Ground-state spin-Hamiltonian parameters, magnetic data, and electronic Raman spectra of hexacoordinate vanadium(III) complexes are calculated with consideration to the ((3)A circle plus E-3) circle times e vibronic interaction and compared to experimental data. It is shown that the zero-field-splitting of the (3)A(g) (S-6) ground term may be reduced significantly by the dynamical Jahn-Teller effect, particularly when the pi-anisotropy of the metal-ligand bonding interaction is significant, and the energy of the Jahn-Teller active vibration is comparable to the diagonal axial field. The dynamical Jahn-Teller effect may also give rise to a significant enhancement in the Raman intensity of overtones and higher harmonics of Jahn-Teller active vibrations, when the energies of these transitions fall in the proximity of intra-T-3(1g) (O-h) electronic Raman transitions. A simple method of conducting vibronic coupling calculations is described, employing ligand field matrices generated by angular overlap model calculations, which may in principle be applied to any transition metal complex.