Acylhydrazone functionalized naphthalene-based self-assembled supramolecular gels for efficient fluorescence detection of Fe3
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Updated: Jul 20, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Jutao Liu1, Shang Wu1, Shuaishuai Fu1
1Key Laboratory for Utility of Environmental Friendly Composite Materials and Biomass in University of Gansu Province, Key Laboratory of Environment-Friendly Composites of the State Ethnic Affairs Commission, Gansu Provincial Biomass Function Composites Engineering Research Center, College of Chemical Engineering, Northwest Minzu University, Lanzhou, Gansu 730030, P. R. China. chwush84@163.com.
Abstract:
A new gel factor (named N) has been successfully designed and synthesized, which contains the conventional fluorophore naphthalene with the acylhydrazone bond as the self-assembly site. It can be self-assembled into stable organogels (named ON) in dimethyl sulfoxide (DMSO) and water mixed medium (V : V = 4 : 1) with a critical gel temperature and concentration (55 °C and 10 mg mL-1). Interestingly, under 365 nm UV light, the ON exhibits bright yellow Aggregation Induced Emission (AIE). The supramolecular organogel ON shows a fluorescent "OFF" response to the metal ions Fe3+, and the state of the gel ON remains constant before and after detection. Notably, the minimum detection limits (LODs) of the gel ON for Fe3+ are as low as 1.30 × 10-7 M. The binding mechanism of supramolecular organogels (ON) to ions has been investigated through a series of characterizations. Meanwhile, the organogel sensor ON can also be used as an ion-responsive membrane for the detection of Fe3+ in the aqueous phase.
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