Abstract: The invention relates to a method for processing mixtures which contain HCl, H2O and siloxanes in the presence of packings comprising fluorinated vinyl polymers.

Abstract: An organic-inorganic composition, which has a backbone containing —Si—O— units with chromophore groups attached directly to at least a part of the silicon atoms. The film forming composition and resulting coating properties can be tailored to suit the specific exposure wavelength and device fabrication and design requirements. By using two different chromophores the refractive index and the absorption co-efficient can be efficiently tuned and a desired Si-content of the anti-reflective coating composition can be obtained—a high Si-content will give good mechanical and thermal properties and also the required wet etch and dry etch properties.

Abstract: The invention relates to organosilane-modified polysiloxanes of the following formula: The invention additionally relates to the use of the organo-modified polysiloxanes for surface coating, and to their preparation.

Abstract: The present invention generally relates to pre-polymer and polymer compositions that can be photopolymerized. In one embodiment, the present invention relates to crosslinking agents that can be used in the photopolymerization of the pre-polymers and polymers disclosed herein. In another embodiment, the present invention relates to processes for producing pre-polymer, polymer and crosslinking compositions useful in photopolymerization reaction schemes. In one instance, the pre-polymers and polymers of the present invention can be crosslinked via a suitable crosslinking agent to produce networks (e.g., amphiphilic networks and/or co-networks).

Abstract: The object of the present invention is to provide a new kind of silicon compound having an ester-type organic functional group and a new method for providing a T8-silsesquioxane compound having a hydroxyl group by using said silicon compound as the starting material. A silicon compound represented by formula (1) is obtained through the production process characterized by using a silicon compound represented by formula (2). wherein: in formula (1), each of seven R1 group is independently selected from the group consisting of hydrogen, alkyl, substituted or unsubstituted aryl, and substituted or unsubstituted arylalkyl and A2 is a hydroxyl-terminal organic functional group, and in formula (2), each of R1 group is the same as R1 in formula (1), and A1 is an organic functional group containing an acyloxy group.

Abstract: The present invention provides a novel organosilicon compound and polysiloxane which are useful as electronic materials, optical materials, coating materials, sealing materials and catalyst carriers and which can be used as additives for improving various physical properties such as flame retardancy, heat resistance, weatherability, light resistance, electric insulating property, a surface characteristic, hardness, a mechanical strength and a chemical resistance of a polymer material.

Abstract: A method for reducing the modulus of polymer siloxane hydrogel compositions by employing monomeric polysiloxanes endcapped with trimethylsilyl to reduce the crosslinking density of the hydrogel. The synthesis consists of a single vessel acid catalyzed ring opening polymerization and may be employed to produce copolymers useful as hydrogel contact lens materials.

Abstract: A highly volatile electrical/electronic parts surfactant containing a polyether-modified silicone having one polyether chain in the molecule, wherein the surface tension at 25° C. of a 0.01 mass % aqueous solution thereof is 25 mN/m or less, the aforesaid silicone is expressed by the following average structural formula (1), and when heated from room temperature to 200° C. at a rate of 5° C./minute to 200° C. and maintained at a temperature of 200° C. for 100 minutes, the polyether-modified silicone completely volatilizes without leaving any remainder, and a method of manufacturing this highly volatile polyether-modified silicone are disclosed. AMe2SiO(MeASiO)nSiMe2A??(1) In formula (1), any one of A is a substituent group expressed by the following general formula (2), the remaining A are methyl groups and n is an integer from 0-2. —CaH2aO(C2H4O)bR??(2) In formula (2), a is 3-4, b is an integer from 1-7 and R is a methyl group or an ethyl group.

Abstract: Disiloxane compounds of the formula MM? Where M comprises either branched allyl hydrocarbon substituents or silanyl substituents and M? comprises an alkylpolyalkyleneoxide substituent. The disiloxane compounds of the invention exhibit an enhanced resistance to hydrolysis outside a pH range ranging from 6 to 7.5, and are useful as surfactants.

Abstract: The invention relates to polyester-modified poly-siloxanes of the general formula (I) where A is an alkyl group having 1 to 8 carbon atoms, Z is an aliphatic group having 1 to 14 carbon atoms, R is an aliphatic and/or cycloaliphatic and/or aromatic poly-ester group containing at least 3 ?and having a weight-average molecular weight of 200 to 4000 g/mol, with no Zerewitinoff hydrogen atoms, Q is a group which contains no Zerewitinoff hydrogen atoms and is free from reactive carbon-carbon multiple bonds, m is 3 to 200 and o+n=2, with both o and n being other than zero. The invention further relates to the use of the compounds of the invention in thermoplastics, moulding compounds and coating materials.

Abstract: Low dielectric materials and films comprising same have been identified for improved performance when used as interlevel dielectrics in integrated circuits as well as methods for making same. In one aspect of the present invention, an organosilicate glass film is exposed to an ultraviolet light source wherein the film after exposure has an at least 10% or greater improvement in its mechanical properties (i.e., material hardness and elastic modulus) compared to the as-deposited film.

Abstract: Chlorosilanes such as dimethyldichlorosilane are hydrolyzed in a first super-azeotropic hydrochloric acid distillation column A to produce cyclosiloxanes, chlorosiloxanes, and hydrogen chloride gas. The cyclosiloxanes and the chlorosiloxanes are washed and separated according to their volatility in a second sub-azeotropic hydrochloric acid distillation column B, to produce a substantially chloride free volatile cyclosiloxane stream and a substantially chloride free non-volatile siloxane stream. The process is substantially chloride efficient.

Abstract: Polysiloxane hydrolyzates are neutralized by treating polysiloxane hydrolyzates containing residual acidic constituents with carbon, and then the carbon is removed from the treated neutralized polysiloxane hydrolyzate. Some examples of polysiloxane hydrolyzates that can be treated are hydride functional polysiloxane hydrolyzates and polydiethylsiloxane hydrolyzates. The carbon neutralizing agent especially preferred is carbon derived from bituminous coal. The carbon is removed from the treated neutralized polysiloxane hydrolyzate by passing it through solid liquid separation devices such as plate and frame filter presses, polishing filters, and post filters for removing fines.

Abstract: In one aspect, the invention relates to silicon-based prepolymers. The disclosed prepolymers exhibit satisfactory solubility in aqueous solutions or hydrophilic solutions and can overcome undesirable shrinkage, expansion, and related problems possessed by conventional silicone monomers and related conventional polymerization techniques by producing hydrogels from a crosslinkable prepolymer. Also disclosed are polymers and molded articles produced from the disclosed prepolymers, which attain a satisfactory oxygen permeability. Also disclosed are methods for producing the disclosed prepolymers. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Abstract: Coating compositions repairable by introduction of energy and comprising defined siloxanes, coatings obtained therewith and repairable by introduction of energy, methods of producing them, and their use.

Abstract: An organopolysiloxane composition comprising an organopolysiloxane, an organosilicon compound having at least three hydrolyzable radicals in the molecule, an acid anhydride and optionally a filler cures at room temperature and exhibits excellent adherence to magnesium alloys.

Abstract: Compounds of formula I may be hydrolyzed to produce metal oxides wherein M is Mg, Al, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, As, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Cd, In, Sn, Sb, La, Hf, Ta, W, Re, Os, Ir, Pt, Hg, Tl, Pb, Bi, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Th, U, or Pu; X is O1/2 or OR; R is alkyl; R1, R2, R3, R4, R5, R6, and R7 are independently H, alkoxy, C1-C10 alkyl, phenyl or R10, R11, R12, R13, R14 and R15 are independently C1-C10 alkyl or phenyl; n is equal to the the value of the oxidation state of M minus q; m and p are independently 0 or an integer from 1 to 5; and q is 0, 1, 2, or 4; with the proviso that when q is 1, X is OR; and when q is 2, X is O1/2, and M is V, Cr, Mn, Fe, As, Nb, Mo, Tc, Ru, Sb, Ta, W, Re, Os, Ir, Pt, Bi, Th, U, or Pu; and when q is 4, X is O1/2, and M is Cr, Mo, W, Ru, Re, Os, U, or Pu.

Abstract: A method is presented for making alkoxy-modified silsesquioxanes (AMS) or co-alkoxy-modified silsesquioxanes (co-AMS,) comprising the steps of (a) combining as a reaction mixture (i) water, (ii) an acid-stable solvent for the water, (iii) a solid strong cationic hydrolysis and condensation catalyst, and (iv) a trialkoxysilane compound, (b) allowing the reaction mixture to react for about 0.5 hours to about 200 hours to form the alkoxy-modified silsesquioxanes; and (c) recovering the alkoxy-modified silsesquioxanes from the reaction mixture. The use of solid strong cationic catalysts in this reaction system is advantageous because they remain as solids throughout the reaction, allowing simplified separation of the solid catalyst from the soluble AMS or co-AMS products, resulting in total or near total recovery of the AMS or co-AMS products, the products being free of, or substantially free of residual acid catalyst, as well as virtual total recovery of the catalyst for recycling.

Abstract: An oriented-film formation apparatus forms an oriented film on a substrate by obliquely evaporating a predetermined material in a vacuum state and includes an evaporation source having an organic-inorganic hybrid material.

Abstract: A foam control composition comprises a polydiorganosiloxane fluid comprising units of the formula where each group R, which may be the same or different, is selected from an alkyl group having 1 to 36 carbon atoms or an aryl group or aralkyl group having up to 36 carbon atoms, the mean number of carbon atoms in the groups R being at least 1.3, and an additive composition having a melting point of at least 35° C. comprising 5-50 parts by weight of a non-polar component (A) and 50-95 parts by weight of a component (B) which is miscible with component (A) and is more polar than component (A), at least one of (A) and (B) being miscible with the polysiloxane fluid.

Abstract: Polysiloxane hydrolyzates are neutralized by treating polysiloxane hydrolyzates containing residual acidic constituents with carbon, and then the carbon is removed from the treated neutralized polysiloxane hydrolyzate. Some examples of polysiloxane hydrolyzates that can be treated are hydride functional polysiloxane hydrolyzates and polydiethylsiloxane hydrolyzates. The carbon neutralizing agent especially preferred is carbon derived from bituminous coal. The carbon is removed from the treated neutralized polysiloxane hydrolyzate by passing it through solid liquid separation devices such as plate and frame filter presses, polishing filters, and post filters for removing fines.

Abstract: Cosmetic formulations comprising alkyl-substituted siloxanes as vaporizable carriers.

Abstract: A compound having the formula: Each R1 is C1-C3 alkyl group or fluoridated C1-C3 alkyl group. The value n is a positive integer. Each R2 is alkylene group or polyethylene glycol group. Y1 is hydrogen, quaternary ammonium-containing group, or phenol-containing group. Y2 is quaternary ammonium-containing group or phenol-containing group. The quaternary ammonium-containing group is non-aromatic and contains no more than one quaternary ammonium.

Abstract: Process for the preparation of a functionalized silicone oil by hydrosilylation of synthons in the presence of at least one organohydrosilicon compound, characterized in that: (1) the synthons hydrosilylated with the organohydrosilicon compound are identical or different, and comprise at least one hydrocarbon-comprising ring in which is included at least one oxygen atom, (2) the said hydrosilylation reaction is carried out in the presence of a homogeneous catalytic system comprising (i) a metal, preferably a complexed metal, chosen from the group consisting of cobalt, rhodium, ruthenium, platinum and nickel and (ii) a heterocyclic organic compound chosen from lactones, lactams, cyclic carbonates and cyclic carbamates.

Abstract: In one aspect, the invention relates to methods of synthesizing acryloyl compounds, comprising the step of hydrosilylating a compound having the structure: with a compound having the structure A-H, wherein A comprises a siloxanyl group, to yield a compound having the structure: Compounds and compositions produced thereby can effectively attain a satisfactory balance between high oxygen permeability and hydrophilicity while achieving an acceptably low concentration of undesirable impurities. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Abstract: This invention is directed to a method of making a composition in which a silane having an unsaturated group and a silane having an aromatic group are hydrolyzed. In this method the more highly reactive silane is continuously added during the hydrolysis reaction of the less reactive silane. The composition can be used in the fabrication of microelectronic devices, particularly as hardmasks or etchstops.

Abstract: A polymer having a repeating unit represented by formula (I) is used for an insulating-film forming material and an insulating film. wherein R1 to R7 each are a monovalent hydrocarbon group, etc.; one of X, Y and Z is a specific siloxane group and the remaining two each are —O— or divalent silyl-containing group that bonds to (I) on the side of the oxygen atom of the group.

Abstract: Chlorosilanes are hydrolyzed to a hydrolysate in a looped system containing a hydrolysis reactor, an HCl purifier, a wash means, and a separator. The steps of the method comprise: (i) feeding chlorosilanes from an external source to the hydrolysis reactor, (ii) feeding water from an external source to the wash means, (iii) feeding a high concentration aqueous HCl of at least 10 percent by weight HCl from an external source to the hydrolysis reactor between the wash means and the hydrolysis reactor, (iv) removing anhydrous hydrogen chloride from the HCl purifier, (v) removing hydrolysate from the wash means, and (vi) removing a low concentration aqueous hydrogen chloride of 0.1 to less than 10 percent by weight HCl from the looped system.

Abstract: Polymerizable silicon-containing compounds of formula (1) wherein R1 is hydrogen, halogen or monovalent organic group are polymerized into polymers.

Abstract: The present invention provides a novel method for the preparation of diorganosilanes by disproportionation of a hydridosiloxanes comprising at least one terminal SiH group and at least one siloxane bond in the presence of Lewis acid catalysts. The reaction is both selective and occurs under mild conditions. The triaryl borane, tris(petafluorophenyl)borane, is especially suited for use as a catalyst in the reaction. Organic catalysts such as tris(pentafluorophenyl)borane are typically preferred owing to their greater solubility and stability in the reaction mixture, relative to inorganic Lewis acid catalysts. The product, diorganosilane may be isolated from the product mixture by conventional techniques such as distillation.

Abstract: Process for preparing highly viscous organopolysiloxanes by reacting siloxanes (1) composed of units of the general formula A a ? R c ? ( OR 1 ) d ? SiO 4 - ( a + c + d ) 2 ( I ) where A is a nitrogen-containing Si—C-bonded radical, R is a C1-18 hydrocarbon radical R1 is hydrogen or a C1-8 alkyl radical, a and d are 0 or 1, c is 0, 1, 2 or 3, a+c+d is <3 and one A and one R1 where of R1 is hydrogen atom are present, optionally siloxanes (2) R c ? ( OR 1 ) d ? SiO 4 - ( c + d ) 2 ( II ) where c+d is ?3 and one R1 radical is hydrogen is present, with silanes (3) BReSi(OR3)3?e??(III) where B is a radical —CR22—Y, R2 is hydrogen or C1-4 alkyl, Y is halogen, a monosubstituted O and S atom, or a substituted N or P atom, R3 is C1-8 alkyl, and e is 0, 1 or 2.

Abstract: Disclosed is a holographic recording medium. The novel holographic recording mediums disclosed herein comprises: a) at least one polyfunctional epoxide monomer or oligomer which undergoes acid initiated cationic polymerization. Each epoxide in the monomer or oligomer is linked by group comprising a siloxane to a silicon atom and each monomer or oligomer has an epoxy equivalent weight of greater than about 300 grams/mole epoxide; b) a binder which is capable of supporting cationic polymerization; c) an acid generator capable of producing an acid upon exposure to actinic radiation; and optionally d) a sensitizer.

Abstract: Mesostructured and microporous to mesoporous organofunctionalized silica compositions are described. The compositions incorporate the organofunctional group L as part of a LSiO3 unit in the framework of the compositions. In addition the compositions incorporate the organofunctional group R as part of a O3Si—R—siO3 unit in the framework of the compositions. The compositions are useful as molecular sieves, supports for catalysts and numerous other applications requiring an organo group on surfaces of a silica.

Abstract: A new silicone condensation reaction, the condensation between an alkoxy silane or siloxane and an organo-hydrosilane or siloxane and catalysts therefore is described and claimed.

Abstract: The invention relates to linear carboxy-functional organosiloxane compounds of the general formula (I) in which a is from 1 to 200, R1 are identical or different aliphatic or aromatic hydrocarbon radicals and R2 is —(Y)[O(C2H4-b(R3)bO)c(CdH2dO)e]fX, and the use thereof for the treatment of the surface of leather.

Abstract: By reacting two types of organosiloxane compounds in the presence of an alkaline compound and under conditions that do not substantially promote equilibration reaction, a linear organosiloxane polymer having a single peak molecular weight distribution is simply and economically produced with minimized formation of cyclics.

Abstract: The invention relates to a process for preparing organosilicon group containing photoinitiators of the formula (I), wherein m is a number from 1 to 200; q is 0 or 1; A is IN-C(O)—O—CHR3—Y— or IN-C(O)—NH—CHR3—Y—; A? is A or R1?; R1 and R1?, R2 and R2? are C1–C18alkyl or phenyl, or —(O)q—SiR1R1?R2; R3 is hydrogen or C1–C6alkyl, Y is a divalent group selected from C1–C10alkeylene, C2–C10alkenylene or —(CH2)b—O—(CH2)a—; and b are each independently of the other a number of 1 to 6; IN is a photolabile functional moiety of the formula (II) or (III), wherein R4 is hydrogen or —C(O)—C(O)—OH or —C(O)—C(O)—OC1–C6alkyl and n is 1–3; R5 and R6 are C1–C12alkyl or together are cycloC5–C7alkyl; R7 is hydroxy, C1–C6alkoxy or morpholinyl; X is —(CH2)a—, —(CH2)b—O—(CH2)a— or —(CH2)b—O—CO—(CH2)a—; a and b are each independently of the other a number of 1 to 6; whereby the process is characterized in that a photolabile functional moiety containing a carboxy group (IN-COOH) or an alkoxycarbonyl group (IN-CO—OC1–C6alkyl) is reacte

Abstract: Three processes for the manufacture of polyhedral oligomeric silsesquioxanes (POSS) which utilize the action of bases that are capable of either attacking silicon or any compound that can react with a protic solvent (e.g. ROH, H2O etc.) and generate hydroxide [OH]?, alkoxide [RO]??, etc. The first process utilizes such bases to effectively redistribute the silicon-oxygen frameworks in polymeric silsesquioxanes [RSiO1.5]28 where ?=1-1,000,000 or higher into POSS nanostructures of formulas [(RSiO1.5)n?#, homoleptic, [(RXSiO1.5)n]?#, functionalized homoleptic, [(RSiO1.5)m(R?SiO1.5)n]?#, heteroleptic, and {(RSiO1.5)m(RXSiO1.0)n}?#, functionalized heteroleptic nanostructures. The second process utilizes base to aid in the formation of POSS nanostructures of formulas [(RSiO1.5)n]?# homoleptic and [(RSiO1.5)m(R?SiO1.5)n]?# heteroleptic and [(RSiO1.5)m(RXSiO1.

Abstract: The method for producing polyorganosiloxane from at least one type of organosilicon compound having a siloxane unit or alkoxysilane by the equilibrating reaction involving cleavage and recombination of the silicon-oxygen bond as a method carried out in the presence of an acidic catalyst capable of giving the product in high productivity and yield, corrosive to the system to a limited extent, and remaining in the product to a limited extent or degrading product quality to a limited extent if it remains, wherein a solid, acidic zirconium oxide catalyst is used as the acidic catalyst.

Abstract: The present invention relates to a low dielectric substance essential for a next generating electrical device such as a semiconductor device having high performance and high density, and particularly to a process for preparing a low dielectric organosilicate polymer, a hydrolysis condensation product of a carbon-bridged oligomer; a process for manufacturing an insulating film using an organosilicate polymer prepared by the process; and an electrical device comprising an insulating film prepared by the process. The organosilicate polymer prepared according the process of the present invention is thermally stable, and has good film-forming prosperities, excellent mechanical strength and crack resistance, and the film manufactured therefrom has excellent insulating properties, film uniformity, dielectric properties, crack resistance, and mechanical strength.

Abstract: Functionalized silsesquioxanes containing from 6 to 24 silicon atoms and minimally about 67 mol percent RSiO3/2 moieties where R is a phenyl group bearing a chemically reactive functional group are highly suitable for use as nanoparticles in producing highly ordered nanocomposites of many types, containing a high proportion of interphase. The nanocomposites have unusual physicochemical properties due to the use of uniform, highly functionalized nanoparticles.

Abstract: Yellow dye moiety-containing prepolymers with blue light absorbing priorities and methods for producing the same for use in the production of relatively high refractive index polymeric compositions are described herein. Polymeric compositions so produced are useful in the production of ophthalmic devices such as for example intraocular lenses and corneal inlays.

Abstract: The present invention relates to polyalkylene oxide porogens having hyper-branches and low dielectric-constant insulators using them. More particularly, the present invention relates to polyalkylene oxide porogens having hyper-branches expressed by the following formula (1), where the polyalkylene oxide porogen has a center molecular (D) having branches (W), and low dielectric-constant insulators having nanopores prepared by coating a mixture of the porogen and a high heat-resistant resin such as polysilsesquioxane and thermal treating the coated substrate at a temperature effective to degrade the porogen.

Abstract: A method of reacting a first non-fluorous compound to produce a second non-fluorous compound includes the steps of: contacting a first non-fluorous phase including the first non-fluorous compound with a first fluorous phase at a first phase interface, the first non-fluorous compound distributing between the first fluorous phase and the first non-fluorous phase; contacting the first fluorous phase with a second non-fluorous phase at a second phase interface; and including at least a third non-fluorous compound in the second non-fluorous phase that reacts with the first non-fluorous compound to produce the second non-fluorous compound, the second non-fluorous compound having a distribution coefficient less than the first non-fluorous compound. For example, the first non-fluorous compound can be dibromine or diiodine, and the second non-fluorous compound can be an alkene.

Abstract: The invention includes a trialkylsilane comprising a hydrocarbon backbone including one to ten carbon atoms; a terminal trialkylsilyl moiety having at least two alkyl groups independently comprising at least six carbon atoms; and a terminal silyl moiety that has at least one hydrolyzable group bound to a silicon of the silyl moiety. At least one of the alkyl groups of the trialkylsilyl moiety may substituted with at least one halogen, and is preferably a perfluoroalkyl group. The invention also provides methods of producing the trialysilane and substrates including the trialkysilane of the invention, as well as columns and substrates for use in chromatographic applications.

Abstract: A cosmetic material comprising as essential cosmetic constituents (A) a silicone-branched silicone compound and (B) a silicone-branched polyether-modified silicone compound.

Abstract: Provided are polyorganosilsesquioxane and process for preparing the same. The polyorganosilsesquioxane is obtained by various methods including polymerization of 1,3-diorganosiloxane, a precursor that is prepared by using silane compounds as starting materials. The polyorganosilsesquioxane has convenience in handling and controlling the rate of polymerization, and structure of highly regular form, and be imparted high functionality and various characteristics as compared to a conventional polyorganosilsesquioxane.

Abstract: Provided are polyorganosilsesquioxane and process for preparing the same. The polyorganosilsesquioxane is obtained by various methods including polymerization of an organosilanetriol as starting materials. The polyorganosilsesquioxane has convenience in handling and controlling the rate of polymerization, and structure of highly regular form, and be imparted high functionality and various characteristics as compared to a conventional polyorganosilsesquioxane.

Abstract: A polyethersilicone represented by the following formula (1), said polyethersilicone being modified at an end of a silicone chain thereof, 1

Abstract: The invention concerns a method for preparing organic-inorganic hybrid materials with controlled porosity and functionality, comprising hydrolysis and condensation polymerisation of at least a compound of formula (I): Z—R1—Si(OR)(OR′)(OR″), wherein: Z represents either an atom selected among chlorine, bromine or iodine atoms, or an amino or phosphino group; R, R′ and R″, independently of one another, represent an alkyl radical comprising on to four carbon atoms; R1 represents a divalent radical derived from an aliphatic hydrocarbon chain comprising 1 to 30 carbon atoms, wherein are optionally interspersed one or several arylene; —O—, —S—, —O—C(═O), —N(R6)—C(═O)— or N(R6), with at least an alkaline or alkaline-earth silicate of (II) in a mol ratio (I)/(II)=1/9 in the presence of at least a non-ionic surfactant in micellar concentration, to form a mesoporous silica represented by formula (III): Z—R1&