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Dimethyldichlorosilane is a tetrahedral organosilicon compound with the formula Si(CH 3) 2 Cl 2. At room temperature it is a colorless liquid that readily reacts with water to form both linear and cyclic Si-O chains. Dimethyldichlorosilane is made on an industrial scale as the principal precursor to dimethylsilicone and polysilane compounds.
LiN(Si(CH 3) 3) 2 Molar mass: 167.33 g·mol −1 Appearance White solid Density: 0.86 g/cm 3 at 25 °C Melting point: 71 to 72 °C (160 to 162 °F; 344 to 345 K) Boiling point: 80 to 84 °C (176 to 183 °F; 353 to 357 K) (0.001 mm Hg)
The chemical formula of PDMS is CH 3 [Si(CH 3) 2 O] n Si(CH 3) 3, where n is the number of repeating monomer [Si(CH 3) 2 O] units. [4] Industrial synthesis can begin from dimethyldichlorosilane and water by the following net reaction: n Si(CH 3) 2 Cl 2 + (n+1) H 2 O → HO[Si(CH 3) 2 O] n H + 2n HCl. The polymerization reaction evolves ...
2 CH 3 Cl + Si → (CH 3) 4−n SiCl n + other products While this reaction is the standard in industrial silicone production and is nearly identical to the first direct synthesis of methyltrichlorosilane, the overall process is inefficient with respect to methyltrichlorosilane. [ 2 ]
Stock and Somieski completed the hydrolysis of dichlorosilane by putting the solution of H 2 SiCl 2 in benzene in brief contact with a large excess of water. [3] [5] A large-scale hydrolysis was done in a mixed ether/alkane solvent system at 0 °C, which gave a mixture of volatile and nonvolatile [H 2 SiO] n.
NaN(Si(CH 3) 3) 2 Molar mass: 183.377 g·mol −1 Appearance off-white solid Density: 0.9 g/cm 3, solid Melting point: 171 to 175 °C (340 to 347 °F; 444 to 448 K) Boiling point: 202 °C (396 °F; 475 K) 2 mmHg
Density: 0.955 g/cm 3: Boiling point: 102–104 °C (216–219 °F; 375–377 K) ... Methyltrimethoxysilane is an organosilicon compound with the formula CH 3 Si(OCH ...
2 Me 3 SiCl + H 2 O → 2 HCl + O[Si(CH 3) 3] 2. It also results from the hydrolysis of silyl ethers and other silyl-protected functional groups. HMDSO can be converted back to the chloride by reaction with Me 2 SiCl 2. [3] Hexamethyldisiloxane is mainly used as source of the trimethylsilyl functional group (-Si(CH 3) 3) in organic synthesis.