4.7 Article

Photo-mediated copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions for forming polymer networks as shape memory materials

Journal

POLYMER
Volume 55, Issue 23, Pages 5880-5884

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2014.08.001

Keywords

Shape memory polymers; Click chemistry; Azide

Funding

  1. National Science Foundation (NSF) [DMR 1310528]
  2. National Institute of Health (NIH) [U01 DE023774]
  3. National Science Foundation Graduate Research Fellowship (NSF GRFP)
  4. Department of Education Graduate Assistance in the Areas of National Need (GAANN)
  5. Direct For Mathematical & Physical Scien
  6. Division Of Materials Research [1310528] Funding Source: National Science Foundation

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The formation of polymer networks polymerized with the Copper (I) - catalyzed azide - alkyne cycloaddition (CuAAC) click reaction is described along with their accompanying utilization as shape memory polymers. Due to the click nature of the reaction and the synthetic accessibility of azide and alkyne functional-monomers, the polymer architecture was readily controlled through monomer design to manipulate crosslink density, ability for further functionalization, and the glass transition temperature (55-114 degrees C). Free strain recovery is used to quantify the shape memory properties of a model CuAAC network resulting in excellent shape fixity and recovery of 99%. The step growth nature of this polymerization results in homogenous network formation with narrow glass transitions ranges having half widths of the transition close to 15 degrees C for these materials resulting in shape recovery sharpness of 3.9%/degrees C in a model system comparable to similarly crosslinked chain growth polymers. Utilization of the CuAAC reaction to form shape memory materials opens a range of possibilities and behaviors that are not readily achieved in other shape memory materials such as (meth) acrylates, thiol-ene, thiol-Michael, and poly(caprolactone) based shape memory materials. (C) 2014 Elsevier Ltd. All rights reserved.

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