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Silane, dimethyldichloro

Figure 2 Most important reaction mechanisms of the reaction of dimethyldichloro-silane with the surface of MCM-48. Figure 2 Most important reaction mechanisms of the reaction of dimethyldichloro-silane with the surface of MCM-48.
It is evident that this process is simpler in its requirements than the Grignard method and involves fewer chemical operations. Since the silicon need not be chlorinated, no free chlorine is required. The hydrochloric acid produced by the hydrolysis of dimethyldichloro-silane is exactly consumed by the reaction with methanol, so that two... [Pg.96]

There is some information in the literature about synthesis of polymers with alternating diorgano-siloxane and organosilsesquioxane units [6-10] in cyclolinear double-stranded macromolecule of the polymer [11], The first series of works has used co-hydrolysis products of dimethyldichloro-silane with phenyltrichlorosilane [6, 7], dimethyldichlorosilane with methyltrichlorosilane [8] or methylphenyldichlorosilane with phenyltrichlorosilane [9] for synthesis of the polymers. [Pg.217]

Silanization should be carried out in a fume hood. Disposable rubber gloves should be worn for protection because dimethyldichloro-silane is volatile and extremely toxic. Place a rubber stopper securely in the bottom of a 16 x 300 mm column. [Pg.189]

The Rochow Process. Rochow found that alkyl and aryl halides react directly with silicon when their vapors contacted silicon at elevated temperatures to produce complex mixtures of organosilicon halides. The reaction is promoted by a wide variety of metals from both the main group and the transition series, but the most efficient catalyst is copper. The most studied reaction of this type is the reaction between methyl chloride and silicon to give dimethyldichlorosilane and methyltrichlorosilane. Dimethyldichloro-silane is major feedstock silane for methylsilicon polymers. [Pg.13]

The synthesis and characterization of enantiomerically pure ansa-cyclopentadienyl organolanthanides Me2Si(ButCp)[(+)- i o-Men-Cp]Ln(CH(SiMe3)2 and their use as precatalysts for asymmetric olefin hydrogenation have been reported. In a one-pot reaction starting from 6,6-dimethylfulvene, methyllithium, and dimethyldichloro-silane the desired product Me2Si(ButCp)Cl was obtained, which was alkylated with Na[(+)-row-Men-Cp] to afford the neutral ligand. Reaction with BunLi afforded the dilithium salt as a colorless crystalline solid (Scheme 161). [Pg.88]

Fig. 4 Structural formulas for perfluorode-canoic acid (PFDA) perfluorooctyltrichl-orosilane (FOTS), dimethyldichloro silane (DDMS), 1-octa decene, and perfluorode-cyl-tris-(dimethylamino)silane (PFIOTAS). Fig. 4 Structural formulas for perfluorode-canoic acid (PFDA) perfluorooctyltrichl-orosilane (FOTS), dimethyldichloro silane (DDMS), 1-octa decene, and perfluorode-cyl-tris-(dimethylamino)silane (PFIOTAS).
A copolymer containing a dimethylsiloxy spacer was prepared by reacting poly(acenaphthylene-co-vinyl alcohol) with dimethyldichloro-silane followed by reaction with 2-naphthol. (See Figure 1). [Pg.358]

Preparation1 The reagent is prepared by refluxing 1 mole of dimethyldichloro-silane with two moles of acetic anhydride for four hours followed by slow distillation of the acetyl chloride produced, and then of unreacted acetic anhydride. The reagent is then isolated by distillation. [Pg.262]

Relative retention volumes and retention indices have been reported399 for silicon tetrachloride, methyltrichloro- and dimethyldichloro-silane, phosphorus trichloride and phosphorus oxychloride at 50 °C on stationary phases containing vaseline oil, poly-siloxane liquids VKZh-94, PFMS-2 and DS-701, fluorosilicone oil 169, dinonyl phthalate and dibutyl phthalate. The retention index for phosphorus oxychloride increased with increase in the polarity of the stationary phase that for silicon tetrachloride remained practically constant. [Pg.426]

Penicillin G, potassium salt 8001, N-13imethylaniline 6001 Phosphorus pentachloride 3001 Dimethyldichloro-silane... [Pg.157]

The other significant aspect of adhesive drag is its relation to the surface contamination present on the surface. For example, an alkyd paint film was painted on a glass surface, cross-linked, and then peeled off. For comparison, the same experiment was carried out on a glass surface coated with dimethyldichloro silane, as shown in Fig. 8.10. [Pg.162]

Various known mixtures of trichlorosilane, silicon tetrachloride, trimethylchlorosilane, methyltrichlorosilane, and dimethyldichloro-silane were used to evaluate the columns. The mixtures were placed in 30ml serum bottles and closed with serum bottle stoppers to facilitate sample removal and to offset hydrolysis of the silanes. Samples with relatively high siloxane content were prepared by storage of chloro- or methyl- chlorosilanes in Teflon screw cap bottles for several months. Aliquots of 5yl were taken with a 5yl Hamilton syringe which was rinsed with chloroform and dried with nitrogen immediately after injection to prevent the plunger from freezing in the barrel because of rapid hydrolysis of the silanes. [Pg.170]

The Silicone oils and gums bleed less at higher temperatures but only those with higher polarity are capable of resolving the chlorosilane mixture. Methyltrichlorosilane and dimethyldichloro-silane elute together when using SF-96, DC-704 and DC-710. Silicon tetrachloride and trimethylchlorosilane are not complete resolved with these substrates. [Pg.172]

Poly(carbosilane)s are usually produced by thermal decomposition of polysilane polymers or cyclic oligomers, optionally in an autoclave to prevent loss of volatile material and enhance the yield. In early work, dodecamethylcyclohexasilane (1), produced by dechlorination of dimethyldichloro-silane using lithium, was employed as the precursor to poly(carbosilane). This compound can be converted to poly(carbosilane) by heating in an autoclave at 400 ""C, but useful spinnable polymer is only obtained after complex purification procedures, and the yield is thus relatively low. ... [Pg.1287]


See other pages where Silane, dimethyldichloro is mentioned: [Pg.233]    [Pg.551]    [Pg.233]    [Pg.551]    [Pg.153]    [Pg.328]    [Pg.445]    [Pg.269]    [Pg.70]    [Pg.155]    [Pg.69]    [Pg.426]    [Pg.699]    [Pg.70]    [Pg.691]    [Pg.300]    [Pg.300]    [Pg.717]    [Pg.406]   
See also in sourсe #XX -- [ Pg.3 , Pg.56 ]




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