CATALYSIS OF TRIPLET-STATE CIS-TRANS ISOMERIZATIONS MAKING A QUANTUM CHAIN PROCESS MORE EFFICIENT

Citation
M. Brink et al., CATALYSIS OF TRIPLET-STATE CIS-TRANS ISOMERIZATIONS MAKING A QUANTUM CHAIN PROCESS MORE EFFICIENT, Journal of photochemistry and photobiology. A, Chemistry, 112(2-3), 1998, pp. 149-153
Citations number
19
Categorie Soggetti
Chemistry Physical
ISSN journal
10106030
Volume
112
Issue
2-3
Year of publication
1998
Pages
149 - 153
Database
ISI
SICI code
1010-6030(1998)112:2-3<149:COTCIM>2.0.ZU;2-1
Abstract
Photocatalysis of cis-trans isomerizations is treated in this paper. T wo systems, 8-( 3,5-ditert-butylstyryl) fluoranthene/camphorquinone/ac ridine and 1,6-bisstyryl-1,3,5-cycloheptatriene/C60 were studied. rn t he first system Z-8-(3,5-ditert-butylstyryl)fluoranthene is photoisome rized with acridine as the catalyst and camphorquinone as triplet sens itizer, and in the second Z,E-1,6-bisstyryl-1,3,5-cycloheptatriene is isomerized with C60 as both catalyst and triplet sensitizer. The quant um efficiencies were found to increase 5.5 times in the first case and to be doubled in the second. The effect of concentration of both the catalyst and the reactant were investigated. The results are explained as an increased efficiency of a quantum chain process, and a theoreti cal model is used to evaluate the results. (C) 1998 Elsevier Science S .A.