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Syntheses, crystal structures, and electrochemical characterizations of two octahedral iron(III) complexes with Schiff base of pyridoxal and aminoguanidine

机译:具有吡ido醛和氨基胍的席夫碱的两种八面体铁(III)配合物的合成,晶体结构和电化学表征

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This article presents the synthesis, physico-chemical, in particular voltammetric, characteristics of two iron(III) complexes with pyridoxal aminoguanidine (PLAG), [Fe(PLAG)Cl_2(H_2O)]Cl (1) and [Fe(PLAG)_2](NO_3)_3 (2). As expected, the zwitterion of the chelate ligand is coordinated tridentate through oxygen of phenol and nitrogen atoms of azomethine and imino groups of the aminoguanidine fragment. In both complexes, Fe(III) is distorted octahedral. [Fe(PLAG)2](NO_3)_3 (2) is the first bis(ligand) complex with this ligand. Cyclic voltammetric characteristics of the ligand and complexes were studied in DMF in the presence of TBAP or LiCl as supporting electrolytes. The complexes are unstable in this solvent, especially in the presence of an excess of chloride, thus forming several reducible species whose stabilities and behaviors were characterized.
机译:本文介绍了具有吡ido醛氨基胍(PLAG),[Fe(PLAG)Cl_2(H_2O)] Cl(1)和[Fe(PLAG)_2]的两种铁(III)配合物的合成,物理化学,特别是伏安特性。 ](NO_3)_3(2)。如所预期的,螯合配体的两性离子通过苯酚的氧和偶氮甲碱的氮原子和氨基胍片段的亚氨基配位成三齿。在两种络合物中,Fe(III)都是八面体扭曲的。 [Fe(PLAG)2](NO_3)_3(2)是具有该配体的第一个双(配体)配合物。在TBAP或LiCl作为支持电解质的情况下,在DMF中研究了配体和配合物的循环伏安特性。络合物在该溶剂中不稳定,尤其是在过量氯化物的存在下,因此形成了几种可还原的物质,其稳定性和行为得到了表征。

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