Реферат: The perfluorinated organoethynylxenon(II) salts, [RC=CXe][BF4] [R = CF3, C3F7, (CF3)(2)CF, cis-, trans-CF3CF=CF; C6F5], were prepared by the reaction of XeF2 with the corresponding perfluoroorganoethynyldifluoroboranes, RC=CBF2, in 1,1,1,3,3-pentafluoropropane (PFP) or CH2Cl2 at -60 to -40 degrees C and isolated in 30-98 % yield. Similarly, the non-fluorinated organoethynylxenon(II) salts [C4H9C=CXe][BF4] and [(CH3)(3)CC=CXe][BF4] were obtained in 20 to 40 % yield. All [RC=CXe][BF4] salts are soluble in anhydrous HE (aHF) and the salts with R = C4H9 or R = (CH3)(3)C display sufficient solubility in the weakly coordinating solvents CH2Cl2 and PFP. The xenonium. salts [RC=CXe][BF4] were unambiguously characterised by their H-1-, B-11-, C-13-, F-19-, and Xe-129 NMR spectra in solution.

Библиографическая ссылка: Frohn H-J. , Bardin V.V.
Organoethynylxenon(II) tetrafluoroborates, [RC CXe][BF4] - The first examples of isolated alkynylxenonium salts: Preparation and multi-NMR characterisation
European Journal of Inorganic Chemistry. 2006. N19. P.3948-3953. DOI: 10.1002/ejic.200600366 WOS Scopus РИНЦ OpenAlex

Даты:

Опубликована в печати:

1 окт. 2006 г.

Идентификаторы БД:

Web of science:	WOS:000241303700019
Scopus:	2-s2.0-33749833538
РИНЦ:	13530578
OpenAlex:	W1995156310

Цитирование в БД:

БД	Цитирований
Web of science	22
Scopus	23
РИНЦ	24
OpenAlex	25

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