The dynamics of simple molecular systems showing glassy properties has been explored by dielectric spectroscopy and nuclear quadrupole resonance (NQR) on the halogenomethanes CBr2Cl2 and CBrCl3 in their low-temperature monoclinic phases. The dielectric spectra display features which correspond to alpha- and beta-relaxation processes, commonly observed in canonical glass formers. NQR experiments, also performed in the ergodic monoclinic phase of CCl4, enable the determination of the microscopic mechanism underlying the beta dynamics in these simple model glasses: Molecules that are nonequivalent with respect to their molecular environment perform reorientational jumps at different time scales. Thus our findings reveal another mechanism that can give rise to typical beta-relaxation behavior, raising some doubt about the existence of a universal explanation of this phenomenon.

Glassy dynamics of rigid molecules is still a matter of controversy: the physics behind the relaxation process at time scales faster than that ruled by the viscosity, the so called Johari-Goldstein process, is not known. In this work we unravel the mechanism of such a process by using a simple molecular model in which the centers of mass of the molecules are forming an ordered lattice, and molecular reorientation is performed by jumps between equilibrium orientations. We have studied the dynamics of simple quasi-tetrahedral molecules CBr(n)Cl(4-n), n = 0, 1, 2, in their monoclinic phases by means of dielectric spectroscopy and nuclear quadrupole resonance: the first technique allows to measure in a broad time scale but it is insensitive to molecular particularities, while the second has a restricted time window but senses the movement of each chlorine atom separately. The dynamic picture emerging from these techniques is that the secondary relaxation process is related to the different molecular surroundings around each nonequivalent atom of the molecule. Dynamical heterogeneities thus seem to be the cause of the secondary relaxation in this simple model of glass.

We present a molecular dynamics study of the liquid and plastic crystalline phases of CCl 3 Br. We investigated the short-range orientational order using a recently developed classification method and we found that both phases behave in a very similar way. The only differences occur at very short molecular separations, which are shown to be very rare. The rotational dynamics was explored using time correlation functions of the molecular bonds. We found that the relaxation dynamics corresponds to an isotropic diffusive mode for the liquid phase, but departs from this behavior as the temperature is decreased and the system transitions into the plastic phase.