From C(58) to C(62) and back: Stability, structural similarity, and ring current.

An increasing number of observations show that non-classical isomers may play an important role in the formation of fullerenes and their exo- and endo-derivatives. A quantum-mechanical study of all classical isomers of C58 , C60 , and C62 , and all non-classical isomers with at most one square or heptagonal face, was carried out. Calculations at the B3LYP/6-31G* level show that the favored isomers of C58 , C60 , and C62 have closely related structures and suggest plausible inter-conversion and growth pathways among low-energy isomers. Similarity of the favored structures is reinforced by comparison of calculated ring currents induced on faces of these polyhedral cages by radial external magnetic fields, implying patterns of magnetic response similar to those of the stable, isolated-pentagon C60 molecule. © 2016 Wiley Periodicals, Inc.

Awaking N-hyperfine couplings in charged yttrium nitride endohedral fullerenes.

The electron spin properties of endohedral metallofullerene molecules have broad potential applications in quantum information and magnetic induction systems due to the high stability and sensitivity. Herein, we synthesized a series of Y3N@C2n (n = 40-44) molecules and studied the hyperfine structures of their anion radicals via ESR measurements and DFT calculations. N-Hyperfine couplings were clearly observed in the ESR spectra of charged Y3N@C80 and Y3N@C86 anion radicals, which are not found in the other metallofullerenes. The ESR results revealed size-dependent spin distributions and hyperfine structures, which are sensitive to subtle changes in the carbon cage and the configuration of the yttrium nitride cluster. BOMD cluster trajectories simulations indicated that the Y3N cluster almost rotates freely in neutral Y3N@C80 but there is a certain degree of limitation in the Y3N@C80 anion.

An atlas of endohedral Sc2S cluster fullerenes.

Structural identification is a difficult task in the study of metallofullerenes, but understanding of the mechanism of formation of these structures is a pre-requisite for new high-yield synthetic methods. Here, systematic density functional theory calculations demonstrate that metal sulfide fullerenes Sc2S@Cn have similar cage geometries from C70 to C84 and form a close-knit family of structures related by Endo-Kroto insertion/extrusion of C2 units and Stone-Wales isomerization transformations. The stabilities predicted for favoured isomers by DFT calculations are in good agreement with available experimental observations, have implications for the formation of metallofullerenes, and will aid structural identification from within the combinatorially vast pool of conceivable isomers.