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首页> 外文期刊>Journal of Fluorescence >Unsymmetrically Substituted Nickel Triazatetra-Benzcorrole and Phthalocynanine Complexes:Conjugation to Quantum Dots and Applications as Fluorescent 'Turn ON' Sensors
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Unsymmetrically Substituted Nickel Triazatetra-Benzcorrole and Phthalocynanine Complexes:Conjugation to Quantum Dots and Applications as Fluorescent 'Turn ON' Sensors

机译:非对称取代的三氮杂镍-苯甲酰镍和邻苯二甲酰亚胺镍配合物:与量子点的共轭及其在荧光“开启”传感器中的应用

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摘要

We report on the design and application of fluorescent nanoprobes based on the covalent linking of L-glutathione-capped CdSe@ZnS quantum dots (QDs) to newly synthesized unsymmetrically substituted nickel mercaptosuccinic acid triazatetra-benzcorrole (3) and phthalocyanine (4) complexes. Fluorescence quenching of the QDs occurred on conjugation to complexes 3 or 4. The nanoprobes were selectively screened in the presence of different cations and Hg~(2+) showed excellent affinity in "turning ON" the fluorescence of the nanoprobes. Experimental results showed that the sensitivity of QDs-4 towards Hg~(2+) was much higher than that of QDs-3 nanoprobe. Themechanismof reaction has been elucidated based on the ability of Hg~(2+) to coordinate with the sulphur atom of the Ni complex ring and apparently "turn ON" the fluorescence of the linked QDs.
机译:我们报告了基于L-谷胱甘肽封端的CdSe @ ZnS量子点(QDs)与新合成的不对称取代的巯基琥珀酸三氮杂苯并(3)和酞菁(4)配合物的共价连接的荧光纳米探针的设计和应用。 QD的荧光猝灭发生在与配合物3或4结合时。在存在不同阳离子的情况下选择性筛选了纳米探针,Hg〜(2+)在“打开”纳米探针的荧光方面显示出极好的亲和力。实验结果表明,QDs-4对Hg〜(2+)的敏感性远高于QDs-3纳米探针。基于Hg〜(2+)与Ni络合物环的硫原子配位并明显“打开”所连接QD荧光的能力,阐明了反应的机理。

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