Alkyl Complexes of Lanthanum and Samarium Supported by a Chiral Binaphthylamido Ligand. Syntheses, Structures, and Catalytic Activity in Hydroamination of Amino-1,3-dienes
2011; American Chemical Society; Volume: 30; Issue: 12 Linguagem: Inglês
10.1021/om2002624
ISSN1520-6041
AutoresIsabelle Aillaud, Clarisse Olier, Yulia Chapurina, Jacqueline Collin, Emmanuelle Schulz, Régis Guillot, Jérôme Hannedouche, Alexander A. Trifonov,
Tópico(s)Asymmetric Hydrogenation and Catalysis
ResumoThe reactions of (R)-(+)-2,2′-bis(cyclopentylamino)-1,1′-binaphthyldiamine with [Li(THF)n]3[LnMe6] (Ln = La, Sm) in THF at 0 °C depending on the metal ion size result in the formation of trinuclear [(R)-C20H12(NC5H9)2]Sm[(μ-Me)2Li(THF)2(μ-Me)Li(THF)] (1) or tetranuclear [(R)-C20H12(NC5H9)2]La{(μ-Me)2Li(THF)[(μ-Me)Li(THF)]2} (2) complexes with methyl ligands μ-bridging lanthanide and lithium atoms. The structures of complexes 1 and 2 were established by single-crystal X-ray diffraction and solution NMR studies. These new complexes were evaluated as catalysts to promote the enantioselective hydroamination of amino-1,3-dienes.
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