Sulfonated surface patches of poly(styrene)-based colloidal particles (CPs) were functionalized with cucurbituril (CB). The macrocycles served as recognition units for diphenyl viologen (DPV2+), a rigid bridging ligand. The addition of DPV2+ to aqueous suspensions of the particles triggered the self-assembly of short linear and branched chainlike structures. The self-assembly mechanism is based on hydrophobic/ion-charge interactions that are established between DPV2+ and surface-adsorbed CB. DPV2+ guides the self-assembly of the CPs by forming a ternary DPV2+(CB)2 complex in which the two CB macrocycles are attached to two different particles. Viologen-driven particle assembly was found to be both directional and reversible. Whereas sodium chloride triggers irreversible particle disassembly, the one-electron reduction of DPV2+ with sodium dithionite causes disassembly that can be reversed via air oxidation. Thus, this bottom-up synthetic supramolecular approach allowed for the reversible formation and directional alignment of a 2D colloidal material.
|Original language||English (US)|
|Number of pages||7|
|State||Published - Jul 19 2016|
ASJC Scopus subject areas
- Materials Science(all)
- Condensed Matter Physics
- Surfaces and Interfaces