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首页> 外文期刊>RSC Advances >An efficient non-reaction based colorimetric and fluorescent probe for the highly selective discrimination of Pd-0 and Pd2+ in aqueous media
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An efficient non-reaction based colorimetric and fluorescent probe for the highly selective discrimination of Pd-0 and Pd2+ in aqueous media

机译:基于高效的非反应基于比色和荧光探针,用于在水性介质中的PD-0和PD2 +的高度选择性辨别

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摘要

A novel anthraquinone-imidazole based colorimetric and fluorogenic probe 1 is synthesized, which can discriminate the oxidation states of palladium(Pd-0 and Pd2+) by naked eye with high selectivity in aqueous media owing to the difference in coordination within the right sized pocket of the probe molecule. The experimental results (fluorescence, UV/Vis and H-1 NMR spectroscopy) aided by density functional theory (DFT) calculations reveal that charge transfer (CT) is the main cause of the selective detection of the oxidation states of palladium. In the 1-Pd2+ complex, which is deficient in electrons, all the electron transitions represent electron transfers from the probe molecule to the central metal atom i.e. partial ligand-to-metal transition excitation while electronically filled Pd-0 shows electron transfers from the metal atom to the probe ligand i.e. partial metal-to-ligand transition excitation.
机译:合成了一种新的Anthraquinone-咪唑基比色和荧光探针1,其可以在右尺寸口袋内的协调差异中,在水性培养基中具有高选择性的肉眼偏离钯(PD-0和PD2 +)的氧化状态 探针分子。 通过密度泛函理论(DFT)计算辅助的实验结果(荧光,UV / VI和H-1 NMR光谱)揭示了电荷转移(CT)是钯氧化态的选择性检测的主要原因。 在缺乏电子的1-Pd2 +复合物中,所有电子转变都代表从探针分子到中央金属原子的电子转移,即部分配体 - 金属转变激发,同时电子填充的PD-0显示电子转移来自金属的电子转移 原子到探针配体,即部分金属与配体过渡激发。

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  • 来源
    《RSC Advances 》 |2016年第65期| 共4页
  • 作者单位

    UNIST Dept Chem Ctr Superfunct Mat Ulsan 44919 South Korea;

    UNIST Dept Chem Ctr Superfunct Mat Ulsan 44919 South Korea;

    UNIST Dept Chem Ctr Superfunct Mat Ulsan 44919 South Korea;

    UNIST Dept Chem Ctr Superfunct Mat Ulsan 44919 South Korea;

    UNIST Dept Chem Ctr Superfunct Mat Ulsan 44919 South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
  • 关键词

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