Transfer hydrogenation of nitroarenes to arylamines catalysed by an oxygen-implanted MoS2 catalyst

被引:32
|
作者
Zhang, Chaofeng [1 ,2 ]
Zhang, Zhixin [1 ]
Wang, Xu [3 ]
Li, Mingrun [1 ]
Lu, Jianmin [1 ]
Si, Rui [3 ]
Wang, Feng [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, State Key Lab Catalysis, Dalian 116023, Liaoning, Peoples R China
[2] Grad Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
基金
中国国家自然科学基金;
关键词
MoS2; MoOx; N2H4; Transfer hydrogenation; Nitro reduction; SUPPORTED GOLD CATALYSTS; AROMATIC NITRO-COMPOUNDS; IRON-OXIDE NANOCRYSTALS; ACTIVE EDGE SITES; SELECTIVE HYDROGENATION; CHEMOSELECTIVE REDUCTION; MOLYBDENUM-DISULFIDE; ROOM-TEMPERATURE; MILD CONDITIONS; AZO-COMPOUNDS;
D O I
10.1016/j.apcata.2016.07.008
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
We present an efficient approach for chemoselective synthesis of various functionalized arylamines from nitroarenes over an oxygen-implanted MoS2 catalyst (O-MoS2). The HRTEM, XRD, XPS, Raman, EXAFS and NH3-TPD characterizations show the existence of (MoOx)-O-Iv structure and abundant coordinative unsaturated (CUS) Mo sites in the 2D-layer structure of O-MoS2. In the transfer hydrogenation of nitroarenes with hydrazine hydrate, the (MoOx)-O-Iv structure works as the catalytic active center. The N2H4 selectively decomposes to the active hydrogen species in polar electronic states (H delta- and He delta+), which show high chemoselectivity toward the nitro reduction over C=C, C=C, and C N groups. The O-MoS2 catalyst can be recovered in a facile manner from the reaction mixture and recycled four times without any significant loss of activity. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:85 / 93
页数:9
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