[RuCl2(dcypb)(CO)](2) 2 (dcypb = 1,4-bis(dicyclohexylphosphino)butane) was prepared in high yield via phosphine exchange between dcypb and RuCl2(CO)(PPh3)(2)(DMF) (1). Reaction of 2 with 8 equiv of (KBHBu3)-Bu-s affords [fac-RuH3(CO)(dcypb)](-) (3), stabilized by interactions with a K+ counterion and an intact (KBHBu3)-Bu-s molecule in the third coordination sphere. Substantial ion pairing accounts for the stability and high hydrocarbon solubility of 3. Complex 3 effects reduction of benzophenone under unprecedentedly mild conditions, at 1 atm of H-2 in refluxing 2-propanol. It is also active for ortho, functionalization of benzophenone under 20 atm of ethylene. Stoichiometric experiments reveal facile formation of orthometalated RuH(CO)[OC(C6H4)(Ph)](dcypb) (5), an intermediate proposed in both types of catalysis. The catalytic activity of isolated 5 supports this hypothesis in the case of hydrogenation but not of Murai catalysis. The X-ray crystal structures of 3 and 5 are reported.
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