Absolute charge transfer and fragmentation cross sections in He2+-C60 collisions
A Rentenier1, L F Ruiz, S Díaz-Tendero
1Laboratoire de Collisions, Agrégats et Reactivité, UMR 5589 CNRS, Université Paul Sabatier 3, 31062 Toulouse, France.
Physical Review Letters
|June 4, 2008
Summary
We studied He2++C60 collisions, finding electron transfer and fragmentation processes are complex. Transfer-ionization is key at low energies, while multifragmentation dominates at higher energies.
Area of Science:
- Atomic and Molecular Physics
- Chemical Physics
- Plasma Physics
Background:
- Understanding ion-molecule collisions is crucial for plasma physics and astrophysics.
- Fullerenes (C60) exhibit unique fragmentation dynamics under energetic ion impact.
Purpose of the Study:
- To determine absolute charge transfer and fragmentation cross sections for He2++C60 collisions.
- To elucidate the underlying mechanisms of electron capture and fragmentation in these collisions.
Main Methods:
- Combined experimental measurements and theoretical calculations.
- Analysis of charge transfer and fragmentation patterns across a wide impact energy range (0.1-250 keV).
Main Results:
- Cross sections for He+ and He0 formation are comparable, indicating significant transfer-ionization.
- Transfer-ionization processes are important even at low impact energies.
- Multifragmentation dominates above 40 keV, while sequential C2 evaporation prevails at lower energies.
Conclusions:
- The dynamics of He2++C60 collisions involve a complex interplay of electron capture and ionization.
- Transfer-ionization plays a critical role across the studied energy spectrum.
- Collision energy dictates the dominant fragmentation pathway of the C60 molecule.
Related Concept Videos
Mass Spectrometry: Molecular Fragmentation Overview
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...
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...
Mass Spectrometry: Alkyne Fragmentation
The fragmentation of alkynes preferentially occurs at the carbon–carbon bond between the α and β carbon of the alkyne bond to generate a 3-propynyl cation (or propargyl cation). In terminal alkynes, there is the only type of fragmentation that yields the 3-propynyl cation. The unsubstituted 3-propynyl cation exhibits a peak at a mass-to-charge ratio of 39. In internal alkynes, the 3-propynyl cation is substituted. For example, 2-pentyne fragments into methyl-substituted 3-propynyl cation, which...
Mass Spectrometry: Cycloalkane Fragmentation
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...
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...
Mass Spectrometry: Cycloalkene Fragmentation
The molecular ions of cycloalkenes undergo fragmentation via a retro-Diels–Alder reaction.
Mass Spectrometry: Carboxylic Acid, Ester, and Amide Fragmentation
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 fragmentation of...
For example, the fragmentation of...
Mass Spectrometry: Alkene Fragmentation
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...


