Hydration and Counterion Binding of [C12MIM] Micelles

Surface-active ionic liquids based on imidazolium cations are promising targets for micellar catalysis in aqueous solution, yielding enhanced rate constants compared to surfactants based on n-alkyltrimethylammonium cations and exhibiting a pronounced counterion dependence ( Bica Chem. Commun. 2012 ,...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 33(2017), 38 vom: 26. Sept., Seite 9844-9856
1. Verfasser: Friesen, Sergej (VerfasserIn)
Weitere Verfasser: Buchecker, Thomas, Cognigni, Alice, Bica, Katharina, Buchner, Richard
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't
Beschreibung
Zusammenfassung:Surface-active ionic liquids based on imidazolium cations are promising targets for micellar catalysis in aqueous solution, yielding enhanced rate constants compared to surfactants based on n-alkyltrimethylammonium cations and exhibiting a pronounced counterion dependence ( Bica Chem. Commun. 2012 , 48 , 5013 - 5015 ; Cognigni Phys. Chem. Chem. Phys. 2016 , 18 , 13375 - 13384 ). Probably most relevant to these effects is the interplay between headgroup hydration and counterion binding. To obtain more detailed information on these effects, aqueous solutions of 1-dodecyl-3-methylimidazolium ([C12MIM]) bromide, iodide, and triflate (TfO-) were investigated at 45 °C using broadband dielectric spectroscopy, viscosity measurements, and small-angle X-ray scattering experiments. Effective hydration numbers were determined, and information on the locations and mobilities of the condensed counterions, X-, was derived. It was found that [C12MIM] halide micelles were less hydrated than the corresponding n-dodecyltrimethylammonium ([C12TA]X) aggregates. Together with their somewhat weaker counterion condensation, this difference probably explains their higher catalytic activity. Whereas [C12MIM]Br micelles remained roughly spherical in the studied concentration range, rodlike aggregates were formed at high concentrations of the iodide and, in particular, the triflate surfactants. It appears that the much lower mobility of condensed TfO- counterions is the reason for the very low catalytic activity of [C12MIM]TfO micelles
Beschreibung:Date Completed 23.07.2018
Date Revised 23.07.2018
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1520-5827
DOI:10.1021/acs.langmuir.7b02201