The Unexpected Role of Cations in the Self-Assembly of Positively Charged Amphiphiles at Liquid/Liquid Interfaces

J Phys Chem Lett. 2022 Nov 24;13(46):10889-10896. doi: 10.1021/acs.jpclett.2c02921. Epub 2022 Nov 17.

Abstract

Conventional wisdom suggests that cations play a minimal role in the assembly of cationic amphiphiles. Here, we show that at liquid/liquid (L/L) interfaces, specific cation effects can modulate the assemblies of hydrophobic tails in an oil phase despite being attached to cationic headgroups in the aqueous phase. We used oligo-dimethylsiloxane (ODMS) methyl imidazolium amphiphiles to identify these specific interactions at hexadecane/aqueous interfaces. Small cations, such as Li+, bind to the O atoms in the ODMS tail and pin it to the interface, thereby imposing a kinked conformation─as evidenced by vibrational sum frequency generation spectroscopy and molecular dynamics simulations. While larger Cs+ ions more readily partition to the interface, they do not form analogous complexes. Our data not only point to ways for controlling amphiphile structure at L/L interfaces but also suggest a means for the separation of Li+, or related applications, in soft-matter electronics.

MeSH terms

  • Cations
  • Hydrophobic and Hydrophilic Interactions
  • Molecular Dynamics Simulation*
  • Water* / chemistry

Substances

  • Cations
  • Water