Sulfonate

The sulfonate ion.

A sulfonate is a salt or ester of a sulfonic acid. It contains the functional group R-SO₃⁻, where R is an organic group. Sulfonates are the conjugate base of sulfonic acids. Sulfonates are generally stable in water, non-oxidizing, and colorless. Many useful compounds and even some biochemicals feature sulfonates.

Contents

• 
  1 Sulfonate salts
  


• 
  2 Sulfonic esters
  
  
  
  • 
    2.1 Sultones
    
  
  
  
  


• 
  3 Examples
  


• 
  4 See also
  


• 
  5 References
  

Sulfonate salts

Alkylbenzene sulfonates are detergents found in shampoos, toothpaste laundry detergent, dishwashing liquid, etc.

Anions with the general formula RSO₃⁻ are called sulfonates. They are the conjugate bases of sulfonic acids with formula RSO₂OH. As sulfonic acids tend to be strong acids, the corresponding sulfonates are weak bases. Due to the stability of sulfonate anions, the cations of sulfonate salts such as scandium triflate have application as Lewis acids.

A classic organic reaction for the preparation of sulfonates is that of alkyl halides with sulfites such as sodium sulfite, first described by Adolph Strecker in 1868 (Strecker sulfite alkylation).^[1] The general reaction is:

RX + M₂SO₃ → RSO₃M + MX

Iodide is used as a catalyst.

Water-softening usually involves removal of calcium ions in water using a sulfonated ion-exchange resin.

Sulfonic esters

Esters with the general formula R¹SO₂OR² are called sulfonic esters. Individual members of the category are named analogously to how ordinary carboxyl esters are named. For example, if the R² group is a methyl group and the R¹ group is a trifluoromethyl group, the resulting compound is methyl trifluoromethanesulfonate.

Sulfonic esters are used as reagents in organic synthesis, chiefly because the RSO₃⁻ group is a good leaving group, especially when R is electron-withdrawing. Methyl triflate, for example, is a strong methylating reagent.

Sulfonates are commonly used to confer water solubility to protein crosslinkers such as N-hydroxysulfosuccinimide (Sulfo-NHS), BS3, Sulfo-SMCC, etc.

Sultones

1,3-Propane sultone

Cyclic sulfonic esters are called sultones.^[2] One example is 1,3-propane sultone. Some sultones are short-lived intermediates, used as strong alkylating agents to introduce a negatively charged sulfonate group. In the presence of water, they slowly hydrolyze to the hydroxy sulfonic acids. Sultone oximes are key intermediates in the synthesis of the anti-convulsant drug zonisamide.^[3]

Tisocromide is an example of a sultone.

Examples

• 
  Mesylate (methanesulfonate), CH₃SO₃⁻
  


• 
  Triflate (trifluoromethanesulfonate), CF₃SO₃⁻
  


• 
  Ethanesulfonate (esilate, esylate), C₂H₅SO₃⁻
  


• 
  Tosylate (p-toluenesulfonate), CH₃C₆H₄SO₃⁻
  


• 
  Benzenesulfonic acid (besylate), C₆H₅SO₃⁻
  


• 
  Closilate (closylate, chlorobenzenesulfonate), ClC₆H₄SO₃⁻
  


• 
  Camphorsulfonate (camsilate, camsylate), (C₁₀H₁₅O)SO₃⁻
  


• 
  Pipsylate (p-iodobenzenesulfonate derivative).^[4]
  


• Nosylate

See also

• Sulfate


• Sulfoxide


• Sulfonyl

References

1. 
   ^ Ueber eine neue Bildungsweise und die Constitution der Sulfosäuren Annalen der Chemie und Pharmacie Volume 148, Issue 1, Pages 90 - 96 (p 90-96) 1868 doi:10.1002/jlac.18681480108
   


2. 
   ^ R. J. Cremlyn “An Introduction to Organosulfur Chemistry” John Wiley and Sons: Chichester (1996). .mw-parser-output cite.citation{font-style:inherit}.mw-parser-output .citation q{quotes:"""""""'""'"}.mw-parser-output .citation .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-maint{display:none;color:#33aa33;margin-left:0.3em}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
   ISBN 0 471 95512 4.
   


3. 
   ^ Mondal, Shovan (2012). "Recent Developments in the Synthesis and Application of Sultones". Chem. Rev. 112: 5339–5355. doi:10.1021/cr2003294.
   


4. 
   ^ Beisler, J. A.; Sato, Y. (1971). "Chemistry of carpesterol, a novel sterol from Solanum xanthocarpum". The Journal of Organic Chemistry. 36 (25): 3946–3950. doi:10.1021/jo00824a022. ISSN 0022-3263.
   

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