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用红外-可见和频振动光谱法探测室温离子液体气/液界面的局部结构:1-烷基-3-甲基咪唑四氟硼酸盐。

Local structure at the air/liquid interface of room-temperature ionic liquids probed by infrared-visible sum frequency generation vibrational spectroscopy: 1-alkyl-3-methylimidazolium tetrafluoroborates.

作者信息

Iimori Toshifumi, Iwahashi Takashi, Kanai Kaname, Seki Kazuhiko, Sung Jaeho, Kim Doseok, Hamaguchi Hiro-o, Ouchi Yukio

机构信息

Research Center for Materials Science, Nagoya University, Nagoya 464-8602, Japan.

出版信息

J Phys Chem B. 2007 May 10;111(18):4860-6. doi: 10.1021/jp067162n. Epub 2007 Apr 12.

Abstract

The air/liquid interface of 1-alkyl-3-methylimidazolium tetrafluoroborates with the general formula [C(n)mim]BF(4) (n = 4-11) was studied using infrared-visible sum frequency generation (SFG) vibrational spectroscopy. The probability of the gauche defect per CH2-CH2 bond in the alkyl chain decreases as the number of carbon atoms in the alkyl chain increases. This observation suggests that the interaction between the alkyl chains is enhanced as the alkyl chain length becomes longer. The frequencies of the C-H stretching vibrational modes observed in the SFG spectra are higher than those of the corresponding peak positions observed in the infrared spectra of the bulk liquids. This shift is consistent with a structure in which the alkyl chain protrudes from the bulk liquid into the air. A local structure, which originates from the intermolecular interaction between the ionic liquid molecules, is proposed to explain these observations.

摘要

采用红外-可见和频振动光谱法研究了通式为[C(n)mim]BF(4)(n = 4 - 11)的1-烷基-3-甲基咪唑四氟硼酸盐的气/液界面。随着烷基链中碳原子数的增加,烷基链中每个CH2-CH2键出现gauche缺陷的概率降低。该观察结果表明,随着烷基链长度变长,烷基链之间的相互作用增强。在和频光谱中观察到的C-H伸缩振动模式的频率高于在本体液体红外光谱中观察到的相应峰位频率。这种位移与烷基链从本体液体中伸向空气的结构一致。提出了一种源于离子液体分子间相互作用的局部结构来解释这些观察结果。

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