Dielectric relaxation and crystallization of nanophase separated 1-propanol-isoamylbromide mixture.

The effects of liquid-liquid phase separation on molecular relaxation of an apparently homogeneous mixture of 1-propanol and isoamylbromide has been studied by dielectric spectroscopy over a broad frequency and temperature range, and its crystallization kinetics investigated in real time. The mixture shows two widely separated relaxation processes, as before, with the faster relaxation due to the orientational diffusion of isoamylbromide and the slower due to that of 1-propanol. In the mixture, the scaled contribution to permittivity from orientation polarization, Deltaepsilon, of isoamylbromide is about the same as in the pure state, but that of 1-propanol decreases by a factor of approximately 3 at 120 K. As the temperature is decreased, this difference remains constant. The relaxation time, tau, of isoamylbromide and its distribution parameter remains the same as for the pure liquid, but that of 1-propanol is longer and increases with decrease in T, becoming approximately 130 times the pure liquid's value at 119 K. This is in contrast to the finding for an isomeric heptanol, whose tau had decreased. Extrapolation suggests that at T>151 K, tau of 1-propanol in the mixture may become less than that in the pure liquid (the isoamylbromide component crystallizes before this temperature could be reached). This indicates that Tg corresponding to tau of 10(3) s for 1-propanol in the mixture would be higher than in the pure liquid. Crystallization of the two components in the mixture occurs at different rates and 1-propanol remains partially uncrystallized while isoamylbromide completely crystallizes. tau of any remaining liquid isoamylbromide does not change in the presence of crystallized states while tau of residual liquid 1-propanol in the mixture is reduced. The mixture phase separates in submicron or nanosize aggregates of the alcohol in isoamylbromide, without affecting the latter's relaxation kinetics, while its own epsilon(s) decreases and tau increases. Consequences of the finding for various relaxation mechanisms are briefly described.

Self-assembled uniaxial and biaxial multilayer structures in chiral smectic liquid crystals frustrated between ferro- and antiferroelectricity.

With a view to obtain a molecular model for the subphases produced by the frustration between ferro- and antiferroelectricity in chiral smectic liquid crystals, we report results on two compounds and observe (i) the staircase character of uniaxial Sm C(*)(alpha) itself in the bulk and (ii) the multipeaked characteristic reflection bands due to the modulated helical structures just above the Sm C(*)(A) temperature range. We suggest the emergence of several uniaxial and biaxial subphases. The results show that both types of subphases can be specified by q(T) = [F] / ( [A] + [F] ) in the zero-order approximation; [A] and [F] are the numbers of antiferroelectric and ferroelectric orderings in the unit cell. We consider the basis of both types of subphases, particularly the description of the short-pitch helical structure of Sm C(*)(alpha), in terms of the molecular models so far proposed and emphasize the important role played by the discrete flexoelectric polarization.