Unknown

Dataset Information

0

Umpolung of an Aliphatic Ketone to a Magnesium Ketone-1,2-diide Complex with Vicinal Dianionic Charge.


ABSTRACT: The new β-diketimine iPrDip nacnacH, HC(iPrCNDip)2 H, Dip=2,6-iPr2 -C6 H3 , was converted to the magnesium(I) complex [{(iPrDip nacnac)Mg}2 ] and reaction with 2-adamantanone (OAd) afforded the ketone-1,2-diide complex [{(iPrDip nacnac)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.

SUBMITTER: Burnett S 

PROVIDER: S-EPMC9541192 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Umpolung of an Aliphatic Ketone to a Magnesium Ketone-1,2-diide Complex with Vicinal Dianionic Charge.

Burnett Stuart S   Bourne Connor C   Slawin Alexandra M Z AMZ   van Mourik Tanja T   Stasch Andreas A  

Angewandte Chemie (International ed. in English) 20220711 34


The new β-diketimine <sup>iPrDip</sup> nacnacH, HC(iPrCNDip)<sub>2</sub> H, Dip=2,6-iPr<sub>2</sub> -C<sub>6</sub> H<sub>3</sub> , was converted to the magnesium(I) complex [{(<sup>iPrDip</sup> nacnac)Mg}<sub>2</sub> ] and reaction with 2-adamantanone (OAd) afforded the ketone-1,2-diide complex [{(<sup>iPrDip</sup> nacnac)Mg}<sub>2</sub> (μ-OAd)]. The complex contains the first stable dianion of an aliphatic ketone with an electropositive metal and shows an OAd<sup>2-</sup> unit with long C-O bo  ...[more]

Similar Datasets

| S-EPMC4105221 | biostudies-literature
| S-EPMC2765497 | biostudies-literature
| S-EPMC5993287 | biostudies-literature
| S-EPMC10031806 | biostudies-literature
| S-EPMC8427630 | biostudies-literature
| S-EPMC12435412 | biostudies-literature
| S-EPMC3338315 | biostudies-literature