{"title":"Perimidine Derivative as a Colorimetric/fluorescence turn-on Sensor for Fe<sup>3+</sup>: Smartphone-assisted Sensing and Quantification of Fe<sup>3</sup>.","authors":"Ruhi Mehta, Rajbir Kaur, Navneet Khetrapal, Sanjay Kumar","doi":"10.1007/s10895-025-04537-y","DOIUrl":null,"url":null,"abstract":"<p><p>A novel perimidine derivative: 2-(isoquinolin-1-yl)-1H-perimidine (sensor 1) was synthesized via a facile, one-step reaction between DAN (1,8 diaminonaphthalene) and 2- quinolinecarboxaldehyde. The as-synthesised sensor 1 was found to be stable under a wide pH range of 2-12, and it behaved as a colorimetric as well as fluorescence turn-on sensor for Fe<sup>3+</sup> with a response range varying from 0 to 200 µM. The fluorescence titration profile was used to calculate the binding constant as 1.3 × 10<sup>4</sup> M<sup>-1</sup> and the LOD was as low as 7.4 nM. Additionally, the interference studies revealed the capability of 1.Fe<sup>3+</sup> complex to sense Cu<sup>2+</sup>, which was accompanied by the fluorescence turn-off response. The binding constant and detection limit of 1.Fe<sup>3+</sup> complex for Cu<sup>2+</sup> were calculated to be 1.44 × 10<sup>3</sup> M and 1.13 × 10<sup>-7</sup> M, respectively. The Fe<sup>3+</sup> induced fluorescence enhancement at different concentrations was also recognized via smartphone, which could benefit in resource-limited areas and could be used as an alternative for complex instrumentation.</p>","PeriodicalId":15800,"journal":{"name":"Journal of Fluorescence","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-09-11","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/s10895-025-04537-y","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
Abstract
A novel perimidine derivative: 2-(isoquinolin-1-yl)-1H-perimidine (sensor 1) was synthesized via a facile, one-step reaction between DAN (1,8 diaminonaphthalene) and 2- quinolinecarboxaldehyde. The as-synthesised sensor 1 was found to be stable under a wide pH range of 2-12, and it behaved as a colorimetric as well as fluorescence turn-on sensor for Fe3+ with a response range varying from 0 to 200 µM. The fluorescence titration profile was used to calculate the binding constant as 1.3 × 104 M-1 and the LOD was as low as 7.4 nM. Additionally, the interference studies revealed the capability of 1.Fe3+ complex to sense Cu2+, which was accompanied by the fluorescence turn-off response. The binding constant and detection limit of 1.Fe3+ complex for Cu2+ were calculated to be 1.44 × 103 M and 1.13 × 10-7 M, respectively. The Fe3+ induced fluorescence enhancement at different concentrations was also recognized via smartphone, which could benefit in resource-limited areas and could be used as an alternative for complex instrumentation.
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.