基于一种酰腙和咪唑配体的铜(Ⅱ)、镍(Ⅱ)配合物的水热合成、晶体结构及体外抗癌活性
Syntheses, Crystal Structures and in Vitro Antitumor Activities of Copper(Ⅱ) and Nickel(Ⅱ) Complexes Based on Acylhydrazone and Imidazole Ligands
作者单位E-mail
高平章 泉州师范学院化工与材料学院, 泉州 362000  
陈雅心 泉州师范学院化工与材料学院, 泉州 362000  
郑敏敏 泉州师范学院化工与材料学院, 泉州 362000  
王景梅 泉州师范学院化工与材料学院, 泉州 362000  
解庆范 泉州师范学院化工与材料学院, 泉州 362000  
陈延民 泉州师范学院化工与材料学院, 泉州 362000 qzucym@163.com 
摘要: 采用水热法合成了5-硝基水杨醛缩噻吩-2-甲酰腙的铜和镍配合物[Cu(Him)L]21)和[Ni(Him)L](2)(H2L=5-硝基水杨醛缩噻吩-2-甲酰腙,Him=咪唑)并经元素分析、红外光谱和紫外光谱表征。X射线单晶衍射分析表明,1的晶体属单斜晶系,空间群P21/c,晶胞参数:a=1.135 68(12)nm,b=0.770 45(8)nm,c=2.140 4(2)nm,β=97.405(3)°。2的晶体属三斜晶系,空间群P1,晶胞参数:a=0.726 91(4)nm,b=0.976 34(6)nm,c=1.265 74(8)nm,α=79.533(2)°,β=82.862(2)°,γ=68.985(2)°。1是中心对称的双核配合物,Cu(Ⅱ)处于四方锥配位环境;2是单核配合物,Ni(Ⅱ)处于平面四边形的配位环境。化合物1通过N-H…O氢键形成一维超分子链,而化合物2通过N-H…O和C-H…O氢键形成二维超分子网络。初步研究了配体和配合物的体外抗癌活性。结果表明,配合物12对人肝癌细胞HEPG2和人结肠癌细胞SW620均有较强的增殖抑制作用。
关键词: 酰腙  配合物  晶体结构  抗癌活性
基金项目: 泉州师范学院学科建设资金和福建省大学生创新创业训练计划项目(No.201510399025,201510399030)资助。
Abstract: Two new complexes[Cu(Him)L]2 (1) and [Ni(Him)L] (2), where H2L is 2-thiophenecarboxylic acid (2-hydroxly-5-nitro-benzylidene)-hydrazide and Him is imidazole, were synthesized by hydrothermal reaction and characterized by elemental analysis, FT-IR and electronic spectra. The structure of complexes has been accomplished by single crystal X-ray diffraction which results confirmed that the crystal of 1 belongs to the monoclinic system,space group P21/c with cell parameters:a=1.135 68(12) nm, b=0.770 45(8) nm, c=2.140 4(2) nm, β=97.405(3)° and the crystal of 2 belongs to the triclinic system, space group P1 with cell parameters:a=0.726 91(4) nm, b=0.976 34(6) nm, c=1.265 74(8) nm, α=79.533(2)°, β=82.862(2)°, γ=68.985(2)°. The X-ray analyses revealed that 1 displays a centrosymmetric binuclear structure with the Cu atoms in square pyramidal coordination. The binuclear units are further linked by hydrogen bonds to generate an infinite 1D chain. The mononuclear units in 2 are linked through weak N-H…O and C-H…O hydrogen bonds to form an infinite 2D network. The in vitro antitumor activities of ligand and complexes were tested by MTT method, which results show that 1 and 2 have strong in vitro antitumor activity against HEPG2 and SW620 cancer cells lines. CCDC:1041671, 1; CCDC 1041672, 2.
Keywords: acylhydrazone  complex  crystal structure  antitumor activity
投稿时间:2016-05-02 修订日期:2016-06-17
摘要点击次数:  1999
全文下载次数:  1976
高平章,陈雅心,郑敏敏,王景梅,解庆范,陈延民.基于一种酰腙和咪唑配体的铜(Ⅱ)、镍(Ⅱ)配合物的水热合成、晶体结构及体外抗癌活性[J].无机化学学报,2016,32(9):1572-1578.
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