Difference between revisions of "Sulfur oxoacids"
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− | The '''sulfur [[oxoacid]]s''' are chemical compounds that contain [[sulfur]], [[oxygen]] and [[hydrogen]]. The best known and most important industrially is [[sulfuric acid]]. Sulfur has a number of | + | The '''sulfur [[oxoacid]]s''' are chemical compounds that contain [[sulfur]], [[oxygen]] and [[hydrogen]]. The best known and most important industrially is [[sulfuric acid]]. Sulfur has a number of oxoacids; however, some of these are known only from their salts (these are shown in italics in the table below).<ref>{{Greenwood&Earnshaw1st|pages=834–54}}.</ref> The acids that have been characterised contain a variety of structural features, for example: |
*tetrahedral sulfur when coordinated to oxygen | *tetrahedral sulfur when coordinated to oxygen | ||
*terminal and bridging oxygen atoms | *terminal and bridging oxygen atoms | ||
*terminal and bridging peroxo groups | *terminal and bridging peroxo groups | ||
*terminal S=S | *terminal S=S | ||
− | *chains of ( | + | *chains of (–S–)<sub>n</sub> |
{| class="wikitable" | {| class="wikitable" | ||
|- | |- | ||
− | + | ! Acid | |
− | + | ! Formula | |
− | + | ! Sulfur oxidation state | |
− | + | ! Structure | |
− | + | ! Related anions | |
− | + | ! Notes | |
|- | |- | ||
− | |[[Sulfuric acid]] | + | | [[Sulfuric acid]] |
− | |H<sub>2</sub>SO<sub>4</sub> | + | | H<sub>2</sub>SO<sub>4</sub> |
| VI | | VI | ||
− | |[[Image:Sulfuric-acid-2D.png|150px|sulfuric]] | + | | [[Image:Sulfuric-acid-2D.png|150px|sulfuric]] |
− | |[[Sulfate]], SO<sub>4</sub><sup> | + | | [[Sulfate]], SO<sub>4</sub><sup>2−</sup> and hydrogen sulfate commonly known as [[bisulfate]] |
− | |Best known and industrially significant | + | | Best known and industrially significant |
|- | |- | ||
− | |[[Disulfuric acid]] or pyrosulfuric acid | + | | [[Disulfuric acid]] or pyrosulfuric acid |
− | |H<sub>2</sub>S<sub>2</sub>O<sub>7</sub> | + | | H<sub>2</sub>S<sub>2</sub>O<sub>7</sub> |
| VI | | VI | ||
− | |[[Image:Disulfuric acid 2-D structure.png|150px|disulfuric]] | + | | [[Image:Disulfuric acid 2-D structure.png|150px|disulfuric]] |
− | |Disulfate commonly known as [[pyrosulfate]], S<sub>2</sub>O<sub>7</sub><sup> | + | | Disulfate commonly known as [[pyrosulfate]], S<sub>2</sub>O<sub>7</sub><sup>2−</sup> |
− | |Pure form melts at | + | | Pure form melts at 36 °C. Present in fuming sulfuric acid, [[oleum]] |
|- | |- | ||
− | |[[Peroxymonosulfuric acid]] | + | | [[Peroxymonosulfuric acid]] |
− | |H<sub>2</sub>SO<sub>5</sub> | + | | H<sub>2</sub>SO<sub>5</sub> |
− | |VI | + | | VI |
− | |[[Image:Peroxomonosulfuric acid 2-D structure.png|150px|peroxymonosulfuric]] | + | | [[Image:Peroxomonosulfuric acid 2-D structure.png|150px|peroxymonosulfuric]] |
− | |[[Peroxymonosulfate]], OOSO<sub>3</sub><sup> | + | | [[Peroxymonosulfate]], OOSO<sub>3</sub><sup>2−</sup> |
− | |"Caro's acid", a solid melting at | + | | "Caro's acid", a solid melting at 45 °C |
|- | |- | ||
− | |[[Peroxydisulfuric acid]] | + | | [[Peroxydisulfuric acid]] |
− | |H<sub>2</sub>S<sub>2</sub>O<sub>8</sub> | + | | H<sub>2</sub>S<sub>2</sub>O<sub>8</sub> |
− | |VI | + | | VI |
− | |[[Image:Peroxodisulfuric_acid_2-D_structure.png|150px|peroxydisulfuric]] | + | | [[Image:Peroxodisulfuric_acid_2-D_structure.png|150px|peroxydisulfuric]] |
− | |[[Peroxydisulfate]], O<sub>3</sub>SOOSO<sub>3</sub><sup> | + | | [[Peroxydisulfate]], O<sub>3</sub>SOOSO<sub>3</sub><sup>2−</sup> |
− | |A solid melting at | + | | A solid melting at 65 °C. |
|- | |- | ||
− | |''[[Dithionic acid]]'' | + | | ''[[Dithionic acid]]'' |
| H<sub>2</sub>S<sub>2</sub>O<sub>6</sub> | | H<sub>2</sub>S<sub>2</sub>O<sub>6</sub> | ||
− | |V | + | | V |
− | |[[Image:Dithionic acid 2-D structure.png|150px|dithionic]] | + | | [[Image:Dithionic acid 2-D structure.png|150px|dithionic]] |
− | |[[Dithionate]], O<sub>3</sub>SSO<sub>3</sub><sup> | + | | [[Dithionate]], O<sub>3</sub>SSO<sub>3</sub><sup>2−</sup> |
− | |Not obtained pure, only concentrated solutions | + | | Not obtained pure, only concentrated solutions |
|- | |- | ||
− | |[[Thiosulfuric acid]] | + | | [[Thiosulfuric acid]] |
− | |H<sub>2</sub>S<sub>2</sub>O<sub>3</sub> | + | | H<sub>2</sub>S<sub>2</sub>O<sub>3</sub> |
| IV | | IV | ||
− | |[[Image:Thiosulfuric acid 2-D structure.png|150px|thiosulfuric]] | + | | [[Image:Thiosulfuric acid 2-D structure.png|150px|thiosulfuric]] |
− | |[[Thiosulfate]], S<sub>2</sub>O<sub>3</sub><sup> | + | | [[Thiosulfate]], S<sub>2</sub>O<sub>3</sub><sup>2−</sup><br />[[Hydrogenthiosulfate]] HS<sub>2</sub>O<sub>3</sub><sup>−</sup> (ammonium salt prepared in anhydrous methanol at −80 °C)<ref>{{citation | title = Raman spectroscopic discovery of the hydrogenthiosulphate anion, HSSO<sub>3</sub><sup>−</sup>, in solid NH<sub>4</sub>HS<sub>2</sub>O<sub>3</sub> | last1 = Steudel | first1 = R. | last2 = Prenzel | first2 = A. | journal = Z. Naturforsch. | year = 1989 | volume = 44 | issue = 12 | pages = 1499–1502}}.</ref> |
− | |Aqueous solutions decompose. | + | | Aqueous solutions decompose. |
|- | |- | ||
− | |''[[Disulfurous acid]]'' | + | | ''[[Disulfurous acid]]'' |
− | |H<sub>2</sub>S<sub>2</sub>O<sub>5</sub> | + | | H<sub>2</sub>S<sub>2</sub>O<sub>5</sub> |
− | |IV | + | | IV |
− | |[[Image:Disulfurous acid 2-D structure.png|150px|disulfurous]] | + | | [[Image:Disulfurous acid 2-D structure.png|150px|disulfurous]] |
− | |Disulfite commonly known as [[metabisulfite]], S<sub>2</sub>O<sub>5</sub><sup> | + | | Disulfite commonly known as [[metabisulfite]], S<sub>2</sub>O<sub>5</sub><sup>2−</sup> |
− | |Not known | + | | Not known |
|- | |- | ||
− | |''[[Sulfurous acid]]'' | + | | ''[[Sulfurous acid]]'' |
| H<sub>2</sub>SO<sub>3</sub> | | H<sub>2</sub>SO<sub>3</sub> | ||
− | |IV | + | | IV |
− | |[[Image:Sulfurous acid 2-D structure.png|150px|sulfurous]] | + | | [[Image:Sulfurous acid 2-D structure.png|150px|sulfurous]] |
− | |[[Bisulfite]], HSO<sub>3</sub><sup> | + | | [[Bisulfite]], HSO<sub>3</sub><sup>−</sup> and [[sulfite]], SO<sub>3</sub><sup>2−</sup> |
− | |Not known | + | | Not known |
|- | |- | ||
− | |''[[Dithionous acid]]'' | + | | ''[[Dithionous acid]]'' |
− | |H<sub>2</sub>S<sub>2</sub>O<sub>4</sub> | + | | H<sub>2</sub>S<sub>2</sub>O<sub>4</sub> |
− | |III | + | | III |
− | |[[Image:Dithionous acid 2-D structure.png|150px|dithionous]] | + | | [[Image:Dithionous acid 2-D structure.png|150px|dithionous]] |
− | |[[Dithionite]], O<sub>2</sub>SSO<sub>2</sub><sup> | + | | [[Dithionite]], O<sub>2</sub>SSO<sub>2</sub><sup>2−</sup> |
− | |Not known. | + | | Not known. |
|- | |- | ||
− | |[[Polythionic acid]] | + | | [[Polythionic acid]] |
− | |H<sub>2</sub>S<sub>x</sub>O<sub>6</sub> | + | | H<sub>2</sub>S<sub>''x''</sub>O<sub>6</sub> |
| | | | ||
− | |[[Image:Polythionic acid 2-D structure.png|150px|polythionic]] | + | | [[Image:Polythionic acid 2-D structure.png|150px|polythionic]] |
− | |[[Polythionate]], O<sub>3</sub>S(S<sub>x | + | | [[Polythionate]], O<sub>3</sub>S(S<sub>''x''−2</sub>)SO<sub>3</sub><sup>2−</sup>. Example [[tetrathionate]]. |
− | |Examples known with x= 3, 4, 5, 6, 7, 8, 10, 12, 14. | + | | Examples known with ''x'' = 3, 4, 5, 6, 7, 8, 10, 12, 14. |
|} | |} | ||
− | == | + | ==References== |
− | + | {{reflist}} | |
− | |||
− | |||
− | |||
[[Category:Sulfur oxoacids|*]] | [[Category:Sulfur oxoacids|*]] | ||
{{Imported from Wikipedia|name=Sulfur oxoacids|id=267814680}} | {{Imported from Wikipedia|name=Sulfur oxoacids|id=267814680}} |
Latest revision as of 18:14, 23 August 2009
The sulfur oxoacids are chemical compounds that contain sulfur, oxygen and hydrogen. The best known and most important industrially is sulfuric acid. Sulfur has a number of oxoacids; however, some of these are known only from their salts (these are shown in italics in the table below).[1] The acids that have been characterised contain a variety of structural features, for example:
- tetrahedral sulfur when coordinated to oxygen
- terminal and bridging oxygen atoms
- terminal and bridging peroxo groups
- terminal S=S
- chains of (–S–)n
Acid | Formula | Sulfur oxidation state | Structure | Related anions | Notes |
---|---|---|---|---|---|
Sulfuric acid | H2SO4 | VI | Sulfate, SO42− and hydrogen sulfate commonly known as bisulfate | Best known and industrially significant | |
Disulfuric acid or pyrosulfuric acid | H2S2O7 | VI | Disulfate commonly known as pyrosulfate, S2O72− | Pure form melts at 36 °C. Present in fuming sulfuric acid, oleum | |
Peroxymonosulfuric acid | H2SO5 | VI | peroxymonosulfuric | Peroxymonosulfate, OOSO32− | "Caro's acid", a solid melting at 45 °C |
Peroxydisulfuric acid | H2S2O8 | VI | Peroxydisulfate, O3SOOSO32− | A solid melting at 65 °C. | |
Dithionic acid | H2S2O6 | V | dithionic | Dithionate, O3SSO32− | Not obtained pure, only concentrated solutions |
Thiosulfuric acid | H2S2O3 | IV | Thiosulfate, S2O32− Hydrogenthiosulfate HS2O3− (ammonium salt prepared in anhydrous methanol at −80 °C)[2] |
Aqueous solutions decompose. | |
Disulfurous acid | H2S2O5 | IV | Disulfite commonly known as metabisulfite, S2O52− | Not known | |
Sulfurous acid | H2SO3 | IV | sulfurous | Bisulfite, HSO3− and sulfite, SO32− | Not known |
Dithionous acid | H2S2O4 | III | Dithionite, O2SSO22− | Not known. | |
Polythionic acid | H2SxO6 | Polythionate, O3S(Sx−2)SO32−. Example tetrathionate. | Examples known with x = 3, 4, 5, 6, 7, 8, 10, 12, 14. |
References
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