首页> 外文期刊>International Journal of Electrochemical Science >Electrocatalytical reduction of bromocyclopentane and iodobenzene using Cobalt(III) and Nickel(II) Tris- and Bis- bidentates Schiff Bases Complexes
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Electrocatalytical reduction of bromocyclopentane and iodobenzene using Cobalt(III) and Nickel(II) Tris- and Bis- bidentates Schiff Bases Complexes

机译:三(钴)和镍(二)三齿和双齿席夫碱配合物对溴环戊烷和碘苯的电催化还原

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The following bidentate Schiff base: 2-[(4-Methoxybenzyl)iminomethyl]-phenol (HL), was employedas an asymmetric ligand in the synthesis of two mononuclear nickel(II) and cobalt(III) complexes(Ni(II)-2L and Co(III)-3L). This ligand has been synthesized via condensation of salicylaldehyde and4-methoxybenzylamine in methanolic solution, while the both complexes result from complexation ofmetal(II) chloride hydrate salts with HL. These coordination compounds were structurallycharacterized by elemental analysis, FT-IR, UV-Vis, 1H NMR and 13C NMR spectral studies.Moreover, the electrochemical properties of both complexes were studied by cyclic voltammetry inDMF solution containing 0.1 M tetra-n-butylammonium tetrafluoroborate (Et4NBF4). This studyreveals that each complex showed successively two redox couples: M(III)/M(II) and M(II)/M(I).Finally, the electrocatalytic activity of these complexes has been examined and it has been found thatthe both complexes worked as effective homogeneous electrocatalysts for the electroreduction ofbromocyclopentane and iodobenzene using glassy carbon as working electrode.
机译:以下双齿席夫碱:2-[(4-甲氧基苄基)亚氨基甲基]-苯酚(HL),在两个单核镍(II)和钴(III)配合物(Ni(II)-2L)的合成中用作不对称配体和Co(III)-3L)。该配体是通过水杨醛和4-甲氧基苄胺在甲醇溶液中的缩合反应合成的,而这两种配合物都是由氯化金属(II)水合物盐与HL的络合产生的。通过元素分析,FT-IR,UV-Vis,1H NMR和13C NMR光谱研究对这些配位化合物进行结构表征。此外,在含0.1 M四正丁基四氟硼酸铵(DMF)的DMF溶液中,通过循环伏安法研究了两种配合物的电化学性质。 Et4NBF4)。这项研究表明,每个配合物依次显示出两个氧化还原对:M(III)/ M(II)和M(II)/ M(I)。最后,研究了这些配合物的电催化活性,发现这两种配合物作为使用玻璃碳作为工作电极的溴环戊烷和碘苯电还原的有效均相电催化剂。

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