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Regioselective preparation of a bis-pyrazolinofullerene by a macrocyclization reaction

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dc.contributor.author Cuesta Gómez, Virginia
dc.contributor.author Urbani, Maxence
dc.contributor.author Cruz, Pilar de la
dc.contributor.author Welte, Lorena
dc.contributor.author Nierengarten, Jean-François
dc.contributor.author Langa, Fernando
dc.date.accessioned 2016-10-13T16:34:20Z
dc.date.available 2016-10-13T16:34:20Z
dc.date.issued 2016
dc.identifier.citation Chemical Communications. 2016 es_ES
dc.identifier.uri http://hdl.handle.net/10578/10833
dc.description.abstract A single isomer of a pyrazolinofullerene bis-adduct was prepared by tether-directed remote functionalization. Specifically, a macrocyclization reaction between C60 and a bis-hydrazone reagent has been carried out to generate a regioisomerically pure fullerene bis-adduct which presents a lower LUMO than pristine C60. es_ES
dc.format text/plain es_ES
dc.language.iso en es_ES
dc.rights info:eu-repo/semantics/openAccess es_ES
dc.subject Pyrazolinofullerene es_ES
dc.subject Macrocyclization reaction es_ES
dc.subject Bis-pyrazolinofullerene es_ES
dc.title Regioselective preparation of a bis-pyrazolinofullerene by a macrocyclization reaction es_ES
dc.type info:eu-repo/semantics/article es_ES
dc.identifier.DOI 10.1039/C6CC06549J


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