Abstract:
The competitive reaction of C4F9CF=CFBF2 (cis : trans = 1.2:1) with XeF2 demonstrated for the first time a remarkably lower reaction rate of the trans isomer with respect to the cis isomer in the xenodeborylation reaction (formation of the [C4F9CF=CFXe]+ cation with a cis : trans ratio of 2.5 to 4:1) and allowed us to develop reaction conditions for the syntheses of [trans-C4F9CF=CFXe]+ salts.
Document Type:
Article
Language: English
Citation:
H. J. Frohn, V. V. Bardin, “Distinct reactivities of cis- and trans-RFCF=CFBF2 towards XeF2 and the first synthesis of a [trans-RFCF=CFXe]+ salt”, Mendeleev Commun., 17:3 (2007), 137–138
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https://www.mathnet.ru/eng/mendc3403
https://www.mathnet.ru/eng/mendc/v17/i3/p137
This publication is cited in the following 4 articles:
Anton Yu Shabalin, Nicolay Yu Adonin, Vadim V Bardin, “Substitution of fluorine in M[C6F5BF3] with organolithium compounds: distinctions between O- and N-nucleophiles”, Beilstein J. Org. Chem., 13 (2017), 703
Hermann-Josef Frohn, Matthias Giesen, Dirk Welting, Vadim V. Bardin, “Bis(perfluoroorganyl)bromonium salts [(RF)2Br]Y (RF=aryl, alkenyl, and alkynyl)”, Journal of Fluorine Chemistry, 131:9 (2010), 922
Hermann‐Josef Frohn, Vadim V. Bardin, “Reactions of Alk‐1‐enylxenonium(II) and Alk‐1‐ynylxenonium(II) Salts [RXe]Y with Bromides and Iodides in Anhydrous HF”, Zeitschrift anorg allge chemie, 633:10 (2007), 1627