Metal-catalyzed cross-coupling chemistry with polyhedral boranes

被引:103
作者
Dziedzic, Rafal M. [1 ]
Spokoyny, Alexander M. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, 607 Charles E Young Dr East, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Calif NanoSyst Inst CNSI, 570 Westwood Plaza, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
CLOSO-DODECABORATE ANIONS; B-H ACTIVATION; X-RAY CRYSTAL; STRUCTURAL-CHARACTERIZATION; PINCER COMPLEXES; SUBSTITUTION-REACTIONS; CARBORANE DERIVATIVES; BOND ACTIVATION; BORON CLUSTER; ARYL HALIDES;
D O I
10.1039/c8cc08693a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Over the past several decades, metal-catalyzed cross-coupling has emerged as a very powerful strategy to functionalize carbon-based molecules. More recently, some of the cross-coupling methodologies have been adapted to inorganic compounds including boron-rich clusters. The development of this chemistry relies on the ability to synthesize halogenated boron-rich clusters which can serve as electrophilic cross-coupling partners with nucleophilic substrates in the presence of a metal catalyst. While the cross-coupling chemistry with boron-clusters is conceptually reminiscent of that of its hydrocarbon counterparts, several key aspects including the spheroidal bulk of clusters and the distinct nature of boron-halogen/boron-heteroatom bonds make this chemistry unique. The utility of metal-catalyzed cross-coupling can be extended to several classes of polyhedral boranes including neutral and anionic carboranes, metallaboranes, and carbon-free boranes. Importantly, cross-coupling enables a suite of boron-heteroatom (C, N, O, P, S) couplings to prepare boron cluster-based systems that can be used for ligand design, medicinal chemistry, and materials applications.
引用
收藏
页码:430 / 442
页数:13
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