A homogeneous catalyst is provided comprising one or more metals; and at least two metal coordinating ligands wherein the homogeneous catalyst is a multi-ligand metal complex adapted for use with an oxidant in an oxidation reaction to catalytically pretreat lignocellulosic biomass. In one embodiment, the homogenous catalyst is copper (II) 2, 2′ bipyridine ethylenediamine (Cu(bpy)en). Related methods are also disclosed.

The present invention is drawn to artificial metalloenzymes for use in cyclopropanation reactions, amination and C—H insertion.

The present invention is drawn to artificial metalloenzymes for use in cyclopropanation reactions, amination and C—H insertion.

This invention relates generally to olefin metathesis catalysts, to the preparation of such compounds, compositions comprising such compounds, methods of using such compounds, and the use of such compounds in the metathesis of olefins and in the synthesis of related olefin metathesis catalysts. The invention has utility in the fields of catalysis, organic synthesis, polymer chemistry, and in industrial applications such as oil and gas, fine chemicals and pharmaceuticals.

The present disclosure provides a quantum-dot ligand, a quantum-dot catalyst and a quantum-dot device. The quantum-dot ligand includes: a first ligand having a first group and a second group and a second ligand having an inorganic ion, in which a coordination bond is formed between the first group and a surface of a quantum dot, a hydrogen bond is formed between the second group and a hydroxyl group; and a coordination bond is formed between the inorganic ion and the surface of the quantum dot. The quantum-dot catalyst of the present disclosure can enhance a catalytic activity of the quantum dots and improve the catalytic performance.

Disclosed is catalyst composition, a process for preparing the catalyst composition, and a use of the catalyst composition. The catalyst composition comprises 1 wt % to 4 wt % of free azacarbene, 1 wt % to 2 wt % of azacarbene iron, 15 wt % to 30 wt % of a phase transfer catalyst, 1 wt % to 5 wt % of a hydrogen donor, 5 wt % to 10 wt % of phosphoric acid, 0.5 wt % to 1 wt % of emulsifier, with the rest being solvent. This disclosure also provides a process for preparing the catalyst composition, comprising: mixing the free azacarbene and the azacarbene iron with the solvent according to a ratio, then adding and mixing the phase transfer catalyst and the hydrogen donor, then adding and mixing the phosphoric acid and the emulsifier to obtain the catalyst composition. The beneficial effect of this disclosure is: only less azacarbene iron and free azacarbene are needed to achieve rapid and efficient viscosity reduction of heavy oil.

The present invention relates to a method of preparing an oxidatively curable coating formulation made from an oxidatively curable alkyd-based resin, a complex comprising one or more manganese ions and one or more triazacyclononane-based ligands; and to the use of triazacyclononane-based ligands for accelerating the rate of curing of an alkyd-based resin formulation by such complexes. The formulations may be paints or other oxidatively curable coating compositions.

The present application provides a mononuclear transition metal complex, a photocatalyst for carbon dioxide reduction including same, and a method for reducing carbon dioxide to formic acid, the method comprising using the photocatalyst for carbon dioxide reduction.

Methods of polymer and/or oligomer depolymerization are described herein which, in some embodiments, enable facile polymer and/or oligomer decomposition under mild, non-energy intensive conditions. Briefly, a method of depolymerization comprises providing a reaction mixture comprising a transition metal catalyst, and a polymer or oligomer having a backbone including cyclobutane units, and decomposing the polymer or oligomer to provide diene monomer or alkene monomer.

The subject invention provides synthetic compounds, and compound complexes having catalytic activities towards oxidation or oxygenation, and/or dehydrogenation of various substrates comprising C—H bonds. The catalysts of the subject invention comprise a dinuclear Cu(I)/Cu(II) center that can convert between a resting state and a reactive species. The subject invention also provides methods of using such catalysts for the oxidation of substrates comprising C—H bonds, e.g., hydrocarbons, to synthesize chemicals for use as pharmaceuticals and industrial feedstock.