An Extensive n, π, σ-Electron Delocalized Si4 Ring

被引:36
作者
Zhang, Shu-Hua [1 ]
Xi, Hong-Wei [2 ]
Lim, Kok Hwa [2 ]
So, Cheuk-Wai [1 ]
机构
[1] Nanyang Technol Univ, Div Chem & Biol Chem, Singapore 637371, Singapore
[2] Nanyang Technol Univ, Div Chem & Biomol Engn, Singapore 637459, Singapore
关键词
aromatic systems; cyclobutadiene; N ligands; silicon; sulfur; X-RAY-STRUCTURE; PHOTOCHEMICAL-TRANSFORMATIONS; CRYSTALLINE MATRIX; DOUBLE-BONDS; CYCLOBUTADIENE; TETRASILACYCLOBUTADIENE; REACTIVITY; 1,3-DIMETHYLCYCLOBUTADIENE; ANTIAROMATICITY; AROMATICITY;
D O I
10.1002/anie.201305567
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The tetrasilacyclobutadiene [LSi(μ-SiL′)2SiL] (L=PhC(NtBu)2, L′=2,6-iPr2C6H 3NSiMe3) consists of an aromatic silicon-containing four-membered ring in which two π, two σ, and two lone-pair electrons are cyclically delocalized. The electron delocalization was illustrated by theoretical studies and reactivity with elemental sulfur to form the allylic zwitterionic cyclic compound [(LSi)2(μ-SiL′)(μ-Si(S) L′)] with 2π-electron delocalization along the Si3 skeleton. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:12364 / 12367
页数:4
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