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Modification of the amino group in polyfluorinated arylenediamines by reactions with aldehydes and quinones Научная публикация

Журнал Fluorine Notes
ISSN: 2071-4807
Вых. Данные Год: 2018, Том: 119, Номер: 4, Страницы: 5-6 Страниц : 1 DOI: 10.17677/fn20714807.2018.04.03
Ключевые слова Polufluorinated arylenediamines, mono-N-benzylidene-polyfluoroarylenediamines, polyfluoroarylaminonaphthoquinones, chromophores
Авторы Vaganova T.A. 1 , Chuikov I.P. 1 , Malykhin E.V. 1
Организации
1 Новосибирский институт органической химии им. Н.Н. Ворожцова СО РАН

Реферат: Reaction of low-reactive polyfluoroaromatic diamines with benzaldehyde and hexafluoronaphthoquinone provide selective preparation of functionalized arylamines. Mono-Nbenzylidene-arylenediamines were prepared in 30-35 % yield, polyfluoroarylaminonaphthoquinones in 50- 55 % yield. The products were characterized by IR, 1H and 19F NMR spectroscopy, mass-spectrometry. Spectral characteristics of the compounds in the UV-visible range were studied and prospects of their usage as signal components of supramolecular sensors were evaluated.
Библиографическая ссылка: Vaganova T.A. , Chuikov I.P. , Malykhin E.V.
Modification of the amino group in polyfluorinated arylenediamines by reactions with aldehydes and quinones
Fluorine Notes. 2018. Т.119. №4. С.5-6. DOI: 10.17677/fn20714807.2018.04.03 РИНЦ OpenAlex
Даты:
Опубликована online: 3 авг. 2018 г.
Идентификаторы БД:
РИНЦ: 35326042
OpenAlex: W2887815182
Цитирование в БД: Пока нет цитирований
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