The molecular orientation and deformation mechanisms of a quenched isotactic polypropylene (iPP) film deformed at temperatures between 303 K and the melting point are studied. At draw temperature T-E less than 400 K where the degree of crystallinity does not change markedly, a linear relationship between molecular orientations of the crystalline and the amorphous phases is revealed and the slope is estimated about 1.82. The interpenetrating network (IPN) model, that takes into account the plastic response of the crystalline (C) network formed by a small portion of crystallites adhered through intercrystalline links and the pseudo-affine deformation of the crystallite enhanced amorphous matrix (CEAM) network, is able to account for inhomogeneous deformation behavior on the mesoscale accompanied with the localized necking in this T-E range. Meanwhile, the initial Young's modulus and the true yield stress exerted by the deformation of the rigid C network exhibit the Arrhenius type of dependence on T-E. The apparent shear modulus of the CEAM network as a function of T-E is discussed in relation to variations in numbers and average molecular weights of the crystalline and the amorphous sequences being manifested by small consecutive endothermic and exothermic peaks in the DSC curve. The IPN model becomes invalid for deformations above T-E = 400 K where morphological changes are induced due to melting of crystallites as proved from the DSC measurement. (c) 2005 Elsevier Ltd. All rights reserved.