Photoinduced Hydrogen Evolution with Hydrogenase and Water-soluble Viologen-linked Zinc Porphyrins

Author(s):  
YUTAKA AMAO ◽  
TOSHIAKI KAMACHI ◽  
ICHIRO OKURA

A series of water-soluble viologen-linked zinc porphyrins with different methylene chain lengths (n = 3−6) between porphyrin and viologen, ZnP ( C n V )4, were synthesized and characterized. The intra- molecular electron transfer rate constants from the porphyrin moiety of ZnP (Cn V )4 to viologen were measured by using fluorescence lifetime and laser flash photolysis. Both the photoexcited singlet state and the triplet state of the porphyrin were quenched by the bonded viologen. These compounds were applied to photoinduced hydrogen evolution in the system containing nicotinamide-adenine dinucleotide phosphate (reduced form NADPH), ZnP ( C n V )4 and hydrogenase under steady-state irradiation.

2001 ◽  
Vol 3 (3) ◽  
pp. 161-169 ◽  
Author(s):  
Peter C. Ford

The discoveries that nitric oxide (a.k.a. nitrogen monoxide) serves important roles in mammalian bioregulation and immunology have stimulated intense interest in the chemistry and biochemistry of NO and derivatives such as metal nitrosyl complexes. Also of interest are strategies to deliver NO to biological targets on demand. One such strategy would be to employ a precursor which displays relatively low thermal reactivity but is photochemically active to release NO. This proposition led us to investigate laser flash and continuous photolysis kinetics of nitrosyl complexes such as the Roussin's iron-sulfur-nitrosyl cluster anionsFe2S2(NO)42−andFe4S3(NO)7−and several ruthenium salen and porphyrin nitrosyls. These include studies using metal-nitrosyl photochemistry as a vehicle for delivering NO to hypoxic cell cultures in order to sensitizeγ-radiation damage. Also studied were the rates and mechanisms of NO “on” reactions with model water soluble heme compounds, the ferriheme protein met-myoglobin and various ruthenium complexes using ns laser flash photolysis techniques. An overview of these studies is presented.


1985 ◽  
Vol 63 (11) ◽  
pp. 3001-3006 ◽  
Author(s):  
D. J. Lougnot ◽  
P. Jacques ◽  
J. P. Fouassier ◽  
H. L. Casal ◽  
Nguyen Kim-Thuan ◽  
...  

Two water-soluble ionic benzophenones containing a quatemized amine and a sulphonate group have been investigated by laser flash photolysis. The decay kinetics and spectra of their triplet states were studied and quenching constants by triethanolamine, isopropanol, and methyl viologen determined. These data are of interest when these benzophenones are used as initiators for photo-polymerizing water-soluble acrylates in homogeneous solution or in reverse micellar assemblies. The high water solubility of these compounds allows the bimolecular deactivations due to triplet–triplet (kTT) and triplet–ground state (kSQ) interactions to be determined more accurately than in the case of benzophenone itself.


1996 ◽  
Vol 225 (2) ◽  
pp. 577-584 ◽  
Author(s):  
Sergei V. Paschenko ◽  
Valery V. Khramtsov ◽  
Mikhail P. Skatchkov ◽  
Viktor F. Plyusnin ◽  
Eberhard Bassenge

2002 ◽  
Vol 76 (5) ◽  
pp. 480 ◽  
Author(s):  
Xavier Damoiseau ◽  
Francis Tfibel ◽  
Maryse Hoebeke ◽  
Marie-Pierre Fontaine-Aupart

2000 ◽  
Vol 72 (4) ◽  
pp. 451 ◽  
Author(s):  
M. Bazin ◽  
F. Bosca ◽  
M. L. Marin ◽  
M. A. Miranda ◽  
L. K. Patterson ◽  
...  

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