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Single Molecule Magnetism with Strong Magnetic Anisotropy and Enhanced Dy∙∙∙Dy Coupling in Three Isomers of Dy-Oxide Clusterfullerene Dy2O@C82.

Wei YangGeorgios VelkosFupin LiuSvetlana M SudarkovaYaofeng WangJiaxin ZhuangHanning ZhangXiang LiXingxing ZhangBernd BüchnerStanislav M AvdoshenkoAlexey A PopovNing Chen
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2019)
A new class of single-molecule magnets (SMMs) based on Dy-oxide clusterfullerenes is synthesized. Three isomers of Dy2O@C82 with C s(6), C 3v(8), and C 2v(9) cage symmetries are characterized by single-crystal X-ray diffraction, which shows that the endohedral Dy-(µ2-O)-Dy cluster has bent shape with very short Dy-O bonds. Dy2O@C82 isomers show SMM behavior with broad magnetic hysteresis, but the temperature and magnetization relaxation depend strongly on the fullerene cage. The short Dy-O distances and the large negative charge of the oxide ion in Dy2O@C82 result in the very strong magnetic anisotropy of Dy ions. Their magnetic moments are aligned along the Dy-O bonds and are antiferromagnetically (AFM) coupled. At low temperatures, relaxation of magnetization in Dy2O@C82 proceeds via the ferromagnetically (FM)-coupled excited state, giving Arrhenius behavior with the effective barriers equal to the AFM-FM energy difference. The AFM-FM energy differences of 5.4-12.9 cm-1 in Dy2O@C82 are considerably larger than in SMMs with {Dy2O2} bridges, and the Dy∙∙∙Dy exchange coupling in Dy2O@C82 is the strongest among all dinuclear Dy SMMs with diamagnetic bridges. Dy-oxide clusterfullerenes provide a playground for the further tuning of molecular magnetism via variation of the size and shape of the fullerene cage.
Keyphrases
  • single molecule
  • atomic force microscopy
  • living cells
  • computed tomography
  • magnetic resonance imaging
  • mass spectrometry
  • room temperature
  • contrast enhanced