On the hyperfine coupling in tetragonal copper(II) complexes

The vibronic effect on the hyperfine coupling (HFC) parameters in tetragonal copper(II) complexes was studied. The parameters of the vibronic contributions from the - and 4s-AOs of the Cu²⁺ ion to the ground-state function were estimated. The anomalous behavior of the isotropic HFC was analyzed in terms of the static model with consideration of the vibronic coupling. The static and vibronic contributions to the anisotropic portions of the components of the HFC tensor were estimated.Translated from Koordinatsionnaya Khimiya, Vol. 31, No. 3, 2005, pp. 204–206.Original Russian Text Copyright © 2005 by Muravev.This revised version was published online in April 2005 with a corrected cover date.This revised version was published online in April 2005 with a corrected cover date.     

Differential polarography of copper(II) complex

A differential polarographic study has been carried out on the interaction product formed in the interaction of copper(II) with bis(2-hydroxymethyl-5-hydroxy-4-pyrone-6)ketone. The data obtained using the differential pulse method show that copper(II) exhibits a coordination number of one and a reproducible formation constant that is fairly consistent over a moderate concentration range.     

Dinuclear copper(II) complex and 1-D copper(II) complex with taurine Schiff base: synthesis,crystal structure,and properties

A dinuclear copper(II) compound, [Cu(btssb)(H₂O)]₂ · 4(H₂O) (1), and a 1-D chain copper(II) compound, [Cu(ctssb)(H₂O)] _n (2) [where H₂btssb is 2-[(5-bromo-2-hydroxy-benzylidene)-amino]-ethanesulfonic acid and H₂ctssb is 2-[(3,5-dichloro-2-hydroxy-benzylidene)-amino]-ethanesulfonic acid], were prepared and characterized. Compound 1 crystallizes in the monoclinic space group P2₁/c, with a = 10.109(2) Å, b = 20.473(4) Å, c = 6.803(1) Å, β = 100.32(3)°, V = 1385.1(5) ų, and Z = 2; R ₁ for 1796 observed reflections [I > 2σ(I)] was 0.0357. The geometry around each copper(II) can be described as slightly distorted square pyramidal. The Cu^II ··· Cu^II distance is 5.471(1) Å. Compound 1 formed a 1-D network through O–H ··· O hydrogen bonds and 1-D water chains exist. The 1-D chain complex 2 crystallizes in the triclinic space group P 1, with a = 5.030(2) Å, b = 7.725(2) Å, c = 17.011(5) Å, α = 92.706(4)°, β = 97.131(4)°, γ = 102.452(3)°, V = 638.6(3) ų, and Z = 2; R ₁ for 1897 observed reflections [I > 2σ(I)] was 0.0171. In 2, Cu(II) was also a slightly distorted square pyramid formed by two oxygens and one nitrogen from ctssb, one oxygen from another ctssb, and one water molecule. The complex formed a 1-D chain through O–S–O bridge of ctssb ligand. The 1-D chain further constructed a double chain through O?H ··· O hydrogen bonds.     

Homogeneous isotope exchange between copper(II) and bis(resacetophenone oxime)copper(II) complex

Isotope exchange behavior of bis(resacetophenone oxime)copper(II) complex with copper(II) in tri-n-butyl-phosphate and methanol medium has been studied. The studies were carried out at different temperatures varying the concentration of both metal ion and complex. The results show that the complex is labile in the kinetic sense. Increase in temperature increases the isotope exchange rate. The increase in concentration also results in enhancement of the rate of reaction.     

A study on dismutation mechanism of superoxide ion by a macrocyclic copper(II) complex of dioxotetraamine

The mechanism of catalytic dismutation of superoxide anion by copper(II) complex of 12-(4′-nitro)-benzyl-1,4,7,10-tetraazacyclotridecane-11,13-dione was studied by using pulse radiolysis and cyclic voltammetry. The redox potential of Cu(II)/Cu(III) was obtained to be E⁰=0.590 V (SCE) in solution of 0.5 mol·dm⁻³ Na₂SO₄. The rate constant of catalytic dismutation was determined to be k_cat=1.9×10⁶ (pH=7.0) and 1.1×10⁶ mol·dm³·s⁻¹ (pH=7.8) by pulse radiolysis and it was suggested that mechanism of catalytic dismutation of O₂⁻ is alternate oxidation and reduction of Cu(II) complex by O₂⁻.     

A copper(II) chloride complex of hexamethylenetetramine

Summary The 3CuCl₂·4hmta·2HCl·2H₂O complex (hmta=hexamethylenetetramine) has been obtained from acid solution. Spectroscopic and magnetic investigations indicate that, in the crystal structure of this compound, the polymeric chains, 3CuCl₂·2hmta·2H₂O, and hmta·HCl groups occur.     

A phenoxyl radical complex of copper(II)

A new N,O-bidentate pro-ligand (HL), [ML2] (M = Cu, Zn) and [CuL2][BF4] have been synthesised; [CuL2].4DMF and [CuL2][BF4].2CH2Cl2 have been crystallographically and spectroscopically characterised; these data indicate that [CuL2]+ cations are constituted as [Cu2+(L.)(L-)]+ and involve the phenoxyl radical L..     

A sugar discriminating binuclear copper(II) complex

We investigated the complex formation between various underivatized carbohydrates and the binuclear copper(II) complex 1, Cu(2)(bpdpo). A combined approach of UV/vis and CD spectroscopic investigations shows a large discrimination ability of 1 for structurally closely related monosaccharides in alkaline solution. The dominating form of the binuclear copper(II) complex consists of a [Cu(2)L(-)(H)(OH)(2)](+) species between pH 11 and 13, as determined from pH-dependent spectrophotometric titration experiments. The binding strengths of the 1:1 sugar-1 complexes, derived from the biologically important monosaccharides d-mannose (3) and d-glucose (5), is about 1.5 orders of magnitude different at pH 12.40. Moreover, a blue- or a red-shift of the absorption maximum of 1 accompanies the sugar binding and highlights the ability of 1 to discriminate carbohydrates. This phenomenon is due to the number of hydroxyl groups of the particular monosaccharide involved in chelation to the binuclear metal complex.     

Carboxylate-bridged copper(II) complexes: synthesis,crystal structures,and superoxide dismutase activity

Two copper(II) complexes, [Cu₂(μ-benzoato)(L¹)₂]NO₃·2H₂O (1) and [Cu₂(μ-succinato)(L²)₂(H₂O)]ClO₄ (2), have been synthesized, where L¹ = N′-[(E)-phenyl(pyridin-2-yl)methylidene]benzoylhydrazone and L² = N′-[(E)-pyridin-2-ylmethylidene]benzoylhydrazone. These complexes were characterized including by single-crystal X-ray diffraction studies. The copper is five-coordinate in 1 while in 2 one copper is five-coordinate and the other is six-coordinate. Electrochemical behavior of these complexes was measured by cyclic voltammetry. The conproportionation equilibrium constants (K_con) for both complexes have been estimated. The superoxide dismutase (SOD) activities of 1 and 2 were measured by nitro blue tetrazolium assay. Complex 1 has better SOD activity than 2.     

Multicomponent assembly of anionic and neutral decanuclear copper(II) phosphonate cages

A multicomponent synthetic strategy involving copper(II) ions, tert-butylphosphonic acid (t-BuPO(3)H(2)) and 3-substituted pyrazole ligands has been adopted for the synthesis of soluble molecular copper(II) phosphonates. The use of six different 3-substituted pyrazoles, 3-R-PzH [R = H, Me, CF(3), Ph, 2-pyridyl (2-Py), and 2-methoxyphenyl (2-MeO-C(6)H(4))] as ancillary ligands afforded nine different decanuclear cages, [Cu(5)(μ(3)-OH)(2)(O(3)P-t-Bu)(3)(3-R-Pz)(2)(X)(2)](2)·(Y) where R = H, X = t-BuPO(3)H, and Y = (Et(3)NH(+))(4)(solvent) (1); R = Me, X = 3-MePzH, and Y = solvent (2); R = Me, X = t-BuPO(3)H, and Y = (Et(3)NH(+))(4)(solvent) (3); R = CF(3), X = t-BuPO(3)H, and Y = (Et(3)NH(+))(4)(solvent) (4); R = Ph, X = 3-PhPzH, and Y = solvent (5); R = 2-Py, X = 0.5 MeOH, and Y = solvent (6); R = 2-Py, X = none, and Y = solvent (7); R = 2-Py, X = H(2)O, and Y = (Et(3)NH(+)·PF(6)(-))(2)(solvent) (8); R = 2-MeO-C(6)H(4), X = MeOH or 0.5:0.5 MeOH/H(2)O, and Y = solvent (9). Compounds 1-6, 8, and 9 were isolated using a direct synthetic method which involves the reaction of copper(II) salts and the ligands, while 7 was obtained from an indirect route involving the reaction of preformed copper-pyridylpyrazolate precursor complexes and t-BuPO(3)H(2). The decametallic compounds 1-9 possess a butterfly shaped core. The core of the cages 1, 3, and 4 are tetraanionic and contain more phosphonates than pyrazole ligands, while the other cages are neutral and contain more pyrazoles than phosphonate ligands. Compounds 1-6 have been studied by electrospray ionization-high-resolution mass spectrometry (ESI-HRMS). The decanuclear cage 6 was shown to be a good plasmid modifier.     

Ion-pair formation of a copper(II)-ammine complex with an anionic surfactant and the recovery of copper(II) from ammonia medium by the surfactant-gel extraction method.

The extraction and separation of copper(II), zinc(II), cobalt(II), and cadmium(II) were investigated. Both copper(II) and zinc(II) formed ammine-complexes, while cadmium(II) and cobalt(II) formed hydroxide precipitates in an ammonia medium. By the addition of sodium dodecylsulfate (SDS), a copper(II) complex formed an ion-pair (copper-ammine-DS), which was extracted into the SDS phase. However, a zinc(II) complex did not form an ion-pair, and was soluble in water. Copper(II) ion was recovered by stripping (back-extraction) after the addition of hydrochloric acid. This method was applied to the separation of copper(II) in a brass alloy.     

The determination of anionic detergents with the bis (ethylenediamine)copper(II) ion

A method is described for the determination of anionic detergents. The detergent anions are extracted into chloroform as an ion-association compound with the bis(ethylenediamine)copper(II) cation. Determinations are completed by colorimetry or atomic absorption spectrometry. With a 150-ml water sample, the limit or detection is 0.03 μg ml^-1 (as LAS) for colorimetry or 0.06 μg ml^-1 for a.a.s. The method requires only one phase separation step and is highly selective. It is directly applicable to brine and sea-water samples.     

Synthesis and spectroscopic characterization of copper(II) tetraazaiminooxime macrocyclic complexes--a tetragonal distortion analysis

Herein we describe the synthesis and spectroscopic (infrared and UV-vis) analysis of [Cu(II)(dohpn)(L)](n+) (dohpn=imineoximic tetraazamacrocyclic ligand 2,3,9,10-tetramethyl-1,4,8,11-tetraazaundecane-1,3,8,10-tetraen-11-ol-1-olate) and L=SCN(-), I(-), Cl(-) (n=0) and 4-aminopyridine (ampy), 4,4'-bipyridine (bipy), imidazole (im), 2-aminopyrazine (ampz) and water (n=1+). The following order of the Jahn-Teller stabilization energy (cm(-1)) was observed: I(-)(6452)相似文献