Degree of branching of highly branched polyurethanes synthesized via the Oligomeric A2 Plus B3 methodology

Ann R. Fornof, Thomas E. Glass, Timothy Edward Long

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

The oligomeric A2 plus monomeric B3 synthetic methodology provided highly branched, poly(ether urethane)s based on IMP (B 3) and isocyanate endcapped polyethers. 13C NMR spectroscopic assignments for the branched polyurethanes were verified using model urethane-containing compounds based on TMP and a monofunctional isocyanate (either cyclohexyl or phenyl isocyanate (PI)). Derivatization of hydroxyl endgroups with trifluoroacetic anhydride enhanced the 13C NMR resolution in spectra for branched polyurethanes. The 13C NMR resonance for the linear unit exhibited a broad shoulder due to quaternary carbons that were attributed to cyclic species in the highly branched polyurethanes. The classical DB calculation revealed the efficiency of the 83 monomer for branching; however, an equation that incorporated the linear contribution of the A2 oligomer provided a more accurate DB for highly branched polyurethanes.

Original languageEnglish
Pages (from-to)1197-1206
Number of pages10
JournalMacromolecular Chemistry and Physics
Volume207
Issue number14
DOIs
Publication statusPublished - 2006 Jul 24
Externally publishedYes

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Keywords

  • C NMR spectroscopy
  • Degree of branching
  • Highly branched
  • Hyperbranched
  • Polyurethanes

ASJC Scopus subject areas

  • Condensed Matter Physics
  • Physical and Theoretical Chemistry
  • Polymers and Plastics
  • Organic Chemistry
  • Materials Chemistry

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