Issue 0, 1979

Stable carbocations. Part 18. Hydride-transfer reactions of [(η5-cyclohexadienyl)(η5-cyclopentadienyl)iron]alkylium ions

Abstract

In solution in CF3CO2H, (η5-cyclohexadienyl)(η5-cyclopentadienyl)iron derivatives containing a C(OH)R1R2 substituent attached either to the cyclopentadienyl ring or to C(1) of the cyclohexadienyl ring are converted into (η6-arene)(η5-cyclopentadienyl)iron cations by hydroxy loss and hydride transfer. The mechanism of the reaction has been investigated using deuterium-labelled substrates.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 1879-1884

Stable carbocations. Part 18. Hydride-transfer reactions of [(η5-cyclohexadienyl)(η5-cyclopentadienyl)iron]alkylium ions

M. M. Khan and W. E. Watts, J. Chem. Soc., Perkin Trans. 1, 1979, 1879 DOI: 10.1039/P19790001879

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