Abstract: The invention relates to a process for the manufacture of organomonosilanes, in particular, bearing both hydrogen and chlorine substituents at the silicon atom by subjecting a silane substrate comprising one or more organomonosilanes, with the proviso that at least one of these silanes has at least one chlorine substituent at the silicon atom, to the reaction with one or more metal hydrides selected from the group of an alkali metal hydride and an alkaline earth metal hydride in the presence of one or more compounds (C) acting as a redistribution catalyst.

Abstract: A process for preparing a halogenated polysilane HpSin?pX(2n+2)?p with n=1 to 50; 0?p?2n+1, and X=F, Cl, Br, I, as an individual compound or a mixture of compounds, from a mixture which includes the halogenated polysilane or in which the halogenated polysilane is formed, additionally includes boron-containing impurities, wherein a) the mixture is admixed with at least 1 ppbw (parts per billion per weight) of a siloxane-forming oxidizing agent or siloxane, the boron-containing impurities forming compounds having a volatility and/or solubility different from the halogenated polysilanes, b) the halogenated polysilane is separated from the compound(s), and c) not more than 1 ppmw of water and not less than 1 ppb of siloxanes are present.

Abstract: The invention provides a process for producing monoalkyltin trihalide or a mixture of monoalkyltin trihalide and dialkyltin dihalide by: (a) contacting dialkyltin dihalide with an alkylation agent and, optionally, tin tetrahalide, to form a tetraalkyltin mixture comprising tetraalkyltin, trialkyltin halide, and dialkyltin dihalide; (b) reacting the tetraalkyltin mixture with tin tetrahalide to form a monoalkyltin trihalide mixture comprising monoalkyltin trihalide, dialkyltin dihalide and optionally triaklyltin halide; (c) processing the monoalkyltin trihalide mixture to separately recover the monoalkyltin trihalide and a dialkyltin dihalide stream optionally containing trialkyltin halide; and (d) recycling at least a portion of the dialkyltin dihalide stream recovered in step (c) to the contacting step (a).

Abstract: The invention relates to a process for the direct preparation of mixtures of monoalkyltin trichlorides RSnCl3 and dialkyltin dichlorides R2SnCl2 in one reaction step by partial alkylation of tin tetrachloride using alkylaluminum compounds in the form of their ether donor complexes, wherein an amount of ether greater than that required for stoichiometric formation of the donor complex is used in the reaction.

Abstract: A process is provided for the production of metalorganic compounds by reacting a Grignard reagent with a Group II, Group III or Group V metal halide in a tertiary alkyl amine solvent to form a metalorganic adduct, isolating the adduct and dissociating the adduct to leave the metalorganic compound.

Abstract: The invention concerns a method of preparing trialkyl-tin hydrides by a process that ensures outstanding long-term stability.Bis-[trialkyl-tin]oxides are dissolved in a solvent that mixes only to some extent, if at all, with water and converted with an aqueous solution of sodium borohydride stabilized with a base. The product is obtained by phase separation and optionally by distillation. The trialkyl-tin hydride is obtained almost quantitatively with a yield of more than 95%.

Abstract: A method is disclosed for the preparation of tetraalkyl-tin wherein tin-tetraacetate is first dispersed in tetrahydrofuran and trialkyl-aluminum is slowly added to the dispersion in an amount sufficient to cause complete reaction. The reaction is carried out at a temperature of <80.degree. C. The reaction mixture is then heated to the reflux temperature of the tetrahydrofuran for about 1 to 2 hours and until complete reaction. The aluminum triacetate is then removed and the tetrahydrofuran is distilled off.

Abstract: A method is disclosed for the production of dialkyl-tin-dichlorides whose alkyl groups have 1 to 22 carbon atoms. Trialkyl-aluminum is slowly added to a solution of tin-diacetate-dichloride and tetrahydrofuran in the mole ratio of about 2:3. The aluminum-triacetate precipitating during the reaction is removed by filtration and the tetrahydrofuran used as solvent is removed by distillation.

Abstract: Organotin stabilizer compositions containing more than 5 percent by weight of monoalkyl tin derivatives of mercaptoacetic acid esters, such as mono-n-octyltin-S,S',S"-tris(isooctyl mercaptoacetate), are useful as food-grade stabilizers for vinyl halide polymers.

Abstract: Vinyl chloride polymers suitable for use in food packaging materials are stabilized against discoloration and embrittlement resulting from exposure to heat using mono-n-octyltin compounds of the general formula H.sub.17 C.sub.8 Sn(SCH.sub.2 COOR').sub.3, wherein R' represents an alkyl radical containing eight carbon atoms.