Abstract: The invention relates to a process for synthesizing tertiary phosphines by reacting halophosphines with organomagnesium compounds in the presence of copper compounds and optionally of salts.

Abstract: The invention relates to novel aminophenylmorpholinone derivates (I) in which S represents an optionally substituted morpholinone radical, to a process for their preparation and to their use.

Abstract: The present invention provides a composition comprising at least one halobutyl elastomer, at least one mineral filler and at least one protected thiol modifier. In another aspect the present invention provides a process which comprises mixing a halobutyl elastomer with at least one mineral filler, in the presence of at least one protected thiol modifier, and curing the resulting filled halobutyl elastomer.

Abstract: The invention describes a process for preparing propoxylated, phosphorus-containing compounds using aluminium chloride catalyst.

Abstract: The present invention relates to an improved process for preparing ring-fluorinated aromatics of the general formula (I) by a halogen exchange reaction (halex reaction) of a plurality of halogen substituents in one stage in the presence of a catalyst.

Abstract: The present invention relates to novel low-monomer-content, low-viscosity preparations composed of isocyanurates which contain isocyanate groups and of phthalate-free plasticizers, to their use as adhesion promoters for coating compositions based on plasticized polyvinyl chloride, and also to coatings and to coated substrates.

Abstract: The present invention relates to silica-filled halogenated butyl elastomers, such as bromobutyl elastomers (BIIR). Further, the present invention also relates to bromobutyl elastomers with improved scorch safety.

Abstract: The present invention relates to a process for preparing aldehydes or ketones using an alkali metal hypochlorite or an alkaline earth metal hypochlorite in the presence of a ruthenium catalysts.

Abstract: The present invention relates to a process for the enantiomeric enrichment of cis-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane with the aid of continuous countercurrent chromatography, which is also described as SMB chromatography (SMB=simulated moving bed). In a further aspect, the invention relates to a process for the preparation of (1S,6R)-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane using the aforementioned process, which furthermore includes a racemization step.

Abstract: Process for preparing pigments of the formula (I) or tautomeric structures thereof and their hydrates, containing melamine as guest, characterized in that a mixture of the azobarbituric mono-cation salt (II) and the azobarbituric di-cation salt (III) is reacted with a nickel compound and melamine, in which cation1, cation2 and cation3 independently of one another are any desired univalent cations or the fraction of any desired multivalent cation that corresponds to a positive charge of one.

Abstract: The present invention relates to a process for preparing monomethylhydrazine by methylating hydrazine or hydrazinium hydrochloride or hydrazinium dihydrochloride with methyl chloride and/or a methano/HCl mixture, characterized in that the reaction mixture formed in the methylation is reacted with an organic base from the group of the alkylamines or alkanolamines and monomethylhydrazine is removed by distillation from the reaction mixture in a low boiler fraction and the low boiler fraction is optionally subjected to a further distillation.

Abstract: The invention relates to a method for the thermal decarboxylation of dicarboxylic acids, in particular to 3,4-ethylene dioxythiophene-2,5-dicarboxylic acid as an educt. According to said method the educt is used in solid form and/or the reaction is carried out in the presence of a plurality of fluidised bed bodies. No solvents are used in the reaction and the decarboxylation product that is formed during the reaction is carried away from the reaction zone in gaseous form.

Abstract: A butyl rubber ionomer having improved adhesion to substrates whose surfaces have polar functional groups. Examples of such substrate materials include stainless steel, glass, mylar or Teflon®. The adhesion of the butyl rubber ionomer to the substrate is at least 25% greater than the adhesion of a non-ionomeric butyl rubber to the same substrate surface and with certain substrates is more than 150% greater. The adhesion is improved with increasing levels of multiolefin content in the butyl rubber ionomer. The adhesion is greatest for butyl rubber ionomers having a high multiolefin content (at least 3.5 mol% of multiolefin monomers or at least 1.5 mol % of residual multiolefins). By taking advantage of these high adhesion levels, a composite article can be formed between the butyl rubber ionomer and the substrate.

Abstract: The invention provides a process for preparing a filled halobutyl elastomer, which includes mixing a halobutyl elastomer with at least one mineral filler that has been reacted with at least one organic compound containing at least one basic nitrogen-containing group and at least one hydroxyl group and, optionally, with at least one silazane compound before admixing the filler with the halobutyl elastomer and optionally curing the filled elastomer with sulfur or other curative systems.

Abstract: A process is described for preparing alkyl thiodiglycolates of the general formula (I) R—OOC—CH2-S—CH2-COO—R??(I) where R is a radical of branched or unbranched C1 to C10-alkyl, characterized in that an alkyl haloacetate of the general formula (II) X—CH2-COO—R??(II) where X is a chlorine or bromine atom and R is as defined for compounds of the formula (I) is reacted with an aqueous solution of alkali metal sulphide or alkali metal hydrogensulphide in the presence of an aqueous pH buffer solution in the pH range between 5 and 8, optionally in the presence of a phase transfer catalyst.

Abstract: Preparation of butyl rubber based graft co-polymers from halobutyl elastomers using phase transfer catalysts in the presence of a solution of an alkali metal salt of an oxygen or sulfur nucleophile that is bound to a polymeric substrate. Graft co-polymers can be produced of a butyl polymer (isobutene-co-isoprene) and polymeric substrates such as polyethylene, polypropylene, polystyrene, polybutadiene, polysilanes, polysiloxanes, polyethylene glycol, polyethylene oxide, polyphosphazenes, polyferrocenes or their hybrids.

Abstract: The present invention relates to an improved process for preparing cyclopropanecarboxylic acid and alcohols.

Abstract: The invention relates to polymeric transition metal catalysts, to processes for preparing them, to intermediates and also to the use of the transition metal catalysts as catalysts in organic reactions, in particular in olefin metathesis reactions.

Abstract: The present invention relates to a process for preparing optionally substituted aromatic or heteroaromatic nitriles starting from haloaromatics. These are reacted in a copper-catalysed reaction with potassium hexacyanoferrate(II) or potassium hexacyanoferrate(III) in the presence of heteroaromatic amines.

Abstract: The invention relates to polymeric transition metal catalysts, to processes for preparing them, to intermediates and also to the use of the transition metal catalysts as catalysts in organic reactions, in particular in olefin metathesis reactions.