Ligand effect on the catalytic activity of ruthenium nanoparticles in ionic liquids
Suspensions of small sized (1-2.5 nm) ruthenium nanoparticles (RuNPs) have been obtained by decomposition, under H(2), of (η(4)-1,5-cyclooctadiene)(η(6)-1,3,5-cyclooctatriene)ruthenium(0), [Ru(COD)(COT)], in the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, [C(1)C(4)Im]...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2012-12, Vol.41 (45), p.13919-13926 |
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creator | Salas, Gorka Campbell, Paul S Santini, Catherine C Philippot, Karine Costa Gomes, Margarida F Pádua, Agílio A H |
description | Suspensions of small sized (1-2.5 nm) ruthenium nanoparticles (RuNPs) have been obtained by decomposition, under H(2), of (η(4)-1,5-cyclooctadiene)(η(6)-1,3,5-cyclooctatriene)ruthenium(0), [Ru(COD)(COT)], in the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, [C(1)C(4)Im][NTf(2)], and in the presence of different compounds acting as ligands: C(8)H(17)NH(2), PPhH(2), PPh(2)H and H(2)O. Previous and new liquid NMR experiments showed that the ligands are coordinated or in the proximity to the surface of the RuNPs. Herein is reported how the ligand affects the catalytic performance (activity and selectivity) compared to a ligand-free system of RuNPs, when RuNPs in [C(1)C(4)Im][NTf(2)] are used as catalysts for the hydrogenation of various unsaturated compounds (1,3-cyclohexadiene, limonene and styrene). It has been observed that σ-donor ligands increase the activity of the nanoparticles, contrarily to π-acceptor ones. |
doi_str_mv | 10.1039/c2dt31644g |
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Previous and new liquid NMR experiments showed that the ligands are coordinated or in the proximity to the surface of the RuNPs. Herein is reported how the ligand affects the catalytic performance (activity and selectivity) compared to a ligand-free system of RuNPs, when RuNPs in [C(1)C(4)Im][NTf(2)] are used as catalysts for the hydrogenation of various unsaturated compounds (1,3-cyclohexadiene, limonene and styrene). 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Previous and new liquid NMR experiments showed that the ligands are coordinated or in the proximity to the surface of the RuNPs. Herein is reported how the ligand affects the catalytic performance (activity and selectivity) compared to a ligand-free system of RuNPs, when RuNPs in [C(1)C(4)Im][NTf(2)] are used as catalysts for the hydrogenation of various unsaturated compounds (1,3-cyclohexadiene, limonene and styrene). 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Previous and new liquid NMR experiments showed that the ligands are coordinated or in the proximity to the surface of the RuNPs. Herein is reported how the ligand affects the catalytic performance (activity and selectivity) compared to a ligand-free system of RuNPs, when RuNPs in [C(1)C(4)Im][NTf(2)] are used as catalysts for the hydrogenation of various unsaturated compounds (1,3-cyclohexadiene, limonene and styrene). It has been observed that σ-donor ligands increase the activity of the nanoparticles, contrarily to π-acceptor ones.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>23023650</pmid><doi>10.1039/c2dt31644g</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8965-825X</orcidid><orcidid>https://orcid.org/0000-0002-7641-6526</orcidid><orcidid>https://orcid.org/0000-0001-8637-6057</orcidid></addata></record> |
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subjects | Catalysis Catalysts Chemical Sciences Hydrogenation Imidazoles - chemistry Ionic liquids Ionic Liquids - chemistry Ligands Liquids Metal Nanoparticles - chemistry Nanoparticles or physical chemistry Organometallic Compounds - chemistry Ruthenium Ruthenium - chemistry Sulfonamides - chemistry Surface chemistry Theoretical and |
title | Ligand effect on the catalytic activity of ruthenium nanoparticles in ionic liquids |
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