Abstract

Vibrational relaxation dynamics of trans-stilbene in the S1 state immediately after photoexcitation is studied by picosecond time-resolved anti-Stokes Raman spectroscopy with several pump and probe wavelengths. Pump-wavelength dependence of the anti- Stokes spectrum indicates that, when pump photons with high excess energy (≈5200cm-1) are used, the anti-Stokes Raman bands at 0 ps delay time arise from vibrationally excited transients with excess vibrational energy not thermally distributed in the molecule. Probe-wavelength dependence suggests that the vibrationally excited transients at 0 ps are mostly on the lowest excited vibrational levels, as far as the olefinic C═C stretching and the C–Ph stretching modes are concerned. The vibrational relaxation process of S1trans-stilbene is discussed on the basis of the observed results.

Highlights

  • Vibrational relaxation dynamics of trans-stilbene in the S state immediately after photoexcitation is studied by picosecond time-resolved anti-Stokes Raman spectroscopy with several pump and probe wavelengths

  • Relative intensities among bands change in a similar time scale. Such temporal behaviour can be attributed to vibrational relaxation toward a thermal equilibrium

  • The anti-Stokes Raman spectra of S trans-stilbene were observed with eight probe wavelengths (580-670nm), all of which were resonant or pre-resonant with the strong Sn+-S absorption

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Summary

Introduction

Vibrational relaxation dynamics of trans-stilbene in the S state immediately after photoexcitation is studied by picosecond time-resolved anti-Stokes Raman spectroscopy with several pump and probe wavelengths. Raman spectra provide important information on the vibrational relaxation dynamics of trans-stilbene in the excited singlet (S1) state. Figure shows the pump-wavelength dependence of the anti-Stokes

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