Ab initio modeling of the solvent influence on the azohydrazone tautomerism

The solvent effect on the azo (A) -hydrazone (H) tautomeric equilibrium of 1-phenylazo-4naphthol is modeled by using ab initio quantum-chemical calculations. It was found that in methanol, methylene chloride and water there exists a strong hydrogen bonding between the particular tautomer and solvent, as well as dipole¯dipole dye-solvent interactions. The results show that the H-form is more stable in water and methylene chloride, while methanol and ioctane stabilize the A-form. The calculational results obtained are in very good agreement with the experimental data in these solvents published previously.