Oxidation of Arsenous Acid by 12-Tungstocobaltate(III) Catalysed by Ruthenium(III) in Aqueous Acid Medium

B. D. Bhosale, G. Gokavi
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引用次数: 3

Abstract

Ruthenium(III)-catalysed arsenic(III) oxidation by 12-tungstocobaltate(III) was found to proceed with transfer of an electron from catalyst to oxidant generating an intermediate ruthenium(IV). In the next step ruthenium(IV) abstract an electron from arsenic(III) leading to form arsenic(IV), which further reacts with oxidant to give arsenic(V). The active catalyst species was RuCl5(H2O) and due to formation of the inactive higher chloro-complex, RuCl6, inhibition of the reaction occurs as chloride ion concentration increases. There was no effect of hydrogen ion concentration on the reaction due to absence of any protonation equilibria under experimental conditions. The reaction was also catalysed by alkali metal cations due to ion pair formation between 12-tungstocobaltate(III) and alkali metal cations.
酸水溶液中钌催化12-钴酸钨(III)氧化亚砷酸的研究
钌(III)催化砷(III)被12-钨钴酸盐(III)氧化,发现电子从催化剂转移到氧化剂,生成中间钌(IV)。下一步,钌(IV)从砷(III)中提取一个电子,形成砷(IV),砷(IV)进一步与氧化剂反应生成砷(V)。活性催化剂为RuCl5(H2O),由于形成了无活性的高氯络合物RuCl6,随着氯离子浓度的增加,反应发生抑制。在实验条件下,由于没有质子化平衡,氢离子浓度对反应没有影响。由于12-钴酸钨(III)与碱金属阳离子之间形成离子对,碱金属阳离子也催化了反应。
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