Influence of the cone angles and the π-acceptor properties of phosphorus-containing ligands in the chemistry of dihydrogen complexes of ruthenium

A series of new dicationic dihydrogen complexes of ruthenium of the type trans-[(dppe)(2)Ru(eta (2)-Hz)(L')][BF4](2) (dppe = Ph2PCH2CH2PPh2; L' = PF(OMe2, PF(OEt)(2), PF((OPr)-Pr-i)(2)) have been prepared by protonating the precursor hydride complexes trans-[(dppe)(2)Ru(H)(L')][BF4] using HBF4. Et2O. The precursor hydride complexes have been obtained from trans-[(dppe)(2)Ru(H)(L')][BF4] (L = P(OMe)(3)), P(OEt)(3), P((OPr)-Pr-i)(3)) via the substitution of a -OR group on the trans phosphorus ligand with a fluoride in the presence of HBF4. Et2O. Coupling of the dihydrogen ligand with the trans phosphorus moiety has been observed. In addition to the complexes bearing trans phosphite groups, the precursor hydrides containing trans phosphine ligands, viz., PMe3 and PMe2Ph, have also been prepared and characterized. It was found that the binding ability of the trans phosphorus ligand in both the hydride and dihydrogen complexes decreases with an increase in the steric congestion of the trans phosphorus moiety. This indicates that the stability of this series of complexes depends on the cone angles of the trans phosphorus ligand. The protonation reactions of the hydride precursors trans[(dppe)(2)Ru(H)(L)][BF4] (L = P(OMe)(3), P(OEt)(3), P((OPr)-Pr-i)(3)) (under certain experimental conditions in the case of P((OPr)-Pr-i)(3)) result in mixtures of the new hydride complexes trans[(dppe)(2)Ru(H)(L')][BF4] (L' = PF(OMe)(2), PF(OEt)(2), PF((OPr)-Pr-i)(2)) and the trans-[(dppe)(2)Ru(eta (2)-H-2)(L')][BF4](2) derivatives. There is a strong dependence on the quantity of the acid used for the isolation of either the new hydrides or the corresponding dihydrogen complexes. Both dihydrogen and the new hydride complexes have been isolated and characterized. On the other hand, the protonation reactions of the starting hydrides that have trans-PMe3, PMe2Ph, or P((OR)-R-i)(3) (under certain experimental conditions) ligands gave a hydride dihydrogen complex, the structure formulation of which could not be established with certainty. The roles of the steric as well as the pi -accepting properties of the trans phosphorus ligands in this series of complexes are discussed. X-ray crystal structures of trans-[(dppe)(2)Ru(H)(P(OMe)(3))][BF4], trans-[(dppe)(2)Ru(H)(PF(OMe)(2))][BF4], and trans-[(dppe)(2)Ru(eta (2)-H-2)(PF-(OEt)(2))][BF4](2) have been determined. trans-[(dppe)(2)Ru(H)(L)][BF4] (L = PMe3, PMe2Ph, P((OPr)-Pr-i)(3)) undergoes substitution of the trans phosphorus ligand with Hz to give trans-[(dppe)(2)Ru(H)(eta (2)-H-2)][BF4] reversibly under very mild conditions.