Issue 26, 2021

Rich-colour mechanochromism of a cyanostilbene derivative with chiral self-assembly

Abstract

Mechanochromic luminophores exhibiting rich-colour transitions among multiple states have important potential applications, but few such compounds are known. Herein, chiral self-assembly fabrication is proposed as a valid method to realize a new type of metastable state, which may bring enriched PL colours. A novel chiral fluorophore, ACNS, was synthesized and assembled into helices with specific handedness, showing a tricolour photoluminescence (PL) transition among yellow, green and blue under grinding and other stimuli. The crystalline ACNS powder (B-phase) emits bright sky-blue light. Interestingly, the luminophore assembles into helical nanofibres (Y-phase) with specific handedness, which present yellow fluorescence at 539 nm. Moreover, upon grinding, both Y-phase and B-phase powder change into green-emitting powder (G-Phase) with a PL peak at 498 nm. This strategy is conceptually simple and affords a promising approach to the development of mechanochromic luminophores with multicolour fluorescence switching.

Graphical abstract: Rich-colour mechanochromism of a cyanostilbene derivative with chiral self-assembly

Supplementary files

Article information

Article type
Paper
Submitted
29 Mar 2021
Accepted
07 Jun 2021
First published
09 Jun 2021

New J. Chem., 2021,45, 11530-11535

Rich-colour mechanochromism of a cyanostilbene derivative with chiral self-assembly

L. Wen, J. Sun, C. Li, C. Zhu, X. Zhang, Z. Wang, Q. Song, C. Lv and Y. Zhang, New J. Chem., 2021, 45, 11530 DOI: 10.1039/D1NJ01528A

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