Issue 15, 1972

The photoreactions of aromatic carbonyl compounds with amines. Part III. The photoreactions of fluorenone with tertiary amines

Abstract

Flash-photolysis experiments have shown that electronically excited fluorenone reacts with NN-dimethylaniline in polar solvents, to give the radical cation of the amine and the radical anion of the ketone. In benzene solution, the only radicals detected were the 9-hydroxyfluorenyl radical and the fluorenone radical anion. By the same technique, excited fluorenone was shown to react with triethylamine in both polar and non-polar solvents to give the fluorenone radical anion and the 9-hydroxyfluorenyl radical. The former radical is probably produced by dissociation of the latter radical. The photoreactions of fluorenone with amines are interpreted in terms of exciplex and radical ion intermediates.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1972, 2355-2359

The photoreactions of aromatic carbonyl compounds with amines. Part III. The photoreactions of fluorenone with tertiary amines

R. S. Davidson and M. Santhanam, J. Chem. Soc., Perkin Trans. 2, 1972, 2355 DOI: 10.1039/P29720002355

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