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首页> 外文期刊>Journal of Molecular Structure >Nickel(II) and copper(II) complexes of N,N-dialkyl-N '-3-chlorobenzoylthiourea: Synthesis, characterization, crystal structures, Hirshfeld surfaces and antimicrobial activity
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Nickel(II) and copper(II) complexes of N,N-dialkyl-N '-3-chlorobenzoylthiourea: Synthesis, characterization, crystal structures, Hirshfeld surfaces and antimicrobial activity

机译:N,N-二烷基-N'-3-氯苯甲酰硫脲的镍(II)和铜(II)配合物:合成,表征,晶体结构,HIRSHFELD表面和抗微生物活性

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We synthesized four new N,N-dialkyl-N'-3-chlorobenzoylthiourea ligands (Alkyl: Dimethyl, diethyl, di-n-propyl and di-n-butyl) and their metal complexes with copper and nickel atoms. The structure of all synthesized compounds was fully characterized by physicochemical, spectroscopic and single crystal X-ray diffraction analysis techniques. The physical, spectral and analytical data of the newly synthesized metal complexes have shown the formation of 1:2 (metal:ligand) ratio. The benzoylthiourea ligands coordinate with metal atoms through oxygen and sulphur atoms. The metal atoms are in slightly distorted square-planar coordination geometry in Ni(II) or Cu(II) complex. Two oxygen and two sulphur atoms are mutually cis to each other in Ni(II) or Cu(II) complex. The intermolecular contacts in the compounds, which are HL1 and HL3, were examined by Hirshfeld surfaces and fingerprint plots using the data obtained from X-ray single crystal diffraction measurement. Besides these, their antimicrobial activities against Gram-positive bacteria (Bacillus subtilis, Staphylococcus aureus, Streptococcus pyogenes and Enterococcus faecalis) and Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa) and anti yeast activity (Candida glabrata, Candida parapsilosis and Candida albicans) were investigated. This exhibited some promising results towards testing organism. Among all the compounds, Ni(L-1)(2) complex showed high activity against Bacillus subtilis with MIC values at 7.81 mu g/mL. (C) 2018 Elsevier B.V. All rights reserved.
机译:我们合成了四种新的N,N-二烷基-N'-3-氯苯甲酰硫脲配体(烷基:二甲基,二乙基,二丙基和二丁基)及其与铜和镍原子的金属配合物。所有合成化合物的结构通过物理化学,光谱和单晶X射线衍射分析技术完全表征。新合成的金属配合物的物理,光谱和分析数据表明,形成为1:2(金属:配体)比。苯甲酰硫脲配体通过氧气和硫原子与金属原子坐标。金属原子在Ni(II)或Cu(II)复合物中略微扭曲的方形平面配位几何体。在Ni(II)或Cu(II)复合物中,两个氧气和两个硫原子相互顺应彼此。使用从X射线单晶衍射测量获得的数据,通过HIRSHFELD表面和指纹图检查化合物中的分子间触点,即HL1和HL3。除此之外,它们对抗革兰氏阳性细菌的抗菌活性(枯草芽孢杆菌,金黄色葡萄球菌,链球菌和肠球菌粪便)和革兰氏阴性细菌(大肠杆菌和假单胞菌铜绿假单胞菌)和抗酵母活性(念珠菌,念珠菌,念珠菌肺病和念珠菌类念珠菌)被调查了。这展示了一些有前途的测试生物体结果。在所有化合物中,Ni(L-1)(2)复合物在7.81μg/ ml下,麦芽芽孢杆菌对枯草芽孢杆菌进行高活性。 (c)2018年elestvier b.v.保留所有权利。

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