The Hamiltonian of the induction effect (dipole-induced dipole interac
tion) in the model proposed by Snels and Reuss is corrected. This mode
l was proposed for the calculation of the frequency shift and transiti
on strength of the IR spectra of clusters of highly symmetric molecule
s such as (SF6)(n), (SiF4)(n) and (SM(4))(n). Disagreement between the
observed frequency shifts and the calculated results obtained using t
his model for (SF6)(3) and (SF6)(4) was found to be caused by the inco
rrect Hamiltonian of the dipole-induced dipole interaction. The calcul
ated results for (SF6)(3) and (SF6)(4) with the corrected Hamiltonian
agree with the observed spectra.