Search results
Results from the WOW.Com Content Network
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.
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.
A science project is an educational activity for students involving experiments or construction of models in one of the science disciplines. Students may present their science project at a science fair, so they may also call it a science fair project. Science projects may be classified into four main types.
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]
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.
A silanol is a functional group in silicon chemistry with the connectivity Si–O–H. It is related to the hydroxy functional group (C–O–H) found in all alcohols. Silanols are often invoked as intermediates in organosilicon chemistry and silicate mineralogy. [1] If a silanol contains one or more organic residues, it is an organosilanol.
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.
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 ...