理论建模Sr{q+) He (q = 0, 1, 2) 范德瓦尔斯系统包括旋转轨道合
Mohamed Bejaoui1, Wissem Zrafi1, Jamila Dhiflaoui1
1Faculty of Science of Monastir, Laboratory of Interfaces and Advanced Materials LR11ES55, Physics Department, University of Monastir, 5019 Monastir, Tunisia.
ACS omega
|August 5, 2024
概括
本研究使用先进的计算方法探索离子与的相互作用. 结果与现有数据有很好的一致性,特别是对于离子-系统.
科学领域:
- 原子和分子物理 原子和分子物理
- 量子化学 是一个量子化学.
- 计算化学的计算化学
背景情况:
- 了解离子-原子相互作用对等离子体物理学和天体物理学至关重要.
- (Sr) 和其与 (He) 等贵气相互作用的离子是基本的系统.
研究的目的:
- 研究中性和带电的 (Srq+,q=0,1,2) 与的相互作用.
- 计算各种电子状态的潜在能量曲线和二极极矩.
- 评估旋转轨道相互作用对光谱性质的影响.
主要方法:
- 一开始的方法包括伪潜能技术和对潜力方法.
- 完整的配置交互计算和合集群单双与扰乱三倍 (CCSD(T)) 级别.
- 旋转轨道效应的半经验方法.
主要成果:
- 计算了SrHe和Sr+He系统的潜在能量曲线和二极点.
- 确定Srq+He状态的光谱常数,有和没有旋转轨道相互作用.
- 观察到与现有的理论和实验研究有很好的一致性,特别是对Sr+He.
结论:
- 计算方法准确地描述了 Sr-He 相互作用.
- 对于某些电子状态,旋转轨道效应是显著的.
- 这项研究为了解-系统提供了有价值的数据.
更多相关视频
相关概念视频
Van der Waals Interactions
63.7K
Atoms and molecules interact with each other through intermolecular forces. These electrostatic forces arise from attractive or repulsive interactions between particles with permanent, partial, or temporary charges. The intermolecular forces between neutral atoms and molecules are ion–dipole, dipole–dipole, and dispersion forces, collectively known as van der Waals forces.
63.7K
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
1.1K
Vicinal or three-bond coupling is commonly observed between protons attached to adjacent carbons. Here, nuclear spin information is primarily transferred via electron spin interactions between adjacent C‑H bond orbitals. This generally favors the antiparallel arrangement of spins, so 3J values are usually positive.
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the...
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the...
1.1K
Van der Waals Equation
4.0K
The ideal gas law is an approximation that works well at high temperatures and low pressures. The van der Waals equation of state (named after the Dutch physicist Johannes van der Waals, 1837−1923) improves it by considering two factors.
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the volume...
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the volume...
4.0K
Valence Bond Theory and Hybridized Orbitals
19.2K
According to valence bond theory, a covalent bond results when: (1) an orbital on one atom overlaps an orbital on a second atom, and (2) the single electrons in each orbital combine to form an electron pair. The strength of a covalent bond depends on the extent of overlap of the orbitals involved. Maximum overlap is possible when the orbitals overlap on a direct line between the two nuclei.
A σ bond (single bond in a Lewis structure) is a covalent bond in which the electron density is...
A σ bond (single bond in a Lewis structure) is a covalent bond in which the electron density is...
19.2K
Spin–Spin Coupling: One-Bond Coupling
951
Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
951
Molecular Orbital Theory II
19.0K
Molecular Orbital Energy Diagrams
19.0K


