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Like other chlorosilanes or silanes, silicon tetrachloride reacts readily with water: . SiCl 4 + 2 H 2 O → SiO 2 + 4 HCl. The reaction can be noticed on exposure of the liquid to air, as SiCl 4 vapour produces fumes as it reacts with moisture to give a cloud-like aerosol of silica and hydrochloric acid. [6]
Trichlorosilane is produced commercially by the reaction of hydrogen chloride with silicon: Si + 3 HCl → HSiCl 3 + H 2. Many alkoxy hydrosilanes are generated by alcoholysis of trichlorosilane. One example is triethoxysilane: HSiCl 3 + 3 EtOH → HSi(OEt) 3 + 3 HCl. Organohydrosilanes can be prepared by partial hydrosilation of silane itself:
The methylchlorosilanes react with water to produce hydrogen chloride, giving siloxanes. In the case of trimethylsilyl chloride, the hydrolyzed product is hexamethyldisiloxane: 2 ((CH 3) 3 SiCl + H 2 O → [(CH 3) 3 Si] 2 O + 2 HCl. The analogous reaction of dimethyldichlorosilane gives siloxane polymers or rings: n (CH 3) 2 SiCl 2 + n H 2 O ...
This also includes water, potentially producing silicon dioxide, chlorine, hydrogen, hydrogen chloride (and its aqueous form hydrochloric acid), and heat. Trichlorosilane can cause hazardous chemical reactions with moisture and humidity alone, and should be handled and stored under inert gas. [8]
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.
CaSi with its zigzag chains of silicon atoms instead reacts to give silanes and polymeric SiH 2, while CaSi 2 with its puckered layers of silicon atoms does not react with water, but will react with dilute hydrochloric acid: the product is a yellow polymeric solid with stoichiometry Si 2 H 2 O. [2]
Silane can be produced by several routes. [7] Typically, it arises from the reaction of hydrogen chloride with magnesium silicide: . Mg 2 Si + 4 HCl → 2 MgCl 2 + SiH 4. It is also prepared from metallurgical-grade silicon in a two-step process.
Reductions with hydrosilanes are methods used for hydrogenation and hydrogenolysis of organic compounds.The approach is a subset of ionic hydrogenation.In this particular method, the substrate is treated with a hydrosilane and auxiliary reagent, often a strong acid, resulting in formal transfer of hydride from silicon to carbon. [1]