Femtosecond studies of vibrationally hot molecules produced by intramolecular proton transfer in the excited state
β Scribed by C. Chudoba; S. Lutgen; T. Jentzsch; E. Riedle; M. Woerner; T. Elsaesser
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 491 KB
- Volume
- 240
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
β¦ Synopsis
The keto-type reaction product of intramolecular proton transfer in the excited state of 2-(2'-hydroxy-5'methylphenyl)benzotriazole is investigated by femtosecond experiments in a wide spectral range. Keto-type molecules produced on a 100 fs time scale show an emission band between 600 and 800 nm that decays with a time constant of 150 fs. The strong spectral overlap of the emission with the absorption spectrum of the keto-type ground state extending from 400 to 700 nm gives evidence of non-equilibrium vibrational excitations of the product molecules. The keto-type species decays by proton back-transfer to the enol ground state with a time constant of 600 fs. Measurements with different excitation wavelengths demonstrate that the rates of this ultrafast reaction cycle are not affected by the initial amount of vibronic excess energy.
π SIMILAR VOLUMES
Sub-microsecond time-resolved infrared spectroscopy has been used to investigate the ground-state relaxation process following the excited-state proton transfer in 2-(2'-naphthyl)-3-hydroxychromone in chloroform. Two transient species with decay times of 5.3 txs (1270 and 1230-1260 cm -1) and 500-60
In this work we analyze how the choice of the active space in the Ε½ CASSCF the complete-active-space multiconfiguration self-consistent-field . Ε½ method and CASPT2 the second-order perturbation theory based on the . CASSCF reference wave function calculations affects the computed potential Ε½ . energ
In~mol~~ 2pn\* + 3dn charge transfer in the excited state of phenyl~e occurs very rapidly (<IO ps) both in ?&Fat 293 K and in EPA glass at 77 K. At room temperature a Iong;lived 425 nm transient (which is assgned to a reananged intermediate) is produced with a nse time of 30 ps, showing that the tra