Ghanbari Bahram, Zarepour-Jevinani Morteza
Department of Chemistry, Sharif University of Technology, PO Box 11155-3516, Tehran, Iran.
J Fluoresc. 2017 Jul;27(4):1385-1398. doi: 10.1007/s10895-017-2075-5. Epub 2017 Apr 20.
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.
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。