English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/52681
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:


Epoxidation of cyclooctene and cyclohexene with hydrogen peroxide catalyzed by bis[3,5-bis(trifluoromethyl)-diphenyl] diselenide: Recyclable catalyst-containing phases through the use of glycerol-derived solvents

AuthorsGarcía-Marín, Héctor ; Mayoral, José A. ; García, José I.
Issue Date2011
CitationJournal of Molecular Catalysis A: Chemical 334: 83-88 (2011)
AbstractA green strategy has been explored for olefin epoxidation which combines renewable solvents (derived from glycerol), aqueous hydrogen peroxide, and catalyst recycling (a seleninic acid derivative). The use of fluorinated glycerol derivatives allows good catalytic activity in the epoxidation of cyclooctene and cyclohexene with aqueous hydrogen peroxide, preventing epoxide hydrolysis to a great extent, which is particularly remarkable in the case of cyclohexene. Furthermore, recycling of the catalytically active phase is possible through distillation of the cyclohexene oxide from the reaction mixture, which can be subsequently recharged with fresh oxidant and substrate. © 2010 Elsevier B.V. All rights reserved.
Identifiersdoi: 10.1016/j.molcata.2010.10.027
issn: 1381-1169
Appears in Collections:(ICMA) Artículos
Files in This Item:
File Description SizeFormat 
Epoxidation of cyclooctene.pdf544,19 kBAdobe PDFThumbnail
Show full item record
Review this work

Related articles:

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.