微波光谱学和1-甲···H2O复合物的结构:两个键使该复合物成为一个刚性旋转器
Surabhi Gupta1, Charlotte N Cummings2, Nicholas R Walker2
1Department of Inorganic and Physical Chemistry, Indian Institute of Science Bangalore, Bengaluru560012, India.
The journal of physical chemistry. A
|September 10, 2025
概括
1-甲和水 (H2O) 复合物的微波光谱显示出一种罕见的刚性旋转器结构. 这项研究确定了弱结复合体中的特定O-H···F和C-H···O键.
科学领域:
- 分子光谱学 分子光谱学
- 物理化学 物理化学
- 超分子化学 超分子化学
背景情况:
- 弱结合复合体为非共价相互作用提供了洞察力.
- 了解化芳香系统中的结是至关重要的.
研究的目的:
- 为了研究1-甲-水复合物的结构和键.
- 分析各种同位素的旋转光谱.
主要方法:
- 破碎的脉冲里埃变换微波光谱学 (CP-FTMW)
- 对四种同位素 (H2O,D2O,DOH,H218O) 的旋转常数分析
- 分子中的原子 (AIM) 和自然键轨道 (NBO) 理论分析.
主要成果:
- 1-甲-水复合体表现出一种罕见的刚性旋转器结构.
- 水既充当键捐赠体 (O-H··F),又充当接受体 (C-H··O).
- 复合体以特定的键类型在平面内方向形成.
结论:
- 通过旋转光谱学确定1-甲-水复合物的结构.
- AIM和NBO的分析证实了发现的键的存在和性质.
- 刚性旋转器的行为是这种弱结合复合体的不寻常特征.
相关概念视频
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
1.3K
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...
1.3K
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR
1.7K
The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.
1.7K
Spin–Spin Coupling Constant: Overview
1.5K
In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
1.5K
Valence Bond Theory
11.2K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
11.2K
¹H NMR: Complex Splitting
1.8K
A proton M that is coupled to a proton X results in doublet signals for M. However, NMR-active nuclei can be simultaneously coupled to more than one nonequivalent nucleus. When M is coupled to a second proton A, such as in styrene oxide, each peak in the doublet is split into another doublet.
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied...
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied...
1.8K
¹H NMR: Interpreting Distorted and Overlapping Signals
1.5K
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...
1.5K


