Lewis Acid-Base Bifunctional Crystals with a Three-Dimensional Framework for Selective Coupling of CO2 and Epoxides under Mild and Solvent-Free Conditions

被引:51
|
作者
Gao, Xiangxiang [1 ]
Liu, Mengshuai [1 ]
Lan, Jianwen [1 ]
Liang, Lin [2 ]
Zhang, Xiao [1 ]
Sun, Jianmin [1 ,3 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, State Key Lab Urban Water Resource & Environm, Harbin 150080, Peoples R China
[2] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150080, Peoples R China
[3] Harbin Inst Technol Shenzhen, Shenzhen Key Lab Organ Pollut Prevent & Control, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; EFFICIENT HETEROGENEOUS CATALYST; DENSITY-FUNCTIONAL THEORY; CARBON-DIOXIDE; CYCLIC CARBONATES; CHEMICAL FIXATION; IONIC LIQUIDS; CYCLOADDITION; CONVERSION; OXIDE;
D O I
10.1021/acs.cgd.6b01132
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two Lewis acidbase bifunctional, isostructural metalorganic frameworks (MOFs), [Zn-3(Hbtc)(2)(atz)(2)].CH3CN.2CH(3)OH (MOF-1) and [Co-3(Hbtc)(2)(atz)(2)].H2O.2DMF (MOF-2), containing NH2 groups and four-coordinated metal sites were fabricated successfully, and the structures were thoroughly characterized by X-ray crystallography, powder X-ray diffraction, thermogravimetric analysis, Fourier transform infrared spectroscopy, and N-2 adsorption/desorption techniques. Satisfactorily, the novel MOFs with a three-dimensional framework were highly efficient and stable heterogeneous catalysts for selective fixation of CO2 to cyclic carbonates under mild conditions in the absence of solvent. The influences of various reaction parameters on catalytic performance were systematically investigated. Also the catalysts showed excellent versatility to epoxides with different substituents and could be easily recyclable with high activity. Additionally, the self-catalyzed mechanism as well as synergistic mechanism with tetrabutylammonium bromide (Bu4NBr) for CO2 conversion was proposed.
引用
收藏
页码:51 / 57
页数:7
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