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Silicon–oxygen single bonds are longer (1.6 vs 1.4 Å) but stronger (452 vs. about 360 kJ mol −1) than carbon–oxygen single bonds. [1] However, silicon–oxygen double bonds are weaker than carbon–oxygen double bonds (590 vs. 715 kJ mol −1) due to a better overlap of p orbitals forming a stronger pi bond in the latter.
[1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.
For example, NH 3 is a Lewis base, because it can donate its lone pair of electrons. Trimethylborane [(CH 3) 3 B] is a Lewis acid as it is capable of accepting a lone pair. In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond. [1]
Hexachlorodisilane is stable under air or nitrogen at temperatures of at least up to 400°C for several hours, but decomposes to dodecachloroneopentasilane and silicon tetrachloride in presence of Lewis bases even at room temperature. [4] 4 Si 2 Cl 6 → 3 SiCl 4 + Si 5 Cl 12
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n, where 0 ≤ x < 2. The family includes orthosilicate SiO 4− 4 ( x = 0 ), metasilicate SiO 2− 3 ( x = 1 ), and pyrosilicate Si 2 O 6− 7 ( x = 0.5 , n = 2 ). The name is also used for any salt of such anions, such as sodium metasilicate ; or any ester containing the corresponding chemical group , such as tetramethyl orthosilicate . [ 1 ]
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Inosilicates (from Greek ἴς is [genitive: ἰνός inos] 'fibre'), or chain silicates, have interlocking chains of silicate tetrahedra with either SiO 3, 1:3 ratio, for single chains or Si 4 O 11, 4:11 ratio, for double chains. The Nickel–Strunz classification is 09.D – examples include: