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dc.contributor.authorGarcía Iglesias, Miguel 
dc.contributor.authorTorres Cebada, Tomás
dc.contributor.authorGonzalez Rodríguez, David
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-11-03T14:44:59Z
dc.date.available2025-11-03T14:44:59Z
dc.date.issued2016-08-04
dc.identifier.issn1359-7345
dc.identifier.issn1364-548X
dc.identifier.otherCTQ-2014-52869-Pes_ES
dc.identifier.otherCTQ-2014-57729-Pes_ES
dc.identifier.urihttps://hdl.handle.net/10902/38057
dc.description.abstractOctameric near-IR dye nanoclusters are produced by complexation of potassium cations with a phthalocyanine-guanosine conjugate. The combination of hydrogen-bonding, K+ coordination, pi-pi stacking and steric interactions between the chiral side groups is responsible for defining a specific helical chromophore arrangement in the clusters, which display high stability and maintain their supramolecular identity onto substrates.es_ES
dc.description.sponsorshipFinancial support from MINECO, Spain (CTQ‐2014‐52869‐P, T.T.; CTQ2014‐57729‐P, D. G.‐R.), the Comunidad de Madrid (S2013/MIT‐2841 FOTOCARBON, T.T.), and the European Research Council (ERC‐StG 279548, D. G.‐R.) is acknowledged.es_ES
dc.format.extent4 p.es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.rights© Royal Society of Chemistryes_ES
dc.sourceChemical Communications, 2016, 52(60), 9446-9449es_ES
dc.titleWell-defined, persistent, chiral phthalocyanine nanoclusters via G-quadruplex assemblyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1039/C6CC04152Ces_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1039/C6CC04152C
dc.type.versionacceptedVersiones_ES


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