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NMR Spectroscopic Evidence for the Intermediacy of XeF3– in XeF2/F– Exchange, Attempted Syntheses and Thermochemistry of XeF3– Salts, and Theoretical Studies of the XeF3– Anion

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Vasdev, N., Moran, M., Chirakal, R., Tuononen, H., Suontamo, R., Bain, A., & Schrobilgen, G. (2010). NMR Spectroscopic Evidence for the Intermediacy of XeF3– in XeF2/F– Exchange, Attempted Syntheses and Thermochemistry of XeF3– Salts, and Theoretical Studies of the XeF3– Anion. Inorganic Chemistry, 49(19), 8997-9004. https://doi.org/10.1021/ic101275m
Published in
Inorganic Chemistry
Authors
Vasdev, Neil |
Moran, Matthew |
Chirakal, Raman |
Tuononen, Heikki |
Suontamo, Reijo |
Bain, Alex |
Schrobilgen, Gary
Date
2010
Discipline
Epäorgaaninen ja analyyttinen kemiaInorganic and Analytical Chemistry
Copyright
© 2010 American Chemical Society. This is a final draft version of an article whose final and definitive form has been published by ACS. Published in this repository with the kind permission of the publisher.

 
The existence of the trifluoroxenate(II) anion, XeF3−, had been postulated in a prior NMR study of the exchange between fluoride ion and XeF2 in CH3CN solution. The enthalpy of activation for this exchange, ΔH⧧, has now been determined by use of single selective inversion 19F NMR spectroscopy to be 74.1 ± 5.0 kJ mol−1 (0.18 M) and 56.9 ± 6.7 kJ mol−1 (0.36 M) for equimolar amounts of [N(CH3)4][F] and XeF2 in CH3CN solvent. Although the XeF3− anion has been observed in the gas phase, attempts to prepare the Cs+ and N(CH3)4+ salts of XeF3− have been unsuccessful, and are attributed to the low fluoride ion affinity of XeF2 and fluoride ion solvation in CH3CN solution. The XeF3− anion would represent the first example of an AX3E3 valence shell electron pair repulsion (VSEPR) arrangement of electron lone pair and bond pair domains. Fluorine-19 exchange between XeF2 and the F− anion has also been probed computationally using coupled-cluster singles and doubles (CCSD) and density functional theory (DFT; PBE1PBE) methods. The energy-minimized geometry of the ground state shows that the F− anion is only weakly coordinated to XeF2 (F2Xe---F−; a distorted Y-shape possessing Cs symmetry), while the XeF3− anion exists as a first-order transition state in the fluoride ion exchange mechanism, and is planar and Y-shaped (C2v symmetry). The molecular geometry and bonding of the XeF3− anion has been described and rationalized in terms of electron localization function (ELF) calculations, as well as the VSEPR model of molecular geometry. Quantum-chemical calculations, using the CCSD method and a continuum solvent model for CH3CN, accurately reproduced the transition-state enthalpy observed by 19F NMR spectroscopy, and showed a negative but negligible enthalpy for the formation of the F2Xe---F− adduct in this medium. ...
Publisher
ACS
ISSN Search the Publication Forum
0020-1669
Keywords
ksenon fluoridit xenon fluorides
DOI
https://doi.org/10.1021/ic101275m
URI

http://urn.fi/URN:NBN:fi:jyu-201511243774

Publication in research information system

https://converis.jyu.fi/converis/portal/detail/Publication/20145015

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