Acceptor less, Reversible Dehydrogenation and Hydrogenation of N-Heterocycles with a Cobalt Pincer Catalyst

被引:226
作者
Xu, Ruibo [1 ,2 ]
Chakraborty, Sumit [1 ]
Yuan, Hongmei [1 ]
Jones, William D. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
[2] Huaihai Inst Technol, Sch Pharm, Lianyungang 222005, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
acceptorless dehydrogenation; hydrogenation; cobalt catalysis; N-heterocycles; pincer ligands; H-2 storage materials; NITROGEN-HETEROCYCLES; STORAGE; COMPLEXES; MILD; ALCOHOLS; RELEASE; INDOLES;
D O I
10.1021/acscatal.5b02002
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
Acceptor less, reversible dehydrogenation and hydrogenation reactions involving N-heterocycles are reported with a well-defined cobalt complex supported by an aminobis(phosphine) [PN(H)P] pincer ligand. Several N-heterocycle substrates have been evaluated under dehydrogenation and hydrogenation conditions. The cobalt-catalyzed amine dehydrogenation step, a key step in the dehydrogenation process, has been independently verified. Control studies with related cycloalkanes suggest that a direct acceptorless alkane dehydrogenation pathway is unlikely. The metal-ligand cooperativity is probed with the related [PN(Me)P] derivative of the cobalt catalyst. These results suggest a bifunctional dehydrogenation pathway and a nonbifunctional hydrogenation mechanism.
引用
收藏
页码:6350 / 6354
页数:5
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