Royal Society of Chemistry, Physical Chemistry Chemical Physics, 35(8), p. 4104
DOI: 10.1039/b602633h
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Pyrazolino[60]fullerene covalently-linked to ferrocene and N,N-dimethylaniline groups has been prepared and studied using time-resolved spectroscopic methods. The fluorescence quenching of the C(60) moiety indicates that charge-separation takes place via the singlet excited state of the C(60) moiety in both polar and non-polar solvents. The charge-separated state, in which an electron is localized on the C(60) sphere and a hole is located on the whole donor moieties of ferrocene, pyrazole, and N,N-dimethylaniline groups, has been confirmed by nanosecond transient spectra in the visible and near-IR spectral region. The lifetimes of the radical ion-pairs are as long as 30 - 50 ns in both polar and non-polar solvents.