Abstract
The new β-diketimine iPrDipnacnacH, HC(iPrCNDip)2H, Dip=2,6-iPr2-C6H3, was converted to the magnesium(I) complex [{(iPrDipnacnac)Mg}2] and reaction with 2-adamantanone (OAd) afforded the ketone-1,2-diide complex [{(iPrDipnacnac)Mg}2(μ-OAd)]. The complex contains the first stable dianion of an aliphatic ketone with an electropositive metal and shows an OAd2− unit with long C−O bond and pyramidal carbon centre. DFT studies reveal an anionic charge on both neighbouring C and O atoms. Reductions of aliphatic ketones with magnesium(I) complexes show that these likely proceed via highly reactive dianions and afforded a 1 : 1 mixture of an alkoxide and an enolate when an enolisable ketone was used, and rapid CH activations reactions, e.g., of stabilising ligand moieties, when non-enolisable ketones were employed.
Author supplied keywords
Cite
CITATION STYLE
Burnett, S., Bourne, C., Slawin, A. M. Z., van Mourik, T., & Stasch, A. (2022). Umpolung of an Aliphatic Ketone to a Magnesium Ketone-1,2-diide Complex with Vicinal Dianionic Charge. Angewandte Chemie - International Edition, 61(34). https://doi.org/10.1002/anie.202204472
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.