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1.
The 12- and 14-membered diazadioxo macrocyclic ligands, 1,2?:?7,8-diphenyl-6,9-diaza-3,12-dioxocyclododecane (L1) and 1,2?:?8,9-diphenyl-7,10-diaza-3,14-dioxocyclotetradecane (L2), were synthesized by condensation between o-phenylenediamine, 1,2-dibromoethane/1,3-dibromopropane, and catechol. Metal complexes [ML1Cl2] and [ML2Cl2] [M?=?Co(II), Ni(II), Cu(II), and Zn(II)] were prepared by interaction of L1 or L2 with metal(II) chlorides. The ligands and their complexes were characterized by elemental analyses, IR, 1H, and 13C NMR, EPR, UV-Vis spectroscopy, magnetic susceptibility, conductivity measurements, and Electrospray ionization-mass spectral (ESI-MS) studies. The results of elemental analyses, ESI-MS, Job's method, and conductivity measurements confirmed the stoichiometry of ligands and their complexes while absorption bands and resonance peaks in IR and NMR spectra confirmed the formation of ligand framework around the metal ions. Stereochemistry was inferred from the UV-Vis, EPR, and magnetic moment studies.  相似文献   

2.
Binuclear cobalt(II), nickel(II), copper(II) and zinc(II) complexes of general composition [M2L1-2(μ-Cl)Cl2] · nH2O with the Schiff-base ligands (where L1H and L2H are the potential pentadentate ligands derived by condensing 2,6-diformyl-4-methylphenol with 4-amino-3-antipyrine and 2-hydroxy-3-hydrazinoquinoxiline, respectively) have been synthesized and characterized. Analytical and spectral studies support the above formulation. 1H-NMR and IR spectra of the complexes suggest they have an endogenous phenoxide bridge, with chloride as the exogenous bridge atom. The electronic spectra of all the complexes are well characterized by broad d–d and a high intensity charge-transfer transitions. The complexes are chloro-bridged as evidenced by two intense far-IR bands centered around 270–280 cm−1. Magnetic susceptibility measurements show that complexes are antiferromagnetic in nature. The compounds show significant growth inhibitory activity against fungi Aspergillus niger and Candida albicans and moderate activity against bacteria Bacillus cirroflagellosus and Pseudomonas auresenosa.  相似文献   

3.
Two new hexadentate N2O4 donor Schiff bases, H4L1 and H4L2, were synthesized by condensation of 4,6-diacetylresorcinol with glycine and alanine, respectively. The structures of the ligands were elucidated by elemental analyses, IR, 1H NMR, electronic, and mass spectra. Reactions of the Schiff bases with copper(II), nickel(II), and iron(III) nitrates in 1 : 2 molar ratio gave binuclear metal complexes and, in the presence of 8-hydroxyquinoline (8-HQ) or 1,10-phenanthroline (Phen) as secondary ligands (L′), mixed-ligand complexes in two molar ratios 1 : 2 : 2 and 1 : 2 : 1 (L1/L2 : M : L′). The complexes were characterized by elemental and thermal analyses, IR, electronic, mass, and ESR spectral studies, as well as conductivity and magnetic susceptibility measurements. The spectroscopic data reveal that the Schiff-base ligands were dibasic or tetrabasic hexadentate ligands. The coordination sites with the metal ions are two azomethine nitrogens, two oxygens of phenolic groups, and two oxygens of carboxylic groups. Copper(II) complexes were octahedral and square planar while nickel(II) and iron(III) complexes were octahedral. The Schiff bases, H4L1 and H4L2, and some of their metal complexes showed antibacterial activity towards Gram-positive (Staphylococcus aureus and Streptococcus pyogenes) and Gram-negative (Pseudomonas fluorescens and Pseudomonas phaseolicola) bacteria and antifungal activity towards the fungi Fusarium oxysporium and Aspergillus fumigatus.  相似文献   

4.
Heteronuclear complexes containing oxorhenium(V), with Fe(III), Co(II), Ni(II), Cu(II), Cd(II) and UO2(VI) ions were prepared by the reaction of the complex ligands [ReO(HL1)(PPh3)(OH2)Cl]Cl (a) and/or [ReO(H2L2)(PPh3)(OH2)Cl]Cl (b), where H2L1?=?1-(2-hydroxyphenyl)butane-1,3-dione-3-(5,6-diphenyl-1,2,4-triazine-3-ylhydrazone) and H3L2?=?1-(2-hydroxyphenyl)butane-1,3-dione-3-(1H-benzimidazol-2-ylhydrazone), with transition and actinide salts. Heterodinuclear complexes of ReO(V) with Fe(III), Co(II), Ni(II), Cu(II) and Cd(II) were obtained using a 1?:?1 mole ratio of the complex ligand and the metal salt. Heterotrinuclear complexes were obtained containing ReO(V) with UO2(VI) and Cu(II) using 2?:?1 mole ratios of the complex ligand and the metal salts. The complex ligands a and b coordinate with the heterometal ion via a nitrogen of the heterocyclic ring and the nitrogen atom of the C=N7 group. All transition metal cations in the heteronuclear complexes have octahedral configurations, while UO2(VI)?complexes have distorted dodecahedral geometry. The structures of the complexes were elucidated by IR, ESR, electronic and 1H NMR spectra, magnetic moments, conductance and TG-DSC measurements. The antifungal activities of the complex ligands and their heteronuclear complexes towards Alternaria alternata and Aspergillus niger showed comparable behavior with some well-known antibiotics.  相似文献   

5.
4,4′-Bis(chloroacetyl)diphenyl ether (HL) was synthesized from chloroacetyl chloride and diphenyl ether in the presence of AlCl3 as catalyst by Friedel-Crafts reaction. Subsequently, its keto oxime (H2L) and glyoxime (H4L) derivatives were also prepared. Then, five new substituted 4,4′-oxy-bis(aminophenyl-glyoximes) (H4L1–5) were synthesized from 4,4′-oxy-bis(chlorophenylglyoxime) and the corresponding amines. The Ni(II), Cu(II), and Co(II) complexes of these ligands were prepared. The structures of these ligands and their complexes were identified by FT-IR, 1H NMR, and ICP-AES spectral data, elemental analyses, and magnetic measurements.  相似文献   

6.
Three new vic-dioximes, [L1H2], N-(4-ethylphenyl)amino-1-acetyl-1-cyclohexenylglyoxime, [L2H2], N-(4-butylphenyl)amino-1-acetyl-1-cyclohexenylglyoxime, and [L3H2], N-(4-methoxyphenyl)amino-1-acetyl-1-cyclohexenylglyoxime were synthesized from 1-acetyl-1-cyclohexeneglyoxime and the corresponding substituted aromatic amines. Metal complexes of these ligands were also synthesized with Ni(II), Cu(II), and Co(II) salts. These new compounds (ligands and complexes) were characterized with FT–IR, magnetic susceptibility measurement, molar conductivity measurements, mass spectrometry measurements, thermal methods (e.g. thermal gravimetric analysis), 1H NMR (Nuclear Magnetic Resonance) and 13C NMR spectral data and elemental analyses.  相似文献   

7.
Zn(II), Co(II) and Ni(II) complexes with some 5-substituted-1,3,4-thiadiazoles (L1-L4) have been prepared and characterized by conductivity, microanalysis, thermal analysis, infrared and electronic spectra measurements. All complexes behave as 1:1 electrolyte and the ligands are coordinated as bidentate molecules. The stability constants and energy of formation are determined and discussed on the basis of the ligands structure.  相似文献   

8.
New transition metal complexes of Co(II), Cu(II), Ni(II), and Fe(III) of the ligands 6,6′-(1E,1′E)-(4,5-dimethyl-1,2-phenylene)bis(azan-1-yl-1-ylidene)bis(methan-1-yl-1-ylidene)bis(7-hydroxy-5-methoxy-2-methyl-4H-chromen-4-one) H2L1 and 6,6’-(1E,1′E)-cyclohexane-1,2-diylbis(azan-1-yl-1-ylidene)bis(methan-1-yl-1-ylidene)bis(7-hydroxy-5-methoxy-2-methyl-4H-chromen-4-one) H2L2 have been prepared and characterized using physio-chemical and spectroscopic methods. The results obtained for the complexes indicated that the geometries of the metal centres are either square planar or octahedral. Cyclopropanation reactions of unactivated olefins by ethyldiazoacetate (EDA) in the presence of [L1Cu]·H2O, [L2Cu]·2H2O and [L2*Co]·2H2O as catalysts were examined. The results showed that only [L2*Co]·2H2O can act as a catalyst for the cyclopropanation reaction of unactivated olefins with very high selectivity (up to 99% based on EDA).  相似文献   

9.
New Schiff bases, N,N′-bis(salicylidene)-4-aminobenzylamine (H2L1), N,N′-bis(3-methoxysalicylidene)-4-aminobenzylamine (H2L2), and N,N′-bis(4-hydroxysalicylidene)-4-aminobenzylamine (H2L3), with their nickel(II), cobalt(II), and copper(II) complexes have been synthesized and characterized by elemental analyses, electronic absorption, FT-IR, magnetic susceptibility, and conductance measurements. For the ligands, 1H and 13C NMR and mass spectra were obtained. The tetradentate ligands coordinate to the metal ions through the phenolic oxygen and azomethine nitrogens. The keto-enol tautomeric forms of the Schiff bases H2L1, H2L2, and H2L3 have been investigated in polar and apolar solvents. All compounds were non-electrolytes in DMSO (~10?3 M) according to the conductance measurements. Antimicrobial activities of the Schiff bases and their complexes have been tested against Acinobacter baumannii, Pseudomonas aeruginosa, Micrococcus luteus, Bacillus megaterium, Corynebacterium xerosis, Staphylococcus aureus, Escherichia coli, Candida albicans, Rhodotorula rubra, and Kluyveromyces marxianus by the disc diffusion method; biological activity increases on complexation.  相似文献   

10.
Cobalt(II), nickel(II), and copper(II) complexes containing 5,12-di(4-bromophenyl)-7,14-dimethyl-1,2,4,8,9,11-hexaazacyclotetradeca-7,14-diene-3,10-dione (H2L1) and 5,12-diphenyl-7,14-dimethyl-1,2,4,8,9,11-hexaazacyclotetradeca-7,14-diene-3,10-dione (H2L2) have been synthesized. All complexes were characterized by elemental analysis, MALDI TOF-MS spectrometry, and electronic absorption spectroscopy. The crystal structures of two compounds, [Cu2(H2L1)Cl4]n and [NiL2], were determined by X-ray powder diffraction. In the polymeric [Cu2(H2L1)Cl4]n, the Cu2Cl4 units and H2L1 molecules are situated on inversion centers. Each Cu(II) has a distorted trigonal-bipyramidal coordination environment formed by N and O from H2L1 [Cu–N 2.340(14)?Å, Cu–O 1.952(11)?Å], two bridging chlorides [Cu–Cl 2.332(5), 2.279(5)?Å] and one terminal chloride [Cu–Cl 2.320(6)?Å]. In the [NiL2] complex, the Ni(II) situated on inversion center has a distorted square-planar coordination environment formed by four nitrogens from L2 [Ni–N 1.860(11), 1.900(11)?Å].  相似文献   

11.
Potentially tetradentate ligands N,N"-di(2-hydroxybenzyl)ethylenediamine (L1) and N,N"-di(2-hydroxybenzyl)o-phenylenediamine (L2) and complexes of Cu(II), Co(II), and Ni(II) with L1and L2were synthesized. The EPR and electronic spectroscopy methods were used to reveal the octahedral structure of the Cu(II) complex with L1in the solid state. In water–alcohol solutions, the Cu(II) and Ni(II) complexes with both ligands have distorted octahedral structures. The Co(II) complexes form dioxygen adduct with L1. In the presence of oxygen, the ligands in the obtained complex compounds can undergo oxidative dehydrogenation with selective formation of the respective disalicylaldimines. In the case of L2, the oxidative dehydrogenation is observed for the complexes of all studied metals in comparatively mild conditions (T= 30°C, methanol and other solvents), while in the case of L1, it occurs only with the Co(II) complexes in the presence of pyridine.  相似文献   

12.
Two Schiff bases, L1 (5,6;11,12-dibenzophenone-2,3,8,9-tetramethyl-1,4,7,10-tetraazacyclododeca-1,3,7,9-tetraene) and L2 (6,7;13,14-dibenzophenone-2,4,9,11-tetramethyl-1,5,8,12-tetraazacyclotetradeca-1,4,8,11-tetraene), bearing functionalized pendant arms have been synthesized by cyclocondensation of 3,4-diaminobenzophenone with 2,3-butanedione and 2,4-pentanedione, respectively. Mononuclear macrocyclic complexes [FeL1Cl2]Cl, [FeL2Cl2]Cl, [ML1Cl2], and [ML2Cl2] (where M?=?Co(II) and Cu(II)) have been prepared by reacting iron(III), cobalt(II), and copper(II) with the preformed Schiff base. The ligands and their corresponding metal complexes were characterized by elemental analyses, ESI-mass spectra, conductivity, magnetic moments, UV-Vis, EPR, IR, 1H-, and 13C-NMR spectral studies, and TGA-DTA/DSC data. The TGA profiles exhibit a two-step pyrolysis, although the iron complexes decompose in three steps, leaving behind metal oxides as the final product. The ligands and complexes were screened in vitro against Gram-positive bacteria, Gram-negative bacteria, and fungi.  相似文献   

13.
We describe the synthesis and characterization of two novel azo ligands, 4,5-dihydroxy-3,6-bis(2-hydroxyphenylazo)-2,7 naphthalene disulfonic acid (H2L) and 4,5-dihydroxy-3,6-bis(2-hydroxy-4-sulfophenylazo)-2,7-naphthalenedisulfonic acid (H2L1). The Cu(II), Ni(II), and Co(II) complexes of these ligands were prepared and characterized by infrared, UV–Vis, 1H- and 13C-NMR spectra, atomic absorption spectroscopy, mass spectrometry, elemental analyses, thermogravimetric analysis, conductivity, cyclic voltammetry, and magnetic measurements. The results suggest that the complexes have a 2:1 (metal:ligand) molar ratio, involving binuclear azo ligands with an ONO donor set. Metal ion uptake studies were conducted with a batch technique. Preliminary histological studies were also made. The results indicate that the azo ligands have high thermal stability, good metal extraction capacity, and favorable dying properties with certain tissues.  相似文献   

14.
Synthesis of four different types of ligands Ar[COC(NOH)R] n (Ar = biphenyl, n = 1, HL1; Ar = biphenyl, n = 2, H2L2; Ar = diphenylmethane, n = 1, HL3; Ar = diphenylmethane, n = 2, H2L4; R = furfurylamine in all ligands) and their dinuclear Co2+, Ni2+, Cu2+, and Zn2+ complexes is reported herein. These compounds were characterized by elemental analysis, ICP-OES, FT-IR spectra, and magnetic susceptibility measurements. The ligands were further characterized by 1H NMR. The results suggest that dinuclear complexes of HL1 and HL3 have a metal to ligand mole ratio of 2: 2 and dinuclear complexes H2L2 and H2L4 have a metal to ligand mole ratio of 2: 1. Square pyramidal or octahedral structures are proposed for complexes of oxime ligands. Furthermore, extraction abilities of the four ligands were also evaluated in chloroform using selected transition metal picrates such as Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg2+, Pb2+. The ligands show strong binding ability towards Hg2+ and Cu2+ ions.  相似文献   

15.
5-Amino-4-arylazo-3-methyl-1-phenylpyrazole (aryl?=?C6H5,o-C6H4COOH,o-C6H4OH) and its complexes with Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II) ions were synthesized. The complexes are in the ratio 1?:?1 and 1?:?2 (metal?:?ligand). Ligands and complexes were subjected to elemental analysis, IR, Raman, UV-Vis and 1H-NMR spectroscopy. The mass spectra of the ligands were discussed. Thermal analysis and magnetic measurements were carried out for the prepared complexes. The X-ray single crystal structure of [Ni(L1)2] was performed. The investigated pyrazole compounds coordinate as bidentate ligands through amino and azo nitrogens or tridentate through NNO. The molar conductance of the chelates is measured and reflected the non-electrolytic nature of the prepared complexes.  相似文献   

16.
Six new Cu(II), Ni(II) and Co(II) macroacyclic Schiff base complexes [MII(H2L)](ClO4)2 (L = L1 and L2) (I–VI) were prepared by the reaction of two new N2O4 Schiff base ligands in equemolar ratios. The ligands H2L1 and H2L2 were synthesized by reaction of 2-[2-(2-formyl phenoxy)ethoxy]benzaldehyde (A1) and/or 2-[2-(3-formylphenoxy)propoxy]benzaldehyde (A2) and ethanol amine and characterized with IR and 1H, 13C NMR spectroscopy. All complexes were characterized by microanalysis, IR and mass spectrometry, whereas complex I was also characterized by single crystal X-ray (CIF file CCDC no. 1020055). The X-ray structure of complex I revealed that all nitrogen and oxygen atoms of ligand (N2O4) have coordinated to the metal ion. However, Cu2+ ion is in six coordination environment that can bedescribed as a distorted octahedral geometry.  相似文献   

17.
Summary Copper(II), nickel(II) and cobalt(II) perchlorate complexes of 5,5-dimethylcyclohexane-1,2,3-trione-2-(p-nitrophenyl-hydrazone) (HL1), 5,5-dimethyl-cyclohexane-1,2,3-trione-2-(p-chlorophenylhydrazone) (HL2), 5,5-dimethylcyclohexane-1,2,3-trione-2-(o-chlorophenylhydrazone) (HL4), 5,5-dimethylcyclohexane-1,2,3-trione-2-(o-methylphenyl-hydrazone) (HL5) and 5,5-dimethylcyclohexane-1,2,3-trione-2-(m-methylphenylhydrazone) (HL6) have been prepared, and characterized using analytical, spectral and magnetic measurements. The data reveal that the reaction of Cu(ClO4)2 (1 mol) in EtOH, with all ligands, produces complexes of the type CuL(ClO4)(H2O).nH2O. Nickel(II) and cobalt(II) perchlorates react only with HL1 and HL2 to produce the complexes ML(ClO4)(H2O)3 (where M = NiII, L = L and L2, M = CoII, L = L1) and Co(HL2)2-(ClO4)2.2H2O. The spectral data show that the ligands behave as monobasic bidentate in their azo forms, except HL2 which reacts with cobalt(II) as a neutral bidentate ligand in its hydrazone form.  相似文献   

18.
Cobalt(II) and copper(II) complexes with three dioxime ligands cyclohexylamine-p-tolylglyoxime (L1H2), tert-butyl amine-p-tolylglioxime (L2H2) and sec-butylamine-p-tolylglyoxime (L3H2), have been prepared. The metal to ligand ratios of the complexes were found to be 1?:?2. The Cu(II) complexes of these ligands are proposed to be square planar; the Co(II) complexes are proposed to be octahedral with water molecules as axial ligands. Ligands and complexes are soluble in common solvents such as DMSO, DMF, CHCl3 and C2H5OH. The ligands have been characterized by elemental analysis, IR, UV-VIS, 1H?NMR, 13C?NMR and thermogravimetric analysis (TGA). The complexes were characterized by elemental analysis, IR, UV-VIS, magnetic susceptibility measurements, thermogravimetric analysis (TGA) and electrochemistry. Electrochemical properties of metal complexes show quasi-reversible one-electron redox processes. However, Co(L1H)2 and Cu(L1H)2 complexes show another oxidation peak in the positive region. This single irreversible oxidation peak is caused by the cyclic ring of the ligand. Data also revealed that the electron transfer rates of metal complexes with L1H2 are higher than the other complexes.  相似文献   

19.
The potassium salt of salicylidene-DL-alanine (KHL), bis(benzylidene)ethylenediamine (A1), thiophene-o-carboxaldene-p-toluidine (A2), and its metal complexes of the formula [(MII(L)(A)(H2O)] (M = Mn(II), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II); A = A1 or A2) are prepared. They are characterized by elemental analysis, magnetic susceptibility measurements, thermogravimetric analysis, and infrared and electronic spectral studies. The electronic spectral and magnetic moment data suggest an octahedral geometry for the complexes. All of these complexes, metal nitrates, fungicides (bavistin and emcarb), and ligands are screened for their antifungal activity against Aspergillus niger, Fusarium oxysporum, and Aspergillus flavus using a plate poison technique. The complexes show higher activity than those of the free ligands, metal nitrate, and the control (DMSO) and moderate activity against bavistin and emcarb. The text was submitted by the authors in English.  相似文献   

20.
Two new soluble vic-dioxime ligands, 4-isopropylanilineglyoxime (L1H2) and 4-benzylpiperidineglyoxime (L2H2) were prepared by reacting 4-isopropylaniline and 4-benzylpiperidine with anti-chloroglyoxime. Ten metal complexes were obtanied by reacting both ligands with Cu(II),Ni(II),Co(II), Zn(II), and Cd(II) cations. The ligands and their metal complexes were elucidated by elemental analysis, IR, UV-vis, 1H NMR, and 13C NMR and also magnetic moments of the complexes were determined. The text was submitted by the authors in English.  相似文献   

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