Abstract: The present invention provides organofunctional siloxane coupling agents, dipodal siloxanes, siloxane block copolymers and a specific method for preparing these organofunctional siloxanes through an addition reaction of hydrido alkoxysilane and organofunctional disiloxanes to an organocyclosiloxane with a catalyst. The addition reaction of the current invention does not result in polymerization and therefore the novel siloxane couplings agents are free of cyclosiloxanes and polymeric siloxanes. This makes them apt for adhesives, coatings and sealant applications. The present invention also relates to the use of these organofunctional siloxane compounds for the treatment of fillers and surfaces.

Abstract: The invention relates to an alkoxysilane polysulfide, of formula (I): (R3O)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OR3)3-n??(I), in which: R1, which are identical or different, each represent a monovalent hydrocarbon group having from 1 to 18 carbon atoms; R2, which are identical or different, each represent a monovalent hydrocarbon group having from 1 to 4 carbon atoms; R3, which are identical or different, each represent a monovalent hydrocarbon group having from 1 to 12 carbon atoms, preferably from 1 to 6 carbon atoms; Z, which are identical or different, each represent a divalent hydrocarbon bonding group comprising from 1 to 16 carbon atoms; x is an integral or fractional number greater than or equal to 2; and n is an integer equal to 0, 1 or 2.

Abstract: An elastomeric composition is based on at least a diene elastomer, an inorganic filler as reinforcing filler and a monohydroxysilane polysulfide as coupling agent of formula (I): (HO)(R1)2Si—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)2(OH) (I), in which: each R1 represents a monovalent hydrocarbon group having from 1 to 18 carbon atoms and can be the same or different from one another; each R2 represents a monovalent hydrocarbon group having from 1 to 4 carbon atoms and can be the same or different from one another; each Z represents a divalent hydrocarbon bonding group comprising from 1 to 16 carbon atoms can be the same or different from one another; and x is an integral or fractional number greater than or equal to 2.

Abstract: The present invention provides organofunctional siloxane coupling agents, dipodal siloxanes, siloxane block copolymers and a specific method for preparing these organofunctional siloxanes through an addition reaction of hydrido alkoxysilane and organofunctional disiloxanes to an organocyclosiloxane with a catalyst. The addition reaction of the current invention does not result in polymerization and therefore the novel siloxane couplings agents are free of cyclosiloxanes and polymeric siloxanes. This makes them apt for adhesives, coatings and sealant applications. The present invention also relates to the use of these organofunctional siloxane compounds for the treatment of fillers and surfaces.

Abstract: The invention relates to an alkoxysilane polysulfide, of formula (I): (R3O)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OR3)3-n??(I), in which: R1, which are identical or different, each represent a monovalent hydrocarbon group having from 1 to 18 carbon atoms; R2, which are identical or different, each represent a monovalent hydrocarbon group having from 1 to 4 carbon atoms; R3, which are identical or different, each represent a monovalent hydrocarbon group having from 1 to 12 carbon atoms, preferably from 1 to 6 carbon atoms; Z, which are identical or different, each represent a divalent hydrocarbon bonding group comprising from 1 to 16 carbon atoms; x is an integral or fractional number greater than or equal to 2; and n is an integer equal to 0, 1 or 2.

Abstract: An elastomeric composition is based on at least a diene elastomer, an inorganic filler as reinforcing filler and a monohydroxysilane polysulfide as coupling agent of formula (I): (HO)(R1)2Si—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)2(OH) (I), in which: each R1 represents a monovalent hydrocarbon group having from 1 to 18 carbon atoms and can be the same or different from one another; each R2 represents a monovalent hydrocarbon group having from 1 to 4 carbon atoms and can be the same or different from one another; each Z represents a divalent hydrocarbon bonding group comprising from 1 to 16 carbon atoms can be the same or different from one another; and x is an integral or fractional number greater than or equal to 2.

Abstract: The present invention is related to a chemical vapor deposition method of depositing layers of materials to provide super-hydrophilic surface properties, or super-hydrophobic surface properties, or combinations of such properties at various locations on a given surface. The invention also relates to electronic applications which make use of super-hydrophobic surface properties, and to biological applications which make use of super-hydrophilic surface properties.

Abstract: A system and methods are provided for a medical diagnostic system that incorporates a genetically encoded digital signature to authenticate a patient. In an illustrative implementation, a platform is provided performing one or more functions including but not limited to patient authentication, diagnostics, transmission, and storage of data in a centralized secure database capable of being accessed by healthcare professionals. In the illustrative implementation, the exemplary medical diagnostic system can comprise a genetic material collector/analyzer. Responsive to inputting genetic material in the collector/analyzer, the collector/analyzer generates a unique genetic-based electronic signature representative of the genetic material. The unique genetic-base electronic signature can then be processed by cooperating parties to authenticate the person providing the genetic sample.

Abstract: The present invention is related to a chemical vapor deposition method of depositing layers of materials to provide super-hydrophilic surface properties, or super-hydrophobic surface properties, or combinations of such properties at various locations on a given surface. The invention also relates to electronic applications which make use of super-hydrophobic surface properties, and to biological applications which make use of super-hydrophilic surface properties.

Abstract: Processes are provided for producing organchlorosilanes and dipodal silanes in which an organic halide or alkene or chloralkene is reacted with a hydridochlorosilane in the presence of a quarternary phosphonium salt catalyst by providing sufficient heat to effect a dehydrohalogenative coupling reaction and/or a hydrosilylation reaction and venting the reaction to control reaction pressure and to remove gaseous byproducts from the reaction. The processes are preferably continuous using a catalyst in fluid form at reaction pressures not exceeding about 600 psi. The reactions may be carried out substantially isothermally and/or isobarically, for example in a plug flow reactor or continuous stirred tank reactor. The processes may produce novel silylated compounds including 1,2-bis(trichlorosilyl)decane or 1,2-bis(trimethoxysilyl)decane.

Abstract: Processes are provided for producing organchlorosilanes and dipodal silanes in which an organic halide or alkene or chloralkene is reacted with a hydridochlorosilane in the presence of a quaternary phosphonium salt catalyst by providing sufficient heat to effect a dehydrohalogenative coupling reaction and/or a hydrosilylation reaction and venting the reaction to control reaction pressure and to remove gaseous byproducts from the reaction. The processes are preferably continuous using a catalyst in fluid form at reaction pressures not exceeding about 600 psi. The reactions may be carried out substantially isothermally and/or isobarically, for example in a plug flow reactor or continuous stirred tank reactor. The processes may produce novel silylated compounds including 1,2-bis(trichlorosilyl)decane or 1,2-bis(trimethoxysilyl)decane.

Abstract: Processes are provided for producing organchlorosilanes and dipodal silanes in which an organic halide or alkene or chloralkene is reacted with a hydridochlorosilane in the presence of a quaternary phosphonium salt catalyst by providing sufficient heat to effect a dehydrohalogenative coupling reaction and/or a hydrosilylation reaction and venting the reaction to control reaction pressure and to remove gaseous byproducts from the reaction. The processes are preferably continuous using a catalyst in fluid form at reaction pressures not exceeding about 600 psi. The reactions may be carried out substantially isothermally and/or isobarically, for example in a plug flow reactor or continuous stirred tank reactor. The processes may produce novel silylated compounds including 1,2-bis (trichlorosilyl)decane or 1,2-bis (trimethoxysilyl)decane.

Abstract: Processes are provided for producing organchlorosilanes and dipodal silanes in which an organic halide or alkene or chloralkene is reacted with a hydridochlorosilane in the presence of a quarternary phosphonium salt catalyst by providing sufficient heat to effect a dehydrohalogenative coupling reaction and/or a hydrosilylation reaction and venting the reaction to control reaction pressure and to remove gaseous byproducts from the reaction. The processes are preferably continuous using a catalyst in fluid form at reaction pressures not exceeding about 600 psi. The reactions may be carried out substantially isothermally and/or isobarically, for example in a plug flow reactor or continuous stirred tank reactor. The processes may produce novel silylated compounds including 1,2-bis(trichlorosilyl)decane or 1,2-bis(trimethoxysilyl)decane.

Abstract: A continuous polymerization process produces hydride-functional siloxane and organofunctional siloxane polymers, copolymers and terpolymers. The cationic polymerization takes place in a plug flow catalytic reactor packed with a heterogeneous acid catalyst. The siloxane polymers produced are optically clear, homogeneous and free of catalyst residues.

Abstract: The present invention provides near quantitative yields of greater than about 95% isomeric purity of poly(3-aminopropylmethylsiloxane)-poly(dimethylsiloxane) copolymers of the general formulae: Me3Si(H2NCH2CH2CH2MeSiO)w(Me2SiO)xOSiMe3 (H2NCH2CH2CH2MeSiO)y(Me2SiO)z wherein Me is methyl, w may range from 1 to about 100, x may range from 1 to about 100, y may range from 1 to about 6, z may range from 1 to about 6 and y+z may range from 3 to about 7.

Abstract: The present invention provides near quantitative yields of greater than about 95% isomeric purity of poly(3-aminopropylmethylsiloxanes) of the general formulae: Me3Si(H2NCH2CH2CH2MeSiO)xOSiMe3 (H2NCH2CH2CH2MeSiO)y wherein Me is methyl, x may range from 2 to about 100 and y may range from 3 to about 7. The present invention also provides a simple method for rapidly producing poly(3-aminopropylmethylsiloxanes) of the general formulae: Me3Si(H2NCH2CH2CH2MeSiO)xOSiMe3 (H2NCH2CH2CH2MeSiO)y wherein Me is methyl, x may range from 2 to over 100 and y may range from 3 to about 7, the method comprising heating of 3-(3-aminopropyl)-1,1,1,3,5,5,5-heptamethyltrisiloxane, of at least 95% isomeric purity, with a basic catalyst, removing hexamethyldisiloxane, and decomposing the catalyst.

Abstract: The invention provides high purity 3-aminopropylmethylsiloxanes of the general formulae: ##STR1## wherein each R may be the same or different aryl group, or monovalent straight or branched chain alkyl group having from 1 to about 18 carbon atoms, Me is methyl, and x may range from about 3 to about 5, the process comprisinghydrosilylating allylamine with a monohydridomethylsiloxane of the general formulae: ##STR2## wherein each R may be the same or different aryl group, or monovalent straight or branched chain alkyl group with 1 to about 18 carbon atoms, and x may range from about 3 to about 5, in the presence of a neutral platinum catalyst.