Amides Do Not Always Work: Observation of Guest Binding in an Amide-Functionalized Porous Metal–Organic Framework
Author(s) -
Oguarabau Benson,
Iván da Silva,
Stephen P. Argent,
Rafel Cabot,
Mathew Savage,
Harry G. W. Godfrey,
Yong Yan,
Stewart F. Parker,
Pascal Manuel,
Matthew J. Lennox,
Tamoghna Mitra,
Timothy L. Easun,
William Lewis,
Alexander J. Blake,
Elena Besley,
Sihai Yang⧫,
Martin Schröder
Publication year - 2016
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.6b08059
Subject(s) - chemistry , amide , adsorption , molecule , porosity , metal organic framework , neutron diffraction , metal , crystallography , functional group , polymer chemistry , chemical engineering , organic chemistry , crystal structure , polymer , engineering
An amide-functionalized metal organic framework (MOF) material, MFM-136, shows a high CO 2 uptake of 12.6 mmol g -1 at 20 bar and 298 K. MFM-136 is the first example of an acylamide pyrimidyl isophthalate MOF without open metal sites and, thus, provides a unique platform to study guest binding, particularly the role of free amides. Neutron diffraction reveals that, surprisingly, there is no direct binding between the adsorbed CO 2 /CH 4 molecules and the pendant amide group in the pore. This observation has been confirmed unambiguously by inelastic neutron spectroscopy. This suggests that introduction of functional groups solely may not necessarily induce specific guest-host binding in porous materials, but it is a combination of pore size, geometry, and functional group that leads to enhanced gas adsorption properties.
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