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合成并通过单晶衍射、元素分析及红外光谱表征了配合物[NiL_2](1),[Zn(HL)_2](NO_3)_2(2),[Cd(HL)_2](NO_3)_2(3),[Cu_2L_2(NO_3)_2](4)和[Cu_2(L)_2(SO_4)]·4CH_3OH (5)的结构(HL为2-乙酰-3-甲基吡嗪-缩N-乙基氨基硫脲)。单晶衍射结果表明,配合物1中,Ni(Ⅱ)离子中心与2个脱氢的缩氨基硫脲配体中的N_2S供体配位,形成扭曲的八面体配位构型。在配合物2和3中,中心Zn(Ⅱ)和Cd(Ⅱ)离子与配合物1中Ni(Ⅱ)离子配位构型相同,但缩氨基硫脲为三齿中性配体。而配合物4和5中均存在双核的Cu_2S_2中心,每个Cu(Ⅱ)均采取扭曲的四方锥配位构型,所不同的是外轴向配位点分别由单齿配位的硝酸根和μ_2-桥联的硫酸根所占据。此外,荧光光谱表明配合物1~5与DNA的相互作用强于配体。 相似文献
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2,4-二羟基苯乙酮缩氨基硫脲及其金属配合物的合成与性质 总被引:5,自引:0,他引:5
2,4-dihydroxyacetophenone thiosemicarbanzone and their complexes of copper(Ⅱ), nickel(Ⅱ) and cobalt(Ⅱ) have been synthesized and characterized by elemental analysis, electronic absorption spectrum, Infro-Red spectrum, molar conductizity and magnetic susce 相似文献
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糠醛缩氨基硫脲合镍配合物的合成、晶体结构及表征 总被引:1,自引:0,他引:1
合成了糠醛缩氨基硫脲的Ni(Ⅱ)单核配合物,通过红外光谱、紫外光谱、X射线单晶衍射和热重-差热分析等手段对其结构进行了表征.单晶结构解析结果表明,标题化合物属于三方晶系,R3-空间群,晶胞参数为:a=1.4097(1)nm,b=1.4097(1)nm,c=2.0952(2)nm,α=90°,β=90°,γ=120°,V=3.6059(4)nm3,Z=9,Dc=1.638Mg/m3,μ=1.488mm-1,F(000)=1818,R1=0.0231,wR2=0.0619.配合物中镍离子采用4配位的平面正方形配位构型,晶体堆积中通过分子间氢键形成三维网状结构. 相似文献
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以往合成芳香醛、酮缩氨基硫脲及其金属配合物多用乙醇作溶剂;电化学氧化法直接合成金属配合物操作简单收率高,还可以得到其它经典方法难以得到的低价金属化合物。本文以金属钛、镍、铜为阳极,2-氯苯甲醛单缩二氨基硫脲为配体,用电化学方法合成了配合物,并探讨电化学反应机理及产物的组成。1 实验部分1.1 仪器与试剂岛津-440型红外分光光度计(KBr压片,4000-300cm 1);XT-4型显微熔点仪;PE-2400型元素分析仪;岛津UV-240紫外可见分光光度计;国产DDS-11A型电导率仪(DMF,25℃);CTP-F82型法拉第磁天平(上海华师科教仪… 相似文献
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Four transition metal(II) complexes with podophyllic acid hydrazide (HL) were prepared and characterized by elemental analysis,
complexometric titration, thermal analysis, conductivity, IR, and 1H NMR. The complexes have the general formula ML2 · nH2O, where M = Zn, Cu, Co, and Ni, n = 2 or 0. Anti-tumor activities of podophyllotoxin, HL, ZnL2 · 2H2O, and NiL2 were tested by both the MTT and the SRB method. The results show that the activities of the complexes against the tumor cells
tested are superior to HL and the anti-tumor activity of NiL2 is even similar to that of podophyllotoxin. 相似文献
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In this work, we aimed to synthesize and characterize a novel tetra-directional ligand, (2E,2′E)-2,2′-((((2-(1,3-bis(4-((E)-(2-carbamothioylhydrazono)methyl)phenoxy)propan-2-ylidene)propane-1,3-diyl)bis(oxy))bis(4,1-phenylene))bis(methanylylidene))bis(hydrazinecarbothioamide) (5), including thiosemicarbazone group and its novel tetra-directional-tetra-nuclear Schiff base complexes. For this purpose, we used 1,4-dibromo-2,3-bis(bromomethyl)but-2-ene (2) as starting material. 4,4′-((2-(1,3-Bis(4-formylphenoxy)propan-2-ylidene)propane-1,3-diyl) bis(oxy))dibenzaldehyde (3) was synthesized by the reaction of an equivalent 1,4-dibromo-2,3-bis(bromomethyl)but-2-ene (2) and 4 equivalents of 4-hydroxybenzaldehyde. Then, compound 5 was synthesized in high yield (86%) by a condensation reaction of compound 3 with thiosemicarbazide (4). Finally, four novel tetra-nuclear Cr(III) or Fe(III) complexes of compound 5 were synthesized. The synthesized compounds were characterized using elemental analyses, 1H NMR, Fourier transform–infrared spectrometry, liquid chromatography–mass spectrometry (ESI+), and thermal analyses. The metal ratios of the prepared complexes were determined using an atomic absorption spectrophotometer. We also investigated their effects on the magnetic behaviors of [salen, salophen, Cr(III)/Fe(III)] capped complexes. The complexes were found to be low-spin distorted octahedral Fe(III) and distorted octahedral Cr(III), all bridged by thiosemicarbazone. 相似文献
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Coordination compounds of Mn (II), Fe (III), Co (II), Ni (II), Cu (II) and Cd (II) ions were synthesized from reaction with Schiff base ligand 4,6‐bis((E)‐(2‐(pyridin‐2‐yl)ethylidene)amino)pyrimidine‐2‐thiol (HL) derived from the condensation of 4,6‐diaminopyrimidine‐2‐thiol and 2‐(pyridin‐2‐yl)acetaldehyde. Microanalytical data, magnetic susceptibility, infrared and 1H NMR spectroscopies, mass spectrometry, molar conductance, powder X‐ray diffraction and thermal decomposition measurements were used to determine the structure of the prepared complexes. It was found that the coordination between metal ions and bis‐Schiff base ligand was in a molar ratio of 1:1, with formula [M (HL)(H2O)2] Xn (M = Mn (II), Co (II), Ni (II), Cu (II) and Cd (II), n = 2; Fe (III), n = 3). Diffuse reflectance spectra and magnetic susceptibility measurements suggested an octahedral geometry for the complexes. The coordination between bis‐Schiff base ligand and metal ions was through NNNN donor sites in a tetradentate manner. After preparation of the complexes, biological studies were conducted using Gram‐positive (B. subtilis and S. aureus) and Gram‐negative (E. coli and P. aeruginosa) organisms. Metal complexes and ligand displayed acceptable microbial activity against both types of bacteria. 相似文献
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A new Schiff base ligand (HL) was prepared via a condensation reaction of quinoline‐2‐carboxaldhyde with 2‐aminophenol in a molar ratio of 1:1. Its transition metal mixed ligand complexes with 1,10‐phenanthroline (1,10‐phen) as co‐ligand were also synthesized in a 1:1:1 ratio. HL and its mixed ligand complexes were characterized using elemental analysis, infrared, 1H NMR, mass and UV–visible spectroscopies, molar conductance, magnetic measurements, solid reflectance, thermal analysis, electron spin resonance and X‐ray diffraction. Molar conductance measurements showed that all complexes have an electrolytic nature, except Cd(II) complex. From elemental and spectral data, the formulae [M(L)(1,10‐phen)(H2O)]Clx?nH2O (where M = Cr(III) (x = n = 2), Mn(II) and Ni(II) (x = 1, n = 2), Fe(III) (x = n = 2), Co(II), Cu(II) and Zn(II) (x = 1, n = 2)) and [Cd(L)(1,10‐phen)Cl]?3H2O for the metal complexes have been proposed. The geometric structures of complexes were found to be octahedral. Powder X‐ray diffraction reflected the crystalline nature of the complexes; however, the Schiff base is amorphous. HL and its mixed ligand complexes were screened against Gram‐positive bacteria (Streptococcus pneumoniae and Bacillus subtilis) and Gram‐negative bacteria (Pseudomonas aeruginosa and Escherichia coli). Antifungal activity was determined against Aspergillus fumigatus and Candida albicans, the data showing that most complexes had activity less than that of the Schiff base while Mn(II), Fe(III) and Ni(II) complexes showed no significant antifungal activity. The anticancer activity of HL and its metal complexes was also studied against breast and colon cell lines. The metal complexes showed IC50 higher than that of HL, especially the Cu(II) complex which showed the highest IC50 against breast cell line. 相似文献
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Formation of nitrogen ligated complexes of types NiL6X2, NiL4X2, NiL2X2 and NiL1X2 (whereL=pyridine, 2-, 3- and 4-methyl-pyridine andX=F, Cl, Br, I) have been studied by traditional preparative methods, i.e. from solutions and by solid-gas phase chemisorption. Quaternary mixed complexes were obtained by chemisorption from heated intermediates. The complexes thus formed were further analysed by simultaneous TG-DTG-DTA. Effects of the ligands on stoichiometry and thermal properties of the complexes are discussed. 相似文献
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New metal based triazoles (1–12) have been synthesized by the interaction of novel Schiff base ligands (L1–L3) with the Co(II), Ni(II), Cu(II) and Zn(II) metal ions. The Schiff base ligands and their all metal(II) complexes have been thoroughly characterized using various physical, analytical and spectroscopic techniques. In vitro bacterial and fungal inhibition studies were carried out to examine the antibacterial and antifungal profile of the Schiff bases in comparison to their metal(II) complexes against two Gram‐positive, four Gram‐negative and six fungal strains. The bioactivity data showed the metal(II) complexes to have more potent antibacterial and antifungal activity than their uncomplexed parent Schiff bases against one or more bacterial and fungal species. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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L. I. Denisovich M. G. Peterleitner A. A. Stepanov S. M. Peregudova 《Russian Chemical Bulletin》2000,49(2):375-377
The electrochemical synthesis of δ-fluoroacyl complexes [M]-δ-CORf(M=C5H5(CO)3W or (CO)5Mn; Rf=CF3 or C4F9) was performed according to two procedures: (1) the preliminary electrochemical synthesis of [M]− from [M]2 followed by reaction with a fluorine-containing compound and (2) the electrochemical synthesis of [M]− in the presence of a fluorine-containing compound. Trifluoroacetic anhydride was demonstrated to be the best acylating agent
in these reactions. The electrochemical properties of the resulting complexes were studied.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 373–375, February, 2000. 相似文献
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《Journal of Coordination Chemistry》2012,65(4):700-712
A new azohydrazone, 2-hydroxy-N′-2-hydroxy-5-(phenyldiazenyl)benzohydrazide (H3L) and its copper(II), nickel(II), cobalt(II), manganese(II), zinc(II), cadmium(II), mercury(II), vanadyl(II), uranyl(II), iron(III), and ruthenium(III) complexes have been prepared and characterized by elemental and thermal analyses as well as spectroscopic techniques (1H-NMR, IR, UV-Vis, ESR), magnetic, and conductivity measurements. Spectral data showed a neutral bidentate, monobasic bidentate, monobasic tridentate, and dibasic tridentate bonding to metal ions via the carbonyl oxygen in ketonic or enolic form, azomethine nitrogen, and/or deprotonated phenolic hydroxyl oxygen. ESR spectra of solid vanadyl(II) complex (2), copper(II) complexes (3–5), and (7) and manganese(II) complex (10) at room temperature show isotropic spectra, while copper(II) complex (6) shows axial symmetry with covalent character. Biological results show that the ligand is biologically inactive but the complexes exhibit mild effect on Gram positive bacteria (Bacillus subtilis), some octahedral complexes exhibit moderate effect on Gram negative bacteria (Escherichia coli), and VO(II), Cd(II), UO(II), and Hg(II) complexes show higher effect on Fungus (Aspergillus niger). When compared to previous results, metal complexes of this hydrazone have a mild effect on microorganisms due to the presence of the azo group. 相似文献