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Solvatochromism of heteroaromatic compounds: XXIX. Configurational isomerism of H complexes of phenols with amides and esters

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Abstract

Phenol and amides and esters in carbon tetrachloride form an H complex with an OH n bond, whose configurational isomers differ from each other by the direction of the hydrogen bond and, as a result, by the value of the spectral shift. Structural details of such configurational isomers and solvatochromism of their IR absorption bands are discussed.

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Authors and Affiliations

  1. Favorskii Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russia

    L. P. Oznobikhina, A. I. Vokin, A. M. Shulunova & V. K. Turchaninov

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  1. L. P. Oznobikhina
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  2. A. I. Vokin
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  3. A. M. Shulunova
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  4. V. K. Turchaninov
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Original Russian Text © L.P. Oznobikhina, A.I. Vokin, A.M. Shulunova, V.K. Turchaninov, 2006, published in Zhurnal Obshchei Khimii, 2006, Vol. 76, No. 5, pp. 803–813.

For communication XXVIII, see [1].

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Oznobikhina, L.P., Vokin, A.I., Shulunova, A.M. et al. Solvatochromism of heteroaromatic compounds: XXIX. Configurational isomerism of H complexes of phenols with amides and esters. Russ J Gen Chem 76, 766–776 (2006). https://doi.org/10.1134/S1070363206050197

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  • DOI: https://doi.org/10.1134/S1070363206050197

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