## Raman spectra of St tnns-stilbcnc and its deutcrotcd nnalogucs were obscrvcd. Assignments of the three olcfinic vihrations have been made on the basis of the isotopic Crcquency shifts. The St Raman spectrn arc intcrpretcd according to the newly cstablishcd vibrational assignments, which arc dif
Observation of transient resonance raman spectra of the S1 state of trans-stilbene
β Scribed by Hiro-o Hamaguchi; Chihiro Kato; Mitsuo Tasumi
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 379 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Transient resonance Raman spectra of transstilbene in n-hexane have been obtained using two pulsed lasers at 266 and 585 nm. The former was used to pump the molecule to the fust excited singlet state (Sr) and the latter to proble spontaneous Raman scattering in resonance with the S, + Sr electronic transition. The dependence of the pump and probe laser power, the temporal behavior, and the excitation profile of the spectra clearly indicate that they are due to the S1 state of trans-stilbene.
π SIMILAR VOLUMES
Anti-Stokes resonance Raman spectra of S 1 trans-stilbene have been measured for vibrational wavenumbers up to 1570 cm-1. Trans-stilbene in n-hexane was excited at 290-310 nm and probed at 580-620 nm, respectively, with 8 ps resolution. All the dominant bands seen in the Stokes spectrum of the S 1 s
Raman spectra and absolute Raman cross sections have been mcasurcd for tram-stilbcne in cyclohcxane and methanol using 282 and 266 nm excitation, and calculations have been performed to model the Raman Intensities and absorption spectra. The only out-of-plane vibration observed in either solvent is