Issue 39, 2021, Issue in Progress

Base-induced multi-state fluorescence of a trefoil-shaped salicylaldehyde azine derivative

Abstract

A trefoil-shaped salicylaldehyde azine derivative bearing multiple acidic protons displays base-induced multi-state luminescence. The azine was prepared through the reaction of 1,3,5-triformylphloroglucinol with 4-methoxysalicylaldehyde hydrazone. 1H NMR spectroscopy revealed that the azine existed in solution at room temperature as an equilibrium mixture of two geometric isomers. The three-step deprotonation (four-state change) of the azine in solution was confirmed using 1H NMR, UV-vis absorption, and emission spectroscopy.

Graphical abstract: Base-induced multi-state fluorescence of a trefoil-shaped salicylaldehyde azine derivative

Supplementary files

Article information

Article type
Paper
Submitted
03 Apr 2021
Accepted
26 Jun 2021
First published
07 Jul 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 24022-24026

Base-induced multi-state fluorescence of a trefoil-shaped salicylaldehyde azine derivative

N. Taniguchi, M. Naito, S. Miyagawa and Y. Tokunaga, RSC Adv., 2021, 11, 24022 DOI: 10.1039/D1RA02627E

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