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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >A Simple and Convenient Route to Arylxenon (II) Tetrafluoroborates
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A Simple and Convenient Route to Arylxenon (II) Tetrafluoroborates

机译:一种简便的四氟硼酸芳基氙(II)路线

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摘要

An improved synthesis of arylxenon (II) salts is reported. The series of fluoro-containing arylxenon (II) tetrafluoroborates (aryl = C_6F_5, 2, 3, 4, 5-C_6HF_4, 3, 4, 5-C_6H_2F_3 and 3, 5-C_6H_3F_2) are prepared by the reaction of xenon difluoride with the corresponding aryldifluoroboranes. The salts [C_6F_5Xe][BF_4] and [2, 3, 4, 5-C_6HF_4Xe][BF_4] are long-term stable in anhydrous HF (aHF) solution at rt, while [3, 4, 5-C_6H_2F_3Xe][BF_4] and [3, 5-C_6H_3F_2Xe] [BF_4] are converted into 1, 2, 3, 5-tetrafluorobenzene and 1, 3, 5-trifluorobenzene, respectively, within a few hours.
机译:据报道,芳基氙(II)盐的合成得到改进。该系列含氟芳基氙(II)四氟硼酸盐系列(芳基= C_6F_5,2,3,4,5-C_6HF_4,3,4,5-C_6H_2F_3和3,5-C_6H_3F_2)是通过二氟化氙与氟的反应制备的。相应的芳基二氟硼烷。盐[C_6F_5Xe] [BF_4]和[2,3,4,5-C_6HF_4Xe] [BF_4]在无水HF(aHF)溶液中于rt长期稳定,而[3,4,5-C_6H_2F_3Xe] [BF_4 ]和[3,5-C_6H_3F_2Xe] [BF_4]在数小时内分别转化为1,2,3,5-四氟苯和1,3,5-三氟苯。

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