Abstract: An apparatus is described for burn-in and/or functional testing of microelectronic circuits of unsingulated wafers. A large number of power, ground, and signal connections can be made to a large number of contacts on a wafer. The apparatus has a cartridge that allows for fanning-in of electric paths. A distribution board has a plurality of interfaces that are strategically positioned to provide a dense configuration. The interfaces are connected through flexible attachments to an array of first connector modules. Each one of the first connector modules can be independently connected to a respective one of a plurality of second connector modules, thereby reducing stresses on a frame of the apparatus. Further features include for example a piston that allows for tight control of forces exerted by terminals onto contacts of a wafer.

Abstract: The invention relates to a process for the making organic aldehyde compounds from an unsaturated compound by hydroformylation and in the presence of a catalyst system comprising a Group VIII metal and a bidentate phosphorus ligand having two trivalent phosphorus atoms bound to salicylanilide groups.

Abstract: Supported bis(phosphorus) ligands are disclosed for use in hydroformylation reactions, including the hydroformylation of olefins. Catalysts are formed when the ligands are complexed with a catalytically active metal (e.g., rhodium or iridium).

Abstract: Process for the preparation of an alkyl pentenoate respectively an aryl pentenoate by contacting an alkoxy-butene respectively an aryloxy-butene compound with carbon monoxide in the presence of a catalyst system comprising palladium, a phosphorus ligand and an acid promotor, wherein the molar ratio of 3-alkoxy-1-butene to 1-alkoxy-2-butene, respectively the molar ratio of 3-aryloxy-1-butene to 1-aryloxy-2-butene, is higher than 4.

Abstract: Process to prepare a pentenoic acid anhydride in the pressence of a catalyst comprising palladium and an organic phosphine ligand, wherein the corresponding alkoxycarbonyl butene is reacted with carbon monoxide at a temperature between 50 and 130.degree. C. and that the phosphine is a monodentate phosphine or a bidentate phosphine.

Abstract: A hydroformylation process for preparating a terminal aldehyde involves reacting an ethylenically unsaturated organic compound with carbon monoxide and hydrogen in the presence of a catalyst system iridium or rhodium and a bidentate organic phosphite ligand wherein the two phosphorus atoms of the phopshite ligand are linked with a 2,2'-dihydroxyl-1,1'-binapthalene bridging group having the following structure (Q): ##STR1## in which R.sup.1 and R.sup.2 are substituents other than hydrogen and in which R.sup.3 and R.sup.4 are the same or different substituted monovalent aryl groups and/or any one of OR.sup.3 and OR.sup.4 connected to one phosphorus atom forms an --O--R.sup.5 --O-group, where R.sup.5 is a divalent organic group containing one or two aryl groups.

Abstract: A hydroformylation catalyst composition comprising iridium or rhodium and a bidentate organic phosphite ligand wherein the two phosphorus atoms of the phopshite ligand are linked with a 2,2'-dihydroxyl-1,1'-binapthalene bridging group having the following structure (Q): ##STR1## in which R.sup.1 and R.sup.2 are substituents other than hydrogen.

Abstract: The invention relates to a process for the preparation of linear aldehydes by hydroformylation of ethylenically unsaturated organic compounds in the presence of a catalyst system comprising a Group VIII metal and a bidentate organic ligand. The bidentate organic ligand is characterized in that it has two trivalent phosphorus atoms each containing at least one P--C or one P--N bond.

Abstract: A hydroformylation process for the production of linear aldehydes from linear olefins, by the reaction of the olefin with hydrogen and carbon monoxide in a solvent containing a catalyst having a platinum component or palladium component, a bidentate diaryl phosphine component where the bridging group is ferrocenyl or 3 to 6 carbon atoms, and a metal promoter component.

Abstract: An improved process for the isomerization of saturated alkyl carboxylic acids is obtained by using aluminum iodide or aluminum bromide promoted rhodium or iridium catalysts.

Abstract: Conversion of certain lactones by reaction with carbon monoxide and water, in the presence of a homogeneous rhodium catalyst and an iodide or bromide promoter, to produce adipic acid.

Abstract: Preparation of 3-pentenoic acid by reacting butadiene and carbon monoxide using a rhodium catalyst and a sulfonic acid catalyst in water and a carboxylic acid solvent.

Abstract: Preparation of 3-pentenoic acid from butadiene, water and carbon monoxide in an organic acid solvent in the presence of a rhodium catalyst and a bromide or iodide promoter.

Abstract: A process for the hydrocarboxylation of alkenes and non-conjugated olefinically unsaturated nitriles and esters using a rhodium catalyst, a bromide or iodide promoter, and a nitrile accelerator.

Abstract: Perfluorinated acid ion-exchange resins are highly effective catalysts for the isomerization of 3-pentenoic compounds to 4-pentenoic compounds, especially if the catalysts contain a group 8 metal in an oxidation state of at least +2.

Abstract: Manufacture of 5-cyanovaleric acid by carbonylation of pentenenitriles from a mixture consisting essentially of pentenenitrile, CO and at least one compound of the formula ROH, where R is hydrogen or alkyl of 1 to 6 carbon atoms, and a cyclic urea and/or a cyclic amide, where the combined weight of the cosolvents is between about 70% and 99% of the total weight of the reaction mixture.

Abstract: Isomerization of branched saturated alkyl carboxylic acids to linear or isomeric branched alkyl carboxylic acids, or vice versa, by heating in the presence of a iodide or bromide promoted rhodium catalyst and carbon monoxide.

Abstract: Manufacture of 5-cyanovaleric acid and its esters by carbonylation of pentenenitriles from a mixture consisting essentially of pentenenitrile, CO and at least one compound of the formula R'OH, where R is hydrogen or alkyl of 1 to 6 carbon atoms.

Abstract: The life of a salcomine catalyst used in the oxidation of phenols to quinones (e.g., of o-phenylphenol to phenyl-p-benzoquinone) is increased by the presence of a water- or acid-removing substance, e.g., a non-acid-forming chemical water scavenger, a molecular sieve, a weak inorganic base, or a sterically hindered organic base, in the reaction medium. Suitable water- or acid-removing substances include carbodiimides, e.g., dicyclohexylcarbodiimide; a Type 3A or 4A molecular sieve; finely divided metal oxides or metal carbonates, e.g., barium carbonate; and 2,6-lutidine. These substances chemically transform by-product carboxylic acids, and/or prevent the formation of such acids, whereby the life of the salcomine catalyst is prolonged.

Abstract: Isomerization of 3-pentenoate esters to 4-pentenoate esters using homogeneous or heterogeneous catalysts of zero valent nickel complexes with an acid promoter.