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Related Concept Videos

Chemical Ionization (CI) Mass Spectrometry01:21

Chemical Ionization (CI) Mass Spectrometry

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...
Ionic Bonding and Electron Transfer02:48

Ionic Bonding and Electron Transfer

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.
Ionization Energy03:12

Ionization Energy

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:
Electrospray Ionization (ESI) Mass Spectrometry01:12

Electrospray Ionization (ESI) Mass Spectrometry

Higher molecular weight biomolecules are nonvolatile compounds that may decompose before ionizing or vaporizing during mass analysis with conventional electron impact ionization methods. Accordingly, electrospray ionization (ESI) is the favored method for vaporizing and ionizing biomolecules as it circumvents rapid fragmentation and enables the recording of mass signals for the entire biomolecule.
ESI utilizes electrical energy to transfer ions from the liquid phase of the sample into the...
Electron Configurations02:46

Electron Configurations

Electron configurations and orbital diagrams can be determined by applying the Aufbau principle (each added electron occupies the subshell of lowest energy available), Pauli exclusion principle (no two electrons can have the same set of four quantum numbers), and Hund’s rule of maximum multiplicity (whenever possible, electrons retain unpaired spins in degenerate orbitals).
The relative energies of the subshells determine the order in which atomic orbitals are filled (1s, 2s, 2p, 3s, 3p, 4s,...
Ionic Radii03:10

Ionic Radii

Ionic radius is the measure used to describe the size of an ion. A cation always has fewer electrons and the same number of protons as the parent atom; it is smaller than the atom from which it is derived. For example, the covalent radius of an aluminum atom (1s22s22p63s23p1) is 118 pm, whereas the ionic radius of an Al3+ (1s22s22p6) is 68 pm. As electrons are removed from the outer valence shell, the remaining core electrons occupying smaller shells experience a greater effective nuclear...

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Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F&#8722;
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Electron ionization of SiCl4.

Simon J King1, Stephen D Price

  • 1Department of Chemistry, University College London, London, United Kingdom. Simon-john.king@bristol.ac.uk

The Journal of Chemical Physics
|February 24, 2011
PubMed
Summary

This study quantifies fragment ion formation from silicon tetrachloride (SiCl4) electron ionization. New data reveal insights into dissociative ionization mechanisms and energetics, including first-time measurements for Cl2+ formation.

Area of Science:

  • Physical Chemistry
  • Atomic and Molecular Physics
  • Mass Spectrometry

Background:

  • Understanding molecular fragmentation under electron impact is crucial for various fields.
  • Silicon tetrachloride (SiCl4) is an important industrial chemical, but its electron ionization fragmentation pathways are not fully elucidated.
  • Previous studies on SiCl4 ionization have limitations in distinguishing fragmentation contributions.

Purpose of the Study:

  • To determine relative partial ionization cross sections (PICS) for fragment ions from SiCl4 electron ionization.
  • To differentiate contributions from single, double, and triple ionization to fragment ion yields.
  • To provide the first quantitative measurements of Cl2+ formation and ion pair production via dissociative double ionization.

Main Methods:

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Analysis of Complex Molecules and Their Reactions on Surfaces by Means of Cluster-Induced Desorption/Ionization Mass Spectrometry
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Analysis of Complex Molecules and Their Reactions on Surfaces by Means of Cluster-Induced Desorption/Ionization Mass Spectrometry

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  • Time-of-flight mass spectrometry combined with an ion coincidence technique.
  • Electron ionization of SiCl4 in the energy range of 30-200 eV.
  • Analysis of 2D ion coincidence data to study dissociation mechanisms.

Main Results:

  • Relative precursor-specific PICS for SiCl4 fragment ions were determined for the first time.
  • Distinguished contributions from single and double ionization to singly charged fragment ions.
  • Reported the first quantitative measurements of Cl2+ fragment ion formation and ion pair production.
  • Identified the lowest energy dicationic precursor state for SiCl4 at 27.4 ± 0.3 eV.

Conclusions:

  • The study provides a comprehensive dataset of relative PICS for SiCl4 fragment ions.
  • Insights into the mechanisms of dissociative ionization, particularly the role of double ionization, were gained.
  • The findings offer valuable data for understanding the fundamental processes of molecular ionization and fragmentation.