化学
超分子化学
堆积
吸附
乙炔
分子间力
金属有机骨架
氢键
结合能
分子
乙二醇
化学物理
计算化学
物理化学
有机化学
物理
核物理学
作者
Sihai Yang⧫,Anibal J. Ramirez‐Cuesta,Ruth Newby,Victoria García Sakai,Pascal Manuel,Samantha K. Callear,Stuart I. Campbell,Chiu C. Tang,Martin Schröder
出处
期刊:Nature Chemistry
[Springer Nature]
日期:2014-12-01
卷期号:7 (2): 121-129
被引量:597
摘要
Supramolecular interactions are fundamental to host-guest binding in many chemical and biological processes. Direct visualization of such supramolecular interactions within host-guest systems is extremely challenging, but crucial to understanding their function. We report a comprehensive study that combines neutron scattering, synchrotron X-ray and neutron diffraction, and computational modelling to define the detailed binding at a molecular level of acetylene, ethylene and ethane within the porous host NOTT-300. This study reveals simultaneous and cooperative hydrogen-bonding, π···π stacking interactions and intermolecular dipole interactions in the binding of acetylene and ethylene to give up to 12 individual weak supramolecular interactions aligned within the host to form an optimal geometry for the selective binding of hydrocarbons. We also report the cooperative binding of a mixture of acetylene and ethylene within the porous host, together with the corresponding breakthrough experiments and analysis of adsorption isotherms of gas mixtures.
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