An oxidative homocoupling method of synthesizing certain 2,2′-bithiophenes from thiophenes using oxygen as the terminal oxidant is disclosed. In non-limiting examples, the method uses oxygen along with a catalytic system that includes palladium, an assistive ligand, and a non-palladium metal additive to catalyze one of the following reactions: ##STR00001## Associated catalytic systems and compositions are also disclosed.

Phosphine phosphonate and phenoxyphosphine ligands bearing polyethylene glycol (PEG) chains are used as described herein to produce heterobimetallic catalysts. The ligands can be metallated selectively with palladium or nickel and secondary metal ions to provide well-defined heterobimetallic compounds. These heterobimetallic complexes exhibit accelerated reaction rates and greater thermal stability in olefin polymerization compared to other catalysts.

The present invention relates to a composition comprising at least one tertiary amino compound (A), and at least one copper(II)-compound (B), a process for the manufacture of said composition, the use of said composition as a catalyst, in particular, as catalyst for the reaction of at least one isocyanate compound with at least one isocyanate-reactive compound, in particular for the manufacture of polyisocyanate polyaddition products, such as polyurethanes, in particular, polyurethane foams.

The present invention relates to a nanomaterial comprising a nanoclay having a layered structure and carbon nanotubes being intercalated between layers of the layered of the nanoclay, and manufacturing method thereof.

Phosphine phosphonate and phenoxyphosphine ligands bearing polyethylene glycol (PEG) chains are used as described herein to produce heterobimetallic catalysts. The ligands can be metallated selectively with palladium or nickel and secondary metal ions to provide well-defined heterobimetallic compounds. These heterobimetallic complexes exhibit accelerated reaction rates and greater thermal stability in olefin polymerization compared to other catalysts.

Disclosed herein is a class of chiral binuclear metal complexes for stereoselective hydrolysis of saccharides and glycosides, and more particular chiral binuclear transition metal complex catalysts that discriminate epimeric glycosides and α- and β-glycosidic bonds of saccharides in aqueous solutions at near physiological pHs. The chiral binuclear metal complexes include a Schiff-base-type ligand derived from a chiral diamino building block, and a binuclear transition metal core, each which can be varied for selectivity. The metal core is a Lewis-acidic metal ion, such as copper, zinc, lanthanum, iron and nickel. The Schiff-base may be a reduced or non-reduced Schiff-base derived from aliphatic linear, aliphatic cyclic diamino alcohols or aromatic aldehydes. The ligand can be a penta- or heptadentate ligand derived from pyridinecarbaldehydes, benzaldehydes, linear or cyclic diamines or diamino alcohols.

An MOFs/MIPs catalyst, an in situ growth preparation method for same, and applications thereof are provided. The method comprises: uniformly mixing template molecules, a functional monomer, and a pore-foaming agent and performing a prepolymerization to produce a prepolymerization reaction product; uniformly mixing a cross-linking agent, an initiator, and the prepolymerization reaction product, heating, eluting the template molecules via a Soxhlet extraction, and drying to produce an imprinted polymer; uniformly mixing dimethylformamide, 2,5-dihydroxyterephthalic acid, ferrous chloride, water, methanol, and the imprinted polymer, heating, washing, using methanol for immersion and washing, and drying to produce the MOFs/MIPs catalyst.

Disclosed are a reduction method and reduction product of an alkenyl active methylene compound. The reduction reaction comprises the following steps: taking an alkenyl active methylene compound as a substrate, a metal hydride as a reducing agent, and a palladium compound as a catalyst, performing a reduction reaction to obtain a reduction product, and then reducing the alkenyl active methylene compound. The reduction system is a simple method for reducing the alkenyl active methylene compound, and the used hydride and palladium compound catalyst are both reagents that could easily be obtained in a laboratory. Compared with conventional hydrogen hydrogenation methods and reduction methods of reducing agents, the method is easier to operate, higher in safety, mild in conditions, and high in reaction yield, a reaction in a one-pot two-step manner can be achieved, and high atom economy and step economy can be obtained.

The invention discloses a visible light responsive titanium dioxide nanowire/metal organic skeleton/carbon nanofiber membrane and preparation method and application thereof. A CNF (Carbon Nano Fiber)/TiO.sub.2 nano-wire/MIL-100 (represented as CTWM) membrane material is prepared and an MIL-100 material is used for adsorbing waste gas to enhance the photocatalytic effect of titanium dioxide on the membrane material; a CNF/TiO.sub.2/MIL-100 membrane catalyst sufficiently utilizes the adsorption capability of MIL-100 on the waste gas, the photocatalytic degradation performance of the TiO.sub.2 and high electrical conductivity of CNF to effectively prolong the service life of photoelectrons and promote the photocatalytic activity of the photoelectrons.

A method for preparing a bi-component, multi-network nanofibrous aerogel-supported heterojunction photocatalyst includes the following steps. Step 1, preparing ammoniated polyacrylonitrile nanofibers. Step 2, dispersing the ammoniated polyacrylonitrile nanofibers in water to obtain a first solution; dispersing cellulose nanofibers in water to obtain a second solution; and mixing, heating and lyophilizing the first solution with the second solution to obtain a bi-component, multi-network nanofibrous aerogel. Step 3, adding graphite carbon nitride, a ferric-iron containing reagent, 2,5-diaminoterephthalic acid, and the bi-component, multi-network nanofiber aerogel obtained in the step 2 into a N, N-dimethylformamide solvent to obtain a third solution, and carrying out a hydrothermal reaction on the third solution for 8-24 hours to obtain the bi-component, multi-network nanofibrous aerogel-supported heterojunction photocatalyst.