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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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Detalles Bibliográficos
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
Descripción
Sumario: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.