Molecular switch based on a cucurbit[6]uril containing bistable [3]rotaxane

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dc.citation.epage1371en_US
dc.citation.issueNumber13en_US
dc.citation.spage1369en_US
dc.contributor.authorTuncel, D.en_US
dc.contributor.authorÖzsar, Ö.en_US
dc.contributor.authorTiftik, H. B.en_US
dc.contributor.authorSalih, B.en_US
dc.date.accessioned2016-02-08T10:15:04Z
dc.date.available2016-02-08T10:15:04Z
dc.date.issued2007en_US
dc.departmentDepartment of Chemistryen_US
dc.description.abstractA bistable CB6-based [3]rotaxane with two recognition sites has been prepared very efficiently in a high yield synthesis through CB6 catalyzed 1,3-dipolar cycloaddition; this rotaxane behaves as a reversible molecular switch and exhibits conformational changes caused by the movement of rings under base, acid and heat stimuli from one location to the other. © The Royal Society of Chemistry.en_US
dc.description.provenanceMade available in DSpace on 2016-02-08T10:15:04Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2007en
dc.identifier.doi10.1039/b616764ken_US
dc.identifier.issn1359-7345
dc.identifier.urihttp://hdl.handle.net/11693/23513
dc.language.isoEnglishen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/b616764ken_US
dc.source.titleChemical Communicationsen_US
dc.subjectAlkane derivativeen_US
dc.subjectCatalysisen_US
dc.subjectChemical modificationen_US
dc.subjectCycloadditionen_US
dc.subjectMolecular recognitionen_US
dc.subjectSupramolecular chemistryen_US
dc.titleMolecular switch based on a cucurbit[6]uril containing bistable [3]rotaxaneen_US
dc.typeArticleen_US

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