Framework-Isomeric Metal-Organic Frameworks Built from Supermolecular Building Blocks for High Iodine Capture

被引:1
作者
Chen, Shuting [1 ]
Wang, Yinyin [1 ]
Huang, Jieqiu [1 ]
Xie, Huanhuan [1 ]
Yuan, Jingjing [1 ]
Song, Mengyao [1 ]
Yang, Bin [1 ]
Pang, Qingqing [2 ]
Tu, Binbin [1 ]
机构
[1] Cent China Normal Univ, Coll Chem, Engn Res Ctr Photoenergy Utilizat Pollut Control &, Minist Educ,Natl Key Lab Green Pesticide, Wuhan 430079, Peoples R China
[2] Wuhan Univ Sci & Technol, Sch Chem & Chem Engn, Key Lab Hubei Prov Coal Convers & New Carbon Mat, Wuhan 430081, Peoples R China
来源
ACS MATERIALS LETTERS | 2024年 / 7卷 / 01期
基金
中国国家自然科学基金;
关键词
ADSORPTION; POLYHEDRA; CHEMISTRY; SELECTION; TOPOLOGY; LIGANDS; DESIGN;
D O I
10.1021/acsmaterialslett.4c01908
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The supermolecular building block approach is powerful in constructing hierarchically porous metal-organic frameworks (MOFs). However, the structural diversity of these extended frameworks built from the same building blocks has never been explored. Herein, we propose a strategy by synergistically tuning the extending direction of metal-organic polyhedra (MOPs) and the linker conformation to achieve MOFs with framework isomerism. Six novel MOFs (CCNUF-1-6) based on an octahedral MOP and different tritopic pyridine-based linkers were successfully synthesized, among which the structural diversity increased with increasing linker flexibility. The topologies (sql, kgd, and rtl) of these materials are unprecedented in MOP-based MOFs. Moreover, highly porous CCNUF-2-6 showed remarkable iodine uptake capacities in the range of 2.51 to 3.11 g g-1. This study emphasizes the potential of MOPs containing open metal sites as versatile platforms for the development of diversified hierarchically porous MOFs with enhanced functional properties.
引用
收藏
页码:304 / 311
页数:8
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