Journal Article10.1021/AR50023A002
Kinetics of organic reactions in micellar systems
Eugene H. Cordes,R. Bruce Dunlap +1 more
204
About: This article is published in Accounts of Chemical Research. The article was published on 01 Nov 1969. The article focuses on the topics: Organic reaction & Kinetics.
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Citations
Physicochemical Foundations of Micellar Catalysis
TL;DR: The structure and properties of micelles of surface-active substances in aqueous solution are briefly surveyed in this paper, with a focus on solubilisation and methods for investigating the location of solubiliised molecules.
409
Aggregation of sensitizing dyes in solution and their adsorption onto silver halides
TL;DR: In this article, the formation of dye dimers and higher aggregates in solution as a function of dye structure and environmental variables are considered, together with silver halide composition and crystal habit.
352
Physicochemical Foundations of Micellar Catalysis
I. Berezin,K. Martinek,A. K. Yatsimirskii +2 more
- 31 Oct 1973
TL;DR: Micellar catalysis kinetics and the structure-solubility relationship of micelles are examined. The solubilization and location of molecules in micelles are discussed. The impact of various factors on micellar catalysis is analyzed.
325
Interactions and reactions in reversed micellar systems
TL;DR: The behavior of surfactants in nonpolar solvents, the consequences of substrate and water solubilization, and the observed rate effects in reversed micelles are summarized in this article.
231
References
Crystallographic Studies of the Activity of Hen Egg-White Lysozyme
TL;DR: The chemical evidence for the enzymic activity of lysozyme will be discussed in detail by other speakers at this meeting, but in order to describe the crystallographic studies of the interactions between the enzyme and its substrates it is necessary to summarize briefly what was known about them at the beginning of the work.
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Synthesis and properties of pentaamminepyridineruthenium(II) and related pentaammineruthenium complexes of aromatic nitrogen heterocycles
TL;DR: Ford and Taube as discussed by the authors showed that the pentaammineruthenium(I1) complex of each of these heterocyclic ligands has an intense absorption band in the visible region which, on the basis of evidence presented below, is assigned to a metal-to-ligand charge transfer transition.