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首页> 外文期刊>RSC Advances >Highly sensitive detection of 2,4,6-trinitrophenol (TNP) based on lysozyme capped CdS quantum dots
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Highly sensitive detection of 2,4,6-trinitrophenol (TNP) based on lysozyme capped CdS quantum dots

机译:基于溶菌酶封端的CdS量子点的高灵敏检测2,4,6-三硝基苯酚(TNP)

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This work presents a novel method for nitroaromatic compound detection using lysozyme-capped CdS quantum dots (Lys-CdS QDs). Cd2+ can react with S2- to generate fluorescent CdS QDs in the presence of lysozyme. The Lys-CdS QDs can bind to 2,4,6-trinitrophenol (TNP) in water via an acid-base pairing interaction between the electron-rich amino ligands and the electron-deficient aromatic ring of TNP. The electrons in the QDs transfer to the TNP molecules, leading to fluorescence quenching. The fluorescence decreases with an increase in TNP concentration and the fluorescence intensity is negatively proportional to the TNP concentration in the range from 0.5 mu mol L-1 to 15 mu mol L-1 with a detection limit of 0.1 mu mol L-1. The newly-developed fluorescence probe shows excellent resistance to the interference of metal ions, such as Cu2+, Fe3+, and Pb2+, when compared with other fluorescence probes. The present method is cost-effective, convenient, and does not require any complicated synthetic procedures.
机译:这项工作提出了使用溶菌酶封端的CdS量子点(Lys-CdS QDs)进行硝基芳香化合物检测的新方法。在溶菌酶的存在下,Cd2 +可以与S2-反应生成荧光CdS QD。 Lys-CdS QD可以通过富电子的氨基配体与TNP的电子缺陷型芳香环之间的酸碱配对作用与水中的2,4,6-三硝基苯酚(TNP)结合。量子点中的电子转移到TNP分子,导致荧光猝灭。荧光随着TNP浓度的增加而降低,并且荧光强度与TNP浓度成反比,范围为0.5μmol L-1至15μmol L-1,检出限为0.1μmol L-1。与其他荧光探针相比,新开发的荧光探针显示出优异的抗金属离子(例如Cu2 +,Fe3 +和Pb2 +)干扰的能力。本方法是成本有效的,方便的,并且不需要任何复杂的合成程序。

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