Simulation of structure and dynamics near the isotropic-nematic transition

We present a computer simulation study of orientational correlations in a molecular liquid approaching the isotropic-nematic transition, including the first calculation of the direct correlation function c(1,2) in this regime. While the second-rank orientational correlation length diverges, the associated component of c(1,2) remains short ranged, and its spatial integral approaches the mechanical instability limit for the isotropic phase as predicted by density-functional theory. Orientational correlation lengths and times are quite well described by Landau-de Gennes theory.