ABSTRACT
The reaction of TpRu(CO)(PPh(3))(OTf) (2) with LiNHPh affords the amido complex TpRu(CO)(PPh(3))(NHPh) (3) in 88% isolated yield. The amido complex 3 has been characterized by (1)H NMR, (13)C NMR, (31)P NMR, elemental analysis, cyclic voltammetry, and a solid-state X-ray diffraction study. Variable temperature NMR studies have revealed a rotational barrier around the ruthenium-amido nitrogen bond of 3 of 12 kcal/mol (transformation of the major isomer to the minor isomer). The solid-state structure of 3 discloses a pyramidal amido moiety. Heating benzene solutions of the amido complex 3 and 1,4-cyclohexadiene or 9,10-dihydroanthracene results in no observable reaction. Reaction of complex 2 with excess aniline yields [TpRu(CO)(PPh(3))(NH(2)Ph)][OTf] (4).
ABSTRACT
The mechanisms for the interconversion of facial diastereomers of a variety of TpRe(CO)(L)(eta(2)-L(Ar)) complexes [L = (t)BuNC, pyridine (py), PMe(3), or 1-methylimidazole (MeIm); L(Ar) = benzene, anisole, naphthalene, 1-methylpyrrole, furan, or thiophene; Tp = hydridotris(pyrazolyl)borate] have been investigated by (1)H NMR spin saturation experiments. In addition, the rates and free energies of activation for these processes were calculated from spin saturation experiments and T(1) measurements. The operative mechanisms for interconversion of the pi diastereomers were found to be nondissociative, undergoing either an interfacial or intrafacial linkage isomerization. A comparison of the kinetic parameters for isomerization of related eta(2)-olefin complexes of the [TpRe(CO)(PMe(3))] and [CpRe(NO)(PPh(3))](+) fragments is also presented.
