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Stress-induced crystal transition of poly(butylene succinate) studied by terahertz and low-frequency Raman spectroscopy and quantum chemical calculation

机译:通过太赫兹和低频拉曼光谱和量子化学计算研究的聚(丁烯琥珀酸盐)的应力诱导的晶体转变

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We measured terahertz (THz) and low-frequency Raman spectra of Poly (butylene succinate) (PBS) which shows the crystal transition from alpha to beta by stretching. For the assignment of the absorption peaks in the low-frequency region, we performed quantum chemical calculations with Cartesian-coordinate tensor transfer (CCT) method. Four major peaks appeared in the THz spectra of PBS at around 58, 76, 90, and 100 cm(-1) and in the low-frequency Raman spectra a peak was observed at 88 cm(-1).The THz peak at 100 cm(-1) and the Raman peak at 88 cm(-1) show a shift to a lower wavenumber region with increasing temperature. The quantum chemical calculation of beta crystal form reveals the new peak appears above 100 cm(-1). It was found that two kinds of peaks overlapped at around 100 cm(-1) in the THz spectra of PBS. One of them can be assigned to a weak hydrogen bond between the C=O and CH2 groups in the intermolecular chains, which is perpendicular to the molecular chain of the alpha crystal form. Another one showed a parallel polarization which can be assigned to the intramolecular interaction between O (ether) and H-C groups in the crystal form. The position of the peak at around 100 cm(-1) in the perpendicular polarization changed to a lower wavenumber region with stretching, because of the weakening of the intermolecular hydrogen bonding by increasing the interatomic distances. On the other hand, that of the parallel polarization shifts to a higher wavenumber region because of the shortening of the interatomic distance from alpha to beta crystal form (the strength of the intramolecular hydrogen bonding became stronger) by stretching. (C) 2018 Elsevier B.V. All rights reserved.
机译:我们测量了聚(丁二烯琥珀酸盐)(PBS)的太赫兹(THz)和低频拉曼光谱,其显示通过拉伸从α至β从α到β的晶体转变。为了在低频区域中的吸收峰分配,我们用笛卡尔坐标张传输(CCT)方法进行量子化学计算。在58,76,90和100cm(-1)约为58,76,90和100cm(-1)的PBS的THz光谱中出现四个主要峰值,在88cm(-1)中观察到峰值的峰值.THz峰值CM(-1)和88cm(-1)处的拉曼峰值显示出在温度升高的下波数区域的转变。 β晶体形式的量子化学计算揭示了新峰值以上100cm(-1)。发现PBS的THz光谱中的两种峰值重叠在约100cm(-1)。其中一个可以分配给分子间链中的C = O和CH2基团之间的弱氢键,其垂直于α晶体形式的分子链。另一个显示了平行偏振,其可以被分配给晶体形式的O(醚)和H-C组之间的分子内相互作用。由于通过增加内部距离,峰值在垂直偏振中变为垂直偏振中的垂直偏振率约为100cm(-1)的位置,而分子间氢粘合的弱化。另一方面,通过缩短从α至β晶体形式的间隙距离(分子内氢粘合强度变得更强的强度),平行偏振的偏移的偏移变换到更高的波数区域。 (c)2018年elestvier b.v.保留所有权利。

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