http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16684
Amino-phosphanes in RhI-Catalyzed Hydroformylation: Hemilabile Behavior of P,N Ligands under High CO Pressure and Catalytic Properties (Articolo in rivista)
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- Label
- Amino-phosphanes in RhI-Catalyzed Hydroformylation: Hemilabile Behavior of P,N Ligands under High CO Pressure and Catalytic Properties (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Alternative label
Andrieu, Jacques; Camus, Jean-Michel; Richard, Philippe; Poli, Rinaldo; Gonsalvi, Luca; Vizza, Francesco; Peruzzini, Maurizio (2006)
Amino-phosphanes in RhI-Catalyzed Hydroformylation: Hemilabile Behavior of P,N Ligands under High CO Pressure and Catalytic Properties
in European journal of inorganic chemistry (Print)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Andrieu, Jacques; Camus, Jean-Michel; Richard, Philippe; Poli, Rinaldo; Gonsalvi, Luca; Vizza, Francesco; Peruzzini, Maurizio (literal)
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- Pagina fine
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- ICCOM-CNR
CNRS Dijon, France (literal)
- Titolo
- Amino-phosphanes in RhI-Catalyzed Hydroformylation: Hemilabile Behavior of P,N Ligands under High CO Pressure and Catalytic Properties (literal)
- Abstract
- The catalytic properties of rhodium complexes containing the ?-, ?-, or ?-amino-phosphane ligands Ph2PCH2NEt2 (?-P,N-
1), Ph2PCH(Ar)NHPh [?-P,N-2; Ar = ?6(o-C6H4Cl)Cr(CO)3], Ph2PCH2NPh2 (?-P,N-3), Ph2PCH2CH(Ph)NHPh (?-P,N), Ph2PCH2(o-C6H4-NMe2) (?-P,N-1), Ph2PCH(o-C6H4-CH2NHPh) (?-P,N-2), and the ?,?-diamino-phosphane ligand Et2NCH2P(Ph)CH2CH(Ph)NHPh (?,?-N,P,N), in styrene hydroformylation have been examined. The results show that the activity increases when the number of backbone carbon atoms linking P and N decreases from 3 to 1. IR and 31P HPNMR studies in solution show that all P,N ligands adopt exclusively a k1-P coordination mode in rhodium chloride carbonyl complexes under high CO pressure. In the solid state a ?1-P-?-amino-phosphane coordination has been ascertained by X-ray methods in trans-[RhCl(CO)(?-P,N-1)2]. In
contrast, an equilibrium between the ?2-P,N and ?1-P-coordination modes has been observed as a function of the CO pressure for the complex containing the ?-P,N ligand. The basicity of the dangling amino group also plays an important role on the catalytic activity and a mechanism involving the nitrogen function in the catalytic cycle is proposed. (literal)
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