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1.
Four copper(II) complexes and one copper(I) complex with pyridine-containing pyridylalkylamide ligands N-(pyridin-2-ylmethyl)pyrazine-2-carboxamide (HLpz) and N-(2-(pyridin-2-yl)ethyl)pyrazine-2-carboxamide (HLpz?) were synthesized and characterized. The X-ray crystal structures of [Cu2(Lpz)2(4,4?-bipy)(OTf)2] (1, OTf?=?trifluoromethanesulfonate, 4,4?-bipy?=?4,4?-bipyridine) and [Cu(Lpz)(py)2]OTf·H2O (2, py?=?pyridine) revealed binuclear and mononuclear molecular species, respectively, while [Cu(Lpz)(μ2-1,1-N3)]n (3), [Cu(Lpz?)(μ2-1,3-N3)]n (4), and [Cu(HLpz)Cl]n (5) are coordination polymer 1-D chains in the solid state.  相似文献   

2.
Three new centrosymmetric dinuclear copper(II) complexes, [Cu2Cl2(L1)2] (1), [Cu2(μ 1,3-NCS)2(L2)2] (2), and [Cu2(μ 1,1-N3)2(L3)2] (3), where L1, L2, and L3 are the deprotonated forms of the Schiff bases 1-[(2-propylaminoethylimino)methyl]naphthalen-2-ol (HL1), 1-[(3-methylaminopropylimino)methyl]naphthalen-2-ol (HL2), and 2-[(2-isopropylaminoethylimino)methyl]phenol (HL3), respectively, have been prepared and characterized by elemental analysis, IR spectra, and single-crystal X-ray crystallography. Each Cu is coordinated by the three donors of the Schiff bases and by two bridging groups, forming a square-pyramidal geometry.  相似文献   

3.
Three new coordination complexes, 2{[Co(L1)2]ClO4} · 0.5CH3OH (1), [Mn(L2)2] (2), and [Cu(HL2)(L2)]ClO4 · 2H2O (3) have been synthesized from two tridentate N,N,O-donor hydrazone ligands HL1, 2-acetylpyridine-salicyloylhydrazone, and HL2, 2-benzoylpyridine-salicyloylhydrazone, respectively and thoroughly characterized by elemental analysis, FT-IR, UV–Vis, electrochemical, and room temperature magnetic susceptibility measurements. Structures of the complexes have been unequivocally established by single crystal X-ray diffraction technique. Structural analysis reveals that 1 consists of two chemically similar but crystallographically independent cationic [Co(L1)2]+ units and 2 consists of a neutral [Mn(L2)2] molecule while 3 consists of a cationic [Cu(HL2)(L2)]+ unit. Metal ions display distorted octahedral geometry in 1 and 2 while in 3 it shows a distorted square pyramidal geometry. Ligand conformations around the metal ions are stabilized by the presence of intra-ligand hydrogen bonding in all the complexes. Structure of 3 reveals that a perchlorate ion linked to the complex by hydrogen bonding via a water molecule.  相似文献   

4.
Four dinuclear cadmium(II) complexes, [Cd2(L1)(μ2-Cl)Cl2] (1), [Cd2(L2)(μ2-Cl)Cl2] (2), [Cd2(L3)(μ2-Cl)Cl2] (3), and [Cd2(L4)3ClO4] (4), where HL1 = 4-methyl-2,6-bis(1-(2-piperidinoethyl)iminomethyl)-phenol, HL2 = 4-methyl-2,6-bis(1-(2-pyrrolidinoethyl)iminomethyl)-phenol, HL3 = 4-methyl-2,6-bis(1-(2-morpholinoethyl)iminomethyl)-phenol and HL4 = 4-methyl-2,6-bis(cyclohexylmethyl)iminomethyl)-phenol, were synthesized. They were characterized by elemental analysis, FT-IR, UV–Vis, fluorescence and electronspray ionization mass spectroscopy. Complexes 1 and 4 were also characterized by single crystal X-ray analysis. The cadmiums atoms in 1 are linked by μ2-chloride in a distorted square pyramidal geometry, whereas cadmium atom in 4 is in a distorted octahedral environment. The complexes show emission bands around 500 nm with excitation at 395 nm.  相似文献   

5.
Novel mononuclear oxovanadium(IV) and manganese(III) complexes [VO(L1)2·H2O] (1); [VO(L2)2·H2O] (2); [VO(L3)2·H2O] (3); [Mn(L1)2]ClO4·H2O (4); [Mn(L2)2] ClO4·H2O (5); [Mn(L3)2]ClO4·H2O (6) were prepared by condensation of 1 mol of VOSO4·5H2O or Mn(OAc)3· 2H2O with 2 mol of ligand HL1, HL2 or HL3 (where HL1 = 4-[(2-hydroxy-ethylamino)-methylene]-5-methyl-2- phenyl-2,4-dihydro-pyrazol-3-one; HL2=4-[(2-hydroxy-ethylamino)-methylene]-5-methyl-2-p-tolyl-2,4-dihydro-pyrazol-3-one; HL3=4-{4-[(2-hydroxy-ethyl-amino)-methyl]-3-methyl-5-oxo-4,5-dihydropyrazol-1-yl} benzene sulfonic acid). The resulting complexes were characterized by elemental analyses, molar conductance, magnetic and decomposition temperature measurements, electron spin resonance, FAB mass, IR and electronic spectral studies. From TGA, DTA and DSC, the thermal behaviour and degradation kinetic were studied. Electronic spectra and magnetic susceptibility measurements indicate distorted octahedral stereochemistry of oxovanadium(IV) complexes and regular octahedral stereochemistry of manganese(III) complexes. Hamiltonian and bonding parameters found from ESR spectra indicate the metal ligand bonding is partial covalent. The X-ray single crystal determination of one of the representative ligand was carried out which suggests existence of amine-one tautomeric form in the solid state. The 1H-NMR spectra support the existence of imine-ol form in solution state. The LC-MS studies sustain the1H-NMR result. The electronic structure of the same representative ligand was optimized using 6-311G basis set at HF level ab initio studies to predict the coordinating atoms of the ligand.  相似文献   

6.
Four new nickel(II), zinc(II), and cobalt(II) complexes, [Zn(L1)2]?·?H2O (1), [Ni(L1)2]?·?H2O (2), [Ni(L2)2] (3), and [Co(L3)2]?·?H2O (4), derived from hydroxy-rich Schiff bases 2-{[1-(5-chloro-2-hydroxyphenyl)methylidene]amino}-2-methylpropane-1,3-diol (HL1), 2-{[1-(2-hydroxy-3-methoxyphenyl)methylidene]amino}-2-ethylpropane-1,3-diol (HL2), and 2-{[1-(5-bromo-2-hydroxyphenyl)methylidene]amino}-2-methylpropane-1,3-diol (HL3) have been synthesized and characterized by elemental analyses, infrared spectroscopy, and single-crystal X-ray determination. Each metal in the complexes is six-coordinate in a distorted octahedral coordination. The Schiff bases coordinate to the metal atoms through the imino N, phenolate O, and one hydroxyl O. In the crystal structures of HL1 and the complexes, molecules are linked through intermolecular O–H···O hydrogen bonds, forming 1-D chains. The urease inhibitory activities of the compounds were evaluated and molecular docking study of the compounds with the Helicobacter pylori urease was performed.  相似文献   

7.
Reactions of the ruthenium complexes [RuH(CO)Cl(PPh3)3] and [RuCl2(PPh3)3] with hetero-difunctional S,N-donor ligands 2-mercapto-5-methyl-1,3,5-thiadiazole (HL1), 2-mercapto-4-methyl-5-thiazoleacetic acid (HL2), and 2-mercaptobenzothiazole (HL3) have been investigated. Neutral complexes [RuCl(CO)(PPh3)2(HL1)] (1), [RuCl(CO)(PPh3)2(HL2)] (2), [RuCl(CO)(PPh3)2(HL3)] (3), [Ru(PPh3)2(HL1)2] (4), [RuCl(PPh3)3(HL2)] (5), and [RuCl(PPh3)3(HL3)] (6) imparting κ2-S,N-bonded ligands have been isolated from these reactions. Complexes 1 and 4 reacted with diphenyl-2-pyridylphosphine (PPh2Py) to give neutral κ1-P bonded complexes [RuCl(CO)(κ1-P-PPh2Py)2(HL1)] (7), and [Ru(κ1-P-PPh2Py)2(HL1)2] (8). Complexes 1-8 have been characterized by analytical, spectral (IR, NMR, and electronic absorption) and electrochemical studies. Molecular structures of 1, 2, 4, and 7 have been determined crystallographically. Crystal structure determination revealed coordination of the mercapto-thiadiazole ligands (HL1-HL3) to ruthenium as κ2-N,S-thiolates and presence of rare intermolecular S-S weak bonding interaction in complex 1.  相似文献   

8.
Two new complexes, [Ni(HL1)(N3)(μ1,1N3)]2 (1) [HL1: NC5H4CH3C=NNH (C=O) NH2] and [Ni(L2)N3] (2) [HL2: NC5H4HC=N NH(C=S)NH2], have been synthesized by reaction of Ni(OAC)2·4H2O and sodium azide with HL1 and HL2 and characterized by elemental analysis, FT-IR, and UV–vis spectral studies. Single-crystal X-ray diffraction reveals that 1 is dinuclear with nickel(II) in an octahedral environment of NNO donors of HL1, two nitrogens of azide bridges and one nitrogen of terminal azide; 2 is mononuclear containing nickel(II) in a distorted square-planar environment of NNS donors of HL2 and one terminal azide. The structures of 1 and 2 have been optimized by density functional theory. The results of antimicrobial activities of ligands, 1 and 2 demonstrated that HL2 and 2 have good antimicrobial activity in contrast with HL1 and 1, related to the presence of sulfur donor in HL2.  相似文献   

9.
Two metal-organic coordination polymers, [Co(tda)(ip)(H2O)2] n (1) and [Mn(tda)(ip)(H2O)] n (2) [H2tda?=?thiophene-2,5-dicarboxylic acid, ip?=?1H-imidazo[4,5-f][1,10]-phenanthroline], have been synthesized and characterized by elemental analyses, IR, PXRD, and X-ray diffraction. Single-crystal X-ray analyses reveal that 2,5-tda is a bridging ligand, exhibiting two coordination modes to link metal ions: μ11?:?η011?:?η0 and μ21?:?η111?:?η0. Compound 1 demonstrates a 1-D structure in which Co2+ centers are connected via tda anions into 1-D chains; the chains are further connected via hydrogen-bonding and π?···?π interactions. Compound 2 displays a 2-D structure in which tda connects two Mn ions forming a dinuclear molecule. In 2 the 3-D supramolecular structure arrays through hydrogen-bonding and π?···?π interactions. In addition, photoluminescence for 1 and 2 is also investigated in the solid state at room temperature.  相似文献   

10.
Transition metal complexes [Zn(L1)2] (I) and [Mn(L2)2] (II), where HL1 = pyridine-2-carboxaldehyde S-methyldithiocarbazate, HL2 = pyridine-2-carboxaldehyde S-benzyldithiocarbazate, have been synthesized. Complex II was characterized by elemental analysis, IR spectra, and single-crystal X-ray diffraction studies. The manganese(II) atom in complex II adopts a distorted octahedral geometry with the Schiff base coordinated to it as a uninegatively charged tridentate chelating agent via the pyridine and azomethine nitrogen atoms and the thiolate sulfur atom. Biological studies carried out in vitro against selected bacteria, fungi, and K562 leukemia cell line, respectively, have shown that the free ligands and their metal complexes exhibited distinctive differences in the biological properties. Ligand HL1 and complex I have the marked and broad antimicrobial activities compared to HL2 and complex II while only HL1 and complex II show significant antitumor activity against K562 leukemia cell line, since they exhibit IC50 values in the μM range.  相似文献   

11.
Two new cobalt(II) complexes, [Co(L3)2]·CH3OH·CH3COCH3 (1) (HL3 = 1-(2-{[(E)-3,5-dichloro-2-hydroxybenzylidene]amino}phenyl)ethanone oxime) and Co(L4)2 (2) (HL4 = 1-(2-{[(E)-3,5-dibromo-2-hydroxybenzylidene]amino}phenyl)ethanone oxime), have been synthesized via complexation of Co(II) acetate tetrahydrate with HL1 and HL2. HL1, HL2, and their corresponding Co(II) complexes were characterized by IR, 1H NMR spectra, as well as by elemental analysis and UV–Vis spectroscopy, respectively. The crystal structures of the complexes have been determined by single-crystal X-ray diffraction. 1 and 2 display that extensive hydrogen bonds and C–X···π bonding interactions construct the 1-D infinite chain [Co(L3)2]·CH3OH·CH3COCH3 and Co(L4)2 into 2-D supramolecular frameworks. The electrochemical properties of two Co(II) complexes were also investigated by cyclic voltammetry.  相似文献   

12.
Three azido-bridged copper(II) complexes, [Cu2(L1)21,1,3-N3)2] n ·2nH2O (1), [Cu4(L2)41,1-N3)21,1,3-N3)2] n (2), and [Cu2(L3)21,1-N3)2] (3), where L1, L2, and L3 are the deprotonated forms of 4-bromo-2-[(2-methylaminoethylimino)methyl]phenol (HL1), 4-bromo-2-[(2-ethylaminoethylimino)methyl]phenol (HL2), and 4-bromo-2-[(2-isopropylaminoethylimino)methyl]phenol (HL3), respectively, have been prepared and structurally characterized by single-crystal X-ray diffraction analysis and IR spectra. The slight differences in the terminal groups of the Schiff bases lead to different bridging modes of the azido groups.  相似文献   

13.
Schiff bases o-vanilidene-1-aminobenzene (HL1) and o-vanilidene-2-methyl-1-aminobenzene (HL2) lead to the formation of mono- and bis-[(Cl)Zn(L1)] (1), [(Cl)Zn(L2)] (2), [(Cl)Hg(L1)] (3), [(Cl)Hg(L2)] (4), [Zn(L1)2] (5), [Zn(L2)2] (6), [Hg(L1)2] (7), and [Hg(L2)2] (8) complexes by reactions of zinc(II) and mercury(II) chlorides in different mole ratio(s). Complexes 18 have been characterized by elemental analyses (Zn, Hg, C, H, Cl, and N), melting point and spectral (IR, 1H-NMR), PXRD, molar conductivity measurement, and TGA. Conductivity measurements suggest non-electrolytes. Structural compositions have been assigned by mass spectral studies. Four-coordinate geometry may be assigned to these complexes tentatively. Structural study reveals that in 14 two metal centers are held together by two bridged (μ2-Cl) chlorides, whereas 58 contain two bidentate Schiff-base ligands around one metal-producing monomers.  相似文献   

14.
[Mn(L)(μ1,1–N3)2]2 n [Mn(H2O)21,1–N3)2] n (1) and [Cd(HL)(μ1,1–N3)2] n (2) have been synthesized from HL (HL: pyridine-2-carbaldehyde semicarbazone) and azide ligands, characterized by FT-IR, UV–vis spectroscopy and X-ray crystallography. Single crystal X-ray diffraction revealed that 1 is a coordination polymer consisting of two infinite 1-D chains: chain A with [Mn(L)(μ1,1–N3)2]2 n and chain B with [Mn(H2O)21,1–N3)2] n . In both chains, Mn centers are connected via two double end-on (EO) azide bridges. 2 is a coordination polymer consisting of a 1-D infinite chain, where Cd centers are connected via two double EO azide bridges. The electrochemistry of HL, 1 and 2 were studied by cyclic voltammetry. Magnetic susceptibility measurements indicate bulk ferromagnetic coupling for 1 below 5?K. Antimicrobial activities of both compounds 1 and 2 were greater than HL, with the strongest effect for 2 consistent with its larger radius and electronegativity of Cd(II) ions.  相似文献   

15.
Three mercury(II) complexes containing double-betaine and halide ligands, [(HgCl2)2(L1)] n (1), [(HgBr2)2(L1)(H2O)2] n (2), and [2HgCl2(HL1)·Hg2Cl6] n (3) [L1=O2CCH2N+(CH2CH2)3-N+H2CO2 ], have been prepared and shown to have polymeric structures by single-crystal X-ray analysis. Complex (1) exhibits an infinite zigzag chain in which each mercury(II) atom is coordinated by pairs of carboxylate oxygen atoms and chloride ligands in a distorted tetrahedral geometry. In complex (2), the mercury(II) atom is in an unusual square-planar coordination geometry, and weak mercury-ligand and hydrogen bonding extend the structural skeletons into a three-dimensional network. Complex (3) consists primarily of an assembly of HgCl2(HL1) moieties and [Hg2Cl6] anions, and the mercury(II) atoms are in planar T-shaped and distorted tetrahedral coordination environments, respectively. The resulting three-dimensional network is based on the cross-linkage of nearly planar, wide ribbons running in thea direction.  相似文献   

16.
Two new cadmium(II) azido complexes, [Cd(2,2′-bipy)(N3)2]n (1) and [Cd(2-acpy)(N3)2]n (2) (2,2′-bipy?=?2,2′-bipyridyl and 2-acpy?=?2-acetylpyridine), have been synthesized and structurally characterized by single-crystal X-ray diffraction methods. The coordination environment of the central cadmium atom is distorted octahedral (MN6) in 1 and (MN5O) in 2, with one-dimensional chains formed through Cd2N2 units and alternatively chelating N,N′-bipyridyl or N,O-2-acetylpyridine groups. The central Cd(II) ion is coordinated to two nitrogen atoms of a chelating bipyridyl group or one nitrogen atom and one acetyl oxygen of 2-acetylpyridine and four nitrogen atoms of four different end-on bridging (μ1,1-N3) groups. Chains in the c direction in 1 are stabilized in b direction by π–π interactions involving the aromatic rings of bipyridyl ligands. IR and NMR spectra of the two complexes are reported.  相似文献   

17.
New complexes of bivalent Co, Ni, and Cu with isatin aminoguanisone (HL) and nitroaminoguanisone (HL1) of the composition ([Co(HL)2]Cl2 (I), [Ni(HL)2]Cl2 (II), [Cu(L)Cl] (III), [Co(L1)2] (IV), [Ni(L1)2] (V), and [Cu(L1)2] (VI) are synthesized. Their molecular conductivities and effective magnetic moments are measured and thermal stabilities are studied. The type of the ligand coordination in IVI is proposed on the basis of IR data. The summary of physicochemical data for IVI and the energy calculations for their molecules by the molecular mechanics method made it possible to establish stoichiometry of the coordination polyhedra of the complexes.  相似文献   

18.
The reaction between tridentate NNO donor hydrazone ligands, (E)-2-cyano-N′-(phenyl(pyridin-2-yl)methylene)acetohydrazide (HL1) and (E)-2-cyano-N′-(1-(pyridin-2-yl)ethylidene)acetohydrazide (HL2), with MnCl2·4H2O in methanol resulted in [Mn(HL1)Cl2(CH3OH)] (1) and [Mn(HL2)Cl2(CH3OH)] (2). Molecular structures of the complexes were determined by single-crystal X-ray diffraction. All of the investigated compounds were further characterized by elemental analysis, FT-IR, TGA, and UV–Vis spectroscopy. These complexes were used as catalysts for olefin oxidation in the presence of tert-butylhydroperoxide (TBHP) as an oxidant. Under similar experimental conditions with equal manganese loading, the presence of [Mn(HL2)Cl2(CH3OH)] (2) resulted in higher conversion than [Mn(HL1)Cl2(CH3OH)] (1).  相似文献   

19.
Hydrothermal reactions of Pb(NO3)2 and 3-fluorophthalic acid (H2Fpht) in the absence or presence of 2,2′-bipyridine (bpy) gave two coordination polymers: Pb5(Fpht)4(Fba)2 (1) and [Pb2(Fpht)2(bpy)(H2O)]·3H2O (2). The 3-fluorobenzoic acid (HFba) results from an in situ decarboxylation of H2Fpht. Solid 1 displays a 2-D structure, comprising center-related hexanuclear [Pb3(COO)6]2 units. There are three crystallographically different Pb(II) ions and two different ligands, Fpht and Fba. The Fpht ligands adopt μ6?:?η5η3 and μ6?:?η3η4 unusual bridging coordination modes. A 3-D supramolecular architecture is formed via C–H?F hydrogen bonds. Solid 2 possesses a 1-D chain structure, comprising center-related tetranuclear [Pb2(COO)4]2 units. There are two crystallographically different Pb(II) ions. The Fpht ligands adopt μ3?:?η2η3 and μ4?:?η3η3 bridging coordination. The free water molecules form (H2O)3 clusters to link the 1-D chain by hydrogen bonds. A 3-D supramolecular assembly is constructed via hydrogen bonds between the free water and the F of Fpht ligands. Fluorescence of the complexes originates from π*–π transitions of the ligands.  相似文献   

20.
Two Co(II) coordination polymers, [CoL(npa)]·2H2O (1) and [CoL(Hnpa)2] (2) (L = 1,4-bis(5,6-dimethylbenzimidazole-1-yl)benzene, H2npa = 5-nitroisophthalic acid), have been synthesized in different solvent systems and characterized by Infrared (IR) spectroscopy, elemental analysis, and powder and single crystal X-ray diffraction. Compound 1 was synthesized under solvothermal conditions with DMF as solvent and had a pair of L ligands adopting a μ2-bridging mode and connecting two Co2+ cations to generate a 26-membered Co2L2 loop. The npa2? link adjacent Co2L2 loops via a bis(monodentate) bridging mode to create a 1-D channel-like chain structure. Compound 2 was obtained under hydrothermal conditions, and the carboxylate of the monodeprotonated Hnpa? adopt a μ1-η0?:?η1 coordination to connect adjacent Co2+ cations into a 2-D polymeric layer. The μ2-bridging L ligands connect adjacent 2-D [Co(Hnpa)]n polymeric layers into a 3-D NaCl-like framework. The Co2+ cations and the L ligands in compounds 1 and 2 exhibit different coordination geometries and conformations. Effects of solvents on the construction of Co(II) coordination polymers were investigated. In addition, the electrochemical behavior of carbon paste electrodes containing 1 and 2 and the thermal stabilities of 1 and 2 were investigated.  相似文献   

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