Chain-end-functionalized polyphosphazenes via a one-pot phosphine-mediated living polymerization

Macromol Rapid Commun. 2014 Jun;35(12):1135-41. doi: 10.1002/marc.201400114. Epub 2014 Apr 4.

Abstract

A simple polymerization of trichlorophosphoranimine (Cl3 P = N-SiMe3 ) mediated by functionalized triphenylphosphines is presented. In situ initiator formation and the subsequent polymerization progress are investigated by (31) P NMR spectroscopy, demonstrating a living cationic polymerization mechanism. The polymer chain lengths and molecular weights of the resulting substituted poly(organo)phosphazenes are further studied by (1) H NMR spectroscopy and size exclusion chromatography. This strategy facilitates the preparation of polyphosphazenes with controlled molecular weights and specific functional groups at the α-chain end. Such well-defined, mono-end-functionalized polymers have great potential use in bioconjugation, surface modification, and as building blocks for complex macromolecular constructs.

Keywords: cationic living polymerization; chain-end functionality; functional polymers; polyphosphazenes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, Gel
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Organophosphorus Compounds / chemical synthesis
  • Organophosphorus Compounds / chemistry*
  • Phosphines / chemistry*
  • Polymerization
  • Polymers / chemical synthesis
  • Polymers / chemistry*
  • Reference Standards

Substances

  • Organophosphorus Compounds
  • Phosphines
  • Polymers
  • poly(phosphazene)
  • phosphine