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dc.contributor.authorDardonville, Christophe-
dc.contributor.authorJimeno, M. Luisa-
dc.contributor.authorAlkorta, Ibon-
dc.contributor.authorElguero, José-
dc.date.accessioned2011-04-26T08:42:09Z-
dc.date.available2011-04-26T08:42:09Z-
dc.date.issued2004-
dc.identifier.citationOrganic and Biomolecular Chemistry 2 : 1587-1591 (2004)es_ES
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/10261/34914-
dc.description.abstractGeometrical and energetic DFT calculations as well as GIAO and NICS chemical shifts have been calculated for 1H-azepine and 5H-dibenz[b, f]azepine and their cations. The last compound has been studied experimentally by 1H and 13C NMR in neutral and acidic conditions establishing that the cation corresponds to an N-protonated structure. The conclusion is that the neutral molecules are antiaromatic while the cations are aromatic (homoheteroaromaticity).es_ES
dc.description.sponsorshipFinancial support was provided by the Spanish DGICYT (Project nos. SAF2003-08003-C02-02 and BQU-2000-0906). C. D. is a recipient of a postdoctoral fellowship from the Spanish Ministerio de Educación, Cultura y Deporte (SB2001-0174).es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.rightsclosedAccesses_ES
dc.subject1H-azepinees_ES
dc.subject5H-dibenz[b, f]azepinees_ES
dc.titleHomoheteroaromaticity: the case study of azepine and dibenzazepinees_ES
dc.typeartículoes_ES
dc.identifier.doi10.1039/b314742h-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1039/B314742Hes_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairetypeartículo-
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