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Observational analysis revealed enhanced catalytic activity and selectivity for vinyl acetate in monometallic Pd catalysts, suggesting importance of Pd-acetate dynamics.
Vinyl acetate monomer (VAM) is a crucial intermediate in the production of various polymers. While molecular Pd-acetate trimers and dimers, such as Pd₃(OAc)₆ and K₂Pd₂(OAc)₆, are known to form on potassium acetate (KOAc)-promoted PdAu catalysts during heterogeneous VAM synthesis, their mechanistic role remains unclear. Here, we study the dynamics of different Pd-acetate species by utilizing in situ and operando crystallographic and spectroscopic characterizations combined with computational modeling on monometallic Pd model catalysts. The promoter-free catalyst expectedly shows low catalytic activity and VAM selectivity, corresponding to the complete reduction of Pdn(OAc)2n species to form Pd⁰ and PdCx nanoparticles. Conversely, noticeable quantities of KnPd₂(OAc)n+4 species remain on the KOAc-promoted catalyst, leading to smaller nanoparticle formation with 10 times the activity and double the selectivity for VAM. This study reveals that molecular Pd-acetate trimers and dimers are significant indicators of catalytic performance and highlights their structurally dynamic nature in heterogeneous vinyl acetate chemistry.
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Jacobs et al. (2025) studied this question.
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