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dc.creatorSilla, Josué M.-
dc.creatorDuarte, Claudimar J.-
dc.creatorFreitas, Matheus P.-
dc.creatorRamalho, Teodorico C.-
dc.creatorCormanich, Rodrigo A.-
dc.creatorSantos, Francisco P.-
dc.creatorTormena, Cláudio F.-
dc.creatorRittner, Roberto-
dc.date.accessioned2020-05-18T15:41:30Z-
dc.date.available2020-05-18T15:41:30Z-
dc.date.issued2011-10-
dc.identifier.citationSILLA, J. M. et al. Theoretical and infrared studies on the conformational isomerism of trans-2-bromo-alkoxycyclohexanes. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, [S.l.], v. 81, n. 1, p. 359-362, Oct. 2011. DOI: 10.1016/j.saa.2011.06.023.pt_BR
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S1386142511005129pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/41026-
dc.description.abstractThe infrared spectra of trans-2-bromo-alkoxycyclohexanes (alcoxy = OMe, OEt, OiPr and OtBu) were obtained for the neat liquid, and the C–Br stretching mode was quantitatively analyzed to give insight about the conformational isomerism of these compounds. Frequency calculations supported the band assignments, and the relative band intensities suggest that the diaxial conformer is prevalent for the methoxy and tert-butoxy derivatives (51 and 56%, respectively), while the diequatorial form is preponderant for the ethoxy and isopropoxy derivatives (76 and 77%, respectively). Therefore, the size of the alkoxy group plays a determinant role in determining the conformational preferences of the title compounds.pt_BR
dc.languageen_USpt_BR
dc.publisherElsevierpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopypt_BR
dc.subjectTrans-2-Bromo-alkoxycyclohexanespt_BR
dc.subjectConformational analysispt_BR
dc.subjectInfrared spectroscopypt_BR
dc.subjectSteric effectspt_BR
dc.subjectAlkoxy groupspt_BR
dc.titleTheoretical and infrared studies on the conformational isomerism of trans-2-bromo-alkoxycyclohexanespt_BR
dc.typeArtigopt_BR
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