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A silicon–oxygen bond (Si−O bond) is a chemical bond between silicon and oxygen atoms that can be found in many inorganic and organic compounds. [1] In a silicon–oxygen bond, electrons are shared unequally between the two atoms, with oxygen taking the larger share due to its greater electronegativity.
The C–Si bond is somewhat polarised towards carbon due to carbon's greater electronegativity (C 2.55 vs Si 1.90), and single bonds from Si to electronegative elements are very strong. [14] Silicon is thus susceptible to nucleophilic attack by O − , Cl − , or F − ; the energy of an Si–O bond in particular is strikingly high.
Orthosilicic acid (/ ˌ ɔːr θ ə s ɪ ˈ l ɪ s ɪ k /) is an inorganic compound with the formula Si(O H) 4. Although rarely observed, it is the key compound of silica and silicates and the precursor to other silicic acids [H 2x SiO x+2] n. Silicic acids play important roles in biomineralization and technology.
The first crystalline silicic acid was prepared from the phyllosilicate natrosilite (Na 2 Si 2 O 5) in 1924. More than 15 crystalline acids are known and comprise at least six modifications of H 2 Si 2 O 5. Some acids can adsorb and intercalate organic molecules, and therefore are interesting alternatives to silica. [10]
Dimethyldichlorosilane (Si(CH 3) 2 Cl 2) is a key precursor to cyclic (D 3, D 4, etc.) and linear siloxanes. [5] The main route to siloxane functional group is by hydrolysis of silicon chlorides: 2 R 3 Si−Cl + H 2 O → R 3 Si−O−SiR 3 + 2 HCl. The reaction proceeds via the initial formation of silanols (R 3 Si−OH): R 3 Si−Cl + H 2 O ...
Alternative depiction of a metasilicate chain emphasizing the Si-O bonds. With two shared oxides bound to each silicon, cyclic or polymeric structures can result. The cyclic metasilicate ring Si 6 O 12− 18 is a hexamer of SiO 3 2-. Polymeric silicate anions of can exist also as long chains.
In the thermodynamically stable room-temperature form, α-quartz, these tetrahedra are linked in intertwined helical chains with two different Si–O distances (159.7 and 161.7 pm) with a Si–O–Si angle of 144°. These helices can be either left- or right-handed, so that individual α-quartz crystals are optically active.
They feature Si-Si bonds. Attracting more interest are the organic derivatives such as polydimethylsilane ((CH 3) 2 Si) n. Dodecamethylcyclohexasilane ((CH 3) 2 Si) 6 is an oligomer of such materials. Formally speaking, polysilanes also include compounds of the type (SiH 2)n, but these less studied. Carbosilanes are polymeric silanes with ...