Incorporation of a carboxyl-functionalized imidazolium-based ionic liquid into a UiO-66 type MOF for chemical fixation of CO2 into carbonates

被引:4
|
作者
Lin, Jianghui [1 ]
Luo, Jiamei [1 ]
Zhang, Mengjia [1 ]
Zhang, Lei [1 ]
Cai, Guohui [1 ]
Zou, Jiahua [1 ]
Li, Ling [1 ]
机构
[1] Fuzhou Univ, Coll Chem Engn, Fuzhou 350008, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; CYCLIC CARBONATES; EFFICIENT CATALYSTS; DIOXIDE CAPTURE; CONVERSION; CYCLOADDITION; SEPARATION; EPOXIDES; SITES; MILD;
D O I
10.1039/d4cy00430b
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
Incorporation of ionic liquids into metal-organic frameworks (MOFs) offers a new platform to construct heterogeneous bifunctional catalytic systems for the chemical capture and conversion of CO2 with epoxides. Herein, an imidazolium-based ionic liquid decorated UiO-66 type MOF (P3[BCMIm]Br@UiO-66) was successfully constructed via solvothermal assembly of the carboxyl-functionalized imidazolium ionic liquid ligand, terephthalic acid ligand and Zr(iv) ions. It exhibits the highest catalytic activity upon the cycloaddition of CO2 (98.2% conversion of propylene oxide and 99% selectivity to propylene carbonate) under optimized conditions (2.2 Mpa CO2, 1.0 wt%, 110 degrees C, reaction time 2 h). Notably, P3[BCMIm]Br@UiO-66 outperformed the original UiO-66 materials and [BCMIm]Br. P3[BCMIm]Br@UiO-66 retained its good catalytic performance for up to five recycling runs with only a little loss in catalytic activity. Furthermore, several additional coupling reactions were investigated with other epoxides as substrates.
引用
收藏
页码:4496 / 4505
页数:10
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