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温度对结晶二苯并[a,h]蒽振动性质的影响。

Temperature effect on vibrational properties of crystalline Dibenz[a,h]anthracene.

作者信息

Zhao Xiao-Miao, Wei Yong-Kai, Zhang Kai, Zhao Zhi-Wei, Wang Shun, Miao Wei, Du Su-Xuan, Zhang Shi-Jie, Li Wen-Feng, Guan Chun-Long, Shi Li-Ping, Lu Xin-Po, Xu San-Kui

机构信息

College of Materials Science and Engineering, Henan University of Technology, Zhengzhou 450001, China; Henan Province Engineering Research Center of New Cermet Matrix Composites, Zhengzhou 450001, China.

College of Science, Henan University of Technology, Zhengzhou 450001, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2022 Jun 5;274:121107. doi: 10.1016/j.saa.2022.121107. Epub 2022 Mar 3.

DOI:10.1016/j.saa.2022.121107
PMID:35259706
Abstract

Vibrational properties associated with the intra- and intermolecular bonding of the crystalline Dibenz[a,h]anthracene at low temperatures are investigated by Raman scattering. A complete characterization of phonon spectra is given for this material. In the 120-150 K temperature region, several lattice modes show abrupt changes of splitting and the discontinuities in the temperature shift, but no emergence of new modes. Moreover, the intensity ratio of I/ is greater than 1 below 130 K. Meanwhile, the aromatic C-C stretching modes exhibit anomalous behaviors in frequencies, widths, and intensities at about 130 K. These spectroscopic results demonstrate a disorder-order transition occurred at about 130 K. However, the modes, corresponding to C-H out-of-plane bending, C-H in-plane bending, and/or C-H rocking, have no significant change in the whole temperature range. It indicates that the transition mainly results from the change of the tilt angle between the molecules. Our work is of great significance to understand the internal vibrational properties of Dibenz[a,h]anthracene, and it also provides considerable supports for the further study of this material.

摘要

通过拉曼散射研究了低温下晶体二苯并[a,h]蒽的分子内和分子间键合相关的振动特性。给出了该材料声子谱的完整表征。在120 - 150 K温度区域,几种晶格模式显示出分裂的突然变化和温度位移的不连续性,但没有新模式出现。此外,在130 K以下,I/的强度比大于1。同时,芳香族C - C伸缩模式在约130 K时在频率、宽度和强度上表现出异常行为。这些光谱结果表明在约130 K发生了无序 - 有序转变。然而,对应于C - H面外弯曲、C - H面内弯曲和/或C - H摇摆的模式在整个温度范围内没有显著变化。这表明该转变主要是由分子间倾斜角的变化引起的。我们的工作对于理解二苯并[a,h]蒽的内部振动特性具有重要意义,也为该材料的进一步研究提供了相当大的支持。

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