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dc.contributor.authorÁlvarez González, Celedonio Manuel 
dc.contributor.authorAullón, Gabriel
dc.contributor.authorBarbero San Juan, Héctor 
dc.contributor.authorGarcía Escudero, Luis Ángel 
dc.contributor.authorMartínez Pérez, Cristina
dc.contributor.authorMartín Álvarez, José Miguel 
dc.contributor.authorMiguel San José, Daniel 
dc.date.accessioned2018-03-20T13:34:38Z
dc.date.available2018-03-20T13:34:38Z
dc.date.issued2015
dc.identifier.citationOrganic Letters 2015, 17 (11), pp 2578–2581es
dc.identifier.issn1523-7060es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/29162
dc.descriptionProducción Científicaes
dc.description.abstractNovel compounds with two or three corannulene subunits have been obtained by “click chemistry”. These exotic systems were synthesized in high yields using the ethynylcorannulene as common reagent. The synergistic action as receptors for fullerenes of several corannulene blocks has been evaluated. It was found that the three-armed derivatives showed efficient complexation abilities toward C60. Furthermore, a new compound having two corannulene subunits linked to a hexahelicene scaffold has a remarkable affinity constant. Finally, theoretical calculations have been performed to evaluate the formation of their relative adducts containing a C60 molecule.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleAssembling Nonplanar Polyaromatic Units by Click Chemistry. Study of Multicorannulene Systems as Host for Fullereneses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1021/acs.orglett.5b01161es
dc.relation.publisherversionhttps://pubs.acs.org/doi/abs/10.1021/acs.orglett.5b01161es
dc.peerreviewedSIes
dc.description.projectMinisterio de Economía, Industria y Competitividad (Projects 258 CTQ2013-41067-P and CTQ2011-23862-C02)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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