Abstract
The substitution of pure metal particles by metal phosphides in catalysis represents a promising opportunity to lower the required metal quantity in the context of a sustainable use of metal resources. Herein we show the synthesis of palladium phosphide, Pd3P, supported on silica, which is tested as catalyst for the Wacker-Tsuji-oxidation of styrene to acetophenone. The synthesized catalyst is characterized by PXRD, SEM-EDX, FTIR, ICP-AES and XPS measurements. Four different reaction systems are investigated in this study including different co-catalysts and reaction media. Conversions of styrene up to 95 % with a selectivity of 73 % towards acetophenone are observed using Pd3P/SiO2 as catalyst, CuCl2 as co-catalyst and O2 as oxidant. An enhanced selectivity up to 100 % towards acetophenone is obtained in other reaction systems. The use of Pd3P/SiO2 leads to an optimized selectivity and conversion in the oxidation reaction in comparison with the purely Pd-based system Pd/SiO2. These results give an insight on how the incorporation of phosphorus has a great effect on the performance of heterogeneous catalysts.
Author supplied keywords
Cite
CITATION STYLE
Neyyathala, A., Flecken, F., & Hanf, S. (2023). A Supported Palladium Phosphide Catalyst for the Wacker-Tsuji-Oxidation of Styrene. ChemPlusChem, 88(2). https://doi.org/10.1002/cplu.202200431
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.