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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2022, том 32, выпуск 3, страницы 371–373 (Mi mendc667)

Эта публикация цитируется в 11 статьях

Communications

New D–A–D luminophores of the [1,2,5]thiadiazolo[3,4-d]pyridazine series

V. M. Korshunova, T. N. Chmovzhbc, G. R. Chkhetianib, I. V. Taidakova, O. A. Rakitinb

a P.N. Lebedev Physical Institute, Russian Academy of Sciences, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c South Ural State University (National Research University), Chelyabinsk, Russian Federation


Аннотация: Three [1,2,5]thiadiazolo[3,4-d]pyridazines containing 4,7-positioned indole-type substituents were synthesized from the corresponding 4,7-dibromo precursor employing the SNAr aromatic nucleophilic substitution. Photophysical properties and DFT calculations showed that the D–A–D dyes based on [1,2,5]thiadiazolo[3,4-d]pyridazine core exhibited fluorescence in the near infrared region of the spectrum, which makes them promising for use as an active emitting layer in NIR-OLEDs as well as for other possible applications as an IR luminophore.

Ключевые слова: [1,2,5]thiadiazolo[3,4-d]pyridazines, indoles, aromatic nucleophilic substitution, luminescence, donor–acceptor–donor structure, synthesis, NIR-OLEDs.

Язык публикации: английский

DOI: 10.1016/j.mencom.2022.05.026



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