Supramolecular binding and separation of hydrocarbons within a functionalized porous metal-organic framework

被引:553
作者
Yang, Sihai [1 ]
Ramirez-Cuesta, Anibal J. [2 ]
Newby, Ruth [1 ]
Garcia-Sakai, Victoria [3 ]
Manuel, Pascal [3 ]
Callear, Samantha K. [3 ]
Campbell, Stuart I. [4 ]
Tang, Chiu C. [5 ]
Schroeder, Martin [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[2] Oak Ridge Natl Lab, Neutron Sci Directorate, Chem & Engn Mat Div, Oak Ridge, TN 37831 USA
[3] STFC Rutherford Appleton Lab, ISIS Neutron Facil, Chilton OX11 0QX, Oxon, England
[4] Oak Ridge Natl Lab, Neutron Sci Directorate, Neutron Data Anal & Visualizat Div NDAV, Oak Ridge, TN 37831 USA
[5] Diamond Light Source, Didcot OX11 0DE, Oxon, England
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
SELECTIVE ADSORPTION; NEUTRON-SCATTERING; DIFFUSION; ETHYLENE; COMBINATION; ACETYLENE; MIL-47(V); ZEOLITES; ETHANE;
D O I
10.1038/nchem.2114
中图分类号
O6 [化学];
学科分类号
0703 ;
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, pi center dot center dot center dot pi 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.
引用
收藏
页码:121 / 129
页数:9
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