A new molecular thermodynamic model is developed of the glass transition temperatures (T-g) of binary polymer-salt complexes by combining configurational entropy theory with Guggenheim's form of the Debye-Mickel theory. The interactions between the polymer chains and the salt as well as those between cations and anions are accounted for by this model. The predictions of this extended configurational entropy theory are compared with the T-g values of poly(2-ethyl-2-oxazoline) (POZ) complexed with AgBF4, AgClO4, AgCF3-SO3, and AgNO3 at various compositions, as obtained by differential scanning calorimetry (DSC). The model accurately predicts the experimental T-g values even at high concentrations of silver salt (i.e., up to a mole ratio of [Ag]/[C=O] = 1/1), where the deviation of the simple configurational entropy theory from experimental data is large. Moreover, the maximum in the glass transition temperature, i.e., the increase in T-g with salt concentration at low salt concentrations but its decrease at high salt concentrations, is explicable with this model.