Influence of temperature on thymine-to-solvent vibrational energy transfer

Abstract

At the instant following the non-radiative deactivation of its ππ* electronic state, the vibrational modes of thymine possess a highly non-equilibrium distribution of excitation quanta (i.e., >4 eV in excess energy). Equilibrium is re-established through rapid (5 ps) vibrational energy transfer to the surrounding solvent. The mechanisms behind such vibrational cooling (VC) processes are examined here using femtosecond transient grating and two-dimensional photon echo spectroscopies conducted at 100 K and 300 K in a mixture of methanol and water. Remarkably, we find that this variation in temperature has essentially no impact on the VC kinetics. Together the experiments and a theoretical model suggest three possible mechanisms consistent with this behavior: (i) vibrational energy transfer from the solute to solvent initiates (directly) in intramolecular modes of the solute with frequencies >300 cm(-1); (ii) the relaxation induced increase in the temperature of the environment reduces the sensitivity of VC to the temperature of the equilibrium system; (iii) the time scale of solvent motion approaches 0.1 ps even at 100 K. Mechanism (i) deserves strong consideration because it is consistent with the conclusions drawn in earlier studies of isotope effects on VC in hydrogen bonding solvents. Our model calculations suggest that mechanism (ii) also plays a significant role under the present experimental conditions. Mechanism (iii) is ruled out on the basis of long-lived correlations evident in the photon echo line shapes at 100 K. These insights into photoinduced relaxation processes in thymine are made possible by our recent extension of interferometric transient grating and photon echo spectroscopies to the mid UV spectral region.