Alkylsilane

Figure C3.2.4. Plot of the log of photocurrent against number of methyl units in a alkylsilane based monolayer self-assembled on a n silicon electrode. The electrode is immersed in a solution witli an electron donor. Best fits of experimental data collected at different light intensities ( ) 0.3 mW cm ( ) 0.05 mW cm. From [10].

This reaction, cataly2ed by uv radiation, peroxides, and some metal catalysts, eg, platinum, led to the production of a broad range of alkyl and functional alkyl trihalosilanes. These alkylsilanes have important commercial value as monomers and are also used in the production of sihcon fluids and resins. Additional information on the chemistry of sihcon hahdes is available (19,21—24). 

Silanes react with alkyllithium compounds, forming various alkylsilanes. Complete substitution is generally favored however, less substituted products can be isolated by proper choice of solvent. AH four methylsHanes, vinylsHane [7291-09-1and divinylsilane [18142-56-8] have been isolated from the reaction of SiH and the appropriate alkyllithium compound with propyl ether as the solvent (35). MethylsHane and ethyldisHane [7528-37-2] have been obtained in a similar reaction (36). 

Nitrodesilyladcn fEq. 2.17 and nitrodeslanyiadon fEq. 2.18 are ef cienl methods for the preparadon of some lands of nitroalkanes from readily available alkylsilanes or ailylslan-nanes. Similar nitradon also lakes place al the vinylic posidons fsee Eq. 2.36 in Secdon 2.1.4. ... 

Xiao, X. D., Hu, J., Chayuch, D. H., and Salmeron, M., Chain Length Dependence of the Frictional Properties of Alkylsilane Molecules Self-Assembled on Mica Studied by Atomic Force Microscopy," Z,angmmr,Vol. 12,1996, pp. 235-240. 

The alkylation of halogen-substituted benzenes such as fluorobenzene and dichlorobenzenes with other (dichloroalkyl)silanes in the presence of aluminum chloride catalyst afforded isomeric mixtures of the corresponding (dihalogen-substituted phenyl)alkylsilanes in moderate yields (Eq. (13)). These results are summarized in Table Xll. 

The transfer of alkylsilane monolayers onto mica was explored by Knobler and coworkers [331]. Monolayers of octadecyltrichlorosilane (OTS) were spread at the water-air interface. The trichlorosilane head groups rapidly undergo hydrolysis and cross-linking reactions to produce two-dimensional polysiloxanes on acidic subphases. On less acidic subphases, the polymerization rate is slower and the monolayer can be spread and transferred before the polymerization is significant. The II-A isotherm for OTS spread on... 

Organosilicon compounds are widely used in our daily life as oil, grease, rubbers, cosmetics, medicinal chemicals, etc. However, these compounds are not naturally occurring substances but artificially produced ones (for reviews of organosilicon chemistry, see [59-64]). Hydrosilylation reactions catalyzed by a transition-metal catalyst are one of the most powerful tools for the synthesis of organosilicon compounds. Reaction of an unsaturated C-C bond such as alkynes or alkenes with hydrosilane affords a vinyl- or alkylsilane, respectively (Scheme 16). 

A kinetic study of the hydrodefluorination of C F H in the presence of EtjSiH indicated a first-order dependence on both [fluoroarene] and [ruthenium precursor] and a zero-order dependence on the concentration of alkylsilane, implying that the rate-limiting step in the catalytic cycle involves activation of the fluoroarene. The regioselectivity for hydrodefluorination of partially fluorinated substrates such as CgFjH has been accounted for by an initial C-H bond activation as shown in the... 

The modification of bentonite with alkylsilanes improves the dispersing properties [991]. Incorporation of phosphonate-type compounds in bentonites for drilling mud permits the blockage of free calcium ions in the form of soluble and stable complexes and the preservation or restoration of the initial fluidity of the mud [1222]. The phosphonates also have dispersing and fluidizing effects on the mud. 

The second approach involves the reaction of enefunctional or multifunctional alkylsilane or cyclosiloxane ... 

Alkylsilanes are not very nucleophilic because there are no high-energy electrons in the sp3-sp3 carbon-silicon bond. Most of the valuable synthetic procedures based on organosilanes involve either alkenyl or allylic silicon substituents. The dominant reactivity pattern involves attack by an electrophilic carbon intermediate at the double bond that is followed by desilylation. Attack on alkenylsilanes takes place at the a-carbon and results in overall replacement of the silicon substituent by the electrophile. Attack on allylic groups is at the y-carbon and results in loss of the silicon substituent and an allylic shift of the double bond. 

This result is further supported by the very short 130 + 10 ps lifetime combined with the remarkably high quantum yield of 0.43, both observed upon excitation at 335 nm, near the long-wavelength edge of the absorption band. These values combine to a radiative lifetime of 300 ps, which corresponds (33a) to an oscillator strength of 1.8. Similarly short emission lifetimes have been observed for other poly(di-n-alkylsilanes) di-n-pentyl, 200 ps, di-n-decyl, 150 ps. The average oscillator... 

See related ALKYLMETALS, ALKYLSILANES j1723. Butylamine (1-Aminobutane)... 

Oxygen, Sodium hydroxide, Water See Oxygen (Gas) Tetramethyldisiloxane See related ALKYLSILANES... 

See Xenon difluoride Silicon-nitrogen compounds See related alkylsilanes... 

Small quantities can be distilled at about 75°C/1.3 mbar, but larger amounts are liable to explode violently owing to local overheating [1], An attempt to prepare an analogous poly(dimethylsilyl) chromate by heating a polydimethylsiloxane with chromium trioxide at 140°C exploded violently after 20min at this temperature [2], See related alkylsilanes, metal oxides... 

Pyridine iV-oxide, Tetrabutylammonium fluoride See Pyridine /V-oxidc Hexamethyldisilane, Tetrabutylammonium fluoride See other alkylsilanes... 

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