Supraphos:  A Supramolecular Strategy To Prepare Bidentate Ligands

We report a new strategy for the preparation of chelating bidentate ligands, which involves just the mixing of two monodentate ligands functionalized with complementary binding sites. In the current example, the assembly process is based on selective metal−ligand interactions, using phosphite zinc(I...

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Veröffentlicht in:Journal of the American Chemical Society 2004-04, Vol.126 (13), p.4056-4057
Hauptverfasser: Slagt, Vincent F, Röder, Marc, Kamer, Paul C. J, van Leeuwen, Piet W. N. M, Reek, Joost N. H
Format: Artikel
Sprache:eng
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Zusammenfassung:We report a new strategy for the preparation of chelating bidentate ligands, which involves just the mixing of two monodentate ligands functionalized with complementary binding sites. In the current example, the assembly process is based on selective metal−ligand interactions, using phosphite zinc(II) porphyrins 1−6 and the nitrogen donor ligands b−i. From only 16 monodentate ligands, a library of 60 palladium catalysts based on 48 bidentate ligand assemblies has been prepared. The relatively small catalyst library gave a large variety in the selectivity of the alkylation of rac-1,3-diphenyl-2-propenyl acetate. Importantly, small variations in the building blocks lead to large differences in the enantioselectivity imposed by the catalyst (up to 97% ee).
ISSN:0002-7863
1520-5126
DOI:10.1021/ja038955f