| Literature DB >> 32785999 |
Filippo Tosi1, José Augusto Berrocal1, Marc C A Stuart1,2, Sander J Wezenberg1,3, Ben L Feringa1.
Abstract
We present the synthesis and self-assembly of a chiral bis(urea) amphiphile and show that chirality offers a remarkable level of control towards different morphologies. Upon self-assembly in water, the molecular-scale chiral information is translated to the mesoscopic level. Both enantiomers of the amphiphile self-assemble into chiral twisted ribbons with opposite handedness, as supported by Cryo-TEM and circular dichroism (CD) measurements. The system presents thermo-responsive aggregation behavior and combined transmittance measurements, temperature-dependent UV, CD, TEM, and micro-differential scanning calorimetry (DSC) show that a ribbon-to-vesicles transition occurs upon heating. Remarkably, chirality allows easy control of morphology as the self-assembly into distinct aggregates can be tuned by varying the enantiomeric excess of the amphiphile, giving access to flat sheets, helical ribbons, and twisted ribbons.Entities:
Keywords: amphiphiles; bis(urea); chirality; ribbons; self-assembly
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Year: 2020 PMID: 32785999 PMCID: PMC7839493 DOI: 10.1002/chem.202003403
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236