Electrochemical method of obtaining copper (II) oxide powders in alkaline electrolyte

Within the framework of these studies, an electrochemical method for the synthesis of highly dispersed powders of copper compounds in aqueous solutions of alkalis is presented. The factors influencing the rate of production of nanoscale copper (II) oxide particles are determined. It is shown that during the anodic oxidation of copper by direct current, the speed of highly dispersed powders formation depends on current density, the nature of alkali cation, and the concentration of electrolyte solution. The mass loss of copper electrodes in NaOH solution is higher than in solutions of potassium hydroxide and lithium hydroxide by 10% and 12%, respectively. This experiment suggests that the studied alkalis act similarly on the anodic behavior of copper and the nature of cation does not significantly affect the speed of anodes destruction. The change in the concentration of alkali solution practically does not affect the mass loss of copper electrodes. The speed of copper oxidation remains almost constant over time, but noticeable weight loss and, accordingly, the speed of copper dissolution is achieved within 15 minutes. The speed of copper oxidation does not depend on current density. It is determined by the amount of electricity that has passed. The current density of 1 A/cm2 can be considered optimal.

Copper complexes as antitumor agents: in vitro and in vivo evidences

: Copper is an essential element for most aerobic organisms, with an important function as a structural and catalytic cofactor, and in consequence, it is implicated in several biological actions. The relevant aspects of chemistry and biochemistry and the importance of copper compounds in medicine give us a comprehensive knowledge of the multifaceted applications of copper in physiology and physiopathology. In this review, we present an outline of the chemistry and the antitumor properties of copper complexes on breast, colon, and lung cancer cells focus on the role of copper in cancer, the relationship between structure-activity, molecular targets, and the study of the mechanism of action involved in its anticancer activity. This overview is expected to contribute to understanding the design, synthesis, uses of copper complexes as antitumor agents in the most common cancers.

Pulse-Modulated Plasma Etching of Copper Thin Films via CH3COOH/Ar

Pulse-modulated plasma etching of copper masked using SIO2 films was conducted via a CH3COOH/Ar. The etch characteristics were examined under pulse-modulated plasma. As the duty ratio of pulse decreased and the frequency of pulse increased, the etch selectivity and etch profile were improved. X-ray photoelectron spectroscopy and indicated that more copper oxides (Cu2O and CuO) and Cu(CH3COO)2 were formed using pulse-modulated plasma than those formed using continuous-wave (CW) plasma. As the concentration of CH3COOH gas in pulse-modulated plasma increased, the formation of these copper compounds increased, which improved the etch profiles. Optical emission spectroscopy confirmed that the active ingredients of the plasma increased with decreasing pulse duty ratio and increasing frequency. Therefore, the optimized pulsed plasma etching of copper via a CH3COOH/Ar gas provides better etch profile than that by CW plasma etching.

Fasulye Bakteriyel Adi Yanıklık Hastalığına Karşı Farklı Bakırlı Bileşiklerin Etkililiği

Common bacterial blight (CBB) caused by Xanthomonas axonopodis pv. phaseoli is the most destructive bacterial disease affecting all bean varieties in production areas. In this study, the effectiveness of different copper preparations against CBB disease on dry beans of Alberto variety, which are widely grown in Konya and Afyonkarahisar provinces with different climatic characteristics, were investigated. In field conditions, after 5-week-old bean plants were inoculated with a bacterial suspension of 108 CFU mL-1 of high virulent Xap k133 isolate, and subsequently twice every with 5 days intervals after inoculation, copper hydroxide, copper sulphate pentahydrate, copper oxychloride + copper hydroxide and copper oxychloride were applied at the doses recommended by the manufacturers. Disease severity (%) and disease score were evaluated using the 0-9 scale, and the effectiveness of the chemicals was compared with the control plants sprayed with water and determined with the help of the Abbott formula. According to the statistical data obtained, the most effective copper compound was determined by the application of copper oxychloride with 42.59-47.25% efficiency rates, copper sulphate pentahydrate had the lowest efficiency with about 7.69-12.96%. In addition to the negative effects of excessive use of copper in agriculture on the environment and human health, copper-resistant strains develops in bacterial pathogens. In order to determine the most effective copper compounds against CBB disease in dry beans in our country, the effectiveness of used as common compounds have been investigated for the first time and an organic and environmentally friendly sustainable bean production is revealed by using less copper.

Crystal structures of two copper(I)–6,6′-dimethyl-2,2′-bipyridyl (dmbpy) compounds, [Cu(dmbpy)2]2[MF6]·xH2O (M = Zr, Hf; x = 1.134, 0.671)

The syntheses and crystal structures of two bimetallic molecular compounds, namely, bis[bis(6,6′-dimethyl-2,2′-bipyridine)copper(I)] hexafluoridozirconate(IV) 1.134-hydrate, [Cu(dmbpy)2]2[ZrF6]·1.134H2O (dmbpy = 6,6′-dimethyl-2,2′-bipyridyl, C12H12N2), (I), and bis[bis(6,6′-dimethyl-2,2′-bipyridine)copper(I)] hexafluoridohafnate(IV) 0.671-hydrate, [Cu(dmbpy)2]2[HfF6]·0.671H2O, (II), are reported. Apart from a slight site occupany difference for the water molecule of crystallization, compounds (I) and (II) are isostructural, featuring isolated tetrahedral cations of copper(I) ions coordinated by two dmbpy ligands and centrosymmetric, octahedral anions of fluorinated early transition metals. The tetrahedral environments of the copper complexes are distorted owing to the steric effects of the dmbpy ligands. The extended structures are built up through Coulombic interactions between cations and anions and π–π stacking interactions between heterochiral Δ- and Λ-[Cu(dmbpy)2]+ complexes. A comparison between the title compounds and other [Cu(dmbpy)2]+ compounds with monovalent and bivalent anions reveals a significant influence of the cation-to-anion ratio on the resulting crystal packing architectures, providing insights for future crystal design of distorted tetrahedral copper compounds.

Anaerobic Degradation of Environmentally Hazardous Aquatic Plant Pistia stratiotes and Soluble Cu(II) Detoxification by Methanogenic Granular Microbial Preparation

The aquatic plant Pistia stratiotes L. is environmentally hazardous and requires effective methods for its utilization. The harmfulness of these plants is determined by their excessive growth in water bodies and degradation of local aquatic ecosystems. Mechanical removal of these plants is widespread but requires fairly resource-intensive technology. However, these aquatic plants are polymer-containing substrates and have a great potential for conversion into bioenergy. The aim of the work was to determine the main patterns of Pistia stratiotes L. degradation via granular microbial preparation (GMP) to obtain biomethane gas while simultaneously detoxifying toxic copper compounds. The composition of the gas phase was determined via gas chromatography. The pH and redox potential parameters were determined potentiometrically, and Cu(II) concentration photocolorimetrically. Applying the preparation, high efficiency of biomethane fermentation of aquatic plants and Cu(II) detoxification were achieved. Biomethane yield reached 68.0 ± 11.1 L/kg VS of Pistia stratiotes L. biomass. The plants’ weight was decreased by 9 times. The Cu(II) was completely removed after 3 and 10 days of fermentation from initial concentrations of 100 ppm and 200 ppm, respectively. The result confirms the possibility of using the GMP to obtain biomethane from environmentally hazardous substrates and detoxify copper-contaminated fluids.

The radioenhancement potential of Schiff base derived copper (II) compounds against lung carcinoma in vitro

For the last years, copper complexes have been intensively implicated in biomedical research as components of cancer treatment. Herewith, we provide highlights of the synthesis, physical measurements, structural characterization of the newly developed Cu(II) chelates of Schiff Bases, Cu(Picolinyl-L-Tryptopahanate)2, Cu(Picolinyl-L-Tyrosinate)2, Cu(Isonicotinyl-L-Tyrosinate)2, Cu(Picolinyl-L-Phenylalaninate)2, Cu(Nicotinyl-L-Phenylalaninate)2, Cu(Isonicotinyl-L-Phenylalaninate)2, and their radioenhancement capacity at kV and MV ranges of irradiation of human lung carcinoma epithelial cells in vitro. The methods of cell growth, viability and proliferation were used. All compounds exerted very potent radioenhancer capacities in the irradiated lung carcinoma cells at both kV and MV ranges in a 100 μM concentration. At a concentration of 10 μM, only Cu(Picolinyl-L-Tyrosinate)2, Cu(Isonicotinyl-L-Tyrosinate)2, Cu(Picolinyl-L-Phenylalaninate)2 possessed radioenhancer properties at kV and MV ranges. Cu(Picolinyl-L-Tryptophanate)2 showed radioenhancer properties only at kV range. Cu(Nicotinyl-L-Phenylalaninate)2 and Cu(Isonicotinyl-L-Phenylalaninate)2 showed remarkable radioenhancer activity only at MV range. All compounds acted in dose-dependent manner at both tested energy ranges. These copper (II) compounds, in combination with 1 Gy irradiation at either 120 kV or 6 MV, are more efficient at delaying cell growth of lung cancer cells and at reducing cell viability in vitro than the irradiation administered alone. Thus, we have demonstrated that the studied copper compounds have a good potential for radioenhancement.

Evolution of the Efficiency of Divalent Cobalt and Copper Chelates Based on Isatin Derivatives and Thiosemicarbazide Ligands as Inhibitors for the Corrosion of Sabic Iron in Acidic Medium

Divalent cobalt and copper chelates of the two ligands 1-(1- Ethoxycarbonylmethyl-2-oxoindolin-3-ylidene) thiosemicarbazide (EOIT) and 1-(1-Benzyl-2-oxoindolin-3-ylidene) thiosemicarbazide (BOIT) are the target compounds of the current study. Identification of the constitution and geometry of these compounds have been performed using the possible physicochemical and analytical instruments. Elemental analysis, molar conductance and thermal analysis assured the composition of the four chelates to be [Co(POIT)Cl]•1.5H2O, [Cu(POIT)Cl], [Co(BOIT)Cl2(H2O)]•5H2O and [Cu(BOIT)Cl]•Cl which was further confirmed by the measurement of mass spectra. The architecture arrangement of the ligand atoms around Co and Cu centers has been determined depending on the UV-Vis spectral measurements and calculation of µeff values assuring the copper compounds to be square plane whereas the cobalt complexes have tetrahedral or octahedral arrangements. These compounds were examined as corrosion inhibitors for the Sabic steel in 1.0 M HCl utilizing potentiodynamic polarization, electrochemical impedance spectroscopy, mass-loss method and scanning electron microscopy at fixed temperature of 298 K. The acquired outcomes disclosed that the inhibition efficiencies (% IEs) of the examined compounds were set to be dependent on both the concentrations and composition of the compounds. The examined compounds were set to have high % IEs, which were interpreted by strong adsorption of the compounds’ molecules on the iron surface and such adsorption was discovered to follow Langmuir adsorption isotherm. The investigational results obtained from all utilized techniques were set to be in a good accord with each other.