Efficient Aliphatic C-H Oxidation and C=C Epoxidation Catalyzed by Porous Organic Polymer-Supported Single-Site Manganese Catalysts

被引:29
|
作者
Wang, Bingyang [1 ,2 ]
Lin, Jin [1 ]
Sun, Qiangsheng [1 ]
Xia, Chungu [1 ]
Sun, Wei [1 ,2 ]
机构
[1] Chinese Acad Sci, Ctr Excellence Mol Synth, Suzhou Res Inst LICP, Lanzhou Inst Chem Phys LICP,State Key Lab Oxo Syn, Lanzhou 730000, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H oxidation; porous organic polymer; manganese catalyst; asymmetric epoxidation; hydrogen peroxide; ENANTIOSELECTIVE EPOXIDATION; ASYMMETRIC EPOXIDATION; HIGHLY EFFICIENT; IRON COMPLEXES; OLEFINS; H2O2; LIGAND; HYDROXYLATION; FE; HYDROFORMYLATION;
D O I
10.1021/acscatal.1c02738
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
Bioinspired manganese complexes have emerged over recent decades as attractive catalysts for a number of selective oxidation reactions. However, these catalysts still suffer from oxidative degradation. In the present study, we prepared a series of porous Mn-N-4 catalysts in which the catalytic units are embedded in the skeleton of porous organic polymers (POPs). These POPbased manganese catalysts demonstrated high reactivity in the oxidation of aliphatic C-H bonds and the asymmetric epoxidation of olefins. Furthermore, these catalysts could be readily recycled and reused due to their heterogeneous nature. Morphological characterization revealed that the Mn-N-4 complex was individually distributed over a porous polymer network. Remarkably, the nature of the single-site catalyst prevented oxidative degradation during the reaction. The present work has thus developed a successful approach for bioinspired single-site manganese catalysts in which the oxidation reaction is confined to a specific channel in an enzyme-like mode.
引用
收藏
页码:10964 / 10973
页数:10
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