Login / Signup

Tuning of Morphology by Chirality in Self-Assembled Structures of Bis(Urea) Amphiphiles in Water.

Filippo TosiJosé Augusto BerrocalMarc C A StuartSander J WezenbergBen L Feringa
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
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.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • high resolution
  • mass spectrometry
  • electron microscopy
  • nk cells
  • healthcare
  • health information
  • single molecule