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

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.