Planar Pentacoordinate versus Tetracoordinate Carbons in Ternary CBe4Li4 and CBe4Li42- Clusters.

Planar hypercoordinate carbon molecules are exotic species, for which the 18-electron counting has been considered a rule. We report herein computational evidence of perfectly planar C2 v CBe4Li4 (1) and D4 h CBe4Li42- (3) clusters. These ternary species contain 16 and 18 electrons, respectively. The dianion is highly symmetric with a planar tetracoordinate carbon (ptC), whereas the neutral features a planar pentacoordinate carbon (ppC). Thus, charge-state alters the coordination environments of a cluster. Chemical bonding analysis shows that both clusters have 2π and 6σ delocalization around the C center, suggesting that ppC or ptC clusters are governed by double π/σ aromaticity, rather than the 18-electron rule. The outer Be4Li4 ring in 1 and 3 also supports 2σ aromaticity, collectively leading to 3-fold π/σ aromaticity for these ppC/ptC clusters. Structural transformation from ptC (3) to ppC (1) is discussed, in which the 16-electron quasi-ptC CBe4Li4 (2) cluster serves as an intermediate. Cluster 2 as a local minimum has severe out-of-plane distortion. Flattening of 2 leads to reorganization of Be4 ring around the C center, which offers space for the fifth atom to coordinate and facilitates ppC formation. The latter arrangement optimizes π aromaticity and better manages intramolecular Coulomb repulsion. This work highlights the geometric factor (and unconventional electron counting) in the design of planar hypercoordinate carbons.