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-09-01

    Los Alamos National Laboratory has developed thermal treatment equipment to treat Navy smoke and dye compounds. Navy smokes were burned in the Los Alamos Controlled Air Incinerator (CAI) in the early 1980s. These test results were used in the development of a portable system consisting of a Thermal Treatment Unit (TTU), feed preparation and pumping skid, utility skid, and control trailer. This equipment was started up at Navy facilities at China Lake, CA where several destruction removal efficiency tests were completed in 1993 burning smoke compositions. The equipment was set up at the Nevada Test Site (NTS) in 1996 where tests were completed burning green Navy spotting dyes. Operating and test results from the NTS efforts resulted in clearer understanding of equipment deficiencies, dye characteristics and composition, and secondary wastes generated. Future tests, scheduled for July, 1996 will demonstrate higher bum rates, better pH measurement and control, and stack emission test results for other colored dyes.

  11. Liquid crystal tunable photonic crystal dye laser

    DEFF Research Database (Denmark)

    Buss, Thomas; Christiansen, Mads Brøkner; Smith, Cameron

    2010-01-01

    We present a dye-doped liquid crystal laser using a photonic crystal cavity. An applied electric field to the liquid crystal provides wavelength tunability. The photonic crystal enhances resonant interaction with the gain medium....

  12. On-chip tunable optofluidic dye laser

    Science.gov (United States)

    Cai, Zengyan; Shen, Zhenhua; Liu, Haigang; Yue, Huan; Zou, Yun; Chen, Xianfeng

    2016-11-01

    We demonstrate a chip-scale tunable optofluidic dye laser with Au-coated fibers as microcavity. The chip is fabricated by soft lithography. When the active region is pumped, a relatively low threshold of 6.7 μJ/mm2 is realized with multimode emission due to good confinement of the cavity mirrors, long active region, as well as total reflectivity. It is easy to tune the lasing emission wavelength by changing the solvent of laser dye. In addition, the various intensity ratios of multicolor lasing can be achieved by controlling flow rates of two fluid streams carried with different dye molecules. Furthermore, the convenience in fabrication and directional lasing emission outcoupled by the fiber make the tunable optofluidic dye laser a promising underlying coherent light source in the integrated optofluidic systems.

  13. Dye laser chain for laser isotope separation

    Science.gov (United States)

    Doizi, Denis; Jaraudias, Jean; Pochon, E.; Salvetat, G.

    1993-05-01

    Uranium enrichment by laser isotope separation uses a three step operation which requires four visible wavelengths to boost an individual U235 isotope from a low lying atomic energy level to an autoionizing state. The visible wavelengths are delivered by dye lasers pumped by copper vapor lasers (CVL). In this particular talk, a single dye chain consisting of a master oscillator and amplifier stages will be described and some of its performance given.

  14. Phytoremediation in education: textile dye teaching experiments.

    Science.gov (United States)

    Ibbini, Jwan H; Davis, Lawrence C; Erickson, Larry E

    2009-07-01

    Phytoremediation, the use of plants to clean up contaminated soil and water, has a wide range of applications and advantages, and can be extended to scientific education. Phytoremediation of textile dyes can be used as a scientific experiment or demonstration in teaching laboratories of middle school, high school and college students. In the experiments that we developed, students were involved in a hands-on activity where they were able to learn about phytoremediation concepts. Experiments were set up with 20-40 mg L(-1) dye solutions of different colors. Students can be involved in the set up process and may be involved in the experimental design. In its simplest forms, they use two-week-old sunflower seedlings and place them into a test tube of known volume of dye solution. Color change and/or dye disappearance can be monitored by visual comparison or with a spectrophotometer. Intensity and extent of the lab work depends on student's educational level, and time constraints. Among the many dyes tested, Evan's Blue proved to be the most readily decolorized azo dye. Results could be observed within 1-2 hours. From our experience, dye phytoremediation experiments are suitable and easy to understand by both college and middle school students. These experiments help visual learners, as students compare the color of the dye solution before and after the plant application. In general, simple phytoremediation experiments of this kind can be introduced in many classes including biology, biochemistry and ecological engineering. This paper presents success stories of teaching phytoremediation to middle school and college students.

  15. Kinetics of Dyes Adsorbed by Chitosan

    Institute of Scientific and Technical Information of China (English)

    CHEN Liang; CHEN Dong-hui; GAO Liang

    2002-01-01

    A study on adsorption of Acidic Blue RAWL and Cationic Blue X-GRRL dyes by chitosan have been conducted.The adsorption kinetic parameters including adsorption rate K and effective diffusing coefficient D'i under the optimal pH ranges have been determined. Analysis through the enthalpy calculation reveals a substantial thermodynamic difference between the adsorption processes of the two dyes, which helps to understand the adsorption mechanism by chitosan.

  16. 花色苷对高糖、高胰岛素下Müller细胞合成VEGF的影响%Effect of cyanin on VEGF in Müller cells under high glucose and high insulin condition

    Institute of Scientific and Technical Information of China (English)

    胡昕倩; 柯敏; 钱志刚

    2011-01-01

    目的 观察高糖、高胰岛素培养下Muller细胞血管内皮生长因子(vascular endothelial growth factor,VEGF)的合成与分泌,以及花色苷对其合成、分泌VEGF的影响.方法 对大鼠视网膜Muller细胞进行原代培养.用50 mmol.L-1葡萄糖和不同浓度的胰岛素处理Muller细胞24 h,分为高胰岛素组(3 KU·L-1胰岛素)、低胰岛素组(3U.L-1胰岛素)和对照组(不含胰岛素).分别用121.1μmol.L-1、22.8μmol.L-1、0μmol.L-1花色苷对各组细胞进行干预.48 h后用酶联免疫吸附法(enzyme linked immunosorbent assay,ELISA)测定上清液中VEGF的含量,免疫细胞化学测定Muller细胞中VEGF的表达.结果 相比对照组,高胰岛素处理Muller细胞后上清液与细胞中的VEGF表达均增加;低浓度和高浓度花色苷均可使该组细胞与上清液中的VEGF表达减少,与未加入花色苷的Muller细胞相比差异均有统计学意义(均为P0.05),2种浓度之间差异亦无统计学意义(均为P>0.05).结论 高浓度胰岛素在短期内即可使Muller细胞合成、分泌VEGF增加,花色苷能有效逆转该过程.%Objective To evaluate expression of vascular endothelial growth factor! VEGF) in cultured rat retinal Muller cells under high glucose and high insulin condition, and effect of cyanin on VEGF expression. Method Muller cells from rat retinas were collected and cultured in vitro. Muller cells were treated with 50 mmol · L-1 glucose and different concentrations of insulin for 24 hours. There were three groups; high insulin group with 3 kU · L-1 insulin,low insulin group with 3 U · L-1 insulin,control group with no insulin. Different concentrations of cyanin( 121.1 μmol · L-1,22. 8 μmol · L-1 and 0 μmol · L-1) were added to the medium in each group. At 48 hours after incubation,enzyme linked immunosorbent assay was used to detect VEGF in the supernatant fluid. Immunocytochemistry was applied to quantify VEGF expression in Muller cells. Results After high insulin

  17. Photocatalytic degradation of synthetic dye under sunlight

    Directory of Open Access Journals (Sweden)

    Mijin Dušan

    2007-01-01

    Full Text Available Synthetic dyes are widely used in the textile industry. Dye pollutants from the textile industry are an important source of environmental contamination. The majority of these dyes are toxic, mostly non-biodegradable and also resistant to decomposition by physico-chemical methods. Among new oxidation methods or "advanced oxidation processes", heterogeneous photocatalysis appears as an emerging destructive technology leading to the total mineralization of many organic pollutants. CI Basic Yellow 28 (BY28, commonly used as a textile dye, could be photocatalytically degraded using TiU2 as catalyst under sunlight. The effect of some parameters such as the initial catalyst concentration, initial dye concentration, initial NaCl and Na2CO3 concentrations, pH, H2O2 and type of catalyst on the degradation rate of BY28 was examined in details. The presence of NaCl and Na2CO3 led to inhibition of the photodegradation process. The highest photodegradation rate was observed at high pH, while the rate was the lowest at low pH. Increase of the initial H2O2 concentration increased the initial BY28 photodegradation efficiency. ZnO was a better catalyst than TiO2 at low dye concentrations.

  18. Degradation of textile dyes by cyanobacteria

    Directory of Open Access Journals (Sweden)

    Priscila Maria Dellamatrice

    Full Text Available Abstract Dyes are recalcitrant compounds that resist conventional biological treatments. The degradation of three textile dyes (Indigo, RBBR and Sulphur Black, and the dye-containing liquid effluent and solid waste from the Municipal Treatment Station, Americana, São Paulo, Brazil, by the cyanobacteria Anabaena flos-aquae UTCC64, Phormidium autumnale UTEX1580 and Synechococcus sp. PCC7942 was evaluated. The dye degradation efficiency of the cyanobacteria was compared with anaerobic and anaerobic-aerobic systems in terms of discolouration and toxicity evaluations. The discoloration was evaluated by absorption spectroscopy. Toxicity was measured using the organisms Hydra attenuata, the alga Selenastrum capricornutum and lettuce seeds. The three cyanobacteria showed the potential to remediate textile effluent by removing the colour and reducing the toxicity. However, the growth of cyanobacteria on sludge was slow and discoloration was not efficient. The cyanobacteria P. autumnale UTEX1580 was the only strain that completely degraded the indigo dye. An evaluation of the mutagenicity potential was performed by use of the micronucleus assay using Allium sp. No mutagenicity was observed after the treatment. Two metabolites were produced during the degradation, anthranilic acid and isatin, but toxicity did not increase after the treatment. The cyanobacteria showed the ability to degrade the dyes present in a textile effluent; therefore, they can be used in a tertiary treatment of effluents with recalcitrant compounds.

  19. Degradation of textile dyes by cyanobacteria.

    Science.gov (United States)

    Dellamatrice, Priscila Maria; Silva-Stenico, Maria Estela; Moraes, Luiz Alberto Beraldo de; Fiore, Marli Fátima; Monteiro, Regina Teresa Rosim

    Dyes are recalcitrant compounds that resist conventional biological treatments. The degradation of three textile dyes (Indigo, RBBR and Sulphur Black), and the dye-containing liquid effluent and solid waste from the Municipal Treatment Station, Americana, São Paulo, Brazil, by the cyanobacteria Anabaena flos-aquae UTCC64, Phormidium autumnale UTEX1580 and Synechococcus sp. PCC7942 was evaluated. The dye degradation efficiency of the cyanobacteria was compared with anaerobic and anaerobic-aerobic systems in terms of discolouration and toxicity evaluations. The discoloration was evaluated by absorption spectroscopy. Toxicity was measured using the organisms Hydra attenuata, the alga Selenastrum capricornutum and lettuce seeds. The three cyanobacteria showed the potential to remediate textile effluent by removing the colour and reducing the toxicity. However, the growth of cyanobacteria on sludge was slow and discoloration was not efficient. The cyanobacteria P. autumnale UTEX1580 was the only strain that completely degraded the indigo dye. An evaluation of the mutagenicity potential was performed by use of the micronucleus assay using Allium sp. No mutagenicity was observed after the treatment. Two metabolites were produced during the degradation, anthranilic acid and isatin, but toxicity did not increase after the treatment. The cyanobacteria showed the ability to degrade the dyes present in a textile effluent; therefore, they can be used in a tertiary treatment of effluents with recalcitrant compounds. Copyright © 2016 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. All rights reserved.

  20. Chitosan derivatives as biosorbents for basic dyes.

    Science.gov (United States)

    Lazaridis, Nikolaos K; Kyzas, George Z; Vassiliou, Alexandros A; Bikiaris, Dimitrios N

    2007-07-03

    The scope of this study was to prepare and evaluate chitosan derivatives as biosorbents for basic dyes. This was achieved by grafting poly (acrylic acid) and poly (acrylamide) through persulfate induced free radical initiated polymerization processes and covalent cross-linking of the prepared materials. Remacryl Red TGL was used as the cationic dye. Equilibrium sorption experiments were carried out at different pH and initial dye concentration values. The experimental equilibrium data for each adsorbent-dye system were successfully fitted to the Langmuir, Freundlich and pH-dependent Langmuir-Freundlich sorption isotherms. Thermodynamic parameters of the adsorption process such as DeltaG degrees, DeltaH degrees, and DeltaS degrees were calculated. The negative values of free energy reflected the spontaneous nature of adsorption. The typical dependence of dye uptake on temperature and the kinetics of adsorption indicated the process to be chemisorption. The grafting modifications greatly enhanced the adsorption performance of the biosorbents, especially in the case of powdered cross-linked chitosan grafted with acrylic acid, which exhibited a maximum adsorption capacity equal to 1.068 mmol/g. Kinetic studies also revealed a significant improvement of sorption rates by the modifications. Diffusion coefficients of the dye molecule were determined to be of the order 10(-13) - 10(-12) m2/s. Furthermore, desorption experiments affirmed the regenerative capability of the loaded material.

  1. Optical properties of natural dyes on the dye-sensitized solar cells (DSSC) performance

    Science.gov (United States)

    Pratiwi, D. D.; Nurosyid, F.; Supriyanto, A.; Suryana, R.

    2016-11-01

    This study reported several natural dyes for application in dye-sensitized solar cells (DSSC). This study aims was to determine the effect of optical absorption properties of natural dyes on efficiency of DSSC. The sandwich structure of DSSC consist of TiO2 as working electrode, carbon layer as counter electrode, natural dyes as photosensitizer, and electrolyte as electron transfer media. The natural dyes used in this experiment were extracted from dragon fruit anthocyanin, mangosteen peels anthocyanin, and red cabbage anthocyanin. The absorbance of dyes solutions and the adsorption of the dye on the surface of TiO2 were characterized using UV-Vis spectrophotometer, the quantum efficiency versus wavelength was characterized using incident photon-to-current efficiency (IPCE) measurement system, and the efficiency of DSSC was calculated using I-V meter. UV-Vis characteristic curves showed that wavelength absorption of anthocyanin dye of red cabbage was 450 - 580 nm, anthocyanin of mangosteen peels was 400 - 480 nm, and anthocyanin of dragon fruit was 400 - 650 nm. Absorption spectra of the dye adsorption on the surface of TiO2 which was resulted in the highest absorbance of red cabbage anthocyanin. IPCE characteristic curves with anthocyanin dye of red cabbage, mangosteen peels anthocyanin, and dragon fruit anthocyanin resulted quantum efficiency of 0.058%; 0.047%; and 0.043%, respectively at wavelength maximum about 430 nm. I-V characteristic curves with anthocyanin dye of red cabbage, mangosteen peels anthocyanin, and dragon fruit anthocyanin resulted efficiency of 0.054%; 0.042%; and 0.024%, respectively.

  2. Chlorine disinfection of dye wastewater: Implications for a commercial azo dye mixture

    Energy Technology Data Exchange (ETDEWEB)

    Vacchi, Francine Inforcato; Albuquerque, Anjaina Fernandes; Vendemiatti, Josiane Aparecida; Morales, Daniel Alexandre [Faculdade de Tecnologia, Universidade Estadual de Campinas, Limeira, SP, 13484-332 (Brazil); Ormond, Alexandra B.; Freeman, Harold S. [Department of Textile Engineering, Chemistry, and Science, North Carolina State University, Raleigh, NC 27695-8301 (United States); Zocolo, Guilherme Juliao; Zanoni, Maria Valnice Boldrin [Departamento de Quimica Analitica, Universidade Estadual Paulista Julio de Mesquita Filho, Instituto de Quimica de Araraquara, Araraquara, SP 14801-970 (Brazil); Umbuzeiro, Gisela, E-mail: giselau@ft.unicamp.br [Faculdade de Tecnologia, Universidade Estadual de Campinas, Limeira, SP, 13484-332 (Brazil)

    2013-01-01

    Azo dyes, the most widely used family of synthetic dyes, are often employed as colorants in areas such as textiles, plastics, foods/drugs/cosmetics, and electronics. Following their use in industrial applications, azo dyes have been found in effluents and various receiving waters. Chemical treatment of effluents containing azo dyes includes disinfection using chlorine, which can generate compounds of varying eco/genotoxicity. Among the widely known commercial azo dyes for synthetic fibers is C.I. Disperse Red 1. While this dye is known to exist as a complex mixture, reports of eco/genotoxicity involve the purified form. Bearing in mind the potential for adverse synergistic effects arising from exposures to chemical mixtures, the aim of the present study was to characterize the components of commercial Disperse Red 1 and its chlorine-mediated decoloration products and to evaluate their ecotoxicity and mutagenicity. In conducting the present study, Disperse Red 1 was treated with chlorine gas, and the solution obtained was analyzed with the aid of LC-ESI-MS/MS to identify the components present, and then evaluated for ecotoxicity and mutagenicity, using Daphnia similis and Salmonella/microsome assays, respectively. The results of this study indicated that chlorination of Disperse Red 1 produced four chlorinated aromatic compounds as the main products and that the degradation products were more ecotoxic than the parent dye. These results suggest that a disinfection process using chlorine should be avoided for effluents containing hydrophobic azo dyes such commercial Disperse Red 1. -- Highlights: Black-Right-Pointing-Pointer Aqueous solutions of Disperse Red 1 were treated with chlorine. Black-Right-Pointing-Pointer The chlorination products of Disperse Red 1 were identified using LC-ESI-MS/MS. Black-Right-Pointing-Pointer Daphnia and Salmonella/microsome were employed for eco/genotoxicity testing. Black-Right-Pointing-Pointer The chlorinated dye was more mutagenic

  3. 水溶性羧苄基甲苄基三甲川菁染料的合成及光谱性能%Synthesis and Spectral Properties of Carboxybenzyl methylbenzyl Trimethine Cyanine Dye

    Institute of Scientific and Technical Information of China (English)

    姜婷婷; 高敬春; 陈辉; 宋波

    2014-01-01

    文章以对肼苯磺酸和3-甲基-2-丁酮为原料合成2,3,3-三甲基-3H-吲哚-5-磺酸,再制得钾盐,由钾盐合成两种N-烷基取代吲哚季铵盐,最后采用一步法合成水溶性三甲川菁染料.所合成的染料经C-18反相柱分离提纯,利用核磁共振氢谱进行结构表征,并测试染料的光谱性能.

  4. 几种半菁染料的合成、光物理性质及在pH检测中的应用研究%Syntheses and Photophysical Properties of Several Cyanine Dyes

    Institute of Scientific and Technical Information of China (English)

    谢普会; 郭丰启; 董兰芬

    2009-01-01

    制备了几种喹啉系列半菁染料和苯并噻唑系列半菁染料,并对其在不同溶剂中的吸收光谱和荧光光谱进行了研究.这类化合物的吸收光谱随pH值的变化发生规律性的变化,这种性质使其在pH检测中具有潜在的应用价值.

  5. 多烯和花菁染料分子设计及其非线性光学性质研究进展%Molecular Design and Nonlinear Optical Properties of Polyene and Cyanine Dyes

    Institute of Scientific and Technical Information of China (English)

    郑庆东; 姚祖光

    2000-01-01

    根据一种新的增强分子非线性光学性质的设计思想,讨论了多烯和花菁染料的结构和性质关系,综述了这类染料的非线性光学性质及其应用进展,并对有机非线性光学材料的发展前景进行了预测.

  6. Syntheses and Spectral Properties of Hemi-cyanine Dyes%一种水溶性苯乙烯半著染料的合成及光谱性能的研究

    Institute of Scientific and Technical Information of China (English)

    陈辉; 吴蓥男; 张超; 宋波

    2015-01-01

    设计和成了一种水溶性的苯乙烯半菁染料,将吲哚啉季铵盐与对氯苯甲醛反应,并采用重结晶的方法得到目标产物.所得的到的菁染料进行了核磁共振氢谱、碳谱以及质谱的结构表征,并对染料的光谱性能进行了初步的研究.

  7. 菁染料和份菁染料的合成及其 溶液的光稳定性研究%SYNTHESIS AND PHOTOSTABILITY OF CYANINE AND MEROCYANINE DYES SOLUTION

    Institute of Scientific and Technical Information of China (English)

    杨松杰; 孟凡顺; 陈孔常; 田禾; 汪文玮

    2001-01-01

    利用UV-Vis吸收光谱仪和光化学反应器,研究了菁染料和份菁染 料的光降解动 力学.研究结果表明,染料在乙腈溶液中的光褪色反应遵循假一级或零级动力学衰减.与相 应的份菁染料相比,携带正电荷的菁染料具有相对较好的光稳定性.

  8. Synthesis and Purification of Unsymmetrical Water-soluble Cyanine Dyes%不对称水溶性菁染料的简便制备与纯化方法

    Institute of Scientific and Technical Information of China (English)

    楼开炎; 钱旭红; 宋恭华

    2002-01-01

    以对肼基苯磺酸为起始原料,经6步反应合成了2个可用于DNA荧光标记的不对称水溶性菁染料.采用三元展开剂体系,用制备薄层色谱方法分离提纯各中间体和产物,得到了与文献报道制备液相色谱方法相当的收率.

  9. 反胶束中菁染料与AgCl粒子相互作用的光谱研究%SPECTRAL INVESTIGATION ON THE INTERACTION OF A CYANINE DYE AND AgCl PARTICLES IN REVERSED MICELLES

    Institute of Scientific and Technical Information of China (English)

    张志颖; 刘春艳

    2000-01-01

    在阴离子型和非离子型表面活性剂组成的反胶束体系中研究了直径为11~14 nm的AgCl微粒子与菁染料之间的作用,讨论了AgCl纳米粒子对菁染料的吸附及荧光猝灭现象.

  10. Comparison of the Sequence-Dependent Fluorescence of the Cyanine Dyes Cy3, Cy5, DyLight DY547 and DyLight DY647 on Single-Stranded DNA: e85605

    National Research Council Canada - National Science Library

    Nicole Kretschy; Mark M Somoza

    2014-01-01

    ..., Förster resonance energy transfer, and labeling for microarray hybridization. Previous research has shown that the fluorescence efficiency of Cy3 and Cy5, covalently attached to the 5' end of single-stranded DNA, is strongly sequence dependent...

  11. Comparison of the sequence-dependent fluorescence of the cyanine dyes Cy3, Cy5, DyLight DY547 and DyLight DY647 on single-stranded DNA

    National Research Council Canada - National Science Library

    Kretschy, Nicole; Somoza, Mark M

    2014-01-01

    ..., Förster resonance energy transfer, and labeling for microarray hybridization. Previous research has shown that the fluorescence efficiency of Cy3 and Cy5, covalently attached to the 5' end of single-stranded DNA, is strongly sequence dependent...

  12. Nucleophilic Addition of Reactive Dyes on Amidoximated Acrylic Fabrics

    Directory of Open Access Journals (Sweden)

    Reda M. El-Shishtawy

    2014-01-01

    Full Text Available Seven reactive dyes judiciously selected based on chemical structures and fixation mechanisms were applied at 2% owf of shade on amidoximated acrylic fabrics. Amidoximated acrylic fabric has been obtained by a viable amidoximation process. The dyeability of these fabrics was evaluated with respect to the dye exhaustion, fixation, and colour strength under different conditions of temperature and dyeing time. Nucleophilic addition type reactive dyes show higher colour data compared to nucleophilic substitution ones. FTIR studies further implicate the binding of reactive dyes on these fabrics. A tentative mechanism is proposed to rationalize the high fixation yield obtained using nucleophilic addition type reactive dyes. Also, the levelling and fastness properties were evaluated for all dyes used. Excellent to good fastness and levelling properties were obtained for all samples irrespective of the dye used. The result of investigation offers a new method for a viable reactive dyeing of amidoximated acrylic fabrics.

  13. Nucleophilic addition of reactive dyes on amidoximated acrylic fabrics.

    Science.gov (United States)

    El-Shishtawy, Reda M; El-Zawahry, Manal M; Abdelghaffar, Fatma; Ahmed, Nahed S E

    2014-01-01

    Seven reactive dyes judiciously selected based on chemical structures and fixation mechanisms were applied at 2% of of shade on amidoximated acrylic fabrics. Amidoximated acrylic fabric has been obtained by a viable amidoximation process. The dyeability of these fabrics was evaluated with respect to the dye exhaustion, fixation, and colour strength under different conditions of temperature and dyeing time. Nucleophilic addition type reactive dyes show higher colour data compared to nucleophilic substitution ones. FTIR studies further implicate the binding of reactive dyes on these fabrics. A tentative mechanism is proposed to rationalize the high fixation yield obtained using nucleophilic addition type reactive dyes. Also, the levelling and fastness properties were evaluated for all dyes used. Excellent to good fastness and levelling properties were obtained for all samples irrespective of the dye used. The result of investigation offers a new method for a viable reactive dyeing of amidoximated acrylic fabrics.

  14. Sorption of dyes from aqueous solutions onto fly ash.

    Science.gov (United States)

    Janos, Pavel; Buchtová, Hana; Rýznarová, Milena

    2003-12-01

    Brown coal fly ashes were tested as potentially low-cost sorbents for the removal of synthetic dyes from waters. It was shown that both basic (cationic) as well as acid (anionic) dyes can be sorbed onto the fly ash. The adsorption can be described by the multi-site Langmuir isotherm. The sorption capacities were in the range of 10(-1)-10(-3)mmol/g and did not differ significantly for basic and acid dyes. The dye sorption decreased in the presence of organic solvents (methanol, acetone). The presence of oppositely charged surfactants exhibited a pronounced effect on the dye sorption-low concentrations of the surfactant enhanced sorption, whereas high concentrations solubilized the dyes and kept them in solution. Inorganic salts exhibited only a minor effect on the dye sorption. The sorption of basic dyes increased at high pH values, whereas the opposite was true for acid dyes.

  15. DYEING COTTON WITH EISENIA BICYCLIS AS NATURAL DYE USING DIFFERENT BIOMORDANTS

    Directory of Open Access Journals (Sweden)

    BONET Mª Ángeles

    2015-05-01

    Full Text Available Natural dyes are known for their use in coloring of food substrate, leather as well as natural protein fibers like wool, silk and cotton as major areas of application since pre-historic times. Nowadays, there has been revival of the growing interest on the application of natural dyes on natural fibers due to worldwide environmental consciousness. Some researchers focus their studies on the improvement of these dyes using mordants. Most works use metallic mordants like aluminum or iron are used, but some of them are hazardous. In this work we used a biomordant to solve environmental problems caused by metallic mordants. The effects of chitosan weight molecular in mordanting on the dyeing characteristics and the UV protection property were examined in this study. Chitosan mordanted Eisenia Bicyclis dyed cotton showed better dyeing characteristic and higher UV protection property compared with undyed cotton fabric. To analyze the differences of the dyeing, reflection spectrophotometer was used, evaluating the results of CIELAB color difference values and the strength color (in terms of K/S value. We conclude that the type of chitosan used affect the dyeing efficiency and the UV protection, showing different behavior between dye sample using chitosan with low or medium molecular weight.

  16. Enzymatic decolorization of spent textile dyeing baths composed by mixtures of synthetic dyes and additives.

    Science.gov (United States)

    Ciullini, Ilaria; Gullotto, Antonella; Tilli, Silvia; Sannia, Giovanni; Basosi, Riccardo; Scozzafava, Andrea; Briganti, Fabrizio

    2012-10-01

    The effects of different components of real dyeing bath formulations, such as the equalizing and fixing additives-acids, salts, and surfactants-on the decolorization catalyzed by Funalia trogii enzymatic extracts, were investigated to understand their influence on the recalcitrance to biodegradation of this type of wastewater. The decolorization of selected dyes and dye mixtures after tissue dyeing was performed in the presence/absence of auxiliary compounds. All spent dyeing baths were enzymatically decolorized to different extents, by the addition of extracts containing laccase only or laccase plus cellobiose dehydrogenase. Whereas surfactant auxiliaries, in some instances, inhibit the decolorization of spent dyeing baths, in several occurrences the acid/salt additives favor the enzymatic process. In general, the complete spent dyeing formulations are better degraded than those containing the dyes only. The comparison of extracellular extracts obtained from spent straws from the commercial growth of Pleurotus sp. mushrooms with those from F. trogii reveals similar decolorization extents thus allowing to further reduce the costs of bioremediation.

  17. Isolation and screening of azo dye decolorizing bacterial isolates from dye-contaminated textile wastewater

    Directory of Open Access Journals (Sweden)

    Shahid Mahmood

    2011-04-01

    Full Text Available Azo dyes are released into wastewater streams without any pretreatment and pollute water and soilenvironments. To prevent contamination of our vulnerable resources, removal of these dye pollutants is of greatimportance. For this purpose, wastewater samples were collected from dye-contaminated sites of Faisalabad. About200 bacterial isolates were isolated through enrichment and then tested for their potential to remove RemazolBlack-B azo dye in liquid medium. Five bacterial isolates capable of degrading Remazol Black-B azo dye efficientlywere screened through experimentation on modified mineral salt medium. Isolate SS1 (collected from wastewater ofSupreme Textile Industry was able to completely remove the Remazol Black-B dye from the liquid medium in 18 h.Further, the isolate showed the best performance at the dye concentration of 100 mg L-1 medium (pH 7 and attemperature 35oC. Similarly, yeast extract proved to be the best carbon source for decolorization purpose. Theresults imply that the isolate SS1 could be used for the removal of the reactive dyes from textile effluents.

  18. Synthesis and dyeing properties of new disazo disperse dyes for polyester and nylon fabrics

    Directory of Open Access Journals (Sweden)

    Tarulata B. Shah

    2014-12-01

    Full Text Available Diazotized aryl amines were coupled with two stenhouse salt namely, N-(5-phenylamino-penta-4-ol-2,4-diene-1-ylideneanilines hydrochloride [S1 (RH or S2 (ROH] to furnish two series of disazo disperse dyes (S1D1–10 and S2D1–10. The structure of all the dyes was established by estimating number of azo groups, elemental analysis and spectral studies (IR, 1H-NMR, UV/Visible. The structure–property relationship was discussed by using electronic absorption spectra of the dyes. These dyes were applied to polyester and nylon fabrics as disperse dyes by using temperature exhaust dyeing method. The relevant dyeing characteristics, such as dyeability on fabrics, wash-fastness and light-fastness were evaluated. Fabrics dyed with these dyes furnished generally deep and bright intense hues ranging from light yellow to orange to reddish brown. The color fastness of the dyed fabric was assessed by determining wash-fastness and light-fastness properties.

  19. Molecular design and photovoltaic performance of organic dyes containing phenothiazine for dye-sensitized solar cells.

    Science.gov (United States)

    Jo, Hyo Jeong; Nam, Jung Eun; Sim, Kyoseung; Kim, Dae-Hwan; Kim, Jae Hong; Kang, Jin-Kyu

    2014-10-01

    We synthesized novel organic photosensitizers based on fluorine-substituted phenothiazine with thiophene bridge units in the chromophore for application in dye-sensitized solar cells (DSSCs). Furthermore, organic dyes with different acceptors exhibited higher molar extinction coefficients, and better light absorption at longer wavelengths. The photovoltaic properties of organic dyes composed of different acceptors in their chromophores were measured to identify their effects on the DSSC performance. The organic dye, PFSCN2 containing multi-cyanoacrylic acid as the electron acceptor, showed a power conversion efficiency of 4.67% under AM 1.5 illumination (100 mW/cm2). The retarded recombination kinetics from TiO2 electrode to electrolyte enhanced the electron life time of the organic dye, PFSCN2 in the photoanode of the DSSC. This was confirmed with impedance analysis.

  20. Ethoxy-substituted Oligo-phenylenevinylene-Bridged Organic Dyes for Efficient Dye-Sensitized Solar Cells

    Institute of Scientific and Technical Information of China (English)

    单益凡; 汤杰; 赖华; 谭宏伟; 刘晓峰; 杨帆; 房强

    2012-01-01

    Organic dyes with ethoxy-substituted oligo-phenylenevinylene as chromophores were synthesized for dye-sensitized solar cells (DSSCs), and the detailed relationships between the dye structures, photophysical properties, electrochemical properties, and performances of DSSCs were described. The dye S3O showed broad IPCE spectra in the spectral range of 350--750 nm, and the dye S1P showed solar energy-to-electricity conversion efficiency (1/) of up to 4.23% under AM 1.5 irradiation (100 mW/cm2) in comparison with the reference Ru-complex (N719 dye) with an r/value of 5.90% under similar experimental conditions.

  1. Unexpected radiation hazard in dyes of textiles.

    Science.gov (United States)

    Abdel Ghany, Hayam A; Ibrahim, Eman M

    2014-01-01

    Textile dyes are among the most problematic pollutants because of their toxicity on several organisms and ecosystems. Many of the chemicals used in the textile industry may represent some health concerns. The determination of the radioactivity in textile dyes is therefore very important for both human health and environment. The study was designated to determine, for the first time, the values of (238)U, (232)Th and (40)K in nine different dyes employed in the textile industry using gamma spectrometry with a Hyper Pure Germanium (HPGe) detector. The mean activity concentrations of (238)U, (232)Th and (40)K were 29.37 ± 4.48, 1.15 ± 0.13 and 565 ± 4 Bq/kg, respectively. The calculated radium equivalents for all samples were lower than the maximum admissible value (370 Bq/kg). The absorbed dose rates due to the natural radioactivity of the investigated samples ranged from 2.94 ± 0.05 to 166 ± 3 nGy/h. So, the absorbed dose rates for all samples of textile dyes were lower than the international recommended value (55 nGy/h) except the yellow dye (166 ± 3 nGy/h), which recorded a significant radiological hazard. The external hazard index was also calculated. Conclusively, the results have indicated that the textile dyes may possess a measurable amount of radioactivity that should be taken into account. Therefore, safety rules and precautions should be applied for dyes used in the textile industry and for people working in this field.

  2. Reactive dye extraction utilizing regenerated bleaching earth

    Directory of Open Access Journals (Sweden)

    M. Shahi

    2017-09-01

    Full Text Available Bentonite bleaching earth is utilized for purifying used motor oil through a recovery process in order to improve the quality and stability of the final product. Indeed, spent bleaching earth is generated due to adsorbing oil impurities. Polluted spent bleaching earth contains 20-40% (w/w oil and is flammable. Its disposal without pre-treatment leads to loss of oil along with environmental impacts. Accordingly, similar studies have been conducted since 1979 until now. This research was a laboratory study on reactive dye adsorption. Cleaning bleaching clay, thermal remediation and acid washing activation methods were utilized. Response surface methodology was used to design the experiments and determine the optimal parameters in order to run the dye adsorption process. The main experimental parameters have been concluded as temperature (200-800 °C, acid solution concentration (0.1-3 M, dye solution concentration (1-35 ppm, and ratio of activated earth to dye solution (0.1-2 %, w/w. Results revealed that dye adsorption process along with oil removal at a temperature of 650 °C, acid solution concentration of 0.83 M, dye solution concentration of 11.75 ppm and ratio of activated earth to dye solution of 1.52 % (w/w results in an adsorption efficiency of 68.57%. This removal efficiency is a bit higher than activated virgin bleaching earth and much higher than virgin bleaching earth, which has adsorption capacities of 66.75% and 51.56%, respectively. Considering this recycling process, the purified material is quite acceptable technically, environmentally and economically.

  3. Review of Recent Progress in Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Fan-Tai Kong

    2007-08-01

    Full Text Available We introduced the structure and the principle of dye-sensitized solar cell (DSC. The latest results about the critical technology and the industrialization research on dye-sensitized solar cells were reviewed. The development of key components, including nanoporous semiconductor films, dye sensitizers, redox electrolyte, counter electrode, and conducting substrate in dye-sensitized solar cells was reviewed in detail. The developing progress and prospect of dye-sensitized solar cells from small cells in the laboratory to industrialization large-scale production were reviewed. At last, the future development of DSC was prospective for the tendency of dye-sensitized solar cells.

  4. The effect of dendrimer on cotton dyeability with direct dyes

    Directory of Open Access Journals (Sweden)

    Khakzar Bafrooei F.

    2014-01-01

    Full Text Available Pretreatment of cotton fabric with poly(propylene imine dendrimer enhanced its colour strength using C.I. Direct Red 81 and C.I. Direct Blue 78. Application of this dendrimer and the direct dye simultaneously on cotton fabric by the exhaust and the continuous dyeing method were studied; slight improvements in the dyeing results were obtained. Pretreatment of the cotton fabric with dendrimer in an emulsion form using the pad-dry method followed by continuous dyeing markedly increased the colour strength. In addition, level dyeing was obtained, and no negative effects on the fastness properties of the dyes used were observed.

  5. Preparation of P(St-BA-VBT)/dye Colored Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    HAN Dong-mei; FANG Kuan-jun

    2015-01-01

    P (St-BA-VBT)/dye colored nanoparticles were prepared by staining P (Styrene-Butyl Acrylate-VinylBenzyl Trimethylammonium chloride) nanoparticles synthesized by soap free cationic emulsion polymerization with reactive dyes. The effects of reactive dyes dosage, dyeing temperature and time on amounts of dyes adsorbed on the nanoparticles were analysed. Results showed that when Reactive Red 195 dosage was 5.25%, the adsorption amounts of dyes on the nanoparticles reached a maximum value of 18.64 mg/g at 65℃for 90 min.

  6. Assessment of Collagen-Induced Arthritis Using Cyanine 5.5 Conjugated with Hydrophobically Modified Glycol Chitosan Nanoparticles: Correlation with 18F-Fluorodeoxyglucose Positron Emission Tomography Data

    Energy Technology Data Exchange (ETDEWEB)

    Cha, Ji Hyeon; Lee, Sang Hoon; Lee, Sheen Woo; Moon, Dae Huk [Asan Medical Center, Ulsan University College of Medicine, Seoul (Korea, Republic of); Park, Kyoung Soon [Biomedical Research Center, Seoul (Korea, Republic of); Biswal, Sandip [Stanford University School of Medicine, Stanford (United States)

    2012-07-15

    To evaluate the potential and correlation between near-infrared fluorescence (NIRF) imaging using cyanine 5.5 conjugated with hydrophobically modified glycol chitosan nanoparticles (HGC-Cy5.5) and {sup 18}F-fluorodeoxyglucose-positron emission tomography ({sup 18}F-FDG-PET) imaging of collagen-induced arthritis (CIA). We used 10 CIA and 3 normal mice. Nine days after the injecting collagen twice, microPET imaging was performed 40 minutes after the intravenous injection of 9.3 MBq {sup 18}F-FDG in 200 {mu}L PBS. One day later, NIRF imaging was performed two hours after the intravenous injection of HGC-cy5.5 (5 mg/kg). We assessed the correlation between these two modalities in the knees and ankles of CIA mice. The mean standardized uptake values of {sup 18}F-FDG for knees and ankles were 1.68 {+-} 0.76 and 0.79 {+-} 0.71, respectively, for CIA mice; and 0.57 {+-} 0.17 and 0.54 {+-} 0.20 respectively for control mice. From the NIRF images, the total photon counts per 30 mm{sup 2} for knees and ankles were 2.32 {+-} 1.54 X 10{sup 5} and 2.75 {+-} 1.51 X 10{sup 5}, respectively, for CIA mice, and 1.22 {+-} 0.27 X 10{sup 5} and 0.88 {+-} 0.24 X 10{sup 5}, respectively, for control mice. These two modalities showed a moderate correlation for knees (r = 0.604, p = 0.005) and ankles (r = 0.464, p = 0.039). Moreover, both HGC-Cy5.5 (p = 0.002) and {sup 18}F-FDG-PET (p = 0.005) imaging also showed statistically significant differences between CIA and normal mice. NIRF imaging using HGC-Cy5.5 was moderately correlated with {sup 18}F-FDG-PET imaging in the CIA model. As such, HGC-Cy5.5 imaging can be used for the early detection of rheumatoid arthritis.

  7. 蓝色素的发酵条件和特性的研究%The research on the fermentation condition and characteristics of cyanine

    Institute of Scientific and Technical Information of China (English)

    全桂静; 孙海娟

    2012-01-01

    对一种蓝色素的发酵条件和特性进行了研究.结果显示,最佳的培养基配方为甘油20g/L,KNO31g/L,K2HPO40.5g/L,NaCl0.5g/L,MgSO4·7H2O 0.5g/L,FeSO4·7H2O0.01g/L,pH8.5;发酵条件为250mL摇瓶装100mL培养基,30℃,150r/min振荡培养96h,发酵液的最高色价为12.6.该色素溶在中性及碱性的水溶液中呈现鲜艳的蓝色;高于60℃时,色素稳定性较差,不宜用于高温处理的食品中;光照对色素稳定性影响较小,保存无需避光;甜味剂、氧化剂及防腐剂等食品添加剂对色素影响较小,而抗坏血酸对色素影响较大.%The fermentation condition and characteristics of Cyanine were studied. The results showed that the best formula of the medium was glycerin 20g/L, KNO31g/L, K2HPO4 0.5g/L, NaCl 0.5g/L, MgSO4 · 7H2O 0.5g/L, FeSO4 · 7 H2O 0.01g/L, pH 8. 5. The fermentation conditions were lOOmL culture medium in 250mL shake flask, 30℃, 150r/min shaking 96h, and the highest color value was 12. 6. The pigment dissolved in the neutral and alkaline solution presented the bright blue. More than 60 t, the stability of pigment was poor. The pigment should nor be applied in the food treated in the high temperature. Light had little effect on the pigment. The food additives, such as sweetener, antioxidants and preservatives had little effects on the pigment, while ascorbic acid affected the pigment more.

  8. ADSORPTION OF DYES ON ACTIVATED CARBON FIBERS

    Institute of Scientific and Technical Information of China (English)

    ChenShuixia; WuChangqing; 等

    1998-01-01

    The adsorption behavior of dyes on a variety of sisal based activated carbon fibers (SACF) has been studied in this paper. The results show that this kind of ACF has excellent adsorption capacities for some organic (dye) molecules.SACF can remove nearly all methylene blue,crystal violet,bromophenol blue and Eriochrome blue black R from water after static adsorption for 24h. at 30℃. The adsorption amounts can reach more than 400mg/g when adding 50 mg SACF into 50 ml dye solution.Under the same conditions,the adsorption amounts of xylenol orange fluorescein and Eriochrome black T wree lower.On the other hand,the adsorption amounts change along with the characteristics of adsorbents.The SACFs activated above 840℃,which have higher specific surface areas and wider pore radii,have higher adsorption amounts for the dyes.The researching results also show that the adsorption rates of dyes onto SACFs decrease by the order of methylene blue,Eriochrome blue black R and crystal violet.

  9. Physical and chemical investigations on natural dyes

    Science.gov (United States)

    Acquaviva, S.; D'Anna, E.; de Giorgi, M. L.; Della Patria, A.; Baraldi, P.

    2010-09-01

    Natural dyes have been used extensively in the past for many purposes, such us to colour fibers and to produce inks, watercolours and paints, but their use declined rapidly after the discovery of synthetic colours. Nowadays we witness a renewed interest, as natural dyes are neither toxic nor polluting. In this work, physical and chemical properties of four selected dyes, namely red (Madder), yellow (Weld and Turmeric) and blue (Woad) colours, produced by means of traditional techniques at the Museo dei Colori Naturali (Lamoli, Italy), have been investigated. The chromatic properties have been studied through the reflectance spectroscopy, a non-invasive technique for the characterisation of chromaticity. Reflection spectra both from powders and egg-yolk tempera models have been acquired to provide the typical features of the dyes in the UV-vis spectral range. Moreover, to assess the feasibility of laser cleaning procedures, tempera layers were investigated after irradiation with an excimer laser. Micro Raman spectroscopy, Scanning Electron Microscopy and Energy Dispersive X-Ray analyses have complemented the survey, returning compositional and morphological information as well. Efforts have been made to give scientific feedback to the production processes and to support the research activity in the restoration of the artworks where these dyes were employed.

  10. Dyes and Materials for Sensitised Electrochemical Photovoltaics

    Science.gov (United States)

    Amirnasr, M.; Brooks, K. G.; McEvoy, A. J.; Nazeeruddin, M. K.; Pechy, P.; Thampi, K. R.; Grätzel, M.

    2001-11-01

    The present concepts evolved in the context of research and development of artificial photosynthetic systems. Our biosphere depends totally on the action of a porphyrin dye, chlorophyll, for its continued existance, since all food resources find their origin in photosynthesis. Equally, for much of our energy resources we rely on the same process, present or past, as stored in fossil fuels. Naturally, therefore, when it comes to the molecular design of dyes for solar photochemical applications the reference to the porphyrins and similar organometallic complexes based on nitrogen ring structures as prototypes is obvious. However, although nature confines itself to magnesium and iron for its principal pigments, chlorophyll and haemoglobin respectively, the synthetic chemist can access the whole range of metallic elements. The use of ruthenium pyridyl complexes has almost thirty years of development history, and although other compounds have been assessed, such as zinc porphyrins and even prussian-blue analogues, the most suitable dyes today are still modifications of the ruthenium-based pyridyl complexes. The molecular engineering of dyes extends the visible spectrum response, enhances stability and promotes chemisorption to oxide semiconductor substrates while maintaining the energetics and kinetics for efficient charge transfer to function in sensitised electrochemical photovoltaic devices. There is also an overview of the present status of the technology, the materials incorporated in current devices, and their reliability in practical applications especially in situations of thermal stress. The conclusion will present the case for ongoing development of dye-sensitised systems in photovoltaic technology.

  11. Chromed Leather Dyeing Peculiarities when Deliming with Peracetic Acid

    Directory of Open Access Journals (Sweden)

    Kęstutis BELEŠKA

    2013-05-01

    Full Text Available The research was aimed to investigate the influence of deliming with peracetic acid on leather dyeing kinetics. Hydrophobic C.I. Acid Red 213 and hydrophilic C.I. Acid Red 423 dyes were used. Sorption of dye depends on hydrophobicity/hydrophility of dye and dyeing temperature. Equilibrium of process is reached faster using hydrophobic C.I. Acid Red 213 at 45 ºC. However, both control and experimental leather fibres adsorb more hydrophilic dye C.I. Acid Red 423 and this fact does not depend on temperature. The diffusion coefficient of dye C.I. Acid Red 423 calculated according to Weisz model is higher when dyeing conventional leather. The change of deliming method has influence on chromed leather dyeing but this influence is not significant. The adsorption ability of control leather fibres at 30 ºC and 45 ºC is higher using both dyes as compared to the dyeing the experimental one. The increase of dyeing temperature increases the adsorption ability independently on the sort of leather fibres. Such dependence of the adsorption ability on the temperature shows that hydrophobic action and van der Waals forces prevail between dye and fibres during dyeing process. The Gibbs energy changes show that adsorption of both dyes by leather fibres independently on their sort is a spontaneous process. The affinity of both dyes to conventional leather fibres is higher comparing with experimental one. The change of enthalpy is positive in all cases, and it means that the driving force of the dyeing is the change of entropy.DOI: http://dx.doi.org/10.5755/j01.ms.19.2.4431

  12. Spectral Studies of UV and Solar Photocatalytic Degradation of AZO Dye and Textile Dye Effluents Using Green Synthesized Silver Nanoparticles.

    Science.gov (United States)

    Mariselvam, R; Ranjitsingh, A J A; Mosae Selvakumar, P; Alarfaj, Abdullah A; Munusamy, Murugan A

    2016-01-01

    The photocatalytic degradation of the chemical dye AZO and dye effluents in different time duration has been investigated using biologically synthesized silver nanoparticles. Dye industry effluents and AZO dye undergo degradation to form harmless intermediate and colourless products following irradiation by UV and solar light in the presence of green synthesized silver nanoparticles. The degree of degradation was tested under the experimental conditions such as P(H), temperature, and absorbance of the dye in UV and solar light was measured. The degradation was higher in the UV light source than in the solar light source. Green synthesized silver nanoparticles in the UV light source were found to expedite the dye degradation process.

  13. Quantum dot-dye hybrid systems for energy transfer applications

    Energy Technology Data Exchange (ETDEWEB)

    Ren, Ting

    2010-07-01

    In this thesis, we focus on the preparation of energy transfer-based quantum dot (QD)-dye hybrid systems. Two kinds of QD-dye hybrid systems have been successfully synthesized: QD-silica-dye and QD-dye hybrid systems. In the QD-silica-dye hybrid system, multishell CdSe/CdS/ZnS QDs were adsorbed onto monodisperse Stoeber silica particles with an outer silica shell of thickness 2-24 nm containing organic dye molecules (Texas Red). The thickness of this dye layer has a strong effect on the total sensitized acceptor emission, which is explained by the increase in the number of dye molecules homogeneously distributed within the silica shell, in combination with an enhanced surface adsorption of QDs with increasing dye amount. Our conclusions were underlined by comparison of the experimental results with Monte-Carlo simulations, and by control experiments confirming attractive interactions between QDs and Texas Red freely dissolved in solution. New QD-dye hybrid system consisting of multishell QDs and organic perylene dyes have been synthesized. We developed a versatile approach to assemble extraordinarily stable QD-dye hybrids, which uses dicarboxylate anchors to bind rylene dyes to QD. This system yields a good basis to study the energy transfer between QD and dye because of its simple and compact design: there is no third kind of molecule linking QD and dye; no spacer; and the affinity of the functional group to the QD surface is strong. The FRET signal was measured for these complexes as a function of both dye to QD ratio and center-to-center distance between QD and dye by controlling number of covered ZnS layers. Data showed that fluorescence resonance energy transfer (FRET) was the dominant mechanism of the energy transfer in our QD-dye hybrid system. FRET efficiency can be controlled by not only adjusting the number of dyes on the QD surface or the QD to dye distance, but also properly choosing different dye and QD components. Due to the strong stability, our QD-dye

  14. Improved Reactive Dye-fixation in Pad-Steam Process of Dyeing Cotton Fabric Using Tetrasodium N, NBiscarboxylatomethyl- L-Glutamate

    OpenAIRE

    Awais Khatri; Mazhar Hussain Peerzada

    2012-01-01

    Pad steam process of dyeing cotton with reactive dyes is known to give lower levels of dye-fixation on the fiber because of excessive dye-hydrolysis. This research presents improved reactive dye-fixation in padsteam process of dyeing cotton found in an effort of using biodegradable organic salts to improve the effluent quality. The CI Reactive Blue 250, a bissulphatoethylsulphone dye and the Tetrasodium N, Nbiscarboxylatomethyl- L-Glutamate, a biodegradable organic salt, were used...

  15. π-Spacer effect in dithiafulvenyl-π-phenothiazine dyes for dye-sensitized solar cells

    Science.gov (United States)

    Zhang, Xiaofeng; Gou, Faliang; Zhao, Dongning; Shi, Jian; Gao, Hong; Zhu, Zhenping; Jing, Huanwang

    2016-08-01

    New dithiafulvenyl-π-phenothiazine dyes have been devised and prepared for dye-sensitized solar cells. Various π-spacers have been successfully introduced into the skeleton of dithiafulvenyl and phenothiazine unit to generate novel D-π-D-A dyes (DPP-1 ∼ 4). All dyes have been characterized with NMR, HRMS, UV-vis and fluorescence spectra, and taken into cyclic voltammetry measurements. The devices of new dyes have been determined by photoelectrochemical experiments (IV, IPCE and EIS), in which, solar cell of DPP-4 with biphenyl ring π-spacer enhances obviously its photoelectric conversion efficiency to 7.66% reaching 94% of N719-based standard cell and displays good long-term stability with quasi-solid-state electrolyte. Density functional theory (DFT) calculations of new dyes provide further insight into the molecular geometries and the impacts of the torsion angles on their photovoltaic performance. Large dihedral angles in DPP dyes induce good charge separation for efficient unidirectional flow of electron from donor to acceptor.

  16. In-situ Decolorization of Residual Dye Effluent in Textile Jet Dyeing Machine by Ozone

    Directory of Open Access Journals (Sweden)

    Irfan Ahmed Shaikh

    2014-12-01

    Full Text Available In this study, a new idea of decolourization was investigated in which residual dyeing effluent from textile dyeing process was treated using O3 in the same machine where it was generated. The novelty comes from the idea of doing dyeing and treatment simultaneously. At the completion of dyeing process, O3 gas was injected directly into the machine to remove colour and COD from the wastewater. To evaluate the effectiveness of new method, pilot-scale studies were performed, and decolourization of residual dyeing effluents containing C.I. Reactive Orange 7, C.I. Reactive Blue 19, and C.I. Reactive Black 5 was carried out in specially built textile jet dyeing machine. The results showed that almost 100% colour removal and 90% COD reduction were achieved when process conditions such as pH, dye concentration (mg/L, ozone production rate (g/hr, and temperature were optimized. The study concludes that new method has a great potential to eliminate the need of a separate end-of-the-pipe wastewater treatment system, thus offering an on-site and cost-effective solution.

  17. Pad ultrasonic batch dyeing of causticized lyocell fabric with reactive dyes.

    Science.gov (United States)

    Babar, Aijaz Ahmed; Peerzada, Mazhar Hussain; Jhatial, Abdul Khalique; Bughio, Noor-Ul-Ain

    2017-01-01

    Conventionally, cellulosic fabric dyed with reactive dyes requires significant amount of salt. However, the dyeing of a solvent spun regenerated cellulosic fiber is a critical process. This paper presents the dyeing results of lyocell fabrics dyed with conventional pad batch (CPB) and pad ultrasonic batch (PUB) processes. The dyeing of lyocell fabrics was carried out with two commercial dyes namely Drimarine Blue CL-BR and Ramazol Blue RGB. Dyeing parameters including concentration of sodium hydroxide, sodium carbonate and dwell time were compared for the two processes. The outcomes show that PUB dyed samples offered reasonably higher color yield and dye fixation than CPB dyed samples. A remarkable reduction of 12h in batching time, 18ml/l in NaOH and 05g/l in Na2CO3 quantity was observed for PUB processed samples producing similar results compared to CPB process, making PUB a more economical, productive and an environment friendly process. Color fastness examination witnessed identical results for both PUB and CPB methods. No significant change in surface morphology of PUB processed samples was observed through scanning electron microscope (SEM) analysis.

  18. Improvement of dye-sensitized solar cells' performance through introducing suitable heterocyclic groups to triarylamine dyes.

    Science.gov (United States)

    Zhang, Ming-Dao; Pan, Hao; Ju, Xue-Hai; Ji, Ya-Jun; Qin, Ling; Zheng, He-Gen; Zhou, Xing-Fu

    2012-02-28

    Dye-sensitized solar cells are currently under intense academic and industrial investigation, owing to their great potential to serve as a low-cost alternative to existing photovoltaic technologies. This paper puts forward a method, which adopts heterocyclic substituted triarylamine units as electronic donor moieties, to design triarylamine dyes for efficient dye-sensitized solar cells. Three novel triarylamine dyes named TTC101, TTC102 and TTC103, were synthesized economically through modification of the structure of a simple triarylamine dye (TC105) using three kinds of heterocyclic groups (4-pyridyl, 2-thienyl and 1-pyrazolyl). The crystal structure of TTC103 indicates that the heterocyclic groups would partly delocalize the positive charge after photooxidation. The overall solar-to-electrical energy conversion efficiencies (η) of TTC102 and TTC103 are 4.92% and 5.21% respectively under AM1.5G irradiation, reaching ∼82.3% and ∼77.7% of a N719-based reference cell under the same conditions. Besides, the energy conversion efficiencies (η) of TTC102 and TTC103 are 1.29 and 1.37 times the efficiency of TC105 respectively. All of the results above demonstrate that photovoltaic performance can be improved by introducing suitable heterocyclic groups to triarylamine dyes. A series of properties were investigated to explain the results, with a special emphasis on the geometric structures, energetics, and charge transfer processes at the dye/titania/electrolyte interface.

  19. Dyeing of Silk with Anthocyanins Dyes Extract from Liriope platyphylla Fruits

    Directory of Open Access Journals (Sweden)

    Huayin Wang

    2014-01-01

    Full Text Available A new source of natural anthocyanins dyes, from Liriope platyphylla fruit, is proposed. This paper analyzes the dye extracts, the primary color components of the extracts, the color features of the extracts under different pH conditions, and their application in silk dyeing. The research shows that, nine anthocyanins are found in  L. platyphylla fruits by analyzing the results of the HPLC/DAD, MS, and MS/MS spectra. The five major anthocyanins related to delphinidin, petunidin, and malvidin derivatives take up 91.72% of total anthocyanin contents. The color of the solution is red under acidic condition (pH < 3.0 and stays in yellow under alkaline condition with pH values above 7.0. The dye extracts applied to silk fabric with mordant free dyeing show different color under different pH conditions, changing between purple, blue, green, and yellow. However, the dyed colors is light and the dyeing rate is low. Metal mordant such as Sn in chelation enhances the dye depth and improves the fastness of the dyed silk fabrics, especially in silk fabrics dyed by premordanting and metamordanting.

  20. Contact dermatitis to hair dye: An update

    Directory of Open Access Journals (Sweden)

    Sanjeev Handa

    2012-01-01

    Full Text Available Exposure to hair dyes has long been known as a significant risk factor for development of allergic contact dermatitis among the exposed population as these lead to severe eczema of face and upper trunk in the consumer and hand eczema in hair-dressers. Currently, para-phenylenediamine (PPD is the main ingredient used in permanent hair color products in the market and is the most important allergen. Prevalence of PPD sensitization is high in patients with contact dermatitis across all continents, with hair dye use being the commonest cause. In order to decrease the burden of disease, use of alternative natural dyeing agents among consumers and use of barrier neoprene gloves among hairdressers should be encouraged apart from stringent legislation to reduce the amount of PPD reaching the consumer.