Redox-Active Ligands in Catalysis

被引:309
作者
Praneeth, Vijayendran K. K. [1 ]
Ringenberg, Mark R. [1 ]
Ward, Thomas R. [1 ]
机构
[1] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
base metals; biomimetic catalysis; homogeneous catalysis; multi-electron transformations; redox-active ligands; TRANSITION-METAL-COMPLEXES; WATER OXIDATION CATALYST; CLUSTER-FREE HYDROGENASE; N-HETEROCYCLIC CARBENES; ELECTRONIC-STRUCTURE; CRYSTAL-STRUCTURE; BOND ACTIVATION; RADICAL LIGANDS; PHOTOSYSTEM-II; C-H;
D O I
10.1002/anie.201204100
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Natures use of redox-active moieties combined with 3d transition-metal ions is a powerful strategy to promote multi-electron catalytic reactions. The ability of these moieties to store redox equivalents aids metalloenzymes in promoting multi-electron reactions, avoiding high-energy intermediates. In a biomimetic spirit, chemists have recently developed approaches relying on redox-active moieties in the vicinity of metal centers to catalyze challenging transformations. This approach enables chemists to impart noble-metal character to less toxic, and cost effective 3d transitional metals, such as Fe or Cu, in multi-electron catalytic reactions.
引用
收藏
页码:10228 / 10234
页数:7
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