STUDY OF THE PROTONATION OF SIMPLE SCHIFF-BASES IN SOLVENTS OF VARIOUS POLARITY BY MEANS OF RAMAN-SPECTROSCOPY

In this study, the protonation of simple Schiff bases by organic acids in various solvents is investigated by Raman spectroscopy and the spectral response of the C = N+ stretching mode is correlated with the macroscopic properties of the medium surrounding the imine. Upon protonation, the unperturbed C = N stretch increases in frequency due to the combination of the coupling with the C = N+H bend and a partial rehybridization of the C = N bond. Depending on the proton location relative to that of its counterion, one mechanism may prevail over the other. Intensity measurements show that protonation is mostly controlled by the hydrogen bonding properties of the solvent and by the polarity of the medium. However, whatever the solvent, full proton transfer cannot be achieved with organic acids with pK(a) similar to the COOH of amino acids found in visual or bacterial pigments, meaning that the protonation mechanism may depend upon particular properties of the protein.