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Related Concept Videos

Mass Spectrometry: Long-Chain Alkane Fragmentation01:18

Mass Spectrometry: Long-Chain Alkane Fragmentation

2.7K
The molecular ions of linear alkanes prefer to fragment at the carbon-carbon bond away from the end of the chain since the cleavage of an inner bond creates a stable carbocation and a stable radical. Consequently, the mass signals of linear alkanes feature intense peaks in the middle of the mass-to-charge ratio plot with weaker peaks on either end. The fragmentation of each carbon-carbon bond with the release of a methyl group in each splitting leads to prominent peaks in the mass spectra...
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Mass Spectrometry: Branched Alkane Fragmentation01:29

Mass Spectrometry: Branched Alkane Fragmentation

1.9K
This lesson delves into the mass spectrometry of branched alkane fragmentation. Branched alkanes possess secondary or tertiary carbon atoms, which generate relatively stable carbocations if the cleavage occurs at the branching point. The high stability of carbocations drives the instant fragmentation of branched alkanes. Accordingly, the branched alkane's molecular ion peak is very weak or invisible in the mass spectra, especially in comparison to a linear alkane.
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Mass Spectrometry: Molecular Fragmentation Overview01:20

Mass Spectrometry: Molecular Fragmentation Overview

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The ionization of a molecule into a molecular ion inside the mass spectrometer causes instability in the molecule's structure due to the loss of an electron. This eventually leads to the fragmentation or breaking of some bonds in the molecule. The fragmentation occurs predominantly at specific bonds to yield relatively stable fragments.
One type of fragmentation pattern is the cleavage of a single bond in the molecular ion. The cleavage leads to a radical and a cation. The cleavage can occur at...
6.2K
Mass Spectrometry: Cycloalkane Fragmentation01:05

Mass Spectrometry: Cycloalkane Fragmentation

2.5K
In mass spectrometry, cycloalkanes exhibit distinct fragmentation patterns due to the inherent stability of their molecular ions compared to linear or branched alkanes. The ring structure of cycloalkanes provides additional stability to the molecular ions, often resulting in prominent ion peaks in the mass spectrum.
For example, cyclohexane molecular ions have a mass-to-charge ratio (m/z) of 84, which tends to produce a stronger signal than linear alkanes like hexane. This stability comes from...
2.5K
Mass Spectrometry: Alkene Fragmentation00:59

Mass Spectrometry: Alkene Fragmentation

3.9K
Alkenes lose one electron from the unsaturated π bond upon ionization and form stable molecular ions. Further fragmentation of alkenes occurs through three different reaction pathways. The most prominent fragmentation is the cleavage at the allylic position. The resultant allylic carbocation is resonance stabilized. In the mass spectra of terminal alkenes, this fragment appears at a mass-to-charge ratio of 41. In the internal alkenes, where there are two choices of allylic cleavage, the...
3.9K
Mass Spectrometry: Carboxylic Acid, Ester, and Amide Fragmentation01:01

Mass Spectrometry: Carboxylic Acid, Ester, and Amide Fragmentation

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The fragmentation patterns observed for compounds such as carboxylic acids, esters, and amides in the mass spectra include ⍺-cleavage and McLafferty rearrangement. Fragmentation by ⍺-cleavage preferentially occurs at the carbon-carbon bond at the ⍺-position next to the carboxylic group to generate a neutral radical and a cation. Long chain compounds with hydrogen at their γ-carbon undergo McLafferty rearrangement to give a radical cation and a neutral alkene.
For example, the...
2.8K

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Methane Hydrate Crystallization on Sessile Water Droplets
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Structure, Reactivity, and Fragmentation of Small Multi-Charged Methane Clusters.

A Sanaa Zaag1, O Yazidi1, N-E Jaidane1

  • 1Laboratoire de Spectroscopie Atomique, Moléculaire et Applications - LSAMA, Université de Tunis Al Manar , Tunis, Tunisia.

The Journal of Physical Chemistry. A
|February 26, 2016
PubMed
Summary
This summary is machine-generated.

Ultrafast laser pulses reveal that small methane clusters, when multiply charged, undergo unique intracluster reactions and fragmentations. These processes differ significantly from isolated methane ions or large ionized clusters.

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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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Area of Science:

  • Physical Chemistry
  • Chemical Physics
  • Laser Physics

Background:

  • Methane clusters exhibit complex behavior under high-energy conditions.
  • Understanding cluster dynamics is crucial for various chemical and physical processes.

Purpose of the Study:

  • To investigate the fragmentation and reaction pathways of small methane clusters (CH4)n upon intense femtosecond laser excitation.
  • To characterize the resulting ionized species and their subsequent reactions.

Main Methods:

  • Irradiation of small methane clusters with intense femtosecond laser pulses at 624 nm.
  • Detection of ionized and fragmented species using time-of-flight mass spectrometry (TOF MS).
  • First-principles calculations ( (R)MP2/aug-cc-pVXZ) for spectral assignment and stability analysis of charged clusters (n=1-4, q=1-4).

Main Results:

  • Evidence for bound, multiply charged methane molecules and clusters formed via Coulomb explosion.
  • Identification of unique intracluster reactions and fragmentation patterns in multiply charged small methane clusters.
  • Calculations confirmed cluster stabilities and potential fragments from intracluster reactivity.

Conclusions:

  • Multiply charged small methane clusters exhibit distinct intracluster reaction and fragmentation dynamics.
  • These dynamics differ from those of isolated methane ions and large ionized methane clusters.
  • Femtosecond laser excitation provides insights into ultrafast processes in molecular clusters.