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Endohedral Metallofullerenes: New Structures and Unseen Phenomena
Author(s) -
Shen Wangqiang,
Hu Shuaifeng,
Lu Xing
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201905306
Subject(s) - endohedral fullerene , lanthanide , actinide , planarity testing , metal , crystallography , cluster (spacecraft) , carbide , materials science , fullerene , nitride , nanotechnology , chemical physics , chemistry , inorganic chemistry , metallurgy , ion , organic chemistry , layer (electronics) , computer science , programming language
Endohedral metallofullerenes (EMFs), namely fullerenes with metallic species encapsulated inside, represent an ideal platform to investigate metal–metal or metal–carbon interactions at the sub‐nanometer scale by means of single‐crystal X‐ray diffraction (XRD) crystallography. Herein, recent progress in the identification of new structures and unprecedented properties are discussed according to the categories of monometallofullerenes, dimetallofullerenes, carbide clusterfullerenes, and nitride clusterfullerenes. In particular, the dimerization and the cage‐isomer dependent oxidation state of the inner metal atom are summarized in terms of pristine monometallofullerenes. Metal–metal bonds involving lanthanide–lanthanides or actinide–actinides are discussed based on both experimental and theoretical studies. The cluster–cage matching and/or mutual selections, as well as the rarely seen M=C double bonds, are discovered in M 2 C 2 @C 2 n , U 2 C@C 80 , M 2 TiC@C 80 , and Ti 3 C 3 @C 80 . Subsequently, the geometries of different M 3 N clusters in various cages are discussed, revealing size‐matching between the internal M 3 N cluster and the outer cage induced by the planarity of the cluster. Finally, an outlook regarding the future developments of the molecular structures and applications of EMFs is presented.