Issue 12, 1978

Redox-photosensitised cleavage of indene dimers using aromatic hydrocarbon–dicyanobenzene systems; catalysis by the cation radical of aromatic hydrocarbons

Abstract

Selective photoexcitation of phenanthrene in the phenanthrene–dicyanobenzene–indene dimer–acetonitrile system resulted in the cleavage of indene dimer to give indene in a limiting quantum yield of 8·2; a mechanism is suggested involving catalysis by the cation radical of phenanthrene.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 490-491

Redox-photosensitised cleavage of indene dimers using aromatic hydrocarbon–dicyanobenzene systems; catalysis by the cation radical of aromatic hydrocarbons

T. Majima, C. Pac, A. Nakasone and H. Sakurai, J. Chem. Soc., Chem. Commun., 1978, 490 DOI: 10.1039/C39780000490

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