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The stereospecific substitution of the xenon atom in cis-perfluoroalk-1-enylxenon(II) salts by hydrogen, halogens, and the phenyl group Научная публикация

Журнал Zeitschrift fur Anorganische und Allgemeine Chemie
ISSN: 0044-2313
Вых. Данные Год: 2004, Том: 630, Номер: 7, Страницы: 1022-1024 Страниц : DOI: 10.1002/zaac.200400056
Ключевые слова noble gas chemistry; xenon-carbon compounds; perfluoroalk-1-enylation reactions; stereochemistry
Авторы Frohn HJ , Bardin VV
Организации
1 (Данные Web of science) Univ Duisburg, Anorgan Chem Inst Chem, D-47048 Duisburg, Germany
2 (Данные Web of science) SB RAS, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk, Russia

Реферат: The substitution of the xenon atom in reactions of [cis-CnF2+1CF=CFXe][Y] salts with benzene, iodide, and bromide anions in propionitrile solution by the phenyl group, or iodine, and bromine atoms, respectively, occurred stereospecifically. When a propionitrile solution of [cis-C2F5CF=CFXe][AsF6] was kept at -40 degreesC without an additional reactant, the fluoroalkene cis-C2F5CF=CFH was the only isomer obtained.
Библиографическая ссылка: Frohn H. , Bardin V.
The stereospecific substitution of the xenon atom in cis-perfluoroalk-1-enylxenon(II) salts by hydrogen, halogens, and the phenyl group
Zeitschrift fur Anorganische und Allgemeine Chemie. 2004. V.630. N7. P.1022-1024. DOI: 10.1002/zaac.200400056 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июл. 2004 г.
Идентификаторы БД:
Web of science: WOS:000222967800011
Scopus: 2-s2.0-4644252703
РИНЦ: 13461676
OpenAlex: W2150130117
Цитирование в БД:
БД Цитирований
Web of science 4
Scopus 6
РИНЦ 7
OpenAlex 6
Альметрики: