Abstract
The i.r. and 1H n.m.r. spectra are reported for the trifluoro-and trichloro-acetates of 12 substituted pyridine N-oxides in dry chloroform. If the centre of gravity of the OH stretching absorption ( H)and the chemical shift of hydrogen-bonded protons (δ) are plotted against the pKa value of the N-oxides, the points fall on two intersecting straight lines. The correlations reflect changes in the hydrogen-bond strength. Plots of H and δ of trifluoroacetates against the corresponding values for the trichloroacetates are used to show that the proton-donor properties of the acids are comparable. A direct plot of δversus H gives a straight line consistent with data for the monomeric acids. This correlation is discussed with respect to the difference between hydrogen bonds in molecular and ion-pair complexes.

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