Disulfur diiodide
 Sulfur, S Iodine, I | |
| Names | |
|---|---|
| IUPAC name Diiododisulfane | |
| Systematic IUPAC name Iodosulfanyl thiohypoiodite | |
| Other names Sulfur monoiodide (incorrect name) | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.053.127 |
| EC Number |
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PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| S2I2 | |
| Molar mass | 317.93 g·mol−1 |
| Appearance | Reddish-brown solid |
| Melting point | −30 °C (−22 °F; 243 K) (decomposes) |
| Solubility | Soluble in carbon tetrachloride, slightly soluble in pentane |
| Structure | |
| C2 | |
| 2 at sulfur atoms | |
| gauche | |
| Related compounds | |
Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Disulfur diiodide is an unstable inorganic chemical compound with the chemical formula S2I2. It is a red-brown solid that decomposes above −30 °C to elemental sulfur and iodine.[1]
Production
Reaction of sulfur and iodine
The first attempt and claim to produce a sulfur iodide were made in 1813 by Bernard Courtois when exploring the properties of his newly discovered element, iodine. He reacted to sulfur and iodine, claiming they had made a compound. However, this production was doubted by Gay-Lussac. Between 1827 and 1896, more attempts were made to make sulfur iodide by combining the elements; however, all were inconclusive on the existence of the compound or failed. Later, when thermal analysis was developed, it was shown that when the elements were combined, it only resulted in a mixture, not a compound.[2]
Production by double replacement
When attempts to produce sulfur iodide by the direct combination of the elements failed to overcome the low thermodynamic stability of the compound, production by double replacement was attempted between 1833 and 1886. Some reactions that were attempted was the reaction of disulfur dichloride and hydroiodic acid:[2]
- S2Cl2 + 2 HI → S2I2 + 2 HCl
The reaction of hydrogen sulfide and iodine trichloride:
- 3 H2S + 2 ICl3 → S3I2 + 6 HCl
The reaction of hydroiodic acid and sulfur:
- 2 HI + 3 S → H2S + S2I2
The reaction of disulfur dichloride and potassium iodide:
- S2Cl2 + 2 KI → S2I2 + 2 KCl
and more, all assumed to have failed to produce sulfur iodide. However, the reaction between S2Cl2 and HI attempted in 1835 was later proven to have produced disulfur diiodide.[2]
In 1940, another production was attempted with the fourth reaction and was reported to have detected various sulfur iodides, such as disulfur diiodide and sulfur diiodide (SI2). When observing the reaction of very dilute disulfur dichloride in carbon tetrachloride and potassium iodide:[2][3]
- S2Cl2 + 2 KI → 2 S + I2 + 2 KCl
they observed a color change from yellow to reddish-brown to finally violet, which was assumed to be evidence for the formation of sulfur iodides. The compound was found to decompose at room temperature slowly in a solution, with the decomposition rate increasing with increasing temperature.[3]
Isolation
Disulfur diiodide was first isolated by the reaction of disulfur dichloride and potassium iodide, sodium iodide, or hydrogen iodide in pentane at −90 °C, and verified by infrared spectroscopy.[4][5]
Properties
Disulfur diiodide is light-sensitive and is soluble in various haloalkanes, such as carbon tetrachloride.[3]
Other sulfur iodides
Sulfur diiodide (SI2) has finally been reported in an argon matrix at 9 K by the reaction of sulfur dichloride and iodine; however, this has been disputed.[6]
Sulfur and iodine react in antimony pentafluoride or arsenic pentafluoride to form the S7I+ ion, which is stable at room temperature, unlike other sulfur-iodine compounds.[7]
The empirical formula of disulfur diiodide is SI. It is therefore sometimes called sulfur monoiodide, but S2I2 is a covalently bound molecule and is not the same as a SI molecule or an ionic salt having 1:1 stoichiometry. The true sulfur monoiodide molecule is a radical.[8]
References
- ^ Wiberg, Egon; Nils Wiberg; Arnold Frederick Holleman (2001). Inorganic chemistry. Academic Press. p. 529. ISBN 978-0-12-352651-9.
- ^ a b c d William B. Jensen (2016). The Search for Sulfur Iodide : Notes from the Oesper Collections, No. 37. University of Cincinnati. Archived from the original on 2022-12-25. Retrieved 2022-12-23.
- ^ a b c M. R. Aswathanarayana Rao (1940). "Investigations on the Iodides of Sulphur". Proceedings of the Indian Academy of Sciences. 11 (3): 162–174.
- ^ Gisela Vahl; Priv.-Doz. Dr. Rolf Minkwitz (1978). "Beiträge zur Chemie der Schwefelhalogenide. IV. Über Versuche zur Darstellung von festem Dijoddisulfan bei tiefen Temperaturen" [Contributions of the Chemistry of Sulfur Halides. IV. On the Preparation of Solid Disulfurdiiodide at Low Temperatures]. Zeitschrift für anorganische und allgemeine Chemie (in German). 443 (1). Wiley: 217–224. doi:10.1002/zaac.19784430124.
- ^ Gisela Krummel; Rolf Minkwitz (1977). "Infrared-spectroscopic investigations on solid disulfurdiiodine". Inorganic and Nuclear Chemistry Letters. 13 (5): 213–215. doi:10.1016/0020-1650(77)80096-2.
- ^ Martin Feuerhahn; Gisela Vahl (1980). "Infrared spectra of matrix isolated sulfur dibromide and sulfur diiodide". Inorganic and Nuclear Chemistry Letters. 16 (1): 5-8. doi:10.1016/0020-1650(80)80082-1.
- ^ T. Klapoetke; J. Passmore (1989). "Sulfur and selenium iodine compounds: from non-existence to significance". Accounts of Chemical Research. 22 (7). ACS Publications: 234–240. doi:10.1021/ar00163a002.
- ^ See SciFinder CAS No 1312-15-8 for main refs