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Mendeleev Communications, 1999, Volume 9, Issue 5, Pages 201–203
DOI: https://doi.org/10.1070/MC1999v009n05ABEH001177
(Mi mendc4597)
 

This article is cited in 8 scientific papers (total in 8 papers)

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

L. Ya. Zakharova, R. A. Shagidullina, F. G. Valeeva, L. A. Kudryavtseva

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Full-text PDF (145 kB) Citations (8)
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.
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Document Type: Article
Language: English


Citation: L. Ya. Zakharova, R. A. Shagidullina, F. G. Valeeva, L. A. Kudryavtseva, “The influence of the structure of ethyl aryl chloromethylphosphonates on the catalytic effect of direct and reverse micellar systems”, Mendeleev Commun., 9:5 (1999), 201–203
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  • https://www.mathnet.ru/eng/mendc/v9/i5/p201
  • This publication is cited in the following 8 articles:
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