Perfluoroorganylxenonium(II) salts from reactions of XeF2 or [FXe][SbF6] with selected perfluorinated alk-1-yn-1-yl- and alk-1-en-1-yltrifluoroborate salts in aHF

Perfluoroorganylxenonium(II) salts from reactions of XeF2 or [FXe][SbF6] with selected perfluorinated alk-1-yn-1-yl- and alk-1-en-1-yltrifluoroborate salts in aHF Научная публикация

Журнал

Journal of Fluorine Chemistry
ISSN: 0022-1139

Вых. Данные

Год: 2012, Том: 138, Страницы: 28-33 Страниц : DOI: 10.1016/j.jfluchem.2012.03.014

Ключевые слова

Alkynylxenonium(II) salts; Alkenylxenonium(II) salts; Alkynyltrifluoroborate salts; Alkenyltrifluoroborate salts; Xenodeboration; Hydrodeboration; NMR spectroscopy

Авторы

Bardin Vadim V. ² , Frohn Hermann-Josef ¹

Организации

1	(Данные Web of science) Univ Duisburg Essen, D-47048 Duisburg, Germany
2	(Данные Web of science) SB RAS, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Xenon difluoride reacted with alkynylborate salts, K[RFC CBF3], in anhydrous HF (aHF) to give alkynylxenonium salts, [RFC CXe][BF4] (R-F = CF3, C3F7, (CF3)(2)CF), in 50-55% yield. Both [FXe][SbF6] and K[C3F7C CBF3] formed the [C3F7C CXe](+) salt in aHF. In the reaction of XeF2 with the alkenylborate salt, K[CF2=C(CF3)BF3], the competitive hydrodeboration reaction (formation of CF2=C(CF3)H in 85% yield) exceeded the xenodeboration reaction (formation of the xenonium salt [CF2=C(CF3)Xe][BF4] in 15% yield only). K[4-BF3C5F4N] did not react with XeF2 in aHF, but underwent fluorine addition in the presence of AsF5. (C) 2012 Elsevier B.V. All rights reserved.

Bardin V.V. , Frohn H-J.
Perfluoroorganylxenonium(II) salts from reactions of XeF2 or [FXe][SbF6] with selected perfluorinated alk-1-yn-1-yl- and alk-1-en-1-yltrifluoroborate salts in aHF
Journal of Fluorine Chemistry. 2012. V.138. P.28-33. DOI: 10.1016/j.jfluchem.2012.03.014 WOS Scopus РИНЦ

Опубликована в печати:

1 июн. 2012 г.

Web of science	WOS:000304691300003
Scopus	2-s2.0-84860487001
РИНЦ	17984094
OpenAlex	W2076671655