基于4,5 -二羟基- 1,3 -苯二磺酸荧光猝灭传感平台的水中Fe2+和Fe3+的总测定和化学形态

IF 3.1 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
K M Alotaibi, Z M Saigl, K S Alblawi, H Alwael, T N Abduljabbar, G I Mohammed, M S El-Shahawi
{"title":"基于4,5 -二羟基- 1,3 -苯二磺酸荧光猝灭传感平台的水中Fe2+和Fe3+的总测定和化学形态","authors":"K M Alotaibi, Z M Saigl, K S Alblawi, H Alwael, T N Abduljabbar, G I Mohammed, M S El-Shahawi","doi":"10.1007/s10895-025-04467-9","DOIUrl":null,"url":null,"abstract":"<p><p>Total quantification and speciation of Fe<sup>2+</sup> and Fe<sup>3+</sup> at trace levels in aqueous environments has emerged as an imperative analytical challenge for ecological systems and public health. Implementation of wavelength-dependent spectrochemical methodologies based on formation of chromogenic Fe<sup>3+</sup> chelate for Fe<sup>3+</sup> quantification in aqueous media also remains intrinsically challenging owing to intrinsic self-absorbance, and spectral convolution. Thus, the current study reports the development of a direct and selective eco-friendly spectrofluorometric probe for Fe<sup>3+</sup> detection in water. The sensor 4, 5- dihydroxy-1, 3-benzenedisulfonic acid (Tiron) displays strong emission which undergoes significant quenching in the fluorescence intensity (at λ<sub>ex/em</sub> = 290/350 nm) upon reaction with Fe<sup>2+</sup> at pH 8-9 in the presence of interfering metal ions, allowing for rapid and efficient detection. The probe was sensitive to implement the produced change in color with a total assay reaction time less than 3 min. Detailed spectroscopic investigation reveal a high binding affinity between the Fe<sup>3+</sup> ions and the sensor, ascribed to specific complex formation. The limit of detection (LOD) and quantitation (LOQ) and linear dynamic rang (LDR) of the assay were 0.015, 0.04 and 0.05-5 mg L<sup>-1</sup> Fe<sup>3+</sup>, respectively. The probe was favorably used for total detection and sequential speciation of trace levels of Fe<sup>2+</sup> & Fe<sup>3+</sup> in water after oxidation of the former to Fe<sup>3+</sup>. Spectroscopic studies suggested high coordinating attraction and stability between the sensor and Fe<sup>3+</sup> ions. The probe was fruitfully validated by comparing the results with the official inductively coupled plasma-optical emission spectrometry (ICP-OES) data using Student t and F tests signifying the high precision, accuracy and reliability for Fe<sup>3+</sup> detection in water samples. The attractive features of the probe comprises its simplicity, no usage of organic solvents, short reaction time; high reactivity, stable response, selective towards Fe<sup>3+</sup>, and sensitive for total quantification of iron species. The probe can assist as a talented tool for application in regions of limiting resources specifically concerning iron pollution.</p>","PeriodicalId":15800,"journal":{"name":"Journal of Fluorescence","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Total Determination and Chemical Speciation of Fe<sup>2+</sup>and Fe<sup>3+</sup> Species in Water Based on the Fluorescence Quenching of 4, 5- Dihydroxy-1, 3-benzenedisulfonic Acid' as a Sensing Platform.\",\"authors\":\"K M Alotaibi, Z M Saigl, K S Alblawi, H Alwael, T N Abduljabbar, G I Mohammed, M S El-Shahawi\",\"doi\":\"10.1007/s10895-025-04467-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Total quantification and speciation of Fe<sup>2+</sup> and Fe<sup>3+</sup> at trace levels in aqueous environments has emerged as an imperative analytical challenge for ecological systems and public health. Implementation of wavelength-dependent spectrochemical methodologies based on formation of chromogenic Fe<sup>3+</sup> chelate for Fe<sup>3+</sup> quantification in aqueous media also remains intrinsically challenging owing to intrinsic self-absorbance, and spectral convolution. Thus, the current study reports the development of a direct and selective eco-friendly spectrofluorometric probe for Fe<sup>3+</sup> detection in water. The sensor 4, 5- dihydroxy-1, 3-benzenedisulfonic acid (Tiron) displays strong emission which undergoes significant quenching in the fluorescence intensity (at λ<sub>ex/em</sub> = 290/350 nm) upon reaction with Fe<sup>2+</sup> at pH 8-9 in the presence of interfering metal ions, allowing for rapid and efficient detection. The probe was sensitive to implement the produced change in color with a total assay reaction time less than 3 min. Detailed spectroscopic investigation reveal a high binding affinity between the Fe<sup>3+</sup> ions and the sensor, ascribed to specific complex formation. The limit of detection (LOD) and quantitation (LOQ) and linear dynamic rang (LDR) of the assay were 0.015, 0.04 and 0.05-5 mg L<sup>-1</sup> Fe<sup>3+</sup>, respectively. The probe was favorably used for total detection and sequential speciation of trace levels of Fe<sup>2+</sup> & Fe<sup>3+</sup> in water after oxidation of the former to Fe<sup>3+</sup>. Spectroscopic studies suggested high coordinating attraction and stability between the sensor and Fe<sup>3+</sup> ions. The probe was fruitfully validated by comparing the results with the official inductively coupled plasma-optical emission spectrometry (ICP-OES) data using Student t and F tests signifying the high precision, accuracy and reliability for Fe<sup>3+</sup> detection in water samples. The attractive features of the probe comprises its simplicity, no usage of organic solvents, short reaction time; high reactivity, stable response, selective towards Fe<sup>3+</sup>, and sensitive for total quantification of iron species. The probe can assist as a talented tool for application in regions of limiting resources specifically concerning iron pollution.</p>\",\"PeriodicalId\":15800,\"journal\":{\"name\":\"Journal of Fluorescence\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-08-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fluorescence\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s10895-025-04467-9\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fluorescence","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s10895-025-04467-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

水环境中痕量Fe2+和Fe3+的总定量和形态已成为生态系统和公共卫生的重要分析挑战。由于固有的自吸性和光谱卷积,基于显色Fe3+螯合物形成的波长依赖光谱化学方法在水介质中定量Fe3+仍然具有本质上的挑战性。因此,本研究报告了一种用于水中Fe3+检测的直接和选择性生态友好型荧光光谱探针的开发。4,5 -二羟基- 1,3 -苯二磺酸(铁)传感器在pH为8 ~ 9的条件下与Fe2+反应,在干扰金属离子存在下,其荧光强度(λex/em = 290/350 nm)发生显著猝灭,实现了快速高效的检测。该探针对所产生的颜色变化非常敏感,总测定反应时间小于3 min。详细的光谱研究揭示了Fe3+离子与传感器之间的高结合亲和力,归因于特定的配合物形成。检测限(LOD)、定量限(LOQ)和线性动态范围(LDR)分别为0.015、0.04和0.05 ~ 5 mg L-1 Fe3+。该探针可用于水中Fe2+和Fe3+氧化后的痕量Fe2+和Fe3+的总检测和顺序形成。光谱研究表明传感器与Fe3+离子之间具有高度的协调吸引力和稳定性。通过与官方电感耦合等离子体光学发射光谱(ICP-OES)数据进行学生t和F测试,验证了探针检测水样中Fe3+的高精度、准确性和可靠性。该探针的吸引人的特点包括其简单,不使用有机溶剂,反应时间短;反应活性高,反应稳定,对Fe3+有选择性,对铁的总量定量敏感。该探针可以作为一种有天赋的工具,用于资源有限的地区,特别是与铁污染有关的地区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Total Determination and Chemical Speciation of Fe2+and Fe3+ Species in Water Based on the Fluorescence Quenching of 4, 5- Dihydroxy-1, 3-benzenedisulfonic Acid' as a Sensing Platform.

Total quantification and speciation of Fe2+ and Fe3+ at trace levels in aqueous environments has emerged as an imperative analytical challenge for ecological systems and public health. Implementation of wavelength-dependent spectrochemical methodologies based on formation of chromogenic Fe3+ chelate for Fe3+ quantification in aqueous media also remains intrinsically challenging owing to intrinsic self-absorbance, and spectral convolution. Thus, the current study reports the development of a direct and selective eco-friendly spectrofluorometric probe for Fe3+ detection in water. The sensor 4, 5- dihydroxy-1, 3-benzenedisulfonic acid (Tiron) displays strong emission which undergoes significant quenching in the fluorescence intensity (at λex/em = 290/350 nm) upon reaction with Fe2+ at pH 8-9 in the presence of interfering metal ions, allowing for rapid and efficient detection. The probe was sensitive to implement the produced change in color with a total assay reaction time less than 3 min. Detailed spectroscopic investigation reveal a high binding affinity between the Fe3+ ions and the sensor, ascribed to specific complex formation. The limit of detection (LOD) and quantitation (LOQ) and linear dynamic rang (LDR) of the assay were 0.015, 0.04 and 0.05-5 mg L-1 Fe3+, respectively. The probe was favorably used for total detection and sequential speciation of trace levels of Fe2+ & Fe3+ in water after oxidation of the former to Fe3+. Spectroscopic studies suggested high coordinating attraction and stability between the sensor and Fe3+ ions. The probe was fruitfully validated by comparing the results with the official inductively coupled plasma-optical emission spectrometry (ICP-OES) data using Student t and F tests signifying the high precision, accuracy and reliability for Fe3+ detection in water samples. The attractive features of the probe comprises its simplicity, no usage of organic solvents, short reaction time; high reactivity, stable response, selective towards Fe3+, and sensitive for total quantification of iron species. The probe can assist as a talented tool for application in regions of limiting resources specifically concerning iron pollution.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信