Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Electron Behavior00:54

Electron Behavior

Electrons are negatively charged subatomic particles that are attracted to an orbit around the positively-charged nucleus of an atom. They reside in locations that are associated with energy levels called shells and are further organized into sub-shells and orbitals within each shell.Electrons Orbit the NucleusElectrons are found in specific locations outside of the nucleus. The shell in which an electron resides indicates the general energy level of the electron: those closer to the nucleus...
Valence Bond Theory02:42

Valence Bond Theory

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...
π Electron Effects on Chemical Shift: Overview01:27

π Electron Effects on Chemical Shift: Overview

An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0, resulting in...
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds01:14

π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds

In aromatic compounds, such as benzene, the circulation of (4n + 2) π-electrons sets up a diamagnetic or diatropic ring current around the perimeter of the molecule. This current induces a magnetic field that opposes the external field inside the ring and reinforces it on the outside. The protons in benzene are deshielded and exhibit high chemical shifts in the range 6.5–8.5 ppm. The shielding effect at the center of the ring is evident in complex aromatic molecules, such as annulenes. In...
Electron Behavior01:09

Electron Behavior

Electrons are negatively charged subatomic particles attracted to and orbit around the positively-charged nucleus of an atom. They reside in spaces associated with energy levels called shells and are further organized into subshells and orbitals within each shell.
Electrons Orbit the Nucleus
Electrons are found in specific locations outside of the nucleus. The shell in which an electron resides indicates the general energy level of the electron: those closer to the nucleus have less energy,...
Deactivation Processes: Jablonski Diagram01:25

Deactivation Processes: Jablonski Diagram

Luminescence, the emission of light by a substance that has absorbed energy, is a process that involves the interaction of molecules with light. The energy-level diagram, or Jablonski diagram, is a graphical representation of these interactions, illustrating the various states and transitions a molecule can undergo. In a typical Jablonski diagram, the lowest horizontal line represents the ground-state energy of the molecule, which is usually a singlet state. This state represents the energies...

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Dynamic breaking of mirror symmetry in spin-dependent electron transport through chiral media causes enantiomeric excesses.

Science advances·2026
Same author

Correction to "Ultrafast Transversal CISS Effect Observed in a Chiral Photoswitching Molecule".

The journal of physical chemistry letters·2025
Same author

Ultrafast Transversal CISS Effect Observed in a Chiral Photoswitching Molecule.

The journal of physical chemistry letters·2025
Same author

Light driven photoswitches: three classes of molecular systems that result in a single photoproduct <i>via</i> a conical intersection and an exothermic reverse reaction.

Physical chemistry chemical physics : PCCP·2024
Same author

Mixed-Valence Bridged Norbornylogous Compounds as Switchable Cells for Molecular Quantum Cellular Automata: A Compromise between High Polarizability and Low Power Dissipation.

The journal of physical chemistry. A·2023
Same author

Spin polarization effects in trigonal mixed-valence complexes exhibiting double exchange supported by external spin-cores.

The Journal of chemical physics·2023

相关实验视频

Updated: Jul 10, 2026

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
11:44

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds

Published on: October 18, 2018

在Jahn-Teller系统中对电子退化的价值键分析:环二烯基基和阴离子基的低状态.

Shmuel Zilberg1, Yehuda Haas

  • 1Department of Physical Chemistry, Farkas Center for Light-Induced Reactions, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.

Journal of the American Chemical Society
|September 5, 2002
PubMed
概括
此摘要是机器生成的。

雅恩-泰勒效应扭曲了来自对称结构的环聚二烯基基和子. 价值债券分析证实,这种扭曲来自于一级的Jahn-Teller效应,确定了特定的扭曲坐标.

更多相关视频

Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
13:56

Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations

Published on: October 12, 2019

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
08:54

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid

Published on: January 25, 2020

相关实验视频

Last Updated: Jul 10, 2026

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
11:44

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds

Published on: October 18, 2018

Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
13:56

Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations

Published on: October 12, 2019

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
08:54

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid

Published on: January 25, 2020

科学领域:

  • 量子化学 是一个量子化学.
  • 分子光谱学 分子光谱学
  • 化学物理 化学物理

背景情况:

  • 环二烯基基 (CPDR) 和离子 (CPDC) 呈现出偏离理想对称几何的电子状态.
  • 雅恩-泰勒效应是一个关键的现象,它导致了电子状态退化的分子中的几何扭曲.

研究的目的:

  • 分析CPDR和CPDC的最低电子状态中的Jahn-Teller扭曲.
  • 通过一种价值键方法来阐明这些扭曲的性质.
  • 为了确定负责观察到的扭曲的特定分子坐标.

主要方法:

  • 使用Longuet-Higgins的相变规则进行价值债券分析.
  • 电子状态和分子几何学的理论研究.
  • 计算化学方法来建模分子行为.

主要成果:

  • 由于第一阶级的Jahn-Teller效应,CPDR和CPDC都经历了扭曲.
  • CPDR表现出一个孤立的Jahn-Teller变性.
  • CPDC显示了一个主要的Jahn-Teller退化,伴随着五个卫星退化.

结论:

  • 一级的Jahn-Teller效应是CPDR和CPDC中扭曲的主要原因.
  • 价值键分析提供了一种化学直观的方法来识别扭曲坐标.
  • 了解这些扭曲对于预测分子特性和反应性至关重要.