Issue 0, 1966

Polyhalogenoallenes. Part IV. Thermal co-dimerisation of tetrafluoroallene with hexafluorobut-2-yne

Abstract

Reaction of tetrafluoroallene with hexafluorobut-2-yne at 80—85° under autogenous pressure in the presence of free-radical scavengers yields, as major product, perfluoro-(1,2-dimethyl-3-methylenecyclobutene), the 19F nuclear magnetic resonance spectrum of which is discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1966, 2051-2052

Polyhalogenoallenes. Part IV. Thermal co-dimerisation of tetrafluoroallene with hexafluorobut-2-yne

R. E. Banks, W. R. Deem, R. N. Haszeldine and D. R. Taylor, J. Chem. Soc. C, 1966, 2051 DOI: 10.1039/J39660002051

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