Synthesis and properties of benzobis(thiadiazole)s with nonclassical pi-electron ring systems

被引:72
作者
Yamashita, Y
Ono, K
Tomura, M
Tanaka, S
机构
[1] Institute for Molecular Science, Myodaiji
基金
日本学术振兴会;
关键词
D O I
10.1016/S0040-4020(97)00356-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Benzo[1,2-c:4,5-c']bis([1,2,5]thiadiazole) containing a hypervalent sulfur atom has a low LUMO energy. The aryl derivatives were synthesized using a Stille coupling reaction, The selenadiazole analogues were also prepared. The electron accepting properties of these nonclassical heterocycles were shown by their high reduction potentials. Introduction of electron-donating groups into the electron-withdrawing heterocycles afforded novel donor-acceptor compounds. Their cyclic voltammograms showed that they are easily both oxidized and reduced. Some of them have the absorption maxima above 700 nm due to the small HOMO-LUMO separation. X-ray structure analysis of the diphenyl derivative revealed the formation of a tape-like network through short S...N contacts. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:10169 / 10178
页数:10
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