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dc.contributor.authorBarbero San Juan, Héctor 
dc.contributor.authorFerrero, Sergio
dc.contributor.authorÁlvarez Miguel, Lucía
dc.contributor.authorGómez Iglesias, Patricia
dc.contributor.authorMiguel San José, Daniel 
dc.contributor.authorÁlvarez González, Celedonio Manuel 
dc.date.accessioned2018-03-20T12:31:29Z
dc.date.available2018-03-20T12:31:29Z
dc.date.issued2016
dc.identifier.citationChemical Communications, 2016, 52 ,12964es
dc.identifier.issn1359-7345es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/29159
dc.descriptionProducción Científicaes
dc.description.abstractSix azobenzene derivatives bearing polyaromatic fragments have been prepared and their reversible photoisomerization has been assessed. Corannulene-functionalized molecules have demonstrated excellent switchable hosting abilities towards fullerenes in which an interesting range of affinities has been found. The success of this design relies upon the reversible formation and destruction of tweezer-like structures.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleAffinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezerses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/c6cc06445kes
dc.relation.publisherversionhttp://pubs.rsc.org/en/content/articlelanding/2016/cc/c6cc06445k#!divAbstractes
dc.identifier.publicationtitleChemical Communicationses
dc.peerreviewedSIes
dc.description.projectMinisterio de Economía, Industria y Competitividad (Project CTQ 2013-41067-P)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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