期刊
COORDINATION CHEMISTRY REVIEWS
卷 269, 期 -, 页码 54-84出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2014.02.016
关键词
Carboranylphosphines; Anionic phosphines; Catalyst; Electron withdrawing groups; Carboranes; Organic-inorganic hybrid phosphines
资金
- Generalitat de Catalunya [2009/SGR/00279]
- Ministerio de Ciencia e Innovacion [CTQ2010-16237]
The accurate selection of a ligand for a metal-catalyzed homogeneous reaction can be as decisive as the selection of the metal. Incorporating a carborane cage as a backbone to produce new phosphines often leads to remarkable properties, which are not accessible employing conventional organic entities. The synergy effects between the o-carborane cluster and the P atom in these closo- and nido-carboranylphosphines is observed from two points of view: the cluster and the P atom. The P atoms in the closo-carboranylmonophosphines grant to the cluster a unique plasticity on the C-cluster-C-cluster distance. The cooperation between the carboranyl moiety and the P atom may result in mono-, di-and tridendicity according to the necessities of the metal, not an ever-available property for organic phosphines. (C) 2014 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据