Issue 5, 1979

Photocyclisation of 1,3-diphenyl-5-(2′-halogenophenyl)pyrazoles: a mechanism of homolytic carbon–halogen bond fission assisted by radical complexation

Abstract

Photocyclisation of 1,3-diphenyl-5-(2′-halogenophenyl)pyrazoles proceeds in high quantum yield from the S0v state followed by homolytic cleavage of the carbon–halogen bond assisted by intramolecular radical complexation whereas that of 1,3-diphenyl-5-(2′-methoxyphenyl)pyrazole proceeds by a different and low quantum yield pathway.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 193-194

Photocyclisation of 1,3-diphenyl-5-(2′-halogenophenyl)pyrazoles: a mechanism of homolytic carbon–halogen bond fission assisted by radical complexation

J. Grimshaw and A. P. de Silva, J. Chem. Soc., Chem. Commun., 1979, 193 DOI: 10.1039/C39790000193

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements