{"title":"通过 RGB 法识别水和土壤样品中铀离子的共轭低聚电解质。","authors":"Lalita Thakur , Lipika Garg , Irshad Mohiuddin , Raghubir Singh , Varinder Kaur , Nikhlesh Thakur","doi":"10.1016/j.saa.2024.125355","DOIUrl":null,"url":null,"abstract":"<div><div>The development of selective and practically applicable sensors for monitoring trace uranyl ions (UO<sub>2</sub><sup>2+</sup>) in an aqueous medium is the biggest challenge. This study presents the development of a conjugated oligoelectrolyte-based probe (COE) for the selective detection of UO<sub>2</sub><sup>2+</sup> ions in water bodies. The COE is a water-soluble probe having an organic backbone with two ionic pendants at the terminal points. It changes its color to a dark yellow selectively in the presence of UO<sub>2</sub><sup>2+</sup> ions. This visible change was integrated with a smartphone RGB color quantification method. The COE displayed an RGB chemo-dosimeter to selectively monitor UO<sub>2</sub><sup>2+</sup> ions without interference from other metal ions. In the parallel experiment, COE displays a spectrofluorimetric emission signal at λ<sub>ems.</sub> = 525 nm (with λ<sub>exc.</sub> = 420 nm), which exhibits quenching of signal when interacted with UO<sub>2</sub><sup>2+</sup> ions. The limit of detection (LOD) is found to be 3.07 × 10<sup>−2</sup> µM and 4.50 µM by spectrofluorimetric and RGB color value methods, respectively. <sup>1</sup>H NMR and XPS analysis investigated the mode of interaction, and it suggested that the quenching of the emission signal was due to the interaction between the electron-rich azomethine site of COE and UO<sub>2</sub><sup>2+</sup> ion. The smartphone-based RGB color analysis makes COE a potential probe with reduced operation time and offers a fresh approach for the immediate, real-time detection of UO<sub>2</sub><sup>2+</sup> ions in aqueous and soil samples.</div></div>","PeriodicalId":433,"journal":{"name":"Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy","volume":"327 ","pages":"Article 125355"},"PeriodicalIF":4.3000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A conjugated oligoelectrolyte for the recognition of uranyl ion in aqueous and soil samples via RGB method\",\"authors\":\"Lalita Thakur , Lipika Garg , Irshad Mohiuddin , Raghubir Singh , Varinder Kaur , Nikhlesh Thakur\",\"doi\":\"10.1016/j.saa.2024.125355\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The development of selective and practically applicable sensors for monitoring trace uranyl ions (UO<sub>2</sub><sup>2+</sup>) in an aqueous medium is the biggest challenge. This study presents the development of a conjugated oligoelectrolyte-based probe (COE) for the selective detection of UO<sub>2</sub><sup>2+</sup> ions in water bodies. The COE is a water-soluble probe having an organic backbone with two ionic pendants at the terminal points. It changes its color to a dark yellow selectively in the presence of UO<sub>2</sub><sup>2+</sup> ions. This visible change was integrated with a smartphone RGB color quantification method. The COE displayed an RGB chemo-dosimeter to selectively monitor UO<sub>2</sub><sup>2+</sup> ions without interference from other metal ions. In the parallel experiment, COE displays a spectrofluorimetric emission signal at λ<sub>ems.</sub> = 525 nm (with λ<sub>exc.</sub> = 420 nm), which exhibits quenching of signal when interacted with UO<sub>2</sub><sup>2+</sup> ions. The limit of detection (LOD) is found to be 3.07 × 10<sup>−2</sup> µM and 4.50 µM by spectrofluorimetric and RGB color value methods, respectively. <sup>1</sup>H NMR and XPS analysis investigated the mode of interaction, and it suggested that the quenching of the emission signal was due to the interaction between the electron-rich azomethine site of COE and UO<sub>2</sub><sup>2+</sup> ion. The smartphone-based RGB color analysis makes COE a potential probe with reduced operation time and offers a fresh approach for the immediate, real-time detection of UO<sub>2</sub><sup>2+</sup> ions in aqueous and soil samples.</div></div>\",\"PeriodicalId\":433,\"journal\":{\"name\":\"Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy\",\"volume\":\"327 \",\"pages\":\"Article 125355\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-10-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S138614252401521X\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"SPECTROSCOPY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S138614252401521X","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SPECTROSCOPY","Score":null,"Total":0}
A conjugated oligoelectrolyte for the recognition of uranyl ion in aqueous and soil samples via RGB method
The development of selective and practically applicable sensors for monitoring trace uranyl ions (UO22+) in an aqueous medium is the biggest challenge. This study presents the development of a conjugated oligoelectrolyte-based probe (COE) for the selective detection of UO22+ ions in water bodies. The COE is a water-soluble probe having an organic backbone with two ionic pendants at the terminal points. It changes its color to a dark yellow selectively in the presence of UO22+ ions. This visible change was integrated with a smartphone RGB color quantification method. The COE displayed an RGB chemo-dosimeter to selectively monitor UO22+ ions without interference from other metal ions. In the parallel experiment, COE displays a spectrofluorimetric emission signal at λems. = 525 nm (with λexc. = 420 nm), which exhibits quenching of signal when interacted with UO22+ ions. The limit of detection (LOD) is found to be 3.07 × 10−2 µM and 4.50 µM by spectrofluorimetric and RGB color value methods, respectively. 1H NMR and XPS analysis investigated the mode of interaction, and it suggested that the quenching of the emission signal was due to the interaction between the electron-rich azomethine site of COE and UO22+ ion. The smartphone-based RGB color analysis makes COE a potential probe with reduced operation time and offers a fresh approach for the immediate, real-time detection of UO22+ ions in aqueous and soil samples.
期刊介绍:
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy (SAA) is an interdisciplinary journal which spans from basic to applied aspects of optical spectroscopy in chemistry, medicine, biology, and materials science.
The journal publishes original scientific papers that feature high-quality spectroscopic data and analysis. From the broad range of optical spectroscopies, the emphasis is on electronic, vibrational or rotational spectra of molecules, rather than on spectroscopy based on magnetic moments.
Criteria for publication in SAA are novelty, uniqueness, and outstanding quality. Routine applications of spectroscopic techniques and computational methods are not appropriate.
Topics of particular interest of Spectrochimica Acta Part A include, but are not limited to:
Spectroscopy and dynamics of bioanalytical, biomedical, environmental, and atmospheric sciences,
Novel experimental techniques or instrumentation for molecular spectroscopy,
Novel theoretical and computational methods,
Novel applications in photochemistry and photobiology,
Novel interpretational approaches as well as advances in data analysis based on electronic or vibrational spectroscopy.