Sulfuryl diazide
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Names | |
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IUPAC name
Sulfuryl diazide
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Other names
Sulfuryl azide; Sulfonyl diazide
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Identifiers | |
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CompTox Dashboard (EPA)
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Properties | |
SO2(N3)2 | |
Molar mass | 148.10 g·mol−1 |
Melting point | −15 °C (5 °F; 258 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Sulfuryl diazide or sulfuryl azide is a chemical compound with the molecular formula SO2(N3)2. It was first described in the 1920s when its reactions with benzene and p-xylene were studied by Theodor Curtius and Karl Friedrich Schmidt.[1][2][3] The compound is reported as having "exceedingly explosive, unpredictable properties" and "in many cases very violent explosions occurred without any apparent reason".[1]
It was not until 2011 that sulfuryl diazide was isolated in a pure enough state to be fully characterized.[4] It was characterized by infrared and Raman spectroscopy; its structure in the solid state was determined by x-ray crystallography.[4] Its melting point is -15 °C.[4] It was prepared by the reaction of sulfuryl chloride (SO2Cl2) with sodium azide (NaN3) using acetonitrile as solvent:
- SO2Cl2 + 2 NaN3 → SO2(N3)2 + 2 NaCl
Sulfuryl diazide has been used as a reagent to perform reactions that remove nitrogen from heterocyclic compounds:[5][6][7]
- R1−NH−R2 + SO2(N3)2 → R1−R2 + SO2 + 2 N2 + HN3
See also
References
- ^ a b Curtius, Theodor; Schmidt, Friedrich (1922). "Action of sulfuryl azide, N3SO2N3, on p-xylene". Berichte der Deutschen Chemischen Gesellschaft B. 55B: 1571–1581.
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: CS1 maint: multiple names: authors list (link) - .
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- ^ PMID 21815651.)
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: CS1 maint: multiple names: authors list (link - PMID 28414236.)
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: CS1 maint: multiple names: authors list (link - ^ Derek Lowe (July 7, 2021). "Carving Out Nitrogens: Pick Your Conditions". In The Pipeline. Science Translational Medicine. Archived from the original on June 5, 2023. Retrieved June 5, 2023.
- S2CID 235746021.