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Names | |||
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IUPAC name
Sulfur monoxide
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Systematic IUPAC name
Oxidosulfur
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Identifiers | |||
3D model (Jmol)
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7577656 | |||
ChEBI | |||
ChemSpider | |||
666 | |||
MeSH | sulfur+monoxide | ||
PubChem CID
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Properties | |||
SO | |||
Molar mass | 48.064 g mol−1 | ||
Appearance | Colourless gas | ||
Reacts | |||
log P | 0.155 | ||
Thermochemistry | |||
Std molar
entropy (S |
221.94 J K−1 mol−1 | ||
Std enthalpy of
formation (ΔfH |
5.01 kJ mol−1 | ||
Related compounds | |||
Related compounds
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Triplet oxygen | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|||
Infobox references | |||
Sulfur monoxide is an inorganic compound with formula SO. It is only found as a dilute gas phase. When concentrated or condensed, it converts to S2O2 (disulfur dioxide). It has been detected in space but is rarely encountered intact otherwise.
The SO molecule has a triplet ground state similar to O2, i.e. each molecule has two unpaired electrons. The S−O bond length of 148.1 pm is similar to that found in lower sulfur oxides (e.g. S8O, S−O = 148 pm) but is longer than the S−O bond in gaseous S2O (146 pm), SO2 (143.1 pm) and SO3 (142 pm).
The molecule is excited with near infrared radiation to the singlet state (with no unpaired electrons). The singlet state is believed to be more reactive than the ground state triplet state, in the same way that singlet oxygen is more reactive than the triplet oxygen.
Production of SO as a reagent in organic syntheses has centred on using compounds that "extrude" SO. Examples include the decomposition of the relatively simple molecule thiirane 1-oxide: as well as more complex examples, such as a trisulfide oxide, C10H6S3O,
The SO molecule is thermodynamically unstable, converting initially to S2O2. SO inserts into alkenes, alkynes and dienes producing molecules with three membered rings containing sulfur.
In the laboratory sulfur monoxide can be produced by treating sulfur dioxide with sulfur vapour in a glow discharge. It has been detected in single bubble sonoluminescence of concentrated sulfuric acid containing some dissolved noble gas.
A chemiluminescence detector for sulfur has been reported that is based on the reactions: