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Mass Analyzers: Common Types01:19

Mass Analyzers: Common Types

The quadrupole mass analyzer consists of four cylindrical metal rods arranged in a diamond carrying a DC voltage and a radio-frequency AC voltage. The motion of ions through the quadrupole depends on the field strength, causing only ions of a certain m/z to resonate successfully and strike the detector at a given field strength. Though the transmission rate for these analyzers is high, the exact elemental composition of the sample is not determined because of low resolution; however, they are...
Double Resonance Techniques: Overview01:12

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Double resonance techniques in Nuclear Magnetic Resonance (NMR) spectroscopy involve the simultaneous application of two different frequencies or radiofrequency pulses to manipulate and observe two distinct nuclear spins. One important application of double resonance is spin decoupling, which selectively suppresses coupling with one type of nucleus while observing the NMR signal from another nucleus, simplifying the spectrum and enhancing resolution.
Spin decoupling is usually achieved by...
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Inductive Effects on Chemical Shift: Overview

The protons in unsubstituted alkanes are strongly shielded with chemical shifts below 1.8 ppm. Methine, methylene, and methyl protons appear at approximately 1.7, 1.2 and 0.7 ppm, while the proton signal from methane appears at 0.23 ppm. An electronegative substituent, such as chlorine, withdraws the electron density from the protons, increasing their chemical shift. Progressive substitution of the hydrogens in methane by chlorine shifts the proton signals increasingly downfield, to 3.05 ppm in...
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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...
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Molecular Orbital Theory II

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Directionality of Nuclear Transport01:42

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Ras-related nuclear protein or Ran is a small G protein that cycles between its GTP and GDP bound states. Ran specific regulators, a Ran GTPase Activating Protein or RanGAP present in the cytosol and a Ran guanine nucleotide exchange factor or RanGEF present inside the nucleus regulate GTP/GDP exchange. A high concentration of GTP inside the cells, in addition to this asymmetric distribution of  Ran-specific regulators, leads to a higher RanGTP concentration inside the nucleus. This...

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Related Experiment Video

Updated: Jun 23, 2026

Direct Imaging of Laser-driven Ultrafast Molecular Rotation
10:52

Direct Imaging of Laser-driven Ultrafast Molecular Rotation

Published on: February 4, 2017

Directional correlation in direct and sequential double ionization of model atoms.

S Haan, N Hoekema, S Poniatowski

    Optics Express
    |May 1, 2009
    PubMed
    Summary

    Investigating two-electron atoms in intense laser fields reveals competing double ionization pathways. Electron-electron repulsion significantly influences whether electrons exit together or sequentially on opposite sides.

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    Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
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    Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers
    08:51

    Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers

    Published on: August 18, 2017

    Area of Science:

    • Atomic Physics
    • Quantum Mechanics
    • Laser-Matter Interactions

    Background:

    • Understanding the behavior of atoms subjected to intense electromagnetic fields is crucial in atomic physics.
    • Double ionization of atoms is a complex process influenced by electron-electron interactions and external fields.
    • Previous studies have explored single and double ionization, but the directional dependence and competing mechanisms in two-electron systems require further investigation.

    Purpose of the Study:

    • To investigate the directional dependence in the time evolution of spatial wavefunctions for two-electron model atoms under intense laser fields.
    • To analyze the competing scenarios of simultaneous and sequential double ionization.
    • To determine the role of electron-electron repulsion in these competing processes across various laser intensities.

    Main Methods:

    • Utilizing a two-electron model atom.
    • Simulating the system's response to intense laser fields.
    • Analyzing the spatial wavefunctions and electron trajectories to identify ionization pathways.
    • Varying laser intensities to observe their effect on the ionization dynamics.

    Main Results:

    • Two distinct competing scenarios for double ionization were identified: simultaneous ejection on the same side and sequential ejection on opposite sides.
    • The electron-electron repulsion plays a critical role in determining which ionization pathway dominates.
    • Directional dependence in wavefunction evolution, including jet formation, was observed.

    Conclusions:

    • The study highlights the complex interplay between electron-electron repulsion and external laser fields in driving double ionization.
    • The findings provide insights into the fundamental mechanisms governing electron emission from atoms in strong fields.
    • The observed directional effects and competing pathways offer a deeper understanding of laser-induced atomic processes.