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Structural proof of a [C–F–C](+) fluoronium cation

Organic fluoronium ions can be described as positively charged molecules in which the most electronegative and least polarizable element fluorine engages in two partially covalent bonding interactions to two carbon centers. While recent solvolysis experiments and NMR spectroscopic studies on a metas...

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Autores principales: Hoffmann, Kurt F., Wiesner, Anja, Müller, Carsten, Steinhauer, Simon, Beckers, Helmut, Kazim, Muhammad, Pitts, Cody Ross, Lectka, Thomas, Riedel, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421340/
https://www.ncbi.nlm.nih.gov/pubmed/34489464
http://dx.doi.org/10.1038/s41467-021-25592-6
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author Hoffmann, Kurt F.
Wiesner, Anja
Müller, Carsten
Steinhauer, Simon
Beckers, Helmut
Kazim, Muhammad
Pitts, Cody Ross
Lectka, Thomas
Riedel, Sebastian
author_facet Hoffmann, Kurt F.
Wiesner, Anja
Müller, Carsten
Steinhauer, Simon
Beckers, Helmut
Kazim, Muhammad
Pitts, Cody Ross
Lectka, Thomas
Riedel, Sebastian
author_sort Hoffmann, Kurt F.
collection PubMed
description Organic fluoronium ions can be described as positively charged molecules in which the most electronegative and least polarizable element fluorine engages in two partially covalent bonding interactions to two carbon centers. While recent solvolysis experiments and NMR spectroscopic studies on a metastable [C–F–C](+) fluoronium ion strongly support the divalent fluoronium structure over the alternative rapidly equilibrating classical carbocation, the model system has, to date, eluded crystallographic analysis to confirm this phenomenon in the solid state. Herein, we report the single crystal structure of a symmetrical [C–F–C](+) fluoronium cation. Besides its synthesis and crystallographic characterization as the [Sb(2)F(11)](−) salt, vibrational spectra are discussed and a detailed analysis concerning the nature of the bonding situation in this fluoronium ion and its heavier halonium homologues is performed, which provides detailed insights on this molecular structure.
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spelling pubmed-84213402021-09-22 Structural proof of a [C–F–C](+) fluoronium cation Hoffmann, Kurt F. Wiesner, Anja Müller, Carsten Steinhauer, Simon Beckers, Helmut Kazim, Muhammad Pitts, Cody Ross Lectka, Thomas Riedel, Sebastian Nat Commun Article Organic fluoronium ions can be described as positively charged molecules in which the most electronegative and least polarizable element fluorine engages in two partially covalent bonding interactions to two carbon centers. While recent solvolysis experiments and NMR spectroscopic studies on a metastable [C–F–C](+) fluoronium ion strongly support the divalent fluoronium structure over the alternative rapidly equilibrating classical carbocation, the model system has, to date, eluded crystallographic analysis to confirm this phenomenon in the solid state. Herein, we report the single crystal structure of a symmetrical [C–F–C](+) fluoronium cation. Besides its synthesis and crystallographic characterization as the [Sb(2)F(11)](−) salt, vibrational spectra are discussed and a detailed analysis concerning the nature of the bonding situation in this fluoronium ion and its heavier halonium homologues is performed, which provides detailed insights on this molecular structure. Nature Publishing Group UK 2021-09-06 /pmc/articles/PMC8421340/ /pubmed/34489464 http://dx.doi.org/10.1038/s41467-021-25592-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hoffmann, Kurt F.
Wiesner, Anja
Müller, Carsten
Steinhauer, Simon
Beckers, Helmut
Kazim, Muhammad
Pitts, Cody Ross
Lectka, Thomas
Riedel, Sebastian
Structural proof of a [C–F–C](+) fluoronium cation
title Structural proof of a [C–F–C](+) fluoronium cation
title_full Structural proof of a [C–F–C](+) fluoronium cation
title_fullStr Structural proof of a [C–F–C](+) fluoronium cation
title_full_unstemmed Structural proof of a [C–F–C](+) fluoronium cation
title_short Structural proof of a [C–F–C](+) fluoronium cation
title_sort structural proof of a [c–f–c](+) fluoronium cation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421340/
https://www.ncbi.nlm.nih.gov/pubmed/34489464
http://dx.doi.org/10.1038/s41467-021-25592-6
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