A novel approach to investigating the theology of miscible polymer ble
nds is described based on complementary infrared polarimetry and mecha
nical rheometry measurements. The method provides a means by which the
blend dynamic modulus G(omega) may be separated into the individiual
contributions due to each of the blend components. This separation is
made possible by converting the observables of dynamic infrared 1,3-d
ichroism and birefringence experiments to those of dynamic shear stres
s experiments through the use of constitutive relations and the applic
ation of the stress-optic rule. The approach is extended to cover blen
d systems which exhibit orientational coupling, an effect which influe
nces the optical anisotropies but does not contribute to the state of
stress. Validity of the analysis technique is demonstrated by studying
highly entangled miscible blends of 1,4-polyisoprene, PI (M(w) = 75 0
00), and 1,2-polybutadiene, 1,2-PB (M(w) = 204 000), containing a frac
tion of deuterium-labeled PI chains (M(w) = 90 000). Orientational cou
pling in this blend is observed and is found to be characterized by a
coupling coefficient epsilon = 0.35 +/- 0.05.