Abstract: What is described is a process for continuously esterifying halosilanes of the formula I with alcohols of the formula II to give silane esters of the formula III in a single column (1) R1aSiHalb??(I) R2—(OH)??(II) R1aS—(OR2)b??(III) in which R1 is hydrogen or a monovalent organic radical, where any two R1 radicals within a molecule may be different within the scope of the given definitions, Hal is a halogen atom, a plurality of Hal atoms within a molecule may be different within the scope of the given definitions, R2 is a monovalent organic radical, a and b are integers from 0 to 4 and the sum total of a and b is 4, comprising the measures of: i) feeding the total amount of the halosilane of the formula I required for the reaction in liquid form through line (6) into the upper third of the column (1), ii) feeding at least 60% by weight of the alcohol of the formula II required for the reaction in liquid form through line (7) into the upper third of the column (1), iii) feeding the remainder of the a

Abstract: The invention relates to a process for dechlorinating alkylsilanes and siloxanes, and also to the use of basic anion exchanger resins for dechlorinating alkyl silanes and alkylsiloxanes.

Abstract: Organosilicon compounds bearing SiOC groups and having low residual silicon-bonded chlorine are prepared continuously by reacting a chlorosilane with alcohol and optionally water by contacting a gaseous phase containing alcohol with a liquid phase containing silane, organosilicon intermediates, organosilicon compounds containing SiOC groups and optional inert solvent in a reaction column in which the gas phase passes through the liquid phase in bubble form, or is provided with a vaporizer operating by a crossflow principle.

Abstract: The present invention provides an organosilicon composition comprising diethoxymethylsilane, a concentration of dissolved residual chloride, and a concentration of dissolved residual chloride scavenger that does not yield unwanted chloride salt precipitate when combined with another composition comprising diethoxymethylsilane.

Abstract: The present invention discloses a method for synthesizing a reversibly protected organometallic compound which comprises (1) reacting an organometallic compound with a hydroxyl group containing compound to produce a solution containing the reversibly protected organometallic compound and hydrogen chloride; (2) reacting the solution containing the reversibly protected organometallic compound and the hydrogen chloride with a trialkyl amine to precipitate the hydrogen chloride from the solution; and (3) recovering the reversibly protected organometallic compound from the solution of the reversibly protected organometallic compound.

Abstract: The present invention relates to an apparatus comprising a) an unbaffled reactor or microreactor having a channel defined by a pathway, and b) an oscillating flow device, wherein the channel pathway comprises a plurality of directional changes. The reactor channel has a hydrolic diameter from 0.1 mm to 10 mm A method of making said apparatus and the use of said apparatus to carry out a process on a suspension is also disclosed.

Abstract: Organosilicon compounds bearing SiOC groups and having low residual silicon-bonded chlorine are prepared continuously by reacting a chlorosilane with alcohol and optionally water by contacting a gaseous phase containing alcohol with a liquid phase containing silane, organosilicon intermediates, organosilicon compounds containing SiOC groups and optional inert solvent in a reaction column in which the gas phase passes through the liquid phase in bubble form, or is provided with a vaporizer operating by a crossflow principle.

Abstract: A hardener for silicone rubber materials comprising a silane compound which comprises a 2-hydroxy-propionic acid alkyl ester radical.

Abstract: The invention relates to a method for producing silicon compounds (A) having hydrocarbon oxy-groups that have at least one unit of the general formula (1) HmSi(OR)n(OR?)oR?pX4-m-n-o-p (1) by conversion of silicon compounds (B) having at least one unit of the general formula (2) Hm+nSi(OR?)oR?pX4-m-n-o-p (2), having an alcohol of the general formula (3) ROH (3) in the presence of a catalyst (K) that is on a carrier material bonded metal selected from Ni, Pd, Pt, wherein per mol formed group OR, at maximum 1 liter of solvent is used and wherein R, R?, R?, X, m, n, o and p have the meanings listed in claim 1.

Abstract: The present invention provides an organosilicon composition comprising diethoxymethylsilane, a concentration of dissolved residual chloride, and a concentration of dissolved residual chloride scavenger that does not yield unwanted chloride salt precipitate when combined with another composition comprising diethoxymethylsilane.

Abstract: Disclosed is a method of storing a fluorine-containing disilanol compound represented by the following formula (3) in the presence of a tertiary amine in such an amount that a molar ratio of the tertiary amine to a silanol group of the fluorine-containing disilanol compound ranges from 0.001 to 20, HO—Z—R1—Rf—R1—Z—OH??(3) wherein Rf is a divalent fluorinated hydrocarbon group or a divalent fluorinated polyether group, R1 may be the same with or different from each other and is a substituted or unsubstituted divalent hydrocarbon group which may have at least one atom selected from the group consisting of oxygen, nitrogen, silicon, and sulfur atoms, and Z is a group represented by the following formula (2) —SiR2R3—??(2) wherein R2 and R3 may be the same with or different from each other and are monovalent organic groups.

Abstract: The present invention discloses a method for synthesizing a reversibly protected organometallic compound which comprises (1) reacting an organometallic compound with a hydroxyl group containing compound to produce a solution containing the reversibly protected organometallic compound and hydrogen chloride; (2) reacting the solution containing the reversibly protected organometallic compound and the hydrogen chloride with a trialkyl amine to precipitate the hydrogen chloride from the solution; and (3) recovering the reversibly protected organometallic compound from the solution of the reversibly protected organometallic compound.

Abstract: A method of preparing a disilanol compound by hydrolyzing a dichlorosilane compound having Si—Cl bonds at both ends, characterized in that the method comprises the step of hydrolyzing the dichlorosilane compound in the presence of a tertiary amine compound.

Abstract: A chromatographic stationary phase for use in reversed-phase chromatography. A process for producing a chromatographic stationary phase for use in reversed-phase chromatography, chromatographic stationary phases prepared according to the methods of the current invention, and liquid chromatography columns, which include the stationary phases, are also provided.

Abstract: The present invention relates to a specific process for preparing organosilane esters of the formula (I) and a composition comprising more than 98% by weight of organosilane esters of the formula (I) and less than 2.0% by weight of at least one hydrocarbon and to the use of such a composition as precursor for producing a layer or film having a dielectric constant of 1<??4.

Abstract: The invention relates to producing an organo alcoxydialkylsilane by a method which consists in introducing by pouring an alcanol in a dialkylhalogenosilane omega-halogenalkyl+an organic solvent (s) phase mixture and in removing a halogen acid formed by entrainment with the aid of said organic solvent(s) phase and is characterised, in particular (i) by selecting a particular phase of solvent(s), for example based on cyclohexane, (2i) by carrying out an alcanol introduction mode which makes it possible to control the drawing off the halogen acid formed during reaction and by (3i) controlling the halogen acid quantity in a reaction medium. The thus obtained dialkylhalogenosilane omega-halogenalkyl is usable, in particular as an initial product for preparing organosilisic sulphur-containing compounds of general formula (IV) by a sulfidising reaction carried out on a alkali metal polysulfur.

Abstract: A process for continuously preparing compounds containing SiOC groups, in which chlorosilane(s) are partially reacted with alcohol and optionally also with water in a prereactor, and the partial reaction product therefrom is fed to a first reaction unit comprising a column, reacted with alcohol and optionally water to give a crude product which still comprises volatile constituents, and the crude product is transferred to a second reaction unit comprising a column in which alcohol is additionally introduced, and freed there of volatile constituents, optionally in the presence of an unreactive organic solvent, the desired end product being removed at the lower end of the second reaction unit.

Abstract: An acetylene alcohol represented by the following formula, wherein R1 represents a monovalent hydrocarbon radical having 4 to 10 carbon atoms with the carbon atom bonded to the silicon atom being a tertiary carbon, R2 and R3 each represents a monovalent group selected from the group consisting of alkyl groups having 1 to 4 carbon atoms and a fluorinated group represented by the formula, Rf—Q—, wherein Rf is a linear or branched perfluoroalkyl group having 3 to 100 carbon atoms which may be interrupted by one or more ether bonds, and Q is a divalent group having 2 to 10 carbon atoms which may be interrupted by one or more nitrogen, oxygen, or sulfur atoms, and n is zero or 1.

Abstract: Alkenylalkoxysilanes such as allyltrimethoxysilane can be made by reacting the corresponding monoalkenyldichlorosilane, i.e., allyldichlorosilane, with a monohydroxy alcohols, i.e., methyl alcohol. No catalyst is required and the reactions can be carried out at room temperature.

Abstract: A mixture of organoalkoxysiloxanes of formula I: wherein R and R″ are identical or different and are methyl, ethyl, vinyl, n-propyl, i-propyl, &ggr;-chloropropyl, n-butyl, i-butyl, n-pentyl, i-pentyl, n-hexyl, i-hexyl, n-heptyl, i-heptyl, n-octyl, i-octyl, hexadecyl, octadecyl or alkoxy, R′ represents methyl or ethyl, n and m are identical or different and each is 0 or an integer ranging from 1 to 20, on the condition that (n+m)≧2, is prepared by: reacting in a first stage the constituents of (i) an organotrichlorosilane or a mixture of organotrichlorosilanes or a mixture of at least one organotrichlorosilane and tetrachlorosilane, (ii) water and (iii) alcohol, combined in a molar ratio (i):(ii):(iii) of 1:(0.59 to 0.95):(0.5 to 100), at a temperature of 0 to 150° C.

Abstract: A process for producing an alkoxysilane-based compound having the general formula: 1

Abstract: The present invention provides a new chemical adsorbent which can form an extremely thin and transparent film in nanometer order which is fixed uniformly and firmly on a substrate, and give an alignment characteristic of high thermal stability to the thin film; as well as a liquid crystal alignment layer and a liquid crystal display device having a desirable alignment characteristic, a superior alignment control force over a liquid crystal molecule, and a superior thermal stability by using the above-mentioned chemical adsorbent. This purpose can be actualized by developing a new compound which is transparent and stable in a range of a visible ray (a wavelength from 400 nm to 700 nm), and has a photosensitivity in a range of an ultraviolet ray and a far-ultraviolet ray (a wavelength from 200 nm to 400 nm), and can form a thin film in a monolayer through a chemisorption on a substrate.

Abstract: A thin film forming chemical absorption material including at least a functional group of the formula CF3—CF2—CH2—O—(benzene)—CH=CH—C(O)—(benzene)— and a —SiX group (X represents halogen) as an end group bonded by siloxane bond. The chemical absorption material can form a monomolecular thin-film having photosensitive groups that are transparent and stable in a visible light region and cause photochemical reaction in an ultraviolet region. A liquid crystal alignment film includes an aggregation of adsorption molecules chemically absorbed directly on a surface with electrodes or chemically adsorbed indirectly thereon through another material layer having a characteristic group the formula above and a —O—Si bond group at a molecular end group.

Abstract: The present invention provides a new chemical adsorbent which can form an extremely thin and transparent film in nanometer order which is fixed uniformly and firmly on a substrate, and give an alignment characteristic of high thermal stability to the thin film; as well as a liquid crystal alignment layer and a liquid crystal display device having a desirable alignment characteristic, a superior alignment control force over a liquid crystal molecule, and a superior thermal stability by using the above-mentioned chemical adsorbent. This purpose can be actualized by developing a new compound which is transparent and stable in a range of a visible ray (a wavelength from 400 nm to 700 nm), and has a photosensitivity in a range of an ultraviolet ray and a far-ultraviolet ray (a wavelength from 200 nm to 400 nm), and can form a thin film in a monolayer through a chemisorption on a substrate.

Abstract: A (polycyclic secondary-amino)dialkoxysilane favorably employable as a catalyst for polymerization of &agr;-olefin can be prepared by reacting tetrachlorosilane, or a mono(C1-C8)alkyltrichlorosilane with a polycyclic secondary-amine in a non-hydrous, non-alcoholic organic solvent in the presence of a hydrogen chloride-trapping reagent, to produce a (polycyclic secondary-amino)chlorosilane and reacting the (polycyclic secondary-amino)chlorosilane with an alkali metal alkoxide or an alkaline earth metal alkoxide in the presence of a lower alcohol.

Abstract: The present invention relates to a process for the preparation of alkoxysilanes in which at least one halogenosilane is reacted with at least one alcohol in the presence of metallic magnesium and the alkoxysilane is isolated from the crude product.

Abstract: Alkoxysilanes are prepared by a process, comprising: (i) reacting a chlorosilane with an alcohol in a water-free and solvent free phase with removal of the liberated hydrogen chloride; (ii) transferring the resultant product mixture into a liquid phase to be distilled and adding a metal alcoholate to the product mixture in the liquid at a temperature in the range from 10-60° C., and thoroughly mixing the neutralized product mixture, said alcoholate being employed in an equimolar amount or in a stoichiometric excess based on the amount of acidic chloride, and (iii) purifying the treated product mixture by distillation under reduced pressure, thereby preparing alkoxysilanes which are low in acidic chloride or essentially free of acidic chloride.

Abstract: A process for preparing an alkoxysilane with an acidic chloride content of less than 10 ppm by weight, comprising:reacting a chlorosilane with an alcohol in a water-free and solvent-free phase to form a product mixture containing alkoxysilane and residual acidic chloride, with removal of resultant hydrogen chloride from the product mixture,then adding liquid or gaseous ammonia, in an amount corresponding to a stoichiometric excess, based on the content of acidic chloride, to form an ammonia-containing product mixture,treating the ammonia-containing product mixture at a temperature between 10 and 50.degree. C., wherein the ammonia and acidic chloride undergo neutralization, to form a crude product, and optionally, then separating off a salt formed in the course of neutralization, from the crude product, andrecovering the alkoxysilane by distilling the crude product.

Abstract: A process for preparing alkoxysilanes by reacting alcohols with halosilanes which are dissolved in a nonpolar solvent that is immiscible with the alcohol.

Abstract: Polyorganosiloxazane is provided which is capable of being converted into a ceramic material having low dielectric constant. The polymer according to the present invention is characterized by comprising the main repeating units of --(RSiN.sub.3)--, --(RSiN.sub.2 O)--, --(RSiNO.sub.2)-- and --(RSiO.sub.3)--, wherein, R represents an alkyl, alkenyl, cycloalkyl, aryl, alkylamino or alkylsilyl group, and by having a number-average molecular weight ranging from 300 to 100,000. The polyorganosiloxazane of the present invention has superior thermal resistance, and a ceramic material obtainable by firing the same at a predetermined temperature shows very low specific dielectric constant of 2.7 or less, making it useful particularly as a material in electronics.

Abstract: There is provided a novel silane compound, di-sec-butoxy-n-propyl methoxysilane. The aforesaid silane compound is prepared by reacting n-propyl trihalosilane with sec-butanol and then reacting a resultant reaction product with methanol.

Abstract: The invention provides high purity alkoxytrimethylsilane fluids of the general formula ROSiMe.sub.3 wherein Me is methyl and R is a monovalent aliphatic hydrocarbon substituent which ranges from 14 to about 20 carbons, the fluid being substantially free of organic and inorganic contaminants, wherein the alkoxytrimethylsilanes are produced by a novel process, and can be readily incorporated into cosmetic formulations containing organic components without heating and provide improved sensory characteristics compared to those provided by the corresponding alcohols.

Abstract: A water soluble water absorption preventing agent mainly comprising an organic silicon compound and/or its partial hydrolytic condensate, represented by the following general formula: ##STR1## wherein R.sup.1 denotes an alkyl group with 1-20 carbon atoms and with a linear chain or branched chain for which a halogen can substitute for part or all of the hydrogen atoms, R.sup.2 denotes a hydrogen atom or an alkyl group with 1-10 carbon atoms and with a linear chain or branched chain, R.sup.3 denotes a hydrogen atom or an alkyl group with 1-8 carbon atoms and with a linear chain or branched chain, m denotes an integer 1-2 and n denotes an integer 1-3 where m+n=3 or 4, p denotes an integer 1-50, and q denotes an integer 0-25.

Abstract: The production of organoxy-functional silanes is carried out by the reaction of (A) halosilanes and (B) hydroxy compounds in the presence of (C) a polymer that includes carbon-bonded fluorine. The presence of (C), the polymer that includes carbon-bonded fluorine, acts to decrease foaming during the reaction and minimizes the production of siloxane oligomer by-products.

Abstract: An ultra thin, water and oil repelling and durable overcoat is easily formed on a substrate surface via covalent bonding by applying a finishing agent of the invention, comprising a chemically adsorptive compound with a chlorosilyl group and a nonaqueous viscous liquid or solid medium, on the substrate surface. A finishing agent, comprising a chemically adsorptive compound with a chlorosilyl group and a nonaqueous viscous liquid or solid medium, is applied on a substrate surface comprising hydrophilic groups. The substrate surface is then reacted with the chemically adsorptive compound at room temperature, and the agent containing unreacted chemically adsorptive compound is removed. The generation of hydrochloric acid gas can be prevented by adding tertiary amine or amide in the molar amount of one to three times more than the chemically adsorptive compound contained in the finishing agent.

Abstract: A process for preparing alkylsilyl and arylsilyl ethers of the formula(R--O--SiR.sup.1 R.sup.2 R.sup.3)wherein R, R1, R2 and R3 are independently selected from the group consisting of hydrogen, alkyl groups containing one to twenty carbon atoms, substituted alkyl groups containing one to twenty carbon atoms, aryl groups containing six to eighteen carbon atoms, substituted aryl groups containing six to eighteen carbon atoms, hetero aryl groups containing four to eighteen carbon atoms, and substituted hetero aryl groups containing four to eighteen carbon atoms, with the proviso that R is never hydrogen, by reacting, in a hydrocarbon solvent, a chlorosilane of the formula R.sup.1 R.sup.2 R.sup.3 Si--Cl wherein R.sup.1, R.sup.2, and R.sup.

Abstract: A novel fluorinated organosilicon compound, exhibiting excellent solvent resistance, chemical resistance and mold release, which is represented by general formula (1): ##STR1## wherein Rf is a divalent group represented by general formula (2): ##STR2## wherein Y is a fluorine atom or CF.sub.3 group; l is an integer of 0-8; k and m are integers of 0-4; j and n are integers of 0 or 1; except when j=k=l=m=n=0.

Abstract: A process for the organooxylation of chlorosilanes. The process comprises contacting in a film a chlorosilane and an alcohol capable of forming an ester with the silicon of the chlorosilane and thereby forming an equilibrium mixture comprising an organooxysilane and hydrogen chloride. The film is heated at a temperature sufficient to cause vaporization of the hydrogen chloride from the equilibrium mixture thereby increasing the yield of organooxysilane in the equilibrium mixture. In a preferred process, the process is run in a falling-film type reactor or a wiped-film type reactor.

Abstract: Novel silane compound, alkoxy cyclopentyl diethoxysilane, is prepared by reacting cyclopentyl trihalosilane with ROH and then with ethanol, or by reacting cyclopentyl triethoxysilane with ROH, wherein alkyl in the alkoxy or R in ROH stands for an organic group selected from tile group consisting of isopropyl, sec-butyl, tert-buryl and tert-amyl groups. The silane compounds are useful as a catalytic component for olefin polymerization and as a silane coupling agent.

Abstract: 3-(Vinylbenzyloxy)propylsilane compounds represented by the general formula, CH.sub.2 CH.PHI. CH.sub.2 OCH.sub. CH.sub.2 CH.sub.2 SiR.sup.1.sub.n (OR.sup.2).sub.3-n (wherein R.sup.1 and R.sup.2 each represent a hydrocarbon residue containing 1 to 4 carbon atoms, and n represents an integer from 0 to 2) are provided as novel styrene skeleton-containing alkoxysilane compounds which are highly useful as silane coupling agent or polymerizing monomer.

Abstract: The present invention is a process for the preparation of hydrido organooxysilanes. The process comprises contacting a chlorosilane having at least one hydrogen atom bonded to the silicon atom with a anhydrous sodium organooxide. In a preferred embodiment, the process comprises adding the anhydrous sodium organooxide to the chlorosilane at a controlled rate. The process is conducted at a temperature within a range of about 0.degree. C. to 70.degree. C.

Abstract: Disclosed herein is a process of recovering hydrogen chloride and monomeric alkoxysilanes from mixtures of chlorine-containing silicon compounds wherein waste chlorine-containing silicon compounds, for example, are converted to useful, valuable silicon intermediates.

Abstract: The invention relates to new cleavable surface-active silane derivatives of the formula ##STR1## in which R.sub.1, n, R.sub.2, R.sub.3, X, m and R.sub.4 have the meaning given in the description, and furthermore processes for the preparation of these silane derivatives and the use of these compounds as surfactants.

Abstract: This present invention relates to a process for the preparation of O-silylated aliphatic hydroxyl, compounds by the reaction of aliphatic hydroxyl compounds with triorganochlorosilanes and removal of the resulting gaseous hydrogen chloride from the reaction mixture, characterized in that the reaction is carried out in the presence of phase transfer catalysts in the absence of solvent.The invention also relates to the use of the O-silylated hydroxyl compounds obtained by this process as starting materials for the preparation of isocyanates containing ester groups by a reaction with isocyanato carboxylic acid chlorides.

Abstract: Novel silane compounds, tert.-butoxy cyclopentyl dimethoxysilane and isopropoxy cyclopentyl dimethoxysilane, are prepared by reacting cyclopentyl trihalosilane with ROH (where R stands for tert.-butyl or isopropyl group) and then with methanol, or by reacting cyclopentyl trimethoxysilane with ROH. The silane compounds are useful as a catlaytic component for olefin polymerization and as a silane coupling agent.

Abstract: Disclosed is a one reactor, continuous system for the manufacture of organoalkoxysilanes. The reactor consists of a fractionating means that allows for completion of the reaction and separation of the HCl formed as a by-product. Also disclosed is a means for removing or reducing any residual hydrolyzable chloride or other acids in the organoalkoxysilanes using ion exchange resins.

Abstract: A method for removing silane compounds from exhaust gases containing silanes comprises treating the silane containing gas with a metal alcholate in alcoholic solution to form a tetraalkoxysilane.

Abstract: Novel organopolysiloxanes are disclosed which comprise ##STR1## wherein R.sup.1 is methyl or phenyl, with the proviso that at least 90% of R.sup.1 is methyl; andR.sup.2 is(a) R.sup.1,(b) linear or branched alkinoxy with 3 to 25 carbon atoms, or(c) a polyalcohol with 2 to 6 hydroxyl groups from which the H-atom of the OH-groups is eliminated, with all but one of the OH-groups being etherified with allyl alcohol.The siloxanes must meet the conditions that at least one--C.tbd.C-- group is contained in the average molecule and that the numerical ratio of the --C.tbd.C-- group to the allyl ether groups is 5:1 to 1:250.The novel organopolysiloxanes, mixed with hydrogenpolysiloxanes and a catalyst, are stable at room temperatures and cure rapidly at elevated temperatures. The cured mixtures have adhesive properties and exhibit no malfunctions due to migration of portions not linked chemically. A process for preparing the organopolysiloxanes is also disclosed.

Abstract: The present invention relates to the preparation of organooxychlorosilanes. They are produced by reacting the corresponding chlorosilane with an alcohol in the presence of a catalyst system consisting of hydrogen chloride and a cocatalyst.

Abstract: In a process for producing an alkoxysilane represented by general formula (III):(CH.sub.3).sub.a H.sub.b Si(OR).sub.c Cl.sub.4-(a+b+c) (III)wherein a represents a number of 0 to 2, b represents a number of 1 to 3, c represents a number of 0 to 2, the sum of a+b+c represents a number of not greater than 4 which comprises reacting a chlorosilane represented by general formula (I):(CH.sub.3).sub.a H.sub.b SiCl.sub.4-(a+b) (I)wherein a and b have the same meanings as described above and a+b represents a number of less than 4, with an alcohol represented by general formula (II);ROH (II)wherein R represents an alkyl group, a process for producing said alkoxysilanes characterized in that the reaction of the chlorosilane and the alcohol is performed in the co-presence of (a) an inert low boiling solvent having a boiling point lower than the boiling point of the objective alkoxysilane represented by general formula (III) and a difference in boiling point is not smaller than 4.degree. C.