PH-Dependent Electronic and Spectroscopic Properties of Pyridoxine (Vitamin B6)

Abstract

The key electronic and spectroscopic properties of vitamin B(6) (pyridoxine) and some of its main charged and protonated/deprotonated species are explored using hybrid density functional theory (DFT) methods including polarized solvation models. It is found that the dominant species at low pH is the N(1)-protonated form and, at high pH, the O(3)(')-deprotonated compound. Computed and experimental UV-spectra for these species (experimental spectra recorded at pH 1.7 and 11.1, respectively) show a very close resemblance. At pH 4.3, the protonated species dominates, but with onset of the zwitterionic oxo form which is also the dominant species at neutral pH. The computational studies furthermore show that neither a polarized continuum model of the polar aqueous solvent or explicit hydrogen bonding through additional water molecules are sufficient to describe accurately the spectrum at physiological pH. Instead, Na(+) and Cl(-) counterions were required to give a blue-shift of approximately 0.15 eV.