首页> 外文期刊>Inorganica Chimica Acta >Structural investigation of discrete solvent protonated vanadium and other transition metal complexes of N '-[(E)-(3-ethoxy-2-hydroxyphenyl) methylidene] benzohydrazide, synthetic, spectroscopic and cytotoxicity studies
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Structural investigation of discrete solvent protonated vanadium and other transition metal complexes of N '-[(E)-(3-ethoxy-2-hydroxyphenyl) methylidene] benzohydrazide, synthetic, spectroscopic and cytotoxicity studies

机译:N' - (E) - (e) - (e) - (3-乙氧基-2-羟基苯基)亚苯肼,合成,光谱和细胞毒性研究的离散溶剂质子钒和其他过渡金属配合物的结构研究

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摘要

A new ligand 3-ethoxysalicylaldehyde benzoic hydrazone (H2ESB) and its copper(II), nickel(II), cobalt(II), zinc (II), and dioxidovanadium(V) complexes have been synthesized and characterized by elemental analysis, IR, UV-Vis and EPR studies. Copper(II) complex (2) contains 2,2'-bipyridine as a coligand. Aroyl hydrazone and its copper and vanadium complexes were characterised by single crystal XRD. The vanadium compound crystallized in triclinic space group P (1) over bar and copper compound in orthorhombic space group P2(1)2(1)2(1). The solvent molecule DMF protonates to form ammonium ion in vanadium complex which neutralises the charge on the vanadium ion. Both complexes copper and vanadium show distorted square pyramidal geometry. From EPR results, spin Hamiltonian and bonding parameters were calculated. The g values in copper complexes indicate the presence of the unpaired electron in the d(x2-y2) orbital. In vitro cytotoxicity studies of aroylhydrazone and its complexes showed that copper, cobalt and vanadium complexes are more cytotoxic than hydrazone and other complexes against Dalton's lymphoma ascites cells (DLA).
机译:已经合成了一种新的配体3-乙醇钠亚甲醛(H2ESB)及其铜(II),镍(II),锌(II),锌(II)和二氧化维蒽铵(V)配合物,并通过元素分析IR,紫外线和EPR研究。铜(II)络合物(2)含有2,2'-硼啶作为Coligand。通过单晶XRD表征芳酰腙及其铜和钒络合物。在正交空间组P2(1)2(1)2(1)中,在三级空间组P(1)中结晶的钒化合物。溶剂分子DMF质子酸盐在钒络合物中形成铵离子,其在钒离子上中和电荷。复合物铜和钒都显示出扭曲的方形金字塔型几何形状。从EPR结果,计算旋转哈密尔顿和键合参数。铜复合物中的G值表明D(X2-Y2)轨道中未配对的电子存在。体外细胞毒性研究的芳酰肼及其复合物表明,铜,钴和钒络合物比腙和对阵Dalton淋巴瘤腹水细胞(DLA)的其他复合物更具细胞毒性。

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