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基于芘-四甲基哌啶基(TEMPO)作为自旋荧光探针,通过其对芘荧光的增强效应来高选择性测定亚铁离子。

High selective determination iron(II) by its enhancement effect on the fluorescence of pyrene-tetramethylpiperidinyl (TEMPO) as a spin fluorescence probe.

作者信息

Chen Jin-Long, Zhuo Shu-Juan, Wu Yu-Qing, Fang Fang, Li Ling, Zhu Chang-Qing

机构信息

College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, PR China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):438-43. doi: 10.1016/j.saa.2005.04.057. Epub 2005 Jun 29.

Abstract

A novel fluorescence method determination for iron(II) with a high selectivity and sensitivity has been proposed, based on the enhancement of fluorescence signals resulting from specific redox reaction between synthesized spin fluorescence probe pyrene-tetramethylpiperidinyl (TEMPO) and iron(II). Under the experimental conditions, fluorescent probe displayed a rapid and linear response for iron(II) over the concentration range from 2.4 x 10(-7) to 3.6 x 10(-6) mol/L. The limit of detection was 4.0 x 10(-8) mol/L. The relative standard deviation of six replicate measurements was 1.90% for 3.0 x 10(-7) mol/L iron(II). Because of the specific redox reaction between developed spin fluorescence probe and iron(II), there are few interference by other ions, especially in the presence of relative high concentration iron(III). The method has been successfully applied for iron(II) determinations in two different kinds of real samples. Results determined by the proposed method agree favorably with those determined UV-vis spectrometry method with 1,10-phenanthroline.

摘要

基于合成的自旋荧光探针芘 - 四甲基哌啶基(TEMPO)与铁(II)之间特定氧化还原反应导致的荧光信号增强,提出了一种具有高选择性和灵敏度的测定铁(II)的新型荧光方法。在实验条件下,荧光探针对铁(II)在2.4×10⁻⁷至3.6×10⁻⁶mol/L的浓度范围内呈现快速线性响应。检测限为4.0×10⁻⁸mol/L。对于3.0×10⁻⁷mol/L的铁(II),六次重复测量的相对标准偏差为1.90%。由于所开发的自旋荧光探针与铁(II)之间的特定氧化还原反应,其他离子的干扰很少,特别是在相对高浓度铁(III)存在的情况下。该方法已成功应用于两种不同实际样品中铁(II)的测定。所提出的方法测定结果与用1,10 - 菲啰啉的紫外 - 可见光谱法测定结果吻合良好。

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