Perimidine Derivative as a Colorimetric/fluorescence turn-on Sensor for Fe3+: Smartphone-assisted Sensing and Quantification of Fe3.

IF 3.1 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Ruhi Mehta, Rajbir Kaur, Navneet Khetrapal, Sanjay Kumar
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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.

吡啶衍生物作为Fe3+的比色/荧光开启传感器:智能手机辅助Fe3的传感和定量。
摘要以丹(1,8二氨基萘)和2-喹啉甲醛为原料,一步反应合成了一种新型的吡啶衍生物:2-(异喹啉-1-基)- 1h -吡啶(传感器1)。合成的传感器1在2-12的宽pH范围内是稳定的,它可以作为Fe3+的比色和荧光开启传感器,响应范围从0到200µM。利用荧光滴定谱计算得到的结合常数为1.3 × 104 M-1, LOD低至7.4 nM。此外,干扰研究揭示了1。Fe3+配合物感应Cu2+,并伴有荧光关闭反应。结合常数和检出限为1。计算出Fe3+对Cu2+的络合物分别为1.44 × 103 M和1.13 × 10-7 M。智能手机还可以识别不同浓度Fe3+诱导的荧光增强,这可以在资源有限的地区受益,并可作为复杂仪器的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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.
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