Steric control of Mg–Mg bond formation vs. N2 activation in the reduction of bulky magnesium diamide complexes

Abstract

Reduction of the magnesium(II) diamide [Mg(^TripNON)] (^TripNON = 4,5-bis(2,4,6-triisopropylanilido)-2,7-diethyl-9,9-dimethyl-xanthene) with 5% w/w K/KI leads to a good yield of a dianionic dimagnesium(I) species, as its potassium salt, [{K(^TripNON)Mg}₂]. An X-ray crystallographic analysis shows the molecule to contain a very long Mg–Mg bond (3.137(2) Å). The formation of [{K(^TripNON)Mg}₂] contrasts with a previously reported reduction of a magnesium(II) complex incorporating a bulkier diamide ligand, which instead afforded a magnesium–dinitrogen complex. In the current study, [{K(^TripNON)Mg}₂] has been shown to be a viable reagent for the reductive activation of CO, H₂ and N₂O.