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Boletín de la Sociedad Chilena de Química

versão impressa ISSN 0366-1644

Resumo

CONTRERAS, J.GUILLERMO  e  MADARIAGA, SANDRA T.. SOLVENT EFFECT ON THE VALENCE TAUTOMERISM OF BENZENE OXIDE/OXEPIN MOLECULAR SYSTEM. Bol. Soc. Chil. Quím. [online]. 2001, vol.46, n.4, pp.471-480. ISSN 0366-1644.  http://dx.doi.org/10.4067/S0366-16442001000400011.

Thermodynamic parameters for the benzene oxide Û oxepin system have been calculated at MP4(SDQ)/6-31+G**//HF/6-31G** level of theory. The calculated enthalpy for this valence tautomeric equilibrium differs from that reported by Vogel et al in 1967, but agree well with the value calculated by Kollman using the MINDO/3 method. Large deviations in the experimental tautomerization entropies lead to unreliable D Go values. The differences in D Ho and D So can be due to the lack of band shape analysis of the 1H-NMR spectra. The effect of solvent polarity on the above equilibrium has been studied using the isodensity polarized continuum method (IPCM). Low polar solvents favor the oxepin formation whereas medium to high polar solvents leads to benzene oxide formation. The transition state for the tautomerization reaction has been fully characterized and the activation energies for the forward and reverse reaction are estimated to be ca. 9.5 and 11.0 kcal/mol,respectively. The solvent polarity exerts a reasonable effect decreasing the activation energies up to 4 kcal/mol.

Palavras-chave : benzene oxide/oxepin; equilibrium; valence tautomerism; solvent effect.

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