Redox Behavior of Cobalt-Phosphine Complexes vs Their Catalytic Activity in Organozinc Compound Formation: Background for Mechanistic Investigations.

Catalytic activity in arylzinc compound formation was studied for eight Co complexes with phosphines along with their redox properties for implementing the idea of rational design. It was found that Co(XantPhos)Cl and Co(-XantPhos)Cl demonstrated distinct reversible Co/Co redox processes and acted as efficient catalysts of arylzinc compound formation. Meanwhile, for Co(DPEphos)Cl, Co(dppf)Cl, Co(dppb)Cl, Co(PPh)Cl, and Co(XantPhos)(Piv) (the latter one without the addition of LiCl), reversible redox processes were not observed.

Catalytic Oxidation of Benzoins by Hydrogen Peroxide on Nanosized HKUST-1: Influence of Substituents on the Reaction Rates and DFT Modeling of the Reaction Path.

In this research, the oxidation of a series of benzoins, R-C(=O)-CH(OH)-R, where R = phenyl, 4-methoxyphenyl, 4-bromophenyl, and 2-naphthyl, by hydrogen peroxide in the presence of nanostructured HKUST-1 (suspension in acetonitrile/water mixture) was studied. The respective benzoic acids were the only products of the reactions. The initial average reaction rates were experimentally determined at different concentrations of benzoin, HO and an effective concentration of HKUST-1.

Cu-Catalyzed Pyridine Synthesis via Oxidative Annulation of Cyclic Ketones with Propargylamine.

A Cu-catalyzed, easily scalable one-pot synthesis of fused pyridines by the reaction of cyclic ketones with propargylamine is described. The protocol was optimized based on the results of more than 30 experiments. The highest product yields were achieved in -PrOH as a solvent in the presence of 5.

Versatile Reactivity of Mn Complexes in Reactions with N-Donor Heterocycles: Metamorphosis of Labile Homometallic Pivalates vs. Assembling of Endurable Heterometallic Acetates.

Reaction of 2,2'-bipyridine (2,2'-bipy) or 1,10-phenantroline (phen) with [Mn(Piv)(EtOH)] led to the formation of binuclear complexes [Mn(Piv)L] (L = 2,2'-bipy (), phen (); Piv is the anion of pivalic acid). Oxidation of or by air oxygen resulted in the formation of tetranuclear Mn complexes [MnO(Piv)L] (L = 2,2'-bipy (), phen ()). The hexanuclear complex [Mn(OH)(Piv)(pym)] () was formed in the reaction of [Mn(Piv)(EtOH)] with pyrimidine (pym), while oxidation of produced the coordination polymer [MnO(Piv)(pym)] ().

Hierarchical Nanoporous Sn/SnO Systems Obtained by Anodic Oxidation of Electrochemically Deposited Sn Nanofoams.

A simple two-step electrochemical method for the fabrication of a new type of hierarchical Sn/SnO micro/nanostructures is proposed for the very first time. Firstly, porous metallic Sn foams are grown on Sn foil via hydrogen bubble-assisted electrodeposition from an acidulated tin chloride electrolyte. As-obtained metallic foams consist of randomly distributed dendrites grown uniformly on the entire metal surface.

Co Complexes with a Tripyridine Ligand, Containing a 2,6-Di--butylphenolic Fragment: Synthesis, Structure, and Formation of Stable Radicals.

Interaction of a tripyridine ligand bearing a 2,6-di--butylphenolic fragment (L, 2,6-di--butyl-4-(3,5-bis(4-pyridyl)pyridyl)phenol) with Co pivalate or chloride led to the formation of one-dimensional coordination polymers [Co(L)Cl] ·EtOH () and [Co(L)(OH)(Piv)] () or a trinuclear complex Co(HO)(L)Cl () (Piv = pivalate). Chemical oxidation of L and - by PbO or K[Fe(CN)], as well as exposure of L (in solution or solid state) and (in solid state) to UV irradiation, led to the formation of free radicals with = 2.0024, which probably originated because of oxidation of 2,6-di--butylphenolic groups.

Modeling of catalytically active metal complex species and intermediates in reactions of organic halides electroreduction.

The results of quantum chemical modeling of organic and metal-containing intermediates that occur in electrocatalytic dehalogenation reactions of organic chlorides are presented. Modeling of processes that take place in successive steps of the electrochemical reduction of representative C1 and C2 chlorides - CHCl3 and Freon R113 (1,1,2-trifluoro-1,2,2-trichloroethane) - was carried out by density functional theory (DFT) and second-order Møller-Plesset perturbation theory (MP2). It was found that taking solvation into account using an implicit solvent model (conductor-like screening model, COSMO) or considering explicit solvent molecules gave similar results.

Porous 2D coordination polymeric formate built up by Mn(II) linking of Fe3O units: influence of guest molecules on magnetic properties.

A first representative of coordination polymers, built from polynuclear carboxylate bridged by mononuclear carboxylate, has been synthesised and structurally characterized. The compound [{Fe(3)O(HCOO)(6)}{Mn(HCOO)(3)(H(2)O)(3)}].3.