Conclusions
Dipole-dipole interaction of the solvent with molecules of aroyl (hydroxymethyl) trifluorosilanes 4-XC6H4COOCH2SiF3 is responsible for changes in frequency of the stretching vibrations of groups included in a five-membered ring, containing an intramolecular coordination bond Si ← 0 (the frequencies νC=O and νSiF a , are lowered, and the frequencies νasCOC are raised). The value of the orientation-induction parameter in the Buckingham equation, reflecting the dependence of νC=O and νSiF a on the parameters of the medium (ɛ, n), increases with increasing electron-donor capability of the substituent X, indicating an increase in the strength of the coordination bond. The coefficient ρ in the Hammett equation is determined by the polar properties of the medium.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2251–2254, October, 1984.
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Gavrilova, G.A., Chipanina, N.N., Frolov, Y.L. et al. Influence of solvent on ir spectra of aroyl(hydroxymethyl)trifluorosilanes. Russ Chem Bull 33, 2052–2055 (1984). https://doi.org/10.1007/BF00954080
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DOI: https://doi.org/10.1007/BF00954080