Nonhydrodynamic molecular motions in a complex liquid: Temperature dependent dynamics in pentylcyanobiphenyl

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Abstract
The isotropic phase of nematogenic substances above the nematic–isotropic phase transition temperature T ni is characterized by short range orientational correlation of the molecules and the existence of pseudonematic domains. This microscopic structure has a strong influence on reorientational dynamics in the liquid. We present time resolved transient gratingoptical Kerr effect measurements of pentylcyanobiphenyl between 35 and 120 °C, which allow us to monitor dynamics on timescales from subpicoseconds to tens of nanoseconds. The well‐known collective component characterizing the reorientational dynamics of the pseudonematic domains follows Landau–deGennes behavior up to 30–35 degrees above T ni where the theoretical correlation length ξ≊three molecular lengths. Additionally fast relaxation channels (with time constants between 1 and 300 ps) are observed which are associated with local reorientational and intermolecular dynamicswithin the pseudonematic domains. The local dynamics are temperature independent in the range where the pseudonematic domains dominate the liquid structure, demonstrating a decoupling of the molecular motions from the bulk viscosity. Only at high temperatures, T≳70 °C, where the pseudonematic domains cease to exist, is a viscosity dependence observed. At these elevated temperatures, the slowest contribution to the fast molecular dynamics approximately follows hydrodynamic theory.