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Chemical Ionization (CI) Mass Spectrometry01:21

Chemical Ionization (CI) Mass Spectrometry

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The molecular ion peak of a molecule in the mass spectrum provides vital information for molecular identification. However, conventional electron impact ionization can lead to the rapid dissociation of some molecular ions before they reach the detector. A milder ionization method is required to increase the lifetime of such ionized analyte molecules. Chemical ionization (CI) is a gas-phase protonation reaction useful for mass-analyzing analyte molecules that are easily protonated to yield the...
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The amount of energy required to remove the most loosely bound electron from a gaseous atom in its ground state is called its first ionization energy (IE1). The first ionization energy for an element, X, is the energy required to form a cation with 1+ charge:
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In an atom, the negatively charged electrons are attracted to the positively charged nucleus. In a multielectron atom, electron-electron repulsions are also observed. The attractive and repulsive forces are dependent on the distance between the particles, as well as the sign and magnitude of the charges on the individual particles. When the charges on the particles are opposite, they attract each other. If both particles have the same charge, they repel each other.
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Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions. 
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在内部外的分子效应连续的双离子化.

Shutao Zhang1,2,3, Ming Zhang1, Ludger Inhester4

  • 1School of Physics, State Key Laboratory for Mesoscopic Physics and Collaborative Innovation Center of Quantum Matter, Peking University, Beijing 100871, China.

The Journal of chemical physics
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概括
此摘要是机器生成的。

我们开发了分子中双光子双电离 (TPDI) 的理论框架. 我们的研究结果表明,分子结构显著影响光离子化动力学,为研究这些过程提供了一种新的方法.

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科学领域:

  • 原子和分子物理 原子和分子物理
  • 量子光学是一种量子光学.
  • 化学物理 化学物理

背景情况:

  • 序列内双光子双电离 (TPDI) 是一个复杂的过程,涉及多个光子与原子或分子相互作用.
  • 了解发射的光电子的角分布为电离化动态提供了关键的见解.
  • 以前的研究往往侧重于原子系统,不太强调分子效应.

研究的目的:

  • 提出分析光电子在分子TPDI中的角分布的理论框架.
  • 为了研究分子结构对电离动力学的影响.
  • 为在多原子系统中模拟和研究TPDI提供计算工具.

主要方法:

  • 开发一个理论框架的连续内部外TPDI.
  • 在CH3I中对的4d外进行序列双电离的数值计算.
  • 使用长度和速度计进行计算.
  • 与原子异进行比较,以突出分子效应.

主要成果:

  • 顺序TPDI的角异性参数被计算为CH3I.
  • 观察到分子结构对第二个电离阶段的异构度参数有显著的影响.
  • 对CH3I的计算参数与原子的参数不同,强调了分子效应.

结论:

  • 分子结构强烈影响了顺序TPDI中的光电子的角分布.
  • 这提供了一种敏感的方法来探测多原子系统中的光离子化动态.
  • 开发的计算代码使得进一步的理论研究分子效应在内双电离.