Journal of the American Chemical Society · 2005 · 30 citations · 18 references
Natural SciencesChemistryMaterials ScienceBiomaterialsMolecular RecognitionSupramolecular ChemistryMacromolecular AssemblySelf-assemblySelf-assembly Of NanomaterialsSupramolecular RecognitionSurface Functionalization Of NanomaterialsSurfactantsHydrogen BondingHydrogen Bonding InteractionsMolecular AggregationMolecular Recognition ElementsMolecular Recognition MaterialsMolecular Recognition MotifsMolecular Self-assemblySurfactant Self-assembly
Here we present a surfactant molecule (1) containing an ammonium headgroup, in which a bis-ureido group is incorporated in its hydrocarbon chain. Due to strong hydrogen bonding interactions, 1 forms well-defined highly ordered ribbon-like aggregates in water. Moreover, we demonstrate that these ribbons can be functionalized via a modular approach through molecular recognition of other bis-urea containing molecules. The dye disperse orange and biotin were coupled to matching bis-ureido groups and incorporated into the ribbon structure. The anchoring of different functionalities in a modular approach proved to be possible using the molecular recognition capabilities of the bis-ureido moiety, thereby opening possibilities to a wide range of applications.
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Atomic and Molecular Manipulation with the Scanning Tunneling Microscope
Joseph A. Stroscio, D. M. Eigler · Science · 1991 · 1.1K citations
Cyclic Bis-Urea Compounds as Gelators for Organic Solvents
Jan H. van Esch, Franck S. Schoonbeek, Maaike de Loos et al. · Chemistry - A European Journal · 1999 · 341 citations · Full text