Tetraorganoarsonium salts
Tetraorganosulfurium salts, commonly referred to as tetraorganosulfonium salts, are a class of chemical compounds with the general formula [RS]4+X?, where R represents an organic group and X is a negatively charged counterion such as PF6? or OTf?. These salts exhibit unique reactivity due to their positively charged sulfur center, making them versatile reagents in organic synthesis. They are often used for activating organosulfur compounds, facilitating various transformations including alkylation, arylation, and sulfuration reactions. The use of tetraorganosulfonium salts allows chemists to explore novel reaction pathways with high functional group tolerance and good yields, making them indispensable tools in synthetic chemistry.
These reagents are typically prepared by reacting organothiol derivatives with Lewis acids or through direct synthesis from organosulfinic compounds. Due to their stability under a wide range of conditions, they offer significant advantages over traditional sulfur-based reagents in terms of operational simplicity and product purity. The ability to selectively activate and transform organosulfur functionalities makes tetraorganosulfonium salts valuable assets for both academic research and industrial applications.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Tetramethyl Arsonium Iodide | 5814-20-0 | C4H12AsI |
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Arsenobetaine Bromide | 71642-15-4 | C5H12AsBrO2 |
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Bromide-Tetramethylarsonium(1+) | 69755-45-9 | C4H12AsBr |
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Arsenocholine Bromide | 71802-31-8 | C5H14AsBrO |
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Bromide-Tetramethylarsonium(1+) | 5814-22-2 | C4H12AsCl |
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(2-Hydroxyethyl)trimethylarsonium(1+); Nitrate | 115195-57-8 | C5H14AsNO4 |
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Arsonium, (2-hydroxyethyl)trimethyl-, chloride | 84796-08-7 | C5H14AsClO |
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Arsonium, [2-(acetyloxy)ethyl]trimethyl-, bromide | 51860-39-0 | C7H16AsBrO2 |
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Bromide-(2-Hydroxyethyl)trimethylarsonium(1+) | 86947-37-7 | C5H14AsIO |
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Bromide-(2-Hydroxyethyl)trimethylarsonium(1+) | 86947-42-4 | C5H15AsO2 |
Related Literature
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Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
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Michael Kappl,Paul M. Young,Daniela Traini,Sanyog Jain RSC Adv., 2016,6, 25789-25798
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Robert P. Davies,Maria A. Giménez,Laura Patel,Andrew J. P. White Dalton Trans., 2008, 5705-5707
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Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
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