Abstract
Reversed micellar systems have borrowed extensively from the nomenclature and concepts used in aqueous detergent systems, and much of the early work on surfactant aggregates in nonpolar solvents arose from the concept of modelling the active site of proteolytic enzymes. Moreover, the readiness with which quite large concentrations of water and substrate were solubilized in the polar interior of reversed micelles led to the attractive possibility of determining reaction order with respect to water.
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O’Connor, C.J., Lomax, T.D., Ramage, R.E. (1982). Kinetic Concepts in Reversed Micellar Systems. In: Mittal, K.L., Fendler, E.J. (eds) Solution Behavior of Surfactants. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-3494-1_4
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