Postmetalation of a new porphyrin ligand-based metal-organic framework for catalytic oxidative carboxylation of olefins

被引:19
|
作者
Jin, Hong-Guang [1 ]
Chen, Fengshi [1 ]
Zhang, Houpeng [1 ]
Xu, Wenjie [1 ]
Wang, Yao [1 ]
Fan, Jincheng [1 ]
Chao, Zi-Sheng [1 ]
机构
[1] Changsha Univ Sci & Technol, Coll Mat Sci & Engn, Changsha 410114, Hunan, Peoples R China
关键词
METALLOPORPHYRIN FRAMEWORK; HETEROGENEOUS CATALYST; CYCLIC CARBONATES; CO2; TRANSFORMATION; EPOXIDATION; EPOXIDES; FIXATION; CAPTURE;
D O I
10.1007/s10853-020-05211-3
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Heterogeneous catalytic reactions based on single metal-organic framework (MOF) material for the oxidative carboxylation of olefins following a tandem process, which involves the epoxidation of olefins and subsequent epoxide-CO2 cycloaddition, are highly desirable and economical for CO2 chemical fixation. In this work, a newtrans-A(2)B(2)-type porphyrin ligand, 5,15-di(m-benzoato)-porphyrin (H2DMBP), was successfully synthesized and utilized for constructing a novel, highly porous, and stable Nd-porphyrin MOF, named CSUST-2. (CSUST stands for Changsha University of Science and Technology.) Furthermore, the coordinatively unsaturated Co(II) ions were implanted into the MOF by exploiting the innate non-metallated porphyrin ligands to generate Co(II)@CSUST-2 framework, which was evidenced to act as an efficient recyclable catalyst for oxidative carboxylation of olefins in the presence oftert-butyl hydroperoxide (TBHP) as an oxidant and tetrabutylammonium bromide (n-Bu4NBr) as a co-catalyst under mild conditions (1 atm CO2, 75 degrees C, and without solvent).
引用
收藏
页码:16184 / 16196
页数:13
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