A catalytic reaction of ethylene oxide (EO) coupling with syngas to produce 1,3-propanediol (1,3-PDO) is disclosed. The catalytic reaction of EO, carbon monoxide and the alcohol uses a N,O-ligand coordinated metal complex catalyst. The reaction is carried out in an organic solvent in the presence of an additive at the temperature of 30-190 C. and the CO pressure of 1-150 atm for 0.1-200 h to prepare 3-hydroxypropinate (3HP). The catalytic reaction of 3HP with dihydrogen uses a copper-containing mixed metal silicon oxide catalyst with a molecular formula of M.sub.uCu.sub.vSi.sub.yO.sub.z. The reaction is carried out at 80-400 C. and 20-150 atm for 0.1-200 h to prepare the 1,3-PDO. The yield of the 1,3-PDO can reach to 73%. The alcohol byproduct generated in the second step catalytic hydrogenation reaction can be recycled to use for the first step catalytic reaction by the ring opening-carbonylation-esterification.

The present invention relates to a novel ligand for forming a ruthenium complex, a ruthenium complex catalyst, a production method therefor and a use thereof. The ligand for forming a ruthenium complex and the ruthenium complex catalyst, according to the present invention, exhibit high catalytic activity, high selectivity, and stability.

A method for preparing sugar-based mono and diesters is described. The process entails the esterification of 2,5-furan-dicarboxylic acid (FDCA) with an alcohol in the presence of low loadings of a homogeneous organotin (IV) catalyst.

The disclosure provides for zirconium terephthalate-based metal organic frameworks with open metal sites, and uses thereof.

Catalyst systems suitable for tetramerizing ethylene to form 1-octene may include a catalyst having a structure according to Formula (VI) or Formula (VII). In Formulas (VI) and (VII), X is a halogen, a (C.sub.2-C.sub.30) carboxylate, acetylacetonate, or a (C.sub.1-C.sub.30) hydrocarbyl; L.sub.1 is a neutral coordinating ligand; n is an integer from 0 to 6; Y is a (C.sub.6-C.sub.20)fluorine-substituted aryl, a (C.sub.6-C.sub.20)fluorine-substituted aryloxy, or a (C.sub.1-C.sub.20)fluorine-substituted alkoxy; and LL is a bidentate chelating ligand. The catalyst system may also include an aluminum containing agent which includes a reaction product of an organoaluminum compound and an antifouling compound. The antifouling compound may include one or more organic acids, organic acid salts, esters, anhydrides, or combinations of these.

The present invention relates to Ziegler-Natta catalyst components for olefin polymerization employing specific carbonate compounds as an element of solid catalyst composition in conjunction with at least one or more internal donor compounds, for producing polyolefins, particularly polypropylene and ethylene-propylene block co-polymer, which exhibits substantially high rubber content with higher stereo-regularity and hydrogen response.

Internal dienes (including supported versions) and their Periodic Groups IX, X and Pt Group Metal Complexes as catalysts for hydrosilylation/coupling reactions. A process for the hydrosilylation of an unsaturated compound comprising reacting (a) a silyl or siloxy hydride with (b) an unsaturated compound in the presence of (c) one or more platinum complex containing said internal dienic ligand or (d) a platinum compound and one or more said internal dienic ligand additive. For Ru, Os, Co, Rh, Ir, Ni, or Pd, catalyzed processes such as CC/CN or CO coupling comprising reacting (a) an aromatic halide/vinyl halide/an aromatic triflate with (b) a primary/secondary amine/amide, an alcohol/aryl boronic acid/aryl boronate/vinyl halide or an activated olefin in the presence of (c) a Group IX or X or Pt Group metal complex containing said dienic ligand(s) or (d) a suitable compound of these metals and of one or more said internal dienic ligand additive.

Provided herein is a coating composition curable by condensation and/or addition reactions and including (A) at least one polymer as binder, (B) at least one crosslinking agent that can be reacted by condensation and/or addition reaction with component (A), and (C) at least one specific complex as catalyst. Also provided herein is a use of the complex for catalyzing the curing of coating compositions curable by condensation and/or addition reaction.

The porphyrin-based catalysts for water splitting are composites of porphyrin or metalloporphyrin active ingredients, conductive carbon (e.g., graphene sheets, vapor grown carbon fiber, carbon black, etc.), and a polymer or binder that may be coated on a glassy carbon electrode. The polymer or binder may be Nafion oil or polyvinylidine difluoride. The porphyrin may be a porphyrin having a transition metal or hydrogen at its center, and may be halogenated and/or have a thiophene substituent.

The present disclosure provides methods for enantioselective synthesis of cyclic and acyclic -quaternary carboxylic acid derivatives via nickel-catalyzed allylic alkylation.