Supramolecular binding and separation of hydrocarbons within a functionalized porous metal–organic framework
Author(s) -
Sihai Yang⧫,
Anibal J. RamirezCuesta,
Ruth Newby,
Victoria García Sakai,
Pascal Manuel,
Samantha K. Callear,
Stuart I. Campbell,
Chiu C. Tang,
Martin Schröder
Publication year - 2014
Publication title -
nature chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.996
H-Index - 232
eISSN - 1755-4349
pISSN - 1755-4330
DOI - 10.1038/nchem.2114
Subject(s) - supramolecular chemistry , chemistry , stacking , acetylene , intermolecular force , hydrogen bond , metal organic framework , adsorption , molecule , ethylene glycol , binding energy , chemical physics , computational chemistry , organic chemistry , physics , nuclear physics
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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