Related Experiment Video
Updated: Mar 24, 2026

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
Published on: October 31, 2019
Fastest non-ionic azo dyes and transfer of their thermal isomerisation kinetics into liquid-crystalline materials
Jaume Garcia-Amorós1, M Cidália R Castro, Paulo Coelho
1Grup de Materials Orgànics, Institut de Nanociència i Nanotecnologia (IN2UB), Departament de Química Orgànica, Universitat de Barcelona, Martí i Franqués 1, E-08028, Barcelona, Spain. dvelasco@ub.edu.
Abstract:
Push-pull bithienylpyrrole-based azo dyes exhibit thermal isomerisation rates as fast as 1.4 μs in acetonitrile at 298 K becoming, thus, the fastest neutral azo dyes reported so far. These remarkably low relaxation times can be transferred into liquid-crystalline matrices enabling light-triggered oscillations in the optical density of the final material up to 11 kHz under ambient conditions.
Related Concept Videos
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Cycloaddition Reactions: MO Requirements for Thermal Activation
Thermal and Photochemical Electrocyclic Reactions: Overview
Polymer Classification: Stereospecificity
Recrystallization: Solid–Solution Equilibria

