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Unité de recherche
COST
Numéro de projet
C07.0117
Titre du projet
Homogeneous hydrogenation catalysts comprising tunable carbene ligands
Titre du projet anglais
Homogeneous hydrogenation catalysts comprising tunable carbene ligands

Textes relatifs à ce projet

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Description succincte
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Partenaires et organisations internationales
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Résumé des résultats (Abstract)
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Références bases de données
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Textes saisis


CatégorieTexte
Mots-clé
(Anglais)
Hydrogenation; late transition metals; N-heterocyclic carbenes; ligand tuning; enantioselectivity; non-classical binding modes; planar asymmetry
Programme de recherche
(Anglais)
COST-Action D40 - Innovative Catalysis: New Processes and Selectivities
Description succincte
(Anglais)
Classical and nonclassical carbene-pyridine C,N coordinating ligand systems, both developed previously in our laboratories, will be functionalized by anellation of metallocenes. This approach offers outstanding opportunities to tune the pielectron density at the ligand and hence also at the metal center, which will have a pronounced effect on metal-mediated hydrogenation catalysis: 1) Activity: the new degree of pi-tunability through the metallocene provides a new methodology to optimize oxidative H–H activation at the metal center and reductive R3C–H elimination, both key steps of the catalytic hydrogenation cycle. 2) Selectivity: the anellated metallocene induced planar asymmetry. This will be exploited in enantioselective hydrogen transfer reactions and also in direct hydrogenation in close cooperation with Prof. Gladiali. At a later stage, this approach will be extended to different reactions such as (asymmetric) C–C bond formation in collaboration with Prof. Claver.
Partenaires et organisations internationales
(Anglais)
AT, BE, CH, DE, DK, ES, FI, FR, GR, HU, IE, IT, LT, MT, NL, PL, PT, RO, SE, SI, SK, TR, UK
Résumé des résultats (Abstract)
(Anglais)
Classical and nonclassical carbene-pyridine C,N coordinating ligand systems, both developed previously in our laboratories, will be functionalized by anellation of metallocenes. This approach offers outstanding opportunities to tune the pielectron density at the ligand and hence also at the metal center, which will have a pronounced effect on metal-mediated hydrogenation catalysis: 1) Activity: the new degree of pi-tunability through the metallocene provides a new methodology to optimize oxidative H–H activation at the metal center and reductive R3C–H elimination, both key steps of the catalytic hydrogenation cycle. 2) Selectivity: the anellated metallocene induced planar asymmetry. This will be exploited in enantioselective hydrogen transfer reactions and also in direct hydrogenation in close cooperation with Prof. Gladiali.
Références bases de données
(Anglais)
Swiss Database: COST-DB of the State Secretariat for Education and Research Hallwylstrasse 4 CH-3003 Berne, Switzerland Tel. +41 31 322 74 82 Swiss Project-Number: C07.0117