Oxidative Cleavage of Vicinal Diols Catalyzed by Monomeric Fe‐Sites Inside MFI Zeolite

Autor: Philipp Treu, Bidyut Bikash Sarma, Jan‐Dierk Grunwaldt, Erisa Saraçi
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: ChemCatChem, 14 (21), e202200993
ChemCatChem 14(21), e202200993 (2022). doi:10.1002/cctc.202200993
ISSN: 1867-3880
1867-3899
DOI: 10.3204/pubdb-2022-07817
Popis: ChemCatChem 14(21), e202200993 (2022). doi:10.1002/cctc.202200993
The oxidative cleavage of vicinal diols to carboxylic acids was investigated over heterogeneous Fe/MFI catalysts in aqueous medium, with green oxidant H2O2 and in mild reaction conditions. High conversions and selectivities (X=90 %, S=79 %) were achieved for the oxidative cleavage of ethylene glycol. Further substrates were also tested broadening the relevance of this catalyst. The employment of non-noble and abundant Fe as the active metal and the MFI-type zeolite as support has a clear advantage over the presently used homogeneous or noble metal-based catalysts. A combination of complementary characterisation techniques with catalytic results is used to show that monomeric Fe species inside zeolite MFI are the active sites for the oxidative cleavage of C−C bonds of vicinal diols. The recyclability of the catalyst and reaction mechanism were also studied.
Published by Wiley-VCH, Weinheim
Databáze: OpenAIRE