4.7 Article

Imine-Based Reactive Mesogen and Its Corresponding Exchangeable Liquid Crystal Elastomer

Journal

MACROMOLECULES
Volume 55, Issue 3, Pages 821-830

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.1c02432

Keywords

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Funding

  1. European Research Council [786659]
  2. European Research Council (ERC) [786659] Funding Source: European Research Council (ERC)

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Researchers have developed a fast synthesis route to produce a new type of reactive mesogen that enables a fast and stable bond-exchange reaction in exchangeable liquid crystalline elastomers (xLCEs). This new xLCE exhibits vitrimer plastic-flow behavior, thermal stability, and the ability to reprogram and realign the mesogen orientation.
To date, exchangeable liquid crystalline elastomers (xLCEs) have been mainly fabricated by combining conventional LCEs with additional exchangeable functional groups in their networks. While conventional LCEs are frequently made from commercially available aromatic-ester reacting mesogens or from mesogens based on a biphenyl core, such reacting monomers are not optimized to fabricating xLCEs whose bond-exchange reaction is fast and clean cut. Here, we develop a fast synthesis route to produce a new type of reactive mesogen based on an aromatic-imine structure that intrinsically enables a fast and stable bond-exchange reaction in the resulting imine-based xLCE. This new xLCE displays vitrimer plastic-flow behavior, and its bond-exchange activation energy is calculated to be 54 kJ/mol. We also demonstrate that this xLCE is thermally stable to withstand many recycling cycles without visible decay, and its liquid crystallinity is preserved. Finally, we demonstrate the reprogramming and realignment of the mesogen orientation in this xLCE with the realigned xLCE capable of reversible thermal actuation.

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