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dc.contributor.author | García-Calvo, Víctor | |
dc.contributor.author | Cuevas, José V. | |
dc.contributor.author | Barbero San Juan, Héctor | |
dc.contributor.author | Ferrero, Sergio | |
dc.contributor.author | Álvarez González, Celedonio Manuel | |
dc.contributor.author | González, Jesús A. | |
dc.contributor.author | Díaz de Greñu, Borja | |
dc.contributor.author | García-Calvo, José | |
dc.contributor.author | Torroba, Tomás | |
dc.date.accessioned | 2024-01-31T15:59:28Z | |
dc.date.available | 2024-01-31T15:59:28Z | |
dc.date.issued | 2019-06-26 | |
dc.identifier.citation | Organic Letters, 2019, 21, 15, 5803–5807 | es |
dc.identifier.issn | 1523-7060 | es |
dc.identifier.uri | https://uvadoc.uva.es/handle/10324/65459 | |
dc.description | Producción Científica | es |
dc.description.abstract | We report the use of a tetraborylated perylenediimide as starting material for the preparation of a tetracorannulene-perylenediimide that is able to bind up to two fullerene-C60 molecules by host–guest molecular recognition with preference over C70. Titration with fullerene-C60 is followed by a dramatic shift of the aromatic signals in 1H NMR and an initial increase in the fluorescence of the system. By this simple mechanism, fluorogenic sensing of fullerene-C60 is easily accomplished by an unprecedented fluorescent turn-on mechanism. | es |
dc.format.mimetype | application/pdf | es |
dc.language.iso | eng | es |
dc.publisher | American Chemical Society | es |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject.classification | Aromatic compounds | es |
dc.subject.classification | Chemical structure | es |
dc.subject.classification | Complexation | es |
dc.subject.classification | Fluorescence | es |
dc.subject.classification | Titration | es |
dc.title | Synthesis of a Tetracorannulene-perylenediimide That Acts as a Selective Receptor for C60 over C70 | es |
dc.type | info:eu-repo/semantics/article | es |
dc.rights.holder | © American Chemical Society | es |
dc.identifier.doi | doi:10.1021/acs.orglett.9b01729 | es |
dc.relation.publisherversion | https://doi.org/10.1021/acs.orglett.9b01729 | es |
dc.identifier.publicationfirstpage | 5803 | es |
dc.identifier.publicationissue | 15 | es |
dc.identifier.publicationlastpage | 5807 | es |
dc.identifier.publicationtitle | Organic Letters | es |
dc.identifier.publicationvolume | 21 | es |
dc.peerreviewed | SI | es |
dc.description.project | Este trabajo forma parte de los proyectos de investigación MCIU/AEI/FEDER PGC2018-096880-A-I00, y PGC2018-099470-B-I00 | es |
dc.identifier.essn | 1523-7052 | es |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
dc.type.hasVersion | info:eu-repo/semantics/acceptedVersion | es |
dc.subject.unesco | 2304 Química Macromolecular | es |
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