Polyethylene Containing Triblock Copolymers Synthesized by Post-polymerization Functionalization

Tianwei Yan, Damien Guironnet

Research output: Contribution to journalArticlepeer-review

Abstract

We report the synthesis of amphiphilic triblock copolymers containing a polyethylene block as the center block. The synthetic methodology consists of performing four consecutive post-polymerization reactions on polyethylene to yield a dihydroxyl-terminated polymer. First, a cross-metathesis reaction converts the olefinic end-group of the polyethylene into an α,β-unsaturated ester followed by isomerization of the double bond and then its hydroformylation. This sequence introduces an aldehyde group randomly distributed along the polymer backbone. Finally, the reduction of the aldehyde- and ester-functionalized polymer yields two terminal hydroxyl groups. The methodology was first established using low-molecular-weight model substrates before being performed on a polyethylene with a molecular weight of Mn = 13 kg mol-1. The functionalized polyethylene was used to initiate the ring-opening polymerizations of ϵ-caprolactone and tert-butyl glycidyl ether to yield the corresponding triblock copolymers. Subsequent hydrolysis of the tert-butyl groups in the polyether yielded an amphiphilic polymer that formed micelles in water.

Original languageEnglish (US)
Pages (from-to)4338-4344
Number of pages7
JournalMacromolecules
Volume53
Issue number11
DOIs
StatePublished - Jun 9 2020

ASJC Scopus subject areas

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

Fingerprint Dive into the research topics of 'Polyethylene Containing Triblock Copolymers Synthesized by Post-polymerization Functionalization'. Together they form a unique fingerprint.

Cite this