Anion-modulated photoswitching of a tetraurea-bridged azobenzene

Abstract

Here, we report a new ortho-phenylene-spaced oligourea receptor, L1, functionalized at its termini with photoresponsive azobenzene units. This peripheral design minimizes steric constraints, increasing conformational freedom and enabling dynamic responsiveness. Complexation of L1 with diverse anions (HPO42−, PO43−, SO42−, Cl, Br) affords stable assemblies (EE-1 to EE-7), and demonstrates robust reversible photoresponse. The distinct photo-dynamic responses elicited by different anions offer new insights for the design of advanced supramolecular photo-reversible materials.

Graphical abstract: Anion-modulated photoswitching of a tetraurea-bridged azobenzene

Supplementary files

Article information

Article type
Research Article
Submitted
01 Sep 2025
Accepted
12 Nov 2025
First published
13 Nov 2025

Inorg. Chem. Front., 2026, Advance Article

Anion-modulated photoswitching of a tetraurea-bridged azobenzene

Y. Wang, Y. Tao, X. Lu, C. Fan, D. Zhang, T. Wang, S. Feng, W. Zhang and C. Jia, Inorg. Chem. Front., 2026, Advance Article , DOI: 10.1039/D5QI01820J

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