Synthesis and Characterization of OsH2Cl[k-N,k-O(ON=CR2)](PiPr3)2 [CR2 = C(CH2)4CH2, R = CH3]: Influence of the L2 Ligand on the Nature of the H2 Unit in OsH2ClL2(PiPr3)2 [L2 = ON=CR2, NH=C(Ph)C6H4] Complexes
Autores: Ricardo Castarlenas, Miguel A. Esteruelas, Enrique Gutiérrez-Puebla, Yves Jean, Agustí Lledós, Marta Martín y Jaume Tomás
Ref. revista: Organometallics, 18, 4296-4303, (1999)
The dihydride-dichloro complex OsH2Cl2(PiPr3)2 (1) reacts with cyclohexanone oxime and acetone oxime in the presence of Et3N to give the dihydride derivatives OsH2Cl{k-N,k-O-[ONdC(CH2)4CH2]}(PiPr3)2 (2) and OsH2Cl{k-N,k-O-[ONdC(CH3)2]}(PiPr3)2 (3), respectively. The structure of 2 has been determined by X-ray diffraction. The geometry around the osmium atom can be described as a distorted pentagonal bipyramid, with the triisopropylphosphine ligands occupying two relative trans positions. The remaining perpendicular plane is formed by the hydride ligands, the chlorine, and the oximate group, which acts with a bite angle of 36.6(1)°. In solution the hydride ligands of 2 and 3 undergo an intramolecular thermally activated site exchange process. The activation parameters of this process are ¢Hq ) 11.9((0.7) kcal mol-1 and ¢Sq ) -0.5((1.4) cal mol-1 K-1 for 2 and ¢Hq) 11.7((0.8) kcal mol-1 and ¢Sq ) -0.8((2.0) cal mol-1 K-1 for 3. To understand why complexes 2 and 3 are dihyride derivatives, while the previously reported complex OsCl-{NHdC(Ph)C6H4}(è2-H2)(PiPr3)2 is an elongated dihydrogen compound, a quantitative theoretical analysis of the interaction between the H2 moiety and the OsClL2(PH3)2(L2)
ONdCH2, NHdCHCHdCH) complex fragments, along the oxidative addition pathway, is also reported.
The dihydride-dichloro complex OsH2Cl2(PiPr3)2 (1) reacts with cyclohexanone oxime and acetone oxime in the presence of Et3N to give the dihydride derivatives OsH2Cl{k-N,k-O-[ONdC(CH2)4CH2]}(PiPr3)2 (2) and OsH2Cl{k-N,k-O-[ONdC(CH3)2]}(PiPr3)2 (3), respectively. The structure of 2 has been determined by X-ray diffraction. The geometry around the osmium atom can be described as a distorted pentagonal bipyramid, with the triisopropylphosphine ligands occupying two relative trans positions. The remaining perpendicular plane is formed by the hydride ligands, the chlorine, and the oximate group, which acts with a bite angle of 36.6(1)°. In solution the hydride ligands of 2 and 3 undergo an intramolecular thermally activated site exchange process. The activation parameters of this process are ¢Hq ) 11.9((0.7) kcal mol-1 and ¢Sq ) -0.5((1.4) cal mol-1 K-1 for 2 and ¢Hq) 11.7((0.8) kcal mol-1 and ¢Sq ) -0.8((2.0) cal mol-1 K-1 for 3. To understand why complexes 2 and 3 are dihyride derivatives, while the previously reported complex OsCl-{NHdC(Ph)C6H4}(è2-H2)(PiPr3)2 is an elongated dihydrogen compound, a quantitative theoretical analysis of the interaction between the H2 moiety and the OsClL2(PH3)2(L2)
ONdCH2, NHdCHCHdCH) complex fragments, along the oxidative addition pathway, is also reported.