The locations of the \( 0_0^0 \) -bands for S1← S0 and S1 → S0 transitions have been found for C60 solutions in hexane. It is shown that the profile of the S1 ← S0 band is mainly shaped by hu(4), t1u(4)- and hg(1), ag(2)- modes that are active in absorption. Bands involving the hu(4)- and t1u(4)-modes in the emission process have also been identified in the fluorescence spectrum. The appearance of the \( 0_0^0 \) -band in the forbidden 11T1g ← 11Ag transition is explained by symmetry reduction in the C60+environment system due to the interaction of electrons with local phonons. The temperature coefficients of the red shift for the 256.3- and 328.3-nm bands of allowed 1T1u ← 11Ag transitions for C60 in hexane are equal to –1.45 and –0.46 cm–1·K–1, respectively. The peak and half-width values of the 337.2-nm band for C60 in polystyrene remain unchanged on cooling to 77 K. Absorption in the 700–800-nm region for concentrated hexane solutions of fullerene at 292 K results from the production of (C60)n-clusters.
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Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 77, No. 3, pp. 362–369, May–June, 2010.
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Pavlovich, V.S., Shpilevsky, E.M. Absorption and fluorescence spectra of C60 fullerene concentrated solutions in hexane and polystyrene at 77–300 K. J Appl Spectrosc 77, 335–342 (2010). https://doi.org/10.1007/s10812-010-9336-2
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DOI: https://doi.org/10.1007/s10812-010-9336-2