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冻结羟基官能化离子液体中的运动——远低于玻璃化转变温度时两种氢键的温度依赖性核磁共振氘核四极耦合常数

Freezing the Motion in Hydroxy-Functionalized Ionic Liquids-Temperature Dependent NMR Deuteron Quadrupole Coupling Constants for Two Types of Hydrogen Bonds Far below the Glass Transition.

作者信息

Khudozhitkov Alexander E, Niemann Thomas, Stange Peter, Donoshita Masaki, Stepanov Alexander G, Kitagawa Hiroshi, Kolokolov Daniil I, Ludwig Ralf

机构信息

Boreskov Institute of Catalysis, Siberian Branch of Russian Academy of Sciences, Prospekt Akademika Lavrentieva 5, Novosibirsk 630090, Russia.

Novosibirsk State University, Pirogova Street 2, Novosibirsk 630090, Russia.

出版信息

J Phys Chem Lett. 2020 Aug 6;11(15):6000-6006. doi: 10.1021/acs.jpclett.0c01731. Epub 2020 Jul 14.

Abstract

We measured the deuteron quadrupole coupling constants (DQCCs) for hydroxy-functionalized ionic liquids (ILs) with varying alkyl chain length over the temperature range between 60 and 200 K by means of solid-state NMR spectroscopy. For all temperatures, the H spectra show two DQCCs representing different types of hydrogen bonds. Higher values, ranging from 220 to 250 kHz, indicate weaker hydrogen bonds between cation and anion (c-a), and lower values varying from 165 to 210 kHz result from stronger hydrogen bonds between the OD groups of cations (c-c), in agreement with recent observations in infrared, neutron diffraction, and NMR studies. We observed different temperature dependencies for (c-a) and (c-c) hydrogen bonding. From the static pattern of the H spectra at the lowest temperatures, we derived the true DQCCs being up to 20 kHz larger than recently reported values measured at the glass transition temperature. We were able to freeze the librational motions of the hydrogen bonds in the ILs. The temperature dependence of the (c-a) and (c-c) cluster populations in the glassy state is opposite to that observed in the liquid state, partly anticipating the behavior of ILs tending to crystallize.

摘要

我们通过固态核磁共振光谱法,在60至200 K的温度范围内,测量了具有不同烷基链长度的羟基官能化离子液体(ILs)的氘核四极耦合常数(DQCCs)。在所有温度下,H谱显示出两个代表不同类型氢键的DQCCs。较高的值,范围为220至250 kHz,表明阳离子与阴离子(c-a)之间的氢键较弱,而较低的值在165至210 kHz之间变化,这是由于阳离子的OD基团之间(c-c)的氢键较强,这与最近在红外、中子衍射和核磁共振研究中的观察结果一致。我们观察到(c-a)和(c-c)氢键具有不同的温度依赖性。从最低温度下H谱的静态模式中,我们得出真实的DQCCs比最近在玻璃化转变温度下测量的值大20 kHz。我们能够冻结离子液体中氢键的振动运动。玻璃态下(c-a)和(c-c)簇群体的温度依赖性与液态中观察到的相反,部分地预示了离子液体趋于结晶的行为。

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