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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 beennmeasured with a time and polarization resolved optical Kerr effect technique. The isotropic andnanisotropic contributions were determined to yield the complete third order response, and thus anmore detailed description of the microscopic liquid dynamics. The anisotropic contributionsnaccurately reproduced previously published results. Both the isotropic and anisotropic Ramannspectral densities shift toward lower frequencies with decreasing molecular weights. The firstnmoment of the isotropic spectral densities scales linearly with the inverse square root of thenmolecular weight, which is consistent with interaction-induced dynamics in these liquids beingndriven mainly by motions with a translational character. Also, the isotropic spectral densities couldnbe fit to a single Bucaro–Litovitz function. The exponent u0001 of this function increases monotonicallynwith the inverse square root of the molecular weight. A possible physical origin of this behavior isndiscussed.
机译:用时间和偏振分辨光学克尔效应技术测量了六种不同芳族分子液体在300波数以下的拉曼光谱。确定各向同性和纳米各向同性以产生完整的三阶响应,从而对微观液体动力学进行了更详细的描述。各向异性贡献准确地复制了以前发表的结果。随着分子量的减小,各向同性和各向异性的拉曼光谱密度都朝着较低的频率移动。各向同性光谱密度的第一阶跃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主要由具有平移特征的运动所驱动是一致的。同样,各向同性的光谱密度可能不适合单个Bucaro-Litovitz函数。该函数的指数u0001与分子量的平方反比单调增加。讨论了这种行为的可能的物理起源。

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