Aqueous Ring-Opening Metathesis Polymerization of Carboximide-Functionalized 7-Oxanorbornenes

Marc A. Hillmyer, Robert H. Grubbs, Christine Lepetit, Dominic V. McGrath, Bruce M. Novak

Research output: Contribution to journalArticle

98 Scopus citations

Abstract

The ring-opening metathesis polymerization (ROMP) of exo-N-methyl-7-oxabicyclo[2.2.1]- hept-5-ene-2,3-dicarboximide (1) was accomplished in aqueous solution under mild conditions using the simple ruthenium(II) coordination complex RuII(H2O)6(tos)2 (tos = p-toluenesulfonate) (2). The polymerization yield was nearly quantitative. The resultant high molecular weight polymer (poly-1) exhibited a glass transition temperature (Tg) of 225 °C and was thermally stable up to 402 °C. The thermal and radiative stabilities of poly-1 were further investigated. Poly-1 was hydrogenated to yield its saturated analogue, which had a lower Tg (170 °C) but a higher temperature of decomposition (430 °C). Complex 2 was deactivated by coordination of free maleimides formed during the polymerization of carboximide-functionalized monomers capable of undergoing retro Diels-Alder chemistry. The scope of this polymerization was therefore limited to carboximide-functionalized monomers that are stable toward retro Diels-Alder reactions at the polymerization temperature. Both ruthenium (II)-1 and ruthenium(II)-N-methylmaleimide olefin complexes were identified.

Original languageEnglish (US)
Pages (from-to)3345-3350
Number of pages6
JournalMacromolecules
Volume25
Issue number13
DOIs
StatePublished - Jun 1 1992

ASJC Scopus subject areas

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

Fingerprint Dive into the research topics of 'Aqueous Ring-Opening Metathesis Polymerization of Carboximide-Functionalized 7-Oxanorbornenes'. Together they form a unique fingerprint.

  • Cite this