A new metal organic complex with coordination unsaturated Co(II) as high-efficiency heterogeneous catalyst for selective oxidation of alkylbenzenes

被引:9
|
作者
Li, Yu-Yao [1 ]
Li, Xiao-Hui [1 ]
Xu, Na [1 ]
An, Zhi-Xuan [1 ]
Chu, Yang [1 ]
Wang, Xiu-Li [1 ]
机构
[1] Bohai Univ, Coll Chem & Mat Engn, Prof Technol Innovat Ctr Liaoning Prov Convers Mat, Jinzhou 121013, Peoples R China
来源
MOLECULAR CATALYSIS | 2023年 / 548卷
基金
中国国家自然科学基金;
关键词
C-H bond oxidation; Cobalt metal-organic complex; Heterogeneous catalysis; AEROBIC OXIDATION; FRAMEWORKS; ALCOHOLS; POLYOXOMETALATE; PORPHYRIN; ACETATE; PD;
D O I
10.1016/j.mcat.2023.113428
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
Converting C-H bonds into valuable compounds is a challenging goal in synthetic chemistry, yet it is both economically and environmentally beneficial. Developing high-efficiency catalysts for the oxidation of saturated C-H bonds is of great significance. Herein, a new cobalt-containing metal-organic complex, [Co-2(L)(0.5)(MTC)(mu(3)-OH)(H2O)(2)]center dot 2H(2)O (1, L = (E)-4,4'-(ethene-1,2-diyl)bis(N-(pyridin-3-yl)benzamide), H3MTC = benzene-1,2,4-tricarboxylic acid), was successfully prepared with Co(NO3)(2), ligand L and H3MTC through one-step hydrothermal synthesis. Complex 1 was found to be a highly effective heterogeneous catalyst for accelerating the oxidation reaction of alkylbenzenes to ketone products. The conversion of diphenylmethane to benzophenone over complex 1 was 95.6%, which was comparable to the highest values of reported transition metal-based catalysts. A possible catalytic reaction mechanism was proposed.
引用
收藏
页数:6
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