Data from: Facile Mechanochemical Cycloreversion of Polymer Cross-linkers Enhances Tear Resistance

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  • The mechanical properties of covalent polymer networks often arise from the permanent end-linking or cross-linking of polymer strands, and molecular linkers that break more easily would likely produce materials that require less energy to tear. We report that cyclobutane-based mechanophore cross-linkers that break via force-triggered cycloreversion lead to networks that are up to 9 times tougher than conventional analogs. The response is attributed to a combination of long, strong primary polymer strands and cross-linker scission forces that are ~ 5-fold smaller than control cross-linkers at the same timescales. The enhanced toughness comes without the hysteresis associated with noncovalent cross-linking, and it is observed in two different acrylate elastomers, in fatigue as well as constant displacement rate tension, and in a gel as well as elastomers. ... [Read More]

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Data Citation
  • Wang, S., Hu, Y., Kouznetsova, T. B., Sapir, L., Chen, D., Herzog-Arbeitman, A., Johnson, J. A., Rubinstein, M., & Craig, S. L. (2023). Data from: Facile Mechanochemical Cycloreversion of Polymer Cross-linkers Enhances Tear Resistance. Duke Research Data Repository. https://doi.org/10.7924/r43r1215n
DOI
  • 10.7924/r43r1215n
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ARK
  • ark:/87924/r43r1215n
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Funding Agency
  • NSF Center for the Chemistry of Molecularly Optimized Networks (MONET)
Grant Number
  • CHE-2116298
Title
  • Data from: Facile Mechanochemical Cycloreversion of Polymer Cross-linkers Enhances Tear Resistance
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