Ruthenium Complexes Stabilized by Bidentate Enamido-Phosphine Ligands: Aspects of Cooperative H2 Activation

Four bidentate, hybrid ligands (R(NP)R′H) featuring imine-nitrogen and alkyl-phosphine donors linked by a cyclopentyl ring were synthesized. The ortho position of the aryl group attached to nitrogen is varied such that R is Me or Pri; additionally, the groups decorating phosphorus (R′) are varied between But or Pri. The addition of each ligand to RuHCl­(PPri3)2(CO) in the presence of KOBut generates four enamido-phosphine complexes RuH­{R(NP)R′}­(PPri3)­(CO) that were characterized by NMR spectroscopy, elemental analyses, and, in the case of R = Pri and R′ = But or Pri, X-ray crystallography. Depending on R′, the reaction of RuH­{R(NP)R′}­(PPri3)­(CO) with H2 generates varying amounts of the imine-phosphine complex RuH2{R(NP)R′H}­(PPri3)­(CO). Insights into the mechanism of H2 activation by these enamido derivatives were explored using RuH­{Pr(NP)Pri}­(PPri3)­(CO), for which an intermediate was identified as the dihydrogen–dihydride complex, RuH2(H2)­{Pri(NP)PriH}­(PPri3)­(CO), on the basis of the T1,min value of 22 ms for the 1H NMR resonance at δ −7.2 at 238 K (measured at 400 MHz). The N donor of the enamine tautomeric form of the ligand is protonated by H2 or D2 and dissociates from Ru. Tautomerization of the enamine to the imine form of the dissociated arm is involved in formation of the final product.