The optically pure Rh(I)-diphosphine complexes [((R)-(R)-BDPBzPSO3)Rh(nbd)] (1), [((+)-DIOP)Rh(nbd)]OTf (2), and [((S)-BINAP)Rh(nbd)]OTf (3) have been tethered to silica via hydrogen-bonding interaction of isolated silanols with a sulphonate group in either the chiral ligand or the counteranion. A preliminary study of the potential of the resulting supported hydrogen-bonded (SHB) catalysts in the heterogeneous enantioselective hydrogenation of prochiral olefins is reported.

Immobilization of optically active rhodium-diphosphine complexes on porous silica via hydrogen bonding

GOBETTO, Roberto;
2001-01-01

Abstract

The optically pure Rh(I)-diphosphine complexes [((R)-(R)-BDPBzPSO3)Rh(nbd)] (1), [((+)-DIOP)Rh(nbd)]OTf (2), and [((S)-BINAP)Rh(nbd)]OTf (3) have been tethered to silica via hydrogen-bonding interaction of isolated silanols with a sulphonate group in either the chiral ligand or the counteranion. A preliminary study of the potential of the resulting supported hydrogen-bonded (SHB) catalysts in the heterogeneous enantioselective hydrogenation of prochiral olefins is reported.
2001
343
41
45
asymmetric catalysis; heterogeneous catalysis; tethered chiral diphosphines; hydrogen-bonded catalysts; olefin hydrogenation
Bianchini, C; Barbaro, P; DAL SANTO, V; Gobetto, Roberto; Meli, A; Oberhauser, W; Psaro, R; Vizza, F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/25213
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