Conformation of 5,6,11,12-tetrahydrodibenzo [a,e ] cyclooctene : an experimental and theoretical NMR study

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dc.centroUniversidad San Pablo-CEU
dc.contributor.authorJimeno, María Luisaes
dc.contributor.authorAlkorta, Ibon
dc.contributor.authorElguero, José
dc.contributor.authorAnderson, J. Edgar
dc.contributor.authorClaramunt, Rosa María
dc.contributor.authorLavandera Díaz, José Luis
dc.date1998es
dc.date.accessioned2013-10-30T05:00:28Z
dc.date.available2013-10-30T05:00:28Z
dc.date.issued1998-10-30
dc.descriptionEn: New Journal of Chemistry. ISSN 1144-0546. n. 22, 1998, págs 1079-1083es
dc.description.abstractHybrid ab initio calculations (GIAO/B3LYP/6-31G*) together with new DNMR experiments (1H and 13C) have been used to clarify the problem of the conformation of 5,6,11,12-tetrahydrodibenzo[a,e]cyclooctene. The carbon-13 chemical shifts have been assigned unambiguously to the chair C and twist-boat TB conformations. Lineshape analysis of the 1H NMR spectra has been carried out at several temperatures using an estimated set of Karplus-type vicinal coupling constants.es_ES
dc.formatapplication/pdfes
dc.identifier000000580790es
dc.identifier.urihttp://hdl.handle.net/10637/5530
dc.language.isoenes
dc.rights.cchttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subjectCompuestos heterocíclicos.es
dc.titleConformation of 5,6,11,12-tetrahydrodibenzo [a,e ] cyclooctene : an experimental and theoretical NMR studyes
dc.typeArtículoes
dspace.entity.typePublicationes
europeana.dataProviderUNIVERSIDAD SAN PABLO CEU
europeana.isShownAthttp://hdl.handle.net/10637/5530
europeana.objecthttp://repositorioinstitucional.ceu.es/visor/libros/580790/thumb_europeana/580790.jpg
europeana.providerHispana
europeana.rightshttp://creativecommons.org/publicdomain/zero/1.0/
europeana.typeTEXT
relation.isAuthorOfPublication4b2f346e-6109-4faa-98e2-394f41e4f7f9
relation.isAuthorOfPublication.latestForDiscovery4b2f346e-6109-4faa-98e2-394f41e4f7f9

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