Glycomacrocycle-Based Azobenzene Derivatives as Chiral Dopants for Photoresponsive Cholesteric Liquid Crystals
Source abstract
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.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Liquid Crystal Research Advancements · Photochromic and Fluorescence Chemistry · Molecular spectroscopy and chirality
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Research Institute for Electronic Science, Hokkaido University, N-20, W-10, Kita-Ku, Sapporo 001-0020, Japan
Photophysique et Photochimie Supramoléculaires et Macromoléculaires, Institut d’Alembert, Université Paris-Saclay, ENS Paris-Saclay, CNRS, 4 Avenue des Sciences, 91190 Gif-sur-Yvette, France
Funding
Mazda Foundation · Hokkaido University · Ministry of Education, Culture, Sports, Science and Technology · Japan Society for the Promotion of Science · Network Joint Research Centre for Materials and Devices
References (52)
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