[NO]- and [NN]-coordination mode rhodium complexes based on a flexible ligand: synthesis, reactivity and catalytic activity

被引:12
|
作者
Yao, Zi-Jian [1 ]
Li, Kuan [1 ]
Zhang, Jian-Yong [1 ]
Deng, Wei [1 ]
机构
[1] Shanghai Inst Technol, Sch Chem & Environm Engn, Shanghai 201418, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
ALPHA-DEHYDROAMINO KETONES; ASYMMETRIC HYDROGENATION; SELECTIVE HYDROGENATION; CHEMOSELECTIVE HYDROGENATION; ADDITION-REACTIONS; IRIDIUM COMPLEXES; AROMATIC KETONES; WATER OXIDATION; BONDS; ALDEHYDES;
D O I
10.1039/c6nj02416e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A flexible [NON]-type ligand was prepared via a stepwise method. Air-and moisture-stable LL-(N, O-coordination mode) (1) and LX-type (N, N-coordination mode) (2) rhodium(I) complexes were synthesized based on this flexible ligand under different reaction conditions. The two rhodium complexes were isolated in good yields and characterized by elemental analysis and IR and NMR spectrometry. The molecular structures of complexes 1 and 2 were confirmed by single-crystal X-ray analysis. The cationic rhodium complex was shown to be a good catalyst for the hydrogenation of acetophenone derivatives without pre-dried solvents and reagents. Good efficiency was achieved for a series of substrates with either electron-donating or electron-withdrawing groups.
引用
收藏
页码:8753 / 8759
页数:7
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