N‐Heterocyclic Carbene (NHC)‐Stabilized Ru 0 Nanoparticles: In Situ Generation of an Efficient Transfer Hydrogenation Catalyst
Autor: | Ashoka G. Samuelson, Lakshay Kathuria, Noor U. Din Reshi |
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Rok vydání: | 2020 |
Předmět: |
In situ
010405 organic chemistry Organic Chemistry Nanoparticle chemistry.chemical_element General Chemistry 010402 general chemistry Transfer hydrogenation 01 natural sciences Catalysis Nanomaterial-based catalyst 0104 chemical sciences Ruthenium Turnover number chemistry.chemical_compound chemistry Polymer chemistry Carbene |
Zdroj: | Chemistry – A European Journal. 26:7622-7630 |
ISSN: | 1521-3765 0947-6539 |
DOI: | 10.1002/chem.202000142 |
Popis: | Tethered and untethered ruthenium half-sandwich complexes were synthesized and characterized spectroscopically. X-ray crystallographic analysis of three untethered and two tethered Ru N-heterocyclic carbene (NHC) complexes were also carried out. These RuNHC complexes catalyze transfer hydrogenation of aromatic ketones in 2-propanol under reflux, optimally in the presence of (25 mol %) KOH. Under these conditions, the formation of 2-3 nm-sized Ru0 nanoparticles was detected by TEM measurements. A solid-state NMR investigation of the nanoparticles suggested that the NHC ligands were bound to the surface of the Ru nanoparticles (NPs). This base-promoted route to NHC-stabilized ruthenium nanoparticles directly from arene-tethered ruthenium-NHC complexes and from untethered ruthenium-NHC complexes is more convenient than previously known routes to NHC-stabilized Ru nanocatalysts. Similar catalytically active RuNPs were also generated from the reaction of a mixture of [RuCl2 (p-cymene)]2 and the NHC precursor with KOH in isopropanol under reflux. The transfer hydrogenation catalyzed by these NHC-stabilized RuNPs possess a high turnover number. The catalytic efficiency was significantly reduced if nanoparticles were exposed to air or allowed to aggregate and precipitate by cooling the reaction mixtures during the reaction. |
Databáze: | OpenAIRE |
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