Please use this identifier to cite or link to this item: http://repositorio.ufla.br/jspui/handle/1/41026
Title: Theoretical and infrared studies on the conformational isomerism of trans-2-bromo-alkoxycyclohexanes
Keywords: Trans-2-Bromo-alkoxycyclohexanes
Conformational analysis
Infrared spectroscopy
Steric effects
Alkoxy groups
Issue Date: Oct-2011
Publisher: Elsevier
Citation: SILLA, 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.
Abstract: The 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.
URI: https://www.sciencedirect.com/science/article/abs/pii/S1386142511005129
http://repositorio.ufla.br/jspui/handle/1/41026
Appears in Collections:DQI - Artigos publicados em periódicos

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