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智能手机辅助新型希夫碱显色法检测钍的研究及其在实时样品中的应用。

Development of the Smartphone-Assisted Colorimetric Detection of Thorium by Using New Schiff's Base and Its Applications to Real Time Samples.

机构信息

Department of Chemistry, School of Advanced Sciences , Vellore Institute of Technology , Vellore 632014 , Tamil Nadu , India.

Indira Gandhi Centre for Atomic Research, Homi Bhabha National Institute , Kalpakkam 603102 , Tamil Nadu , India.

出版信息

Inorg Chem. 2018 Dec 17;57(24):15270-15279. doi: 10.1021/acs.inorgchem.8b02564. Epub 2018 Dec 5.

DOI:10.1021/acs.inorgchem.8b02564
PMID:30516379
Abstract

In this paper, a new Th ion-selective chromogenic sensor (L) was developed by reacting 1,10-phenanthroline-2,9-dicarbohydrazide with 2-hydroxy naphthaldehyde. The sensing ability of L toward Th was investigated in solution and paper strips loaded with L using spectrophotometric and colorimetric methods. The selective interaction of L was examined with various f-metal ions and other selected metal ions from s-block and d-block elements. Results show that by the colorimetric method in solution-phase dimethyl sulfoxide/HO (7:3, v/v) and paper strip methods, the naked-eye detectable color change of L occurred from colorless solution to yellow-orange and pale yellow colour upon interacting with Th and Al, respectively, whereas other metal ions did not interfere. The ligand L exhibits two absorbance bands at 320 and 375 nm because of ligand-to-ligand charge transfer. Upon interaction with Th, L undergoes red shift of both absorption bands and the formation of a new UV-vis band at 335 and 440 nm. The UV-visible spectral studies indicate the formation of a 1:1 host-guest complex between L and Th with an association constant of 4.7 × 10 M. The limit of quantification and limit of detection of L for the analysis of Th are found to be 167 and 50 nM, respectively. The visually detectable color change of L has been well integrated with a smartphone RGB color value to make it an analytical signal for real-time analysis of Th with the detection limit down to 116 nM. Besides, L was applied for the analysis of Th content present in various real water samples, monazite, and lantern mantle samples by spectrophotometry and RGB color values. The binding mode of L with Th is investigated by H NMR, electrospray ionization-mass, and theoretical studies.

摘要

在本文中,通过将 1,10-菲咯啉-2,9-二羧酸二酰肼与 2-羟基萘醛反应,开发了一种新的 Th 离子选择性显色传感器(L)。使用分光光度法和比色法在溶液中和负载有 L 的纸条上研究了 L 对 Th 的传感能力。研究了 L 与各种 f 金属离子以及来自 s 块和 d 块元素的其他选定金属离子的选择性相互作用。结果表明,通过在溶液相二甲基亚砜/HO(7:3,v/v)和纸条方法中的比色法,L 与 Th 和 Al 相互作用时,从无色溶液到黄色橙色和淡黄色的肉眼可检测颜色变化,而其他金属离子则没有干扰。配体 L 由于配体到配体的电荷转移而具有两个吸收带,在 320nm 和 375nm 处。与 Th 相互作用时,L 的两个吸收带均发生红移,并且在 335nm 和 440nm 处形成新的紫外可见带。紫外可见光谱研究表明,L 与 Th 之间形成了 1:1 的主体-客体络合物,其缔合常数为 4.7×10^M。L 用于 Th 分析的定量下限和检测限分别为 167nm 和 50nm。L 的可见颜色变化已与智能手机 RGB 颜色值很好地集成在一起,使其成为实时分析 Th 的分析信号,检测限低至 116nm。此外,L 还通过分光光度法和 RGB 颜色值用于分析各种实际水样、独居石和灯笼罩样品中的 Th 含量。通过 H NMR、电喷雾电离质谱和理论研究研究了 L 与 Th 的结合模式。

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