Visible-light-initiated one-pot clean synthesis of nitrone from nitrobenzene and benzyl alcohol over CdS photocatalyst

被引:26
作者
Yu, Weiwei [1 ]
Guo, Xinwen [1 ]
Song, Chunshan [1 ,2 ,3 ]
Zhao, Zhongkui [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, PSU DUT Joint Ctr Energy Res, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Penn State Univ, PSU DUT Joint Ctr Energy Res, EMS Energy Inst, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Energy & Mineral Engn & Chem Engn, University Pk, PA 16802 USA
基金
中国国家自然科学基金;
关键词
One-pot strategy; Clean synthesis; Nitrone; Imine and secondary amine; Nitrobenzene and benzyl alcohol; Photocatalysis; CATALYTIC-REACTIONS; HYDROGEN EVOLUTION; SECONDARY-AMINES; EFFICIENT; NITROARENES; OXIDATION; REDUCTION; IMINES; NITROAROMATICS; NANOPARTICLES;
D O I
10.1016/j.jcat.2018.12.011
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
The controlled visible-light mediated conversion of nitroaromatics to versatile nitrogen-containing intermediates is of great significance but still remains a challenge. Herein, we report for the first time a facile visible-light-initiated one-pot strategy for clean and efficient synthesis of nitrone from nitrobenzene and benzyl alcohol. It integrates the controlled photocatalytic reduction of nitrobenzene to phenylhydroxylamine by photogenerated electrons with the selective photocatalytic oxidation of benzyl alcohol to benzaldehyde by photoinduced holes over a low-cost CdS photocatalyst with a suitable reduction capability, followed by spontaneous condensation of the as-formed hydroxylamine and aldehyde at ambient pressure and room temperature. Furthermore, by modulating cocatalyst and illumination time, for the conversion of the same reactants, the other two useful nitrogen-containing compounds, imine and secondary amine, were also successfully synthesized. The reaction mechanisms for flexible synthesis of the three target products are proposed. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:97 / 106
页数:10
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