Bergen A, Tavera Méndez CL, Eichhorn V, Maier P, Harrer E, Scheurer A, Heinemann FW, Zahn D, Hartmann M, Wisser D, Meyer K (2026)
Publication Type: Journal article
Publication year: 2026
Article Number: e71585
DOI: 10.1002/chem.71585
Heterogenized molecular catalysts commonly rely on covalent grafting to solid supports. Cleavage of these linkages under catalytic conditions, however, can compromise structural definition and control at the interface. Here, we introduce a ligand-encoded anchoring strategy in which a platinum(II) bis(NHC) complex is immobilized on mesoporous silica (SBA-15) exclusively through directional, non-covalent F–Si interactions. The molecular pre-catalyst trans-[Pt(LF)2Cl2] was structurally characterized by single-crystal X-ray diffraction and multinuclear solution-state NMR spectroscopy. Advanced solid-state MAS NMR experiments, including 19F{29Si} REDOR, combined with molecular dynamics simulations, establish well-defined F–Si contacts with internuclear distances on the Å-scale and reveal the organization of the pre-catalyst at the silica interface. A model hydrosilylation reaction demonstrates catalytic activity and retention of the molecular species on the support during turnover. This work establishes non-covalent interface engineering as a viable strategy for structurally defined heterogenized catalysis.
APA:
Bergen, A., Tavera Méndez, C.L., Eichhorn, V., Maier, P., Harrer, E., Scheurer, A.,... Meyer, K. (2026). Non-Covalent Fluorine–Silica Anchoring of a Molecular Platinum(II) bis(NHC) Catalyst: Structure, Interface Control, and Hydrosilylation Activity. Chemistry - A European Journal. https://doi.org/10.1002/chem.71585
MLA:
Bergen, Alexander, et al. "Non-Covalent Fluorine–Silica Anchoring of a Molecular Platinum(II) bis(NHC) Catalyst: Structure, Interface Control, and Hydrosilylation Activity." Chemistry - A European Journal (2026).
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