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A coumarin-pyrazolone based fluorescent probe for selective colorimetric and fluorimetric fluoride detection: Synthesis, spectroscopic properties and DFT calculations

机译:基于香豆素 - 吡唑酮的荧光探针,用于选择性比色和氟化氟化物检测:合成,光谱性质和DFT计算

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摘要

A novel coumarin based fluorescence anion chemosensor (P-1) bearing pyrazolone as a receptoric part was synthesized and characterized by using FT-IR, H-1/C-13 NMR and HRMS for the purpose of recognition of anions in DMSO. P-1 has four tautomeric structures and the most stable tautomeric form of P-1 was determined experimentally and theoretically. The chemosensor P-1 consists two receptoric parts as free amide N-H and enamine N-H which is stabilized intramolecular H-bonding with coumarin carbonyl oxygen. P-1 interacts selectively with fluoride anion via amide N-H. The selectivity and sensitivity of probe to various anions were determined with spectrophotometric and H-1 NMR titration techniques as experimentally and all results were also explained by theoretical calculations. (C) 2018 Elsevier B.V. All rights reserved.
机译:用FT-IR,H-1 / C-13 NMR和HRMS合成并表征了作为接受部分的新型香豆素基荧光阴离子化学传感器(P-1)轴承吡唑酮作为接受部分,以识别DMSO中的阴离子。 P-1具有四个互变异构型结构,并且在实验和理论上测定最稳定的p-1的互变异构形式。 Chemosensor P-1由两种接受零件组成,作为游离酰胺N-H和烯胺N-H,其与香豆素羰基氧稳定的分子内H键合。 P-1通过酰胺N-H选择性地用氟化物阴离子相互作用。 用分光光度法和H-1 NMR滴定技术确定探针对各种阴离子的选择性和敏感性,如实验,也通过理论计算解释了所有结果。 (c)2018年elestvier b.v.保留所有权利。

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