TY - JOUR
T1 - SF6 Negative Ion Formation in Charge Transfer Experiments
AU - Kumar, Sarvesh
AU - Hoshino, Masamitsu
AU - Kerkeni, Boutheïna
AU - Garcia, Gustavo
AU - Ouerfelli, Ghofrane
AU - Al-Mogren, Muneerah Mogren
AU - Limão-Vieira, Paulo
N1 - info:eu-repo/grantAgreement/FCT/OE/PD%2FBD%2F142831%2F2018/PT#
info:eu-repo/grantAgreement/FCT/OE/COVID%2FBD%2F152673%2F2022/PT#
info:eu-repo/grantAgreement/FCT/Concurso de avaliação no âmbito do Programa Plurianual de Financiamento de Unidades de I&D (2017%2F2018) - Financiamento Base/UIDB%2F00068%2F2020/PT#
Partial financial support from the Spanish Ministerio de Ciencia e Innovación Project No. PID2019-104727RB-C21 (G.G.) is also acknowledged. The authors would like to acknowledge the Deanship of Graduate Studies and Scientific Research, Taif University for funding this work and extend their appreciation to the Researchers Supporting Project (RSPD2024R808) of King Saud University, Riyadh, Saudi Arabia.
© 2024 by the authors.
Licensee MDPI, Basel, Switzerland.
PY - 2024/8/24
Y1 - 2024/8/24
N2 - In the present work, we report an update and extension of the previous ion-pair formation study of Hubers, M.M.; Los, J. Chem. Phys. 1975, 10, 235–259, noting new fragment anions from time-of-flight mass spectrometry. The branching ratios obtained from the negative ions formed in K + SF6 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 SF5− and contributing to more than 70% of the total ion yield, followed by the non-dissociated parent anion SF6− and F−. Other less intense anions amounting to <20% are assigned to SF3− and F2−, while a trace contribution at 32u is tentatively assigned to S− 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.
AB - In the present work, we report an update and extension of the previous ion-pair formation study of Hubers, M.M.; Los, J. Chem. Phys. 1975, 10, 235–259, noting new fragment anions from time-of-flight mass spectrometry. The branching ratios obtained from the negative ions formed in K + SF6 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 SF5− and contributing to more than 70% of the total ion yield, followed by the non-dissociated parent anion SF6− and F−. Other less intense anions amounting to <20% are assigned to SF3− and F2−, while a trace contribution at 32u is tentatively assigned to S− 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.
KW - Anion formation
KW - Charge transfer
KW - Energy loss
KW - Mass spectrometry
KW - Sulphur hexafluoride
KW - sulphur hexafluoride
KW - mass spectrometry
KW - energy loss
KW - anion formation
KW - charge transfer
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=nova_api&SrcAuth=WosAPI&KeyUT=WOS:001312841300001&DestLinkType=FullRecord&DestApp=WOS_CPL
UR - http://www.scopus.com/inward/record.url?scp=85204139149&partnerID=8YFLogxK
U2 - 10.3390/molecules29174118
DO - 10.3390/molecules29174118
M3 - Article
C2 - 39274966
SN - 1420-3049
VL - 29
JO - Molecules
JF - Molecules
IS - 17
M1 - 4118
ER -