Construction of hexanuclear Ce(III) metal-porphyrin frameworks through linker induce strategy for CO2 capture and conversion

被引:18
|
作者
Zhang, Liangliang [1 ,2 ,3 ]
Feng, Yang [4 ]
He, Huihui [1 ,2 ]
Liu, Yang [1 ,2 ]
Weng, Jiena [1 ,2 ]
Zhang, Peng [3 ]
Huang, Wei [1 ,2 ]
机构
[1] Northwestern Polytech Univ, Frontiers Sci Ctr Flexible Elect FSCFE, Shaanxi Inst Flexible Elect SIFE, 127 West Youyi Rd, Xian 710072, Peoples R China
[2] Northwestern Polytech Univ, Shaanxi Inst Biomed Mat & Engn SIBME, 127 West Youyi Rd, Xian 710072, Peoples R China
[3] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
[4] China Univ Petr East China, Sch Mat Sci & Engn, Qingdao 266580, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks (MOFs); Linker induce strategy; CO2; ORGANIC FRAMEWORKS; MOF; PLATFORM; CYCLOADDITION; EPOXIDES; DESIGN; SIZE; NET;
D O I
10.1016/j.cattod.2020.12.038
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this article, we report a series of hexanuclear rare-earth MOFs based on Ce (III) and 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin, namely Ce-PCN-224, with a new zln topology through linker induce strategy. Ce-PCN224 exhibits permanent porosity, high water and thermal stabilities, and the ability to adsorb dye molecules in the aqueous environment. Moreover, after post-metallation with Fe, Co, and Ni, Ce-PCN-224(Fe) and Ce-PCN224(Co) were proved to be efficient heterogeneous catalysts for the cycloaddition of CO2 with epoxides, attributed to the combination of multiple Lewis acidic sites.
引用
收藏
页码:38 / 43
页数:6
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