Liquid
crystal elastomers (LCEs) are excellent polymer
materials
for a wide range of applications, including soft actuators and shape
memory materials. At present, some dynamic covalent bonds (DCBs) have
been introduced into LCEs to achieve reprogrammability. However, the
contradiction between reprogrammability and stable actuation performance
is still a challenge. One of the solutions is to introduce photoactivated
DCBs into thermotropic LCEs to maintain their thermal adaptability.
Therefore, it is meaningful to find a DCB with thermal stability and
mild photoresponse for application in thermotropic LCEs. Herein, we
adopt dynamic chemistry of allyl selenide, which not only achieves
the separation of network reconfiguration conditions (light) from
LC phase transition conditions (heat) but also achieves multiple network
reconfiguration of LCEs under visible light conditions (405–450
nm). This dynamic covalent chemistry with mild stimulation conditions
and sustainable dynamic exchange capability offers great possibilities
for the application and design of covalently adaptable LCEs.