B01J31/226

Hydrogen Generation Method, System, and Solution Used Therein

A hydrogen generation method including steps as follows: adding a nitrogen-substituted derivative of an alkyldithiolate ruthenium complex as a biomimetic hydrogenase photocatalyst into a solution, adding an organic acid into the solution, adding a P-ligand into the solution, adding an electron donor into the solution, and irradiating the solution with light in order to generate hydrogen.

Iron-sulfur complex and method for producing hydrogen using the same as catalyst
10016748 · 2018-07-10 · ·

This invention relates to an iron-sulfur complex that is capable of efficiently catalyzing formation of hydrogen, and a method for producing hydrogen using the complex as a catalyst. The iron-sulfur complex provided herein comprises: a structure of formula (I) ##STR00001## wherein the ligands L.sup.1 to L.sup.3, L.sup.5 and L.sup.6 and the groups X.sup.1 to X.sup.3 are each selected from the group consisting of alkyl, alkenyl, alkynyl and aryl that are substituted or unsubstituted, hydroxyl, carbonyl, aldehyde, and so on; L.sup.4 is a bridging ligand selected from the group consisting of hydroxyl, carbonyl, and so on; and the symbol z means the charge, which is an integer with the range of 3 to +2. X.sup.1 and X.sup.2 may join together to form a bridging group between the two sulfur atoms. X.sup.3 may alternatively be a vacant site.

CATALYST FOR PRODUCING METHANOL PRECURSOR, METHANOL PRECURSOR PRODUCED USING THE CATALYST AND METHANOL PRODUCED USING THE METHANOL PRECURSOR

Disclosed is a novel catalyst for producing a methanol precursor. The use of the catalyst enables the production of a methanol precursor and methanol with high efficiency under low temperature and low pressure conditions. Also disclosed are a methanol precursor produced using the catalyst and methanol produced using the methanol precursor.

Bimetallic catalytic complexes for the polymerisation of carbon dioxide and an epoxide

The present invention provides a novel catalyst of formula (I): wherein M is selected from Zn(H), Co(II), Mn(II), Mg(II), Fe(II), Cr(III)-X or Fe(III)-X, and the use thereof in polymerizing carbon dioxide and an epoxide.

CHIRAL SPIRO PHOSPHORUS-NIROGEN-SULPHUR TRIDENTATE LIGAND, PREPARATION METHOD AND APPLICATION THEREOF
20180141966 · 2018-05-24 ·

The present invention relates to a chiral spiro phosphine-nitrogen-sulfur (PNS) tridentate ligand, preparation method and application thereof. The PNS tridentate ligand is a compound represented by Formula I or Formula II, their racemates, optical isomers, or catalytically acceptable salts thereof. The ligand has a primary structure skeleton characterized as a chiral spiro indan skeleton structure with a thio group. The chiral spiro phosphine-nitrogen-sulfur tridentate ligand can be synthesized by reacting racemic or optical active compound 7-diary/alkyl phosphine-7-amino-1,1-spiro-dihydro-indene compound having a spiro-dihydro-indene skeleton as the starting material. The chiral spiro PNS tridentate ligand being complex with transition metal salt can be used in an asymmetric catalytic hydrogenation reaction for catalyzing carbonyl compound. In particular, in asymmetric hydrogenation reaction process, being complex with iridium for catalyzing -alkyl--keto ester can obtain a high catalytic activity (a catalyst amount of 0.0002% mol) and high enantioselectivity (up to 99.9% ee) result. So the present invention has a practical value for industrial and commercial production.

##STR00001##

Catalytic hydrogenation process for the synthesis of terminal diols from terminal dialkyl aliphatic esters

A phosphorus ligand-free, mild, efficient and complete catalytic hydrogenation process is for the sustainable production of terminal diols from renewable terminal dialkyl esters with improved yield. Soluble, phosphorus ligand free Ru (II)-pincer type complexes can be used as catalysts in the hydrogenation process.

Olefin hydroboration

A process comprising contacting a) an alkene, b) a hydrogen-boron bond containing compound, c) an -diimine metal salt complex comprising an -diimine iron salt complex or an -diimine cobalt salt complex, and d) a group 1 metal borohydride under conditions suitable to form an alkylboron compound. A process comprising contacting a) an alkene, b) a hydrogen-boron bond containing compound, and c) an -diimine metal salt complex comprising an -diimine iron methylenetrihydrocarbylsilyl complex or an -diimine cobalt methylenetrihydrocarbylsilyl complex, to form an alkyl-boron compound under conditions suitable to form an alkylboron compound. A process comprising contacting an alkene, a hydrogen-boron bond containing compound, and an -diimine metal salt complex to form an alkyl-boron compound under conditions suitable to form an alkylboron compound.

Catalysts for efficient Z-selective metathesis

The present application provides, among other things, compounds and methods for metathesis reactions. In some embodiments, provided compounds promote highly efficient and highly Z-selective metathesis. In some embodiments, provided compounds and methods are particularly useful for producing allyl alcohols. In some embodiments, provided compounds have the structure of formula I. In some embodiments, provided compounds comprise ruthenium, and a ligand bonded to ruthenium through a sulfur atom.

PLASMONIC VIS-NIR PHOTOTHERMAL ACTIVATION OF OLEFIN METATHESIS ENABLING PHOTORESPONSIVE MATERIALS

text missing or illegible when filed plasmonic ROM polymer composites optionally comprising a latent catalyst, precursors thereof and uses thereof as a catalyst, are disclosed.

Ruthenium-based complexes, their preparation and use as catalysts

The present invention relates to novel Ruthenium-based complex compounds which represent viable catalysts, in particular for all sorts of metathesis reactions. Such complex compounds can be prepared by a novel, very favorable and cost efficient method which includes the introduction of an alkylidene ligand into the complex by using vinyl sulfides or vinyl ethers.