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质子化可离子化杯[4]芳烃荧光团对 Hg2+ 的选择性传感。

Selective sensing of Hg2+ by a proton-ionizable calix[4]arene fluoroionophore.

机构信息

Dipartimento di Scienze Chimiche, Università degli Studi di Catania, Catania, Italy.

出版信息

Anal Bioanal Chem. 2013 Jan;405(2-3):1133-7. doi: 10.1007/s00216-012-6378-8. Epub 2012 Sep 12.

Abstract

A fluorogenic derivative of a calix[4]arene with two proton-ionizable N-(phenyl)sulfonyl carboxamide-containing side arms in the 1,3-positions on the lower rim is employed for the selective sensing of Hg(2+) at low concentration levels in water/MeCN (1:1, v/v) solutions containing Pb(2+) and Cd(2+). All three metal ions quench the fluorescence of the ligand in pure MeCN. However, in water/MeCN mixed solvent, the recognition of such cations occurs differently as only Hg(2+) complexation quenches the fluorescence of the calixarene. Experiments carried out in the presence of an acid and a bulky non-complexing cation shows that the quenching of the calixarene fluorescence upon Hg(2+) addition is likely due to proton displacement from the proton-ionizable side arms of the ligand. The system may be employed as a simple tool for the selective and efficient mercury sensing in mixed water/organic solvent.

摘要

一种在 1,3-位的低边缘上具有两个质子可电离的 N-(苯基)磺酰基羧酰胺的杯[4]芳烃的荧光衍生试剂,用于在含有 Pb(2+)和 Cd(2+)的水/MeCN(1:1,v/v)溶液中选择性地检测低浓度的 Hg(2+)。所有三种金属离子都会在纯 MeCN 中猝灭配体的荧光。然而,在水/MeCN 混合溶剂中,对这些阳离子的识别方式不同,只有 Hg(2+)的络合会猝灭杯芳烃的荧光。在存在酸和大体积非络合阳离子的情况下进行的实验表明,配体质子可电离侧臂上的质子被 Hg(2+)取代可能导致杯芳烃荧光猝灭。该体系可作为一种在混合水/有机溶剂中选择性和高效检测汞的简单工具。

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