Coordinatively Unsaturated Cobalt Complexes with Acyclic Aminooxycarbene Ligation: Synthesis and Characterization

Acyclic aminooxycarbene (AAOC) ligands, analogues of N-heterocyclic carbene (NHC), are believed to possess superior σ-donating and π-accepting abilities over those of NHCs. Their coordination chemistry, however, remains largely unexplored. In this study, we demonstrate that AAOC ligands can effectively stabilize coordinatively unsaturated cobalt complexes. The equimolar reactions of CoCl2 with the AAOC ligands, N,N-diisopropyl-2,6-dimethylphenoxylmethylidene (LiPrXyl) and N,N-diisopropyl-2,6-diisopropylphenoxylmethylidene (LiPrDipp), in THF afford the tetrahedral cobalt(II) complexes [(AAOC)(THF)CoCl2] (AAOC = LiPrXyl, 1; LiPrDipp, 2) in good yields, whereas the reaction of CoCl2 with N,N-diisopropyl-1-adamantanoxylmethylidene (LiPrAd) yields the dimeric complex devoid of THF coordination [(LiPrAd)Co(Cl)(μ-Cl)2Co(Cl)(LiPrAd)] (3). The solvent affects the reaction outcome as the interaction of CoCl2 with two equiv of LiPrDipp in toluene produces the square planar cobalt(II) complex [trans-(LiPrDipp)2CoCl2] (4). Reduction of 4 with Mg in THF yields the three-coordinate cobalt(I) complex [(LiPrDipp)2CoCl] (5), which further reacts with NaBPh4 to form the two-coordinate cobalt(I) complex [(LiPrDipp)2Co][BPh4] (6). Moreover, the three-coordinate cobalt(0) complexes with AAOC ligation [(AAOC)Co(dvtms)] (dvtms = divinyltetramethyldisiloxane, AAOC = LiPrXyl, 7; LiPrDipp, 8; LiPrAd, 9) proved accessible from the reduction reactions of 1-3 with Mg in the presence of dvtms. Complexes 1–9 have been fully characterized by 1H NMR spectroscopy, magnetic susceptibility measurement, single-crystal X-ray diffraction, and elemental analysis.