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