Taming the Oxidative Power of SeO3 in 1,4-Dioxane, Isolation of Two New Isomers of Mixed-Valence Selenium Oxides, and Two Unprecedented Cyclic Esters of Selenic Acid


Por: Richtera L., Jancik V., Martínez-Otero D., Pokluda A., Zak Z., Taraba J., Touzin J.

Publicada: 7 jul 2014
Resumen:
The reaction of (SeO3)(4) with 1,4-dioxane (diox, dioxane) with or without diluting solvent led to the isolation of the unprecedented esters of selenic acid-1,2-ethyl selenate (CH2O)(2)SeO2 and the glyoxal diselenate O2Se[(OCHO)(2)]SeO2. It was possible to isolate an unknown dimeric form of Se2O5 (Se4O10-(diox)(2)) and a geometrical isomer of the mixed-valence oxide trans-Se3O7, both stabilized by dioxane. The dioxane adduct of monomeric selenium trioxide SeO3-diox was obtained from the reaction of (SeO3)(4) with dioxane in liquid SO2. The reaction mechanism for the formation of these compounds was elucidated, and the molecular structure of the unstable form of the selenium trioxide was determined, consisting in a trimeric arrangement (SeO3)(3).

Filiaciones:
Richtera L.:
 Institute of Materials Chemistry, Faculty of Chemistry, Brno University of Technology, Purkynova 118, 612 00 Brno, Czech Republic

Jancik V.:
 UAEM UNAM, Ctr Conjunto Invest Quim Sustentable, Toluca 50200, Estado De Mexic, Mexico

Martínez-Otero D.:
 UAEM UNAM, Ctr Conjunto Invest Quim Sustentable, Toluca 50200, Estado De Mexic, Mexico

Pokluda A.:
 Department of Chemistry, Masaryk University, Kotlarska 2, 61137 Brno, Czech Republic

Zak Z.:
 Department of Chemistry, Masaryk University, Kotlarska 2, 61137 Brno, Czech Republic

Taraba J.:
 Department of Chemistry, Masaryk University, Kotlarska 2, 61137 Brno, Czech Republic

Touzin J.:
 Department of Chemistry, Masaryk University, Kotlarska 2, 61137 Brno, Czech Republic
ISSN: 00201669
Editorial
AMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 53 Número: 13
Páginas: 6569-6577
WOS Id: 000338748100022
ID de PubMed: 24940821