胆二酸盐的相位过渡:振动光谱学和周期性DFT研究
Vitor H Paschoal1, Mauro C C Ribeiro1
1Laboratório de Espectroscopia Molecular, Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, 05513-970 São Paulo, Brazil.
The Journal of chemical physics
|March 6, 2024
概括
胆二酸盐 ([Chol][H2PO4]) 呈现复杂的相位过渡. 拉曼光谱揭示了20°C的过渡涉及形状变化和离子重新排列,而不是在更高的温度下化.
科学领域:
- 材料科学 材料科学 材料科学
- 固态化学 固态化学
- 频谱学是一种光谱学.
背景情况:
- 胆二酸盐 ([Chol][H2PO4]) 是一种导质子的离子塑料晶体,热性能和相位转换的理解不佳.
- 现有的文献对其热行为提出了相互矛盾的解释,需要进一步调查.
研究的目的:
- 用先进的光谱技术澄清[][H2PO4]的热性质和相变.
- 为了协调文献中关于其相变性质的差异.
主要方法:
- 拉曼和红外显微镜被用来分析[Chol][H2PO4]的振动特性.
- 进行周期密度函数理论计算,以根据已知的低温晶体结构确定振动频率.
- 拉曼映射被用来评估在环境温度下材料内的形状分布.
主要成果:
- 在20°C的固体-固体过渡与[Chol]+离子从反向左向变形体和局部离子重排的变形变化有关.
- 拉曼光谱显示,在20°C过渡时,格子模式带消失,表明结构变化.
- 拉曼映射揭示了环境温度样本中的反和左合体的共存,这是由于易于形成转移稳定的晶体.
- 高达120°C的加热导致了离子环境的持续变化,与融化过渡不一致.
结论:
- 在[Chol][H2PO4]中的相过渡涉及形状变化和阳离子重新排列,而不是突然化.
- 光谱证据支持材料结构随温度的不断演变,与低聚变和离子导电性数据保持一致.
相关概念视频
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
1.1K
When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
1.1K
UV–Vis Spectroscopy: Molecular Electronic Transitions
1.4K
In Ultraviolet–Visible (UV–Vis) spectroscopy, the absorption of electromagnetic radiation is used to probe the electronic structure of molecules. This technique provides insights into molecular electronic transitions, particularly the movement of electrons between different molecular orbitals. Radiation is absorbed if the energy of the electromagnetic radiation passing through the molecule is precisely equal to the energy difference between the excited and ground states. During this...
1.4K
¹H NMR: Interpreting Distorted and Overlapping Signals
1.0K
Spin systems where the difference in chemical shifts of the coupled nuclei is greater than ten times J are called first-order spin systems. These nuclei are weakly coupled, and their chemical shifts and coupling constant can generally be estimated from the well-separated signals in the spectrum.
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are...
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are...
1.0K
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
839
At room temperature, the chair conformer of cyclohexane undergoes rapid ring flipping between two equivalent chair conformers at a rate of approximately 105 times per second. These two chair conformers are in equilibrium. The rapid ring flipping results in the interconversion of the axial proton to an equatorial proton and an equatorial to the axial proton. Such interconversions are too rapid and cannot be detected on the NMR timescale. Hence, the NMR spectrometer cannot distinguish between the...
839
Double Resonance Techniques: Overview
203
Double resonance techniques in Nuclear Magnetic Resonance (NMR) spectroscopy involve the simultaneous application of two different frequencies or radiofrequency pulses to manipulate and observe two distinct nuclear spins. One important application of double resonance is spin decoupling, which selectively suppresses coupling with one type of nucleus while observing the NMR signal from another nucleus, simplifying the spectrum and enhancing resolution.
Spin decoupling is usually achieved by...
Spin decoupling is usually achieved by...
203
IR Spectrum Peak Splitting: Symmetric vs Asymmetric Vibrations
1.0K
Identical bonds within a polyatomic group can stretch symmetrically (in-phase) or asymmetrically (out-of-phase). Similar to hydrogen bonding, these vibrations also influence the shape of the IR peak. Generally, asymmetric stretching frequencies are higher than symmetric stretching frequencies. For example, primary amines exhibit two distinct IR peaks between 3300–3500 cm−1 corresponding to the symmetric and asymmetric N-H stretching, while secondary amines exhibit a single...
1.0K


