超分子化学
多孔性
氢键
灵活性(工程)
材料科学
结晶学
分子
氢
吸附
分子间力
吸附
晶体工程
Crystal(编程语言)
晶体结构
化学工程
化学
有机化学
复合材料
物理化学
计算机科学
工程类
统计
数学
程序设计语言
作者
Chenghao Jiang,Jia‐Xin Wang,Di Liu,Enyu Wu,Xiao‐Wen Gu,Xu Zhang,Bin Li,Banglin Chen,Guodong Qian
标识
DOI:10.1002/anie.202404734
摘要
Abstract The 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 C 3 H 8 and n‐C 4 H 10 molecules rather by C 2 H 6 and CH 4 . This leads to notably higher C 3 H 8 and n‐C 4 H 10 uptakes with enhanced selectivities than C 2 H 6 over CH 4 under ambient conditions, affording one of the highest n‐C 4 H 10 /CH 4 selectivities. The gas‐loaded single‐crystal structures coupled with theoretical simulations reveal that the loading of n‐C 4 H 10 can induce an obvious framework expansion along with pore pocket opening to improve n‐C 4 H 10 uptake and selectivity, while not for C 2 H 6 adsorption. This work suggests an effective strategy of designing flexible‐robust HOFs for improving gas separation properties.
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