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NHC ligand-based half-sandwich iridium complexes: synthesis, structure and catalytic activity in acceptorless dehydrogenation and transfer hydrogenation
被引:7
|作者:
Li, Rong-Jian
[1
,2
]
Wang, Yang
[1
]
Jin, Yan
[1
,2
]
Deng, Wei
[1
]
Liu, Zhen-Jiang
[1
]
Yao, Zi-Jian
[1
,3
]
机构:
[1] Shanghai Inst Technol, Sch Chem & Environm Engn, Shanghai 201418, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Transducer Technol, Shanghai 200050, Peoples R China
[3] Anhui Normal Univ, Coll Chem & Mat Sci, Anhui Lab Mol Based Mat, Wuhu 241002, Peoples R China
基金:
中国国家自然科学基金;
关键词:
N-HETEROCYCLIC CARBENES;
RUTHENIUM COMPLEXES;
HOMOGENEOUS RUTHENIUM;
HIGHLY EFFICIENT;
ELECTRON-RICH;
ALCOHOLS;
ALDEHYDES;
METHANOL;
OSMIUM;
IR;
D O I:
10.1039/d1nj03824a
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A set of neutral C,C-chelate half-sandwich iridium(iii) complexes have been prepared with NHC ligands that contain pendant aromatic rings as potentially chelating donor sites. The catalytic activity of such iridium complexes has been investigated for the acceptorless dehydrogenation (AD) reactions of alcohols and for the transfer hydrogenation reactions of ketones. The prepared iridium(iii) complexes show excellent catalytic activity for AD reactions of a wide range of secondary alcohols, and they are also shown to be effective for the synthesis of aldehydes from primary alcohols without the observation of undesired byproducts such as esters. Additionally, these complexes are also highly efficient in transfer hydrogenation of ketones and aldehydes, which give the alcohols in good yields under mild conditions. The exact structure and bonding mode of the NHC-based iridium complexes was identified using various spectroscopic methods and single crystal X-ray analysis.
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页码:19002 / 19010
页数:9
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