Related Experiment Video
Updated: Dec 2, 2025

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
Published on: October 31, 2019
Glycomacrocycle-Based Azobenzene Derivatives as Chiral Dopants for Photoresponsive Cholesteric Liquid Crystals
Yuna Kim1, Noushaba Nusrat Mafy1, Stéphane Maisonneuve2
1Research Institute for Electronic Science, Hokkaido University, N-20, W-10, Kita-Ku, Sapporo 001-0020, Japan.
Abstract:
We demonstrate photoresponsive cholesteric liquid crystals (CLCs) doped with glycomacrocyclic azobenzene derivatives, which exhibit large conformational changes, providing dynamic control of helical superstructures in response to a light stimulus. An unprecedented shortening of the helical pitch length and the empowerment of helical twisting power up to 500% are observed upon trans (E) to cis (Z) photoisomerization. Light-driven dynamic helix twisting and untwisting behavior affords the first example of glycomacrocyclic azobenzene-based CLCs, which can drive the mechanical movement of micro-objects. Two modes of rotation-two-directional or one-directional rotational motion (crankshaft mode)-are realized. In particular, the latter mode based on the reversible cholesteric texture transition between homogeneous stripes and focal conics leads to the accumulation of the rotation angles achieving the amplified mechanical movements.
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Prochirality
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Properties of Enantiomers and Optical Activity
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

