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首页> 外文期刊>Bulletin of the Korean Chemical Society >Effect of Transition Metal(¥±)-N,N-Bis(salicylaldehyde)phenylenediimines on the Electrochemical Reduction of Thionyl Chloride
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Effect of Transition Metal(¥±)-N,N-Bis(salicylaldehyde)phenylenediimines on the Electrochemical Reduction of Thionyl Chloride

机译:过渡金属(¥±)-N,N-双(水杨醛)苯二胺对亚硫酰氯电化学还原的影响

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Catalytic effects of transition metal (Co2+, Ni2+) complexes of N,N-bis(salicylaldehyde)-o-phenylenediimine (SOPD), N,N-bis(salicylaldehyde)-m-phenylenediimine (SMPD), and N,N-bis(salicylaldehyde)-p-phenylenediimine (SPPD), on the reduction of thionyl chloride at glassy carbon electrode, are evaluated by determining the kinetic parameters with cyclic voltammetric technique. The charge transfer process for the reduction of thionyl chloride is strongly affected by the concentration of the catalysts. Some quadridentate Schiff base-M(ケ) complexes show sizable catalytic activities for the reduction of thionyl chloride. Catalytic effects of [M(ケ)(SOPD)] complexes are slightly larger compared to [M(ケ)2(SMPD)2] and [M(ケ )2(SPPD)2] complexes. On those electrodes deposited with the catalysts, the observed exchange rate constants (ko) are in the range of 0.89-2.28 】 10-7 cm/s, while it is 1.24 】 10-7 cm/s on the bare glassy carbon electrode.
机译:N,N-双(水杨醛)-邻苯二甲胺(SOPD),N,N-双(水杨醛)-间苯二胺(SMPD)和N,N-双的过渡金属(Co2 +,Ni2 +)络合物的催化作用(水杨醛)-对苯二胺(SPPD)在玻璃碳电极上亚硫酰氯的还原反应中,通过循环伏安法测定动力学参数来进行评估。还原亚硫酰氯的电荷转移过程受催化剂浓度的强烈影响。一些四齿席夫碱-M(ケ)配合物显示出可观的催化活性,可减少亚硫酰氯。与[M(ケ)2(SMPD)2]和[M(ケ)2(SPPD)2]配合物相比,[M(ケ)(SOPD)]配合物的催化作用稍大。在那些沉积有催化剂的电极上,观察到的交换速率常数(ko)在0.89-2.28】10-7 cm / s的范围内,而在裸露的玻璃碳电极上则为1.24)10-7 cm / s。

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