Double Modification of Polymer End Groups through Thiolactone Chemistry

Macromol Rapid Commun. 2016 Jun;37(12):947-51. doi: 10.1002/marc.201600150. Epub 2016 May 4.

Abstract

A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of telechelic polymers is performed through amine-thiol-ene conjugation. Thiolactone end-functionalized polymers are prepared via two different methods, through controlled radical polymerization of a thiolactone-containing initiator, or by modification of available end-functionalized polymers. Next, these different linear polymers are treated with a variety of amine/acrylate-combinations in a one-pot procedure, creating a library of tailored end-functionalized polymers. End group conversions are monitored via SEC, NMR, and MALDI-TOF analysis, confirming the quantitative modification after each step. Finally, this strategy is applied for the synthesis of block copolymers via polymer-polymer conjugation and the successful outcome is analyzed via LCxSEC measurements.

Keywords: amine-thiol-ene conjugation; end group functionalities; one-pot double modification; polymer-polymer conjugation.

MeSH terms

  • Lactones / chemistry*
  • Molecular Structure
  • Polymers / chemical synthesis
  • Polymers / chemistry*
  • Sulfhydryl Compounds / chemistry*

Substances

  • Lactones
  • Polymers
  • Sulfhydryl Compounds