Extraction and complexation of copper(II) with para-tert-butylbenzhydrazide and its N′,N′-dimethyl derivative

The extraction of copper(II) with the para-tert-butylbenzoic acid hydrazide and related N??,N??-dimethyl derivative was studied. The composition and structure of the extracted complexes were determined, the mechanism of extraction of copper(II) in different media was suggested, the extraction constant was calculated. The copper(II) complex compounds with these reagents were isolated.     

Complexation of copper(II) with 2′,2′-dialkyl-para-tert-butylbenzohydrazides

The complexation of copper(II) with 2′,2′-dimethyl-, 2′,2′-dibutyl-, and 2′,2′-diisobutyl-para-tert-butylbenzohydrazide in water-ethanol media was studied. The reagents (HL) formed [Cu(HL)]²⁺ and [Cu(HL)₂]²⁺ cationic complexes in a weakly acidic medium and uncharged CuL₂ complexes in an alkaline medium. logK _st was calculated for these complexes. The effect of 2′,2′-alkyl radicals on the stability of the complexes was considered. The obtained results were compared with data on the complexation of copper(II) ions with 2′,2′-dialkylbenzohydrazides.     

Crystal structure of copper(II) chelate with para-(tert-butyl)benzoic acid N′,N′-dimethylhydrazide

X-Ray diffraction analysis was performed for the copper(II) chelate with para-(tert-butyl)benzoic acid N??,N??-dimethylhydrazide, Cu(p-(tert-Bu)C₆H₄CONHNMe₂)₂ (I). The reagent functions as a bidentate (O,N(2)) ligand giving a five-membered copper-containing ring. The molecule is centrosymmetric. The Cu atom and the metal rings lie in the same plane. The coordination polyhedron of copper is a slightly distorted square. The crystals are monoclinic: a = 16.2634(14) ?, b = 9.0415(8) ?, c = 9.6415(9) ?, ?? = 90°, ?? = 100.052(7)°, Z = 2, space group P2₁/c.     

Five coordinate complexes of N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamide with copper Crystal and molecular structures of dichloro(N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamido)copper(II) and chloro(perchlorato)(N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamido)copper(II)

The title compound N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamide (DEAP) forms a 1:1 complex with anhydrous CuCl₂, [Cu(DEAP)Cl₂], (1) which was crystallized from EtOH solution in the monoclinic space group P2_{1/ n} with cell constant, a = 10.024(1); b = 13.122(1); c = 14.404(1) Å β = 101.31(1)° V = 1857.8(3) ų and Z = 4. The chloro-perchlorato complex, [Cu(DEAP)Cl(ClO₄)], (2) obtained in near quantitative yield by reacting (1) with an excess of NaClO₄ in EtOH, crystallized in the monoclinic space group P2_{1/ n} with cell constants, a = 7.965(1); b = 25.827(2); c = 10.046(1) Å β = 98.81(1)° V = 2042.2(4) ų and Z = 4. Both (1) and (2) contain 5-coordinated copper linked to DEAP through O～N～O donor set of atoms with covalently bonded chlorine atoms in (1) and chlorine and perchlorate groups in (2). The coordination geometry is intermediate between square pyramidal and trigonal bipyramidal, and is probably best described as a trigonally distorted rectangular pyramid.     

Manganese(II), nickel(II) and copper(II) complexes of (1,3-bis-aminomethyl) cyclohexane-N,N,N′,N′-tetrakisbenzimidazole

Summary Mn^II, Ni^II and Cu^II complexes of (1,3-bis-aminomethyl)-cyclohexane-N,N,N,N-tetrakisbenzimidazole (CDTB) have been prepared and characterized by spectral techniques. The complexes are monomeric and pseudo-octa-hedral, as evidenced by their e.p.r. spectra and analytical data. Parameters ², ², ² and for Cu^II complexes, and the crystal field splitting parameter (10 Dq) together with the Nephelauxetic ratio (), for Ni^II complexes, are reported.     

Catalase activity of cobalt(II) complexes with N,N,N′,N′-tetrasubstituted thiocarbamoylsulfenamides

On the base of the kinetic and activation parameters of the hydrogen peroxide decomposition in the presence of chelates of CoX₂ salts (X = Cl, Br, I, NCS) with N,N,N′,N′-tetrasubstituted thiocarbamoylsulfenamides containing exocyclic (out-of-chelate) fragments of dimethylamine (I), piperidine (II), and piperazine (III) the nature of acido-ligands influence on catalase activity of complexes I–III was revealed, depending on the structure and composition of the chelating ligand. Mononuclear complexes I(Br) and II(Br) can transform into 10-membered binuclear macrochelate intermediates.     

Thermal decomposition kinetics of polymeric complexes of copper(II) and mercury(II) with N,N′-bis(dithiocarboxy)piperazine

The thermal decomposition behaviour of polymeric complexes of Cu(II) and Hg(II) with N,N-bis(dithiocarboxy)piperazine is investigated in air by thermogravimetric (TG), derivative thermogravimetric (DTG) and differential thermal analysis (DTA) techniques. The kinetic parameters (non-isothermal method) for their decomposition have been evaluated by graphical as well as by least-squares methods. The equations of Coats-Redfern, Freeman-Carroll and Horowitz-Metzger have been applied. The results indicate that the values ofE,A and S obtained by these three different methods agree well. It was also found that the decomposition of these metal chelates follow first-order kinetics.

---

Zusammenfassung Mittels TG, DTG und DTA wurde das thermische Zersetzungsverhalten von Polymerkomplexen aus Cu(II) bzw. Hg(II) mit N,N-Bis(dithiocarboxy)piperazin an Luft untersucht. Für ihre Zersetzung (nichtisotherme Methode) wurden die kinetischen Parameter sowohl graphisch als auch durch Methoden mit den kleinsten Fehlerquadraten ermittelt. Dabei wurden die Gleichungen von Coats-Redfern, Freeman-Carroll und von Horowitz-Metzger angewendet. Alle drei Verfahren zeigen übereinstimmende Resultate fürE, A undS. Es wurde weiterhin gefunden, daß diese Metallchelate einer Reaktion erster Ordnung unterliegen.

---

---

The authors are thankful to Prof. C. G. R. Nair, Head of the Department of Chemistry, University of Kerala and Dr. M. P. Kannan, Department of Chemistry, University of Calicut for some helpful discussions.     

Spectroscopic characterization and crystal structure of cis-Bis(N-(2-benzoyl)-N′,N′-diphenylthioureato-k 2O,S)nickel(II)

The title compound [Ni(C₂₀H₁₅N₂OS)₂] is prepared by the reaction of metal acetate with the corresponding acylthiourea derivative. The complex is characterized by elemental analysis, IR, ¹H and ¹³C NMR, and its structure is determined by single crystal X-ray diffraction. The Ni(II) ion is coordinated by the S and O atoms of two N-benzoyl-N??,N??-diphenylthiourea ligands in a slightly distorted square-planar coordination geometry. The two O and two S atoms are mutually cis to each other. The substance crystallizes triclinic (P-1 space group) with cell dimensions a = 10.7262(9) ?, b = 12.938(3) ?, c = 14.2085(12) ?, ?? = 74.650(4)°, ?? = 78.398(4)°, ?? = 68.200(5)°, and two formula units in the unit cell. The structure is very close to the related N-(2-furoyl) Ni complex reported previously.     

Cobalt(III), nickel(II) and copper(II) complexes of N,N′-didodecildithiooxamide

The complexes of N,N′-didodecildithiooxamide (L): CoL₃(ClO₄)₃, NiL₂X₂ (X = Cl, Br, I, ClO₄, HSO₄), CuL₂X₂ (X = ClO₄, HSO₄) and CuLX₂ (X = Cl, Br) were prepared. The cobalt and nickel complexes are diamagnetic, with octahedral and planar coordination respectively. The copper complexes are paramagnetic with normal magnetic moments corresponding to a tetragonal coordination. The i.r. and far i.r. spectra are discussed.     

Extraction of U(VI) and Th(IV) from nitric acid solutions with N,N,N′,N′-tetrahexylsuccinylamide

The results of monitoring of⁸⁵Kr volume activity in ground-level air of Prague over the period 1989–1995 are summariyed. Seasonal dependence with a maximum in late spring and summer months and a gradual increase of⁸⁵Kr concentration in the atmosphere were observed. Linear approximation of long-term trend in the period 1983–1995 gives the growth rate of 35 mBq·m^–3 per year. Exponential approximation provides an inter-year growth by 3.7% The measured values were compared to the prognosis of⁸⁵Kr contamination development of the atmosphere from the early 1980s. They were found to be near to the low estimate of the assumed development.     

Synthesis and magnetic properties of heterobinuclear copper(II)–iron(II) complexes with N,N′-bis(2-aminopropyl)oxamidocopper(II)

Six new -oxamido heterobinuclear complexes, namely [Cu(oxap)Fe(L)2]SO4, where oxap denotes the N,N-bis(2-aminopropyl)oxamido dianion and L represents 1,10-phenanthroline (phen); 5-nitro-1,10-phenanthroline (NO2-phen); 5-chloro-1,10-phenanthroline (Cl-phen); 5-methyl-1,10-phenanthroline (Me-phen); 2,2-bipyridine (bpy); and 4,4-dimethyl-2,2-bipyridine (Me2bpy), have been synthesized and characterized by elemental analyses, i.r. spectra, electronic spectra, magnetic moments (at room temperature) and molar conductivity measurements. The temperature dependent magnetic susceptibilities of [Cu(oxap)Fe(bpy)2]SO4 (1) and [Cu(oxap)Fe(phen)2]SO4 (2) have been studied in the 4.2–300K range, giving the exchange integrals J=–20.9cm–1 for (1) and J=–22.5cm–1 for (2). These results are commensurate with antiferromagnetic interactions between adjacent metal ions within each molecule.     

Syntheses and structures of cobalt(II), nickel(II), and copper(II) complexes with N,N,N′,N′-tetraalkylpyridine-2,6-dicarboxamides (O-daap) containing nitrate as the counter ion

Reactions of M(NO₃)₂?·?xH₂O [M?=?Co(II), Ni(II), and Cu(II)] with N,N,N′,N′-tetraalkylpyridine-2,6-dicarboxamides(O-daap) in CH₃CN yield [Co(O-dmap)(NO₃)₂] (1), [Co(O-deap)(NO₃)₂] (2), [Co(O-dpap)(NO₃)₂] (3), [Ni(O-dmap)(H₂O)₃](NO₃)₂] (4), [Ni(O-deap)(H₂O)₂(NO₃)](NO₃)] (5), [Cu(O-deap)(NO₃)₂] (6), and [Cu(O-dpap)(NO₃)₂] (7). X-ray crystal structures of 1, 2, 4, 5, and 7 reveal that O-daap ligands coordinate tridentate to each metal, O–N–O, with nitrate playing a vital role in molecular and crystal structures of all the complexes. The coordination geometry in the two Co(II) complexes, 1 and 2, is approximately pentagonal bipyramidal with nitrate bonded in a slightly unsymmetrical bidentate chelating mode. [Ni(dmap)(H₂O)₃](NO₃)₂ (4) and [Ni(deap)(H₂O)₂(NO₃)](NO₃) (5) exhibit octahedral geometry, the former containing uncoordinated nitrate while the latter has one nitrate coordinated unidentate and the other nitrate outside the coordination sphere. The Cu(II) in [Cu(dpap)(NO₃)₂] (7) occupies a distorted square pyramidal geometry and is linked to two unidentate nitrates, although one nitrate is also involved in a weak interaction with the metal through its other oxygen. IR spectra and other physical studies are consistent with their crystal structural data. O-dmap?=?N,N,N′,N′-tetramethylpyridine-2,6-dicarboxamides; O-deap?=?N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamides; and O-dpap?=?N,N,N′,N′-tetraisopropylpyridine-2,6-dicarboxamides.     

Synthesis and structural features of copper(II) complexes of N,N,N′,N′-tetramethylethylenediamine with 2-chlorobenzoate1− and 2-hydroxybenzoate1−

Abstract

Two copper(II) coordination complexes, formulated as [Cu(tmen)(Clba)₂] (1) and [Cu(tmen)(Hsal)₂·H₂O] (2) (where tmen?=?N,N,N′,N′-tetramethyl ethylenediamine (C₆H₁₆N₂), Clba^1? = 2-chlorobenzoate (C₇H₄ClO₂^1?), and Hsal^1? (C₇H₅O₃^1? = monoanion of o-hydroxybenzoic acid (salicylic acid)), have been synthesized and characterized by elemental combustion analysis, spectroscopic techniques, thermal studies, and single crystal X-ray analyses. Complex 1 consists of two distinct monomeric units in which the coordination environment around the central copper(II) ion is a distorted octahedron with a CuN₂O₄ chromophore, constituted by a chelating tmen molecule, and two 2-chlorobenzoate^1? anions coordinated through their carboxylate-O atoms in an asymmetrical bidentate fashion. Complex 2 is also a monomer and consists of an CuN₂O₃ chromophore, in which tmen is coordinated to Cu(II) through its two N atoms in a chelating bidentate fashion, and an aqua-O and the two o-hydroxybenzoate^1? (HSal^1?) anions are coordinated through one of their carboxylate-O atoms in a monodentate mode, forming a square pyramidal structure. Hydrogen bonding interactions especially of O–H…O, N–H…O, and C–H…Cl types interweave monomeric units and stabilize the overall crystal structures in both complexes. Thermal analysis and antibacterial activities of 1 and 2 against various bacterial strains were also investigated.     

Kinetics of the oxidation of [N-(2-hydroxyethyl)-ethylene-diamine-N,N′,N′-triacetato]cobalt(II) by N-bromosuccinimide

The kinetics of the oxidation of [N-(2-hydroxyethyl)-ethylene-diamine-N,N,N-triacetato] cobalt(II), [Co^II-(HEDTA)]^–, by N-bromosuccinimide, NBS, have been studied in aqueous solutions and water-methanol solvent mixtures under various conditions. The reaction stoichiometry indicates that one mole of NBS reacts with one mole of [Co^II(HEDTA)]^–. In aqueous solutions the reaction obeys the following rate law:

Mixed valence copper(I)–copper(II) complexes of N,S donor ligands and their 7,7′,8,8′-tetracyanoquinodimethane derivatives

The reaction of the CuCl2·2H2O with the N,S donor ligands bis(o-aminobenzenethio)ethane, bis(o-aminoben-zenethio)propane and bis(o-aminobenzenethio)butane (abbreviated as eN2S2, pN2S2 and bN2S2, respectively) yielded mononuclear CuII complexes of stoichiometry Cu(L)Cl2 (L=eN2S2, pN2S2 or bN2S2). When the reactions were performed in the presence of 2,6–diacetylpyridine and NaClO4, binuclear mixed valence CuI–CuII complexes of stoichiometry [Cu2(L)][ClO4]3 (L=eN6S4, pN6S4 or bN6S4) were formed. Metatheses between the binuclear complexes and the lithium salt of 7,7,8,8-tetracyanoquinodimethane (TCNQ) yielded complexes of stoichiometry Cu2(L)(TCNQ)2 (L=eN6S4, pN6S4 or bN6S4). All of the complexes were characterised by analytical and spectroscopic techniques.     

Protolytic equilibria of N-(β-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid

The heats of the successive dissociation of N-(β-hydroxyethyl)ethylenediamine-N,N′, N′-triacetic acid at T = 298.15 K and I = 0.1, 0.5, and 1.0 (KNO₃) have been determined directly by calorimetry. Standard thermodynamic characteristics of the protolytic equilibria have been derived from thermochemical and potentiometric data obtained under identical conditions. The results are compared with the corresponding data for similar compounds and are discussed with reference to the structural features of the diamine chelants.     

Extraction of copper(II) ions from ammonia solutions with a β-diketone extractant

The extraction of copper(II) ions from ammonia solutions with a new β-diketone extractant, DX-510A, has been studied. Kinetic features of the copper(II) extraction and back extraction have been established: the reaction orders have been determined, and extraction and stripping rate constants have been calculated to be k_e1 = 4.14 × 10^–2 s^–1 and k_be1 = 3.20 × 10^–2 s^–1, respectively. It has been demonstrated that the extraction of copper(II) ions is not accompanied by the coextraction of ammonia. The type of extracted complex has been determined and its formula has been suggested.     

Extraction of Uranium(VI) with N,N′-Dilauroylpiperazine in Carbon Tetrachloride

A novel extractant, N,N-dilauroylpiperazine (DLPEZ), was synthesized for the first time. The extraction of uranium(VI) with the novel extractant in carbon tetrachloride from aqueous nitric acid media has been studied. The dependence of extraction distribution ratio on the concentration of aqueous nitric acid, extractant, salting-out agent and temperature was investigated and the enthalpy of the extraction was determined.     

Extraction behavior of strontium from nitric acid solution with N,N,N′,N′-Tetraisobutyl diglycolamide

The extraction behaviors of strontium from nitric acid solution were investigated with N,N,N′,N′-tetraisobutyl diglycolamide (TiBDGA). Effects of acidity, diluents, concentration of extractant and temperature on the distribution ratio of strontium (D _Sr) were examined. The stoichiometry of the extracted molecule was Sr²⁺:TiBDGA of 1:3. The apparent extraction equilibrium concentration constant logK _ex was 3.25. The enthalpy change ΔH and entropy change ΔS were ?55.6 kJ mol^-1 and ?124 J mol^-1 K^-1, respectively. The extraction is an exothermic process. Through two strip stages, strontium could be stripped effectively by 0.01 M nitric acid solution.