Cobalt(II)-Catalyzed Transfer Hydrogenation of Simple Alkenes

被引:4
|
作者
Tian, Jing [1 ,2 ]
Xu, Daqian [3 ]
Sun, Wei [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Lanzhou City Univ, Sch Chem & Chem Engn, Lanzhou 730070, Peoples R China
基金
中国国家自然科学基金;
关键词
transfer hydrogenation; ammonia-borane; cobalt complex; terminal olefin; cobalt hydride; CATALYZED ASYMMETRIC HYDROGENATION; OLEFIN HYDROGENATION; AMMONIA-BORANE; COBALT; LIGAND; IRON; COMPLEXES; MECHANISM; ALKYNES; AMINE;
D O I
10.1002/adsc.202200712
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Several cobalt(II) complexes supported by tetradentate aminobenzimidazole (N4) ligands and a tridentate nitrogen (N3) ligand have been prepared and characterized. X-ray crystallographic analysis indicates that the cobalt complex of BPMB (BPMB=1,2-bis((S)-2-(1-methyl-1H-benzo[d]imidazol-2-yl) pyrrolidin-1-yl)ethane) ligand shows a distorted octahedral configuration. These cobalt(II) complexes can catalyze the transfer hydrogenation reaction of simple olefins with ammonia borane as a hydrogen source, and a variety of terminal olefins can be reduced to corresponding alkanes in good to excellent yields under mild reaction conditions. Note that Co-N3 complex provides an inferior outcome than those of Co-N4 complexes.
引用
收藏
页码:3874 / 3880
页数:7
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