Abstract
A new class of low molecular mass organogelators, the fluorous derivatives of gallic acid 13, is described. The gelation properties have been examined in a large variety of organic liquids. The corresponding analogs possessing alkyl instead of semiperuluoroalkyl chains (46) do not display any gelation properties, thus revealing the key role of perfluorinated chains in the aggregationgelation process. Gels have been studied by scanning electron microscopy, revealing the presence of three-dimensional networks of nanosized fibers. In the case of an instable gel, SEM images showed that these elongated fibers curl up into nanoballs, failing to create the entangled network responsible for solvent entrapment. © 2010 Elsevier Ltd.
Original language | English |
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Pages (from-to) | 5190-5195 |
Journal | Tetrahedron |
Volume | 66 |
Issue number | 27-28 |
DOIs | |
Publication status | Published - 3 Jul 2010 |
Keywords
- Fluorous compounds
- Nanostructures
- Organogels
- Supramolecular chemistry