Visible Light-Induced Oxidation of Alcohols by a Luminescent Osmium(VI) Nitrido Complex: Evidence for the Generation of PhIO plus as a Highly Active Oxidant in the Presence of PhIO

被引:4
|
作者
Xiang, Jing [1 ,2 ]
Pan, Yi [3 ]
Liu, Lu-Lu [2 ]
Wang, Li-Xin [2 ]
Yang, Huan [2 ]
Cheng, Shun-Cheung [3 ]
Yiu, Shek-Man [3 ]
Leung, Chi-Fai [4 ]
Ko, Chi-Chiu [3 ]
Lau, Kai-Chung [3 ]
Lau, Tai-Chu [3 ,5 ]
机构
[1] Jianghan Univ, Key Lab Optoelect Chem Mat & Devices, Minist Educ, Wuhan 430056, Peoples R China
[2] Yangtze Univ, Coll Chem & Environm Engn, Jingzhou 434020, Hubei, Peoples R China
[3] City Univ Hong Kong, Dept Chem, Tat Chee Ave, Hong Kong 999077, Peoples R China
[4] Educ Univ Hong Kong, Dept Sci & Environm Studies, Hong Kong 00000, Peoples R China
[5] Dongguan Univ Technol, Res Ctr Ecoenvironm Engn, Dongguan 523808, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
REACTIVITY; MECHANISM; RADICALS; STATE; HEME; ATOM;
D O I
10.1021/jacs.3c00760
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although alcohols are readily oxidized by a variety of oxidants, their oxidation by metal nitrido complexes is yet to be studied. We report herein visible-light-induced oxidation of primary and secondary alcohols to carbonyl compounds by a strongly luminescent osmium(VI) nitrido complex (OsN). The proposed mechanism involves initial rate-limiting hydrogen-atom transfer (HAT) from the alpha-carbon of the alcohol to OsN*. Attempts to develop catalytic oxidation of alcohols by OsN* using PhIO as the terminal oxidant resulted in the formation of novel osmium(IV) iminato complexes in which the nitrido ligand is bonded to a 6-carbon of the alcohol. Experimental and theoretical studies suggest that OsN* is reductively quenched by PhIO to generate PhIO+, which is a highly active oxidant that readily undergoes alpha- and 6- C-H activation of alcohols.
引用
收藏
页码:9129 / 9135
页数:7
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