A series of homoleptic Ni bis-1,1-dithiolates, [Ni(SCRR')] (R=CN, R'=CN, COEt, CONH, Ph, Ph-4-Cl, Ph-4-OMe, Ph-4-NO, Ph-3-CF, Ph-4-CF, Ph-4-CN; R=NO, R'=H; R=R'=COEt) have been synthesized from the reaction of the alkali metal salt of the ligand and nickel chloride, and isolated as tetraphenylphosphonium or tetrabutylammonium salts. The complexes were characterized by X-ray crystallography, high-resolution mass spectrometry, and infrared (IR), nuclear magnetic resonance (NMR) and electronic absorption spectroscopies. The molecular structures show a rigidly square planar Ni(II) center linking two four-membered chelate rings whose dimensions are constant across the series.
View Article and Find Full Text PDFInorg Chem
February 2024
The two-electron reductive activation of O to O is of particular interest to the scientific community mainly due to the use of peroxides as green oxidants and in powerful fuel cells. Despite of the great importance of vanadium(IV) species to activate the two-electron reductive activation of O, the mechanism is still unclear. Reaction of VO species with the tridentate-planar carboxamide (ΗL) ligands in solution (CHOH:HO) under atmospheric O, at room temperature, resulted in the quick formation of [V(═O)(η-O)(κ-L)(HO)] and -[V(═O)(κ-L)] compounds.
View Article and Find Full Text PDFOrganometallic molecules offer some of the most promising scaffolds for interaction with G-quadruplex nucleic acids. We report the efficient synthesis of a family of organoplatinum(II) complexes, featuring a 2-([2,2'-bipyridin]-6-yl)phenyl tridentate (N N C) ligand, that incorporates peripheral side-chains aiming at enhancing and diversifying its interaction capabilities. These include a di-isopropyl carbamoyl amide, a morpholine ethylenamide, two enantiomeric proline imides and an oxazole.
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