共 50 条
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
相关论文