Mono-and Binuclear Cobalt(II) Mixed Ligand Complexes of 2,2’-Bipyridine and Ethylenediamine: Synthesis, Characterization and Biological Application

Antibiotic resistance of pathogens to the current commercially available drugs is a serious problem. To curve this problem, the discovery of active compounds with a new mode of action is insistent. In line with this, we report two new complexes; mononuclear [Co(L1)2(L2)(H2O)]Cl2 and binuclear [Co2(L1)4(L2)(H2O)2]Cl4 using precursor complex, [Co(L1)2(H2O)2]Cl2, synthesized before; where L1: 2,2’-bipyridine and L2: ethylenediamine. The precursor complex was prepared from CoCl2.6H2O and L1 in ethanol, treated with a different mole of L2 under optimized reaction conditions to give the corresponding mono-and binuclear cobalt(II) mixed ligand complexes. These complexes were characterized using the spectroscopic technique (ICP-OES, UV-Vis, FT-IR) and physicochemical methods (chloride determination, thermal analysis, and conductance measurement). Their antibacterial activities were also tested against two Gram-negative (Escherichia coli (E. coli) and Klebsiella pneumoniae (K. pneumoniae)) and two Gram-positive (Staphylococcus aureus (S. aureus), Streptococcus pyogenes (S. pyogenes)) bacteria using the disc diffusion method. The new complexes showed better activities against K. pneumoniae than the reference Gentamycin. Furthermore, [Co(L1)2(L2)(H2O)]Cl2 demonstrated better activity than Gentamycin against S. aureus and E. coli.

Synthesis of Copper Sulfide Nanoparticles by Thermal Decomposition Approach and Morphology Dependent Peroxidase-Like Activity

Copper sulfide nanoparticles have been employed as artificial mimics for peroxidase-like activity. In the present study, copper sulfide nanoparticles with four different morphologies have been synthesized by thermal decomposition of cyclo-tri-μ-thioacetamide-tris(chlorocopper(I)) complex ([Cu3TAA3Cl3]) at 200 °C in different solvents such as diphenyl ether, ethylene glycol, 1-octadecene and also without any solvent. Hierarchical copper sulfide nanostructures are formed when the complex is decomposed in the absence of solvent, in diphenyl ether, and 1-octadecene while in the case of ethylene glycol, randomly agglomerated nanoparticles are formed. The precursor complex ([Cu3TAA3Cl3]) as well as copper sulfide nanoparticles were characterized using an array of techniques and after characterization, the peroxidase-like activity of copper sulfide nanoparticles was investigated.Morphologically different copper sulfide nanoparticles possess different exposed facets and due to this, the peroxidase-like activity was different among different morphologies.

Generation of a zinc and rhodium containing metallomacrocycle by rearrangement of a six-coordinate precursor complex

Two pentadentate N3,P2 ligands coordinate zinc(ii) by their N3 pocket.

Selective surface functionalization generating site-isolated Ir on a MnOx/N-doped carbon composite for robust electrocatalytic water oxidation

Through designing the precursor complex, single Ir atoms can be selectively accommodated in hybrid materials, providing higher stability and activity in electrocatalysis.

Novel green synthesis and improved solar-blind detection performance of hierarchical γ-Ga2O3 nanospheres

High-quality γ-Ga2O3 nanospheres (diameter, 130 nm) were successfully synthesized by direct conversion of a precursor complex of Ga3+ ions and tartrate ions (L2−) in water.

Controlled stepwise synthesis of a Cu-MOF: Transmetallation of a magnesium precursor to a three-dimensional framework with very high solvent content

A copper metal-organic framework (MOF) was synthesized by transmetalation. The ditopic ligand 3-(3,5-dimethyl-pyrazol-4-yl)pentane-2,4-dione is introduced via its Mg precursor complex in which it is oxygen-coordinated. After transmetallation, the ligand acts as