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A widely applicable synthetic approach to alk-1-yn-1-yl(polyfluoroorganyl)iodonium salts [(RC C)(R')I][BF4] Full article

Journal Zeitschrift fur Anorganische und Allgemeine Chemie
ISSN: 0044-2313
Output data Year: 2008, Volume: 634, Number: 1, Pages: 82-86 Pages count : 5 DOI: 10.1002/zaac.200700319
Tags alkynyldifluoroboranes; polyfluoroorganyliodine difluorides; alkynyl(organyl)iodonium salts; electrophilic iodonium cations; NMR spectroscopy
Authors Frohn Hermann-Josef 1 , Bardin Vadim V. 2
Affiliations
1 (Данные Web of science) Univ Duisburg Essan, Fachbereich Chem, Dept Chem Inorgan Chem, D-47048 Duisburg, Germany
2 (Данные Web of science) SB RAS, NN Vorozhtsov Novosibirsk Inst Org Chem, Novosibirsk, Russia

Abstract: The reaction of alkynyldifluoroboranes RC CBF2 (R= (CH3)(3)C, CF3, (CF3)(2)CF) with organyliodine difluoride R'IF2 bearing electron-withdrawing polyfluoroorganyl groups R'=C6F5, (CF3)(2)CFCF=CF, C4F9, and CF3CH2 leads to the corresponding alkynyl(organyl)iodonium salts [(RC C)(R')I][BF4]. This approach uses a widely applicable method as demonstrated for a representative series of polyfluorinated aryl-, alkenyl-, and alkyliodine difluorides. Generally, these syntheses proceed with good yields and deliver pure iodonium salts. The distinct electrophilic nature of their [(RC C)(R')I](+) cations is deduced from multinuclear magnetic resonance data. Within the series of new iodonium salts [CF3C C(C4F9)I][BF4] is an intrinsic unstable one and decomposed forming CF3C CI and C4F10.
Cite: Frohn H-J. , Bardin V.V.
A widely applicable synthetic approach to alk-1-yn-1-yl(polyfluoroorganyl)iodonium salts [(RC C)(R')I][BF4]
Zeitschrift fur Anorganische und Allgemeine Chemie. 2008. V.634. N1. P.82-86. DOI: 10.1002/zaac.200700319 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Jan 1, 2008
Identifiers:
Web of science: WOS:000252283700012
Scopus: 2-s2.0-38149062101
Elibrary: 13576740
OpenAlex: W2021322889
Citing:
DB Citing
Web of science 11
Scopus 12
Elibrary 13
OpenAlex 11
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