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.
- This article is part of the themed collection: Chiral Nanomaterials