Highly Selective and Efficient Ring Hydroxylation of Alkylbenzenes with Hydrogen Peroxide and an Osmium(VI) Nitrido Catalyst

被引:23
|
作者
Kwong, Hoi-Ki [1 ,2 ]
Lo, Po-Kam [1 ,2 ]
Yiu, Shek-Man [1 ,2 ]
Hirao, Hajime [1 ,2 ,3 ]
Lau, Kai-Chung [1 ,2 ]
Lau, Tai-Chu [1 ,2 ]
机构
[1] City Univ Hong Kong, Dept Biol & Chem, Tat Chee Ave, Kowloon Tong, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Inst Mol Funct Mat, Tat Chee Ave, Kowloon Tong, Hong Kong, Peoples R China
[3] Nanyang Technol Univ, Div Chem & Biol Chem, Sch Phys & Math Sci, 21 Nanyang Link, Singapore 637371, Singapore
关键词
alkylbenzenes; hydrogen peroxide; hydroxylation; nitrido; osmium complexes; OXIDATION; COMPLEXES; OXIDANTS; BENZENE; ALKANES; TOLUENE; PHENOL; H2O2;
D O I
10.1002/anie.201705986
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Os-VI nitrido complex, Os-VI(N)(quin)(2)(OTs) (1, quin=2-quinaldinate, OTs=tosylate), is a highly selective and efficient catalyst for the ring hydroxylation of alkylbenzenes with H2O2 at room temperature. Oxidation of various alkylbenzenes occurs with ring/chain oxidation ratios ranging from 96.7/3.3 to 99.9/0.1, and total product yields from 93% to 98%. Moreover, turnover numbers up to 6360, 5670, and 3880 can be achieved for the oxidation of p-xylene, ethylbenzene, and mesitylene, respectively. Density functional theory calculations suggest that the active intermediate is an Os-VIII nitrido oxo species.
引用
收藏
页码:12260 / 12263
页数:4
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