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Electron-transfer reactions of C[sub 60]F[sub 48]

Journal Article · · Journal of the American Chemical Society; (United States)
DOI:https://doi.org/10.1021/ja00091a069· OSTI ID:7101932
;  [1];  [2]
  1. Oak Ridge National Lab., TN (United States)
  2. Univ. of North Carolina, Charlotte, NC (United States)
We now report the first cyclic voltammetric study of C[sub 60]F[sub 48] and the characterization of the products formed in the successive addition of electrons to C[sub 60]F[sub 48] in solution by various electron donors using electrospray mass spectrometry (ES-MS). Cyclic voltammograms (CVs) of C[sub 60]F[sub 48] was performed in a CH[sub 2]Cl[sub 2] solution. The reduction of C[sub 60]F[sub 48] to its anion radical occurs at E[sub 1/2]=-0.43 V with respect to the 9,10-diphenylanthracene (DPA)/9,10-diphenylanthracene radical cation (DPA[sup [sm bullet]+]) reference redox couple used in this experiment, or 0.79 V with respect to the SCE. The peak current ratio, i[sub pa]/i[sub pc], of 0.98 and the peak separation, [Delta]E[sub p], of 66 mV ([Delta]E[sub p] of the DPA/DPA[sup [sm bullet]+], a reversible couple, is 80 mV)indicated that C[sub 60]F[sub 48] undergoes a reversible reduction to form C[sub 60]F[sub 48][sup [sm bullet][minus]]. The reduction potential of C[sub 60]F[sub 48] is 1.38 V more positive than that of the first reduction wave of C[sub 60], indicating that C[sub 60]F[sub 48] is much easier to reduce than C[sub 60]. Moreover, this potential is also more positive than that of most other neutral organic electron acceptors known to the authors. 22 refs., 2 figs.
DOE Contract Number:
AC05-84OR21400
OSTI ID:
7101932
Journal Information:
Journal of the American Chemical Society; (United States), Journal Name: Journal of the American Chemical Society; (United States) Vol. 116:12; ISSN JACSAT; ISSN 0002-7863
Country of Publication:
United States
Language:
English