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A turn-on AIE dual-channel fluorescent probe for sensing Cr3+/ClO- and application in cell imaging
Huizhen Wang1, Yan Tang2, Kezhen Gou3
1School of Science, Asymmetric Synthesis and Chiral Technology Key Laboratory of Sichuan Province, Xihua University, Chengdu 610039, PR China; State Key Laboratory of Environment-friendly Energy Materials, School of Materials and Chemistry, Southwest University of Science and Technology, Mianyang 621010, PR China.
Abstract:
A Cr3+/ClO--enhanced fluorescent probe, DNS (5-(dimethylamino)-N'-(2-hydroxy-4,6-dimethoxybenzylidene)-naphthalene-1-sulfonyl hydrazide), with aggregation-induced emission (AIE) properties was synthesized using dansylhydrazide and 4,6-dimethoxysalicylaldehyde as starting materials. The probe rapidly and selectively detects Cr3+ and ClO- in a solvent system of H2O/DMSO (2:8). Upon binding with Cr3+/ClO-, the probe exhibits a significant fluorescence enhancement, with minimal interference from other ions. The detection limits (LOD) were determined to be 5.36 × 10-7 mol/L for Cr3+ and 3.65 × 10-7 mol/L for ClO-. The binding mechanisms of DNS with Cr3+/ClO- were investigated through Job's plot, 1H NMR titration, and mass spectrometry. Furthermore, the probe's low cytotoxicity and biocompatibility suggest its potential for detecting exogenous Cr3+/ClO- and endogenous ClO- in living cells. DNS shows promise for real-time detection and bioimaging applications.
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