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Self-Stabilized Giant Aggregates in Water from Room-Temperature Ionic Liquids with an Asymmetric Polar-Apolar-Polar Architecture.

Geping ZhangHongxia ZhuJingfei ChenMengjun ChenTomasz KalwarczykRobert HołystHongguang LiJingcheng Hao
Published in: The journal of physical chemistry. B (2020)
We report the assembly of four imidazolium bromides, each of which bears a naphthyl on one side of the imidazolium cation and a branched alkyl chain on the other. This design creates a new type of amphiphilic ionic liquid with an apolar-polar-apolar structure and a low melting point (mp, <-20 °C), which has not been achieved by reported counterparts bearing linear alkyl chains. In solvent-free states, microphase segregation occurs where polar and apolar domains arrange bicontinuously as proved by molecular dynamics (MD) simulations. When dispersed in water, self-stabilized giant aggregates formed with ultrahigh colloidal stability (up to years). MD simulations provide clues of discrete bicontinuous phases within the giant aggregates. These newly discovered self-assemblies provide a heterogeneous reservoir that can accommodate guest molecules including the highly apolar fullerene C60, paving the way for a wide range of potential applications.
Keyphrases
  • ionic liquid
  • molecular dynamics
  • room temperature
  • density functional theory
  • high resolution
  • rare case
  • risk assessment
  • mass spectrometry
  • solid state