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Far-infrared study of the Jahn-Teller distorted C60 monoanion in C60 tetraphenylphosphoniumiodide

机译:Jahn-Teller扭曲的C60四苯基膦腈铝中C60单阴离子的远红外研究

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摘要

We report high-resolution far-infrared transmission measurements on C(60)-tetraphenylphosphoniumiodide as a function of temperature. In the spectral region investigated (20-650 cm(-1)), we assign intramolecular modes of the C(60) monoanion and identify low-frequency combination modes. The well-known F(1u)(1) and F(1u)(2) modes are split into doublers at room temperature, indicating a D(5d) or D(3d) distorted ball. This result is consistent with a dynamic Jahn-Teller effect in the strong-coupling limit or with a static distortion stabilized by low-symmetry perturbations. The appearance of silent odd modes is in keeping with symmetry reduction of the hall, while activation of even modes is attributed to interband electron-phonon coupling and orientational disorder in the fulleride salt. Temperature dependences reveal a weak transition in the region 125-150 K in both C(60)(-) and counterion modes, indicating a bulk, rather than solely molecular, effect. Anomalous softening (with decreasing temperature) in several modes may correlate with the radial character of those vibrations. [S0163-1829(98)03245-7].
机译:我们报告C(60)-四苯基膦腈铝酸盐的高分辨率远红外透射测量与温度的关系。在调查的光谱区域(20-650 cm(-1)),我们分配C(60)单阴离子的分子内模式,并确定低频组合模式。众所周知的F(1u)(1)和F(1u)(2)模式在室温下被分成两个倍增器,表示D(5d)或D(3d)变形的球。此结果与强耦合极限中的动态Jahn-Teller效应或通过低对称扰动稳定的静态失真相符。静音奇数模式的出现与霍尔的对称性降低保持一致,而偶数模式的激活归因于富勒酸盐中的带间电子-声子耦合和取向紊乱。温度依赖性揭示了在C(60)(-)和抗衡离子模式下,区域125-150 K的转换都很弱,表明存在整体效应,而不仅仅是分子效应。几种模式下的异常软化(随温度降低)可能与这些振动的径向特征相关。 [S0163-1829(98)03245-7]。

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