Which polyesters can mimic polyethylene?

Macromol Rapid Commun. 2013 Jan 11;34(1):47-50. doi: 10.1002/marc.201200611. Epub 2012 Nov 19.

Abstract

Self-metathesis of erucic acid by [(PCy(3))(η-C-C(3)H(4)N(2)Mes(2))Cl(2)Ru = CHPh] (Grubbs second- generation catalyst) followed by catalytic hydrogenation and purification via the ester yields 1,26-hexacosanedioate (>99% purity). Polyesterification with 1,26-hexacosanediol, generated from the diester, affords polyester-26,26, which features a T(m) of 114 °C (T(c) = 92 °C, ΔH(m) = 160 J g(-1)). Ultralong-chain model polyesters-38,23 (T(m) = 109 °C) and -44,23 (T(m) = 111 °C), generated via multistep procedures including acyclic diene metathesis polymerization, underline that melting points of such aliphatic polyesters do not gradually increase with methylene sequence chain length. Available data suggest that to mimic linear polyethylenes thermal properties, even longer sequences, amounting to at least four times a fatty acid chain, fully incorporated in a linear fashion are required.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Erucic Acids / chemistry
  • Hydrogenation
  • Models, Chemical
  • Polyesters / chemical synthesis
  • Polyesters / chemistry*
  • Polyethylene / chemical synthesis
  • Polyethylene / chemistry*
  • Polymerization
  • Transition Temperature

Substances

  • Erucic Acids
  • Polyesters
  • erucic acid
  • Polyethylene