Abstract
This work consisted of finalizing simple strategies of synthesis to obtain new double-chain perfluoroalkylated amphiphiles having a modular structure and in studying their ability to form membrane bilayers as a function of their molecular structure. The synthesis of F-alkylated isocyanates and the corresponding F-alkylated ureas are described. Amphiphiles are prepared by quaternization of F-alkylated ureas by 1-bromoalkanes and 2-(F-hexyl) ethylbromoacetamide and sonicated in water. The sonicated solutions are viewed by freeze fracture electron micrography.
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© 1999 Springer-Verlag
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Szönyi, S., Jouani, M.A., Cambon, A. (1999). Bilayer formation in water from new urea-based double-chain dimethylammonium amphiphiles containing perfluorinated moieties. In: Težak, D., Martinis, M. (eds) Trends in Colloid and Interface Science XIII. Progress in Colloid and Polymer Science, vol 112. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-48953-3_13
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DOI: https://doi.org/10.1007/3-540-48953-3_13
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