Exxon Research and Engineering Company

Pfizer Corporation

Givaudan Corporation

Chem Systems Inc.

Exxon Research & Engineering

I-Der Huang

Alexis A Oswald

Andrew A Westner

Krishna K Rao

Torris G Jermansen

Tai-Cheng Yang

Torris G Jermasen

Martin B Sherwin

Harry H Teng

Leon M Polinski

Catherine McCooey

Hsuan L Labowsky

Andrew Westner

Compositions of matter are disclosed which are highly useful in hydroformylation processes. The compositions are non-charged, non-chelated bis- and tris-(alkyl diaryl phosphine) rhodium carbonyl hydrides. The substituents of the alkyl group include heteroorganic radicals containing silane, silicone, ether, ester, keto and hydroxy oxygen, phosphine oxide and phosphorus ester phosphorus, amine, amide, amine oxide and heterocyclic nitrogen groups. These compositions are highly stable and selective catalysts for the hydroformylation of olefins under certain conditions. The disclosed catalyst systems contain a large excess of phosphine ligand and employ alpha-olefin plus synthesis gas reactant mixtures having a high H.sub.2 /CO ratio at relatively low pressures. They produce mostly aldehydes derived from terminal attack on the alpha-olefin reactant. In the case of low olefins, such as butene-1, the products can be advantageously removed in a continuous manner, as distillate components from a ligand reaction mixture kept at an elevated temperature and continuously fed by an appropriate mixture of the reactants.

Ligand exchange process for producing alkyl diaryl phosphine rhodium

Compositions of matter are disclosed which are highly useful in hydroformylation processes. The compositions are non-charged, non-chelated bis- and tris-(alkyl diaryl phosphine) rhodium carbonyl hydrides. The substituents of the alkyl group include heteroorganic radicals containing ether, ester, keto and hydroxy oxygen, phosphine oxide and phosphorus ester phosphorus, amine, amide, amine oxide and heterocyclic nitrogen groups. These compositions are highly stable and selective catalysts for the hydroformylation of olefins under certain conditions. The disclosed catalyst systems contain a large excess of phosphine ligand and employ alpha-olefin plus synthesis gas reactant mixtures having a high H.sub.2 /CO ratio at relatively low pressures. They produce mostly aldehydes derived from terminal attack on the alpha-olefin reactant. In the case of low olefins, such as butene-1, the products can be advantageously removed in a continuous manner, as distillate components from a ligand reaction mixture kept at an elevated temperature and continuously fed by an appropriate mixture of the reactants.

Selective hydroformylation process using alkyl diaryl phosphine rhodium

Compositions of matter are disclosed which are highly useful in hydroformylation processes. The compositions are non-charged, non-chelated bis- and tris-(alkyl diaryl phosphine) rhodium carbonyl hydrides. The substituents of the alkyl group includes heteroorganic radicals containing ether, ester, keto and hydroxy oxygen, phosphine oxide and phosphorus ester phosphorus, amine, amide, amine oxide and heterocyclic nitrogen groups. These compositions are highly stable and selective catalysts for the hydroformylation of olefins under certain conditions. The disclosed catalyst systems contain a large excess of phosphine ligand and employ alpha-olefin plus synthesis gas reactant mixtures having a high H.sub.2 /CO ratio at relatively low pressures. They produce moslty aldehydes derived from terminal attack on the alpha-olefin reactant. In the case of low olefins, such as butene-1, the products can be advantageously removed in a continuous manner, as distillate components from a ligand reaction mixture kept at an elevated temperature and continuously fed by an appropriate mixture of the reactants.

Transition metal complex catalysts

Heterocycle-substituted alkyl diaryl phosphine rhodium caronyl hydride

Branched alkyl diaryl phosphine rhodium carbonyl hydride complexes are surprisingly effective, stable and selective hydroformylation catalysts particularly in the presence of a large excess of t-phosphine ligands. As such, they are advantageously employed as catalysts in a novel low pressure rhodium hydroformylation process producing normal and iso aldehydes by reacting olefins with H.sub.2 and CO.

Hydroformylation catalysis by branched alkyl diaryl phosphine rhodium

A process for preparing a vanadium, phosphorus oxygen containing catalyst composition capable of partially oxidizing hydrocarbons (e.g., n-butane) to form a carboxylic anhydride (e.g., maleic anhydride), and a process for using this catalyst to form such anhydrides is disclosed. The catalyst composition is prepared by an organic solution technique followed by activation in an air-hydrocarbon atmosphere.

Process for preparing a vanadium phosphorus oxygen catalyst composition

A vanadium, phosphorus oxygen containing catalyst composition capable of partially oxidizing hydrocarbons (e.g., n-butane) to form a carboxylic anhydride (e.g., maleic anhydride), a process for preparing this catalyst, and a process for using this catalyst to form such anhydrides is disclosed. The catalyst composition is prepared by an organic heterogenous technique followed by a water treatment step and activation.

Process for the synthesis of carboxylic anhydrides using a vanadium,

A heterogeneous process for preparing a vanadium-phosphorus-oxygen containing catalyst for use in the preparation of carboxylic anhydrides is disclosed. This process employs an activation procedure in an air-hydrocarbon atmosphere.

Process for oxidizing a carboxylic anhydride with heterogeneously

Described is a carbonylation process using novel homogeneous trihydrocarbyl silyl-substituted alkyl diaryl phosphine transition metal complexes of the general formula:

Trihydrocarbyl silyl substituted alkyl diaryl phosphine transition metal

A process for preparing a metal oxygen composition capable of dehydrocoupling toluene wherein metal oxides such as Sb.sub.2 O.sub.3, PbO, and Bi.sub.2 O.sub.3 are admixed with an organic media such as isobutanol and heated to form a metal oxygen precursor composition which is recovered and calcined is disclosed.

Process for preparing inorganic metal oxygen composition capable of

Homogeneous hydroformylation catalysis with silyl substituted alkyl

Heterogeneous process for preparing vanadium phosphorus oxygen

A process for dehydrocoupling a hydrocarbon, such as toluene, using oxygen as the oxidant, in the presence of a crystalline zeolite of the faujasite structure containing a cation such as cesium, and a promoter, such as boron and/or phosphorus is disclosed.

Growing community of inventors

Upper Saddle River, NJ, United States of America

I-Der Huang