Regulation of Catenation in Metal-Organic Frameworks with Tunable Clathrochelate-Based Building Blocks

被引:9
|
作者
Chen, Zhijie [1 ,2 ]
Idrees, Karam B. [1 ,2 ]
Shetty, Suchetha [3 ]
Xie, Haomiao [1 ,2 ]
Wasson, Megan C. [1 ,2 ]
Gong, Wei [1 ,2 ]
Zhang, Xuan [1 ,2 ]
Alameddine, Bassam [3 ]
Farha, Omar K. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
[3] Gulf Univ Sci & Technol, Dept Math & Nat Sci, Hawally 32093, Kuwait
关键词
POROUS MATERIALS; INTERPENETRATION; DESIGN; ADSORPTION; CHEMISTRY; ACCESS; NETS;
D O I
10.1021/acs.cgd.1c01151
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inherent pore structures and pore environment of metal-organic frameworks (MOFs) have a significant impact on the macroscopic functionalities. In this regard, it is valuable to explore the regulation of catenation and then tune the pore structures and pore environment, optimally at the molecular level. Here we report regulating the catenation of Zn-MOFs based on the primitive cubic (pcu) net, isoreticular to MOF-5, via fine-tuning the clathrochelate-based ditopic building blocks. The use of clathrochelate-based carboxylate ligands with bulky cores of n-butyl groups led to the synthesis of a Zn-MOF with the pcu net, while clathrochelate linkers with relatively fewer bulky cores give a twofold interpenetrated Zn-MOF structure under similar conditions.
引用
收藏
页码:6665 / 6670
页数:6
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