THE EFFECT OF SPIN MULTIPLICITY ON THE PHOTOCHEMICAL-REACTION OF A 2-VINYLNAPHTHALENE-DICHLOROMALEIC ANHYDRIDE SYSTEM

被引:3
作者
SATOH, SI
NAKAJIMA, T
SHIROTA, Y
机构
[1] Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka, 565, Yamadaoka
关键词
D O I
10.1163/156856795X00585
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The photochemical reaction of a 2-vinylnaphthalene-dichloromaleic anhydride system has been studied in order to elucidate the correlation between the spin multiplicity of an excited-state molecule and reaction pathways in electron donor - acceptor systems. Direct irradiation of the system resulted mostly in the recovery of the starting materials. By contrast, the triplet-sensitized reaction using benzophenone as a sensitizer produced a copolymer and two stereoisomeric cycloadducts of 2-vinylnaphthalene with dichloromaleic anhydride. It is suggested that electron transfer takes place both in the electronically excited singlet and triplet states, although a tripler-state reaction also proceeds simultaneously in the benzophenone-sensitized reaction, and that the reaction pathway of the radical-ion pair generated in the excited singlet state is greatly different from that generated in the excited triplet state.
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收藏
页码:939 / 949
页数:11
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