We extend the self-consistent two-state model, already proposed to describe
linear and nonlinear spectral properties of push-pull chromophores in solu
tion, to describe vibrational spectra and to account for inhomogeneous broa
dening effects occurring in polar solvents. The model, not relying on pertu
rbative expansions of the solute-solvent interaction, offers a simple and i
nternally consistent description of electronic and vibrational spectra. Exo
tic and apparently unrelated phenomena, like the narrowing of time-resolved
emission bands and the dispersion of resonant Raman frequencies with the e
xcitation line find a natural explanation in the proposed approach.