The material is formed by heating silicon and sulfur or by the exchange reaction between SiO2 and Al2S3. The material consists of chains of edge-shared tetrahedra, -Si(μ-S)2Si(μ-S)2-.[2]
Like other silicon sulfur-compounds (e.g., bis(trimethylsilyl)sulfide) SiS2 hydrolyzes readily to release H2S.
In liquid ammonia it is reported to form the imide Si(NH)2 and NH4SH,[3] but a recent report has identified crystalline (NH4)2[SiS3(NH3)]·2NH3 as a product which contains the tetrahedral thiosilicate anion, SiS3(NH3)2-.[4]
SiS2 is claimed to occur in certain interstellar objects.[6]
References
^Weiss, A.; Weiss, A. (1954). "Über Siliciumchalkogenide. VI. Zur Kenntnis der faserigen Siliciumdioxyd-Modifikation". Zeitschrift für Anorganische und Allgemeine Chemie. 276 (1–2): 95–112. doi:10.1002/zaac.19542760110.
^Holleman, A. F.; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN0-12-352651-5. A printing error in this book states that rSiSi is 214 picometers, when in fact that distance describes rSiS.
^Meier, Martin; Korber, Nikolaus (2009). "The first thiosilicate from solution: synthesis and crystal structure of (NH4)2[SiS3(NH3)]·2NH3". Dalton Transactions (9): 1506–1508. doi:10.1039/b818856d. ISSN1477-9226. PMID19421590.
^R. Piękoś, W. Wojnowski (1962). "Untersuchungen über die Alkoholyse des SiS2. II. Darstellung von Trialkoxysilanthiolen und Tetraalkoxycyclodisilthianen aus den tertiären Alkoholen". Z. Anorg. Allg. Chem. 318 (3–4): 212–216. doi:10.1002/zaac.19623180310.