5-Oxo-7,7-Dimethyl-5,6,7,8-Tetrahydro-4-H-Chromene Bearing N, N-Dimethylaniline as Turn-Off Fluorescent Chemosensor for Picric Acid in Real Water Sample.

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Eswaran Rajendran, Selvaraj Loganathan, Ramasamy Santhiya, Gandhi Sivaraman, Muthu Seenivasa Perumal
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Abstract

We have synthesized a one-pot, three-component pyran-based fluorescence chemosensor using onion extract as a green catalyst. The confirmed structure of the 1:2 binding of receptor SPR-2-picric acid adduct revealed that the pyran-based receptor accommodated two guest picric acid molecules through non-covalent interactions. UV-Vis and fluorescence spectroscopy show high selectivity and sensitivity towards picric acid. The 1D/2D NMR and Job's plot analysis show the complexation and stoichiometric binding of the receptor SPR-2 with picric acid are 1:2. The 1H NMR spectral studies confirm that the formation of receptor SPR-2-picric acid adduct via weak hydrogen bonding. The cooperativity of the receptor SPR-2-picric acid adduct shows negative cooperativity due to the weak hydrogen bonding of receptor SPR-2 and picric acid. Further, the density functional theory (DFT) confirmed the molecular level interaction of the SPR-2 and receptor SPR-2-Picric acid adduct. The receptor was effectively used to assess picric acid concentrations in real water samples.

Abstract Image

含有 N, N-二甲基苯胺的 5-氧代-7,7-二甲基-5,6,7,8-四氢-4-H-色烯作为实际水样中苦味酸的关闭荧光化学传感器。
我们利用洋葱提取物作为绿色催化剂,合成了一种单锅三组分吡喃基荧光化学传感器。受体 SPR-2 与苦味酸加合物 1:2 结合结构的确认表明,吡喃基受体通过非共价作用容纳了两个客体苦味酸分子。紫外可见光谱和荧光光谱显示了对苦味酸的高选择性和高灵敏度。一维/二维核磁共振和约伯图分析表明,受体 SPR-2 与苦味酸的络合度和化学计量结合度为 1:2。1H NMR 光谱研究证实,受体 SPR-2 与苦味酸的加合物是通过弱氢键形成的。由于受体 SPR-2 与苦味酸的氢键作用较弱,受体 SPR-2 与苦味酸加合物的合作性呈现负合作性。此外,密度泛函理论(DFT)证实了 SPR-2 和受体 SPR-2 与苦味酸加合物在分子水平上的相互作用。该受体被有效地用于评估实际水样中的苦味酸浓度。
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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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