Issue 20, 1976

Chemical evidence of a triplet mechanism in the photoisomerization of nitrostibenes. Formation of singlet oxygen from triplet states of nitrostilbenes

Abstract

In the presence of oxygen several photoexcited (λ > 300 nm)trans-4-nitrostilbenes give rise to the formation of singlet excited oxygen whereas trans-stilbenes substituted other groups as well as unsubstituted trans-stilbene do not.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 824-825

Chemical evidence of a triplet mechanism in the photoisomerization of nitrostibenes. Formation of singlet oxygen from triplet states of nitrostilbenes

H. J. Kuhn, R. Straatmann and D. Schulte-Frohlinde, J. Chem. Soc., Chem. Commun., 1976, 824 DOI: 10.1039/C39760000824

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