ELECTROSYNTHESIS, AN ALTERNATIVE FOR THE SYNTHESIS OF POLYCARBOSILANES

被引:21
作者
BORDEAU, M
BIRAN, C
PONS, P
LEGER, MP
DUNOGUES, J
机构
[1] Laboratoire de Chimie organique et organométallique (U.R.A., 35 CNRS), Université de Bordeaux I
关键词
D O I
10.1016/0022-328X(90)80225-O
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The electrochemical reduction of chloromethyldimethylchlorosilane affords polycarbosilanes in high yields and this route constitutes a competitive route to 1,1,3,3-tetramethyl-1,3-disilacyclobutane formed in 34% crude yield. The solvent mixture was varied to yield its precursor, Cl(CH2SiMe2)2Cl, in 43% yield after distillation, while electrosynthesis in the presence of dimethyldichlorosilane provided bis(dimethyl-chlorosilyl)methane, another polycarbosilane precursor, in 60% yield after distillation. © 1990.
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页码:C21 / C24
页数:4
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