Heteroatom-Free Arene-Cobalt and Arene-Iron Catalysts for Hydrogenations

被引:125
作者
Gaertner, Dominik [1 ]
Welther, Alice [1 ]
Rad, Babak Rezaei [1 ]
Wolf, Robert [1 ]
Jacobi von Wangelin, Axel [1 ]
机构
[1] Univ Regensburg, Fak Chem, D-93040 Regensburg, Germany
关键词
arene complexes; cobalt; homogeneous catalysis; hydrogenations; iron; ASYMMETRIC TRANSFER HYDROGENATION; ELECTRONIC-STRUCTURE; CARBONYL-COMPLEXES; OLEFINS; DEHYDROGENATION; NANOPARTICLES; CHEMISTRY; MECHANISM; RELEVANT; KINETICS;
D O I
10.1002/anie.201308967
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
75 years after the discovery of hydroformylation, cobalt catalysts are now undergoing a renaissance in hydrogenation reactions. We have evaluated arene metalates in which the low-valent metal species is-conceptually different from heteroatom-based ligands-stabilized by pi coordination to hydrocarbons. Potassium bis(anthracene)cobaltate 1 and -ferrate 2 can be viewed as synthetic precursors of quasi-"naked" anionic metal species; their aggregation is effectively impeded by (labile) coordination to the various p acceptors present in the hydrogenation reactions of unsaturated molecules (alkenes, arenes, carbonyl compounds). Kinetic studies, NMR spectroscopy, and poisoning studies of alkene hydrogenations support the formation of a homogeneous catalyst derived from 1 which is stabilized by the coordination of alkenes. This catalyst concept complements the use of complexes with heteroatom donor ligands for reductive processes.
引用
收藏
页码:3722 / 3726
页数:5
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