We report on the structure and the viscoelastic properties of two side-chai
n liquid-crystalline polymers with different spacer length in the melt and
fiber states and of their Copolymers with a semicrystalline block. Optical
microscopy, X-ray scattering, and differential scanning calorimetry are emp
loyed for the structure investigation and rheology for the dynamics. The sm
ectic and nematic liquid-crystalline polymers exhibit non-Newtonian low-fre
quency response and violate the empirical principle of time-temperature sup
erposition with the effect being more pronounced in the former. Fibers draw
n from the melt exhibit significantly different structure from the melt sam
ples. In the diblock copolymer composed of smectic/crystalline blocks, the
strong first-order isotropic-to-smectic transition induces the weak disorde
r-to-lamellar transition between the dissimilar blocks in the diblock.