Time-resolved resonance raman spectrum of all-trans-diphenylbutadiene in the lowest excited singlet state
โ Scribed by Robert Wilbrandt; Niels-Henrik Jensen; Frans W. Langkilde
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 506 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
โฆ Synopsis
The resonance Raman spectrum of all-trans-diphenylbutadiene in its lowest exited St state exited in resonance with the S1 + S,, absorption band at 650 nm in non-pohr solvents is reported_ Three vldrational bands at 1572,1481 and 1165 Cm-l are observed. A possible assignment of the the 1481 cm-l the lowest S, state being of "Ai-band to the C=C double-bond stretching mode may support symmetry_
๐ SIMILAR VOLUMES
The lowest cxcluzd [riplet stales or 3ll-lrans-2.4.6-oclaIrlene. alloocimene and nw-nlloocimenc have kn studled by Ilme-resolved resonance Raman spec~oscopy. The spec~n showed bands al 1574. 1264. 1252, 1205. and 1136 cm-' for oclalnene. al 1560 cm-' for allooclmene. and al 1559 cm-' for neo-alloocl
Time-resolved resonance Raman spectra were observed with the pump/probe technique using two 7 ns pulsed lasers for octaethylporphinato Cu(II) [(OEP)Cu] and its isotopomers (OEP-meso-d 4 and OEP-lSN) in the lowest excited triplet state. Raman bands were assigned on the basis of depolarization ratios
The resonance Raman spectrum of tetramethylbutadiene in its lowest excited triplet state, with a reported lifetime of 80 ns, is presented. The triplet state was produced by laser flash photolysis using acetone as sensitizer in acetonitrile.