NONHYDRODYNAMIC MOLECULAR MOTIONS IN A COMPLEX LIQUID - TEMPERATURE-DEPENDENT DYNAMICS IN PENTYLCYANOBIPHENYL

被引:90
作者
DEEG, FW [1 ]
GREENFIELD, SR [1 ]
STANKUS, JJ [1 ]
NEWELL, VJ [1 ]
FAYER, MD [1 ]
机构
[1] STANFORD UNIV,DEPT CHEM,STANFORD,CA 94305
关键词
D O I
10.1063/1.458832
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The isotropic phase of nematogenic substances above the nematic-isotropic phase transition temperature Tni 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 grating optical 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 Tni 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 dynamics within 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. © 1990 American Institute of Physics.
引用
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页码:3503 / 3514
页数:12
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