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Polysiloxane-encapsulated “Pd”-nanoclusters were generated by reduction of Pd(OAc)2 with polymethylhydrosiloxane, which functions as a reducing agent as well as a capping material for production and stabilization of catalytically active “Pd”-nanoparticles. Chemoselective hydrogenation of functional conjugated alkenes was achieved by in-situ- or ex-situ-generated polysiloxane-stabilized “Pd”- nanoclusters under mild reaction conditions in high yields. Electron microscopy, UV-vis, and NMR studies of the reaction mixture during the catalytic transformation were performed and, in conjunction with catalyst poisoning experiments, demonstrated unequivocally the role of polysiloxane-encapsulated “Pd”-nanoclusters as the real catalytic species. The recyclability of the “Pd”-nanoclusters was established by reusing the solid left after the reaction.

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Reference:
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion