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Reactions of methyl(pentafluorophenyl)- and methyl(pentafluorophenyl)phenylsilanes with electrophiles. A convenient preparative route to halogeno(methyl)pentafluorophenylsilanes C6F5SiMe2X and C6F5SiMeX2 (X = F, Cl and Br) Full article

Journal Journal of Organometallic Chemistry
ISSN: 0022-328X
Output data Year: 1998, Volume: 570, Number: 2, Pages: 255-263 Pages count : 9 DOI: 10.1016/S0022-328X(98)00805-5
Tags silanes; electrophilic substitution
Authors Frohn H.J. 1 , Lewin A. 1 , Bardin V.V. 2
Affiliations
1 Fachgebiet Anorganische Chemie, Gerhard-Mercator-Universität Duisburg, Lotharstrasse 1, D-47048 Duisburg, Germany
2 Institute of Organic Chemistry, 630090 Novosibirsk, Russia

Abstract: Halogeno(methyl)pentafluorophenylsilanes C6F5SiMenX3-n (n = 1, 2) (X = F, Cl, Br) were prepared in good yields from the corresponding phenylsilanes C6F5SiMenPh3-n by reactions with the electrophiles aHF, HCl-AlCl3, Br-2-AlBr3 or AlX3 (X = Cl, Br) halogenated hydrocarbons. Additionally, reactions of C6F5SiMe3 and (C6F5)(2)SiMe2 with selected electrophiles were studied. (C) 1998 Elsevier Science S.A. All rights reserved.
Cite: Frohn H.J. , Lewin A. , Bardin V.V.
Reactions of methyl(pentafluorophenyl)- and methyl(pentafluorophenyl)phenylsilanes with electrophiles. A convenient preparative route to halogeno(methyl)pentafluorophenylsilanes C6F5SiMe2X and C6F5SiMeX2 (X = F, Cl and Br)
Journal of Organometallic Chemistry. 1998. V.570. N2. P.255-263. DOI: 10.1016/S0022-328X(98)00805-5 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Nov 1, 1998
Identifiers:
Web of science: WOS:000076724200012
Scopus: 2-s2.0-0011873437
Elibrary: 13279795
OpenAlex: W2026513762
Citing:
DB Citing
Web of science 6
Scopus 6
Elibrary 8
OpenAlex 6
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