Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog-Weg 2, 8093, Zürich, Switzerland.
Institute of Chemistry and Biochemistry, Université de Lyon, Université Lyon 1, CNRS, 43 Bd du 11 Novembre 1918, 69622, Villeurbanne, France.
Angew Chem Int Ed Engl. 2019 Dec 19;58(52):18937-18941. doi: 10.1002/anie.201910594. Epub 2019 Nov 18.
The TCICA/KF approach to oxidative fluorination of heteroatoms has emerged as a surprisingly simple, safe, and versatile surrogate to classically challenging fluorination reactions. Although polyfluorination (or chlorofluorination) of diaryl disulfides, diaryl diselenides, diaryl ditellurides, aryl iodides, and aryl(perfluoroalkyl)tellanes has been described, the application of this TCICA/KF methodology to aryl(perfluoroalkyl)sulfanes and selanes remains an area of unexplored chemical space. Accordingly, to address the "missing links" in the developing series of chalcogen-based substrate reactivity, we report mild syntheses of metastable difluoro(aryl)(perfluoroalkyl)-λ -sulfanes and selanes. As only limited examples of these species exist in the current literature (accessible only by using F or XeF /HF), we have carried out detailed structural analyses, primarily using NMR and SC-XRD data. In addition, we investigate the effect of the perfluoroalkyl chain on the outcome of oxidative fluorination, and, finally, we provide preliminary evidence that difluoro(aryl)(trifluoro-methyl)-λ -sulfanes may act as fluorinating reagents.
TCICA/KF 方法在杂原子的氧化氟化中,作为一种简单、安全且多功能的替代方法,已成为经典氟化反应的令人惊讶的替代方法。虽然已经描述了二芳基二硫代物、二芳基二硒代物、二芳基二碲代物、芳基碘化物和芳基(全氟烷基)碲烷的多氟化(或氯氟化),但这种 TCICA/KF 方法在芳基(全氟烷基)硫代和硒代物中的应用仍然是一个未开发的化学空间。因此,为了解决正在发展的基于硫属元素的底物反应系列中的“缺失环节”,我们报告了亚稳二氟(芳基)(全氟烷基)-λ-硫代和硒代物的温和合成方法。由于在当前文献中只有这些物种的有限实例(仅可通过使用 F 或 XeF/HF 获得),我们进行了详细的结构分析,主要使用 NMR 和 SC-XRD 数据。此外,我们研究了全氟烷基链对氧化氟化结果的影响,最后,我们提供了初步证据表明二氟(芳基)(三氟甲基)-λ-硫代物可能作为氟化试剂。