Abstract
Quasi-block copolymers (q-BCPs) are block copolymers consisting of conventional and supramolecular blocks, in which the conventional block is end-terminated by a functionality that interacts with the supramolecular monomer (a “chain stopper” functionality). A new design of q-BCPs based on a general polymeric chain stopper, which consists of polystyrene end-terminated with a sulfonate group (PS-SO3Li), is described. Through viscosity measurements and a detailed diffusion-ordered NMR spectroscopy study, it is shown that PS-SO3Li can effectively cap two types of model supramolecular monomers to form q-BCPs in solution. Furthermore, differential scanning calorimetry data and structural characterization of thin films by scanning force microscopy suggests the existence of the q-BCP architecture in the melt. The new design considerably simplifies the synthesis of polymeric chain stoppers; thus promoting the utilization of q-BCPs as smart, nanostructured materials.
| Original language | English |
|---|---|
| Pages (from-to) | 10203-10210 |
| Number of pages | 8 |
| Journal | Chemistry - A European Journal |
| Volume | 22 |
| Issue number | 29 |
| DOIs | |
| State | Published - 11 Jul 2016 |
Bibliographical note
Publisher Copyright:© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Keywords
- block copolymers
- diffusion-ordered NMR spectroscopy
- self-assembly
- supramolecular chemistry
- supramolecular polymers