Evonik Operations Gmbh

Evonik Degussa Gmbh

Chemetall Gmbh

Matthias Wagner

Hans-Wolfram Lerner

Julian Teichmann

Ulrich Wietelmann

Jens Röder

Jan Tillmann

Hannes Vitze

Maximilian Moxter

Wolfram Lerner

A process can be used for the preparation of tris(trichlorosilyl)dichlorogallylgermane, which is a chlorinated, uncharged substance.

Tris(trichlorosily1)dichlorogallylgermane, process for the preparation thereof and use thereof

A novel process provides for the preparation of the chlorinated, uncharged substance tetrakis(trichlorosilyl)germane, and for the use thereof.

Tetrakis(trichlorosilyl)germane, process for the preparation thereof and use thereof

A trichlorogermanide of formula (I): [RN]/[RP]Cl[GeCl] (I), where R is Me, Et, iPr, nBu, or Ph, tris(trichlorosilyl)germanide of formula (II): [RN]/[RP][Ge(SiCl)] (II), where R is Me, Et, iPr, nBu, or Ph, a tris(trichlorosilyl)germanide adduct of GaClof formula (III): [PhP][Ge(SiCl)*GaCl], and a tris(trichlorosilyl)germanide adduct of BBrof formula (IV): [PhP][Ge(SiCl)*BBr]. Also, methods for preparing the trichlorogermanides of formula (I), the tris(trichlorosilyl)germanide of formula (II), the tris(trichlorosilyl)germanide adduct of BBrof formula (IV).

Halogermanides and methods for the preparation thereof

A trichlorogermanide of formula (I): [RN]/[RP]Cl[GeCl] (I), where R is Me, Et, iPr, nBu, or Ph, tris(trichlorosilyl)germanide of formula (II): [RN]/[RP][Ge(SiCl)] (II), where R is Me, Et, iPr, nBu, or Ph, a tris(trichlorosilyl)germanide adduct of GaClof formula (III): [Php][Ge(SiCl)*GaCl], and a tris(trichlorosilyl)germanide adduct of BBrof formula (IV): [PhP[]Ge(SiCl)*BBr]. Also, methods for preparing the trichlorogermanides of formula (I), the tris(trichlorosilyl)germanide of formula (II), the tris(trichlorosilyl)germanide adduct of BBrof formula (IV).

The present invention relates to a process for the production of perhalogenated hexasilane anion by reacting halogenated monosilane in the presence of organosubstituted ammonium and/or phosphonium halide at temperatures in a range from 100 to 120&#xb0; C., wherein no solvent is used, and a process for the production of a cyclic silane compound of the formula SiR, by reacting [X][SiCl] with AlRin at least one organic solvent, wherein R is chlorine or methyl and X, the same or different, is a counter-cation and is preferably selected from organosubstituted ammonium, organosubstituted phosphonium, alkali metal ions and [(PEDETA)(HSiCl)]+.

Method for producing perhalogenated hexasilane anion and method for producing a cyclic silane compound

Triphenylgermylsilane (PhGe&#x2014;SiH) is useful for the production of germanium-silicon layers (Ge&#x2014;Si) or as transfer agent of silane groups (SiH). Further, a method describes the production of triphenylgermylsilane (PhGe&#x2014;SiH) by reducing trichlorosilyl-triphenylgermane (PhGe&#x2014;SiCl) with a hydride in solution, and another method describes the production of trichlorosilytrichlorogermane (ClGe&#x2014;SiCl) by reacting trichlorosilyltriphenyigermane (PhGe&#x2014;SiCl) with hydrogen chloride (HCl) in the presence of AlClin solution. In addition, trichlorosilyltrichlorogermane is also used for the production of germanium-silicon layers (Ge&#x2014;Si).

Triphenylgermylsilane and trichlorosilyl-trichlorogermane for the production of germanium-silicon layers, and method for the production thereof from trichlorosilyl-triphenylgermane

A novel compound chlorosilylarylgermane, a method for preparing the compound, and the use of the compound are described. A method for preparing trichlorosilyltrichlorogermane and the use of trichlorosilyltrichlorogermane are also described.

Chlorosilylarylgermanes, method for preparation thereof and use thereof

A coordination compound of an element of the boron group, the production of the compound and methods of using the compound as an additive, stabilizer, catalyst, co-catalyst, activator for catalyst systems, conductivity improver, and electrolyte.

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Auburn Hills, MI, United States of America

Matthias Wagner