3.3.2. 1-(邻苯二嗪-1(2H)- 1)[(吡啶-2-基)乙基]腙及其钴(III)配合物的合成、晶体结构和生物活性

F. Majoumo-Mbe, E. Nfor, Eric B. Sengeh, R. N. Njong, O. E. Offiong
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引用次数: 0

摘要

合成了一种新的钴(III)(2)与1-(邻苯二嗪-1(2H)- 1)[(吡啶-2-基)乙基]腙配体(1)的单核配合物,并用元素分析、红外光谱和质谱技术对其进行了表征。用单晶x射线衍射技术测定了自由配体(1)及其配合物(2)的晶体结构。在配合物2中,腙配体通过氮原子以三叉状方式与钴(III)离子螯合,形成八面体,其中钴(II)被氧化为钴(III)。配体1及其配合物2对黑曲霉、黄曲霉和白色念珠菌的抗真菌活性进行了研究。结果表明,与游离配体1相比,配合物2对黑曲霉、黄曲霉和白色念珠菌的抑制区分别为12、11和12 mm,其抑制区分别为14、15和14 mm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
3.3.2. Synthesis, crystal structure and biological activity of 1-(phthalazin-1(2H)-one)[(Pyridin-2-yl)ethylidene]hydrazone and its cobalt (III) complex
A new mononuclear complex of cobalt (III) (2) with 1-(phthalazin-1(2H)-one)[(Pyridin-2-yl) ethylidene] hydrazone ligand ( 1 ) has been synthesized and characterized by elemental analysis, IR and mass spectroscopic techniques. The crystal structures of the free ligand (1) and its complex ( 2 ) have been determined by single crystal X-ray diffraction technique. In complex 2 the hydrazone ligand chelates to the cobalt (III) ion through nitrogen atoms in a tridentate manner, giving an octahedral geometry where the cobalt (II) was oxidized to cobalt (III). The antifungal activity of ligand 1 and its complex 2 was studied against Aspergillus niger , Aspergillus flavus and Candida albicans . The results revealed modest activity of complex 2 against the tested organism with inhibition zones of 14, 15 and 14 mm, compared to the free ligand 1 with the inhibition zones of 12, 11 and 12 mm for A. niger, A. flavus, C. albicans respectively.
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