Cobalt-Catalyzed Acceptorless Dehydrogenation of Primary Amines to Nitriles

被引:16
|
作者
Tian, Haitao [1 ]
Ding, Cai-Yun [1 ]
Liao, Rong-Zhen [1 ]
Li, Man [1 ]
Tang, Conghui [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGENATION; RUTHENIUM; ALCOHOLS; CONVERSION; COOPERATION; COMPLEXES; CHEMISTRY; MECHANISM; ALDEHYDES; CYANIDE;
D O I
10.1021/jacs.4c00493
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct double dehydrogenation from primary amines to nitriles without an oxidant or hydrogen acceptor is both intriguing and challenging. In this paper, we describe a non-noble metal catalyst capable of realizing such a transformation with high efficiency. A cobalt-centered N,N-bidentate complex was designed and employed as a metal-ligand cooperative dehydrogenation catalyst. Detailed kinetic studies, control experiments, and DFT calculations revealed the crucial hydride transfer, proton transfer, and hydrogen evolution processes. Finally, a tandem outer-sphere/inner-sphere mechanism was proposed for the dehydrogenation of amines to nitriles through an imine intermediate.
引用
收藏
页码:11801 / 11810
页数:10
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