The stable silylene Si[(NCH2tBu)2C6H4-1,2]:: insertion into Li-C or Li-Si bonds of lithium alkyls LiR or [LiSi(SiMe3)3(THF)3] [R = Me, tBu or CH(SiMe3)2]

被引:8
作者
Cai, XP [1 ]
Gehrhus, B [1 ]
Hitchcock, PB [1 ]
Lappert, MF [1 ]
Slootweg, JC [1 ]
机构
[1] Univ Sussex, Chem Lab, Brighton BN1 9QJ, E Sussex, England
基金
英国工程与自然科学研究理事会;
关键词
amino-functionalised silyl anions; lithium; alkyls; sisyls;
D O I
10.1016/S0022-328X(01)01273-6
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The new crystalline amino-functionalised lithium silyls Li[Si{(NCH2'Bu)(2)C6H4-1,2}R](L) [R = Si(SiMe3)(3) (sisyl), L = (THF)(2) (2); R = Me, L = (OEt2)(2) (3); R = 'Bu, L = (THF)(3) (4a) or THF(OEt2) (4b); R = CH(SiMe3)(2), L = (THF)(2) (5)] have been obtained in high yield from the silylene Si[(NCH2'Bu)(2)C6H4-1,2] and Li-R under mild conditions. A by-product in the reaction leading to 4 was the crystalline disilane [1,2-C6H4(NCH2'Bu)(2)('Bu)Si](2) (6). Each of 2-6 was fully characterised by microanalysis, multinuclear NMR spectra and X-ray structures. Each of the compounds 3-6 was thermally stable in solution. whereas the sisyl derivative 2 retained its integrity only at low temperatures, being completely dissociated into its factors at ambient temperature. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:272 / 277
页数:6
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