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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8421340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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