Redox characteristics of Schiff base manganese and cobalt complexes related to water-oxidizing complex of photosynthesis

S. Hotchandani , U. Ozdemir , C. Nasr , S.I. Allakhverdiev , N. Karacan , V.V. Klimov , P.V. Kamat , R. Carpentier
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引用次数: 29

Abstract

In an effort to obtain synthetic analogues of water-oxidizing complex (WOC) of photosystem II (PS II) of plant photosynthesis, a Schiff base manganese and a cobalt complex, employing Niten, a SALEN type ligand, have been prepared. Cyclic and square wave voltammetric measurements have been performed to assess their redox characteristics. Both complexes undergo several reduction processes in cathodic negative potential region at more or less similar potentials. In view of these reductions being independent of the nature of the metal, they are thought to be ligand-localized. Although similar in negative region, a marked difference in the behavior of the complexes is observed in anodic region. While the cobalt complex is electrochemically inactive in the positive potentials up to +1.0 V vs. Ag/AgCl, the manganese complex displays two oxidation waves at +0.25 and +0.5 V vs. Ag/AgCl. The presence of oxidation wave in manganese complex at +0.5 V vs. Ag/AgCl or +0.7 V vs. NHE suggests that this complex can catalyze the oxidation of water and can, thus, simulate the WOC of PS II.

与光合作用水氧化配合物有关的希夫碱锰钴配合物的氧化还原特性
为了合成植物光合作用光系统II (PS II)的水氧化配合物(WOC),采用SALEN型配体Niten制备了一种希夫碱锰钴配合物。循环伏安法和方波伏安法测量已被执行,以评估其氧化还原特性。这两种配合物都在阴极负电位区以或多或少相似的电位经历了多次还原过程。鉴于这些还原与金属的性质无关,它们被认为是配体局部化的。虽然在负区相似,但在阳极区观察到配合物的行为有显着差异。而钴配合物在+1.0 V vs Ag/AgCl的正电位下表现出电化学活性,锰配合物在+0.25 V和+0.5 V vs Ag/AgCl的正电位下表现出两个氧化波。在+0.5 V vs Ag/AgCl或+0.7 V vs NHE条件下,锰配合物中存在氧化波,表明锰配合物可以催化水的氧化,从而可以模拟PS II的WOC。
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