Dynamics of the Kerr effect in the isotropic phase of comb-shaped nematic polymers

The equilibrium Kerr effect and its dynamics are investigated in isotropic melts of the comb-shaped LC polymer poly(4-[(4′-cyano-1,1′-biphenyl-4-yl)oxy]butyl-2-acrylate) and its copolymers with acrylic acid or methyl methacrylate and isotropic melts of the LC ionomer containing rubidium ions in a wide temperature range. A sharp change in the temperature dependence of relaxation times for the induced macroscopic orientational order is found for the LC copolymers and the LC ionomer in the temperature range 10–15 K higher than the temperature of the nematic-isotropic phase transition. In contrast, the phenomena caused by the small-scale dynamics, such as electric conductivity and dipole relaxation, are approximated by the conventional Arrhenius type dependence, and the equilibrium electrooptical properties of the copolymers are well characterized via the Landau-De Gennes model. The nonclassical behavior of macroscopic relaxation times may be associated with temperature variations in the contribution of main polymer chains to the orientation macroscopic dynamics of the melt, in which the decisive role is played by side mesogenic groups.