Synthesis, characterization and biological evaluation of methyl dithiocarbonate-acenaphthenequinone (MDTCZ-ACQ) schiff base ligand and its coordination complexes with copper, nickel, zinc, and cobalt
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引用次数: 0
Abstract
This study presents the characterization of a novel Schiff base ligand, methyl dithiocarbonate with acenaphthenequinone (MDTCZ-ACQ), and its coordination complexes with copper (Cu), nickel (Ni), zinc (Zn), and cobalt (Co). The ligand and its metal complexes were synthesized and characterized through techniques such as UV–vis spectroscopy, FTIR, and NMR. Structural analysis indicated a tetrahedral geometry for the metal complexes. The electronic spectrum of the ligand showed a characteristic azomethine group absorption around 282 nm, along with a CS stretch at 1148 cm⁻1, and an N–N group at 1045 cm⁻1. The Schiff base ligand exhibited a strong peak at 1603 cm⁻1, attributed to the ν(CN) bond, suggesting that the dithiocarbazate acenaphthenequinone moiety acts as a bidentate ligand coordinating through azomethine nitrogen and an oxygen atom. Biological investigations demonstrated that the Schiff base complexes showed enhanced activity against Escherichia coli, with a resistance zone of 19 mm, while the copper and zinc complexes exhibited superior antibacterial efficacy compared to nickel and cobalt complexes.
本文研究了一种新型希夫碱配体——苊烯醌二硫代碳酸甲酯(MDTCZ-ACQ)及其与铜(Cu)、镍(Ni)、锌(Zn)和钴(Co)的配位配合物的表征。合成了配体及其金属配合物,并通过紫外可见光谱、红外光谱和核磁共振等技术对其进行了表征。结构分析表明金属配合物呈四面体结构。该配体的电子光谱显示,在282nm处有一个典型的亚甲基吸收基团,在1148 cm - 1处有一个CS延伸,在1045 cm - 1处有一个N-N基团。希夫碱配体在1603 cm - 1处表现出一个很强的峰,这是由ν(CN)键引起的,表明二硫代氨基甲酸酯苊醌部分作为双齿配体通过亚甲基氮和氧原子配位。生物学研究表明,希夫碱配合物对大肠杆菌的抗性增强,抗性区为19 mm,而铜和锌配合物的抗菌效果优于镍和钴配合物。
期刊介绍:
The Journal of the Indian Chemical Society publishes original, fundamental, theorical, experimental research work of highest quality in all areas of chemistry, biochemistry, medicinal chemistry, electrochemistry, agrochemistry, chemical engineering and technology, food chemistry, environmental chemistry, etc.