A p-styrenyl substituent attached to the ligand framework allows the diphosphine moiety −(C6H4)CH2OCH2C(CH3)(CH2PPh2)2 to be introduced as a pendant group in cross-linked styrene/divinylbenzene matrixes via free-radical copolymerization. In conjunction with rhodium(I), the POLYDIPHOS material forms an effective heterogeneous catalyst for the hydrogenation of benzylideneacetone to benzylacetone and of quinoline to a mixture of 1,2,3,4-tetrahydroquinoline, 5,6,7,8-tetrahydroquinoline, and decahydroquinoline. The homogeneous behavior of related 1,3-bis(diphenylphosphino)propane rhodium complexes is different in both activity and selectivity.
Synthesis of Polymer-Supported Rhodium(I)-1,3-Bis(diphenylphosphino)propane Mojeties and Their Use in the Heterogeneous Hydrogenation of Quinoline and Benzylideneacetone / C. BIANCHINI; M. FREDIANI; G. MANTOVANI; F. VIZZA. - In: ORGANOMETALLICS. - ISSN 0276-7333. - STAMPA. - 20:(2001), pp. 2660-2662. [10.1021/om0010868]
Synthesis of Polymer-Supported Rhodium(I)-1,3-Bis(diphenylphosphino)propane Mojeties and Their Use in the Heterogeneous Hydrogenation of Quinoline and Benzylideneacetone
FREDIANI, MARCO;
2001
Abstract
A p-styrenyl substituent attached to the ligand framework allows the diphosphine moiety −(C6H4)CH2OCH2C(CH3)(CH2PPh2)2 to be introduced as a pendant group in cross-linked styrene/divinylbenzene matrixes via free-radical copolymerization. In conjunction with rhodium(I), the POLYDIPHOS material forms an effective heterogeneous catalyst for the hydrogenation of benzylideneacetone to benzylacetone and of quinoline to a mixture of 1,2,3,4-tetrahydroquinoline, 5,6,7,8-tetrahydroquinoline, and decahydroquinoline. The homogeneous behavior of related 1,3-bis(diphenylphosphino)propane rhodium complexes is different in both activity and selectivity.File | Dimensione | Formato | |
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