Abstract: The invention relates to a process comprising the following process steps: a) introducing an ethylenically unsaturated compound; b) adding a monophosphine ligand and a compound which comprises Pd, or adding a complex comprising Pd and a monophosphine ligand; c) adding an aliphatic alcohol; d) supplying CO; e) heating the reaction mixture, the ethylenically unsaturated compound being reacted to form an ester; where the monophosphine ligand is a compound of formula (I) where R1 is selected from —(C1-C12)-alkyl, —O—(C1-C12)-alkyl, —O—(C6-C20)-aryl, —(C6-C20)-aryl, —(C3-C12)-cycloalkyl, —(C3-C12)-heterocycloalkyl, —(C3-C20)-heteroaryl; R2 is selected from —(C6-C20)-aryl, —(C3-C12)-cycloalkyl, —(C3-C12)-heterocycloalkyl, —(C3-C20)-heteroaryl; R3 is —(C3-C20)-heteroaryl; and R1, R2 and R3 may each independently be substituted by one or more substituents selected from —(C1-C12)-alkyl, —(C3-C12)-cycloalkyl, —(C3-C12)-heterocycloalkyl, —O—(C1-C12)-alkyl, —O—(C1-C12)-alkyl-(C6-C20)-aryl, —O—(C3-C12)-cyclo

Abstract: Process for the direct conversion of diisobutene to a carboxylic acid.

Abstract: The invention relates to bisphosphites having 2,4-tert-butylphenyl units and a method for the preparation thereof. Furthermore, the invention relates to the use of the compounds as ligands in a ligand-metal complex. The compound, and also the complex, may be used as a catalytically active composition in hydroformylation reactions.

Abstract: Process for Pd-catalyzed hydroxycarbonylation of diisobutene:acetic acid/diisobutene ratio.

Abstract: Process for Pd-catalyzed hydroxycarbonylation of diisobutene:ligand/Pd ratio.

Abstract: Process for methoxycarbonylation with formic acid and methanol.

Abstract: The present invention relates to a method for preparing saturated Cn- and C2n-alcohols, wherein the ratio of Cn- to C2n-alcohols is controlled by the diversion of substreams in individual method steps.

Abstract: Process for Pd-catalyzed hydroxycarbonylation of diisobutene:sulfuric acid/ligand ratio.

Abstract: A process for Pd-catalyzed hydroxycarbonylation of diisobutene in an acetic acid solvent in the presence of a ligand having the following structure: In contrast to reaction solvents such as formic acid or 3,5,5 hexanoic acid the conversion rates were improved and greater than 90% at a reaction temperature of 120° C. and CO pressure of 40 bar.

Abstract: The invention relates to a process comprising the following process steps: a) introducing an ether having 3 to 30 carbon atoms; b) adding a phosphine ligand and a compound which comprises Pd, or adding a complex comprising Pd and a phosphine ligand; c) adding an alcohol; d) supplying CO; e) heating the reaction mixture, the ether being reacted for form an ester; where the phosphine ligand is a compound of formula (I) where m and n are each independently 0 or 1; R1, R2, R3, R4 are each independently selected from —(C1-C12)-alkyl, —(C3-C12)-cycloalkyl, —(C3-C12)-heterocycloalkyl, —(C6-C20)-aryl, —(C3-C20)-heteroaryl; at least one of the R1, R2, R3, R4 radicals is a —(C3-C20)-heteroaryl radical; and R1, R2, R3, R4, if they are —(C1-C12)-alkyl, —(C3-C12)-cycloalkyl, —(C3-C12)-heterocycloalkyl, —(C6-C20)-aryl or —(C3-C20)-heteroaryl, may each independently be substituted by one or more substituents selected from —(C1-C12)-alkyl, —(C3-C12)-cycloalkyl, —(C3-C12)-heterocycloalkyl, —O—(C1-C12)-alkyl, —O—(C

Abstract: A heat exchanger system can be used for removal or introduction of heat from or into a chemical reactor in which a chemical reaction is proceeding. The system further provides an apparatus for controlling the temperature of a reactor and a process for performing a chemical reaction, in each case using a heat exchanger system with a thermally insulated inner tube.

Abstract: Process for Pd-catalyzed hydroxycarbonylation of diisobutene: ratio of 3,5,5-trimethylhexanoic acid/H2O.

Abstract: An electrochemical method for C—C coupling a phenol and an aniline in a reaction vessel containing a suitable solvent or solvent mixture and a conductive salt to produce biaryls having both hydroxyl and amino functions, wherein the difference in the oxidation potentials ?E of the substrates ranges from 10 mV to 450 mV and the substrate with the highest oxidation potential is in excess, which method dispenses with multi-step syntheses using metallic reagents.

Abstract: The invention relates to an oligomerization catalyst comprising nickel oxide and silica-alumina support material and to a process for oligomerization of C3- to C6-olefins using the oligomerization catalyst.

Abstract: A process for preparing an oligomerization catalyst is based on using nickel aluminosilicate that has high activity and selectivity coupled with adequate service life in the heterogeneously catalysed oligomerization of C3 to C6 olefins or olefin-containing feed mixtures based thereon.

Abstract: The invention relates to an oligomerization catalyst comprising nickel oxide and silica-alumina support material and to a process for oligomerization of C3- to C6-olefins using the oligomerization catalyst.

Abstract: The invention relates to a process for producing an oligomerization catalyst comprising nickel oxide and a silicon-alumina support material, wherein the silica-alumina support material is in the ammonium form. The present invention further relates to a process for oligomerization of C3- to C6-olefins using the oligomerization catalyst produced according to the invention.

Abstract: A catalytic process for the methoxycarbonylation of olefins where formic acid is the CO source. The process includes the steps of forming a reaction mixture where methanol and formic acid are added at a volume ratio in the range from 1.55:0.45 to 1.1:09. The methanol-formic acid ratio enhances both the rate of conversion and methyl ester yield ether produced. The catalysts used is a palladium/benzene-base diphosphine ligand complex.

Abstract: Propyl-bridged diphosphine compounds, metal complexes of these compounds and the use thereof for alkoxycarbonylation.

Abstract: Process for Pd-catalyzed hydroxycarbonylation of diisobutene:acetic acid/diisobutene ratio.