Abstract: Aminoalkylsilanes of formula I: R1R2N—(CH2)y—Si(OR3)3−nR4n  (I), wherein R1 and R2 are each independently, identical of different, hydrogen, aryl, arylalkyl or C1-4-alkyl; R3 and R4 are each independently, identical or different, C1-8-alkyl or aryl; y is 2, 3 or 4 and n is 0 or 1, 2 or 3, are prepared by a process comprising: reacting an organosilane of formula II: X—(CH2)y—Si(OR3)3−nR4n  (II), wherein X is Cl, Br, I or F; and R3, R4, y and n are each as defined above with ammonia or an organic amine compound of the formula: HNR1R2  (III),  wherein R1 and R2 are each as defined above with at least one of R1 and R2 not being hydrogen in a liquid phase; evaporating ammonia or organic amine under reduced pressure while ammonium chloride or aminohydrochloride by-products, produced in the reaction of the first step, remains dissolved in the liquid phase; transferring the product mixture after said evaporation to another vessel operate

Abstract: Dialkyldihalosilane formation during direct method alkylhalosilane production is promoted by effecting reaction between alkyl halide and powdered silicon in the presence of a catalyst comprising copper, zinc, and aluminum and further comprising an amount of phosphorus and tin wherein the amount of phosphorus and tin substantially enhances the selectivity of dialkyldihalosilane formation in comparison to the selectivity of dialkyldihalosilane formation in the presence of the catalyst comprising copper, zinc, aluminum and tin without phosphorus.

Abstract: The invention relates to a process for the preparation of organosilylalkylpolysulfanes, of the general formula I (R1R2R3SiR4)2Sx (I) by reaction of organosilylalkylpolysulfanes of the general formula II (R1R2R3SiR4)2Sy (II) with an ionic sulfide of the general formula M+2S2− (III) and an organosilylalkyl halide of the general formula R1R2R3SiR4X (IV), the long-chain organosilylalkylpolysulfane of the general formula (II) and the organosilylalkyl halide of the general formula (IV) being initially introduced into the reaction vessel and the ionic sulfide of the general formula (III) being added to this solution in several portions.

Abstract: A method for the preparation of triorganooxysilanes containing one silicon-hydrogen bond is provided which comprises reacting at least one tetraorganooxysilane with at least one metal hydride.

Abstract: A method of preparing a reduced product by efficiently reducing an unsaturated organic compound by using, as a reducing agent, a trichlorosilane which is industrially cheaply available and is easy to handle, and a reducing agent therefor. A reduced product of an unsaturated organic compound is obtained by mixing the unsaturated organic compound and a trichlorosilane together to reduce the unsaturated organic compound in the presence of a compound that forms a silicon complex having five coordinations upon acting on the trichlorosilane such as an N-formylated product of a secondary amine having not less than 3 carbon atoms. The invention further provides a reducing agent comprising a particular silicon complex.

Abstract: Catalyst compositions, systems and methods, useful in polymerization processes, are disclosed, which utilize bridged metallocene catalysts, preferably including indenyl groups, bound to the transition metal and a vinyl group bound to the bridge.

Abstract: Ortho-substituted arylmetal compounds are prepared by deprotonation of aromatics which have a hydrogen atom in the ortho position relative to at least one halogen atom, one trifluoromethoxy group, one dialkylamino group, one nitrile group, one alkoxy group or one dialkylamido group. The arylmetal compounds can then be reacted with electrophilic reagents. Deprotonation of the aromatics is carried out using alkyl- or arylmetal compounds or metal hydrides in the presence of a catalytic amount of a secondary metal amide.

Abstract: A process is provided for preparing a bis(silylorgano)amine in which a cyanoorganosilane is reacted with hydrogen under hydrogenation conditions in the presence of a catalytically effective amount of hydrogenation catalyst selected from the group consisting of rhodium, ruthenium, palladium and platinum to produce the secondary aminoorganosilane.

Abstract: Compounds having the formula: wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (e.g., m-phenylene), produced by reacting a compound having the formula: with an R-ylating agent (e.g., R2 SO4) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: are produced by reacting a compound having the formula: with wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula are produced by reacting a compound of the formula with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups.

Abstract: Novel silicon amphiphilic compounds which comprise a silicon residue. The silicon amphiphilic compounds are particularly suitable for use in compositions for diagnostic imaging, such as ultrasound. Compositions of the silicon amphiphilic compounds comprise a gas or gaseous precursor, and may take the form of vesicle compositions, such as micelles or liposomes.

Abstract: Hypervalent silane and siloxane reagents (preformed or generated in situ) for transmetalation in palladium catalyzed reactions with derivatives of allylic alcohols, aryl halides, electron-withdrawing aryl bromides, and aryl triflates derived from phenols are disclosed. Also disclosed are methods of preparing glycosyl azides by reaction of an azide with a silyl ester in the presence of a phoshine.

Abstract: In the process for the preparation of vinylsilanes by reacting acetylenic hydrocarbons with silanes which have at least one silicon-bonded hydrogen atom in the liquid phase in the presence of a catalyst, the silane is added to the liquid phase. In particular, the reaction is carried out at superatmospheric pressure, and the spent acetylenic hydrocarbon is replenished during the reaction while maintaining a pressure which is constant during the entire reaction.

Abstract: The invention relates to block copolymers of the general average formula with siloxane blocks which are linked via rigid spacers, and to their use as surface-active agents.

Abstract: This invention includes a process for producing an alkylsilane, comprising reducing an alkoxysilane in the presence of an alkali metal hydride in the presence of a high boiling solvent. The alkylsilane has a boiling point lower than the boiling point of the solvent, which is typically diglyme. This invention also includes a chloride-free alkylsilane formed from the reduction of an alkoxysilane in the presence of an alkali metal hydride. The alkylsilane produced according to the process of the present invention may be useful in microelectronic applications, such as in the production of chloride-free low dielectric constant materials which may be produced by the chemical vapor deposition of such silanes.

Abstract: A process for preparing boratabenzene derivatives is provided. The process includes the hydrogenation of a compound containing a boranaphthalene functional group to form a boratabenzene-containing compound. Depending on the compound containing a boranaphthalene functional group, the resulting boratabenzene compound may be converted into a catalyst suitable for olefin polymerization. A process for forming a boratabenzene derivative from a halo-dioxaborolane is also provided. In this process, a halo-dioxaborolane is reacted with a piperylide salt for form a pentadienyl dioxaborolane. The pentadienyl-dioxaborolane is reacted with a strong base to form an intermediate boratacyclohexanediene salt. The intermediate boratacyclohexanediene salt is then reacted with a trialkylaluminum compound to form an alkylboratabenzene salt.

Abstract: In a process for preparing trialkoxysilanes by reaction of silicon metal with an alcohol in an inert solvent in the presence of a copper catalyst, the copper catalyst used is a copper salt whose anion contains at least one nonhydrolyzable fluorine atom, or a mixture thereof with other salts.

Abstract: The present invention is related to diimino compounds of formulae (I) R2—N═C(R1)(R3)nC(R1)═N—R2 and (II) (R1)2C═N—(CR24)m—N═C(R1)2 functionalized with at least one siloxy group. Said diimino compounds are useful for obtaining a solid catalyst component for polymerizing olefins wherein the diimino compound of formulae (I) or (II) is bonded to a porous inorganic support and to a transition metal selected from groups 8, 9 and 10 of the periodic table. This invention also relates to a process for preparing said diimino compounds of formulae (I) or (II), to a process for obtaining said solid catalyst component comprising the combination of the diimino compound and a porous inorganic support. Further, the invention also relates to the use of said solid catalyst in combination with a cocatalyst to polirnenrze olefins.

Abstract: A continuous method for performing a hydrosilylation reaction comprising effecting a hydrosilylation reaction between a liquid organosilicon compound (A) having in each molecule at least one silicon-bonded hydrogen atom and a liquid organosilicon compound (B) having in each molecule at least one aliphatic unsaturated bond in the presence of a platinum catalyst (C) continuously in a tubular reactor equipped with a stirring and plug-flow maintaining apparatus located within the reactor.

Abstract: An organosilane preparation, comprising a mixture of one or more organosilanes and one or more fillers, has a fines content of less than 2%.

Abstract: A series of emitting materials used for organic EL based on tridentate ligands are characterized as Formula 1, Formula 2 and Formula 3, where: the group O-I-N is a bidentate ligand such as 8-hydroxyquinoline and 2-(o-hydroxyphenyl)-benzoxazole, II, III are unsubstituted or substituted aryl groups. The substituted groups can have 1-8 carbon atoms, halogen, cyano, amino, amido, sulfonyl, carbonyl, aryl, or heteroalkyl groups. The ligand including II and III is a tridentate ligand with three chelate atoms: two oxygen atoms and one nitrogen atom. The central metal atoms can be trivalent or tetravalent atoms such as Al, In, Ga, Tl, and Sn. These materials can be used as emitting materials or electronic transport materials in organic EL devices.