SF6 Negative Ion Formation in Charge Transfer Experiments

In the present work, we report an update and extension of the previous ion-pair formation study of Hubers, M.M.; Los, J. <i>Chem. Phys.</i><b>1975</b>, <i>10</i>, 235-259, noting new fragment anions from time-of-flight mass spectrometry. The branching ratios obtained from the negative ions formed in K + SF<sub>6</sub> collisions, in a wide energy range from 10.7 up to 213.1 eV in the centre-of-mass frame, show that the main anion is assigned to SF<sub>5</sub><sup>-</sup> and contributing to more than 70% of the total ion yield, followed by the non-dissociated parent anion SF<sub>6</sub><sup>-</sup> and F<sup>-</sup>. Other less intense anions amounting to <20% are assigned to SF<sub>3</sub><sup>-</sup> and F<sub>2</sub><sup>-</sup>, while a trace contribution at 32u is tentatively assigned to S<sup>-</sup> formation, although the rather complex intramolecular energy redistribution within the temporary negative ion is formed during the collision. An energy loss spectrum of potassium cation post-collision is recorded showing features that have been assigned with the help of theoretical calculations. Quantum chemical calculations for the lowest-lying unoccupied molecular orbitals in the presence of a potassium atom are performed to support the experimental findings. Apart from the role of the different resonances participating in the formation of different anions, the role of higher-lying electronic-excited states of Rydberg character are noted.

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Journal
Molecules
Published
2024-08-30
DOI
https://doi.org/10.3390/molecules29174118
Citations
1
Primary Topic
Mass Spectrometry Techniques and Applications
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article
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SF6 Negative Ion Formation in Charge Transfer Experiments

M. Hoshino, Sarvesh Kumar, Ghofrane Ouerfelli, Boutheı̈na Kerkeni et al.
1 citations
Molecules
Mass Spectrometry Techniques and Applications
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article

SF6 Negative Ion Formation in Charge Transfer Experiments

M. Hoshino, Sarvesh Kumar, Ghofrane Ouerfelli, Boutheı̈na Kerkeni, P. Limão-Vieira, G. Garcı́a, Muneerah Mogren Al‐Mogren
article en
1 citations

Abstract

In the present work, we report an update and extension of the previous ion-pair formation study of Hubers, M.M.; Los, J. <i>Chem. Phys.</i><b>1975</b>, <i>10</i>, 235-259, noting new fragment anions from time-of-flight mass spectrometry. The branching ratios obtained from the negative ions formed in K + SF<sub>6</sub> collisions, in a wide energy range from 10.7 up to 213.1 eV in the centre-of-mass frame, show that the main anion is assigned to SF<sub>5</sub><sup>-</sup> and contributing to more than 70% of the total ion yield, followed by the non-dissociated parent anion SF<sub>6</sub><sup>-</sup> and F<sup>-</sup>. Other less intense anions amounting to <20% are assigned to SF<sub>3</sub><sup>-</sup> and F<sub>2</sub><sup>-</sup>, while a trace contribution at 32u is tentatively assigned to S<sup>-</sup> formation, although the rather complex intramolecular energy redistribution within the temporary negative ion is formed during the collision. An energy loss spectrum of potassium cation post-collision is recorded showing features that have been assigned with the help of theoretical calculations. Quantum chemical calculations for the lowest-lying unoccupied molecular orbitals in the presence of a potassium atom are performed to support the experimental findings. Apart from the role of the different resonances participating in the formation of different anions, the role of higher-lying electronic-excited states of Rydberg character are noted.

MoleculesVol. 29(17)
Tunis University (TN), Consejo Superior de Investigaciones Científicas (ES), Lawrence Berkeley National Laboratory (US), Taif University (SA), King Saud University (SA), Instituto de Física Fundamental (ES), Sophia University (JP), Tunis El Manar University (TN), Manouba University (TN), Universidade Nova de Lisboa (PT)
Affordable and clean energy
Openalex Percentile: Top 50%
Mass Spectrometry Techniques and Applications
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