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Ratiometric phosphorescence imaging of Hg(II) in living cells based on a neutral iridium(III) complex

机译:基于中性铱(III)络合物的活细胞中汞(II)的比例荧光成像

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摘要

In this work, a neutral iridium(III) complex [Ir(bt)2(acac)] (Hbt = 2-phenylbenzothiazole; Hacac = acetylacetone) has been realized as a Hg(II)-selective sensor through UV-vis absorption, phosphorescence emission, and electrochemical measurements and was further developed as a phosphorescent agent for monitoring intracellular Hg(II). Upon addition of Hg(II) to a solution of [Ir(bt)_2(acac)], a noticeable spectral blue shift in both absorption and phosphorescent emission bands was measured. 1H NMR spectroscopic titration experiments indicated that coordination of Hg(II) to the complex induces fast decomposition of [Ir(bt)_2(acac)] to form a new complex, which is responsible for the significant variations in optical and electrochemical signals. Importantly, cell imaging experiments have shown that [Ir(bt)_2(acac)] is membrane permeable and can be used to monitor the changes in Hg(II) levels within cells in a ratiometric phosphorescence mode.
机译:在这项工作中,中性铱(III)络合物[Ir(bt)2(acac)](Hbt = 2-苯基苯并噻唑; Hacac =乙酰丙酮)已通过UV-vis吸收作为Hg(II)选择性传感器实现,磷光发射和电化学测量,并被进一步开发为用于监测细胞内Hg(II)的磷光剂。将汞(II)添加到[Ir(bt)_2(acac)]的溶液中后,在吸收和磷光发射带中均测量到明显的光谱蓝移。 1 H NMR光谱滴定实验表明,Hg(II)与配合物的配位诱导了[Ir(bt)_2(acac)]的快速分解,从而形成了新的配合物,这是光学和电化学信号的显着变化的原因。重要的是,细胞成像实验表明,[Ir(bt)_2(acac)]是膜可渗透的,可用于以比例磷光模式监控细胞内Hg(II)水平的变化。

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