The term can also refer to organyl substituted species of type H–+F–R, R–+F–R, or R2C=F+. In contrast to the heavier halogens, which have long been known to form open-chain halonium ions (such as [Me2Cl]+[Al(OTeF5)4]–)[4] as well as cyclic haliranium ions, fluorine was not believed to form fluoronium ions of type R–+F–R until the recent characterization of a fluoronium ion locked in a designed cage structure by Lectka and coworkers.[5] Recent solvolysis experiments and NMR spectroscopic studies on a metastable [C–F–C]+ fluoronium ion strongly support the dicoordinated fluoronium structure over the alternative rapidly equilibrating classical carbocation. Definitive structural proof of the symmetrical [C–F–C]+ was reported by Riedel, Lectka, and coworkers by single crystal X-ray diffraction analysis. Besides its synthesis and crystallographic characterization as the [Sb2F11]− salt, vibrational spectra could be recorded and a detailed analysis concerning the nature of the bonding situation in this fluoronium ion and its heavier halonium homologues was reported.[6]
References
^Esteves, Pierre M.; Ramírez-Solís, Alejandro; Mota, Claudio J. A. (March 2002). "The Nature of Superacid Electrophilic Species in HF/SbF5: A Density Functional Theory Study". Journal of the American Chemical Society. 124 (11): 2672–2677. doi:10.1021/ja011151k. ISSN0002-7863. PMID11890818.
^Mootz, Dietrich; Bartmann, Klemens (1988). "The Fluoronium Ions H2F+ and H 3F+ 2: Characterization by Crystal Structure Analysis". Angewandte Chemie. 27 (3): 391–392. doi:10.1002/anie.198803911.
^Diercksen, G. H. F.; von Niessen, W.; Kraemer, W. P. (1973). "SCF LCGO MO studies on the fluoronium ion FH+ 2 and its hydrogen bonding interaction with hydrogen fluoride FH". Theoretical Chemistry Accounts: Theory, Computation, and Modeling. 31 (3): 205–214. doi:10.1007/BF00526510. S2CID98637994.
^Pitts, Cody Ross; Holl, Maxwell Gargiulo; Lectka, Thomas (2018-02-12). "Spectroscopic Characterization of a [C−F−C]+ Fluoronium Ion in Solution". Angewandte Chemie International Edition. 57 (7): 1924–1927. doi:10.1002/anie.201712021. PMID29316122.