Supramolecular assemblies constructed by cucurbituril-catalyzed click reaction

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dc.citation.epage532en_US
dc.citation.issueNumber5-6en_US
dc.citation.spage525en_US
dc.citation.volumeNumber51en_US
dc.contributor.authorTuncel, D.en_US
dc.contributor.authorÜnal, Ö.en_US
dc.contributor.authorArtar, M.en_US
dc.date.accessioned2018-04-12T13:44:28Z
dc.date.available2018-04-12T13:44:28Z
dc.date.issued2011en_US
dc.departmentDepartment of Chemistryen_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.description.abstractCucurbituril homologues are multi-functional macrocycles that can find applications in many areas and have numerous interesting features setting them apart from the other macrocycles. Among them, the ability of one of the cucurbituril homologues, cucurbit[6]uril (CB6), to catalyze 1,3- dipolar cycloaddition in a regiospecific fashion is truly exceptional. Using this feature, small molecules can be clicked together to form complex structures in a very efficient way. Accordingly, in this article we review recent research involving the use of CB6-catalyzed 1,3-dipolar cycloaddition or the click reaction of CB6 in the construction of supramolecular assemblies including rotaxanes, pseudorotaxanes, polyrotaxanes, polypseudorotaxanes, molecular switches, machines, and nanovalves.en_US
dc.identifier.doi10.1002/ijch.201100034en_US
dc.identifier.eissn1869-5868
dc.identifier.issn0021-2148
dc.identifier.urihttp://hdl.handle.net/11693/38101
dc.language.isoEnglishen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/ijch.201100034en_US
dc.source.titleIsrael Journal of Chemistryen_US
dc.subject1,3-dipolar cycloadditionen_US
dc.subjectClick chemistryen_US
dc.subjectCucurbiturilsen_US
dc.subjectRotaxanesen_US
dc.subjectSupramolecular chemistryen_US
dc.titleSupramolecular assemblies constructed by cucurbituril-catalyzed click reactionen_US
dc.typeArticleen_US

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Department of Chemistry
Institute of Materials Science and Nanotechnology (UNAM)