B01J31/2291

Selective reduction catalyst of ?,?-unsaturated ketone using electronically weakly coupled 4,4′-divinylazoarylene-bridged diruthenium complex bearing two Ru(CO)(8-mercaptoquinolato(PiPr3)2 moieties
11986810 · 2024-05-21 · ·

A 4,4-divinylazoarylene-bridged diruthenium complex with a general formula [{Ru(CO)(L-?.sup.2[N,S].sup.?)(P.sup.iPr.sub.3).sub.2}.sub.2(?{CH?CHC.sub.6H.sub.2(.sup.iPr).sub.2-2,6}.sub.2N?N-4,4)], its synthesis, and its use as an catalyst in inorganic processes.

4,4-divinylazoarylene-bridged diruthenium complex bearing Ru(CO)Cl(PiPr3)2 as an inorganic catalyst

A 4,4-divinylazoarylene-bridged diruthenium complex bearing two Ru(CO)Cl(P.sup.iPr.sub.3).sub.2 moieties, its synthesis, and its use as an catalyst in organic processes.

4,4′-divinylazobenzene-bridged diruthenium complex bearing Ru(CO)Cl(P.SUP.i.Pr.SUB.3.).SUB.2 .moieties as an inorganic catalyst
11980877 · 2024-05-14 · ·

A 4,4-divinylazobenzene-bridged diruthenium complex bearing two Ru(Co)Cl(P.sup.iPr.sub.3).sub.2 moieties, its synthesis, and its use as an catalyst in organic processes.

YLIDE-FUNCTIONALISED PHOSPHANES FOR USE IN METAL COMPLEXES AND HOMOGENEOUS CATALYSIS
20240149256 · 2024-05-09 ·

The invention relates to ylide-functionalized phosphane ligands, the production of same and use in transition metal compounds, as well as the use of same as catalysts in organic reactions.

Chemoselective hydrogenation catalyst of ?,?-unsaturated ketone and polyelectrochromism of electronically weakly coupled 4,4′divinylazoarylene-bridged diruthenium complex bearing two Ru(CO)(8-hydroxyquinolato)(P.SUP.i.Pr.SUB.3.).SUB.2 .moieties
11975311 · 2024-05-07 · ·

A 4,4-divinylazoarylene-bridged diruthenium complex bearing two Ru(CO) (8-hydroxyquinolato)(P.sup.iPr.sub.3).sub.2 moieties, its synthesis, and its use as a catalyst.

Selective hydrogenation catalyst of ?,?-unsaturated ketone using electronically weakly coupled 4,4′-divinylazoarylene-bridged diruthenium complex bearing two Ru(CO)(2-mercaptoquinolato)(P.SUP.i.Pr.SUB.3.).SUB.2 .moieties
11975312 · 2024-05-07 · ·

A 4,4-divinylazoarylene-bridged diruthenium complex bearing two Ru(CO)(2-mercaptoquinolato)(P.sup.iPr.sub.3).sub.2 moieties, its synthesis, and its use as a catalyst.

Process for preparing tris[3-(alkoxysilyl)propyl]isocyanurates
10377776 · 2019-08-13 · ·

A process can prepare an isocyanurate compound by hydrosilylation. The compound is a tris[3-(trialkoxysilyl)propyl] isocyanurate, a tris[3-(alkyldialkoxysilyl)propyl] isocyanurate, and/or a tris[3-(dialkylalkoxysilyl)propyl] isocyanurate. The process includes (A) preparing a mixture of at least one carboxylic acid, a platinum catalyst, and 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; (B) heating the mixture to a temperature in the range of 40 to 140 C.; (C) adding at least one H-silane among a hydrotrialkoxysilane, a hydroalkyldialkoxysilane, and a hydrodialkylalkoxysilane to the mixture; (D) adding at least one alcohol to the mixture prepared in step (C); and (E) isolating the isocyanurate compound.

PROCESS FOR PREPARING TRIS[3-(ALKYLDIALKOXYSILYL)PROPYL]ISOCYANURATES
20190233445 · 2019-08-01 · ·

A process can prepare an isocyanurate compound by hydrosilylation. The compound is a tris[3-(trialkoxysilyl)propyl] isocyanurate, a tris[3-(alkyldialkoxysilyl)propyl] isocyanurate, and/or a tris[3-(dialkylalkoxysilyl)propyl] isocyanurate, The process includes (A) preparing a mixture of at least one carboxylic acid, a platinum catalyst, and 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; (B) heating the mixture to a temperature in the range of 40 to 140 C.; (C) adding at least one H-silane among a hydrotrialkoxysilane, a hydroalkyldialkoxysilane, and a hydrodialkylalkoxysilane to the mixture; (D) adding at least one alcohol to the mixture prepared in step (C); and (E) isolating the isocyanurate compound.

OPTICALLY PURE ENANTIOMERS OF RUTHENIUM COMPLEXES AND USES THEREOF

The present invention relates to an optically pure (+) or (?) enantiomer of a ruthenium complex having formula (I) as well as the preparation method of said enantiomer, and uses thereof as catalyst, in particular in asymmetric olefin metathesis.

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UNSYMMETRICAL N-HETEROCYCLIC CARBENE CATALYSTS AND METHODS USING SAME

The present disclosure relates in part to novel complexes of unsymmetrical N-heterocylic carbene (NHC) ligands and group 10 or 11 metals. The present disclosure further relates to methods of electrophilic functionalization of alkynes and/or nitriles using the NHC catalysts described herein.