Dipolar interactions in liquids and linear dielectric relaxation spectroscopy.

Linear dielectric relaxation studies performed on two isotropic liquids composed of the molecules of the same moment of inertia and a quite different polarity: C10H21-O-Ph-COO-Ph-CN (the dipole moment of about 5 D) and C10H21-O-Ph-OOC-Ph-CN (2.5 D) showed that, at given temperature, the relaxation times corresponding to the rotation around the short axis of the two kinds of molecules coincide to each other, regardless the polarity of the molecules and their abilities to accomplish dipolar aggregation. The studies allow one to estimate the lifetime of the intermolecular aggregates due to the dipolar interactions in liquids as no longer than 0.

Static and dynamic dielectric properties of strongly polar liquids in the vicinity of first order and weakly first order phase transitions.

The paper presents the results of measurements of the linear dielectric properties of the compounds from the homologous series of alkylcyanobiphenyls (C(n)H(2n+1)PhPhCN, nCB) in the vicinity of the first order transition (from the isotropic liquid to the crystalline phase) of nonmesogenic nCB's (n=2-4) and the weakly first order transition (from the isotropic liquid to the nematic phase) of 5CB. The experimental method for the separation of the critical part of the static permittivity derivative and the activation energy for rotation of the mesogenic molecules, in the vicinity of weakly first order phase transition, is proposed. It is shown that the critical temperature dependence of the permittivity and the activation energy can be described with a function of (T-T*)(-alpha) type, with the same values of the temperature of virtual transition of the second order (T*) and the critical exponent (alpha).