新取代恶唑硫代氨基脲配体及其Co (II)和Ni (II)配合物的合成、结构表征和抗菌活性

M. M. Mohammed, M. B. Hussein, Y. Sulfab, Abdelwahab Abuelgasim Mohammed Adam
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摘要

合成了新配体5-甲基-2-(2-噻吩基)-1,3-恶唑-4-甲醛硫代氨基脲(HL)(1)。该配体与Co(II)和Ni(II)氯化物以1:2的比例反应:配体产生两个配合物,[Co(LH)]Cl2(2)和[Ni(HL)2]Cl2(3)。用光谱技术对配体及其金属(II)配合物进行了表征。x射线结构研究表明,两种配合物中游离配体均以硫酮形式存在,并与NNS供体原子保持中性三叉构型,同时配合物晶格空腔中存在不配位的氯离子。在配合物(2)中,其中一种氯化物与配体胺的一个质子成氢键。而在配合物(3)中,氯与亚胺(-N2H)的质子键合,配位环境呈扭曲的八面体。两个配合物中的恶唑N和S原子是顺式的,而亚甲基N原子是反式配位的。该配体及其金属配合物在100 μ g/ml浓度下对6种标准微生物进行了体外生物活性测试:2种革兰氏阳性菌(枯草芽孢杆菌和黄体微球菌)、1种革兰氏阴性菌(大肠杆菌)和3种真菌(酿酒酵母、毛霉和黑曲霉)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Structural Characterization and Antimicrobial Activity of New Substituted Oxazole Thiosemicarbazone Ligand and its Co (II) and Ni (II) Complexes
The New ligand 5-methyl-2-(2-thienyl)-1,3-oxazole-4-carbaldehyde thiosemicarbazone (HL)(1) was synthesized. This ligand reacted with Co(II) and Ni(II) chloride in ratio 1:2 metal:ligand afforded two complexes, [Co(LH)]Cl2 (2) and [Ni(HL)2]Cl2 (3). The ligand and its metal (II) complexes have been characterized by spectroscopic techniques. The X-ray structural studies revealed that the free ligand exist in thione form and remain as neutral tridentate with NNS donor atoms in the tow complexes beside presence of uncoordinated chloride ions in the cavities of the crystal lattice of the complexes. One of these chlorides in complex (2) is hydrogen bonded to a proton of the amine of the ligand. While in complex (3) the chloride bonded to proton of imine (-N2H) of the ligand and the coordination environment has a distorted octahedral. The oxazole N and S atoms in the two complexes are cis to each other whereas the azomethine N atoms are trans coordinated. The ligand and its metal complexes were tested for their in vitro biological activity against six standard microorganisms: two Gram positive namely Bacillus subtilis and Micrococcus luteus, and one Gram negative bacteria Escherichia coli and three fungi: Saccharomyces cerevisiae (Baker’s yeast), Mucor spec., and Aspergillus niger, at a concentration 100µg/ml.
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