Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties
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Otros documentos de la autoría: Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitry; Peris, Eduardo
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/141972
comunitat-uji-handle4:10234/141976
INVESTIGACIONMetadatos
Título
Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic propertiesAutoría
Fecha de publicación
2015-06Editor
Royal Society of ChemistryISSN
2052-4110Cita bibliográfica
Mejuto, C., García-Eleno, M. A., Guisado-Barrios, G., Spasyuk, D., Gusev, D., & Peris, E. (2015). Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties. Organic Chemistry Frontiers, 2(8), 936-941.Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
http://pubs.rsc.org/en/content/articlehtml/2015/qo/c5qo00137dPalabras clave / Materias
Efficient hydrogenation | Bond activation | Chiral alcohols | Esters | Mild | Co2 | Reduction | Oxidation | Methanol | Ketones
Resumen
1-Methyl-3-(2-((pyridin-2-ylmethylene)amino)ethyl)-1H-imidazol-3-ium bromide was prepared and used as an N-heterocyclic carbene NNC-pincer ligand precursor. Depending on the coordination strategy, a monometallic ... [+]
1-Methyl-3-(2-((pyridin-2-ylmethylene)amino)ethyl)-1H-imidazol-3-ium bromide was prepared and used as an N-heterocyclic carbene NNC-pincer ligand precursor. Depending on the coordination strategy, a monometallic [Ru(NNC)(CO3)(PPh3)] complex, or the [Ru(μ-Cl)(NNC)]2(2Cl−) dimer, was obtained. A di-silver complex in which two ligands are monocoordinated to the metal center through the NHC groups was also obtained and characterised. The dimetallic ruthenium complex reacts with alcohols yielding a monohydride species. The preliminary studies on the catalytic activity of the ruthenium dimer indicate that the complex is active in the reduction of ketones and aldehydes under transfer hydrogenation conditions. [-]
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Organic Chemistry Frontiers, 2(8), 2015Derechos de acceso
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Reproduced by permission of The Royal Society of Chemistry
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