Capturing the Missing Carbon Cage Isomer of C84via Mutual Stabilization of a Triangular Monometallic Cyanide Cluster

Monometallic cyanide clusterfullerenes (CYCFs) represent a unique branch of endohedral clusterfullerenes with merely one metal atom encapsulated, offering a model system for elucidating structure–property correlation, while up to now only C82and C76cages have been isolated for the pristine CYCFs. C84is one of the most abundant fullerenes and has 24 isomers obeying the isolated pentagon rule (IPR), among which 14 isomers have been already isolated, whereas the C2v(17)-C84isomer has lower relative energy than several isolated isomers but never been found for empty and endohedral fullerenes. Herein, four novel C84-based pristine CYCFs with variable encapsulated metals and isomeric cages, including MCN@C2(13)-C84(M = Y, Dy, Tb) and DyCN@C2v(17)-C84, have been synthesized and isolated, fulfilling the first identification of the missing C2v(17)-C84isomer, which can be interconverted from the C2(13)-C84isomer through two steps of Stone–Wales transformation. The molecular structures of these four C84-based CYCFs are determined unambiguously by single-crystal X-ray diffraction. Surprisingly, although the ionic radii of Y3+, Dy3+, and Tb3+differ slightly by only 0.01 Å, such a subtle difference leads to an obvious change in the metal–cage interactions, as inferred from the distance between the metal atom and the nearest hexagon center of the C2(13)-C84cage. On the other hand, upon altering the isomeric cage from DyCN@C2(13)-C84to DyCN@C2v(17)-C84, the Dy–cage distance changes as well, indicating the interplay between the encapsulated DyCN cluster and the outer cage. Therefore, we demonstrate that the metal–cage interactions within CYCFs can be steered via both internal and external routes.