<abstract xmlns="http://www.w3.org/1999/xhtml"><p> A systematic comparative theoretical study has been performed on a series of fourteen metasubstituted selenophenols. The optimal geometries were calculated using the density functional theory (DFT) and the Nuclear Magnetic Resonance parameters were computed by applying the Gauge Including Atomic Orbital (GIAO) method. The calculated NMR shifts were correlated with the Hammett constants. The obtained results were also compared with the theoretical data obtained for thiophenols and phenols. Our results indicate the linear dependence between the gas-phase NMR shifts and Hammett constants. However, the presence of large selenium atoms is able to suppress significantly the substituent effect in meta position. Therefore six substituents (Me, OH, MeCO, COOMe, COOEt and CF3 groups) were excluded from the data evaluation. Correlations with the fundamental stretching vibration frequencies of the mode with the dominant Se-H vibration have not been found.</p></abstract>

A systematic comparative theoretical study has been performed on a series of fourteen metasubstituted selenophenols. The optimal geometries were calculated using the density functional theory (DFT) and the Nuclear Magnetic Resonance parameters were computed by applying the Gauge Including Atomic Orbital (GIAO) method. The calculated NMR shifts were correlated with the Hammett constants. The obtained results were also compared with the theoretical data obtained for thiophenols and phenols. Our results indicate the linear dependence between the gas-phase NMR shifts and Hammett constants. However, the presence of large selenium atoms is able to suppress significantly the substituent effect in meta position. Therefore six substituents (Me, OH, MeCO, COOMe, COOEt and CF3 groups) were excluded from the data evaluation. Correlations with the fundamental stretching vibration frequencies of the mode with the dominant Se-H vibration have not been found.

Theoretical 1H(Se—H) NMR shifts in meta-substituted Ph—XH (X = O, S, Se)

Institute of Physical Chemistry and Chemical Physics, Slovak Technical University, SK-81237 Bratislava, Slovakia

Acta Chimica Slovaca

A systematic comparative theoretical study has been performed on a series of fourteen metasubstituted selenophenols. The optimal geometries were calculated...

Theoretical 1H(Se—H) NMR shifts in meta-substituted Ph—XH (X = O, S, Se)

Publicado en línea: 14 dic 2012

Páginas: 159 - 163

DOI: https://doi.org/10.2478/v10188-012-0024-0

Palabras clave
chemical shift, NMR, Hammett constant, selenophenol, B3LYP

This content is open access.

Theoretical 1H(Se—H) NMR shifts in meta-substituted Ph—XH (X = O, S, Se)

Publicado en línea: 14 dic 2012

Páginas: 159 - 163

DOI: https://doi.org/10.2478/v10188-012-0024-0

Palabras clavechemical shift, NMR, Hammett constant, selenophenol, B3LYP

This content is open access.

Palabras clave
chemical shift, NMR, Hammett constant, selenophenol, B3LYP