Loading AI tools
Ion From Wikipedia, the free encyclopedia
The dithionate (or metabisulfate) anion, S
2O2−
6, is a sulfur oxoanion[3] derived from dithionic acid, H2S2O6. Its chemical formula is sometimes written in a semistructural format, as [O3SSO3]2−. It is the first member of the polythionates.
| |||
Names | |||
---|---|---|---|
IUPAC name
Dithionate | |||
Systematic IUPAC name
Bis(trioxidosulfate)(S—S)(2−)[1] | |||
Identifiers | |||
3D model (JSmol) |
|||
ChEBI | |||
ChemSpider | |||
PubChem CID |
|||
CompTox Dashboard (EPA) |
|||
| |||
| |||
Properties | |||
S 2O2− 6 | |||
Molar mass | 160.126 g mol−1 | ||
Acidity (pKa) | 0.5[2] | ||
Conjugate acid | Dithionic acid | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
The sulfur atoms of the dithionate ion are in the +5 oxidation state due to the presence of the S–S bond. Generally, dithionates form stable compounds that are not readily oxidised or reduced. Strong oxidants oxidise them to sulfates and strong reducing agents reduce them to sulfites and dithionites.[4] Aqueous solutions of dithionates are quite stable and can be boiled without decomposition.[5]
The γ-irradiation of crystalline dithionates produces SO•−
3 radical ions.[6] The unpaired electron in the SO•−
3 radical can be detected with electron paramagnetic resonance and barium dithionate has been proposed as the basis for a radiation dosimeter.[7]
The dithionate ion can act as a bidentate ligand.[8]
The structure of the dithionate ion in the solid state is staggered in Na2S2O6·2H2O, whereas in the anhydrous potassium salt it is nearly eclipsed.[4]
Compounds containing the dithionate ion include:
Seamless Wikipedia browsing. On steroids.
Every time you click a link to Wikipedia, Wiktionary or Wikiquote in your browser's search results, it will show the modern Wikiwand interface.
Wikiwand extension is a five stars, simple, with minimum permission required to keep your browsing private, safe and transparent.