journal article·2020-11-18Open access

Glycomacrocycle-Based Azobenzene Derivatives as Chiral Dopants for Photoresponsive Cholesteric Liquid Crystals

Yuna Kim, Noushaba Nusrat Mafy, Stéphane Maisonneuve, Chaoqi Lin, Nobuyuki Tamaoki, Juan Xie

ACS Applied Materials & Interfaces· Volume 12· Issue 46

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.
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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

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