A versatile cobalt catalyst for the reductive amination of carbonyl compounds with nitro compounds by transfer hydrogenation

被引:120
|
作者
Zhou, Peng [1 ]
Zhang, Zehui [1 ]
Jiang, Liang [1 ]
Yu, Changlin [2 ]
Lv, Kangle [1 ]
Sun, Jie [1 ]
Wang, Shuguo [1 ]
机构
[1] South Cent Univ Nationalities, Minist Educ, Key Lab Catalysis & Mat Sci, Wuhan 430074, Peoples R China
[2] Jiangxi Univ Sci & Technol, Sch Met & Chem Engn, 86 Hongqi Rd, Ganzhou 341000, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-noble heterogeneous catalyst; Nitro compounds; Hydrogenation; Transfer hydrogenation; Reductive coupling reaction; FORMIC-ACID; NANOPARTICLES; EFFICIENT; NITROARENES; LIGANDS; METALS; GREEN;
D O I
10.1016/j.apcatb.2017.04.026
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
Co nanoparticles embedded in mesoporous nitrogen-doped carbon (abbreviated as Co@CN-800) were prepared and found to be resistant to acid. The Co@CN-800 catalyst was found to be active and selective for the one-pot reductive amination of carbonyl compounds with nitro compounds by transfer hydrogenation with formic acid as the hydrogen donor, affording the corresponding secondary amines with excellent yields (89.6-99%). Both nitrogen atoms and Co nanoparticles were of great importance in the one-pot reductive amination over the Co@CN-800 catalyst by formic acid, and the protic N-H+ and hydridic Co-H- were proposed to be the active species for the transfer hydrogenation reactions. Furthermore, the Co@CN-800 catalyst was highly stable without loss of its activity. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:522 / 532
页数:11
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