什么非线性IR实验可以告诉你关于水的IR频谱不能告诉你
Ivan R Piletic1, David E Moilanen, Nancy E Levinger
1Department of Chemistry, Stanford University, Stanford, California 94305, USA.
Journal of the American Chemical Society
|August 10, 2006
概括
即使具有相似的红外光谱,水的动态也可以显著不同. 非线性红外光谱学揭示了水系统中不同的振动寿命和放松时间,突出了它对研究键的重要性.
科学领域:
- 物理化学 物理化学
- 频谱学是一种光谱学.
- 材料科学 材料科学 材料科学
背景情况:
- 红外 (IR) 光谱法通常用于研究水的键网络结构和强度.
- 然而,相似的吸收光谱可以掩盖水系统的潜在动态差异.
研究的目的:
- 为了研究水的动态在具有非常相似的吸收光谱的系统中可以变化的程度.
- 为了确定振动寿命和定向放松是否与溶液中的水度相关.
主要方法:
- 利用非线性IR光谱学探测了四个不同的水系统的动态.
- 分析了振动寿命和定向放松时间尺度.
主要成果:
- 在四个样本中观察到振动寿命和定向放松时间尺度的巨大变化.
- 没有发现这些动态特性与相对数量的水,表面活性剂或溶液之间的相关性.
- 证明类似的吸收光谱并不意味着类似的水动力学.
结论:
- 非线性IR光谱对于识别结系统中的微妙动态差异至关重要.
- 这些先进的技术提供了基本的信息,超出了传统的红外光谱所能提供的水性环境的特征.
相关概念视频
Infrared (IR) Spectroscopy: Overview
When electromagnetic radiation passes through a material, atoms or molecules transition from a lower to a higher energy state by absorbing radiation corresponding to the energy difference between the two states. The absorption of infrared (IR) radiation causes transitions between vibrational energy levels in a molecule. Therefore, IR spectroscopy is a useful analytical tool for determining the molecular structure of molecules.
Different compounds display unique properties due to their...
Different compounds display unique properties due to their...
IR Spectrum
When infrared (IR) radiation passes through a molecule, the bonds stretch or bend by absorbing the radiation. This absorption creates the molecule's absorption spectrum, which is the plot of its percentage transmittance versus wavenumber.
Transmittance is defined as the ratio of the radiant power passing through a sample to that from the radiation's source. Multiplying the transmittance by 100 gives the percent transmittance (%T), which varies between 100% (no absorption) and 0% (complete...
Transmittance is defined as the ratio of the radiant power passing through a sample to that from the radiation's source. Multiplying the transmittance by 100 gives the percent transmittance (%T), which varies between 100% (no absorption) and 0% (complete...
IR Spectroscopy: Molecular Vibration Overview
When Infrared (IR) radiation passes through a covalently bonded molecule, the bonds transition from lower to higher vibrational levels. The fundamental vibrational motions that result in infrared absorption can be classified as stretching or bending vibrations.
Stretching vibrations are vibrational motions that occur along the bond line, changing the bond length or distance between two bonded atoms. They are further distinguished as symmetric or asymmetric. In symmetric stretching, the...
Stretching vibrations are vibrational motions that occur along the bond line, changing the bond length or distance between two bonded atoms. They are further distinguished as symmetric or asymmetric. In symmetric stretching, the...
IR Spectrometers
There are two main infrared (IR) spectrophotometers: dispersive IR spectrometers and Fourier transform infrared (FTIR) spectrometers. In a dispersive IR spectrometer, a beam of infrared radiation produced by a hot wire is divided into two parallel equal-intensity beams using mirrors. One beam passes through the sample, while another is a reference beam. The beams then move through the monochromator, which separates the radiations into a continuous spectrum of different frequencies. The...
IR Frequency Region: X–H Stretching
In IR spectroscopy, signals produced by the X−H bonds (such as C−H, O−H, or N−H) can be observed in the frequency range of 2700–4000 cm–1. The C−H stretching vibration forms sharp bands in the region 2850–3000 cm–1. The presence of the O−H stretching vibration leads to the forming of an absorption band in the frequency range 3650–3200 cm−1. At the same time, N−H stretching can be confirmed by absorption bands in the 3500–3100 cm−1 range. Even though both O−H and N−H bonds vibrate at a similar...
IR Frequency Region: Fingerprint Region
IR spectra are divided into two main regions: the diagnostic region and the fingerprint region. The diagnostic region of the spectrum lies above 1500 cm−1. The absorptions resulting from single-bond vibrations of the N–H, C–H, and O–H stretch at higher wavenumbers and appear on the left side of the spectrum. The stretching absorptions of the C≡C and C≡N occur between 2100–2300 cm−1. In contrast, those arising from stretching absorptions of the C=O, C=N, and C=C occur between 1600–1850 cm−1.
The...
The...


