Metal-Metal Bonds in Catalysis

被引:292
作者
Powers, Ian G. [1 ]
Uyeda, Christopher [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
catalysis; metal-metal bonds; cooperativity effects; multinuclear complexes; organometallic chemistry; C-H BOND; OXIDATIVE-ADDITION-REACTIONS; DINUCLEAR NICKEL-COMPLEXES; REDOX-ACTIVE LIGANDS; CRYSTAL-STRUCTURE; MULTIPLE BONDS; HETEROBIMETALLIC COMPLEX; SUBSTITUTION-REACTIONS; HIGH REGIOSELECTIVITY; MECHANISTIC INSIGHTS;
D O I
10.1021/acscatal.6b02692
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transition metals can assemble to form multi nuclear complexes by engaging in direct metal-to-metal interactions. Metal metal covalent bonds provide a large perturbation in electronic structure, relative to mononuclear metal ions, and the unique properties of these dinuclear fragments can be harnessed in a broad range of applications for example, as chromophores in photochemical processes, redox centers in molecular electronics, or structural elements in metal organic materials. There is a growing body of evidence that metal metal bonds may also be formed under conditions relevant to catalysis and play a key role in transformations that were previously assumed to only involve mononuclear species. These findings have stimulated interest in characterizing multinuclear reaction pathways and developing well-defined multinuclear platforms as catalytic active sites. In this Perspective, we present case studies in this emerging area of catalysis research, emphasizing the impact of metal metal bonding in either enhancing or depressing the rate and/or selectivity of a catalytic organic transformation.
引用
收藏
页码:936 / 958
页数:23
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