190
Views
18
CrossRef citations to date
0
Altmetric
Original Articles

FUNCTIONAL TELECHELIC POLYMER SYNTHESIS VIA ADMET POLYMERIZATION

&
Pages 745-758 | Published online: 07 Feb 2007
 

ABSTRACT

Acyclic Diene METathesis (ADMET) polymerization of 1,9-decadiene with epoxy-containing monoolefins using ruthenium based Grubbs' catalyst gave epoxy terminated telechelic polymers. The number of methylene spacers between the olefin and the epoxy from the oxygen side of the epoxy-containing monoolefins was varied from one to three. The optimal condition for the present ADMET polymerization was determined as monomer/catalyst ratio of 200/1 for 96 hr at 90°C. All polymer structures were characterized by FT-IR and 1H NMR spectroscopy. It is quite interesting that even 1,2-epoxy-4-pentene with one methylene spacer metathesizes successfully using ruthenium catalyst despite this monoolefin suffers a stronger negative neighboring group effect than the other monoolefins. The telechelic polymer was reacted with toluene diisocyanate to give a higher molecular weight segmented copolymer connected with oxazolidone linkage.

ACKNOWLEDGMENTS

We acknowledge to Dr. K. B. Wagener for his helpful discussions and suggestions. A part of this research was financially supported by the Kansai University Special Research Fund, 1999.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 1,060.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.