The lifetime of excited diphenyl ketyl radicals is lengthened by deuterium substitution. The largest effect is obyrved by substitution at the hydroxyllc positioni for example, the lifetimes are 3.9, 4.2, 8.7 and 10.5 ns for (C6H5)2COH, (C&)#OH, (C6Hs)2COD and (C&)2COD, respectively, in toluene or to
The laser versus the lamp: Reactivity of the diphenyl ketyl radical in the ground and excited states
β Scribed by H. Baumann; C. Merckel; H.-J. Timpe; A. Graness; J. Kleinschmidt; I.R. Gould; N.J. Turro
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 442 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The diphenyl ketyl radical which is formed upon photolysis of a-phenyl benzoin is produced in its excited state upon intense pulsed laser irradiation. Using the techniques of time-resolved absorption and emission spectroscopy, reaction rate constants for the ground and excited states of this radical were obtained. For the radical quenchers employed, the excited state reactivity is found to be typically several orders of magnitude greater than that of the sound state. It is concluded that the excited state of diphenyl ketyl radical reacts predominantly by electron transfer processes.
π SIMILAR VOLUMES
## Lehn-tuhl ftir lleoreridle Chemie der Oiliversitiit Sorm.
Ab initio SCF c&zulations using the generalized coupling operator method have been p&formed OR the ground and two excited states of methyl radical. Geometries of the ground and one excited state have been optimized. Vertical transition energies have also been calculated.