Abstract: The present invention relates to a catalyst which comprises a support material and an oxidic composition containing at least one alkali metal and tungsten, a process for producing such catalysts and also a process for preparing alkyl mercaptans by reaction of alkanols with hydrogen sulphide in the presence of such a catalyst.

Abstract: A nonaqueous electrolyte battery is provided and includes a positive electrode, a negative electrode, and an electrolyte. The electrolyte contains a nonaqueous solvent, an electrolyte salt, a matrix polymer and a ceramic powder, and further contains a polyacid and/or a polyacid compound.

Abstract: The present invention provides modified multifunctional thiol-ene monomers wherein one or more thiols are reacted with a Michael addition reactive double bond compound. The present invention further discloses photocurable thiol-ene formulations comprising thiol-ene monomers including the modified multifunctional thiols. The present invention further discloses photocurable thiol-ene formulations comprising thiol-ene monomers and Michael addition reactive double bond molecules and a Michael catalyst. The formulations of the present invention can be photocured to make films or coatings. In a further disclosure, the formulations, including those comprised of unmodified multifunctional thiols and multifunctional enes, are photocured to form films applied to non-flexible or flexible polymer or non-polymer substrates suitable for food packaging, electronic products, optical products and other applications and free-standing films.

Abstract: The process for preparing a mercaptan from an olefin and hydrogen sulphide is carried out in the presence of hydrogen and a catalyst composition comprising a strong acid, such as a heteropolyacid, and at least one metal belonging to group VIII of the Periodic Table.

Abstract: A process for selectively making 2-thiols from alpha olefins is described. The process includes contacting a linear or branched alpha olefin having with H2S in the presence of a catalyst and recovering the 2-thiol from a product mixture. The catalyst includes a support and at least one metal selected from Group IIIA-VIIIA and the branched olefin is branched at the 3-position or higher with respect to the olefin double bond. Compositions wherein the 2-thiols are substantially free of 1-thiol and 3-thiol isomers are also described.

Abstract: Chiral ligands and metal complexes based on such chiral ligands useful in asymmetric catalysis are disclosed. The metal complexes according to the present invention are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition; epoxidation, kinetic resolution and [m+n] cycloaddition. Processes for the preparation of the ligands are also described.

Abstract: Chiral ligands and metal complexes based on such chiral ligands useful in asymmetric catalysis are disclosed. The metal complexes according to the present invention are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition; epoxidation, kinetic resolution and [m+n] cycloaddition. Processes for the preparation of the ligands are also described.

Abstract: A process is disclosed for the preparation of primary mercaptans by reacting hydrogen sulfide with an alpha-olefin in the presence of a reaction initiating amount of a borane represented by the formula R.sub.2 BH or R.sub.3 B where R is a linear or cyclic aliphatic or aryl group.

Abstract: A process is disclosed for continuously preparing dialkyl disulfides and dialkyl polysulfides by reacting at elevated temperature and in the presence of a solid, particulate catalyst an alkene and hydrogen sulfide in a first reaction zone, and then passing the reactor effluent into a second reaction zone where it is reacted at elevated temperature with molten, elemental sulfur in the presence of a solid, particulate catalyst.

Abstract: A process is disclosed for the preparation of secondary thiols by the addition of H.sub.2 S to C.sub.10 to C.sub.30 linear olefins in the presence of certain zeolite catalysts. The process achieves high selectivity to the secondary thiol and minimizes formation of dialkyl sulfide by-products. The secondary thiol products are of particular advantage for use as intermediates in the preparation of surfactant chemicals.

Abstract: A process for making alkyl mercaptans in high yield while minimizing the formation of dialkyl sulfides is conducted by reacting an olefin with hydrogen sulfide in an inert solvent (e.g. CH.sub.2 Cl.sub.2) containing a Lewis Acid catalyst (e.g. BF.sub.3). Best results are obtained when the olefin is added to the hydrogen sulfide solution at a rate that keeps the amount of unreacted olefin below about 0.05 moles per mole of hydrogen sulfide.

Abstract: A process is provided for the preparation of dialkyl sulfides by reacting alkenes and hydrogen sulfide at elevated temperature in the presence of a Type X, Y or L zeolite containing from about 5 to 15 percent by weight of alkali metal, expresed as Me.sub.2 O (where Me is an alkali metal).

Abstract: Process for the synthesis of a mercaptan from an olefin, by the action of hydrogen sulphide thereon, in the presence of a catalyst comprising a cation exchange resin, characterized in that this resin is dry and that the reaction is effected at a temperature ranging between 45.degree. and 75.degree. C.

Abstract: Vinylidene olefins are selectively removed from a mixture of olefins containing vinylidene olefins by reacting the mixture with either hydrogen sulfide or a hydrocarbyl mercaptan and then distilling the resultant mixture to obtain a substantially vinylidene olefin-free product.