LASER INDUCED FLUORESCENCE OF CYCLOHEXADIENYL RADICALS
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Date
1979
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Ohio State University
Abstract
The assignment of the lowest electronic transitions of cyclohexadienyl and phenylcyclohexadienyl radicals will be presented. These radicals are prepared by the bombardment of benzene crystals with high energy electron beams. The radical product are oriented substitutionally in the solid lattice. Laser induced fluorescence of these radicals were obtained at the liquid heluim temperature. Their orgins are located at 5586 and 6571{\AA}, respectively. A brief summary of other benz-cyclohexadienyl radicals in their corresponding crystal lattice will also be presented.
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