Abstract
The femtosecond dynamics of 4-(N,N-dimethylamino)-4′-cyanostilbene (DCS) in acetonitrile and methanol solvent was studied by fluorescence upconversion and pump-probe absorption spectroscopy. The spectral evolution observed provides strong evidence for a fast internal charge-transfer (CT) process dominating the dynamics in the first few picoseconds, while Stokes shift dynamics seem to play only a minor role. The initially excited state seems to have already a large amount of CT character, in line with observations in jet-cooled DCS-solvent clusters. The non-exponential CT-state formation contains components significantly faster than longitudinal dielectric relaxation rates in the solvents studied, indicating a possible contribution by high-frequency vibrational modes.
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