Synthesis of New Azo–Schiff Base Complexes and Study of their Antibacterial Activity

T. I. Mohammed
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Abstract

In this research, we synthesized new azo-schiff base derivatives (4-9). These derivatives of azo compounds (1-3) that synthesized from 4-ethoxyaniline and drivatives of aldehyde such as, 4-aminobenzaldehyde, 4- hydroxybenzaldehyde and 4-ethoxybenzaldehyse to produce azo compounds (1-3). The compounds (1-3) reacted with differents aldehyde such as, isonicotinic hydrazide to produce N'-[(Z)-{3-[(E)-(4-ethoxyphenyl)diazenyl]-4-subs.phenyl}-methylidene]pyridine-4-carbohydrazide derivatives (4-6) and 3-amino pyridine to produce 2-[(E)-(4-ethoxyphenyl)diazenyl]-4-{(E)-[(pyridin-3-yl)imino]-methyl}subsbenzene derivatives (7-9). These compounds were characterization by spectroscopy methods such as, FTIR and 1HNMR. Some compounds (4, 6 and 9) that synthesized tested as antibacterial via used differents types such as, E. coli, Bacillus subtilis, and S. aureus. The activities of these compounds with different bacteria are known by the excellent diffusion methodology applied and derivative (6) gives a more activites from other derivatives.
新型偶氮席夫碱配合物的合成及其抗菌活性研究
在这项研究中,我们合成了新的偶氮希夫碱衍生物(4-9)。这些偶氮化合物(1-3)的衍生物是由4-乙氧基苯胺和醛的衍生物如4-氨基苯甲醛、4-羟基苯甲醛和4-乙氧基苯甲醛合成的偶氮化合物(1-3)。化合物(1-3)与异烟碱肼等不同醛反应生成N′-[(Z)-{3-[(E)-(4-乙氧基苯基)二氮基]-4-亚基。苯基}-甲基]吡啶-4-碳肼衍生物(4-6)和3-氨基吡啶生成2-[(E)-(4-乙氧基苯基)二氮基]-4-{(E)-[(吡啶-3-基)亚氨基]-甲基}亚苯衍生物(7-9)。用FTIR、1HNMR等光谱方法对化合物进行了表征。合成的一些化合物(4、6和9)通过使用不同的类型,如大肠杆菌、枯草芽孢杆菌和金黄色葡萄球菌,被测试为抗菌。这些化合物与不同细菌的活性是通过应用优秀的扩散方法而已知的,衍生物(6)给出了比其他衍生物更多的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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