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Title: Artificial photosynthesis using chlorophyll based carotenoid-quinone triads: Final technical progress report

Technical Report ·
OSTI ID:5780386

Goal of this last year was the synthesis and study of a molecular tetrad consisting of a porphyrin or chlorophyll derivative covalently linked to both a carotenoid polyene and a rigid diquinone moiety. Photosynthesis converts light into chemical potential energy in the form of long-lived charge separation across a bilayer membrane. Recombination of the charge-separated state is prevented by the large distance between the final electron donor and acceptor. Reaction centers employ a series of electron transfer steps, each of which occurs over a short distance with high quantum yield. Synthetic carotenoid-porphyrin-quinone triad molecules and other molecular systems which begin to model this approach have recently been reported by our group and other researchers. In photosynthetic bacteria, the charge separation sequence includes electron donation from a bacteriopheophytin to a quinone which then transfers an electron to a second quinone. The proposed carotenoid-porphyrin-diquinone (C-P-Q-Q) tetrad was designed to model this portion of the natural photosynthetic electron transport system, and to be the next step in the evolution of increasingly complex synthetic mimics of natural solar energy conversion. Such a tetrad has been prepared. Nanosecond laser flash photolysis and picosecond fluorescence decay studies were carried out. Electron transfer reactions in C-P dyads and C-P-Q triads were studied.

Research Organization:
Arizona State Univ., Tempe (USA). Dept. of Chemistry
DOE Contract Number:
FG02-84CH10198
OSTI ID:
5780386
Report Number(s):
DOE/CH/10198-T1; ON: DE88001660
Resource Relation:
Other Information: Portions of this document are illegible in microfiche products
Country of Publication:
United States
Language:
English