Issue 2, 1997

Reactions involving fluoride ion. Part 41.1,2 Synthesis of hexakis(trifluoromethyl)cyclopentadiene and derived cyclopentadienide salts

Abstract

An efficient synthesis of hexakis(trifluoromethyl)cyclopentadiene 4, which shows a remarkably low reduction potential, is described. Various donors promote one-electron transfer to 4, leading to corresponding salts of pentakis(trifluoromethyl)cyclopentadienide 5. A novel approach to the synthesis of metal derivatives involves heating, or photolysis, of 4 directly with metals (including Cu, Ni, Fe and Co), leading to the corresponding ionic salts. X-Ray structural analysis was difficult because of rotation of trifluoromethyl groups in these salts, but structural data on 20, 24 and 30 has been obtained that reveals interesting conformations and stacking of the ions.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 135-146

Reactions involving fluoride ion. Part 41.1,2 Synthesis of hexakis(trifluoromethyl)cyclopentadiene and derived cyclopentadienide salts

R. D. Chambers, W. K. Gray, J. F. S. Vaughan, S. R. Korn, M. Médebielle, A. S. Batsanov, C. W. Lehmann and J. A. K. Howard, J. Chem. Soc., Perkin Trans. 1, 1997, 135 DOI: 10.1039/A604087J

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