The Speciation of Homochiral and Heterochiral Diastereomers of Homoleptic Cobalt(II) and Zinc(II) PyBox Complexes

Homochiral [M((R)-LR)2]2+ and heterochiral [M((R)-LR)((S)-LR)]2+ isomers of [Zn(LPh)2][BF4]2, [Zn(LiPr)2][BF4]2, [Co(LPh)2][BF4]2, and [Co(LiPr)2][BF4]2 (LPh = 2,6-bis(4-phenyloxazolinyl)pyridine; LiPr = 2,6-bis(4-isopropyloxazolinyl)pyridine) have been prepared and characterised. Six of the eight compounds were crystallographically characterised, showing that steric repulsions between ligand substituents lead to more distorted coordination geometries in the homochiral isomers, especially in the LiPr complexes. Heterochiral [M((R)-LiPr)((S)-LiPr)]2+ (M = Zn or Co) undergoes partial racemisation in CD3CN through ligand redistribution reactions, whereas [M((R)-LPh)((S)-LPh)]2+ does not (in agreement with previous reports). This may be a consequence of intramolecular π... π - interactions in [M((R)-LPh)((S)-LPh)]2+, whereby each pyridyl group is sandwiched between two phenyl substituents from the other LPh ligand. These π... π -interactions are disrupted in homochiral [M((R)-LR)2]2+, owing to the aforementioned steric clash between phenyl substituents in that isomer.