Results 311 to 320 of about 112,449 (386)
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Inorganic Chemistry, 2015
A high-yield synthesis of the class of (trimethylsilyl)chalcogenolate organic salts [Cat][TMS-E] (E = S, Se, Te; Cat = BMPyr, DMPyr, NMe4, nBu3MeP) is presented.
Lars H. Finger+2 more
semanticscholar +1 more source
A high-yield synthesis of the class of (trimethylsilyl)chalcogenolate organic salts [Cat][TMS-E] (E = S, Se, Te; Cat = BMPyr, DMPyr, NMe4, nBu3MeP) is presented.
Lars H. Finger+2 more
semanticscholar +1 more source
Trimethylsilylation of hemimorphite
Journal of Inorganic and Nuclear Chemistry, 1979Trimethylsilyl derivatives were prepared from hemimorphite by the reaction between the mineral and the trimethylsilylating reagent which was the reaction mixture of hexamethyldisiloxane, chlorotrimethylsilane and an organic solvent (the direct method of trimethylsilylation of silicates). The silylated derivatives were analyzed by gas chromatography and
Chuzo Kato, Kazuyuki Kuroda
openaire +2 more sources
Journal of the American Chemical Society, 2014
Electron-rich organosilicon compounds, such as 1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2a), 2,5-dimethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2b), 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2c)
Teruhiko Saito+5 more
semanticscholar +1 more source
Electron-rich organosilicon compounds, such as 1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2a), 2,5-dimethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2b), 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2c)
Teruhiko Saito+5 more
semanticscholar +1 more source
Bis (trimethylsilyl) thioketone
Tetrahedron Letters, 1985Abstract Tris (trimethylsilyl) methylsulphenylbromide undergoes facile Me 3 SiBr elimination to give bis (trimethylsilyl) thioketone.
A. Ricci+6 more
openaire +3 more sources
2007
[3385-94-2] C6H18SSi2 (MW 178.44) InChI = 1S/C6H18SSi2/c1-8(2,3)7-9(4,5)6/h1-6H3 InChIKey = RLECCBFNWDXKPK-UHFFFAOYSA-N (reduction of S, Se, and Te oxides;4 formation of thiocarbonyl derivatives under mild conditions;7 formation of allylsilanes from ketones or allylic alcohols13) Alternate Name: TMS2S.
M. A. Matulenko+2 more
openaire +4 more sources
[3385-94-2] C6H18SSi2 (MW 178.44) InChI = 1S/C6H18SSi2/c1-8(2,3)7-9(4,5)6/h1-6H3 InChIKey = RLECCBFNWDXKPK-UHFFFAOYSA-N (reduction of S, Se, and Te oxides;4 formation of thiocarbonyl derivatives under mild conditions;7 formation of allylsilanes from ketones or allylic alcohols13) Alternate Name: TMS2S.
M. A. Matulenko+2 more
openaire +4 more sources
Trimethylsilylation of Biotite
Clays and Clay Minerals, 1977AbstractOrganic solvent soluble organosilicate compounds retaining silicate backbone were obtained by the reaction between biotite and trimethylsilylating reagent. The soluble product which was formed at room temperature or at reflux temperature was a viscous liquid and was soluble in a wide range of organic solvents, but insoluble in water.
Chuzo Kato, Kazuyuki Kuroda
openaire +2 more sources
, 2015
Tris(trimethylsilyl) phosphite (TMSP) is well known as an effective electrolyte additive that significantly improves the electrochemical performance of high-voltage lithium-ion batteries.
Young‐Kyu Han, Jaeik Yoo, Taeeun Yim
semanticscholar +1 more source
Tris(trimethylsilyl) phosphite (TMSP) is well known as an effective electrolyte additive that significantly improves the electrochemical performance of high-voltage lithium-ion batteries.
Young‐Kyu Han, Jaeik Yoo, Taeeun Yim
semanticscholar +1 more source
ChemInform Abstract: 2,3‐Bis(trimethylsilyl)‐ and 2,3,8,9‐Tetrakis(trimethylsilyl)[4]phenylene. [PDF]
AbstractCobaltcatalyzed [2+2+2] cycloaddition of the biphenylene (I) and the acetylene (H) yields the [Slphenylene (III), which is convened to the diyne (V).
M. Hirthammer, K. P. C. Vollhardt
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Structures and optical properties of tris(trimethylsilyl)silylated oligothiophene derivatives.
Journal of Organic Chemistry, 2014The structures and optical properties of tris(trimethylsilyl)silylated oligothiophenes were examined by spectroscopies, theoretical calculations, and single-crystal X-ray measurements.
Hikaru Inubushi+3 more
semanticscholar +1 more source
Preparation and regioselective metalation of bis(trimethylsilyl)methyl-substituted aryl derivatives.
Chemistry, 2014A range of bis(trimethylsilyl)methyl-substituted aryl derivatives was prepared by using a Kumada-Corriu cross-coupling reaction. The regioselective metalation of the resulting bis(trimethylsilyl)methyl-substituted aryl derivatives bearing this bulky ...
V. Werner+5 more
semanticscholar +1 more source