Thiosulfonate
Appearance
![](http://upload.wikimedia.org/wikipedia/commons/thumb/f/fb/RSO2SR%27.png/220px-RSO2SR%27.png)
Thiosulfonates are organosulfur compounds with the formula RSO2SR'. Thiosulfonate esters are produced by oxidation of disulfides or by the reaction or organosulfonyl halides with thiolates.[1]
Alkali metal thiosulfonates are the conjugate base of thiosulfuric acid. They are prepared by the reaction of organosulfonyl chlorides with sources of sulfide.[1][2]
See also
- Bunte salts are related organosulfur compounds with the formula RSSO3-
- Thiosulfinate a structurally analogous functional group in a lower oxidation state, with the formula RSS(O)R
References
- ^ a b Nikolai S. Zefirov, Nikolai V. Zyk, Elena K. Beloglazkina, Andrei G. Kutateladze (1993). "Thiosulfonates: Synthesis, Reactions and Practical Applications". Sulfur Reports. 14: 223-240. doi:10.1080/01961779308055018.
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: CS1 maint: multiple names: authors list (link) - ^ "Trimethylene Dithiotosylate And Ethylene Dithiotosylate". Org. Synth. 54: 33. 1974. doi:10.15227/orgsyn.054.0033.
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