Actinide endohedral metallofullerenes (EMFs) are a fullerene
family
that possess unique actinide–carbon cage host–guest
molecular and electronic structures. In this work, a novel actinide
EMF, U@C
s(4)-C82, was successfully
synthesized and characterized, and its chemical reactivity was investigated.
Crystallographic analysis shows that U@C
s(4)-C82, a new isomer of U@C82, has a C
s(4)-C82 cage, which has never been
discovered in the form of empty or endohedral fullerenes. Its unique
chemical reactivities were further revealed through the Bingel–Hirsch
reaction and carbene addition reaction studies. The Bingel–Hirsch
reaction of U@C
s(4)-C82 shows
exceptionally high selectivity and product yield, yielding only one
major addition adduct. Moreover, the addition sites for both reactions
are unexpectedly located on adjacent carbon atoms far away from the
actinide metal, despite the nucleophilic (Bingel–Hirsch) and
electrophilic (carbene addition) nature of either reactant. Density
functional theory (DFT) calculations suggest that this chemical behavior,
unprecedented for EMFs, is directed by the unusually strong interaction
between U and the sumanene motif of the carbon cage in U@C
s(4)-C82, which makes the energy increase when
it is disrupted. This work reveals remarkable chemical properties
of actinide EMFs originating from their unique electronic structures
and highlights the key role of actinide–cage interactions in
the determination of their chemical behaviors.