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A mononuclear copper(II) complex [CuLa] (1), and three mononuclear nickel(II) complexes [NiLa] (2), [NiLa]·CH3OH (2·CH3OH) and [NiLb] (3), where La and Lb are the dianionic form of N,N'-bis(4-bromosalicylidene)-1,2-cyclohexanediamine (H2La) and N,N'-bis(4-fluorosalicylidene)-1,2-cyclohexanediamine (H2Lb), respectively, were prepared and structurally characterized by spectroscopy method and elemental analyses. The detailed structures were determined by X-ray single crystal diffraction. All the copper and nickel complexes are mononuclear compounds. The metal ions in the complexes are in square planar coordination, with the two phenolate oxygens and two imine nitrogens of the Schiff base ligands. The biological effect of the four complexes were assayed on the bacteria strains Staphylococcus aureus, Escherichia coli and Candida albicans.
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http://dx.doi.org/10.17344/acsi.2023.8359 | DOI Listing |
Org Lett
September 2025
School of Molecular Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
We report the synthesis of three nickel complexes based on Ni(NHC)[P(OR)](Ar)Cl and their application in C()-N cross-coupling reactions. Reactions involving secondary amines proceeded at room temperature, while anilines and primary alkyl amines coupled under mild heating. The reported complexes are air-stable as solids, operate at low catalytic loading, and do not require an exogenous ligand.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
Department of Chemistry, Taras Shevchenko National University of Kyiv, Volodymyrska Street 64, Kyiv, 01601, Ukraine.
The unit cell of the title compound, [Ni(CHNO)]·2CHOH, consists of a neutral complex and two methanol mol-ecules. In the complex, the two tridentate 2-[3-(benzo[][1,3]dioxol-5-yl)-1-1,2,4-triazol-5-yl]-6-(1-pyrazol-1-yl)pyridine ligands coordinate to the central Ni ion through nitro-gen atoms of the pyrazole, pyridine and triazole groups, forming a pseudo-octa-hedral coordination sphere. Neighbouring mol-ecules are linked through weak C-H(pz)⋯π(ph) inter-actions into monoperiodic chains, which are further linked through weak C-H⋯H/N/C inter-actions into diperiodic layers.
View Article and Find Full Text PDFJ Inorg Biochem
August 2025
Faculty of Chemistry, University of Wroclaw, F. Joliot - Curie 14, 50-383 Wroclaw, Poland.
This study presents the synthesis, structural characterization, and biological evaluation of three nickel(II) complexes containing bioactive ligands: two bidentate pyridyl alcohols (2-pymetH and 2-pyetH) and a mixed-ligand system with memantine and acetylacetone. Single-crystal X-ray diffraction revealed that all complexes adopt a distorted octahedral geometry with a {NiN₂O₄} coordination core, differing in ligand orientation, symmetry, and supramolecular packing. Complementary spectroscopic techniques, including FT-IR, Raman, and UV-Vis, confirmed successful ligand coordination and complex integrity.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, The University of Hong Kong, Hong Kong 999077, China.
While intricate designs have been implemented to transform noble-metal complexes and sophisticated organic molecules into reactive photocatalysts for the single-electron reduction of unactivated alkyl halides, the development of highly reducing photocatalytic systems based on earth-abundant metals is still in its early stages. Herein, we show that a simple terpyridine-ligated nickel(II) complex, integrated into an imine-linked covalent organic framework, can be readily reduced by photoexcited Hantzsch esters to produce a heterogeneous nickel(I) photocatalyst with a fairly low excited-state oxidation potential of approximately -3.5 V (referenced to the saturated calomel electrode).
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Inorganic, Analytical Chemistry and Electrochemistry, Faculty of Chemistry, Silesian University of Technology, B. Krzywoustego 6, 44-100 Gliwice, Poland. Electronic address:
A novel nickel-modified chitosan sorbent (CsNi), highly efficient in phosphates removal from aqueous solutions, was proposed. Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and point of zero charges of sorbent were employed to determine its structure and properties. Batch sorption experiments allowed to identify the CsNi high phosphate sorption capacity, exceeding 62.
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