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Low-frequency isotropic and anisotropic Raman spectra of aromatic liquids

机译:芳香族液体的低频各向同性和各向异性拉曼光谱

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摘要

The Raman spectra below 300 wavenumbers of six different aromatic molecular liquids have been measured with a time and polarization resolved optical Kerr effect technique. The isotropic and anisotropic contributions were determined to yield the complete third order response, and thus a more detailed description of the microscopic liquid dynamics. The anisotropic contributions accurately reproduced previously published results. Both the isotropic and anisotropic Raman spectral densities shift toward lower frequencies with decreasing molecular weights. The first moment of the isotropic spectral densities scales linearly with the inverse square root of the molecular weight, which is consistent with interaction-induced dynamics in these liquids being driven mainly by motions with a translational character. Also, the isotropic spectral densities could be fit to a single Bucaro-Litovitz function. The exponent δ of this function increases monotonically with the inverse square root of the molecular weight. A possible physical origin of this behavior is discussed.
机译:六种不同的芳香族分子液体在300波数以下的拉曼光谱已通过时间和偏振分辨光学Kerr效应技术进行了测量。确定各向同性和各向异性贡献以产生完整的三阶响应,从而更详细地描述微观液体动力学。各向异性的贡献准确地再现了以前发表的结果。随着分子量的降低,各向同性和各向异性拉曼光谱密度都向较低的频率移动。各向同性谱密度的一阶矩与分子量的平方根成反比,这与这些液体中相互作用诱导的动力学一致,这些动力学主要由具有平移特性的运动驱动。同样,各向同性光谱密度可以适合单个Bucaro-Litovitz函数。该函数的指数δ与分子量的平方根成反比。讨论了此行为的可能的物理起源。

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