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一种用于检测水中汞的独特的灵敏且高选择性荧光萘二氮杂冠醚大环配体化学传感器。

A Unique Sensitive and Highly Selective Fluorescent Naphthodiaza-Crown Macrocyclic Ligand Chemosensor for Hg in Water.

作者信息

Ghanbari Bahram, Zarepour-Jevinani Morteza

机构信息

Department of Chemistry, Sharif University of Technology, PO Box 11155-3516, Tehran, Iran.

出版信息

J Fluoresc. 2017 Jul;27(4):1385-1398. doi: 10.1007/s10895-017-2075-5. Epub 2017 Apr 20.

Abstract

The noticeable enhancement in fluorescence emission of ON-donor naphthodiaza-crown macrocyclic ligand (L) in the presence of Hg was observed in which the fluorescence quantum yield of free ligand L as well as L/Hg complex were found to be as 0.29 and 0.49, respectively. The observed ultra-low limit of detection (LOD) for Hg by L was determined as low as 1.0 × 10 M in water. A 1:1 stoichiometry was also established for L/Hg together with a binding constant K  = 66,543 by employing fluorescence spectrophotometry. The competition experiments on L/Hg demonstrated highly selective detection of Hg in the presence of the library cations. A two path mechanism for detection of metal ion in terms of coordination of metal ion to L and/or the formation of counter ion was proposed by using of H NMR and fluorescence spectroscopy. Graphical Abstract pH dependence mechanism of interaction between Hg and macrocyclic ligand L.

摘要

在汞存在的情况下,观察到供体萘二氮杂冠大环配体(L)的荧光发射显著增强,其中发现游离配体L以及L/Hg配合物的荧光量子产率分别为0.29和0.49。通过L对汞的检测限极低,在水中低至1.0×10⁻⁷M。通过荧光分光光度法还确定了L/Hg的化学计量比为1:1,结合常数K = 66543。L/Hg的竞争实验表明在库阳离子存在下对汞具有高度选择性检测。利用¹H NMR和荧光光谱法提出了一种基于金属离子与L配位和/或抗衡离子形成的检测金属离子的双路径机制。图形摘要:汞与大环配体L相互作用的pH依赖性机制。

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