Stereochemical effect revealed in self-assemblies based on archaeal lipid analogues bearing a central five-membered carbocycle : a SAXS study

The relative stereochemistry (cis or trans) of a 1,3-disubstituted cyclopentane unit in the middle of tetraether archaeal bipolar lipid analogues was found to have a dramatic influence on their supramolecular self-assembly properties. SAXS studies of two synthetic diastereomeric archaeal lipids bear...

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Publié dans:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 28(2012), 20 vom: 22. Mai, Seite 7591-7
Auteur principal: Jacquemet, Alicia (Auteur)
Autres auteurs: Mériadec, Cristelle, Lemiègre, Loïc, Artzner, Franck, Benvegnu, Thierry
Format: Article en ligne
Langue:English
Publié: 2012
Accès à la collection:Langmuir : the ACS journal of surfaces and colloids
Sujets:Journal Article Research Support, Non-U.S. Gov't Cyclopentanes Lipids