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Shpolski Effect in Optical Spectra of Frozen Solutions of the Organic C60 Fullerene Derivative in Toluene

机译:Shpolski效应在甲苯中有机C60富勒烯衍生物的冷冻溶液的光谱中

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摘要

The optical spectra of a solution of the C_(60) ethyl acetate (C_(60)-EA) in toluene are investigated. The absorption spectra measured at T= 80 K reveal a combination of an intense featureless background pedestal deriving from absorption of charge-transfer cluster complexes on which weakly structured molecular absorp_tion is superposed. A decrease in the temperature from 80 to 2 K leads to the appearance of a multiplet of narrow lines (with a width of down to 5 cm~(-1)) corresponding to the optical excitation of C_(60)-EA molecules occu_pying different inequivalent positions in the matrix. A similar structure is observed in the luminescence spectrum of the C_(60)- EA solution at T= 2 K. The structural luminescence spectrum is in mirror symmetry with the absorption bands. The frequencies of the corresponding transitions and the related molecular vibrations are determined. The allowed character of both mirror-symmetry spectra combined with the exact matching of their constituent frequencies suggests that the vibronic interaction in the molecule is determined by the Frank-Condon mechanism.
机译:研究了C_(60)乙酸乙酯(C_(60)-EA)在甲苯中的溶液的光谱。在T = 80 K处测得的吸收光谱揭示了强烈的无特征背景基座的组合,该基座来自电荷转移簇复合物的吸收,在其上叠加了弱结构的分子吸收。温度从80 K降低到2 K导致出现多条细线(宽度减小到5 cm〜(-1)),对应于C_(60)-EA分子的光激发,矩阵中的不等价位置。在T = 2 K时,C_(60)-EA溶液的发光光谱中观察到相似的结构。结构发光光谱与吸收带成镜像对称。确定相应跃迁的频率和相关的分子振动。两种镜面对称光谱的允许特征与它们的组成频率的精确匹配相结合,表明分子中的振动相互作用是由Frank-Condon机制决定的。

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