脱质子化
苯并恶唑
荧光
化学
离子
氰化物
部分
化学计量学
光化学
分析化学(期刊)
无机化学
立体化学
物理化学
色谱法
有机化学
物理
量子力学
作者
Najmin Tohora,Manas Mahato,Tuhina Sultana,Sabbir Ahamed,Susanta Ghanta,Sudhir Kumar Das
标识
DOI:10.1016/j.jphotochem.2023.114807
摘要
This article introduced a benzoxazole-based (NT) photoluminescence 'off–on-off' probe for sequential detection of cyanide (CN–) and iron (III) (Fe3+) ions, respectively in H2O/DMSO (1:1 v/v) medium. Probe NT quickly produced a strong blue fluorescence due to the introduction of CN– ions, found to be 1:1 binding stoichiometry, mainly due to the disruption of excited state intramolecular proton transfer (ESIPT) because of deprotonation of hydroxy (–OH) functional group present in the salicylimine moiety. The resulting deprotonated NT is further employed for detecting Fe3+ ions by turn-off fluorescence response and binding affinity found in the 1:3 stoichiometry ratio. The detection thresholds for CN– and Fe3+ ions are estimated to be 23 nM and 5.70 μM, respectively, much lower than the permissible maximum contamination level predicted by Environmental Protection Agency (EPA). For the practical utilization of our fluorescence sensor NT as an on-site detector, we have demonstrated a paper strip-based test kit experiment to quantify traces of CN– ions in stocks of related analytes. The ability of NT and deprotonated NT to detect CN– and Fe3+ ions, respectively, demonstrated that it might be a sensing tool for real sample analysis.
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