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2

Magnetic resonance studies of photosynthetic reaction centers and porphyrins  

Science.gov (United States)

During the period covered by this report research has been concerned with the study of photo-induced electron transfer reactions from porphyrins to acceptor molecules with time-resolved Electron Paramagnetic Resonance (EPR) methods. Excited-state electron transfer reactions are of importance from a fundamental point of view and in connection with applications in homogeneous and heterogeneous photosensitization, photopolymerization, and solar energy conversions. For this reason, the study of photo-induced electron transfer reactions is of considerable interest.

1989-11-01

3

Supramolecular selectivity of [60]-fullerene among equivalently photoactive porphyrins  

International Nuclear Information System (INIS)

The photophysical investigation of different para-substituted tetraphenylporphyrins (TP), viz., meso-tetra(4'-hydroxyphenyl)-21H-23H-porphyrin(1),meso-tetrakis (4'-hex-5-enyloxyphenyl)-21H-23H-porphyrin(2), meso-tetrakis(4'-oct-7-enyloxyphenyl)-21H-23H-porphyrin(3) and meso-tetrakis(4'-undecyloxyphenyl)-21H-23H-porphyrin (4) revealed that except for quantum yield (#phi#) the para-substitution has little effect on any other photophysical properties like lifetime, excitation, emission wavelength, etc. The host-guest type interactions of these tetraarylporphyrins (TP 1-4), with [60]-fullerene (F) have been studied with "1H NMR and fluorescence spectrometric techniques in carbon tetrachloride medium. Fluorescence studies revealed that the Q band of the TPs was sufficiently quenched upon addition of F. All the fullerene/porphyrin systems were found to produce stable complexes with 1:1 ...

2010-10-01

4

Enterococcus faecalis Heme-Dependent Catalase  

UK PubMed Central (United Kingdom)

Enterococcus faecalis cells cannot synthesize porphyrins and do not rely on heme for growth but can take up heme and use it to synthesize heme proteins. We recently described a cytochrome...Full Text Available

2002-11-01

5

Investigations of biomimetic light energy harvesting pigments  

Energy Technology Data Exchange (ETDEWEB)

This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). Nature uses chlorophyll and other porphyrinic pigments to capture and transfer light energy as a preliminary step in photosynthesis. The design of synthetic assemblies of light harvesting and energy directing pigments has been explored through synthesis and characterization of porphyrin oligomers. In this project, pigment electronic and vibrational structures have been explored by electrochemistry and dynamic and static optical measurements. Transient absorption data reveal energy transfer between pigments with lifetimes on the order of 20--200 picoseconds, while Raman data reveal that the basic porphyrin core structure is unperturbed relative to the individual monomer units. These two findings, along with an extensive series of experiments on the oxidized oligomers, reveal that ...

1998-12-01

6

Induction of Porphyrin Synthesis in Etiolated Bean Leaves by Chelators of Iron 12  

UK PubMed Central (United Kingdom)

Primary leaves of 7- to 9-day-old etiolated seedlings of Phaseolus vulgaris L. var. Red Kidney infiltrated in darkness with aqueous solutions of α, α′-dipyridyl,...Full Text Available

1974-02-01

7

Electrosynthesis of adherent poly(3-amino-1,2,4-triazole) films on brass prepared in nonaqueous solvents  

Energy Technology Data Exchange (ETDEWEB)

The kinetics of the electropolymerization of 3-amino-1,2,4-triazole on a brass substrate in alkaline solution containing methanol was investigated using cyclic polarization, chronoamperometry, electrochemical impedance techniques and scanning electronic microscopy. The polymeric film was prepared by successive cycles of potential of a 60Cu-Zn electrode between 0 and 1.6 V. During the second cycle, the oxidation peak of the monomer disappears indicating the formation of the insulating film. We have also shown that the monomer oxidation reaction is essentially irreversible and controlled by a diffusion process. The protective effect of the film formed on brass has been studied in a 3%NaCl and 3%NaCl + S{sup 2-} solution. The results showed important inhibition efficiency, about 96% for 4 h of testing time.

2008-06-15

8

Electrosynthesis of adherent poly(3-amino-1,2,4-triazole) films on brass prepared in nonaqueous solvents  

British Library Electronic Table of Contents (United Kingdom)

The kinetics of the electropolymerization of 3-amino-1,2,4-triazole on a brass substrate in alkaline solution containing methanol was investigated using cyclic polarization, chronoamperometry, electrochemical impedance techniques and scanning electronic microscopy. The polymeric film was prepared by successive cycles of potential of a 60Cu-Zn electrode between 0 and 1.6V. During the second cycle, the oxidation peak of the monomer disappears indicating the formation of the insulating film. We have also shown that the monomer oxidation reaction is essentially irreversible and controlled by a diffusion process. The protective effect of the film formed on brass has been studied in a 3%NaCl and 3%NaCl+S2- solution. The results showed important inhibition efficiency, about 96% for 4h of testing ...

2008-01-01

9

Comparison of radiationless decay processes in osmium and platinum porphyrins  

International Nuclear Information System (INIS)

Two osmium porphyrin complexes, Os(OEP)L_2 [OEP = octaethylporphin, L = py(pyridine) or NO], and PtOEP were investigated by picosecond laser spectroscopy with use of a double-beam, mode-locked Nd:glass system delivering 6-ps (fwhm) pulses at 527 nm with 1-2mJ/pulse. Time-resolved excited-state spectra were recorded from the time of photoexcitation to 5 ns after photoexcitation. The initial excited state, S_1, decayed in less than or equal to9 ps for the two osmium complexes and in less than or equal to15 ps for the platinum porphyrin. A second excited state, T_1, lived for 1, 9, and >50 ns respectively for Os(OEP)(py)_2, Os(OEP)(NO)_2, and PtOEP. The #DELTA#A spectra of the T_1 states of the osmium complexes were similar to those of previously reported (d/sub #pi#/,#pi#*) states for Os(OEP)(py)_2 and (#pi#,#pi#*) states for Os(OEP)(NO)_2. This finding supports prior assignments of these states on the basis of expected axial and equatorial ...

10

Strong coupled organic microcavities  

International Nuclear Information System (INIS)

Strong coupled organic-inorganic microcavities device has been realized and studied. One of the two cavities contains an organic thin film of tetrakis(4-methoxyphenyl)porphyrin, whereas the other microcavity is a dielectric structure coupled to the organic one by means of a LiF/ZnS Bragg mirror. Reflectivity spectra show the presence of two well defined cavity dips. We observe an energy splitting of the two cavity-modes. Despite only one cavity contains the active layer, the photoluminescence spectra display two peaks at the same energy of the reflectivity dips. These observations indicate the strong coupling of the two cavities. The comparison of the diagonalized effective Hamiltonian with the observed resonances further confirms the strong coupling.

2010-02-01

11

Photodynamic therapy against cyanobacteria  

British Library Electronic Table of Contents (United Kingdom)

This study explores the use of photosensitizers and reactive oxygen species (ROS) to limit growth of cyanobacteria. We chose 12 phthalocyanines, tetraphenol porphyrine, and methylene blue as compounds producing singlet oxygen. Hydrogen peroxide was chosen as another source of ROS. These compounds were tested using algal toxicity tests in microplates on three cultures of green algae (Pseudokirchneriella subcapitata, Scenedesmus quadricauda, and Chlorella kessleri) and on three cultures of cyanobacteria (Synechococcus nidulans, Microcystis incerta, and Anabaena sp.). Results indicate that photosensitizers and singlet oxygen could be highly toxic for some selected phytoplankton species. Green alga Scenedesmus quadricauda was highly sensitive (EC50 = 0.07 mg/L) to compounds producing singlet o...

2007-01-01

12

Effect of biodegradation on vanadylporphyrin distribution  

Energy Technology Data Exchange (ETDEWEB)

Oils, tars, and degraded oils of varying degrees of biodegradation occur in the Permian Phosphoria Formation along the eastern flank of the Wind River mountains, Wyoming, US. Biodegradation has altered the isomer distributions of steranes, the hopanes, and the mono- and triaromatised steroids in these oils. The conventional maturity parameters based on these biomarkers are of limited use in estimating their maturity. On the other hand, even in severely biodegraded oils the vanadylporphyrin distributions are unaltered. Because of this, the Porphyrin Maturity Parameter (PMP) derived from the vanadylporphyrin distribution is an ideal parameter for estimating the maturity of these oils. This study also confirms the previous observation that T[sub s] and T[sub m] are unaffected by even severe biodegradation. 14 refs., 5 figs., 2 tabs.

1993-05-01

13

New dioxomolybdenum(VI) complexes with tridentate dibasic ONO donor schiff bases  

International Nuclear Information System (INIS)

Several dioxomolybdenum(VI) complexes of the schiff bases derived from salicylaldehyde, 2-hydroxy-1-naphthaldehyde, o-hydroxyacetophenone or pyridoxal and o-aminobenzylalcohol, o-aminophenol, o-hydroxybenzylamine, o-hydroxy(methylbenzyl)amine or 3-amino-2-naphthoic acid have been synthesized and characterized by elemental analysis, electrical conductance, molecular weight, IR and electronic spectral and magnetic susceptibility measurements. The schiff bases behave as dibasic, tridentate ligands and coordinate through ONO donor system forming complexes of the type MoO_2L.X (where LH_2=schiff base, X=H_2O or Ch_3OH). The compounds MoO_2L.Ch_3OH react with 2,2'-dipyridyl to form heterochelates of the type MoO_2L.dipyridyl. The complexes are non-electrolytes, monomers, diamagnetic and possess a cis-MoO_2 structure. The complexes exhibit a ligand-to-metal charge-transfer transition around 25000 cm"-"1. The complexes MoO_2L.X and MoO_2L.dipyridyl are ...