A new approach to the synthesis of unsymmetrical disilenes and germasilene:: Unusual 29Si NMR chemical shifts and regiospecific methanol addition

被引:75
作者
Ichinohe, M
Arai, Y
Sekiguchi, A [1 ]
Takagi, N
Nagase, S
机构
[1] Univ Tsukuba, Dept Chem, Tsukuba, Ibaraki 3058571, Japan
[2] Inst Mol Sci, Dept Theoret Studies, Okazaki, Aichi 4448585, Japan
关键词
D O I
10.1021/om010419d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of dilithiosilanes ((Pr3Si)-Pr-i)(2)SiLi2 (1a) and ((Bu2MeSi)-Bu-t)2SiLi2 (1b) with diaryldichlorosilanes [Ar2SiCl2, Ar = Mes (2,4,6-trimethylphenyl) and Tip (2,4,6-triisopropylphenyl)] quantitatively produced the corresponding unsymmetrical 1,1-diaryl-2,2-bis(trialkylsilyl)disilenes, Ar2Si=Si(SiR3)(2) (2, R3Si = (Pr3Si)-Pr-i; 3, R3Si = (Bu2MeSi)-Bu-t). A stable germasilene, Mes(2)Ge = Si((SiMeBu2)-Bu-t)(2) (4), was also synthesized by the reaction of lb with dimesityldichlorogermane. These compounds reveal unusual Si-29 NMR shifts and regioselective methanol additions.
引用
收藏
页码:4141 / 4143
页数:3
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