Issue 5, 1972

Evidence for the formation of triplet 1,3-biradicals on photolysis of cis- and trans-3,4-dimethyl-Δ1-pyrazoline

Abstract

The stereochemistry of the cis- and trans-1,2-dimethylcyclopropanes produced on photolysis of cis-and trans-3,4-dimethyl-Δ1-pyrazoline indicates that triplet biradicals are intermediates; the results also indicate that triplet biradical production becomes more important on photolysis at shorter wavelengths.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 273-274

Evidence for the formation of triplet 1,3-biradicals on photolysis of cis- and trans-3,4-dimethyl-Δ1-pyrazoline

S. D. Nowacki, P. B. Do and F. H. Dorer, J. Chem. Soc., Chem. Commun., 1972, 273 DOI: 10.1039/C39720000273

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