The isolated-pentagon rule (IPR) is a determining structural feature that accounts for hollow fullerene stabilization and properties related to Cn (n≥60) cages. The recent characterization of an unprecedented non-IPR hydrofullerene, C2v C66 H4 , bearing two heptagons with adjacent fused-pentagon motifs, largely dismisses this feature. Herein, employing DFT calculations, the 13 C NMR spectroscopy and aromatic behavior of C2v C66 H4 are explored. The results show the presence of three π-aromatic circuits at the bottom boat section of C66 H4 , indicating the unique features of this hydrofullerene in comparison to those of pristine C60 . In addition, under specific orientations of the external field, certain π-aromatic circuits are enabled, resulting in a more aromatic fullerene than that of C60 , but lower than that of the spherical aromatic C60 6- fulleride. Notably, under a field aligned with the saturated carbon atoms, nonaromatic characteristics are exposed. This reveals that spherical-like cages can involve a complex magnetic response that heavily depends on the orientation of the applied field.
Keywords: aromaticity; density functional calculations; fullerenes; hydrofullerenes; ring currents.
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