Abstract
A coupling between the librations of the methyl groups or proton tetrahedra (e.g., CH4 and NH4+) in a solid is shown to explain the experimentally observed decrease of the librational tunneling splitting without significant lifetime broadening when the temperature is raised at low temperatures. Due to the same coupling, the libration amplitude of a given group is influenced by neighboring groups. The amplitude can momentarily increase so much that the group undergoes random jumps to other equilibrium orientations even at liquid-helium temperatures. This model agrees with the nearly temperature-independent spin-lattice relaxation time T1 of protons in some samples for T4 K and with the temperature-dependent T1 described by the activation energy equal to the separation between the ground and first-excited-librational levels at somewhat higher temperatures.