Energy Balance in the Photochemistry of Benzene
- 15 January 1967
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 46 (2), 674-680
- https://doi.org/10.1063/1.1840724
Abstract
Quantum yields of triplet‐state formation in benzene vapor have been determined at several wavelengths by the method of Cundall. From 2520 to 2668 Å, values average about 0.63 if one excludes those at a single wavelength of 2535.5 Å. At this wavelength a higher value is obtained, and its possible significance is briefly discussed. At 2420 Å the triplet‐state yield is small and may be zero. Fluorescent yields have been scanned for ranges of a few Angstrom units from 2400 to 2600 Å. Above 2520 Å there is no significant change with wavelength. The trends in these results are briefly discussed, and it is pointed out that a detailed discussion of the theory of the photochemistry of benzene has little value because data now available are not sufficient to test any theory.Keywords
This publication has 29 references indexed in Scilit:
- Conjugated Dienes as Quenchers for Excited Singlet States of Aromatic Hydrocarbons1Journal of the American Chemical Society, 1966
- The Vapor Phase Photolysis of Benzene at 1849 AJournal of the American Chemical Society, 1966
- A Photochemical 1,3 Cycloaddition of Olefins to Benzene1Journal of the American Chemical Society, 1966
- Triplet state yields for benzene and benzene-d 6 in the vapour phaseTransactions of the Faraday Society, 1966
- Absorption spectrum of triplet benzeneTransactions of the Faraday Society, 1966
- Triplet State of FluorobenzeneThe Journal of Physical Chemistry, 1965
- Photoisomerization of Tri-t-butylbenzenes. Prismane and Benzvalene Isomers1Journal of the American Chemical Society, 1965
- Phototransposition of Carbon Atoms in the Benzene Ring1Journal of the American Chemical Society, 1965
- Photoisomerization of DialkylbenzenesJournal of the American Chemical Society, 1964
- Chemistry of Dewar Benzene. 1,2,5-Tri-t-Butylbicyclo[2.2.0]Hexa-2,5-DieneJournal of the American Chemical Society, 1962