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Ruthenium(II) complexes of optically active P, N donor ligands. Synthesis and evaluation in the catalytic hydrogenation of acetophenone

✍ Scribed by Hong Yang; Noël Lugan; René Mathieu


Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
603 KB
Volume
2
Category
Article
ISSN
1387-1609

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✦ Synopsis


The reaction of 2 equiv of the optically active P, N bidentate ligands l-3 with RuC1,(PPh,)3 gives the RuCl,(l-3)2 (4-6) complexes in good yield as a mixture of isomers. The solid state structure of RuC1,( 2), (SC) is described: the two chlorine atoms are in tram position and due to steric crowding, one of the two ligands 2 is more weakly bound to Ru. The complexes 4-6 show moderate to good catalytic activity for the hydrogenation of acetophenone in basic media in hydrogen transfer conditions, from propanol-2, or under dihydrogen, but the enantiomeric excesses are low. 0 Acadtmie des sciences/Elsevier, Paris


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## Abstract Achiral P‐donor pincer‐aryl ruthenium complexes ([RuCl(PCP)(PPh~3~)]) 4c,d were synthesized __via__ transcyclometalation reactions by mixing equivalent amounts of [1,3‐phenylenebis(methylene)]bis[diisopropylphosphine] (2c) or [1,3‐phenylenebis(methylene)]bis[diphenylphosphine] (2d) and