Sulfonamido−phosphoramidite ligands in cooperative dinuclear hydrogenation catalysis

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2009

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Patureau, F.W.
de Boer, Sandra
Kuil, M.
Meeuwissen, J.
Breuil, P.-A.R.
Siegler, Maxime A.ISNI 0000000396450817
Spek, A.L.ISNI 0000000389231413
de Bruin, B.
Reek, J.N.H.

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Abstract

Sulfonamido−phosphoramidite ligands lead to the formation of Rh−Rh dinuclear complexes through the anionic P−N− bridging character. The resulting “boat-shaped” dinuclear catalysts activate molecular H2 through a cooperative dinuclear endocyclic mechanism, resulting in one bridging and one classical hydride on the dinuclear complex. These new complexes are very active hydrogenation catalysts that operate via a new cooperative hydrogenation activation mechanism, as calculated with density functional theory, and they display unequaled high selectivities in the hydrogenation of hindered cyclic acetamidoalkenes.

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Patureau, F W, de Boer, S, Kuil, M, Meeuwissen, J, Breuil, P-AR, Siegler, M A M, Spek, A L, de Bruin, B & Reek, J N H 2009, 'Sulfonamido−phosphoramidite ligands in cooperative dinuclear hydrogenation catalysis', Journal of the American Chemical Society, vol. 131, no. 19, pp. 6683-6685.