The leapfrog principle for boron fullerenes: a theoretical study of structure and stability of B112

Abstract

Two leapfrog isomers of a B₁₁₂ boron fullerene are constructed from small C₂₈ fullerenes (T_d and D₂ symmetries) by the leapfrog transformation combined with omnicapping of the new hexagons. Their electronic structure is analyzed using the density functional theory at the B3LYP/SVP and BHLYP/SVP levels. Both isomers are characterized as minima on the potential energy hypersurface with a HOMO–LUMO gap at B3LYP/SVP of 1.7 eV and 1.6 eV (3.1 and 3.0 eV at BHLYP/SVP), respectively. The optimized structure of the helical D₂-leapfrog is asymmetric, due to radial displacements of the capping atoms. The computed cohesive energies amount to −4.2 eV (∼0.04 eV lower than B₈₀). The B₁₁₂ isomers are isoelectronic to T_d-C₈₄ and D₂-C₈₄, and HOMO and LUMO orbitals in both isomers closely resemble those of their C₈₄ homologues. Energetic stability of leapfrogboron fullerenes depends on the isolation of empty hexagon criterion, which is defined by the empty hexagon index based on the total number of empty hexagon pairs and empty hexagon–pentagon fused pairs. The switch of the cap atom to the nearest or farthest empty hexagon destabilizes the cage by 1.6 and 2.7 eV, respectively. The destabilization becomes more enhanced in non-leapfrog structures wherein more caps are displaced.