Issue 42, 2024

Flexible organic crystals with multi-stimuli-responsive CPL for broadband multicolor optical waveguides

Abstract

Flexible organic crystals, capable of transmitting light and responding to various external stimuli, are emerging as a new frontier in optoelectronic materials. They hold immense potential for applications in molecular machines, sensors, displays, and intelligent devices. Here, we report on flexible organic crystals based on single-component enantiomeric organic compounds, demonstrating multi-stimuli-responsive circularly polarized light (CPL). These crystals exhibit remarkable elasticity, responsiveness to light and acid vapors, and tunable circularly polarized optical signals. Upon exposure to acid vapors, the fluorescence of the crystals shifts from initial yellow emission to green emission, attributable to the protonation-induced inhibition of excited-state intramolecular proton transfer. Under UV irradiation, the fluorescence emission undergoes a red-shift, resulting from the molecular transformation from an enol configuration to a ketone configuration. Notably, both processes are reversible and can be restored under daylight. The integration of reversible fluorescence changes under light and acid vapors stimuli, CPL signals, and flexible optical waveguides within a single crystal paves the way for the application of organic crystals as all-organic chiral functional materials.

Graphical abstract: Flexible organic crystals with multi-stimuli-responsive CPL for broadband multicolor optical waveguides

Supplementary files

Article information

Article type
Edge Article
Submitted
27 Jul 2024
Accepted
26 Sep 2024
First published
27 Sep 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2024,15, 17444-17452

Flexible organic crystals with multi-stimuli-responsive CPL for broadband multicolor optical waveguides

X. Pan, L. Lan and H. Zhang, Chem. Sci., 2024, 15, 17444 DOI: 10.1039/D4SC05005C

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