Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/80517
Type: Artigo de periódico
Title: Infrared and theoretical calculations in 2-halocycloheptanones conformational analysis
Author: Rozada, TC
Gauze, GF
Favaro, DC
Rittner, R
Basso, EA
Abstract: 2-Halocycloheptanones (Halo = F, Cl, Br and I) were synthesized and their conformational analysis was performed through infrared spectroscopy data. The corresponding conformers geometries and energies were obtained by theoretical calculations at B3LYP/aug-cc-pVDZ level of theory in the isolated state and in solution. It was observed, by both approaches, that the conformational preferences were very sensitive to the solvent polarity, since its increase led to an increase in the population of the more polar conformer. An analysis of these conformational equilibria showed they suffer also the influence of stereoelectronic effects, like hyperconjugation and steric effects. These results were interpreted using natural bond orbital (NBO) analysis, which indicated that the electronic delocalization to the orbital pi*c=o is directly involved in the stability increase of conformers I and II. The relative effect of the period of the halogen can also be noted, with changes in the conformational preferences and in the energies involved in the interactions of NBO. (C) 2012 Elsevier B.V. All rights reserved.
Subject: 2-Halocycloheptanones
Conformation analyses
Infrared
Theoretical calculations
NBO
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.saa.2012.03.027
Date Issue: 2012
Appears in Collections:Unicamp - Artigos e Outros Documentos

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