Tridentate hydrazido-hydrazones vanadium complexes. Synthesis, properties and biological activity

Nine new vanadium complexes, with tridentate Schiff base ligand based on 3,5-di-tert-butyl-2-hydroxybenzaldehyde and different hydrazides, are described and characterized. The X-ray crystal structure of complex 8 shows distorted octahedral geometry of vanadium, with ONO ligand in equatorial position. The tridentate Schiff base ligand forms six membered and five-membered chelate rings at the V(V) acceptor center, with the corresponding bite angles being 82.97(9)˚ and 74.48(9)˚. The molecules are gathered by means of intermolecular O-H∙∙∙N hydrogen bond and layered by π∙∙∙π interactions involving the pyridine and phenolate rings. Such interactions expand the structure along the crystallographic a axis. The complexes were characterized by the elemental analyses, IR, UV-Vis, EPR spectroscopy, cyclic voltammetry, thermogravimetry and magnetic susceptibility measurements. The stabilization role of co-ligands is discussed. The cytotoxicity versus HepG2 hepatocytes and inhibition of human recombinant PTP1B was studied.

Influence of ligand substitution at the donor and acceptor center on MMCT in a cyanide-bridged mixed-valence system

A series of cyanide-bridged complexes [TpmRu(LD)(μ-CN)Ru(LP)Cp*][PF6]2 were investigated by changing the substitutions of the donor and acceptor sites to systemically tune MMCT.

Extractants Based on Coordinating Liquid Polar Solvents for Removal of Sulfur Compounds from Diesel Fuels

To remove sulfur-containing compounds (SCC) from the diesel fraction 200–360 °C extraction systems have been created based on coordinating organic solvents—dimethylformamide and dimethylsulfoxide, metal chlorides (CoCl2, CuCl2, CdCl2, MnCl2 and CrCl3), and metal trifluoroacetates (Co(TFA)2, Cu(TFA)2 and Mn(TFA)2). Using PMR spectroscopy the coordination of metal chloride and metal trifluoroacetate on the oxygen atom in the carbonyl group of DMF was shown to redistribute electron density in the solvent molecule and to enhance properties of the acceptor center localized on the nitrogen atom. The removal of sulfur-containing compounds from the diesel fraction proceeded under mild conditions—at the temperature of 25 °C and atmospheric pressure. The degree of SCC removal from the diesel fraction in 30 minutes extraction was more than 90%. The interaction of organic solvents with metal salts and sulfur-containing compounds of the diesel fraction was considered within the framework of the concept of “hard and soft acids and bases” (HSAB). The most complete SCC extraction was carried out with DMF-Mn(TFA)2, MnCl2 and CrCl3 systems, that was probably connected with the implementation of the ‘hard base–hard acid’ system.

Extractants Based on Coordinating Liquid Polar Solvents for Removal of Sulfur Compounds from Diesel Fuels

To remove sulfur-containing compounds (SCC) from the diesel fraction 200-360 °C extraction systems have been created based on coordinating organic solvents - dimethylformamide and dimethylsulfoxide and chlorides (CoCl2, CuCl2, CdCl2, MnCl2 and CrCl3) and metal trifluoroacetates (Co (TFA)2, Cu(TFA)2 and Mn(TFA)2). Using PMR spectroscopy the coordination of chloride and metal trifluoroacetate on the oxygen atom in the carbonyl group of DMFA was shown to redistribute electron density in the solvent molecule and to enhance properties of the acceptor center localized on the nitrogen atom. The removal of sulfur-containing compounds from the diesel fraction proceeded under mild conditions - at the temperature of 25 °C and atmospheric pressure. The degree of SCC removal from the diesel fraction in 30 minutes extraction was more than 90%. The interaction of organic solvents with metal salts and sulfur-containing compounds of the diesel fraction was considered within the framework of the concept of "hard and soft acids and bases" (HSAB). The most complete SCC extraction was carried out by "DMFA - Mn(TFA)2, MnCl2 and CrCl3 systems, that was probably connected with the implementation of the" hard base - hard acid "system.