Abstract
We report studies on several methylated uracils and thymines and thymine−water complexes in the gas phase using resonantly enhanced multiphoton ionization (REMPI) and laser-induced fluorescence (LIF) spectroscopy. Results from two different REMPI experiments provided strong evidence that, after photoexcitation to the S1 state, bare molecules were funneled into and trapped in a dark state via fast internal conversion. Lifetimes of this dark state were determined to be tens to hundreds of nanoseconds, depending on the internal energy and the degree of methyl substitution. The mass spectra of hydrated thymine clusters demonstrated dependence on the excitation wavelength, and the gradual loss of the ion signal with increasing water content across the absorption region of the S1 state indicated a reduced lifetime of the S1 state by the water solvent. In addition, the lifetime of the dark state also decreased gradually as thymine became more hydrated. On the basis of these results, we conclude that, in water so...
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