方解石
沸石咪唑盐骨架
笼子
结晶学
拓扑(电路)
化学
咪唑酯
材料科学
金属有机骨架
化学物理
沸石
无机化学
吸附
物理化学
有机化学
催化作用
组合数学
数学
作者
Meizhen Gao,Rui‐Kang Huang,Bin Zheng,Pengfei Wang,Qi Shi,Wei‐Xiong Zhang,Jinxiang Dong
标识
DOI:10.1038/s41467-022-32332-x
摘要
Abstract The flexibility and guest-responsive behavior of some metal-organic frameworks (MOFs) indicate their potential in the fields of sensors and molecular recognition. As a subfamily of MOFs, the flexible zeolitic imidazolate frameworks (ZIFs) typically feature a small displacive transition due to the rigid zeolite topology. Herein, an atypical reversible displacive transition (6.4 Å) is observed for the sodalite (SOD) cage in flexible ZIF-65(Zn), which represents an unusually large breathing effect compared to other ZIFs. ZIF-65(Zn) exhibits a stepwise II → III → I expansion between an unusual ellipsoidal SOD cage (8.6 Å × 15.9 Å for II) and a spherical SOD cage (15.0 Å for I). The breathing behavior of ZIF-65(Zn) varies depending on the nature of the guest molecules (polarity and shape). Computational simulations are employed to rationalize the differences in the breathing behavior depending on the structure of the ZIF-65(Zn) cage and the nature of the guest-associated host–guest and guest–guest interactions.
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