Addition of Isocyanides to Tetramesityldigermene: A Comparison of the Reactivity between Surface and Molecular Digermenes

被引：9

作者：

Tashkandi, Nada Y. ^{[1
]}

Cook, Emily E. ^{[1
]}

Bourque, Jeremy L. ^{[1
]}

Baines, Kim M. ^{[1
]}

机构：

[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada

来源：

CHEMISTRY-A EUROPEAN JOURNAL | 2016年 / 22卷 / 39期

基金：

加拿大自然科学与工程研究理事会;

关键词：

germanium; inorganic chemistry; isocyanide ligands; main-group elements; surface chemistry; IV SEMICONDUCTOR SURFACES; N-HETEROCYCLIC CARBENE; GE(100)-2 X-1 SURFACE; BIRADICAL INTERMEDIATE; ORGANIC FUNCTIONALIZATION; CYCLOPROPYL ALKYNE; CARBONYL-COMPOUNDS; DISILENE; GE; CYCLOTRIGERMANES;

D O I：

10.1002/chem.201602222

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The reaction of benzyl isocyanide, tert-butyl isocyanide, and 2,6-dimethylphenyl isocyanide with tetramesityl-digermene (Mes(2)Ge=GeMes(2)) was examined. Whereas the addition of benzyl isocyanide gave the C-NC activation product, Mes(2)Ge(CH2Ph) Ge(CN) Mes(2), tert-butyl isocyanide, and 2,6-dimethylphenyl isocyanide did not give stable ad-ducts, rather the rate of conversion of the digermene to the corresponding cyclotrigermane was accelerated. A comparison between the reactivity of the isocyanides with Mes(2)Ge=GeMes(2) and the Ge(100)-2 x 1 surface was made and some insights into the surface chemistry are offered.

引用

页码：14006 / 14012

页数：7

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