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HERO ID
4340505
Reference Type
Journal Article
Title
Epoxidation of Butadiene with Hydrogen Peroxide Catalyzed by the Salts of Phosphotungstate Anions: Relation Between Catalytic Activity and Composition of Intermediate Peroxo Complexes
Author(s)
Kuznetsova, LI; Kuznetsova, NI; Maksimovskaya, RI; Aleshina, GI; Koscheeva, OS; Utkin, VA
Year
2011
Is Peer Reviewed?
Yes
Journal
Catalysis Letters
ISSN:
1011-372X
EISSN:
1572-879X
Volume
141
Issue
10
Page Numbers
1442-1450
DOI
10.1007/s10562-011-0676-1
Web of Science Id
WOS:000295519500006
Abstract
Epoxidation of 1,3-butadiene has been studied in acetonitrile solutions of aqueous H2O2 and tetrabutylammonium or 1-ethyl-3-methylimidazolium salts of phosphotungstate anions: [(n-C4H9)(4)N](3){PO4[WO(O-2)(2)](4)}, [(n-C4H9)(4)N](5)Na0.6H1.4[PW11O39] or [(C2H5)(CH3)C3H3N2](5)NaH[PW11O39]. The selectivity of the 1,3-butadiene to 3,4-epoxy-1-butene (EpB) conversion attains 97% at nearly 100% efficiency of the H2O2 consumption. The rate of the EpB formation has been correlated with the solution compositions as found by P-31 NMR under the reaction conditions.
Keywords
Epoxidation; 1,3-Butadiene; Hydrogen peroxide; Phosphotungstates; Tetrabutylammonium; 1-Ethyl-3-methylimidazolium; P-31 NMR
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