Electrophilic Aromatic Substitution by the Fluorofullerene C60F18

The FeCl3‐catalysed arylation of C60F18 gives tri‐substituted compounds C60F15Ar3, where Ar=phenyl, 4‐tolyl, 4‐methoxyphenyl, 4‐phenoxyphenyl, 4‐chlorophenyl, 3,4‐dichlorophenyl, 2‐biphylenyl and 2‐fluorenyl, together with some bis‐ and mono‐substituted product. Bis‐substitution was achieved with biphenylene and fluoranthene, and mono‐substitution with biphenylene (2‐position), pyrene (1‐position), and naphthalene (1‐ and 2‐positions); the tris‐phenyl and tris‐biphenylene derivatives are fluorescent. The 2‐naphthyl substituent freely rotates at 328 K, whereas rotation of the 1‐naphthyl substituent is prevented by interaction of the peri‐hydrogen atom with fluorine. The 1‐naphthyl derivative eliminates a molecule of HF during EI mass spectrometry, whilst the 2‐naphthyl derivative eliminates HF and all fluorenes to give a naphthaleno[60]fullerene. The reaction rate is relatively unaffected by electron supply in the aryl rings, but no product was obtained with benzotrifluoride which defines the lower reactivity limit. The low discrimination between aromatics makes it possible to isolate derivatives having different aryl groups attached to the cage. Reactions occur mainly when the reagent solutions (or solutions in 1,2‐dichlorobenzene) are evaporated to dryness. In most FeCl3‐catalysed reactions, unreacted C60F18 was recovered, more if the less effective SnCl4 was used as a catalyst; use of AlCl3 resulted in polyarylation and degradation of the C60F18. The structure of C60F17(1‐biphenylyl) was confirmed by single‐crystal X‐ray analysis. Reaction of C60F18 with perylene/FeCl3/o‐dichlorobenzene gave red fluorescent “tagliatelli”‐like threads (up to 1 cm long) of self‐assembled π‐stacked tetrachloroperylene arising from chlorination by FeCl3. A range of mono‐, bis‐ and tris‐aryl substituted derivatives is produced when C60F18 reacts with various aromatic compounds in the presence of FeCl3 (see picture).