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

The exploration of metal-doped boron clusters has a great significance to design high coordination number (CN) compounds. Actinide-dopted boron clusters are probably candidates for achieving high CNs. In this work, we systematically explored a series of actinide metal atoms (U, Np, Pu) doped B20 boron clusters An@B20 (An = U, Np, 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 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 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 dopted boron clusters, and provide new clues for developing stable high CN boron-based nanomaterials.