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Protonation Behavior and Solution Properties of Amine Oxide Surfactants Containing a Pyridyl Group
Organic Materials Research Division, Osaka Municipal Technical Research Institute, 1-6-50 Morinomiya, Joto-ku, Osaka 836-8553, Japan.
Organic Materials Research Division, Osaka Municipal Technical Research Institute, 1-6-50 Morinomiya, Joto-ku, Osaka 836-8553, Japan.
Department of Applied Chemistry, Faculty of Engineering, Osaka Institute of Technology, 5-16-1 Omiya, Asahi-ku, Osaka 535-8585, Japan.
Department of Applied Chemistry, Faculty of Engineering, Osaka Institute of Technology, 5-16-1 Omiya, Asahi-ku, Osaka 535-8585, Japan.
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2013 (English)In: Journal of Oleo Science, ISSN 1345-8957, E-ISSN 1347-3352, Vol. 62, no 3, 123-132 p.Article in journal (Refereed) Published
Abstract [en]

Hydrogen bonding between surfactant molecules plays an important role in self-assembly formation. For long alkyl chain amine oxide surfactants, the specific protonation degree dependence of some solution properties has been considered to be due to hydrogen bonding between protonated and deprotonated species. In addition to this type of hydrogen bonding, we introduced a pyridyl group into an alkylamine oxide molecule as a new hydrogen-bonding site. The pyridyl group has three different structural isomers based on the position of the substituent. An amine oxide group in pyridylamine oxides was preferentially protonated. In addition, protonation of the pyridyl group revealed a pronounced substituent position effect on the critical micelle concentration, micellar size, and solubilization of oil-soluble dye into micelles. The intermolecular or intramolecular hydrogen bond formation could be controlled by altering the substituent position.

Place, publisher, year, edition, pages
2013. Vol. 62, no 3, 123-132 p.
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Chemical Sciences
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URN: urn:nbn:se:uu:diva-196325ISI: 000315362000002OAI: oai:DiVA.org:uu-196325DiVA: diva2:609857
Available from: 2013-03-11 Created: 2013-03-07 Last updated: 2017-12-06Bibliographically approved

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Karlsson, Göran

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