Two confining phosphane ligands derived from either a- or b-cyclodextrin produce singly PIII-ligated metal complexes with unusual coordination spheres. High-pressure NMR studies have revealed that rhodium hydride complexes of the same type are also formed under hydroformylation conditions. This unique feature strongly favors the formation of the branched aldehyde at the expense of the linear one with high enantioselectivity in the rhodium-catalyzed hydroformylation of styrene

Confining Phosphanes Derived from Cyclodextrins for Efficient Regio-and Enantioselective Hydroformylation

Oberhauser Werner;
2014

Abstract

Two confining phosphane ligands derived from either a- or b-cyclodextrin produce singly PIII-ligated metal complexes with unusual coordination spheres. High-pressure NMR studies have revealed that rhodium hydride complexes of the same type are also formed under hydroformylation conditions. This unique feature strongly favors the formation of the branched aldehyde at the expense of the linear one with high enantioselectivity in the rhodium-catalyzed hydroformylation of styrene
2014
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Hydroformylation
phosphanes
cyclodextrins
enantioselectivity
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/263892
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