4.7 Article

Synthesis and Degradation Behavior of Cyclic Poly(ε-caprolactone)

Journal

MACROMOLECULES
Volume 42, Issue 17, Pages 6406-6413

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma9011076

Keywords

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Funding

  1. Petroleum Research Fund
  2. American Chemical Society [47108-G7]
  3. Tulane University
  4. Louisiana Board of Regents [graduate fellowship]
  5. NSF-MRI [0619770]
  6. Tulane Institute for Macromolecular Engineering and Science [NNC06AA18A]
  7. Division Of Chemistry
  8. Direct For Mathematical & Physical Scien [0619770] Funding Source: National Science Foundation

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Narrow polydisersity cyclic poly(caprolactone) was synthesized by cyclization of linear alpha, omega-functionalized poly(caprolactone), The linear precursors were prepared via ring-opening polymerization from an azido-functionalized initiator, followed by end group modification to attach a terminal alkyne. Click coupling afforded the cyclic polymer in high yields and provided linear and cyclic poly(caprolactone) with exactly identical molecular weight distributions. The thermal and acid-catalyzed degradation of analogous linear and cyclic poly(caprolactone) samples were investigated to determine the effect of architccture.

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