Aluminum complexes incorporating bidentate amido phosphine ligands.

A series of aluminum complexes supported by o-phenylene-derived amido phosphine ligands, N-(2-diphenylphosphinophenyl)-2,6-dimethylanilide ([Me-NP]-) and N-(2-diphenylphosphinophenyl)-2,6-diisopropylanilide ([iPr-NP]-), have been prepared. The reactions of trialkylaluminum with H[Me-NP] and H[iPr-NP], respectively, in refluxing toluene produced the corresponding dialkyl complexes [Me-NP]AlR(2) and [iPr-NP]AlR(2) (R = Me, Et). Deprotonation of H[Me-NP] with n-BuLi in THF at -35 degrees C followed by addition of AlCl(3) in toluene at -35 degrees C afforded [Me-NP]AlCl(2), which was subsequently reacted with 2 equiv of trimethylsilylmethyllithium in toluene to give [Me-NP]Al(CH(2)SiMe(3))(2). The aluminum complexes were all characterized by (1)H, (13)C, (31)P, and (27)Al NMR spectroscopy. The solid-state structures of monomeric, four-coordinate [Me-NP]AlEt(2) and [iPr-NP]AlMe(2) and five-coordinate [Me-NP]AlCl(2)(THF) were determined by X-ray crystallography. The (1)H NMR studies of [Me-NP]AlEt(2), [Me-NP]Al(CH(2)SiMe(3))(2), and [iPr-NP]AlEt(2) indicate diastereotopic alpha-hydrogen atoms in these molecules. Heteronuclear COSY and NOE experiments suggest that the phosphorus donor in [Me-NP]Al(CH(2)SiMe(3))(2) and [iPr-NP]AlEt(2) is coupled to only one of the diastereotopic alpha-hydrogen atoms that is virtually antiperiplanar with respect to the phosphorus atom.