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dc.contributor.authorBarbero San Juan, Héctor 
dc.contributor.authorMasson, Eric
dc.date.accessioned2024-01-30T15:25:27Z
dc.date.available2024-01-30T15:25:27Z
dc.date.issued2021
dc.identifier.citationChem. Sci., 2021, 12, 9962es
dc.identifier.issn2041-6520es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/65374
dc.descriptionProducción Científicaes
dc.description.abstractPlatinum terpyridyl complexes, stacked on top of one another and secured as dimers with cucurbit[8]uril (CB[8]) in aqueous medium, were functionalized quantitatively and in situ with a pair of pentapeptides Phe-(Gly)3-Cys by grafting their cysteine residues to the Pt centers. The resulting CB[8]·(Pt·peptide)2 assemblies were used to target secondary hosts CB[7] and CB[8] via their pair of phenylalanine residues, again in situ. A series of well-defined architectures, including a supramolecular “pendant necklace” with hybrid head-to-head and head-to-tail arrangements inside CB[8], were obtained during the self-sorting process after combining only 3 or 4 simple building units.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/3.0/*
dc.titleDesign and recognition of cucurbituril-secured platinum-bound oligopeptideses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/d1sc02637bes
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2021/sc/d1sc02637bes
dc.identifier.publicationfirstpage9962es
dc.identifier.publicationissue29es
dc.identifier.publicationlastpage9968es
dc.identifier.publicationtitleChemical Sciencees
dc.identifier.publicationvolume12es
dc.peerreviewedSIes
dc.identifier.essn2041-6539es
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Unported*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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