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1.
Zhen‐Guo Zhao Xiao‐Yuan Wu Quan‐Guo Zhai Li‐Juan Chen Quan‐Zheng Zhang Wei Li Yi‐Ming Xie Can‐Zhong Lu 《无机化学与普通化学杂志》2008,634(2):288-294
Three new nickel(II) complexes constructed with N‐(2‐hydroxybenzyl)‐β‐alanine (H2L), namely [NiL(phen)H2O]·H2O ( 1 ) (phen = 1.10‐phenanthroline), [Ni4L4(H2O)4]·5H2O ( 2 ) and K[Ni4L4(NCS)(H2O)5]·5.42H2O ( 3 ) have been synthesized and characterized by single‐crystal X‐ray diffraction analysis. Complex 1 exhibits a discrete structure, and the structures are bound together through hydrogen bonding to a one‐dimensional chain in ladder‐like fashion. Complexes 2 and 3 contain similar [Ni4(μ2‐O)6] cores with “zig‐zig” arrangement. In complex 3 , the tetranuclear nickel units [Ni4L4(H2O)4] and [Ni4L4(NCS)(H2O)] are alternately bridged by potassium atoms to a one‐dimensional chain. The neighboring chains are further linked up by {K2O2} units to a two‐dimensional layer structure. Moreover, the IR, XRD, TGA and the temperature‐dependent magnetic susceptibility for 2 and 3 have also been studied. 相似文献
2.
合成了2个含三齿Schiff碱配体和单齿N-杂环分子的多核过渡金属配合物:1个含5-氯水杨醛缩对硝基苯甲酰腙(H2L1)和吗啡啉(Mf)的镍髤配合物[Ni(L1)(Mf)](1),1个含5-氯水杨醛缩水杨酰腙(H2L2)和吡啶(Py)的铜髤配合物[Cu2(L2)2(Py)2](2),并通过元素分析、红外光谱、紫外光谱以及单晶衍射等手段进行表征。在配合物1中,中心Ni髤与酰腙配体(L12-)的酚氧、亚胺氮、去质子酰胺氧原子以及中性吗啡啉氮原子配位形成平面四方形的N2O2配位构型,相邻配合物通过分子间氢键作用构筑成一维超分子链状结构。配合物2中含有2个晶体学上独立的双核铜髤配合物,相邻配合物分子的酚氧原子分别桥联2个[Cu(L2)(Py)]基本单元,形成2个含有Cu2(μ-O)2核心的配合物。每个Cu髤原子具有五配位的NONO(O)四角锥配位构型。 相似文献
3.
Four novel Schiff base nickel(II) and copper(II) complexes, derived from the end‐on (μ1,1‐N3) azide, end‐to‐end (μ1,3‐NCS) thiocyanate, or phenolate oxygen bridges, have been synthesized and their crystal structures determined by X‐ray diffraction methods. They are the dinuclear double end‐on azide‐bridged [Ni2(L1)2(MeCN)2(μ1,1‐N3)2]·MeOH ( 1 ), the dinuclear double end‐on azide‐bridged [Ni2(L2)2(MeOH)2(μ1,1‐N3)2][Ni2(L2)2(OH2)2(μ1,1‐N3)2]·MeOH ( 2 ), the dinuclear double end‐to‐end thiocyanate‐bridged [Cu2(L3)2(μ1,3‐NCS)2] ( 3 ), and the dinuclear double phenolate O‐bridged [Cu2(L4)2(NCS)2] ( 4 ), where HL1, HL2, HL3 and HL4 are four tridentate Schiff bases obtained by the condensation of 3,5‐dibromosalicylaldehyde with N‐ethylethane‐1,2‐diamine, of 3,5‐dichlorosalicylaldehyde with N‐methylpropane‐1,3‐diamine, of 3‐bromo‐5‐chlorosalicylaldehyde with 2‐aminomethylpyridine, and of 5‐nitrosalicylaldehyde with 2‐aminomethylpyridine, respectively. Each nickel(II) atom in 1 and 2 is in an octahedral coordination, while each copper(II) atom in 3 and 4 is in a square pyramidal coordination. There exists crystallographic inversion centre symmetry in each of the complexes. 相似文献
4.
1 INTRODUCTION The insulin-mimetic property of vanadium complexes is the most noteworthy finding and the relationship between vanadium and diabetes mellitus has been extensively studied in the past decades[1~5]. Vanadium complexes are capable of increa… 相似文献
5.
6.
Synthesis,Crystal Structure,DNA‐binding Properties and Antioxidant Activity of a Copper(II) Complex with Naphthalimide Schiff Base 下载免费PDF全文
The Schiff N‐allylamine‐4‐(ethylenediamine‐5‐methylsalicylidene)‐1,8‐naphthalimide (H2L) and its copper(II) complex, [Cu(HL)2] · 0.5DMF, were synthesized and characterized. The crystal structure of the CuII complex reveals a slightly distorted square‐planar arrangement provided by two N and O donors from two deprotonated ligands. In addition, the DNA‐binding properties of the ligand and CuII complex were investigated by fluorescence spectra, electronic absorption, and viscosity measurements. The experimental studies of the DNA‐binding properties indicated that the ligand and CuII complex reacted with DNA via intercalation binding mode, and binding affinity for DNA takes the order: ligand > CuII complex. The antioxidant assay in vitro suggested that both exhibited potential intensely antioxidant properties, and the ligand is more effective than its CuII complex. 相似文献
7.
1 INTRODUCTION Schiff base ligands have been studied for a longtime due to the instant and enduring popularity fromtheir easy synthesis and versatility complexes. Theyplay an important role in the development of coor-dination chemistry as well as inorganic biochemistry,catalysis, optical materials and so on[1, . Consider- 2]able attention has been focused on the syntheses andstructures of copper(II) and nickle(II) complexes.The nickel complexes with multidentate Schiff baseligands have … 相似文献
8.
Four Schiff base complexes, [Cu2(L1)2(μ‐NCS)2] ( 1 ), [Cu2(L2)2(μ‐N3)2] ( 2 ), Cu[Cu(CH3COO)(L3)]2 ( 3 ), and [Zn{Zn(C3H4N2)(L3)}2(NO3)](NO3) ( 4 ) (where L1 = 2‐[(pyridin‐2‐ylmethylimino)methyl]phenol, L2 = 1‐[(pyridin‐2‐ylmethylimino)methyl]naphthalen‐2‐ol, and L3 = bis(salicylidene)‐1, 3‐propanediamine), were synthesized and characterized by elemental analyses, infrared spectroscopy, and single crystal X‐ray determinations. Both 1 and 2 are structurally similar di‐nuclear complexes, which are located at crystallographic inversion centers (with the center of the central Cu2N2 ring). In 1 , each copper atom has a slightly distorted square pyramidal configuration, coordinated by two nitrogen atoms and one oxygen atom from L1 and another two terminal nitrogen atoms from two bridging thiocyanate anions. The Cu···Cu separation is 3.466(3) Å. The structure of 2 is similar to that of 1 , with Cu···Cu separation of 3.368(2) Å. Both 3 and 4 are linear tri‐nuclear complexes. In 3 , the central Cu2+ ion is located on an inversion centre and has a distorted octahedral coordination involving four bridging O atoms from two Schiff base ligands (L3) in the equatorial plane and one O atom from each bridging acetate group in the axial positions. The coordination around the terminal Cu2+ ions is irregular‐square pyramidal, with two O and two N atoms of L3 in the basal plane and one O atom from an acetate group in the apical position. The acetate bridges linking the central and terminal Cu2+ ions are mutually trans. The Cu···Cu separation is 3.009(3) Å. In 4 , the coordination configuration of the central and the terminal zinc atoms are similar to that of the 3 , with Zn···Zn separation of 3.153(4) Å. The three Schiff bases and the corresponding three copper complexes exhibit good antibacterial properties, while the zinc complex 4 has nearly no. 相似文献
9.
M. I. Fernndez García M. Fondo A. M. García Deibe M. B. Fernndez Fernndez A. M. Gonzlez 《无机化学与普通化学杂志》2000,626(9):1985-1991
New copper(II) complexes of asymmetrical tetradentate Schiff bases containing pyrazine have been prepared and thoroughly characterised by elemental analysis, IR and electronic spectroscopy, mass spectrometry and magnetic measurements. Two alternative methods were used in the isolation of the complexes: template synthesis in the preparation of Cu(SalDpyz)ClO4 (HSalDPyz = derived from the condensation of salicylaldehyde, acetylpyrazine and 1,2‐ethylendiamine, 2‐methyl‐1,2‐propylendiamine, 1,2‐phenylendiamine) and direct interaction between copper perchlorate and the corresponding Schiff base, as in the isolation of Cu(AEPyz)(ClO4) (HAEPyz = (Z)‐4‐[2‐{[2‐{[(E)‐1‐(pyrazinyl)ethylidene]amino} ethyl)amino]‐3‐penten‐2‐one)]. [Cu(SalEn)(py)(OClO3)][Cu(SalEn)(py)]ClO4 ( 1 ) (SalEn = 4‐(2‐hydroxyphenyl)‐3‐aza‐3‐buten‐1‐amino, py = pyridine), metal precursor in the preparation of Cu(SalEnpyz)(ClO4) (HSalEnpyz = 2‐{E(2‐{[(E)‐1‐(2‐pyrazinyl)ethylidene]amino}ethyl)imino]methyl}phenol), was crystallographically characterised. The crystal structure of [Cu(AEpyz)]ClO4 ( 2 ) is also reported. 相似文献
10.
A new bi‐nucleating Schiff base ligand, 2‐(((3‐(dimethylamino)propyl)imino)methyl)‐6‐methoxyphenol (HL1) was prepared by a one‐pot condensation reaction, which was further used in the construction of three trinuclear Schiff base transition metal(II) complexes [Cu3(L1)2(OH)2(H2O)2](NO3)2 ( 1 ), [Co3(L1)2(OH)2(H2O)2](NO3)2 ( 2 ), and [Cu3(L1)2(N3)4] ( 3 ). Furthermore, a green hand grinding technique was implemented to reduce the particle size of the coordination complexes to generate the nanoscale compounds. The SEM studies reveal the formation of square and spherical particles for nano 1 and 2 , and nanorod for nano 3 . In addition, the anti‐proliferation activity of nano 1 – 3 was detected on the human cervical cancer Hela cells with CCK‐8 assay. The cell viability curves and IC50 values indicated that only nano 1 has anti‐proliferation activity on Hela cells. To further investigate the mechanism of nano 1 induced Hela cell death, the Annexin V‐FITC/PI double staining assay, western blot assay, and ROS level detection was conducted. 相似文献
11.
Four Schiff base complexes, [Zn2L2(NCS)2] ( 1 ), [Cd2L2(NCS)2]n ( 2 ), [Zn4L2(N3)2Cl4(OH2)(CH3OH)] ( 3 ), and [Cu4L2(N3)2Cl4(OH2)(CH3OH)] ( 4 ) (where L = 2‐[(2‐dimethylaminoethylimino)methyl]phenol), were synthesized and characterized by elemental analyses, infrared spectroscopy, and single crystal X‐ray determinations. Both 1 and 2 are structurally similar polynuclear complexes. In 1 , each Zn atom has a slightly distorted square‐pyramidal coordination configuration. In the basal plane, the Zn atom is coordinated by one O and two N atoms of one L, and by one O atom of another L. The apical position is occupied by one terminal N atom of a coordinated thiocyanate anion. The Zn···Zn separation is 3.179(3) Å. While in 2 , the Cd1 atom is six‐coordinated in an octahedral coordination. In the equatorial plane, the Cd1 atom is coordinated by one O and two N atoms of one L, and by one O atom of another L. The axial positions are occupied by the terminal N and S atoms from two bridging thiocyanate anions. The coordination of Cd2 atom in 2 is similar to those of the zinc atoms in 1 . The Cd···Cd separation is 3.425(2) Å. Both 3 and 4 are novel tetra‐nuclear complexes. Each metal atom in the complexes has a slightly distorted square‐pyramidal coordination. The arrangements of the terminal metal atoms are similar, involving one O and two N atoms of one L ligand and one bridging Cl atom defining the basal plane, and one O atom of a coordinated water molecule or MeOH molecule occupying the apical position. The coordinations of the central metal atoms are also similar. The basal plane of each metal atom involves one O atom of one L ligand, one terminal Cl atom, and two terminal N atoms from two bridging azide groups. The apical position is occupied by a bridging Cl atom which also acts as a basal donor atom of the terminal metal atom. The Schiff base ligand and the four complexes showed high selectivity and antibacterial activities against most of the bacteria. 相似文献
12.
Mitra Ghassemzadeh Masoomeh Tabatabaee Samaneh Soleimani Bernhard Neumüller 《无机化学与普通化学杂志》2005,631(10):1871-1876
The reaction of 4‐amino‐5‐methyl‐2H‐1,2,4‐triazole‐3(4H)‐thione (AMTT, 1 ) with 4‐methoxy benzaldehyde and 3‐methoxybenzaldehyde in methanol led to the iminic derivatives 4‐(4‐methoxybenzylideneamino)‐5‐methyl‐2H‐1,2,4‐triazole‐3(4H)thione ( 2 , L1) and 4‐(3‐methoxybenzylideneamino)‐5‐methyl‐2H‐1,2,4‐triazole‐3(4H)‐thione ( 3 , L2). The reaction of the latter with [(PPh3)2CuCl] in methanol solution gave the first CuI complex of 3 , [(PPh3)2CuCl(L2)] ( 4 ) and in chloroform solution the complex [(PPh3)2CuCl(L2)]·2CHCl3 ( 5 ). All compounds were characterized by infrared spectroscopy, elemental analyses as well as by X‐ray diffraction studies. Crystal data for 2 at ?80 °C: space group P21/c with a = 1351.3(3), b = 399.4(1), c = 2225.2(5) pm, β = 96.50(2)°, Z = 4, R1 = 0.0667, for 3 at ?80 °C: space group R3c with a = b = 3020.4(2), c = 708.2(1) pm, Z = 18, R1 = 0.0435, for 4 at ?80 °C: space group P21/c with a = 1427.8(1), b = 1129.0(1), c = 2622.8(2) pm, β = 97.19(1)°, Z = 4, R1 = 0.0517 and for 5 at ?80 °C: space group with a = 1280.5(1), b = 1316.1(1), c = 1731.4(1) pm, α = 78.14(1)°, β = 86.06(1)°, γ = 64.69(1)°, Z = 2, R1 = 0.0525. 相似文献
13.
Bao‐Li Fei Qing‐Ling Yan Jiang‐Hong Wang Qing‐Bo Liu Jian‐Ying Long Yang‐Guang Li Kui‐Zhan Shao Zhong‐Min Su Wei‐Yin Sun 《无机化学与普通化学杂志》2014,640(10):2035-2040
Two copper(II) complexes, namely [Cu(HL)Cl] ( 1 ) and [Cu(HL)Br] ( 2 ), where HL is the multidentate Schiff base N‐[(2‐oxy‐acetate)benzyl]‐2‐aminothanol, were synthesized and fully characterized. The CuII ions in 1 and 2 are pentacoordinate and the coordination arrangement is best described as distorted square‐pyramidal. The degradation of methyl orange (MO) was investigated using 1 and 2 as homogeneous photo‐Fenton‐like catalysts. 1 and 2 exhibited similar catalytic activity at neutral pH. The results suggest that they have advantages on catalyzing efficient degradation of organic dye through photo‐Fenton‐like reaction. 相似文献
14.
Two new zinc(II) complexes, [Zn2L2Cl4]·2[ZnL(CH3OH)Cl2] 1 and [ZnL2(NO3)2] 2, were synthesized by reacting ZnX2·nH2O (X = Cl-, NO3-) and a Schiff base ligand 2-[(4-me- thylphenylimino)methyl]-6-methoxyphenol (C15H15NO2, L) which was obtained by the condensation of o-vanillin (2-hydroxy-3-methoxybenzaldehyde) with p-toluidine. Both 1 and 2 were characterized by single-crystal X-ray diffraction technique, elemental analysis, molar conductance, FT-IR, UV-Vis, 1H-NMR spectra and thermogravimetric analysis. The Schiff base ligand and its zinc(II) complexes have been tested in vitro to evaluate their antibacterial activity against bacteria, viz., Escherichia Coli, Staphylococcus aureus and Bacillus Subtilis. The results show that these complexes have higher activity than the corresponding free Schiff base ligand against the same bacteria. 相似文献
15.
S‐allyl‐β‐N‐(benzylidene)dithiocarbazate (sabdtc, 1 ), prepared from hydrazine hydrate, carbon disulfide, allyl bromide and benzaldehyde, reacts with copper(II) nitrate in ethanol solution to form the complex Cu(sabdtc)2 ( 2 ). 1 function as a single negatively charged bidentate chelating ligand and coordinates via the azomethine nitrogen atom and thioenolate sulfur atom to the metal ion. 1 and 2 were characterized by elemental analyses, 1H NMR, 13C NMR, UV/Vis, IR, and mass spectra. Spectroscopic evidences suggest a four‐coordinate distorted square planar structure for 2 . The molecular and crystal structure of 2 was determined by single crystal X‐ray analysis. Crystallographic data for 2 at 291(2) K: space group C2/c, a = 20.340(3), b = 15.503(3), c = 7.659(1) Å, β = 95.96(2)°, Z = 4, R1 = 0.044 and wR2 = 0.0689. 相似文献
16.
A Schiff base ligand 1‐salicylideneamino‐1,3,4‐triazole (L) was prepared. Two new complexes with Schiff base, [Zn(L)2(SCN)2] ( 1 ) and [Co2(L)5(SCN)4]·H2O ( 2 ) have been synthesized and structurally characterized. Complex 1 takes a mononuclear zinc structure and the coordination geometry of zinc atom exhibits a distorted tetrahedron, in which a zig‐zag chain is constructed through hydrogen bonding interactions. A 2D supramolecular network is formed through Π‐Π stacking between triazole planes and phenyl planes of adjacent chains, and a 3D supramolecular network is further constructed by these non‐covalent Π‐Π stacking interactions between the triazole planes of neighboring layers. Complex 2 takes a dinuclear structure with the bidentate‐bridging Schiff base ligands, and cobalt site exhibits a distorted octahedron. The lattice water molecules and neutral complex 2 units form a dimer with hydrogen bonding interactions. In addition, IR and thermal gravimetric analysis are presented. 相似文献
17.
Rasoul Vafazadeh Fariba Jafari Mohammad Mehdi Heidari Anthony C. Willis 《Journal of Coordination Chemistry》2016,69(8):1313-1325
Two tridentate Schiff base ligands were synthesized by condensation of equimolar amounts of benzoylacetone and 2-amino-1-ethanol or 3-amino-1-propanol, H2L1 and H2L2, respectively. The reaction of the Schiff base ligands with Cu(CH3COO)2 in methanol leads to (CuL1)4, 1 and (CuL2)2, 2. In the tetranuclear cubane species, the tridentate H2L has both a chelating and a bridging mode, after double deprotonation of the enolic OH groups. The copper(II) centers are five-coordinate with a NO4 donor set from the ligands. The coordination geometry around each copper ion is essentially square pyramidal with one nitrogen and two oxygens from one ligand and two oxygens of adjacent ligands from the next unit of the cubane. In dinuclear 2, H2L2 has chelating and bridging modes after double deprotonation of the enolic OH groups. The dianionic form of the Schiff base coordinates forming a six-membered chelate ring with Cu(II). Two such monomeric CuL2 entities are eventually linked through the alkoxo bridges to produce dinuclear 2. The absorption spectra strongly suggest that 2 interacts with CT-DNA. Both 1 and 2 appear to be more efficient than the parent compound in DNA cleavage. 相似文献
18.
Three novel thiocyanato‐bridged polynuclear cadmium(II) complexes, [Cd(HL1)(NCS)2(μ1,3‐NCS)]n ( 1 ), [CdL2(μ1,3‐NCS)2]n ( 2 ), and [CdL3(μ1,3‐NCS)2]n ( 3 ) (L1 = N‐methyl‐N′‐(1‐pyridin‐2‐ylmethylidene)ethane‐1,2‐diamine, L2 = 2‐(cyclopropyliminomethyl)‐6‐methoxyphenol, L3 = 2‐(cyclopentyliminomethyl)‐6‐methoxyphenol), have been synthesized and structurally characterized by elemental analysis, IR spectra and single‐crystal X‐ray diffraction. Each cadmium(II) atom in the complexes is in an octahedral coordination. The urease inhibitory activities of the complexes were evaluated. All of them showed potent inhibitions against jack bean urease. 相似文献
19.
Mehmet Gülcan Mehmet Sönmez 《Phosphorus, sulfur, and silicon and the related elements》2013,188(9):1962-1971
Abstract Monobasic tridentate Schiff base ligand having ONS donor sequence was prepared by condensing N-aminopyrimidine-2-thione with o-vanillin. The complexes were formed by reacting ligand and the metal acetates of Cu(II), Ni(II), Co(II), Mn(II), and Cd(II) in methanol to get a series of mononuclear and dinuclear complexes. The characterization of ligand and metal complexes were carried out by elemental analyses, conductivity measurements, magnetic susceptibility data, FTIR, UV-vis, NMR, and API-ES mass spectral data. The structure of the complexes was confirmed on the basis of elemental analyses, magnetic susceptibility, API-ES mass spectral data and thermal gravitational analysis (TGA). GRAPHICAL ABSTRACT 相似文献
20.
ZHANG Xin-Li 《结构化学》2013,32(2)
<正>Two new Cu(II) complexes have been synthesized with two different bidentate N_2O_2 donor Schiff base ligands HL_1 (2-((E)-(4-chlorophenylimino)methyl)-6-bromo-4-chlorophenol) and HL_2 (2-((E)-(2-chlorophenylimino)methyl)-6-bromo-4-chlorophenol), respectively. Both complexes 1 and 2 have been characterized by elemental analysis and single-crystal X-ray diffraction studies. Structural studies reveal that in both complexes the metal centers are four-coordinated with N_2O_2 donor set of Schiff base ligands. Complex 1 belongs to the tetragonal system, space group P4(3)2(1)2 with a = 10.2379(2), b = 10.2379(2), c = 24.9623(90) , V = 2616.41(12) ~3, Z = 4, D_c = 1.908 g/cm~3, μ(MoKα) = 4.3327 mm~(-1), F(000) = 1468, S = 0.999, the final R = 0.0345 and wR = 0.0835 for 3506 unique reflections (R_(int) = 0.0428) with 3249 observed ones (I > 2σ(I)). Complex 2 is of monoclinic system, space group P21/c with a = 11.064(3), b = 9.437(2), c = 13.277(4), β = 108.997(3)°, V = 1310.8(6) ~3 , Z = 2, D_c = 1.904 g/cm~3, μ(MoKα) = 4.319 mm~(-1), F(000) = 734, S = 0.997, the final R = 0.0282 and wR = 0.0619 for 3491 unique reflections (R_(int) = 0.0428) with 2777 observed ones (I > 2σ(I)). The units of the complex are linked via weak interactions, such as C-H…Br hydrogen bonds together with Cl…Cl and Cu…Cl interactions, leading to the formation of one-dimensional chain and two-dimensional network and stabilizing the crystal structure. 相似文献