Molecular Motion of the Junction Points in Model Networks Prepared by Acyclic Triene Metathesis

Macromol Rapid Commun. 2016 Mar;37(6):527-31. doi: 10.1002/marc.201500642. Epub 2016 Jan 20.

Abstract

The junction dynamics in a selectively deuterated model polymer network containing junctions on every 21st chain carbon is studied by solid state (2) H echo NMR. Polymer networks are prepared via acyclic triene metathesis of deuteron-labeled symmetric trienes with deuteron probes precisely placed at the alpha carbon relative to the junction point. The effect of decreasing the cross-link density on the junction dynamics is studied by introduction of polybutadiene chains in-between junctions. The networks are characterized by swelling, gel content, and solid state (1) H MAS NMR. Line shape analysis of the (2) H quadrupolar echo spectra reveals that the degree of motion anisotropy and the distribution of motion correlation times depend on the cross-link density and structural heterogeneity of the polymer networks. A detailed model of the junction dynamics at different temperatures is proposed and explained in terms of the intermolecular cooperativity in densely-packed systems.

Keywords: NMR; cross-linking; dynamics; metathesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Anisotropy
  • Butadienes / chemistry*
  • Deuterium / chemistry*
  • Elastomers / chemistry*
  • Magnetic Resonance Spectroscopy
  • Models, Chemical*
  • Molecular Structure
  • Motion
  • Temperature

Substances

  • Butadienes
  • Elastomers
  • polybutadiene
  • Deuterium