Catalytic auto-oxidation of o-hydroxyphenylthiourea by Iridium(III): A photometric sensing platform for Iridium

Chemistry of Inorganic Materials Pub Date : 2024-12-01 Epub Date: 2024-11-19 DOI:10.1016/j.cinorg.2024.100081
A. Sunil, Ashish Deep Chettri, S. Jagadeeswara Rao
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Abstract

o-Hydroxyphenylthiourea (HPTU) undergoes oxidative dimerization to form a yellow-colored disulfide in the presence of Iridium(III), a process significantly enhanced by the activator 1,10-phenanthroline. This catalytic oxidation was monitored spectrophotometrically at 416 ​nm under ambient conditions, employing both tangent and fixed-time methods. The method's performance was optimized by investigating factors like pH, reagent concentration, temperature, and potential interferents. A linear relationship between the rate of reaction and Iridium(III) concentration was observed in the range of 0.001 ​ng–5.0 ​mg of Iridium per mL, enabling the detection of Iridium(III) down to 0.001 ​ng/mL at pH 11.7. The method's simplicity, cost-effectiveness, and sensitivity make it suitable for the determination of Iridium(III) in real-time samples, eliminating the need for additional reagents, complex procedures, or preconcentration steps.

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铱(III)催化邻羟基苯硫脲的自氧化作用:铱的光度传感平台
邻羟基苯基硫脲(HPTU)在铱(III)存在下发生氧化二聚反应,形成黄色的二硫化物,活化剂 1,10-菲罗啉显著增强了这一过程。在环境条件下,采用正切法和固定时间法在 416 纳米波长处对这种催化氧化作用进行分光光度法监测。通过研究 pH 值、试剂浓度、温度和潜在干扰物等因素,对该方法的性能进行了优化。在每毫升 0.001 纳克-5.0 毫克铱的范围内,反应速率与铱(III)浓度之间呈线性关系,在 pH 值为 11.7 时,可检测到低至 0.001 纳克/毫升的铱(III)。该方法简便、经济、灵敏,适用于实时样品中铱(III)的测定,无需额外的试剂、复杂的程序或预浓缩步骤。
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