Synthesis, spectral, DFT and anticancer studies on bis(N-(3-methoxybenzyl)-N-(pyridin-3-ylmethyl)dithiocarbamato-S,S’)M(II) (M= Pd, Pt)

IF 3.2 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Journal of the Indian Chemical Society Pub Date : 2024-09-03 DOI:10.1016/j.jics.2024.101357
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Abstract

We reported synthesis of bis(N-(3-methoxybenzyl)-N-(pyridin-3-ylmethyl)dithiocarbamato-S,S’)M(II) (where M(II) = palladium(II) (1), platinum(II) (2)). Both the complexes were characterized by elemental analysis, FTIR, UV–visible, 1H and 13C NMR spectroscopy. Based on FTIR spectral studies, bidentate coordination of dithiocarbamate ligand was proposed for both complexes. UV–visible spectral data confirm the formation of square planar complexes. The structure properties, frontier molecular orbital (FMO), molecular electrostatic potential (MEP), chemical reactivities and Mulliken charges were investigated using density functional theory (DFT)/B3LYP methods with 6-31+G (d, p) basis sets and LanL2DZ for light atoms and heavy atoms, respectively. FMO and Mulliken charges recognize the chemical active sites of 1 and 2 responsible for its chemical activity. In vitro anticancer activity of complexes 1 and 2 were analyzed on MCF-7 by MTT assay method. Results show that platinum complex 2 has higher activity compared to these of palladium complex 1.

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双(N-(3-甲氧基苄基)-N-(吡啶-3-基甲基)二硫代氨基甲酸-S,S')M(II) (M= Pd, Pt) 的合成、光谱、DFT 和抗癌研究
我们报告了双(N-(3-甲氧基苄基)-N-(吡啶-3-基甲基)二硫代氨基甲酸-S,S')M(II)(其中 M(II) = 钯(II) (1),铂(II) (2))的合成。这两种复合物都通过元素分析、傅立叶变换红外光谱、紫外-可见光谱、1H 和 13C NMR 光谱进行了表征。根据傅立叶变换红外光谱研究,这两种配合物都含有二硫代氨基甲酸配体的双齿配位。紫外-可见光谱数据证实了方形平面配合物的形成。利用密度泛函理论(DFT)/B3LYP 方法,分别用 6-31+G (d, p) 基集和 LanL2DZ 对轻质原子和重质原子进行了结构性质、前沿分子轨道(FMO)、分子静电位(MEP)、化学反应活性和 Mulliken 电荷的研究。FMO 和 Mulliken 电荷识别出了 1 和 2 的化学活性位点,这些位点负责其化学活性。采用 MTT 检测法分析了铂络合物 1 和 2 对 MCF-7 的体外抗癌活性。结果表明,与钯复合物 1 相比,铂复合物 2 具有更高的活性。
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来源期刊
CiteScore
3.50
自引率
7.70%
发文量
492
审稿时长
3-8 weeks
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.
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