Issue 0, 1968

Unstable intermediates. Part LII. The reaction of tetracyanoethylene with dimethyl sulphoxide

Abstract

Solutions of tetracyanoethylene in dimethyl sulphoxide exhibit an e.s.r. spectrum characteristic of the tetracyanoethylene anion-radical. The presence of this species in the system is due to a chemical reaction between tetracyanoethylene and dimethyl sulphoxide and not to dissociation of the tetracyanoethylene–dimethyl sulphoxide charge-transfer complex in a thermally populated triplet state, as previously supposed.

Article information

Article type
Paper

J. Chem. Soc. A, 1968, 1134-1135

Unstable intermediates. Part LII. The reaction of tetracyanoethylene with dimethyl sulphoxide

R. N. Butler, J. Oakes and M. C. R. Symons, J. Chem. Soc. A, 1968, 1134 DOI: 10.1039/J19680001134

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