Hierarchical self-assembly of two-length-scale multiblock copolymers

J Phys Condens Matter. 2011 Jul 20;23(28):284110. doi: 10.1088/0953-8984/23/28/284110. Epub 2011 Jun 27.

Abstract

The self-assembly in diblock copolymer-based supramolecules, obtained by hydrogen bonding short side chains to one of the blocks, as well as in two-length-scale linear terpolymers results in hierarchical structure formation. The orientation of the different domains, e.g. layers in the case of a lamellar-in-lamellar structure, is determined by the molecular architecture, graft-like versus linear, and the relative magnitude of the interactions involved. In both cases parallel and perpendicular arrangements have been observed. The comb-shaped supramolecules approach is ideally suited for the preparation of nanoporous structures. A bicontinuous morphology with the supramolecular comb block forming the channels was finally achieved by extending the original approach to suitable triblock copolymer-based supramolecules.

MeSH terms

  • Hydrogen Bonding
  • Micelles
  • Molecular Conformation
  • Molecular Structure
  • Polymers / chemical synthesis*
  • Polymers / chemistry*

Substances

  • Micelles
  • Polymers