Abstract
Steering the cluster configuration inside a fullerene cage has been one of most interesting topics in the field of fullerenes, since the physical property of a cluster fullerene may be modified accordingly. It has been well-recognized that the cluster configuration can be tuned via altering the cage size.
Typically, the carbide cluster and the oxide cluster are experimentally seen to be curled up within a small fullerene cage whereas they are expanded in a large cage. In this work, a new oxide cluster fullerene Ho2O@C-2(13333)-C-74 is prepared and isolated.
The single crystal X-ray diffraction (XRD) study reveals that the Ho2O cluster, however, expands within the small non-IPR cage of C-2(13333)-C-74 with a Ho-O-Ho angle of >170 degrees indicating that cluster configuration is highly related to the cage shape and cage structure as well. The DFT computation demonstrates that the cluster-to cage electron-transfer obviously enhances the aromaticity of the motif containing the fused-pentagon pair and hence stabilizes the non-IPR cage of C-2(13333)-C-74.
In addition, the electrochemical and magnetic properties of Ho(2)OpC(2)(13333)-C-74 are studied to further investigate the effect of endohedral Ho2O cluster.