• Arene ligands;
  • Hydrides;
  • O ligands;
  • Reactive intermediates;
  • Ruthenium


[RuCl26-arene)(PR3)] complexes react with K2CO3 in the presence of water to afford the carbonatoruthenium(II) derivatives [Ru(η2-O2CO)(η6-arene)(PR3)] (2; arene = p-cymene, R = Cy, Ph, or Me; arene = hexamethylbenzene, R = Me) involving a planar Ru(η2-O2CO) moiety as shown by X-ray crystal structure determination of 2a (p-cymene, PCy3) and 2d (hexamethylbenzene, PMe3). The complex [Ru(η2-O2CO)(p-cymene)(PCy3)] is cleanly converted in hot methanol into the dihydride [RuH2(p-cymene)(PCy3)]. The related complexes [Ru(η2-O2CO)(η6-arene)(IMes)] [arene = p-cymene or hexamethylbenzene, IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene] are straightforwardly prepared by treating [RuCl26-arene)]2 precursors with 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride and K2CO3 in THF at reflux. The removal of the carbonato ligand from complexes 2 with HBF4 in the presence of acetonitrile leads to the dicationic derivatives [Ru(η6-arene)(L)(MeCN)2][BF4]2 (L = PR3 or IMes). (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)