dc.creatorMangione, Maria Ines
dc.creatorSpanevello, Rolando Angel
dc.creatorAnzardi, M. B.
dc.date.accessioned2018-06-28T20:00:37Z
dc.date.accessioned2018-11-06T11:24:22Z
dc.date.available2018-06-28T20:00:37Z
dc.date.available2018-11-06T11:24:22Z
dc.date.created2018-06-28T20:00:37Z
dc.date.issued2017-10
dc.identifierMangione, Maria Ines; Spanevello, Rolando Angel; Anzardi, M. B.; Efficient and straightforward click synthesis of structurally related dendritic triazoles; Royal Society of Chemistry; RSC Advances; 7; 75; 10-2017; 47681-47688
dc.identifier2046-2069
dc.identifierhttp://hdl.handle.net/11336/50499
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1850819
dc.description.abstractA simple, rapid and efficient copper-catalyzed 1,3-dipolar cycloaddition reaction is described for the synthesis of a novel family of twelve triazolic dendrimers structurally related. The products were the result of the click reaction of three cores and four different azides in tetrahydrofuran applying a homogeneous copper catalysis. The reaction intermediates and products were obtained in very good to excellent yields using straightforward and simple work-up procedures. This new family of compounds contain electroactive moieties such as carbazole and triphenylamine which may turn them into excellent candidates for the development of optoelectronic organic materials.
dc.languageeng
dc.publisherRoyal Society of Chemistry
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2017/RA/C7RA09558A#!divAbstract
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/C7RA09558A
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectDendritic triazoles
dc.subjectDendrimers
dc.subject1,3-dipolar cycloadditions
dc.subjectOrganic materials
dc.titleEfficient and straightforward click synthesis of structurally related dendritic triazoles
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución