Fluoride binding modulated supramolecular chirality of urea-containing triarylamine and photo manifestation

Abstract

In recent years, the regulation of anion-mediated chiral assembly has gained significant interest. This study investigated the modulation of supramolecular chiroptical signals and chiral assembled structures in triarylamine system containing urea moiety through fluoride ion-urea bond interactions, aiming to understand the chiral sense amplification in the supramolecular assemblies. Chiral triarylamine derivatives containing urea or amide units were synthesized and the self-assembly were examined in the absence and presence of fluoride ion. The results revealed that the addition of F- led to an increase in the circular dichroism (CD) intensity for the triarylamine compounds containing urea, accompanied by a transformation of the nanofiber structure into chiral twists. Comparative studies with other anions confirmed the selective specificity for F-. Additionally, the combination of photo-induced triarylamine cation radicals allowed the F- in the system to be visualized through photoirradiation, resulting in distinct colour changes that were detectable by the naked eye. The research demonstrates that F- can selectively amplified supramolecular chirality through urea-F- interactions, which may have promising applications in the fields of sensing and chiroptical devices.

Supplementary files

Article information

Article type
Paper
Submitted
10 oct. 2024
Accepted
23 déc. 2024
First published
27 déc. 2024

Nanoscale, 2025, Accepted Manuscript

Fluoride binding modulated supramolecular chirality of urea-containing triarylamine and photo manifestation

S. Ma, X. Wen, Y. Jiang, J. Jiang, W. Hao, L. Zhang and M. Liu, Nanoscale, 2025, Accepted Manuscript , DOI: 10.1039/D4NR04175E

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