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1.
2.
1,2-bis(p-aminophenoxy)ethane was obtained with reduction of 1,2-bis(p-nitrophenoxy)ethane and Pd/C as catalyst in hydrazine hydrate. Co(II), Cu(II), and Ni(II) complexes of aromatic bidentate
diamine were prepared. The structure of the ligand and its complexes were characterized by IR, elemental analysis, magnetic
susceptibility, conductivimetry, UV-Vis and 1H NMR spectroscopy. The metal/ligand mole ratios were found to be 1:1. The general compositions of these complexes are found
to be [CoLCl2], [CuLCl2], and [CoLCl2].
The text was submitted by the authors in English. 相似文献
3.
E. V. Tretyakov S. E. Tolstikov G. V. Romanenko A. S. Bogomyakov R. Z. Sagdeev V. M. Novotortsev V. I. Ovcharenko 《Journal of Structural Chemistry》2013,54(1):104-109
Previously unknown [ML2(H2O) n ] bischelates, where M is Mn(II), Co(II), Ni(II), or Cu(II) and L is deprotonated triformylmethane, are studied by X-ray diffraction analysis. It is revealed that in the crystals of all compounds there are multiple hydrogen bonds linking bischelate molecules into polymer layers or a single framework. The character of the temperature dependence of the effective magnetic moment [ML2(H2O) n ] indicates the existences of weak intracrystalline exchange interactions between the unpaired electrons of the paramagnetic centers. 相似文献
4.
Under the thermolysis condition, 5-phenyl-2,3-dihydro-2,3-furandione (IV) in inert aprotic solvents as p-xylene at 130–140°C yields 3-benzoyl-4-hydroxy-6-phenyl-2H-pyran-2-one (VI) via phenyl ketene (V). The compound (VI) was converted into the corresponding 3-benzoyl-4-hydroxy-6-phenylpyridin-2(1H)-one (VII), and 3-benzoyl-2-oxo-6-phenyl-2H-pyran-4-yl acetate (VIII), by its reactions with ammonium hydroxyde, and acetic anhydride, respectively. On the other hand, a series of new various
metal complexes (IX-XIa, XIb) of VI was synthesized. The results suggest that the compound VI as bidentate ligand indicate a binuclear structure for the Cu(II) complex with square-planar geometry. The Ni(II) and Zn(II)
complexes are of tetrahedral and the Co(II) complex is also octahedral geometry with water molecules at the axial positions.
The structures of compounds and complexes were characterized on the basis of elemental analysis, Mass, IR, 1H, and 13C NMR spectra.
The text was submitted by the authors in English. 相似文献
5.
Ma del Carmen Fernández-Fernández Alejandro Macías Laura Valencia 《Journal of organometallic chemistry》2009,694(22):3608-3613
The coordination capability of the new tetrapyridyl pendant-armed azamacrocyclic ligand L, towards Co(II), Ni(II), Cu(II) and Cd(II) ions was studied. The ligand and the complexes were characterized by microanalysis, LSI mass spectrometry, IR, UV-Vis and NMR spectroscopy, magnetic studies and conductivity measurements. Crystal structures of [Co2L(CH3CN)2](ClO4)4·2CH3CN and [Cd2L(NO3)2](NO3)2·2H2O complexes have been determined. The X-ray studies show the presence of dinuclear endomacrocyclic complexes with the metal ion in a similar distorted octahedral environment, coordinated by one pyridyl bridgehead group, two amine nitrogen atoms and two pyridyl pendant-arms. The sixth coordination position around the metal ion is completed by one acetonitrile molecule in [Co2L(CH3CN)2](ClO4)4·2CH3CN and by one monodentate nitrate anion in [Cd2L(NO3)2](NO3)2·2H2O. Different sort of intramolecular non-classical hydrogen bonds were found in the crystal lattice of both structures. 相似文献
6.
Jesús Ma Martínez-Snchez Rufina Bastida de la Calle Alejandro Macías Paulo Prez-Lourido Laura Valencia Matarranz 《Polyhedron》2006,25(18):3495-3500
Hydrated nitrate and perchlorate salts of the transitional metal ions Co2+, Ni2+ and Cu2+ have been used to investigate the coordination capability of the octaaza macrocycle L derived from 2,6-diformylpyridine and diethylenetriamine. The synthesis of the metal complexes was carried out in 1:1 and 2:1 metal:ligand molar ratios, but dinuclear complexes were obtained in all cases due to the size of the 24-membered ligand. The complexes have been characterized by elemental analysis, molar conductivity, mass spectrometry, IR spectroscopy, diffuse reflectance and magnetic measurements. The dinuclear nature of the compounds was confirmed by X-ray diffraction. The crystal structures of [Ni2L(NO3)2](NO3)2, [Cu2L(NO3)4] and [Cu2L(ClO4)4], were determined. 相似文献
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A new ligand, 4‐(1‐methyl‐1‐mesityl‐3‐cyclobutanyl)‐2‐(2‐hydroxy‐1‐naphthylideneimino)thiazole (LH), has been synthesized starting from 1‐methyl‐1‐mesityl‐3‐(2‐chloro‐1‐oxoethyl)cyclobutane and thiourea and subsequently 2‐hydroxy‐1‐napthalaldehyde. Mononuclear complexes with a metal‐ligand ratio of 1:2 have been prepared with Co(II), Cu(II), Ni(II), and Zn(II) metals. The authenticity of the ligand and its complexes are proposed based on elemental analyses, IR, UV‐vis, 13C and 1H NMR spectra, magnetic susceptibility measurements, thermogravimetric analyses, and differential scanning calorimetry. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:42–46, 2001 相似文献
9.
《Journal of Coordination Chemistry》2012,65(21):3454-3462
4-Bromo-N-(di-R-carbamothioyl)benzamide (R = methyl, ethyl, n-propyl, n-butyl and phenyl) ligands and their Ni(II) and Cu(II) complexes have been synthesized and characterized by elemental analyses, FT-IR and 1H-NMR spectroscopy. The crystal and molecular structure of bis(4-bromo-N-(di-n-propylcarbamothioyl)benzamido)nickel(II) has been determined from single crystal X-ray diffraction data. It crystallizes in the triclinic, space group P 1, Z = 2 with a = 9.286(2) Å, b = 13.215(3) Å, c = 14.125(3) Å, α = 64.180(5)°, β = 85.483(6)°, γ = 83.067(5)°, V = 1548.3(7) Å3 and D Calcd = 1.594 mg m?3. Loss of the N–H proton resonance and the N–H stretching vibration and the shift of the ν C=O and ν C=S stretching vibrations confirm formation of the metal complexes. These studies have shown that the metal complexes are neutral cis-[ML2]. 相似文献
10.
New metal complexes of Fe(III), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II) with salicylidine-2-aminobenzimidazole (SABI) are
synthesized and their physicochemical properties are investigated using elemental and thermal analyses, IR, conductometric,
solid reflectance and magnetic susceptibility measurements. The base reacts with these metal ions to give 1:1 (Metal:SABI)
complexes; in cases of Fe(III), Co(II), Cu(II), Zn(II) and Cd(II) ions; and 1:2 (Metal:SABI) complexes; in case of Ni(II)
ion. The conductance data reveal that Fe(III) complex is 2:1 electrolyte, Co(II) is 1:2 electrolyte, Cu(II), Zn(II) and Cd(II)
complexes are 1:1 electrolytes while Ni(II) is non-electrolyte. IR spectra showed that the ligand is coordinated to the metal
ions in a terdentate mannar with O, N, N donor sites of the phenloic -OH, azomethine -N and benzimidazole -N3. Magnetic and
solid reflectance spectra are used to infer the coordinating capacity of the ligand and the geometrical structure of these
complexes. The thermal decomposition of the complexes is studied and indicates that not only the coordinated and/or crystallization
water is lost but also that the decomposition of the ligand from the complexes is necessary to interpret the successive mass
loss. Different thermodynamic activation parameters are also reported, using Coats-Redfern method.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
11.
O. G. Shakirova L. G. Lavrenova N. V. Kuratieva D. Yu. Naumov A. S. Bogomyakov L. A. Sheludyakova T. F. Mikhailovskaya S. F. Vasilevsky 《Russian Journal of Coordination Chemistry》2012,38(8):552-559
New cobalt(II), nickel(II), and copper(II) complexes based on 5-methoxycarbonyl-3-me-thylpyrazole (MePzCOOMe), [Co(MePzCOOMe)2(H2O)2](NO3)2 (I), [Ni(MePzCOOMe)2(H2O)2] (NO3)2 (II), and [Cu(MePzCOO)2(H2O)] · 3H2O (III), were synthesized. The compounds were studied by X-ray diffraction analysis, IR spectroscopy, and static magnetic susceptibility. The molecular and crystal structures of complexes I and III were determined by X-ray structure analysis. 相似文献
12.
Satish M. Annigeri M. P. Sathisha Vidyanand K. Revankar 《Transition Metal Chemistry》2007,32(1):81-87
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
13.
《Journal of Coordination Chemistry》2012,65(16):2728-2735
A new Schiff base, {1-[(2-hydroxy-naphthalen-1-ylmethylene)-amino]-4-phenyl-2-thioxo-1, 2-dihydro-pyrimidin-5-yl}-phenyl-methanone, has been synthesized from N-amino pyrimidine-2-thione and 2-hydroxynaphthaldehyde. Metal complexes of the Schiff base were prepared from acetate/chloride salts of Cu(II), Co(II), Ni(II), Zn(II), and Cd(II) in methanol. The chemical structures of the Schiff-base ligand and its metal complexes were confirmed by elemental analyses, IR, 13C-NMR, 1H-NMR, API-ES, UV-Visible spectroscopy, magnetic susceptibility, and thermogravimetric analyses. The electronic spectral data and magnetic moment measurements suggest mononuclear octahedral and mononuclear or binuclear square planar structures for the metal complexes. In light of these results, it was suggested that this ligand coordinates to each metal atom by hydroxyl oxygen, azomethine nitrogen, and thione sulfur to form octahedral complexes with Cd(II) and Zn(II). 相似文献
14.
The ligand has been
prepared from ω-chloroisonitrosoacetophenone and 1,4-phenylenediamine
in the presence of NaHCO3. The ligand have a C=O group
and an –NH–R group adjacent to the oxime group. The Ni(II), Cu(II)
and Co(II) complexes of the synthesized ligand were prepared and their structures
were identified using FTIR, UV-Vis spectral data, elemental analysis, thermal
analysis and magnetic moment measurements. The metal-ligand ratios were found
to be 3:2. The ligands were found to coordinate to the metal ions via the
oxime nitrogen, oxime oxygen, one of the carbonyl group and amide nitrogen
atoms. Thermal analyses data reveals that the water in the complexes was found
to be non-coordinated to the metal ions. In the trinuclear structures, the
metals have the tetrahedral environments. 相似文献
15.
Gresser R Hoyer A Hummert M Hartmann H Leo K Riede M 《Dalton transactions (Cambridge, England : 2003)》2011,40(14):3476-3483
The synthesis of five homoleptic transition metal complexes of bis-(phenyl)-diisoindol-aza-methene is described together with the optical, electrochemical and thermal properties of these compounds. Additionally, crystal structures for the Co and the Zn complex are reported. 相似文献
16.
Gondolova G. G. Ismailova S. Z. Fatullaeva P. A. Mejidov A. A. 《Russian Journal of General Chemistry》2019,89(3):546-548
Russian Journal of General Chemistry - Co(II), Ni(II), and Cu(II) complexes with N-(2-hydroxybenzamido)phthalimide (LH2) were synthesized and studied by IR, electron absorption, EPR spectroscopy,... 相似文献
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18.
《Journal of Analytical and Applied Pyrolysis》1986,9(2):159-170
The thermal behaviour of 6-amino-1,3-dimethyl-5-phenylazouracil complexes of Co(II), Ni(II), Cu(II) and Ag(I) ions was studied by IR, thermogravimetric and differential scanning calorimetric techniques. IR spectroscopy applied to these complexes heated in air allowed the elucidation of the decomposition steps and the nature of the intermediate products. The Cu(II) complexes led to the same products on heating at 225°C [bis(1,3-dimethyl-2,4-dioxo-5-phenylazo-1,2,3,4- tetrahydropyrimidine-6-oxido)copper(II)]. 相似文献
19.
The cobalt, nickel, copper and zinc atoms in bis(1,10-phenanthroline)bis(salicylato-O)metal(II) monomeric octahedral complexes
[M(Hsal)2(phen)2]·nH2O, (M: Co(II), n=1; Cu(II), n=1.5 and Ni(II), Zn(II), n=2) are coordinated by the salicylato monoanion (Hsal) through the carboxyl oxygen in a monodentate fashion and by the 1,10-phenanthroline (phen) molecule through the two amine
nitrogen atoms in a bidentate chelating manner. On the basis of the DTGmax, the thermal stability of the hydrated complexes follows order: Ni(II) (149°C)>Co(II) (134°C)>Zn(II) (132°C)>Cu(II) (68°C)
in static air atmosphere. In the second stage, the pyrolysis of the anhydrous complexes takes place. The third stage of decomposition
is associated with a strong exothermic oxidation process (DTA curves: 410, 453, 500 and 450°C for the Co(II), Ni(II), Cu(II)
and Zn(II) complexes, respectively). The final decomposition products, namely CoO, NiO, CuO and ZnO, were identified by IR
spectroscopy.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
20.
《Polyhedron》1988,7(5):337-343
The new Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes with tridentate Schiff base, the product of condensation of o-aminobenzyl alcohol with salicylaldehyde have been synthesized and characterized by elemental analysis, IR, electronic, EPR and Mössbauer spectra, thermal analysis, magnetic susceptibility and molecular weight measurements. Dimeric or polymeric structures for the investigated complexes were proposed. The interaction of the cobalt complex with dioxygen is also described. 相似文献