Electrochemical synthesis of network polygermanes and polysilanes

被引:20
作者
Okano, M [1 ]
Fukai, H [1 ]
Arakawa, M [1 ]
Hamano, H [1 ]
机构
[1] Tokyo Inst Polytech, Fac Engn, Dept Photoopt Engn, Atsugi, Kanagawa 2430297, Japan
关键词
polygermane; polygermyne; polysilane; polysilyne; electro-reduction;
D O I
10.1016/S1388-2481(99)00045-4
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Network sigma-conjugated polymers, i.e., a butyl substituted network polygermane, (BuHxGe)(n) (x=0-2), a butyl substituted network polysilane, (BuHxSi)(n) (x = 0-2), and an octyl substituted network polysilane, (OctH(x)Si)(n) (x = 0-2), were synthesized by electrochemical reduction of butyltrichlorogermane, butyltrichlorosilane, and octyltrichlorosilane, respectively, for the first lime. A polymer of (BuHxGe)(n), (x= 0-2) had absorption which extended to 900 nm, while a polymer of (BuHxSi)(n) (x= 0-2) and a polymer of (OctH(x)Si)(n) (x= 0-2) had absorption which extended to 500 and 800 nms, respectively. It was found that the reported electrochemical method gave a-conjugated polymers with more highly developed network structures compared to the other synthetic pathways. The structure of the polymers was successfully controlled from linear to highly developed network structures by controlling the charge for electrosynthesis. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:223 / 226
页数:4
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