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Highly optically selective and electrochemically active chemosensor for copper (II) based on triazole-linked glucosyl anthraquinone

机译:基于三唑连接的葡糖基蒽醌的铜(II)的高光学选择性和电化学活性化学传感器

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摘要

A novel triazole-linked acetyl-β-N-glucosyl anthraquinone 1 was conveniently synthesized through one-step click chemistry. The functionalized glycoconjugate (1) exhibited a remarkable blue shift absorption and quenching fluorescence in the presence of trace amounts of Cu~(2+), presumably attributable to intramolecular charge transfer (ICT), which also displayed high selectivity over a series of other metal cations tested in acetonitrile. The result yielded by fluorescence spectroscopy titration suggested a 2:1 ligand-to-metal complex which was further demonstrated by NMR spectroscopy titration. Moreover, the addition of Cu~(2+) to 1 also significantly altered its electrochemical behavior which was reflected via differential pulse voltammetry (DPV) measurements. Such optically and electrochemically detectable metal-mediated sugar derivatives could be further used as biosensors for the recognition of multivalent carbohydrate-protein interactions.
机译:通过一步点击化学反应方便地合成了新型的三唑连接的乙酰基-β-N-葡萄糖基蒽醌1。功能化的糖缀合物(1)在痕量Cu〜(2+)的存在下表现出显着的蓝移吸收和猝灭荧光,可能归因于分子内电荷转移(ICT),它对一系列其他金属也具有高选择性阳离子在乙腈中测试。荧光光谱滴定产生的结果表明2:1的配体与金属的络合物,这可以通过NMR光谱滴定进一步证明。此外,向1中添加Cu〜(2+)还显着改变了其电化学行为,这通过差分脉冲伏安法(DPV)测量得到反映。这样的光学和电化学可检测的金属介导的糖衍生物可以进一步用作生物传感器,以识别多价碳水化合物-蛋白质相互作用。

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