Postsynthetic Modification of a Metal-Organic Framework for Stabilization of a Hemiaminal and Ammonia Uptake

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dc.contributor.authorMorris, Williamko
dc.contributor.authorDoonan, Christian J.ko
dc.contributor.authorYaghi, Omar M.ko
dc.date.accessioned2013-03-09T10:13:52Z-
dc.date.available2013-03-09T10:13:52Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-08-
dc.identifier.citationINORGANIC CHEMISTRY, v.50, no.15, pp.6853 - 6855-
dc.identifier.issn0020-1669-
dc.identifier.urihttp://hdl.handle.net/10203/96067-
dc.description.abstractIn our study, we show by solid-state (15)N NMR measurements that an important zirconium metal-organic framework (UiO-66) with amino-functionalized links is composed of a mixture of amino and -NH(3)(+)Cl(-) salt functionalities rather than all amino functionality to give a composition of Zr(6)O(4)(OH)(4)(BDC-NH(2))(4)(BDC-NH(3)(+)Cl(-))(2) (UiO-66-A). UiO-66-A was postsynthetically modified to form a mixture of three functionalities, where the hemiaminal functionality is the majority species in UiO-66-B and aziridine is the majority functionality in UiO-66-C. UiO-66-A-C are all porous with surface areas ranging from 780 to 820 m(2)/g and have chemical stability, as evidenced by reversible ammonia uptake and release showing capacities ranging from 134 to 193 cm(3)/g.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectFUNCTIONALIZATION-
dc.subjectSTABILITY-
dc.titlePostsynthetic Modification of a Metal-Organic Framework for Stabilization of a Hemiaminal and Ammonia Uptake-
dc.typeArticle-
dc.identifier.wosid000293036000003-
dc.identifier.scopusid2-s2.0-79960793591-
dc.type.rimsART-
dc.citation.volume50-
dc.citation.issue15-
dc.citation.beginningpage6853-
dc.citation.endingpage6855-
dc.citation.publicationnameINORGANIC CHEMISTRY-
dc.identifier.doi10.1021/ic200744y-
dc.contributor.nonIdAuthorMorris, William-
dc.contributor.nonIdAuthorDoonan, Christian J.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusSTABILITY-
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