Theoretical probing of twenty-coordinate actinide-centered boron molecular drums

Abstract

The exploration of metal-doped boron clusters has a great significance in the design of high coordination number (CN) compounds. Actinide-doped boron clusters are probable candidates for achieving high CNs. In this work, we systematically explored a series of actinide metal atom (U, Np, and Pu) doped B₂₀ boron clusters An@B₂₀ (An = U, Np, and Pu) by global minimum structural searches and density functional theory (DFT). Each An@B₂₀ cluster is confirmed to be a twenty-coordinate complex, which is the highest CN obtained in the chemistry of actinide-doped boron clusters so far. The predicted global minima of An@B₂₀ are tubular structures with actinide atoms as centers, which can be considered as boron molecular drums. In An@B₂₀, U@B₂₀ has a relatively high symmetry of C₂, while both Np@B₂₀ and Pu@B₂₀ exhibit C₁ symmetry. Extensive bonding analysis demonstrates that An@B₂₀ has σ and π delocalized bonding, and the U–B bonds possess a relatively higher covalency than the Np–B and Pu–B bonds, resulting in the higher formation energy of U@B₂₀. Therefore, the covalent character of An–B bonding may be crucial for the formation of these high CN actinide-centered boron clusters. These results deepen our understanding of actinide metal doped boron clusters and provide new clues for developing stable high CN boron-based nanomaterials.