新型含酚羟基酰基探针的合成及其对S2-的比色荧光检测

IF 1.4 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
Xiaohua Cai , Benyue Yao , Mei Han , Le Liang , Xiaohong Li , Yanli Leng
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引用次数: 0

摘要

过量的S2-可导致多种严重的生理疾病,因此快速检测S2-对人类具有重要意义。本文以肼和取代水杨醛为原料,设计并合成了一种简单易探测的新型Y。该方法在高含水溶液(DMSO/H2O, v/v = 1/9)中检测S2-性能良好,添加50倍的S2-后比色和荧光光谱变化明显,其他常见的15种阴离子对检测几乎没有影响。利用荧光滴定数据计算其检出限为3.88 μmol/L,络合常数为3.68×106 L/mol。Job的plot实验表明,宿主与S2-的结合比例为1:1。用核磁共振滴定法验证了识别机理,添加过量的S2-后,2个羟基(- oh)和1个亚胺(- nh)中的3个质子消失,表明探针Y发生了去质子化过程。初步应用实验表明,Y型探针可以探测水样和土壤中的S2-。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis of new phenolic-containing hydroxyacyl probe and its colorimetric fluorescence detection of S2-

Synthesis of new phenolic-containing hydroxyacyl probe and its colorimetric fluorescence detection of S2-
The excessive S2- can lead to a variety of serious physiological diseases, so the quickly detection of S2- is of great significance for human. In this paper, a new simple and easily probe Y was designed and synthesized with hydrazine and substituted salicylaldehyde. It can detect S2- with good performance in a highly water contain solution (DMSO/H2O, v/v = 1/9), both colorimetric and fluorescence spectroscopy have obvious changes after adding 50-folds of S2-, and other common fifteen anions have almost no influence in the detection. The detection limit and complexation constant were calculated using fluorescence titration data to be 3.88 μmol/L and 3.68×106 L/mol, respectively. Job’s plot experiment showed that the binding ratio of the host with S2- is 1:1. The NMR titration was employed to verify the recognition mechanism, three protons in two hydroxyl groups (-OH) and one imine (-NH) are disappeared after adding excessive S2-, which shown that probe Y undergo a deprotonation process. Preliminary application experiments show that probe Y can detect S2- in water samples and soil.
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来源期刊
CiteScore
2.60
自引率
7.70%
发文量
103
审稿时长
2.1 months
期刊介绍: Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.
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