We examine the phase behavior of diblock copolymers of arbitrary flexi
bility near their order-disorder transition. Our approach is based on
a free energy functional calculated from a microscopic model of rigid
rods connected with free joints and depends only on a small set of par
ameters, including the Flory chi parameter, a Maier-Saupe parameter, a
nd the rod lengths and molecular weights of each block. By analyzing s
pinodals within this model, we have explored the effect of differences
in flexibility between the two blocks, as well as the stiffness of th
e diblock as a whole, on the phase behavior. We find that nematic and
microphase fluctuations can significantly affect transition temperatur
es and phase boundaries when the difference in stiffness is large.