SYNTHESIS AND STRUCTURE OF IRON(III) COMPLEX WITH 2-ACETYLPYRIDINE-AMINOGUANIDINE

M. Radanović, Ljiljana S. Vojinović-Ješić, M. Rodić, V. Leovac
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Abstract

Schiff bases represent an interesting class of compounds due to a wide range of possible applications, especially their biological activity. Having in mind that the biological activity of the ligand could be closely related to its coordinating properties, we examined the synthesis and structure of a novel Fe(III) complex with the Schiff base of aminoguanidine and 2-acetylpyridine. Bis(ligand) complex of iron(III), of the formula [Fe(L–H)2]2(NCS)Cl, was obtained by the reaction of FeCl3 and the thiocyanate ligand salt in a mole ratio 1:1 in the presence of lithium-acetate as a deprotonating agent. The complex is obtained in the form of brown single crystals and is characterized by elemental analysis data, conductometric measurements, IR spectra, and X-ray analysis. The latter revealed that the chelating ligand is coordinated in its monoanionic form via pyridine, azomethine, and nitrogen atoms of the aminoguanidine fragment, forming octahedral environment.
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2-乙酰吡啶-氨基胍配合物铁(iii)的合成与结构
希夫碱由于其广泛的应用前景,特别是其生物活性而成为一类有趣的化合物。考虑到配体的生物活性可能与其配位性质密切相关,我们研究了一种新型的含氨基胍和2-乙酰吡啶席夫碱的Fe(III)配合物的合成和结构。在醋酸锂作为去质子剂的情况下,FeCl3与硫氰酸盐以摩尔比1:1的比例反应得到了式为[Fe(L-H)2]2(NCS)Cl的铁(III)二(配体)配合物。该配合物以棕色单晶的形式获得,并通过元素分析数据、电导测量、红外光谱和x射线分析进行了表征。后者揭示了螯合配体通过氨基胍片段的吡啶、亚甲基和氮原子以单阴离子形式配位,形成八面体环境。
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