Synthesis, crystal structures and antimicrobial activity of dioxidomolybdenum(VI) complexes derived from aroylhydrazones.

IF 1.2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Zhi-Tong Li, Xiao-Jie Wu, Qiong Wu, Yong-Peng Yu, Zhen Cong, Xin-Yu Min, Xin-Yi Du, Zhong-Lu You, Jian Jiang
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引用次数: 0

Abstract

Two new aroylhydrazone compounds (E)-N'-(3-ethoxy-2-hydroxybenzylidene)-3-(trifluoromethyl)benzohydrazide (H2La) and (E)-2-bromo-N'-(3,5-dichloro-2-hydroxybenzylidene)benzohydrazide (H2Lb) were prepared and characterized by 1H NMR spectroscopy. Reaction of the aroylhydrazones with MoO2(acac)2 afforded two new dioxidomolybdenum(VI) complexes with general formula [MoO2L(CH3OH)] (L = La for 1, Lb for 2). The complexes were characterized by IR and UV-Vis spectroscopy. Molecular structures of the aroylhydrazones and two dioxidomolybdenum(VI) complexes were further characterized by single crystal X-ray determination. The aroylhydrazone ligands coordinate to Mo through the phenolate oxygen, imine nitrogen, and enolate oxygen atom. The Mo atom displays a distorted octahedral geometry, with the three donors of the aroylhydrazone ligands and one oxo defining the equatorial plane, and one methanol and the other oxo occupying the axial positions. The effective antimicrobial activity of the compounds against the bacteria strains B. subtilis, S. aureus, E. coli, P. fluorescens and on the fungal strains C. albicans and A. niger was observed.

芳基腙衍生的二氧化钼(VI)配合物的合成、晶体结构和抗菌活性。
制备了两个新的芳基腙化合物(E)- n′-(3-乙氧基-2-羟基苄基)-3-(三氟甲基)苯并肼(H2La)和(E)-2-溴- n′-(3,5-二氯-2-羟基苄基)苯并肼(H2Lb),并用1H NMR对其进行了表征。芳基腙与MoO2(acac)2反应得到两种新的二氧化钼(VI)配合物,其通式为[MoO2L(CH3OH)] (L = La = 1, Lb = 2)。用红外光谱和紫外可见光谱对配合物进行了表征。用单晶x射线进一步表征了芳基腙和两种二氧化钼配合物的分子结构。芳基腙配体通过苯酚氧、亚胺氮和烯醇化氧原子与Mo配位。Mo原子呈现出扭曲的八面体结构,其中三个芳基腙配体的给体和一个氧占据赤道面,一个甲醇和另一个氧占据轴向位置。观察了化合物对枯草芽孢杆菌、金黄色葡萄球菌、大肠杆菌、荧光假单胞菌以及真菌白色念珠菌和黑曲霉的有效抑菌活性。
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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来源期刊
Acta Chimica Slovenica
Acta Chimica Slovenica 化学-化学综合
CiteScore
2.50
自引率
25.00%
发文量
80
审稿时长
1.0 months
期刊介绍: Is an international, peer-reviewed and Open Access journal. It provides a forum for the publication of original scientific research in all fields of chemistry and closely related areas. Reviews, feature, scientific and technical articles, and short communications are welcome.
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