在烯-Br2pi复合体中的极化效应和分散相互作用
Cinzia Chiappe1, Heiner Detert, Dieter Lenoir
1Dipartimento di Chimica Bioorganica e Biofarmacia, Università di Pisa, I-56126 Pisa, Italy. cinziac@farm.unipi.it
Journal of the American Chemical Society
|March 6, 2003
概括
弱结合的分子复合体在科学中至关重要. 这项研究发现了极化性和pi复合物的稳定性之间的直接联系,提出了一个新的预测方程.
科学领域:
- 分子相互作用分子相互作用.
- 化学物理 化学物理
- 超分子化学 超分子化学
背景情况:
- 弱结合的分子复合体是整个化学,物理和生物科学的基础.
- 了解这些相互作用是预测化学反应性和材料性能的关键.
研究的目的:
- 量化研究各种和之间形成的平衡前pi复合体.
- 为了建立这些复合物的稳定性和烯的特性之间的定量关系.
主要方法:
- 对与的烯的平衡前pi复合物的分析.
- 对关联常数 (KF) 的定量检查.
- 与olefin极化性和电离潜力的相关性分析.
主要成果:
- 发现-烯pi复合物的关联常数 (KF) 与烯的极化性之间存在直接关系.
- 这些pi复合体的稳定性受捐赠者电离潜力和烯的极化性影响.
结论:
- 该研究提出了一个新的方程来预测Br2-olefin pi-complexes的稳定性,包括分极性和电离潜力.
- 这为理解和预测这些重要的分子复合物的行为提供了更准确的方法.
相关概念视频
VSEPR Theory and the Effect of Lone Pairs
Effect of Lone Pairs of Electrons on Molecule Geometry
Valence Bond Theory
Overview of Valence Bond Theory
Hybridization of Atomic Orbitals I
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
¹H NMR: Complex Splitting
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 first.
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 first.
NMR Spectroscopy of Benzene Derivatives
Simple unsubstituted benzene has six aromatic protons, all chemically equivalent. Therefore, benzene exhibits only a singlet peak at δ 7.3 ppm in the 1H NMR spectrum. The observed shift is far downfield because the aromatic ring current strongly deshields the protons. Any substitution on the benzene ring makes the aromatic protons nonequivalent, and the protons split each other. The peak is, therefore, no longer a singlet and the splitting pattern and their associated coupling constants depend...
Spin–Spin Coupling Constant: Overview
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 have a...
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 have a...


