Absorption, fluorcsccncc cwtauon and emwon spectra, quantum yields, and fluorescence decay times have been measurcd for several derwauvcs of all-trans 1,6dlphenyl-1,3,5hexatriene (DPH) III a number of solvents. Emlsslon occurs from the low-lymg IA: state and the I B,\* which IS at shghtly hgher ener
Evidence for S1/S2 electronic state mixing in the S1 ←l S0 fluorescence excitation spectrum of 1-naphthol
✍ Scribed by Susan J. Humphrey; David W. Pratt
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 413 KB
- Volume
- 257
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
Rotationatly resolved fluorescence excitation spectra of two vibronic bands at AE= 410.5 and 414.9 cm -l in the S l ~ S O electronic transition of trans-l-naphthol have been recorded and analyzed. The analysis reveals that the in-plane transition dipole moment of the 410 cm-1 band makes an angle of -36 ° with the a inertial axis, the same as the origin band, whereas the corresponding angle of the 414 cm-1 band is + 55 °. Additionally, the spectrum of the 414 cm-1 band is perturbed. These effects are attributed to a coupling of the 414 cm-1 vibrational level of the S 1 electronic state to the S 2 electronic state which may influence the proton transfer behavior of 1-naphthol.
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