Thioketone
In organic chemistry, thioketones (from Ancient Greek θεῖον (theion) 'sulfur';[1] also known as thiones or thiocarbonyls) are organosulfur compounds related to conventional ketones in which the oxygen has been replaced by a sulfur.[2] Instead of a structure of R2C=O, thioketones have the structure R2C=S, which is reflected by the prefix "thio-" in the name of the functional group. Thus the simplest thioketone is thioacetone, the sulfur analog of acetone. Unhindered alkylthioketones typically tend to form polymers or rings.[3][4]
- ^ θεῖον Archived 2017-05-10 at the Wayback Machine, Henry George Liddell, Robert Scott, A Greek–English Lexicon
- ^ IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (2006–) "Thioketones". doi:10.1351/goldbook.T06356
- ^ Kuhn, N.; Verani, G. (2007). "Chalcogenone C=E compounds". Handbook of Chalcogen Chemistry: New Perspectives in Sulfur, Selenium and Tellurium. Royal Society of Chemistry. doi:10.1039/9781847557575-00107.
- ^ Whittingham, William G. (1995). "Thioaldehydes and Thioketones". Comprehensive Organic Functional Group Transformations. pp. 329–380. doi:10.1016/B0-08-044705-8/00169-2. ISBN 978-0-08-044705-6.