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Mendeleev Communications, 2017, Volume 27, Issue 3, Pages 265–267
DOI: https://doi.org/10.1016/j.mencom.2017.05.016
(Mi mendc1963)
 

This article is cited in 7 scientific papers (total in 7 papers)

Communications

White electroluminescence from polyfluorenes copolymerized with carbazole derivatives of Nile Red and 1,8-naphthalimide

G. I. Nosovaa, D. M. Ilgacha, I. A. Berezina, E. V. Zhukovaa, T. N. Kopylovab, E. N. Nikonovab, R. M. Gadirovb, R. Yu. Smyslova, A. V. Yakimanskiiac

a Institute of Macromolecular Compounds, Russian Academy of Sciences, St. Petersburg, Russian Federation
b V.D. Kuznetsov Siberian Physical-Technical Institute, Tomsk State University, Tomsk, Russian Federation
c Department of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation
Full-text PDF (336 kB) Citations (7)
Abstract: Seven polyfluorenes containing new carbazole derivatives of Nile Red dye and 1,8-naphthalimide in the chain (obtained by the Suzuki and Yamamoto coupling) are characterized by the Nile Red emission band being less intense in their electroluminescence spectra than in photoluminescence spectra. In the optimal composition, 0.15 mol% fraction of Nile Red and 0.5 mol% fraction of N-[6-(2,7-dibromocarbazol-9-yl)hexyl]-4-diethylamino-1,8-naphthalimide provide a nearly white light electroluminescence (CIE coordinates x = 0.28; y = 0.36) with the brightness of 3278 cd m–2 and the current efficiency of 1.86 cd A–1.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (838.4 Kb)


Citation: G. I. Nosova, D. M. Ilgach, I. A. Berezin, E. V. Zhukova, T. N. Kopylova, E. N. Nikonova, R. M. Gadirov, R. Yu. Smyslov, A. V. Yakimanskii, “White electroluminescence from polyfluorenes copolymerized with carbazole derivatives of Nile Red and 1,8-naphthalimide”, Mendeleev Commun., 27:3 (2017), 265–267
Linking options:
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  • https://www.mathnet.ru/eng/mendc/v27/i3/p265
  • This publication is cited in the following 7 articles:
    1. 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  mathnet  crossref
    2. Sergey Miltsov, Alexander Yakimansky, Alexander Mitroshin, Vladislav Gurzhiy, Julian Alonso-Chamarro, Mar Puyol, “N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes”, Tetrahedron, 140 (2023), 133485  crossref
    3. M. A. Simonova, D. M. Ilgach, K. I. Kaskevich, M. I. Nepomnyashaya, L. S. Litvinova, A. P. Filippov, A. V. Yakimansky, “Self-assembly of Polyfluorene Molecular Brushes with Poly(methacrylic acid) Side Chains in Ethanol and Water”, Polym. Sci. Ser. C, 64:2 (2022), 189  crossref
    4. R. R. Valiev, D. A. Sunchugashev, R. M. Gadirov, R. T. Nasibullin, V. N. Cherepanov, “Vibronic Spectra of Bifluorene and Terfluorene”, Russ Phys J, 64:11 (2022), 2082  crossref
    5. Maria Simonova, Dmitry Ilgach, Ksenia Kaskevich, Maria Nepomnyashaya, Larisa Litvinova, Alexander Filippov, Alexander Yakimansky, “Novel Amphiphilic Polyfluorene-Graft-(Polymethacrylic Acid) Brushes: Synthesis, Conformation, and Self-Assembly”, Polymers, 13:24 (2021), 4429  crossref
    6. D. A. Lypenko, G. I. Nosova, I. A. Berezin, A. R. Tameev, E. I. Mal'tsev, “Role of benzothiadiazole substituents in white electroluminescent single macromolecules of fluorene-based copolymers”, Mendeleev Commun., 30:2 (2020), 165–167  mathnet  crossref
    7. R. M. Gadirov, A. V. Odod, A. E. Kurtsevich, D. M. Ilgach, A. V. Yakimansky, T. N. Kopylova, “Multilayer Light-Emitting Diodes Based on Organic Semiconductor Polymers”, Russ Phys J, 61:8 (2018), 1541  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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