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Electrochemical Investigation of Quinone Complexation by Lewis Acids in a Chloroaluminate Ionic Liquid

机译:氯铝酸盐离子液体中路易斯酸对醌络合的电化学研究

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The electrochemical behavior of 9,10-anthraquinone (AQ) hasbeen investigated in the initially neutral aluminum chloride : 1-ethyl-3-methylimidazolium chloride ionic liquid. It has beenfound that AQ is characterized by a single irreversible redoxprocess in the neutral melt. Additions of AlCl_3 cause a positivepotential shift, first by the formation of two reversible redoxprocesses corresponding to AlCl_3 complexes of AQ under mildlyacidic conditions, and then by the appearance of a shiftedirreversible redox process in an acidic melt. HfCl4 additions causesimilar behavior, except that the reversible systems persist athigher Lewis acid levels than for AlCl_3. At the 11:1 Lewis acid:AQpoint, AQ is still soluble as an orange solution for AlCl_3 additions,but a yellow solid precipitates from a yellow (amber) solution forHfCl4 additions.
机译:9,10-蒽醌(AQ)的电化学行为 在最初的中性氯化铝中进行了研究:1- 乙基-3-甲基咪唑鎓氯化物离子液体。它一直 发现AQ的特征是单一不可逆的氧化还原 在中性熔体中的过程。 AlCl_3的添加导致阳性 势移,首先通过形成两个可逆的氧化还原 轻度下与AQ的AlCl_3配合物相对应的过程 酸性条件下,再由外观转变 在酸性熔体中不可逆的氧化还原过程。 HfCl4添加的原因 类似的行为,除了可逆系统在 的路易斯酸含量比AlCl_3高。在11:1路易斯酸:AQ 因此,对于添加AlCl_3而言,AQ仍可溶解为橙色溶液, 但黄色固体从黄色(琥珀色)溶液中沉淀出来 HfCl4添加。

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