化学
吡咯
金属有机骨架
连接器
锆
分子
星团(航天器)
结晶学
纳米技术
组合化学
拓扑(电路)
材料科学
无机化学
有机化学
吸附
组合数学
程序设计语言
操作系统
计算机科学
数学
作者
Yiyang Li,Xiaoteng Li,Shuping Jia,Chong Zhang,Yuxin Luo,Zhihua Lin,Yonggang Zhao,Wei Huang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-07-26
卷期号:60 (16): 12129-12135
被引量:14
标识
DOI:10.1021/acs.inorgchem.1c01336
摘要
To date, numerous zirconium cluster-based metal–organic frameworks (Zr-MOFs) with attractive physical properties have been achieved thanks to tailorable organic linkers and versatile Zr clusters. Nevertheless, in comparison with the most-used high-symmetry organic linkers, low-symmetry linkers have rarely been exploited in the construction of Zr-MOFs. Despite challenges in predicting the structure and topology of the MOF, linker desymmetrization presents opportunities for the design of Zr-MOFs with unusual topologies and unexpected functionalities. Herein, we report for the first time the construction of two robust Zr-MOFs (IAM-7 and IAM-8) from two pyrrolo-pyrrole-based low-symmetry tetracarboxylate linkers with a rare rhombic shape. The low symmetry of the linkers arises from the asymmetric pyrrolo-pyrrole core and the varying branch lengths, which play a critical role in the structural diversity between IAM-7 and IAM-8 seen from the structural analysis and lead to hydrophilic channels that contain uncoordinated carboxylate groups in the structure of IAM-7. Furthermore, the proton conductivity of IAM-7 displays a high temperature and humidity dependence where the proton conductivity increases from 2.84 × 10–8 S cm–1 at 30 °C and 40% relative humidity (RH) to 1.42 × 10–2 S cm–1 at 90 °C and 95% RH, making it among one of the most conductive Zr-MOFs. This work not only enriches the library of Zr-MOFs but also offers a platform for the design of low-symmetry linkers toward the structural diversity or irregularity of MOFs as well as their structure-related properties.
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