Issue 1, 1991

Hydrolysis of toxic organophosphorus esters. The behaviour of the perborate anion

Abstract

It has been observed that in the hydrolysis of the organophosphorus esters such as paraoxon 1 and ethyl p-nitrophenylmethylphosphonate (2), by aqueous sodium or phosphonium perborate, it is not possible to obtain a complete understanding of the results obtained if the perhydroxide anion is considered to be the sole nucleophilic reagent. In this work we investigate the possibility of perborate anion participation. We propose a new kinetic expression for this kind of hydrolysis taking into account the effectiveness of the perborate anion as a reactive entity.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1991, 13-16

Hydrolysis of toxic organophosphorus esters. The behaviour of the perborate anion

H. Cristau, E. Torreilles and J. Ginieys, J. Chem. Soc., Perkin Trans. 2, 1991, 13 DOI: 10.1039/P29910000013

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