The present invention relates to the technical field of chiral synthesis, and specifically provides the synthesis and use of a new type of oxa-spirodiphosphine ligands. The bisphosphine ligand is prepared with oxa-spirobisphenol as a starting material after triflation, palladium catalyzed coupling with diaryl phosphine oxide, reduction of trichlorosilane, further palladium catalyzed coupling with diaryl phosphine oxide, and further reduction of trichlorosilane. The oxa-spiro compound has central chirality, and thus includes L-oxa-spirodiphosphine ligand and R-oxa-spirodiphosphine ligand. The racemic spirodiphosphine ligand is capable of being synthesized from racemic oxa-spirobisphenol as a raw material. The present invention can be used as a chiral ligand in the asymmetric hydrogenation of unsaturated carboxylic acids. The complex of the ligand with ruthenium can achieve an enantioselectivity of greater than 99% in the asymmetric hydrogenation of methyl-cinnamic acid.

A titanium catalyst and a synthesizing method of polyester resins are provided in the present disclosure. The titanium catalyst has a chemical structure represented by Formula (I), Formula (II) or Formula (III). ##STR00001##
The symbols shown in the Formula (I), the Formula (II) or the Formula (III) are defined in the description. The synthesizing method of polyester resins includes providing the titanium catalyst, performing a feeding step, performing a heating and pressurizing step and performing a heating and vacuuming step. The titanium catalyst and a heat stabilizer are added into an autoclave before the feeding step or before the heating and vacuuming step.

The instant disclosure provides an organometallic compound of Formula I: ##STR00001##
wherein R is selected from C.sub.1-10 alkyl or C(O)C.sub.1-10 alkyl; R.sub.1 is selected from C.sub.1-10 alkyl, C(O)C.sub.1-10 alkyl, C(O)C.sub.1-10 alkylN.sup.+R.sub.aR.sub.bCl.sup.?, C(O)C.sub.1-10 alkylN(CO)R.sub.a, C.sub.1-10 alkylN.sup.+R.sub.aR.sub.bCl, or C.sub.1-10 alkylN(CO)R.sub.a, wherein R.sub.a, and R.sub.b is independently selected from H, C.sub.6-12 aryl, C.sub.1-10 alkyl, C.sub.6-12 aryl, or C.sub.1-10 alkyl; R, and R.sub.1 can be taken together to form a monocyclic 6-8 membered ring; M is selected from Group VI-B metals; and m and n is independently 1 to 3. A process for obtaining the organometallic compound is also provided.

The invention relates to a process for the preparation of a deuterated ethanol from ethanol, D.sub.2O, a ruthenium catalyst, and a co-solvent.

A method for making organo-metal material involves providing a metal ion source in a medium that removes metal ions from the source and forms 1D metal-containing coordination polymers that self-assemble and precipitate as at least one of a 2D and 3D coordination polymer material that can be thermally treated to produce a porous metal oxide material.

The present invention relates to an organic zinc catalyst which exhibits more improved catalytic activity than conventional organic zinc catalysts during a polymerization process for the preparation of a polyalkylene carbonate resin and is capable of preventing an aggregation phenomenon during a reaction, a method for preparing the same, and a method for preparing a polyalkylene carbonate resin using the organic zinc catalyst.

The method for preparing an organic zinc catalyst includes the step of reacting a zinc precursor with a dicarboxylic acid in the presence of a polyether derivative to form a zinc dicarboxylate-based catalyst.

The present disclosure relates to a catalyst system for ethylene oligomerization and a method for producing ethylene oligomerization using the same and more particularly, to a catalyst system for ethylene oligomerization including a transition metal or transition metal precursor with a new structure, a ligand with a backbone structure expressed by the following Chemical Formula 1 or Chemical Formula 2, and a co-catalyst for providing an ethylene oligomer and a method for producing ethylene oligomerization using the same. [Chemical Formula 1] R.sup.1OC(O)Y.sup.1C(O)OR.sup.2 Herein, R.sup.1, R.sup.2 are each independently hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, or substituted heterohydrocarbyl, and Y.sup.1 represents a group connecting CO(O). [Chemical Formula 2] R.sup.1OY.sup.2OR.sup.2 Herein, R.sup.1, R.sup.2 are each independently hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, or substituted heterohydrocarbyl, and Y.sup.2 represents a group connecting O and is a linear, branched, or cyclic alkyl group having 3 or more carbon atoms, or hetero hydrocarbyl, or substituted heterohydrocarbyl. The catalyst system of the present disclosure has an excellent catalytic activity and in the distribution of the produced -olefins, C8-C18 -olefins are highly distributed.

Embodiments of the invention relate to a method for preparing a hydroprocessing catalyst including supporting a carrier with one or more hydrogenation metal components selected from the group consisting of VIB, VIIB, and VIII group metals of the periodic table; drying and calcining the supported carrier having the hydrogenation metal components; supporting the supported carrier having the hydrogenation metal components with an organic compound, and drying and calcining the supported carrier having the hydrogenation metal components and the organic compound. The hydrogenation metal components and the organic compound are supported in the carrier. The organic compound is selected from the group consisting of methyl acetoacetate, ethyl acetoacetate and a mixture thereof. The hydrogenation metal components supported in the carrier is sulfide. An amount of the organic compound is 15 wt % to 90 wt % based on the total amount of the hydroprocessing catalyst.

Methods and compositions of catalysts for sulfoxidation reaction processes are disclosed. The sulfoxidation reaction process can be performed in an aqueous medium, and the catalysts can be recycled for further use. In some embodiments, a method of making a catalyst may include contacting a transition metal compound with an oxidizing agent to form a first solution, contacting a carboxylic acid compound with a cationic surfactant to form a second solution, mixing the first solution and the second solution to form a precipitate, and isolating the precipitate.

The present disclosure relates to a method of using homogenous rhodium-BIPHEPHOS catalysts comprising for the hydroformylation of an allyl alcohol. In some aspects, the methods provided herein relate to the hydroformylation of allyl alcohol to produce 4-hydroxybutyraldehyde in a continuous process.