AbstractWe report the isolation and spectroscopic identification of the eight-coordinated alkaline earth metal–dinitrogen complexes M(N₂)₈ (M=Ca, Sr, Ba) possessing cubic (O_h) symmetry in a low-temperature neon matrix. The analysis of the electronic structure reveals that the metal-N₂ bonds are mainly due to [M(d_π)]→(N₂)₈ π backdonation, which explains the observed large red-shift in N-N stretching frequencies. The adducts M(N₂)₈ have a triplet (³A_1g) electronic ground state and exhibit typical bonding features of transition metal complexes obeying the 18-electron rule. We also report the isolation and bonding analysis of the charged dinitrogen complexes [M(N₂)₈]⁺ (M=Ca, Sr).