Patent classifications
C07F7/04
Amino-containing organosilicon compound and making method
An amino-containing organosilicon compound having formula (1) is used for surface treatment of an inorganic filler for thereby rendering the filler more compatible with and adhesive to a polymer material. In formula (1), R.sup.1 is alkyl, alkenyl, aryl or aralkyl, R.sup.2 is alkenyl, aryl or aralkyl, R.sup.3 and R.sup.4 each are a monovalent hydrocarbon group, and n is 0, 1 or 2. ##STR00001##
Method for producing siloxane resin
A method for producing a siloxane resin, by hydrolyzing and condensing a silane compound containing a hydrolyzable silyl group represented by R.sub.nSiX.sub.4-n using a neutral salt as a catalyst. In the formula R.sub.nSiX.sub.4-n, R represents an organic group having a carbon atom directly bonded to Si, X represents a hydroxyl group or a hydrolyzable group, and n represents an integer of 0 to 3, provided that when n is 2 or greater each R may be the same as or different from each other, and when (4-n) is 2 or greater, each X may be the same as or different from each other.
HYDROSILYLATION REACTION CATALYST
A hydrosilylation reaction catalyst prepared from: a prescribed transition metal compound such as iron pivalate, cobalt pivalate, iron acetate, cobalt acetate, or nickel acetate; a ligand comprising t-butylisocyanide or another isocyanide compound; and a borane compound, Grignard reagent, alkoxysilane, or other prescribed promoter makes it possible to promote a hydrosilylation reaction under moderate conditions, and has exceptional handling properties and storage stability.
DIRECT SYNTHESIS OF ALKOXYSILANES USING COPPER-ALUMINUM ALLOY CATALYSTS
An improved catalyzed reaction of silicon metal with alcohol is provided for the formation of alkoxysilanes, particularly trialkoxysilanes. The Direct Synthesis reaction of silicon metal and alcohol employs a catalytically effective amount of a copper-aluminum alloy as a catalyst precursor and further benefits from an effective catalyst-promoting amount of a catalyst promoter.
Substituted angular bistetracenes and substituted angular bisoligoacenes and electronic devices made with same
We report the synthesis and characterization of novel bistetracenes, an unconventional, linearly extended conjugated core with eight fused rings. Also described are bisoligoacenes. In general, the properties and stability of large polycyclic aromatic hydrocarbons (PAHs) strongly depend on the mode of ring annellation and the topology of their it-electron systems, which are usually associated with the resonance stabilization energy in large PAHs.
Hydrosilylation reaction catalyst
A hydrosilylation reaction catalyst prepared from: a catalyst precursor comprising a transition metal compound, excluding platinum, belonging to group 8-10 of the periodic table, e.g., iron acetate, cobalt acetate, nickel acetate, etc.; and a ligand comprising an isocyanide compound such as t-butyl isocyanide. The hydrosilylation reaction catalyst has excellent handling and storage properties. As a result of using this catalyst, a hydrosilylation reaction can be promoted under gentle conditions.
Platinum catalyzed hydrosilylation reactions utilizing cyclodiene additives
A process and composition for the hydrosilylation of an unsaturated compound comprising reacting (a) a silyl hydride with (b) an unsaturated compound in the presence of (c) a platinum compound and (d) a cyclodiene, with the proviso that when the unsaturated compound is a terminal alkyne, the silyl hydride is other than a halosilane. The process and composition optionally comprise an inhibitor (e). The process and composition may be employed to form a variety of hydrosilylation products.
Method for producing tetraalkoxysilane
An object of the present invention is to provide a method for producing tetraalkoxysilane while saving energy at a high yield. Tetraalkoxysilane can be produced while saving energy at a high yield by the method including a first step of reacting alcohol with carbon dioxide in the presence of a dehydrating agent and/or in a reactor provided with a dehydrating means, and a second step of reacting a reaction mixture obtained in the first step with silicon oxide.
Method for producing tetraalkoxysilane
An object of the present invention is to provide a method for producing tetraalkoxysilane while saving energy at a high yield. Tetraalkoxysilane can be produced while saving energy at a high yield by the method including a first step of reacting alcohol with carbon dioxide in the presence of a dehydrating agent and/or in a reactor provided with a dehydrating means, and a second step of reacting a reaction mixture obtained in the first step with silicon oxide.
Hydrosilylation reaction catalyst
A hydrosilylation reaction catalyst prepared from: a catalyst precursor comprising a transition metal compound, excluding platinum, belonging to group 8-10 of the periodic table, e.g., iron acetate, cobalt acetate, nickel acetate, etc.; and a ligand comprising a carbine compound such as 1,3-dimesitylimidazol-2-ylidene, etc.. The hydrosilylation reaction catalyst has excellent handling and storage properties. As a result of using this catalyst, a hydrosilylation reaction can be promoted under gentle conditions.