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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Acylthiourea derivatives as colorimetric sensors for anions: Synthesis, characterization and spectral behaviors
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Acylthiourea derivatives as colorimetric sensors for anions: Synthesis, characterization and spectral behaviors

机译:酰基硫脲衍生物作为阴离子比色传感器:合成,表征和光谱行为

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摘要

Several acylthioureas have been synthesized to develop colorimetric sensors for detection of biologically important anions. UV-vis titration experiments indicated that the absorbance values have a good linear relationship with concentration of anions when the anions were added in AR-1, AR-4 and AR-6 sensor molecules. The detection limit to AcO- and F- is 5 x 10(-6) mol/L when the concentration of receptors are 2 x 10(-5) mol/L. Especially, compounds AR-1 and AR-4, decorated with strong electron-withdrawing NO2 substituent, showed augmented anion sensing properties, being capable of naked-eye detecting of F- and AcO- when the water content is lower than 15%. The recognition details of anion sensing were also assessed using H-1 NMR technique and confirmed that the basic anions induced deprotonation of N-H. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经合成了几种酰基硫脲,以开发用于检测生物学上重要阴离子的比色传感器。 UV-vis滴定实验表明,当在AR-1,AR-4和AR-6传感器分子中添加阴离子时,吸光度值与阴离子浓度具有良好的线性关系。当受体浓度为2 x 10(-5)mol / L时,AcO-和F-的检出限为5 x 10(-6)mol / L。尤其是,装饰有强吸电子NO2取代基的化合物AR-1和AR-4显示出增强的阴离子感测性能,当水含量低于15%时,可以肉眼检测F-和AcO-。阴离子感测的识别细节也使用H-1 NMR技术进行了评估,并证实了碱性阴离子诱导了N-H的去质子化。 (C)2015 Elsevier B.V.保留所有权利。

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