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Harnessing entropy to direct the bonding/debonding of polymer systems based on reversible chemistry

Chemical Science, ISSN: 2041-6539, Vol: 4, Issue: 7, Page: 2752-2759
2013
  • 49
    Citations
  • 0
    Usage
  • 52
    Captures
  • 0
    Mentions
  • 48
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    49
    • Citation Indexes
      49
  • Captures
    52
  • Social Media
    48
    • Shares, Likes & Comments
      48
      • Facebook
        48

Article Description

The widely accepted approach for controlling polymer debonding/rebonding properties in responsive materials has been to purposefully engineer the functional end-groups responsible for monomer dynamic bonding. Here, however, we evidence that the debonding temperature of a polymer can also be tuned by changing the chain length of the polymer building blocks, thus altering the entropy released on debonding. Entropy driven debonding, as governed by building block chain length, is suggested theoretically and realized experimentally for two Diels-Alder polymer systems, each based on a different difunctional diene and a common difunctional dienophile. In each case a significant decrease (as much as 60 °C) in the retro Diels-Alder temperature was observed when the chain length of the difunctional dienophile building block was increased. These results have the potential to fundamentally change the approach utilized to design materials capable of bonding reversibly on demand. © 2013 Royal Society of Chemistry.

Bibliographic Details

Nathalie K. Guimard; Jan O. Mueller; Kim K. Oehlenschlaeger; Christopher Barner-Kowollik; Junming Ho; Ching Yeh Lin; Mansoor Namazian; Daniel G. Nocera; Michelle L. Coote; Josef Brandt; Albena Lederer; Stefan Hilf; Friedrich G. Schmidt

Royal Society of Chemistry (RSC)

Chemistry

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