Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/72341
Type: Artigo de periódico
Title: The relevant effect of an intramolecular hydrogen bond on the conformational equilibrium of cis-3-methoxycyclohexanol compared to trans-3-methoxycyclohexanol and cis-1,3-dimethoxycyclohexane
Author: de Oliveira, PR
Rittner, R
Abstract: H-1 NMR data show that an increase in the concentration of cis-3-methoxycyclohexanol (cis-3-MCH) shifts the conformational equilibrium from the 1aa conformer, stabilized by an intramolecular hydrogen bond (IAHB), to the fee conformer [X-ee = 44% (at 0.05 mol L-1) to 59% (at 0.40 mol L-1), in CCl4], which forms intermolecular hydrogen bonds (IEHB), as confirmed by IR data. The percentage of lee conformer increases with the solvent polarity, from 33% (Delta G(ee-aa) = 1.72 kJ mol(-1)) in cyclohexane (C6D12) to 97% (Delta G(ee-aa) = -8.41 kJ mol(-1)) in DMSO. For trans-3-methoxycyclohexanol (trans-3-MCH), lae and lea conformers are almost equally present in the studied solvents, lae increasing from 41%, in C6D12 (Delta G(ae-ea) = 0.84 kJ mol(-1)), to 49%, in DMSO (Delta G(ae-ea), = 0.13 kJ mol-1). A value of 18.4 kJ mol(-1) for the strength of IAHB in cis-3-MCH was obtained, from the theoretical data, through the CBS-4M method. (c) 2004 Elsevier B.V. All rights reserved.
Subject: conformational analysis
theoretical calculations
intramolecular hydrogen bond
NMR spectroscopy
IR spectroscopy
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.saa.2004.07.004
Date Issue: 2005
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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