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Discriminating Chemosensor for Detection of Fe3+ in Aqueous Media by Fluorescence Quenching Methodology

机译:荧光猝灭法鉴别水相中Fe3 +的化学传感器

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The Schiff base as chemosensor (B) namely 2‐((anthracen‐1‐ylimino) methyl) phenol was designed and synthesized. The spectral properties of chemosensor B were confirmed by using IR, 1H NMR, 13C NMR, and LC–MS techniques. The chemosensor B shows a significant fluorescence quenching with incremental addition of Fe3+. The present chemosensor B shows unaffected fluorescence response induced by Fe3+ even in the presence of other competing ions in mixed solvent system. The binding mode and stoichiometry (2:1) between chemosensor B and Fe3+ were analyzed by recording 1H NMR and Job's plot respectively. The ground state complexation of chemosensor B and Fe3+was confirmed by absorption titration and fluorescence lifetime measurement in the absence and presence of various concentration of Fe3+ ion to chemosensor B. The lower detection limit for Fe3+ found to be 0.59?μM with correlation coefficient R2?=?0.9815. The present chemosensor B successfully applied for quantitative determination of the Fe3+ ion from ordinary water samples.
机译:设计并合成了Schiff碱作为化学传感器(B)的2-((蒽-1-ylimino)甲基)苯酚。化学传感器B的光谱特性通过IR,1H NMR,13C NMR和LC-MS技术得到证实。化学传感器B随添加Fe3 +的增加而显示出明显的荧光猝灭。即使在混合溶剂系统中存在其他竞争离子,本发明的化学传感器B仍显示出Fe3 +诱导的不受影响的荧光响应。通过分别记录1 H NMR和Job's图来分析化学传感器B与Fe3 +之间的结合模式和化学计量比(2:1)。在不存在和存在各种浓度的Fe3 +离子的情况下,通过吸收滴定和荧光寿命测量,证实了化学传感器B和Fe3 +的基态络合。发现Fe3 +的下限为0.59?μM,相关系数为R2 = 0.9815。本化学传感器B成功地用于定量测定普通水样中的Fe3 +离子。

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