Synthesis, structure, and theoretical study of trifluoromethyl derivatives of C84(22) fullerene.

Trifluoromethylation of higher fullerene mixtures with CF(3)I was performed in ampoules at 400 to 420 and 550 to 560 °C. HPLC separation followed by crystal growth and X-ray diffraction studies allowed the structure elucidation of nine CF(3) derivatives of D(2)-C(84) (isomer 22). Molecular structures of two isomers of C(84)(22)(CF(3))(12), two isomers of C(84)(22)(CF(3))(14), four isomers of C(84)(22)(CF(3))(16), and one isomer of C(84)(22)(CF(3))(20) were discussed in terms of their addition patterns and relative formation energies. DFT calculations were also used to predict the most stable molecular structures of lower CF(3) derivatives, C(84)(22)(CF(3))(2-10). It was found that the addition of CF(3) groups to C(84)(22) is governed by two rules: additions can only occur at para positions of C(6)(CF(3))(2) hexagons and no additions can occur at triple-hexagon-junction positions on the fullerene cage.
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