One‐Pot Synthesis of Rh Nanoparticles in Polycationic‐Shell, Triphenylphosphine Oxide‐Functionalized Core‐Crosslinked Micelles for Aqueous Biphasic Hydrogenation

Cationic‐shell core‐crosslinked micelles (CCM−C) with rhodium nanoparticles (RhNPs) anchored to core‐linked triphenylphosphine oxide (TPPO) ligands were synthesized by a facile one‐pot approach by the reduction of [Rh(COD)(μ‐Cl)]2/toluene in the presence of an aqueous TPPO@CCM−C latex. The resulting...

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Bibliographic Details
Published inChemCatChem Vol. 16; no. 15
Main Authors Abou‐Fayssal, Chantal J., Schill, Leonhard, Poli, Rinaldo, Manoury, Eric, Philippot, Karine, Riisager, Anders
Format Journal Article
LanguageEnglish
Published 12.08.2024
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Summary:Cationic‐shell core‐crosslinked micelles (CCM−C) with rhodium nanoparticles (RhNPs) anchored to core‐linked triphenylphosphine oxide (TPPO) ligands were synthesized by a facile one‐pot approach by the reduction of [Rh(COD)(μ‐Cl)]2/toluene in the presence of an aqueous TPPO@CCM−C latex. The resulting RhNP‐TPPO@CCM−C latex showed to be performant for the aqueous biphasic hydrogenation of styrene with an average corrected turnover frequency (cTOF) up to 23600 h−1 based on the RhNP surface atoms. The catalyst system also proved reusable in multiple catalytic runs without any visible RhNP loss during the recycling process as well as applicable to the hydrogenation of other selected alkenes, alkynes and carbonyl substrates (average cTOF of 1000–3200 h−1), thus demonstrating a high versatility. Polymeric nanoreactors consisting of core‐crosslinked micelles with Rh nanoparticles (RhNPs) anchored to core‐linked triphenylphosphine oxide (TPPO) ligands are active, selective, and reusable catalysts for the aqueous biphasic hydrogenation of styrene. The nanoreactors also prove applicable to the selective hydrogenation of other selected unsaturated substrates, including alkynes and carbonyls.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.202400189