ELECTRONIC-SPECTRA AND TRANSITIONS OF THE FULLERENE C-60

Absorption spectra of C60 have been measured in the ranges (a) 190-700 nm in n-hexane solutions at 300 K, (b) 390-700 nm in n-hexane and in 3-methylpentane solutions at 77 K. 40 vibronic bands were observed. They exhibit a large range of bandwidths and intensities, whose significance is discussed. Assignment of electronic transitions has been carried out using the results of theoretical calculations. Vibronic structures have been analyzed within the framework of theories of electronic transitions of polyatomic molecules applied to the I(h) symmetry group. Nine allowed 1T1u-1A(g) transitions have been assigned in the 190-410 nm region. Observed and calculated allowed transition energies and oscillator strengths are compared. Detailed vibronic analyses of the 1 1T1u-1 1A(g) and 2 1T1u-1 1A(g) transitions illustrate the role of Jahn-Teller couplings. Orbitally forbidden singlet-singlet transitions are observed between 410 and 620 nm. Their vibronic structures were analyzed in terms of concurrent Herzberg-Teller and Jahn-Teller vibronic interactions. The 77 K spectra provided useful information on hot bands and on other aspects of the analyses. Vibronic bands belonging to triplet <-- singlet transitions were detected between 620 and 700 nm.