Supramolecular Entanglement in a Hydrogen‐Bonded Organic Framework Enables Flexible‐Robust Porosity for Highly Efficient Purification of Natural Gas

Author:

Jiang Chenghao1,Wang Jia‐Xin1,Liu Di1,Wu Enyu1,Gu Xiao‐Wen1,Zhang Xu2,Li Bin1,Chen Banglin3ORCID,Qian Guodong1

Affiliation:

1. State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou 310027 China

2. Jiangsu Engineering Laboratory for Environmental Functional Materials School of Chemistry and Chemical Engineering Huaiyin Normal University Huaian 223300 China

3. Fujian Provincial Key Laboratory of Polymer Materials College of Chemistry and Materials Science Fujian Normal University Fuzhou 350007 China

Abstract

AbstractThe development of porous materials with flexible‐robust characteristics shows some unique advantages to target high performance for gas separation, but remains a daunting challenge to achieve so far. Herein, we report a carboxyl‐based hydrogen‐bonded organic framework (ZJU‐HOF‐8a) with flexible‐robust porosity for efficient purification of natural gas. ZJU‐HOF‐8a features a four‐fold interpenetrated structure with dia topology, wherein abundant supramolecular entanglements are formed between the adjacent subnetworks through weak intermolecular hydrogen bonds. This structural configuration could not only stabilize the whole framework to establish the permanent porosity, but also enable the framework to show some flexibility due to its weak intermolecular interactions (so‐called flexible‐robust framework). The flexible‐robust porosity of ZJU‐HOF‐8a was exclusively confirmed by gas sorption isotherms and single‐crystal X‐ray diffraction studies, showing that the flexible pore pockets can be opened by C3H8 and n‐C4H10 molecules rather by C2H6 and CH4. This leads to notably higher C3H8 and n‐C4H10 uptakes with enhanced selectivities than C2H6 over CH4 under ambient conditions, affording one of the highest n‐C4H10/CH4 selectivities. The gas‐loaded single‐crystal structures coupled with theoretical simulations reveal that the loading of n‐C4H10 can induce an obvious framework expansion along with pore pocket opening to improve n‐C4H10 uptake and selectivity, while not for C2H6 adsorption. This work suggests an effective strategy of designing flexible‐robust HOFs for improving gas separation properties.

Funder

National Natural Science Foundation of China

Science and Technology Department of Zhejiang Province

Publisher

Wiley

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