The thermal and dynamic mechanical behaviour of ordered stoichiometric as w
ell as off-stoichiometric polyurethane networks based on mesogenic diol - 6
,6'-[ethylenebis(1,4-phenyleneoxy)]dihexanol (D), 2(4)-methyl-1,3-phenylene
diisocyanate (DI) and poly(oxypropylene) triol (T) is reviewed. The effect
s of various initial molar ratios of the reactive groups ([OH](T)/[NCO](DI)
/[OH](D)) and of the ordered or isotropic state of the diol on the critical
gel structure at the sol-gel transition and a power-law mechanical behavio
ur is discussed. The effects of amount of mesogenic diol in the elastically
active network chains (EANCs) on the conformational rearrangements require
d for ordering, the concentration of permanent physical interactions (trapp
ed entanglements) and on the intensity of the slow relaxation process in th
e rubbery region are shown.