Magnesium aryloxides: synthesis, structure, solution behavior and magnesiate ion formation

Abstract

The heteroleptic magnesium complexes [{Ar′OMgBu}2] 1 and [{Ar′OMgN(i-Pr)2}2] 2, where OAr′ = 2,6-di-tert-butylphenoxy, have been prepared and found to be dimeric in the solid state, with tri-coordinate metal centers. Complex 1 utilizes the aryloxide anions as bridging groups whereas the amido anions connect the metals in 2. Addition of THF or TMEDA to hydrocarbon solutions containing 2 results in disproportionation and the exclusive precipitation of the homoleptic, solvated, complexes [Mg(OAr′)2·2THF] 3 or [Mg(OAr′)2·TMEDA] 4. Both 3 and 4 are monomeric in the solid state with tetra-coordinate magnesium centers. Solution NMR spectroscopic studies of 1 and 2 reveal that disproportionation to the homoleptic complexes is promoted in THF-d8 but that the main component still appears to be the heteroleptic species. Dissolution of the unsolvated dimeric complex [Mg(OAr′)2] 5 in THF-d8 results in partial formation of the magnesiate complex [Ar′OMg]+[(Ar′O)3Mg]−10, along with the monomer 3. In contrast, no magnesiate is formed on dissolution of 3 in THF-d8, indicating that magnesiate formation most likely proceeds via unsymmetrical cleavage of the dimer. Ab initio calculations (HF/6-31G*) have been used to investigate the possible structures of the magnesiate species.