Abstract
Herein, we performed the reactions of M3N@Ih-C80 (M = Sc and Lu) with the methanol (CH3OH) solution of TBAOH (note that both CH3O- and OH- are nucleophiles) in benzonitrile (PhCN) and dimethylformamide, respectively. It is found that OH- ions rather than CH3O- ions selectively attacked the fullerene cage to form the M3N@C80--O- intermediate. Although the fullerene cage is initially attacked by OH- in both PhCN and DMF solvents, the products are quite different. In PhCN, two isomeric Sc3N@Ih-C80 fullerooxazoline heterocyclic products (1 and 2) were synthesized. Whereas, in DMF, an epoxide of Lu3N@Ih-C80 (3) was obtained. The preference for fullerooxazoline formation over that of fullerene epoxy in PhCN is well explained by density functional theory calculations. Plausible reaction mechanisms for the formation of metallofullerene oxazoline and epoxide were proposed based on the experimental and theoretical results.
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