1997
DOI: 10.1007/s003960050063
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A proton NMR study on aggregation of cationic surfactants in water: effects of the structure of the headgroup

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Cited by 55 publications
(51 citation statements)
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“…This is perhaps the reason that CDBACl is adsorbed on mercury and forms the condensed film in region A, while this is not possible for CTAB. NMR results have indicated that the benzyl group of CDBACl lies more or less parallel to the interface [43]. It is remarkable that the condensed film in the potential region A is formed in substances that have the benzene ring in their molecules.…”
Section: Discussionmentioning
confidence: 98%
“…This is perhaps the reason that CDBACl is adsorbed on mercury and forms the condensed film in region A, while this is not possible for CTAB. NMR results have indicated that the benzyl group of CDBACl lies more or less parallel to the interface [43]. It is remarkable that the condensed film in the potential region A is formed in substances that have the benzene ring in their molecules.…”
Section: Discussionmentioning
confidence: 98%
“…The "medium effect" results from the substitution of a sizable part of the hydrocarbon/water contact in the monomer by hydrocarbon/hydrocarbon contact in the aggregate, and the "conformation effect" results from a change in conformation of the alkyl chain. The two effects generally lead to a downfield shift of the 1 H NMR peaks of the aggregated surfactant [72][73][74][75][76].…”
Section: Isotropic L1 Phasementioning
confidence: 98%
“…Considering that these two surfactant classes differ only in headgroup architecture, the changes in Acmc can be ascribed to the effect of adding an extra -CH2 -to the surfactant hydrophilic part. Because of the presence of the -CH2 -spacer in the surfactant headgroup, the glutarate surfactants have slightly larger headgroups [48].…”
Section: Limiting Surface Tension One Important Function Of the Surfmentioning
confidence: 99%