新型Hg2+特异性“开启”荧光传感器:通过实时比色分析在水样和测试条中的应用

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Nirawit Kaewnok, Pimpisa Tabphan, Jitnapa Sirirak, Krit Setthakarn, Nantanit Wanichacheva
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引用次数: 0

摘要

汞污染仍然是全球关注的问题,对环境和人类健康造成危害。因此,必须开发一种快速、灵敏、有效的检测环境中Hg2+的方法。本研究成功合成了一种基于硫羰基功能化罗丹明(TRS)的新型Hg2+特异性荧光传感器。该传感器在甲醇水溶液中表现出强烈的荧光增强和对Hg2+的显色变化。同时,TRS可以将Hg2+与其他竞争离子区分开来,检测限为8.7 nM (1.7 ppb)。传感器以1:1的化学计量比识别Hg2+,这一点得到了Job的图的证实。FTIR、1H NMR和13C NMR谱分析充分证明了其感应机理包括Hg2+络合物的形成和随后的脱硫机理。用不同的实际样品验证了TRS在比色法和荧光法中监测Hg2+含量的有效性。该传感器开发的试纸条也显示出高选择性的比色Hg2+检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel Hg2+‐Specific “turn-on” fluorescence sensor: Applications in water samples and test strips via real‐time colorimetric assay

Novel Hg2+‐Specific “turn-on” fluorescence sensor: Applications in water samples and test strips via real‐time colorimetric assay
Mercury pollution remains a global concern that causes harm to the environment and human health. Therefore, a rapid, sensitive, and effective method for detecting Hg2+ in the environment must be developed. This study successfully synthesized a new Hg2+-specific fluorescence sensor based on thiocarbonyl-functionalized rhodamine (TRS). The sensor exhibits drastic fluorescence enhancement and a chromogenic change toward Hg2+ in an aqueous methanol solution. Meanwhile, TRS can distinguish Hg2+ from other competing ions with a detection limit of 8.7 nM (1.7 ppb). The sensor recognizes Hg2+ with a 1:1 stoichiometric ratio, confirmed by Job's plot. Its sensing mechanism involves forming the Hg2+ complex and later desulfurization mechanism, as intensively proved by FTIR, 1H NMR, and 13C NMR spectral analysis. The efficacy of TRS in colorimetric and fluorometric assays for monitoring Hg2+ contents was validated using different real samples. A paper test strip developed from this sensor also demonstrated high selectivity for colorimetric Hg2+ detection.
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
期刊介绍: The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid. We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.
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