The treatment of C60 with the tertiary amine 1,8-diazabicyclo [5.4.0]u
ndec-7-ene results in the formation of a diamagnetic zwitterion salt [
DBU]C60. This addition reaction was monitored in solution by UV/VIS/NI
R and ESR spectroscopy. It is shown that in the first step a single el
ectron transfer occurs leading to the C60-. monoradical anion and the
DBU radical cation. In a subsequent step [DBU]C60 is formed upon a rad
ical recombination process. The represented results give evidence for
the reaction mechanism of nucleophilic amine additions to C60 proposed
earlier.