Expanding the Structural Topologies of Rare-Earth Porphyrinic Metal-Organic Frameworks through Ligand Modulation

被引:8
|
作者
Wu, Wei [1 ,2 ]
Xie, Yabo [1 ,2 ]
Lv, Xiu-Liang [1 ,2 ]
Xie, Lin-Hua [1 ,2 ]
Zhang, Xin [1 ,2 ]
He, Tao [1 ,2 ]
Si, Guang-Rui [1 ,2 ]
Wang, Kecheng [1 ,2 ]
Li, Jian-Rong [1 ,2 ]
机构
[1] Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
[2] Beijing Univ Technol, Dept Chem Engn, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-organic frameworks; porphyrin; rare-earth metals; topology; heterogeneous catalysis; DESIGN; SERIES;
D O I
10.1021/acsami.2c21576
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Expanding the structural diversity of porphyrinic metal-organic frameworks (PMOFs) is essential to develop functional materials with novel properties or enhanced performance in different applications. Herein, we establish a strategy to construct rare-earth (RE) PMOFs with unprecedented topology via rational functionalization of porphyrinic ligands. By introducing phenyl/pyridyl groups to the meso-positions of the porphyrin core, the symmetries and connectivities of the ligands are tuned, and three RE-PMOFs (BUT 224/-225/-226) with new topologies are successfully obtained. In addition, BUT-225(Co), with both the Lewis basic and acidic sites, exhibits enhanced CO2 uptake and higher catalytic activity for the cycloaddition of CO2 and epoxides under mild conditions. This work reveals that the RE-PMOFs with novel topologies can be rationally designed and constructed through ligand functionalization, which provides insights into the construction of tailored PMOFs for various applications.
引用
收藏
页码:5357 / 5364
页数:8
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