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首页> 外文期刊>Journal of chemical crystallography >Synthesis, spectroscopy, in vitro biological activity and X-ray structure of (4-Methylpiperidine-dithiocarbamato-S,S ')triphenyltin(IV)
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Synthesis, spectroscopy, in vitro biological activity and X-ray structure of (4-Methylpiperidine-dithiocarbamato-S,S ')triphenyltin(IV)

机译:(4-甲基哌啶-二硫代氨基甲酸酯-S,S')三苯基锡(IV)的合成,光谱,体外生物学活性和X射线结构

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摘要

(4-Methylpiperidine-dithiocarbamato-S,S')triphenyltin(IV) derivative of 4-methyl-1-piperidine carbodithioic acid (4-MePCDTA) have been synthesized and characterized by elemental, IR, multinuclear NMR (H-1 and C-13) and mass spectrometric studies. The crystal structure of the complex has been determined by X-ray single crystal analysis, which shows unsymmetrical nature of the ligand towards coordination to tin. It crystallizes in monoclinic P21/c space group with the crystal cell parameters: a = 10.1863(10) angstrom, b = 21.200(2) angstrom, c = 11.7332(11) angstrom, beta = 111.2020(10)degrees, Z = 4 and V = 2,362.2(4) angstrom(3). The tin atom is coordinated to the two sulfur atoms of the dithiocarbamate ligand and three carbon atoms of the phenyl groups are in distorted trigonal bipyramid geometry. This complex was tested for its antimicrobial activity against six different plant and human pathogens. The screening results show that the complex exhibit higher antibacterial and antifungal activity than the free ligand.
机译:合成了4-甲基-1-哌啶碳二硫酸(4-MePCDTA)的(4-甲基哌啶-二硫代氨基甲酸酯-S,S')三苯基锡(IV)衍生物,并通过元素红外,多核NMR(H-1和C -13)和质谱研究。配合物的晶体结构已通过X射线单晶分析确定,表明配体对锡的配位具有不对称性。它在具有晶体晶胞参数的单斜P21 / c空间群中结晶:a = 10.1863(10)埃,b = 21.200(2)埃,c = 11.7332(11)埃,beta = 111.2020(10)度,Z = 4 V = 2,362.2(4)埃(3)。锡原子与二硫代氨基甲酸酯配体的两个硫原子配位,苯基的三个碳原子呈扭曲的三角双锥几何形状。测试了该复合物对六种不同植物和人类病原体的抗菌活性。筛选结果表明,该复合物比游离配体具有更高的抗菌和抗真菌活性。

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