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氰离子在高碱性介质中的选择性和灵敏荧光检测及其测定

Selective and Sensitive Fluorescent Detection of Cyanide Ions and their Estimation in a Highly Alkaline Medium.

作者信息

Ponlakshmi P, Dharaniprabha V, Elango Kuppanagounder P

机构信息

Department of Chemistry, Gandhigram Rural Institute (Deemed to be University), Gandhigram, 624302, India.

出版信息

J Fluoresc. 2025 Aug 22. doi: 10.1007/s10895-025-04513-6.

DOI:10.1007/s10895-025-04513-6
PMID:40844581
Abstract

Accurate detection of cyanide ions in food and water is indispensable to avert detrimental effects on human health and minimize environmental defilement. In response to this pressing need, we reported a novel fluorescent chemosensor (PPL1) to detect cyanide ions in highly alkaline solutions with a unique and instant fluorescence response (dull green to bright yellow) with great selectivity and sensitivity. The 1:1 binding fashion of PPL1 with CN was signified by Job analysis. The limit of detection (0.49 µM) and the interference assay of PPL1 certified its selectivity and suitability for the detection of CN in actual samples. The selectivity of PPL1 towards CN was ascribed to the deprotonation followed by nucleophilic addition mechanism as proven by H and C NMR and LC-MS. The PPL1 demonstrated exceptional performance even under extreme pH circumstances and enabled us to quantify cyanide in alkaline water samples in line with the US EPA standard cyanide estimation protocol and in food samples such as sprouting potatoes, cassava, and almonds. The DFT/TD-DFT computations that shed light on the electronic transitions and interaction sites involved in the sensing process robustly validate our experimental findings and proposed mechanism. The PPL1 emerges as an advancing candidate for environmental monitoring and food safety applications due to its strong mechanistic validation (deprotonation followed by nucleophilic addition), low detection limit (0.49 µM), rapid response time (instant response), and swift fluorescence switching with CN ions (green to yellow instantaneously in contact with CN).

摘要

准确检测食品和水中的氰离子对于避免对人类健康产生有害影响以及最大限度地减少环境污染至关重要。为满足这一迫切需求,我们报道了一种新型荧光化学传感器(PPL1),用于在高碱性溶液中检测氰离子,它具有独特且即时的荧光响应(从暗绿色变为亮黄色),具有很高的选择性和灵敏度。Job分析表明PPL1与CN的结合方式为1:1。检测限(0.49 μM)和PPL1的干扰试验证明了其对实际样品中CN检测的选择性和适用性。PPL1对CN的选择性归因于去质子化后亲核加成机制,这已通过氢谱和碳谱以及液相色谱 - 质谱得到证实。即使在极端pH条件下,PPL1也表现出优异的性能,使我们能够根据美国环境保护局标准氰化物估计协议对碱性水样以及发芽土豆、木薯和杏仁等食品样品中的氰化物进行定量。密度泛函理论/含时密度泛函理论计算揭示了传感过程中涉及的电子跃迁和相互作用位点,有力地验证了我们的实验结果和提出的机制。由于其强大的机理验证(去质子化后亲核加成)、低检测限(0.49 μM)、快速响应时间(即时响应)以及与氰离子的快速荧光切换(与CN接触时瞬间从绿色变为黄色),PPL1成为环境监测和食品安全应用中一个有前景的候选者。

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