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dc.contributor.authorLutton Gething, A. R. Bonity J.
dc.contributor.authorSpencer, Ben F.
dc.contributor.authorWhitehead, George F. S.
dc.contributor.authorVitorica-Yrezabal, Iñigo Javier
dc.contributor.authorLee, Daniel
dc.contributor.authorAttfield, Martin P.
dc.date.accessioned2024-05-15T10:00:15Z
dc.date.available2024-05-15T10:00:15Z
dc.date.issued2024-02-08
dc.identifier.citationA. R. Bonity J. Lutton-Gething, Ben F. Spencer, George F. S. Whitehead, Iñigo J. Vitorica-Yrezabal, Daniel Lee, and Martin P. Attfield Chemistry of Materials 2024 36 (4), 1957-1965 DOI: 10.1021/acs.chemmater.3c02849es_ES
dc.identifier.urihttps://hdl.handle.net/10481/91809
dc.description.abstractRare-earth (RE) metal−organic frameworks (MOFs) synthesized in the presence of fluorine-donating modulators or linkers are an important new subset of functional MOFs. However, the exact nature of the REaXb core of the molecular building block (MBB) of the MOF, where X is a μ2 or 3-bridging group, remains unclear. Investigation of one of the archetypal members of this family with the stable fcu framework topology, Y-fum-fcu-MOF (1), using a combination of experimental techniques, including high-field (20 T) solid-state nuclear magnetic resonance spectroscopy, has determined two sources of framework disorder involving the μ3-X face-capping group of the MBB and the fumarate (fum) linker. The core of the MBB of 1 is shown to contain a mixture of μ3-F− and (OH)− groups with preferential occupation at the crystallographically different facecapping sites that result in different internally lined framework tetrahedral cages. The fum linker is also found to display a disordered arrangement involving bridging− or chelating−bridging bis-bidentate modes over the fum linker positions without influencing the MBB orientation. This linker disorder will, upon activation, result in the creation of Y3+ ions with potentially one or two additional uncoordinated sites possessing differing degrees of Lewis acidity. Crystallographically determined host−guest relationships for simple sorbates demonstrate the favored sorption sites for N2, CO2, and CS2 molecules that reflect the chemical nature of both the framework and the sorbate species with the structural partitioning of the μ3-groups apparent in determining the favored sorption site of CS2. The two types of disorder found within 1 demonstrate the complexity of fluoride-containing RE-MOFs and highlight the possibility to tune this and other frameworks to contain different proportions and segregations of μ3-face-capping groups and degrees of linker disorder for specifically tailored applications.es_ES
dc.description.sponsorshipEPSRC and the University of Manchester for the award of a DTG PhD studentship (EPSRC EP/R513131/1) and funding the dual source Rigaku FR-X diffractometer (EPSRC EP/P001386/1)es_ES
dc.description.sponsorshipHenry Royce Institute, funded through EPSRC grants EP/R00661X/1, EP/P025021/1, and EP/P025498/1es_ES
dc.description.sponsorshipEPSRC and BBSRC (EP/T015063/1)es_ES
dc.description.sponsorshipUniversity of Warwickes_ES
dc.description.sponsorshipBirmingham Science City Advanced Materials Projects 1 and 2 supported by Advantage West Midlands (AWM) and the European Regional Development Fund (ERDF)es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleDisorder and Sorption Preferences in a Highly Stable Fluoride- Containing Rare-Earth fcu-Type Metal−Organic Frameworkes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1021/acs.chemmater.3c02849
dc.type.hasVersionVoRes_ES


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