Robust acid-base Ln-MOFs: searching for efficient catalysts in cycloaddition of CO2 with epoxides and cascade deacetalization-Knoevenagel reactions

被引:10
|
作者
Si, Xuezhen [1 ]
Pan, Xuze [1 ]
Xue, Jintang [1 ]
Yao, Qingxia [1 ]
Huang, Xianqiang [1 ]
Duan, Wenzeng [1 ]
Qiu, Yi [2 ]
Su, Jie [2 ]
Cao, Minglei [3 ]
Li, Jun [1 ]
机构
[1] Liaocheng Univ, Sch Chem & Chem Engn, Liaocheng 252000, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Shandong Ruijie New Mat Co Ltd, Liaocheng 252000, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYSTS; SITES; SEPARATION;
D O I
10.1039/d2ra06545b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A family of microporous and robust Ln(iii)-based metal-organic frameworks (1-Ln, Ln = Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) have been obtained using 4,4',4''-nitrilotribenzoic acid (H3NTB) in NMP-HCl solvent. Both single-crystal and powder X-ray diffraction analyses demonstrate that 1-Ln are isostructural and possess 3D frameworks with permanent porosity for Ar and CO2 adsorption. Strikingly, the incorporation of both Lewis acidic lanthanide ions and the basic triphenylamine group into 1-Ln makes them efficient acid-base catalysts for both cycloaddition of epoxides with CO2 and one-pot cascade deacetalization-Knoevenagel reactions. The systematic catalytic studies show that 1-Tb and 1-Yb possess the best catalytic activities for both reactions, indicating the catalytic activities of these Ln-MOFs are strongly dependent on metal Lewis acid sites embedded in the frameworks.
引用
收藏
页码:33501 / 33509
页数:9
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