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Anthraquinone catalysis in the glucose-driven reduction of indigo to leuco-indigo

机译:蒽醌催化葡萄糖驱动的靛蓝还原为隐色靛蓝

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摘要

Anthraquinone immobilised onto the surface of indigo microcrystals enhances the reductive dissolution of indigo to leuco-indigo. Indigo reduction is driven by glucose in aqueous NaOH and a vibrating gold disc electrode is employed to monitor the increasing leuco-indigo concentration with time. Anthraquinone introduces a strong catalytic effect which is explained by invoking a molecular "wedge effect" during co-intercalation of Na~+ and anthraquinone into the layered indigo crystal structure. The glucose-driven indigo reduction, which is ineffective in 0.1 M NaOH at 65 °C, becomes facile and goes to completion in the presence of anthraquinone catalyst. Electron microscopy of indigo crystals before and after reductive dissolution confirms a delamination mechanism initiated at the edges of the plate-like indigo crystals. Catalysis occurs when the anthraquinone-indigo mixture reaches a molar ratio of 1:400 (at 65 °C; corresponding to 3 μM anthraquinone) with excess of anthraquinone having virtually no effect. A strong temperature effect (with a composite E_A ≈ 120 kJ mol~(-1)) is observed for the reductive dissolution in the presence of anthraquinone. The molar ratio and temperature effects are both consistent with the heterogeneous nature of the anthraquinone catalysis in the aqueous reaction mixture.
机译:固定在靛蓝微晶表面上的蒽醌增强了靛蓝还原为无色-靛蓝的溶解性。靛蓝还原是由NaOH水溶液中的葡萄糖驱动的,振动金盘电极用于监测随着时间的推移,隐色-靛蓝浓度的增加。蒽醌具有很强的催化作用,这可以通过在Na〜+和蒽醌共插入层状靛蓝晶体结构中调用分子“楔效应”来解释。在蒽醌催化剂的存在下,葡萄糖驱动的靛蓝还原反应(在0.1 M NaOH中于65°C时无效)变得容易,并且可以完成。在还原溶解之前和之后,靛蓝晶体的电子显微镜检查证实了在板状靛蓝晶体的边缘开始的分层机制。当蒽醌-靛蓝混合物的摩尔比达到1:400(在65°C时,对应于3μM蒽醌)且过量的蒽醌几乎没有作用时,就会发生催化作用。在蒽醌存在下,还原性溶解观察到强烈的温度效应(复合E_A≈120 kJ mol〜(-1))。摩尔比和温度效应均与水性反应混合物中蒽醌催化的非均相性质一致。

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