“…A detailed microscopic picture of the origin of various relaxation mechanisms cannot be easily reconstructed due to significant disagreement in the experimental values of the measured parameters such as electron spin-lattice relaxation time, T 1 , or rotational correlation time, τ = τ ∞ exp( E/kT ) of the CH 3 group. For example, it can be demonstrated (10) that literature data for the CH 3 dynamics of the SAR1 center (1,4,5,7,12) differ in activation energy, E/k, from 1100 to 2100 K and even more for the preexponential factor, τ ∞ , from 0.1 to 0.001 ps. On the other hand, several characteristic relaxation times were measured and origins of the corresponding relaxation mechanisms are not completely clear (8,9).…”