Reactivity of alkali and alkaline earth metal tetrafluorobromates towards aromatic compounds and pyridine / V. I. Sobolev, V. D. Filimonov, R. V. Ostvald [et al.]

Set Level: Journal of Fluorine ChemistryCoauthor: Sobolev, V. I., Chemical Engineer, Engineer-designer of Tomsk Polytechnic University, 1989-, Vasily Igorevich;Filimonov, V. D., Russian chemist, Professor of the TPU, 1945-, Viktor Dmitrievich;Ostvald, R. V., Chemical Engineer, Associate Professor of Tomsk Polytechnic University, Candidate of chemical sciences, 1980-, Roman Vyacheslavovich;Radchenko, V. B., Vyacheslav Borisovich;Zherin (Gerin), I. I., Russian chemist, Professor of Tomsk Polytechnic University, Doctor of сhemical sciences (DSc), 1955-, Ivan IgnatyevichCorporate Author (Secondary): Национальный исследовательский Томский политехнический университет (ТПУ), Физико-технический институт (ФТИ), Кафедра химической технологии редких, рассеянных и радиоактивных элементов (№ 43) (ХТРЭ);Национальный исследовательский Томский политехнический университет (ТПУ), Институт физики высоких технологий (ИФВТ), Кафедра биотехнологии и органической химии (БИОХ)Language: английский.Country: Netherlands.Abstract: The bromination activity of tetrafluorobromates of alkali and alkali-earth metals increases in the order KBrF4, CsBrF4, RbBrF4 and Ba(BrF4)2. The most active tetrafluorobromate-Ba(BrF4)2 is able to selectively brominate the deactivated aromatic compounds nitrobenzene and 4-nitrotoluene, but not the activated compounds benzene and toluene. In all cases bromination of methyl groups of methylbenzenes does not occur. Ba(BrF4)2 forms the known complex C6H5N·BrF3 when reacted with pyridine. Due to dilution by inert BaF2, this pyridine-based complex is air stable and can be considered as safer and more convenient reagent in comparison with the original fluorobromates; it can selectively brominate benzene and toluene in contrast with tetrafluorobromates..Bibliography: [References: p. 123 (16 tit.)].Audience: .Subject: электронный ресурс | труды учёных ТПУ | bromine trifluoride | tetrafluorobromates | bromination | fluorine | arenes | трифторид брома | бромирование | фтор Online Resources:Click here to access online
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[References: p. 123 (16 tit.)]

The bromination activity of tetrafluorobromates of alkali and alkali-earth metals increases in the order KBrF4, CsBrF4, RbBrF4 and Ba(BrF4)2. The most active tetrafluorobromate-Ba(BrF4)2 is able to selectively brominate the deactivated aromatic compounds nitrobenzene and 4-nitrotoluene, but not the activated compounds benzene and toluene. In all cases bromination of methyl groups of methylbenzenes does not occur. Ba(BrF4)2 forms the known complex C6H5N·BrF3 when reacted with pyridine. Due to dilution by inert BaF2, this pyridine-based complex is air stable and can be considered as safer and more convenient reagent in comparison with the original fluorobromates; it can selectively brominate benzene and toluene in contrast with tetrafluorobromates.

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