dc.creatorCoelho, JV
dc.creatorFreitas, MP
dc.creatorRamalho, TC
dc.creatorMartins, CR
dc.creatorBitencourt, M
dc.creatorCormanich, RA
dc.creatorTormena, CF
dc.creatorRittner, R
dc.date2010
dc.date39995
dc.date2014-11-15T04:04:07Z
dc.date2015-11-26T17:35:54Z
dc.date2014-11-15T04:04:07Z
dc.date2015-11-26T17:35:54Z
dc.date.accessioned2018-03-29T00:18:13Z
dc.date.available2018-03-29T00:18:13Z
dc.identifierChemical Physics Letters. Elsevier Science Bv, v. 494, n. 41699, n. 26, n. 30, 2010.
dc.identifier0009-2614
dc.identifierWOS:000279368000005
dc.identifier10.1016/j.cplett.2010.05.097
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/78106
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/78106
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/78106
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1285734
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.descriptionThe infrared spectrum of 2-bromocyclohexanone in the vapor phase was obtained for the first time, and the nu(C=O) intensity for the more polar equatorial conformer was surprisingly found to be higher than for the axial form, suggesting its larger population, opposite to calculations. Theoretical data for dimeric models showed that attractive intermolecular interactions in the equatorial-equatorial dimer are dominant, but this is not enough to explain the spectroscopic behavior, since the axial-axial dimer remains more stable. The higher C=O molar absorptivity in the equatorial form is therefore invoked to explain its more intense C=O band, as confirmed by charge calculations. (C) 2010 Elsevier B.V. All rights reserved.
dc.description494
dc.description41699
dc.description26
dc.description30
dc.descriptionFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.languageen
dc.publisherElsevier Science Bv
dc.publisherAmsterdam
dc.publisherHolanda
dc.relationChemical Physics Letters
dc.relationChem. Phys. Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectNmr
dc.subjectIr
dc.subject2-halocyclohexanones
dc.subjectSolvation
dc.titleThe case of infrared carbonyl stretching intensities of 2-bromocyclohexanone: Conformational and intermolecular interaction insights
dc.typeArtículos de revistas


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