Issue 5, 1999

The influence of the structure of ethyl aryl chloromethylphosphonates on the catalytic effect of direct and reverse micellar systems

Abstract

The reactivity of ethyl aryl chloromethylphosphonates in the basic hydrolysis reactions in direct micelles of cetyltrimethylammonium bromide depends on both electronic and hydrophobic properties of the substituent in the aryl group, while in the sodium dodecyl sulfate–hexanol–water micellar system it depends only on the electronic nature.

Article information

Article type
Paper

Mendeleev Commun., 1999,9, 201-203

The influence of the structure of ethyl aryl chloromethylphosphonates on the catalytic effect of direct and reverse micellar systems

L. Y. Zakharova, R. A. Shagidullina, F. G. Valeeva and L. A. Kudryavtseva, Mendeleev Commun., 1999, 9, 201 DOI: 10.1070/MC1999v009n05ABEH001177

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