Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/180409
Título: SF6 Negative Ion Formation in Charge Transfer Experiments
Autor: Kumar, Sarvesh
Hoshino, Masamitsu
Kerkeni, Boutheïna
Garcia, Gustavo
Ouerfelli, Ghofrane
Al-Mogren, Muneerah Mogren
Limão-Vieira, Paulo
Palavras-chave: Anion formation
Charge transfer
Energy loss
Mass spectrometry
Sulphur hexafluoride
sulphur hexafluoride
mass spectrometry
energy loss
anion formation
charge transfer
Drug Discovery
Analytical Chemistry
Chemistry (miscellaneous)
Molecular Medicine
Physical and Theoretical Chemistry
Pharmaceutical Science
Organic Chemistry
Data: 24-Ago-2024
Resumo: 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.
Descrição: 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.
Peer review: yes
URI: http://hdl.handle.net/10362/180409
DOI: https://doi.org/10.3390/molecules29174118
ISSN: 1420-3049
Aparece nas colecções:Home collection (FCT)

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