RESUMO
In the present study, the electronic structures of a series of binuclear sandwich complexes based on the cyclooctatetraene ligand M12(η8-C8H8)2M22 (M1 = Na, K and M2 = Ca, Mg) are studied theoretically. Each cyclooctatetraene ligand binds with the metal in the η8 binding mode. The M2-M2 bond length agrees well with the reported bimetallic covalent Ca2 and Mg2 bond lengths. The Wiberg bond index (WBI) also indicates the presence of covalent M2-M2 bonds, which gives additional stability to the complex. A non-nuclear attractor (NNA) is found in-between the M2-M2 bond and the negative Laplacian of the electron density is found at the NNA. Noncovalent interaction (NCI) plot shows that electron density is localized at the M2-M2 bond. Based on the performed analysis, we have concluded that the designed sandwich complexes are electrides. We herein report, for the first time, the electride sandwich complexes of the cyclooctatetraene ligand. Due to the presence of a diffuse electron system, the electride complexes exhibit higher values of the static second hyperpolarizability within the range of 2.6 × 105 to 1.4 × 106 a.u. Among the studied complexes, M12(η8-C8H8)2Ca2 exhibit a higher value of static second hyperpolarizability.