Deuteron NMR study of dynamics and order in the columnar phase of a fluorinated discotic liquid crystal

Abstract

Measurements have been made of deuteron quadrupolar splitting and spin—lattice relaxation times T 1Q and T 1z in the columnar phase of a ring deuterated 1-fluoro-2,3,6,7,10,11-hexahex-yloxytriphenylene (F-HAT6) as a function of temperature and at two different Larmor frequencies. The disc-like molecules are stacked, with only short range positional order, into columns which are arranged on a 2-dimensional hexagonal lattice. To describe small step reorientations of these molecules, a rotational diffusion model which uses a space-fixed frame to diagonalize the molecular diffusion tensor is adopted. The principal diffusion constants in this so called ‘anisotropic viscosity model’ Dα and Dβ are for rotations of a molecule around and perpendicular to the columnar axis, respectively. A global target analysis of the spectral densities J 1(ω0) and J 2(2ω0) at seven temperatures and two Larmor frequencies in a single minimization procedure was carried out. It was found that Dα Dβ, which is consistent with the picture that the motion towards or away from the local director (i.e., the columnar axis) tends to disrupt the packing of molecules within the column. Furthermore, the activation energies Eαβ and Eβa for these motions were found to be 67.7 kJmol−1 and 56.3kJmol−1. That these values are higher in comparison with those for HAT6 is interesting, and believed to be a result of a strong lateral dipole in F-HAT6.