首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Self-enhanced electrogenerated chemiluminescence of ruthenium(II) complexes conjugated with Schiff bases
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Self-enhanced electrogenerated chemiluminescence of ruthenium(II) complexes conjugated with Schiff bases

机译:与席夫碱偶联的钌(II)配合物的自增强电致化学发光

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摘要

In this work, we obtain two ruthenium(II) complexes with Schiff base cavities that exhibit significantly enhanced electrochemiluminescence (ECL) intensity and quantum efficiency due to Ru(bpy)(3)(2+) in aqueous solution, without the addition of tri-n-propylamine (TPrA). The great increase in ECL intensity is confirmed to be due to the electrochemical oxidation of phenolic hydroxyl groups and the resonant structure of imino radicals. Thus, the electrons are transferred intramolecularly to the Ru(III) center, leading to efficient generation of the excited state of Ru(II)*. Subsequently, we find that Co2+ bonding with the salen cavity can selectively and quickly quench the ECL signal. Furthermore, we study the mechanism of the process by which Co2+ hinders the oxidation of phenolic groups and blocks the electron transfer from imino radicals to the Ru center. Thus, a highly sensitive and selective ECL probe for the recognition of Co2+ was developed with a stable response over a concentration range of 0.9 mu M to 6.3 mu M and a detection limit as low as 21 nM.
机译:在这项工作中,我们获得了两个具有席夫碱腔的钌(II)配合物,由于Ru(bpy)(3)(2+)在水溶液中的存在而没有添加三价锡,它们的电化学发光(ECL)强度和量子效率显着提高。 -正丙胺(TPrA)。证实ECL强度的极大提高是由于酚羟基的电化学氧化和亚氨基自由基的共振结构。因此,电子被分子内转移到Ru(III)中心,从而导致Ru(II)*激发态的有效产生。随后,我们发现与Salen腔的Co2 +键可选择性且快速地消除ECL信号。此外,我们研究了Co2 +阻止酚基氧化并阻止电子从亚氨基自由基转移到Ru中心的过程机理。因此,开发出了一种用于识别Co2 +的高灵敏度,选择性ECL探针,该探针在0.9μM至6.3μM的浓度范围内具有稳定的响应,检测限低至21 nM。

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