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Updated: Nov 26, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
2-Hydroxynaphthalene based acylhydrazone as a turn-on fluorescent chemosensor for Al3+ detection and its real sample
Yucun Liu1, Lili Zhang2, Lei Chen1
1Key Laboratory of Preparation and Applications of Environmental Friendly Materials (Jilin Normal University), Ministry of Education, Changchun 130103, China; College of Chemistry, Jilin Normal University, Siping 136000, China.
Abstract:
Developing high performance fluorescent chemosensor for Al3+ detection is highly desirable, due to the excess of Al3+ will lead to many diseases. In this paper, a simple 2-hydroxynaphthalene-based fluorescent chemosensor has been synthesized and characterized by different spectroscopic methods. The compound exhibited an "turn-on-type" fluorescent chemosensing for the detection of Al3+, which was ascribed to the chelation-enhanced fluorescence (CHEF). The high selectivity and sensitivity of the compound for Al3+ were verified by fluorescence spectra in its DMF solution, and the enhancement of fluorescent intensity could be observed by naked-eye from non-fluorescence to green light. The detection limit of the compound for Al3+ was found to be 4.22 × 10-8 M and the stability constant was 4.82 × 104 M-1. The 1:1 binding stoichiometry of the compound to Al3+ was confirmed from the Job's plot based on fluorescence titrations. Additionally, the sensing process of the compound to Al3+ was chemically reversible by adding Na2EDTA. Importantly, the probe was successfully applied to quantitative analysis of Al3+ in real drug and potable water samples.
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