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Halogen-bonded shape memory polymers

Author

Listed:
  • Hongshuang Guo

    (Tampere University)

  • Rakesh Puttreddy

    (Tampere University)

  • Turkka Salminen

    (Tampere University)

  • Alons Lends

    (Latvian Institute of Organic Synthesis)

  • Kristaps Jaudzems

    (Latvian Institute of Organic Synthesis)

  • Hao Zeng

    (Tampere University)

  • Arri Priimagi

    (Tampere University)

Abstract

Halogen bonding (XB), a non-covalent interaction between an electron-deficient halogen atom and a Lewis base, is widely adopted in organic synthesis and supramolecular crystal engineering. However, the roadmap towards materials applications is hindered by the challenges in harnessing this relatively weak intermolecular interaction to devise human-commanded stimuli-responsive soft materials. Here, we report a liquid crystalline network comprising permanent covalent crosslinks and dynamic halogen bond crosslinks, which possess reversible thermo-responsive shape memory behaviour. Our findings suggest that I···N halogen bond, a paradigmatic motif in crystal engineering studies, enables temporary shape fixation at room temperature and subsequent shape recovery in response to human body temperature. We demonstrate versatile shape programming of the halogen-bonded polymer networks through human-hand operation and propose a micro-robotic injection model for complex 1D to 3D shape morphing in aqueous media at 37 °C. Through systematic structure-property-performance studies, we show the necessity of the I···N crosslinks in driving the shape memory effect. The halogen-bonded shape memory polymers expand the toolbox for the preparation of smart supramolecular constructs with tailored mechanical properties and thermoresponsive behaviour, for the needs of, e.g., future medical devices.

Suggested Citation

  • Hongshuang Guo & Rakesh Puttreddy & Turkka Salminen & Alons Lends & Kristaps Jaudzems & Hao Zeng & Arri Priimagi, 2022. "Halogen-bonded shape memory polymers," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34962-7
    DOI: 10.1038/s41467-022-34962-7
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    References listed on IDEAS

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    1. Alexander S. Mikherdov & Alexander S. Novikov & Vadim P. Boyarskiy & Vadim Yu. Kukushkin, 2020. "The halogen bond with isocyano carbon reduces isocyanide odor," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
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