Modification of the amino group in polyfluorinated arylenediamines by reactions with aldehydes and quinones Full article
| Journal |
Fluorine Notes
ISSN: 2071-4807 |
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| Output data | Year: 2018, Volume: 119, Number: 4, Pages: 5-6 Pages count : 1 DOI: 10.17677/fn20714807.2018.04.03 | ||
| Tags | Polufluorinated arylenediamines, mono-N-benzylidene-polyfluoroarylenediamines, polyfluoroarylaminonaphthoquinones, chromophores | ||
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Abstract:
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.
Cite:
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
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
Dates:
| Published online: | Aug 3, 2018 |
Identifiers:
| Elibrary: | 35326042 |
| OpenAlex: | W2887815182 |
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