Synthesis and Properties of Aromatic CompoundsLiquid Crystal Research AdvancementsMolecular spectroscopy and chirality

Honoka Akiyama, Kosuke Kaneko, S. Naya, Yoshitane Imai

2026.1.1Asian Journal of Organic Chemistry

DOI: 10.1002/ajoc.70303

Abstract

Chiral liquid crystal (LC) materials are indispensable functional components of advanced optoelectronic devices. In this study, we fabricated chiral nematic liquid crystal (N*‐LC) devices by introducing perylene and its N,N ‐di‐ n ‐octyl‐3,4,9,10‐perylenetetracarboxylic diimide (OPDI) derivative, as achiral luminophores, into an N*‐LC host composed of the achiral 4'‐pentyl‐4‐cyanobiphenyl (5CB) LC and the planar‐chiral 4,12‐dihydroxy[2.2]paracyclophane ([2.2]‐PCP) dopant. Remarkably, both perylene and OPDI exhibited pronounced circularly polarized luminescence (CPL) within the planar‐chiral‐dopant‐induced N*‐LC environment, despite the use of achiral luminophores. Furthermore, the handedness of the CPL can be controlled by the planar chirality of the [2.2]‐PCP dopant. In addition, the resulting N*‐LC materials exhibited rapid and reversible inversion of CPL handedness when a direct‐current (DC) electric field was applied and then removed. This reversible behavior is ascribable to the electric‐field‐induced phase transition between the helical N*‐LC structure of 5CB and another ordered phase. These findings provide a new material design principle in which a planar‐chiral dopant induces the N*‐LC phase in 5CB, thereby enabling high‐speed, reversible CPL modulation based on the application of an electric field.

Citation format

AKIYAMA, Honoka, et al. Fast and reversible circularly polarized luminescence switching in planar chirality‐induced chiral nematic liquid crystals in a DC electric field. Asian Journal of Organic Chemistry, 2026, 15(1).