Neutral and cationic alkylmanganese(II) complexes containing 2,6-bisiminopyridine ligands

Manganese alkyl complexes stabilised by 2,6-bis(N,N'-2,6-diisopropyl-phenyl)acetaldiminopyridine ((iPr)BIP) have been selectively prepared by reacting suitable alkylmanganese(II) precursors, such as homoleptic dialkyls (MnR(2))(n)] or the corresponding THF adducts {MnR(2)(thf)}(2)] with the mentioned ligand. For R=CH(2)CMe(2)Ph or CH(2)Ph, formally Mn(I) derivatives are produced, in which one of the two R groups migrates to the 4-position of the central pyridine ring in the (iPr)BIP ligand. In contrast, a true dialkyl complex MnR(2)((iPr)BIP)] can be isolated for R=CH(2)SiMe(3). In solution, this compound slowly evolves to the corresponding Mn(I) monoalkyl derivative. A detailed study of this reaction provides insights on its mechanism, showing that it proceeds through successive alkyl migrations, followed by spontaneous dehydrogenation. Protonation of Mn(CH(2)SiMe(3))(2)((iPr)BIP)] with the pyridinium salt H(Py)(2)]BAr'(4)] (Ar'=3,5-C(6)H(3)(CF(3))(2)) leads to the cationic species Mn(CH(2)SiMe(3))(Py)((iPr)BIP)](+). Alternatively, the same complex can be produced by reaction of the pyridine complex {Mn(CH(2)SiMe(3))(2)(Py)}(2)] with the protonated ligand salt H(iPr)BIP](+)BAr'(4)](-). This last reaction allows the synthesis of analogous cationic alkylmanganese(II) derivatives, when precursors of type MnR(2)((iPr)BIP)] are not available. Treatment of these neutral and cationic (iPr)BIP alkylmanganese derivatives with a range of typical co-catalysts (modified methylaluminoxane (MMAO), B(C(6)F(5))(3), trimethyl or triisobutylaluminum) does not lead to active ethylene polymerisation catalysts.