Synthesis,structural characterization and biological activities of metal(II) complexes with Schiff bases derived from 5-bromosalicylaldehyde: Ru(II) complexes transfer hydrogenation

In this study, two novel Schiff base ligands (L¹ and L²) derived from condensation of methyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate and methyl 2-amino-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate, both starting matter with 5-bromo-salicylaldehyde, and their Zn(II) and Ni(II) metal complexes have been prepared using a molar ratio of ligand:metal as 1:1 except the Ru(II) complexes 1:0.5. The structures of the obtained ligands and their metal complexes were characterized by elemental analysis, FT-IR, ¹H NMR, ¹³C NMR, UV–vis, thermal analysis methods, mass spectrometry, and magnetic susceptibility measurements. Antioxidant and antiradical activity of Schiff base ligands and their metal complexes were been evaluated in vitro tests. Antioxidant activities of metal complexes generally were more effectives than free Schiff bases. 1c and 2c were used as catalysts for the transfer hydrogenation (TH) of ketones. 1c, 2c complexes were found to be efficient catalyst for transfer hydrogenation reactions.     

Synthesis,crystal structures,characterization and antimicrobial activities of 5-hydroxyisophthalate complexes

Two 5-hydroxyisophthalate complexes of nickel(II), formulated as [Ni(μ-Hhip)(2-hepy)₂] _n (1) and [Ni₂(μ-Hhip)₂(dap)₄] _n (2) (H₃hip = 5-hydroxyisophthalic acid, 2-hepy = 2-(2-hydroxyethyl)pyridine, dap = 1,3-diaminopropane), have been synthesized and characterized by chemical and spectroscopic methods. The molecular structures of the complexes have been determined by single-crystal X-ray diffraction analysis. The Ni(II) centres have distorted octahedral geometries in both crystals. Furthermore, both complexes have 1D chain structures in which the individual chains are linked together via hydrogen bonds to give 3D frameworks. Evaluation of the complexes by the agar diffusion method showed that they have weak antibiotic activities against the tested microorganisms.     

Amide-based tripodal receptors for selective anion recognition

The binding properties of ethylester derivative of p-tetraphenyl tetrahomodioxacalix[4]arenes (1) towards alkali, alkaline-earth, transition and heavy metal cations using UV-absorption spectrophotometry and ¹H-NMR spectroscopy are reported.     

Facile and green fabrication of silver nanoparticles on a polyoxometalate for Li-ion battery

In the present study, we report the green and one-pot synthesis of silver nanoparticles (AgNPs) on as-prepared novel polyoxometalate {[Ni_2,5(Hpen)₄(PW₉O₃₄)]?·?5H₂O} (POM) without any reducing agent and its application as improved anode material for lithium-ion batteries (LIBs). The structure of the AgNPs involved POM (AgNPs/POM) nanocomposite was characterized by transmission electron microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. The synthesized POM was also characterized by elemental analysis and thermal analysis. The electrochemical performances of the POM, AgNPs, and AgNPs/POM composites were measured for charge/discharge specific capacities at different current rates in CR2032 coin-type cells. The prepared AgNPs/POM composite showed a high specific gravimetric capacity of about 1760 mAh g^?1 and long-term cycle stability.     

Synthesis and characterization of erbia and ceria doped calcia stabilized nanocrystalline zirconia based ceramics

Er₂O₃ doped calcia stabilized zirconia based inert matrix fuel containing CeO₂ as a surrogate for PuO₂ was fabricated for a wide range of concentration using the polymer-to-ceramic conversion technique via metal acetate preceramic hybrid polymer solutions. Samples were characterized by XRD, SEM and AFM techniques. Nanocrystallite size variation in the samples was evaluated using peak broadening values by means of the Scherrer formula. The smallest lattice constant was obtained for the sample containing Zr/Ca/Ce/Er atomic weight ratio of 74/11/10/5. The average grain diameters varied between 64 nm and 129 nm. SEM results show that, the smallest grain size was obtained for the sample containing Zr/Ce/Er atomic weight ratio of 22/2/1. Moreover, surface roughness characteristics of the samples were evaluated by different definitions using intermittent contact mode AFM.     

Some metal chelates with Schiff base ligand: synthesis,structure elucidation,thermal behavior,XRD evaluation,antioxidant activity,enzyme inhibition,and molecular docking studies

Molecular Diversity - Schiff bases are well-known compounds for having significant biological properties. In this study, a new Schiff base ligand and its metal complexes were synthesized, and their...     

Hydrogen bonding networks and proton transfer compounds of cobalt(II) and copper(II) with pyridine-2,5-dicarboxylate

Three Co(II) and Cu(II)-pyridine-2,5-dicarboxylate (pydc) proton transfer compounds with 1,4-butanediamine (ben) and 2,2-dimethylpropane-1,3-diamine (dmpen), trans-(H₂ben)[Co(pydc)₂(H₂O)₂]·4H₂O (1), trans-(H₂dmpen)[Co(pydc)₂(H₂O)₂]·2H₂O (2) and (H₂ben)₂[Cu₂(μ-pydc)₄(H₂O)₂] (3) have been synthesized and characterized by the methods of elemental, spectroscopic (IR and UV-Vis), thermal (TG/DTG, DTA) analysis, magnetic measurement and single crystal X-ray diffraction. The crystallographic analysis revealed that the complexes consist of [Co(pydc)₂(H₂O)₂]²⁻ anion, bis(protonated) diamine cation (H₂ben for 1 and H₂dmpen for 2) and four and two crystal water molecules, respectively. The Co(II) ions are coordinated by two pydc and two aqua ligands. The bis(deprotonated) pydc ligands coordinate to the Co(II) ions through the nitrogen atom of pyridine ring and the oxygen atom of carboxylate group, creating a chelate ring. The distorted octahedral geometries are completed by two trans aqua ligands at axial positions. The molecular structure of the complex 3 consists of dinuclear [Cu₂(μ-pydc)₄(H₂O)₂]⁴⁻ units and bis(protonated) 1,4-butanediammonium cation. In the structure, each Cu(II) ion is coordinated by two nitrogen and two oxygen atoms from two pydc ligands and one oxygen atom from aqua ligand, forming a distorted square pyramidal geometry.     

Synthesis, characterization, structures and cytotoxic activity of palladium(II) and platinum(II) complexes containing bis(2-pyridylmethyl)amine and saccharinate

New palladium(II) and platinum(II) complexes containing bis(2-pyridylmethyl)amine (bpma) and saccharinate (sac), [Pd(bpma)(sac)](sac)·2H₂O (1), [Pt(bpma)(sac)](sac)·2H₂O (2), [Pd(bpma)Cl](sac)·2H₂O (3) and [Pt(bpma)(sac)]Cl·1.5H₂O (4), were synthesized and characterized by elemental analysis, IR, NMR and TG-DTA. A single-crystal X-ray analysis of 3 and 4 proved a distorted square-planar geometry around the metal ions with one tridentate bpma ligand and one Cl or sac monoanion. The [Pd(bpma)Cl]⁺ ions in 3 form dimers by intermolecular N-H?Cl and Pd?Pd interactions. The cations reside in the centers of a hydrogen-bonded honeycomb network formed by the uncoordinated sac ions and the lattice water molecules, while the cations of 4 are connected by N-H?Cl and OW-H?O hydrogen bonds into one-dimensional chains. Cyclic planar tetrameric and trimeric water clusters were observed in 3 and 4, respectively. Cytotoxicity of 1-4 was tested against A549, C6 and CHO cells. Although 2 and 4 have no cytotoxicity, the best results were achieved for 1 and 3. In particular, the cyctotoxic activity of 3 is comparable to cisplatin.     

Generalized difference sequence spaces and their dual spaces

The definition of the pα-, pβ- and pγ-duals of a sequence space was defined by Et [Internat. J. Math. Math. Sci. 24 (2000) 785-791]. In this paper we compute pα- and N-duals of the sequence spaces Δ^m_v(X) for X=?_∞, c and c₀, and compute β- and γ-duals of the sequence spaces Δ^m_v(X) for X=?_∞, c and c₀.     

Sampling hazelnuts for aflatoxin: effect of sample size and accept/reject limit on reducing the risk of misclassifying lots

About 100 countries have established regulatory limits for aflatoxin in food and feeds. Because these limits vary widely among regulating countries, the Codex Committee on Food Additives and Contaminants began work in 2004 to harmonize aflatoxin limits and sampling plans for aflatoxin in almonds, pistachios, hazelnuts, and Brazil nuts. Studies were developed to measure the uncertainty and distribution among replicated sample aflatoxin test results taken from aflatoxin-contaminated treenut lots. The uncertainty and distribution information is used to develop a model that can evaluate the performance (risk of misclassifying lots) of aflatoxin sampling plan designs for treenuts. Once the performance of aflatoxin sampling plans can be predicted, they can be designed to reduce the risks of misclassifying lots traded in either the domestic or export markets. A method was developed to evaluate the performance of sampling plans designed to detect aflatoxin in hazelnuts lots. Twenty hazelnut lots with varying levels of contamination were sampled according to an experimental protocol where 16 test samples were taken from each lot. The observed aflatoxin distribution among the 16 aflatoxin sample test results was compared to lognormal, compound gamma, and negative binomial distributions. The negative binomial distribution was selected to model aflatoxin distribution among sample test results because it gave acceptable fits to observed distributions among sample test results taken from a wide range of lot concentrations. Using the negative binomial distribution, computer models were developed to calculate operating characteristic curves for specific aflatoxin sampling plan designs. The effect of sample size and accept/reject limits on the chances of rejecting good lots (sellers' risk) and accepting bad lots (buyers' risk) was demonstrated for various sampling plan designs.