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Sulfur trioxide (alternative spelling sulphur trioxide) is the chemical compound with the formula SO 3. It has been described as "unquestionably the most [economically] important sulfur oxide". [ 1 ] It is prepared on an industrial scale as a precursor to sulfuric acid .
The Parikh–Doering oxidation is an oxidation reaction that transforms primary and secondary alcohols into aldehydes and ketones, respectively. [1] The procedure uses dimethyl sulfoxide (DMSO) as the oxidant and the solvent, activated by the sulfur trioxide pyridine complex (SO 3 •C 5 H 5 N) in the presence of triethylamine or diisopropylethylamine as base.
Sulfur trioxide pyridine complex is the compound with the formula C 5 H 5 NSO 3. It is a colourless solid that dissolves in polar organic solvents. It is the adduct formed from the Lewis base pyridine and the Lewis acid sulfur trioxide. The compound is mainly used as a source of sulfur trioxide, for example in the synthesis of sulfate esters ...
Sulfur trioxide, SO 3, a chemical compound of sulfur and the anhydride of sulfuric acid; Sulfite, SO 2− 3, a chemical ion composed of sulfur and oxygen with a 2− charge; SO(3), the special orthogonal group in 3 dimensions; the rotations that can be given an object in 3-space; Star Ocean: Till the End of Time, the third main game in the Star ...
Oleum (Latin oleum, meaning oil), or fuming sulfuric acid, is a term referring to solutions of various compositions of sulfur trioxide in sulfuric acid, or sometimes more specifically to disulfuric acid (also known as pyrosulfuric acid). [1] Oleums can be described by the formula ySO 3 ·H 2 O where y is the
Sulfur oxide refers to many types of sulfur and oxygen containing compounds such as SO, SO 2, SO 3, S 7 O 2, S 6 O 2, S 2 O 2, etc. Sulfur oxide (SO x) refers to one or more of the following: Lower sulfur oxides (S n O, S 7 O 2 and S 6 O 2) Sulfur monoxide (SO) and its dimer, Disulfur dioxide (S 2 O 2) Sulfur dioxide (SO 2) Sulfur trioxide (SO 3)
In biology, sulfation is typically effected by sulfotransferases, which catalyze the transfer of the equivalent of sulfur trioxide to substrate alcohols and phenols, converting the latter to sulfate esters. [5] [6] The source of the SO 3 group is usually 3'-phosphoadenosine-5'-phosphosulfate (PAPS).
The two principal sulfur oxides are obtained by burning sulfur: S + O 2 → SO 2 (sulfur dioxide) 2 SO 2 + O 2 → 2 SO 3 (sulfur trioxide). Many other sulfur oxides are observed including the sulfur-rich oxides include sulfur monoxide, disulfur monoxide, disulfur dioxides, and higher oxides containing peroxo groups.
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