基于使用光谱,结构,基于QTAIM和基于NBO的描述符的方程来量化键能量的量化,这些描述符通过分子量身定制方法校准
Andrei V Afonin1, Danuta Rusinska-Roszak2
1A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Division of Russian Academy of Sciences, Irkutsk, Russia.
Journal of molecular modeling
|December 30, 2023
概括
这项研究使用光谱,结构,QTAIM和NBO描述器量化了分子内键能量. 一个新的方程系统提供了可靠的能量估计基碳化合物.
科学领域:
- 计算化学的计算化学
- 分子建模分子建模
- 量子化学 是一个量子化学.
背景情况:
- 键对于分子结构和性质至关重要.
- 精确量化键能量仍然是一个挑战.
- 这项研究的重点是基碳化合物中的O−H···O=C分子内键.
研究的目的:
- 开发一种可靠的方法来量化分子内键能量.
- 为了建立各种分子描述符和键能量之间的关系.
- 为预测键能量创建一个方程系统.
主要方法:
- 计算的光谱 (振动频率,化学转移) 和结构 (纽带长度,距离) 描述器.
- 利用分子中的原子量子理论 (QTAIM) 和自然键轨道 (NBO) 分析.
- 采用分子量身定制方法来量化能量.
主要成果:
- 光谱,结构,QTAIM和NBO描述符显示了相关的变化.
- 这些描述符在功能上与分子内键能量有关.
- 为了估计键能量,推导出一个方程系统.
结论:
- 开发的方程系统能够可靠地和可靠地量化分子内键能量.
- 这种方法整合了多种描述符类型,以提高准确性.
- 这些发现促进了对键的理解和计算评估.
更多相关视频
相关概念视频
Bond Energies and Bond Lengths
25.3K
Stable molecules exist because covalent bonds hold the atoms together. The strength of a covalent bond is measured by the energy required to break it, that is, the energy necessary to separate the bonded atoms. Separating any pair of bonded atoms requires energy — the stronger a bond, the greater the energy required to break it.
25.3K
IR Spectroscopy: Hooke's Law Approximation of Molecular Vibration
1.3K
A covalently bonded heteronuclear diatomic molecule can be modeled as two vibrating masses connected by a spring. The vibrational frequency of the bond can be expressed using an equation derived from Hooke's law, which describes how the force applied to stretch or compress a spring is proportional to the displacement of the spring. In this case, the atoms behave like masses, and the bond acts like a spring.
According to Hooke's law, the vibrational frequency is directly proportional to...
According to Hooke's law, the vibrational frequency is directly proportional to...
1.3K
Hydrogen Bonds
8.5K
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
8.5K
IR Spectrum Peak Broadening: Hydrogen Bonding
1.0K
The vibrational frequency of a bond is directly proportional to its bond strength. As a result, stronger bonds vibrate at higher frequencies, while weaker bonds vibrate at lower frequencies. The stretching vibration of the strong O–H bond in alcohols and phenols (very dilute solution or gas phase) appears as a sharp peak at 3600–3650 cm−1.
However, the extent of hydrogen bonding influences the observed stretching frequency and band broadening. Intermolecular or intramolecular...
However, the extent of hydrogen bonding influences the observed stretching frequency and band broadening. Intermolecular or intramolecular...
1.0K
Molecular Orbital Theory II
19.2K
Molecular Orbital Energy Diagrams
19.2K
Noncovalent Attractions in Biomolecules
50.9K
Noncovalent attractions are associations within and between molecules that influence the shape and structural stability of complexes. These interactions differ from covalent bonding in that they do not involve sharing of electrons.
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
50.9K


