New Anionic Rhodium Complexes as Efficient Hydroboration and Hydrosilylation Catalysts

This paper presents the synthesis and characterization of anionic rhodium(I) complexes obtained by the reaction of a homogeneous Wilkinson catalyst or a rhodium cyclooctadiene dimer with ionic liquids as precursors. All newly produced complexes were characterized spectroscopically (NMR, ESI-MS, FT-IR) and their thermal stability was examined (TGA, melting point). Moreover, their catalytic activity was determined in the hydrosilylation of octene or allyl glycidyl ether with 1,1,1,3,3,5-heptamethyltrisiloxane and in the hydroboration reaction of styrene with pinacolborane (HBpin). All catalysts used were insoluble in the reactants, which allowed for their isolation and repeated use. Their activity was compared in subsequent 10 (hydrosilylation) or 5 (hydroboration) catalytic cycles. The obtained results allowed the selection of the most effective catalytic systems, which can be a real alternative to traditional homogeneous catalysts, offering greater ease of recovery and reuse.

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Publication Details

Journal
Catalysts
Published
2025-12-23
DOI
https://doi.org/10.3390/catal16010012
Primary Topic
Organoboron and organosilicon chemistry
Type
article
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article

New Anionic Rhodium Complexes as Efficient Hydroboration and Hydrosilylation Catalysts

Izabela Dąbek, Hieronim Maciejewski, Anna Schulmann, Karol Szubert et al.
Catalysts
Organoboron and organosilicon chemistry
article

New Anionic Rhodium Complexes as Efficient Hydroboration and Hydrosilylation Catalysts

Izabela Dąbek, Hieronim Maciejewski, Anna Schulmann, Karol Szubert, Błażej Rubiś, Magdalena Jankowska-Wajda
article en

Abstract

This paper presents the synthesis and characterization of anionic rhodium(I) complexes obtained by the reaction of a homogeneous Wilkinson catalyst or a rhodium cyclooctadiene dimer with ionic liquids as precursors. All newly produced complexes were characterized spectroscopically (NMR, ESI-MS, FT-IR) and their thermal stability was examined (TGA, melting point). Moreover, their catalytic activity was determined in the hydrosilylation of octene or allyl glycidyl ether with 1,1,1,3,3,5-heptamethyltrisiloxane and in the hydroboration reaction of styrene with pinacolborane (HBpin). All catalysts used were insoluble in the reactants, which allowed for their isolation and repeated use. Their activity was compared in subsequent 10 (hydrosilylation) or 5 (hydroboration) catalytic cycles. The obtained results allowed the selection of the most effective catalytic systems, which can be a real alternative to traditional homogeneous catalysts, offering greater ease of recovery and reuse.

CatalystsVol. 16(1)
Poznan University of Medical Sciences (PL), Adam Mickiewicz University in Poznań (PL)
Clean water and sanitation
Openalex Percentile: Top 33%
Organoboron and organosilicon chemistry
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