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]
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]
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]
^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.