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• W1997354677 abstract "The transient spectra of azulene in solution have been measured in the spectral region 600−350 nm at room temperature, pumping into the S1 and S2 states with femtosecond pulses and probing with a delayed femtosecond white light continumm. The spectra are a combination of ground-state bleaching, stimulated emission, and excited-state absorption. The latter component gives a direct information on excited states which may be not active in the ground-state absorption. S1 → Sn and S2 → Sn absorptions have been discussed with the help of ab initio calculations of the MCSCF/CAS type with the 6-31G* basis set and including perturbative corrections. The calculated S0 → Sn, S1,eq → Sn, and S2,eq → Sn vertical excitation energies and oscillator strengths are in satisfactory agreement with the experimental results. It has been found that electronic states, weakly active in the ground-state absorption, occur with high intensity in the femtosecond transient spectra, in particular in the energy range 36000−44000 cm-1 above the ground-state energy." @default.
• W1997354677 created "2016-06-24" @default.
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• W1997354677 date "2003-02-25" @default.
• W1997354677 modified "2023-10-18" @default.
• W1997354677 title "S₁ → S<i>_n</i> and S₂ → S<i>_n</i> Absorption of Azulene: Femtosecond Transient Spectra and Excited State Calculations" @default.
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• W1997354677 doi "https://doi.org/10.1021/jp021313e" @default.
• W1997354677 hasPublicationYear "2003" @default.
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