Selenium oxydichloride
──────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────
top
Selenium oxydichloride is the inorganic compound with the formula SeOCl2. It is a colorless liquid. With a high dielectric constant (55) and high specific conductance, it is an attractive solvent. Structurally, it is a close chemical relative of thionyl chloride SOCl2, being a pyramidal molecule.
Contents
• See also
──────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────────
Preparation and reactions
Selenium oxydichloride can be prepared by several methods, and a common one involves the conversion of selenium dioxide to dichloroselenious acid followed by dehydration:cite-ref-3[3]
SeO2 + 2 HCl → Se(OH)2Cl2
Se(OH)2Cl2 → SeOCl2 + H2O
The original synthesis involved the redistribution reaction of selenium dioxide and selenium tetrachloride.
Pure selenium oxydichloride autoionizes to a dimer:cite-ref-footnoteaudriethkleinberg1953237-4-0[4]
SeOCl2 ↔ (SeO)2Cl+ 3 + Cl−
The SeOCl2 is generally a labile Lewis acid and solutions of sulfur trioxide in SeOCl2 likely form [SeOCl]+[SO3Cl]− the same way.cite-ref-footnoteaudriethkleinberg1953239-242-5-0[5]
The compound hydrolyzes readily to form hydrogen chloride and selenium dioxide, and very few organic compounds dissolve in it without reaction. At elevated temperatures, it is a strong oxidizer, yielding a chloride, selenium dioxide, and diselenium dichloride.cite-ref-6[6]
See also
References
cite-note-11. "Selenium compounds (as Se)". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
cite-note-22. "Selenium oxychloride". pubchem.ncbi.nlm.nih.gov. Retrieved 12 December 2021.
cite-note-footnoteaudriethkleinberg1953237-44. ↑ Audrieth & Kleinberg 1953, p. 237.
cite-note-footnoteaudriethkleinberg1953239-242-55. ↑ Audrieth & Kleinberg 1953, pp. 239–242.