Issue 17, 1973

Some insertion reactions of platinum hydrido-complexes with olefins: hydrolysis of platinum–carbon σ-bonds

Abstract

The insertion of olefins into the Pt–H bond of trans-PtH(NO3)(PEt3)2 occurs via preliminary substitution of nitrate by olefin, and the intermediate trans-[PtH(C2H4)(PEt3)2]BPh4 has been isolated. Butadiene and allene give π-allylic complexes and cyclo-octa-1,5-diene and norbornadiene give enyl-systems. Whereas PhN:CH·CH:CHPh gives [PtH(PhN:CH·CH:CHPh)(PEt3)2]BPh4 with no insertion, CH2:CHCOMe gives [Pt(CH2·CH2·-COMe)(PEt3)2]BPh4, the Pt–C σ-bond of which is readily hydrolysed to give [Pt2(OH)2(PEt3)4]2+ and ethyl methyl ketone.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1973, 1848-1852

Some insertion reactions of platinum hydrido-complexes with olefins: hydrolysis of platinum–carbon σ-bonds

A. J. Deeming, B. F. G. Johnson and J. Lewis, J. Chem. Soc., Dalton Trans., 1973, 1848 DOI: 10.1039/DT9730001848

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