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.
Образец цитирования:
V. M. Korshunov, T. N. Chmovzh, G. R. Chkhetiani, I. V. Taidakov, O. A. Rakitin, “New D–A–D luminophores of the [1,2,5]thiadiazolo[3,4-d]pyridazine series”, Mendeleev Commun., 32:3 (2022), 371–373
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc667
https://www.mathnet.ru/rus/mendc/v32/i3/p371
Эта публикация цитируется в следующих 11 статьяx:
Vladislav M. Korshunov, Timofey N. Chmovzh, Alisia V. Tsorieva, Gleb A. Gruzdev, Dadozhon M. Rakhimkulov, Ilya V. Taydakov, Oleg A. Rakitin, “Towards deep NIR emissive simple D–A–D dyes: a novel acceptor block providing anti-Kasha's rule emission”, J. Mater. Chem. C, 12:47 (2024), 19200
Oleg A. Rakitin, Advances in Heterocyclic Chemistry, 142, 2024, 227
T. N. Chmovzh, T. A. Kudryashev, L. V. Mikhalchenko, O. A. Rakitin, “[1,2,5]Thia(selena)diazolo[3,4-c]pyridine-4,7-dicarbonitriles: synthesis and electrochemical reduction to radical anions”, Russ Chem Bull, 73:5 (2024), 1280
A. A. Yakimanskiy, A. M. Mitroshin, T. G. Chulkova, S. A. Miltsov, A. V. Yakimanskii, “Fluorene-based π-conjugated polymers for OLEDs: advances, opportunities, and challenges”, Mendeleev Commun., 34:5 (2024), 609–629
Timofey N. Chmovzh, Karim S. Gaisin, Oleg A. Rakitin, “5,6-Dihydro-[1,2,5]oxadiazolo[3,4-d]pyridazine-4,7-dione”, Molbank, 2023:2 (2023), M1649
Mozhgan Hosseinnezhad, Mehdi Ghahari, Ghazal Mobarhan, Mohsen Fathi, Arvydas Palevicius, Venkatramaiah Nutalapati, Giedrius Janusas, Sohrab Nasiri, “New Insights into Improving the Photovoltaic Performance of Dye-Sensitized Solar Cells by Removing Platinum from the Counter Electrode Using a Graphene-MoS2 Composite or Hybrid”, Micromachines, 14:12 (2023), 2161
A. S. Kozlov, O. I. Afanasyev, M. A. Losev, M. I. Godovikova, D. A. Chusov, “Nitrogen ligand influence on the CO-assisted ruthenium-catalyzed reductive amination”, Mendeleev Commun., 33:2 (2023), 174–176
Timofey N. Chmovzh, Timofey A. Kudryashev, Oleg A. Rakitin, “4,4′-([1,2,5]Thiadiazolo[3,4-d]pyridazine-4,7-diyl)bis(N,N-bis(4-methoxyphenyl)aniline)”, Molbank, 2022:4 (2022), M1479
Timofey N. Chmovzh, Oleg A. Rakitin, “4,7-Bis(2,3,3a,8b-tetrahydrocyclopenta[b]indol-4(1H)-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine”, Molbank, 2022:3 (2022), M1441
Timofey N. Chmovzh, Timofey A. Kudryashev, Karim S. Gaisin, Oleg A. Rakitin, “4,7-Di(9H-carbazol-9-yl)-[1,2,5]oxadiazolo[3,4-d]pyridazine”, Molbank, 2022:3 (2022), M1428
Timofey N. Chmovzh, Daria A. Alekhina, Timofey A. Kudryashev, Oleg A. Rakitin, “Efficient Synthesis of 4,8-Dibromo Derivative of Strong Electron-Deficient Benzo[1,2-d:4,5-d']bis([1,2,3]thiadiazole) and Its SNAr and Cross-Coupling Reactions”, Molecules, 27:21 (2022), 7372
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