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Aromatic interactions of allenyl-anthracene derivatives with pi-electron acceptor molecules: an experimental and computational study

dc.contributor.authorVidal Vidal, Ángel
dc.contributor.authorAlonso Gómez, José Lorenzo 
dc.contributor.authorCid Fernández, María Magdalena 
dc.contributor.authorMarín Luna, Marta 
dc.date.accessioned2024-01-24T13:19:23Z
dc.date.available2024-01-24T13:19:23Z
dc.date.issued2020
dc.identifier.citationSupramolecular Chemistry, 32(1): 39-48 (2020)spa
dc.identifier.issn10610278
dc.identifier.issn10290478
dc.identifier.urihttp://hdl.handle.net/11093/5796
dc.description.abstractElectrostatic effects play an important role in aromatic interactions towards molecular recognition. Anthraceno-allenophanes are cyclic π-conjugated aromatic systems able to recognise complementary molecules through aromatic interactions. A computational and experimental study has shown that the dispersive contribution is the predominant stabilising term in the interaction of an allenyl-anthracene derivative with relevant π-acceptor molecules, such as pentafluorophenol, picric acid and 2,3-dichloro-5,6-dicyano-1,4-quinone.spa
dc.description.sponsorshipAgencia Estatal de Investigación | Ref. CTQ2017-85919-Rspa
dc.description.sponsorshipXunta de Galicia | Ref. ED431C 2017/7spa
dc.description.sponsorshipXunta de Galicia | Ref. ED431E 2018/07spa
dc.description.sponsorshipXunta de Galicia | Ref. ED481B 2016/166-0spa
dc.language.isoengspa
dc.publisherSupramolecular Chemistryspa
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-85919-R/ES/RECONOCIMIENTO SUPRAMOLECULAR HELICOIDAL: COMPLEJOS HOSTGUEST RIGIDOS Y SISTEMAS MOLECULARES AUTO-ENSAMBLADOS
dc.rightsAttribution-NonCommercial-NoDerivs 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleAromatic interactions of allenyl-anthracene derivatives with pi-electron acceptor molecules: an experimental and computational studyeng
dc.typearticlespa
dc.rights.accessRightsopenAccessspa
dc.identifier.doi10.1080/10610278.2019.1685672
dc.identifier.editorhttps://doi.org/10.1080/10610278.2019.1685672spa
dc.publisher.departamentoQuímica orgánicaspa
dc.publisher.grupoinvestigacionNovos Materiaisspa
dc.publisher.grupoinvestigacionSíntese, Estructura e Simulación (S3)spa
dc.subject.unesco2306.16 Esteroquímica y Análisis Conformacionalspa
dc.date.updated2024-01-22T14:02:21Z
dc.computerCitationpub_title=Supramolecular Chemistry|volume=32|journal_number=1|start_pag=39|end_pag=48spa
dc.referencesThis is an accepted manuscript of the article published by Taylor & Francis in Supramolecular Chemistry on 01 Nov 2019, available at https://doi.org/10.1080/10610278.2019.1685672spa


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