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首页> 外文期刊>ACS Omega >Characteristic Spectroscopic Features because of Cation–Anion Interactions Observed in the 700–950 cm–1 Range of Infrared Spectroscopy for Various Imidazolium-Based Ionic Liquids
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Characteristic Spectroscopic Features because of Cation–Anion Interactions Observed in the 700–950 cm–1 Range of Infrared Spectroscopy for Various Imidazolium-Based Ionic Liquids

机译:由于各种咪唑基离子液体的红外光谱在700–950 cm–1范围内观察到的阳离子-阴离子相互作用所致的光谱特征

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The 700–950 cm–1 range in infrared spectroscopy was investigated for various imidazolium-based ionic liquids (ILs). Two main vibrational modes of the methylimidazolium cation exist in this region. At 700–800 cm–1, there is an out-of-plane +C(2)–H and +C(4,5)–H bending mode with a larger motion of +C(4,5)–H in the imidazolium ring, whereas at 800–950 cm–1, there is an out-of-plane +C(2)–H and +C(4,5)–H bending mode with a larger motion of +C(2)–H in the imidazolium ring. The molar-concentration-normalized absorbance spectrum of the former band at 700–800 cm–1, which is related to the bending mode with a large +C(4,5)–H motion in the imidazolium ring, is not particularly sensitive to the interactions with anions. The molar-concentration-normalized absorbance spectrum of the latter band at 800–950 cm–1 was nearly identical for ILs that have methylimidazolium cations with carbon chains of different lengths and the same anions. The band shape of the latter band, which is related to the bending mode with a large out-of-plane +C(2)–H bending motion, was highly sensitive to the interactions with anions and, interestingly, both blue- and red-shifted tendencies in the spectrum for each system were observed.
机译:研究了各种咪唑基离子液体(IL)在红外光谱中的700–950 cm–1范围。该区域存在两种主要的甲基咪唑鎓阳离子振动模式。在700–800 cm–1处,存在平面外+ C(2)–H和+ C(4,5)–H弯曲模式,其中+ C(4,5)–H较大咪唑环,而在800–950 cm–1处,存在一个平面外的+ C(2)–H和+ C(4,5)–H弯曲模式,其中+ C(2)的运动较大咪唑环中的-H。前条带在700–800 cm-1处的摩尔浓度归一化吸收光谱与对咪唑环中+ C(4,5)–H运动较大的弯曲模式有关,对与阴离子的相互作用。对于具有甲基咪唑鎓阳离子,碳链长度不同且阴离子相同的离子液体,在800–950 cm-1处,后者的摩尔浓度归一化吸收光谱几乎相同。后一个带的带形状与大平面外+ C(2)–H弯曲运动的弯曲模式有关,对阴离子与阴离子的相互作用非常敏感,有趣的是,蓝色和红色观察到每个系统的光谱变化趋势。

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