Diazine-based thermally activated delayed fluorescence chromophores

被引:36
作者
Achelle, Sylvain [1 ]
Hodee, Maxime [1 ]
Massue, Julien [2 ]
Fihey, Arnaud [1 ]
Katan, Claudine [1 ]
机构
[1] Univ Rennes, Inst Sci Chim Rennes, CNRS, ISCR,UMR 6226, F-35000 Rennes, France
[2] Inst Chim & Proc Energie Environnement & Sante IC, Ecole Europeenne Chim Polymeres & Mat, Equipe Chim Organ Biol Mat & Opt COMBO, CNRS,UMR 7515, 25 Rue Becquerel, F-67087 Strasbourg 02, France
关键词
Diazine; Pyrimidine; Pyrazine; Thermally activated delayed fluorescence; TD-DFT; Push-pull; LIGHT-EMITTING-DIODES; ACRIDINE-CARBAZOLE HYBRID; TADF EMITTERS; HIGH-PERFORMANCE; CHARGE-TRANSFER; PYRIMIDINE; BLUE; EFFICIENCY; EMISSION; SINGLET;
D O I
10.1016/j.dyepig.2022.110157
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Diazines are electron deficient six-membered aromatic rings heterocycles which have successfully been employed in the design of a wide range of push-pull chromophores for various applications in the field of organic electronics and optoelectronics. For instance, some have been specifically designed to be inserted in the electroluminescent emission layer of organic light emitting diodes (OLED). OLED technology has continuously evolved and is currently used in industry for display and lighting purposes, offering many advantages including low turn on voltage and power consumption. In the prospect to further reduce energy waste, a third generation of OLED based on thermally activated delayed fluorescence (TADF), which allows harvesting both triplet and singlet excitons, attracts increasing attention from the scientific community. In this review, we provide a comprehensive overview of the present status of diazine-based dyes developed for TADF. The pyrimidine core is by far the most used and has demonstrated deep blue, blue or sky-blue and green emission when combined with carbazole, acridan and phenoxazine fragments, respectively. Further design of TADF emitters is desirable to afford red OLED and both the pyrazine and pyridazine cores have been scarcely explored.
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页数:19
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共 108 条
  • [1] Tuning the Photophysical Properties of Push-Pull Azaheterocyclic Chromophores by Protonation: A Brief Overview of a French-Spanish-Czech Project
    Achelle, Sylvain
    Rodriguez-Lopez, Julian
    Bures, Filip
    Robin-le Guen, Francoise
    [J]. CHEMICAL RECORD, 2020, 20 (05) : 440 - 451
  • [2] Photoluminescence Properties of Aryl-, Arylvinyl-, and Arylethynylpyrimidine Derivatives
    Achelle, Sylvain
    Rodriguez-Lopez, Julian
    Guen, Francoise Robin-le
    [J]. CHEMISTRYSELECT, 2018, 3 (06): : 1852 - 1886
  • [3] Emission properties of diazines chromophores: Structure-properties relationship
    Achelle, Sylvain
    Robin-le Guen, Francoise
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2017, 348 : 281 - 286
  • [4] Luminescent materials incorporating pyrazine or quinoxaline moieties
    Achelle, Sylvain
    Baudequin, Christine
    Ple, Nelly
    [J]. DYES AND PIGMENTS, 2013, 98 (03) : 575 - 600
  • [5] Pyrimidine Ring as Building Block for the Synthesis of Functionalized II-Conjugated Materials
    Achelle, Sylvain
    Ple, Nelly
    [J]. CURRENT ORGANIC SYNTHESIS, 2012, 9 (02) : 163 - 187
  • [6] Incorporation of pyridazine rings in the structure of functionalized π-conjugated materials
    Achelle, Sylvain
    Ple, Nelly
    Turck, Alain
    [J]. RSC ADVANCES, 2011, 1 (03) : 364 - 388
  • [7] Nearly 100% internal phosphorescence efficiency in an organic light-emitting device
    Adachi, C
    Baldo, MA
    Thompson, ME
    Forrest, SR
    [J]. JOURNAL OF APPLIED PHYSICS, 2001, 90 (10) : 5048 - 5051
  • [8] Arjona-Esteban A., 2019, TADF technology for efficient blue OLEDs: status and challenges from an industrial point of view, P1, DOI [10.5772/intechopen.86534, DOI 10.5772/INTECHOPEN.86534]
  • [9] Excitonic singlet-triplet ratio in a semiconducting organic thin film
    Baldo, MA
    O'Brien, DF
    Thompson, ME
    Forrest, SR
    [J]. PHYSICAL REVIEW B, 1999, 60 (20): : 14422 - 14428
  • [10] Highly efficient phosphorescent emission from organic electroluminescent devices
    Baldo, MA
    O'Brien, DF
    You, Y
    Shoustikov, A
    Sibley, S
    Thompson, ME
    Forrest, SR
    [J]. NATURE, 1998, 395 (6698) : 151 - 154