Facile Generation of Thermally Activated Delayed Fluorescence and Fabrication of Highly Efficient Non‐Doped OLEDs Based on Triazine Derivatives
A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a...
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Published in | Chemistry : a European journal Vol. 25; no. 72; pp. 16699 - 16711 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
20.12.2019
Wiley Subscription Services, Inc |
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Online Access | Get full text |
ISSN | 0947-6539 1521-3765 1521-3765 |
DOI | 10.1002/chem.201904411 |
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Abstract | A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D–D/A–A‐type π–π interactions, resulting in the intermolecular D–A charge transfer. The weak aggregation‐caused quenching (ACQ) effect caused by the suppressed intermolecular D–D/A–A‐type π–π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (ΔEST). As a result, blue‐emitting devices with TH‐2DMAC and TH‐2DPAC non‐doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (λpeak<475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances.
Getting the blues: A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. |
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AbstractList | A series of donor-acceptor-donor triazine-based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue-emitting OLEDs with non-doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D-D/A-A-type π-π interactions, resulting in the intermolecular D-A charge transfer. The weak aggregation-caused quenching (ACQ) effect caused by the suppressed intermolecular D-D/A-A-type π-π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (ΔE
). As a result, blue-emitting devices with TH-2DMAC and TH-2DPAC non-doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (λ
<475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances. A series of donor-acceptor-donor triazine-based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue-emitting OLEDs with non-doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D-D/A-A-type π-π interactions, resulting in the intermolecular D-A charge transfer. The weak aggregation-caused quenching (ACQ) effect caused by the suppressed intermolecular D-D/A-A-type π-π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (ΔEST ). As a result, blue-emitting devices with TH-2DMAC and TH-2DPAC non-doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (λpeak <475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances.A series of donor-acceptor-donor triazine-based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue-emitting OLEDs with non-doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D-D/A-A-type π-π interactions, resulting in the intermolecular D-A charge transfer. The weak aggregation-caused quenching (ACQ) effect caused by the suppressed intermolecular D-D/A-A-type π-π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (ΔEST ). As a result, blue-emitting devices with TH-2DMAC and TH-2DPAC non-doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (λpeak <475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances. A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D –D/A–A‐type π–π interactions, resulting in the intermolecular D–A charge transfer. The weak aggregation‐caused quenching (ACQ) effect caused by the suppressed intermolecular D –D/A–A‐type π–π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (Δ E ST ). As a result, blue‐emitting devices with TH‐2DMAC and TH‐2DPAC non‐doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters ( λ peak <475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances. A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D–D/A–A‐type π–π interactions, resulting in the intermolecular D–A charge transfer. The weak aggregation‐caused quenching (ACQ) effect caused by the suppressed intermolecular D–D/A–A‐type π–π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (ΔEST). As a result, blue‐emitting devices with TH‐2DMAC and TH‐2DPAC non‐doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (λpeak<475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances. A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D–D/A–A‐type π–π interactions, resulting in the intermolecular D–A charge transfer. The weak aggregation‐caused quenching (ACQ) effect caused by the suppressed intermolecular D–D/A–A‐type π–π interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (ΔEST). As a result, blue‐emitting devices with TH‐2DMAC and TH‐2DPAC non‐doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (λpeak<475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances. Getting the blues: A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue‐emitting OLEDs with non‐doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. A series of donor-acceptor-donor triazine-based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly efficient blue-emitting OLEDs with non-doped emitting layers (EMLs). The targeted molecules use a triazine core as the electron acceptor, and a benzene ring as the conjugated linker with different electron donors to alternate the energy level of the HOMO to further tune the emission color. The introduction of long alkyl chains on the triazine core inhibits the unwanted intermolecular D-D/A-A-type pi-pi interactions, resulting in the intermolecular D-A charge transfer. The weak aggregation-caused quenching (ACQ) effect caused by the suppressed intermolecular D-D/A-A-type pi-pi interaction further enhances the emission. The crowded molecular structure allows the electron donor and acceptor to be nearly orthogonal, thereby reducing the energy gap between triplet and singlet excited states (Delta E-ST). As a result, blue-emitting devices with TH-2DMAC and TH-2DPAC non-doped EMLs showed satisfactory efficiencies of 12.8 % and 15.8 %, respectively, which is one of the highest external quantum efficiency (EQEs) reported for blue TADF emitters (lambda(peak)<475 nm), demonstrating that our tailored molecular designs are promising strategies to endow OLEDs with excellent electroluminescent performances. |
Author | Chang, Chih‐Hao Hsieh, Yi‐Chun Chih, Hsin‐Yun Lu, Chin‐Wei Li, Wei‐Cheng Chen, Ying‐Wei Liao, Chia‐Wei Lin, Chun‐Han Tsai, Wei‐Wen Chiu, Ting‐Ya |
Author_xml | – sequence: 1 givenname: Hsin‐Yun surname: Chih fullname: Chih, Hsin‐Yun organization: Providence University – sequence: 2 givenname: Ying‐Wei surname: Chen fullname: Chen, Ying‐Wei organization: Providence University – sequence: 3 givenname: Yi‐Chun surname: Hsieh fullname: Hsieh, Yi‐Chun organization: Providence University – sequence: 4 givenname: Wei‐Cheng surname: Li fullname: Li, Wei‐Cheng organization: Yuan Ze University – sequence: 5 givenname: Chia‐Wei surname: Liao fullname: Liao, Chia‐Wei organization: Yuan Ze University – sequence: 6 givenname: Chun‐Han surname: Lin fullname: Lin, Chun‐Han organization: Yuan Ze University – sequence: 7 givenname: Ting‐Ya surname: Chiu fullname: Chiu, Ting‐Ya organization: Yuan Ze University – sequence: 8 givenname: Wei‐Wen surname: Tsai fullname: Tsai, Wei‐Wen organization: DuPont de Nemours, Inc – sequence: 9 givenname: Chin‐Wei orcidid: 0000-0003-1516-8685 surname: Lu fullname: Lu, Chin‐Wei email: cwlu@pu.edu.tw organization: Providence University – sequence: 10 givenname: Chih‐Hao orcidid: 0000-0002-5586-9526 surname: Chang fullname: Chang, Chih‐Hao email: chc@saturn.yzu.edu.tw organization: Yuan Ze University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31638288$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.orgel.2018.11.018 10.1002/ange.201709125 10.1016/j.dyepig.2016.08.023 10.1002/adma.201301603 10.1063/1.3558906 10.1021/cm4011597 10.1002/adma.201807388 10.1039/C6CS00368K 10.1002/adom.201600749 10.1002/adma.201605444 10.1002/adom.201800568 10.1039/C8TC01139G 10.1002/adfm.201300547 10.1103/PhysRevB.62.10967 10.1002/adma.201402532 10.1021/acsami.7b08258 10.1021/acs.chemmater.7b03371 10.1002/asia.201601384 10.1002/anie.201709125 10.1063/1.1751232 10.1016/j.dyepig.2018.11.042 10.1002/adfm.201802031 10.1002/anie.201509231 10.3389/fchem.2019.00199 10.1016/j.orgel.2018.09.023 10.1021/acsomega.8b03296 10.1021/acs.chemmater.6b05324 10.1002/ange.201509231 10.1021/acsami.8b00053 10.1021/acsami.9b07820 10.1039/C7TC00119C 10.1002/chem.201800822 10.1039/C8SC04991B 10.1016/j.dyepig.2015.02.014 10.1002/adfm.201101907 10.1002/jsid.598 10.1039/C4TC00865K 10.1016/j.orgel.2017.06.029 10.1039/C9TC02491C 10.1021/acsami.8b20699 10.1039/C6TC02702D 10.1117/1.JPE.8.032104 10.1002/adma.201803524 10.1021/jacs.7b00873 10.1002/adfm.201705813 10.1016/j.cap.2003.11.091 10.1021/am401694s 10.1016/j.dyepig.2016.10.029 10.1038/natrevmats.2018.20 10.1002/chem.201805952 10.1021/cm703682q 10.1038/nature11687 10.1002/adma.200701730 10.1039/c3cp52255e 10.1063/1.1568146 10.1039/c7tc00119c 10.1039/c9tc02491c 10.1039/c6tc02702d 10.1039/c6cs00368k 10.1039/c4tc00865k 10.1039/c8sc04991b 10.1039/c8tc01139g |
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Keywords | DESIGN BLUE ORGANIC ELECTROPHOSPHORESCENCE blue-emitting OLEDs EMITTERS organic light-emitting diodes LIGHT-EMITTING-DIODES TRIPLET EXCITON CONFINEMENT donor-acceptor systems triazines fluorescence AGGREGATION-INDUCED EMISSION BIPOLAR HOST MATERIALS CHARGE-TRANSFER ROLL-OFF |
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References | 2017; 5 2019; 7 2018; 28 2019; 4 2013; 25 2019; 31 2017; 48 2017; 25 2019; 11 2019; 10 2013; 23 2017; 46 2014; 26 2011; 98 2018; 63 2017; 29 2017 2017; 56 129 2019; 163 2013; 5 2017; 9 2017; 137 2017; 139 2018; 24 2016; 4 2012; 492 2018; 6 2018; 8 2018; 3 2013; 15 2016 2016; 55 128 2004; 95 2014; 2 2019; 65 2019; 25 2017; 12 2005; 5 2016; 134 2000; 62 2015; 117 2008; 20 2003; 82 2018; 10 2012; 22 e_1_2_7_5_1 e_1_2_7_3_1 e_1_2_7_9_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_17_1 e_1_2_7_15_1 e_1_2_7_41_1 e_1_2_7_1_1 e_1_2_7_13_1 e_1_2_7_43_1 e_1_2_7_11_1 e_1_2_7_45_1 e_1_2_7_47_1 e_1_2_7_26_1 e_1_2_7_49_1 e_1_2_7_28_1 e_1_2_7_50_1 e_1_2_7_25_1 e_1_2_7_31_1 e_1_2_7_52_1 e_1_2_7_23_1 e_1_2_7_33_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_37_1 e_1_2_7_39_1 e_1_2_7_6_1 e_1_2_7_4_1 e_1_2_7_8_1 e_1_2_7_18_1 e_1_2_7_16_1 e_1_2_7_40_1 e_1_2_7_2_1 e_1_2_7_14_1 e_1_2_7_42_1 e_1_2_7_12_1 e_1_2_7_44_1 e_1_2_7_10_1 e_1_2_7_46_1 e_1_2_7_48_1 e_1_2_7_27_1 e_1_2_7_48_2 e_1_2_7_29_1 e_1_2_7_51_1 e_1_2_7_30_1 e_1_2_7_53_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_22_2 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_20_1 e_1_2_7_36_1 e_1_2_7_38_1 Chen, DG (WOS:000430642100083) 2018; 10 Lu, CW (WOS:000457666300017) 2019; 163 Serevicius, T (WOS:000324412300020) 2013; 15 Cha, JR (WOS:000383526000069) 2016; 134 Liang, X (WOS:000467079100003) 2019; 25 Su, SJ (WOS:000257044600018) 2008; 20 Liu, YC (WOS:000430173500006) 2018; 3 Tsai, CC (WOS:000449270700024) 2018; 63 Su, SJ (WOS:000253727400011) 2008; 20 Tao, Y (WOS:000346263100001) 2014; 26 Wang, JS (WOS:000453572400026) 2019; 65 Wang, XD (WOS:000461509800003) 2019; 10 Tsujimoto, H (WOS:000398764000044) 2017; 139 Shiu, YJ (WOS:000370656200004) 2016; 55 Jeon, SK (WOS:000481877300012) 2019; 31 Wong, MY (WOS:000402963400023) 2017; 29 Zhang, QS (WOS:000304749600013) 2012; 22 Xiang, YP (WOS:000387229000011) 2016; 4 Lv, XL (WOS:000462260000035) 2019; 11 Wang, JS (WOS:000405458400037) 2017; 48 Chen, XL (WOS:000445812900038) 2017; 56 Chang, CH (WOS:000323241100079) 2013; 5 Cheng, Z (WOS:000480498600067) 2019; 11 Matsushima, H (WOS:000227690700003) 2005; 5 Hu, J (WOS:000390182700055) 2017; 137 Huang, TY (WOS:000434260700001) 2018; 6 Lee, J (WOS:000411918900044) 2017; 29 Tang, XY (WOS:000427110100016) 2018; 28 Kobayashi, T (WOS:000456697900005) 2018; 8 Li, YF (WOS:000398950500007) 2017; 5 Holmes, RJ (WOS:000182104900018) 2003; 82 Braveenth, R (WOS:000475453000018) 2019; 7 Murawski, C (WOS:000328424600002) 2013; 25 Im, Y (WOS:000396639400006) 2017; 29 Park, YS (WOS:000327480000009) 2013; 23 Uoyama, H (WOS:000312259300038) 2012; 492 Yang, ZY (WOS:000395629200010) 2017; 46 Kim, HG (WOS:000393209600007) 2017; 5 Park, IS (WOS:000442205200010) 2018; 28 Grybauskaite-Kaminskiene, G (WOS:000437730300021) 2018; 24 Baldo, MA (WOS:000165058600057) 2000; 62 Zhang, PP (WOS:000463468900001) 2019; 7 Zou, Y (WOS:000453512700001) 2018; 6 Endo, A (WOS:000287764300088) 2011; 98 Suzuki, K (WOS:000413667400003) 2017; 25 Rao, JC (WOS:000460214700204) 2019; 4 CHEN XL (WOS:000501147800001.9) 2017; 129 Xu, YW (WOS:000462619000015) 2019; 31 Liao, JL (WOS:000340353700005) 2014; 2 Ban, XX (WOS:000393434200009) 2017; 12 Goushi, K (WOS:000221843400037) 2004; 95 Huang, B (WOS:000352664900018) 2015; 117 SHIU YJ (WOS:000501147800001.36) 2016; 128 Komino, T (WOS:000323193000018) 2013; 25 Lien, YJ (WOS:000408178400049) 2017; 9 |
References_xml | – volume: 56 129 start-page: 15006 15202 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 95 start-page: 7798 year: 2004 publication-title: J. Appl. Phys. – volume: 29 start-page: 8012 year: 2017 publication-title: Chem. Mater. – volume: 31 start-page: 1803524 year: 2019 publication-title: Adv. Mater. – volume: 98 start-page: 083302 year: 2011 publication-title: Appl. Phys. Lett. – volume: 20 start-page: 1691 year: 2008 publication-title: Chem. Mater. – volume: 15 start-page: 15850 year: 2013 publication-title: Phys. Chem. Chem. Phys. – volume: 9 start-page: 27090 year: 2017 publication-title: ACS Appl. Mater. Interfaces – volume: 82 start-page: 2422 year: 2003 publication-title: Appl. Phys. Lett. – volume: 5 start-page: 3480 year: 2017 publication-title: J. Mater. Chem. C – volume: 5 start-page: 305 year: 2005 publication-title: Curr. Appl. Phys. – volume: 139 start-page: 4894 year: 2017 publication-title: J. Am. Chem. Soc. – volume: 28 start-page: 1705813 year: 2018 publication-title: Adv. Funct. Mater. – volume: 25 start-page: 480 year: 2017 publication-title: J. Soc. Inf. Disp. – volume: 117 start-page: 141 year: 2015 publication-title: Dyes Pigm. – volume: 48 start-page: 262 year: 2017 publication-title: Org. Electron. – volume: 20 start-page: 2125 year: 2008 publication-title: Adv. Mater. – volume: 7 start-page: 7672 year: 2019 publication-title: J. Mater. Chem. C – volume: 31 start-page: 1807388 year: 2019 publication-title: Adv. Mater. – volume: 4 start-page: 1861 year: 2019 publication-title: ACS Omega – volume: 10 start-page: 12886 year: 2018 publication-title: ACS Appl. Mater. Interfaces – volume: 492 start-page: 234 year: 2012 publication-title: Nature – volume: 28 start-page: 1802031 year: 2018 publication-title: Adv. Funct. Mater. – volume: 29 start-page: 1946 year: 2017 publication-title: Chem. Mater. – volume: 2 start-page: 6269 year: 2014 publication-title: J. Mater. Chem. C – volume: 6 start-page: 5577 year: 2018 publication-title: J. Mater. Chem. C – volume: 23 start-page: 4914 year: 2013 publication-title: Adv. Funct. Mater. – volume: 46 start-page: 915 year: 2017 publication-title: Chem. Soc. Rev. – volume: 25 start-page: 6801 year: 2013 publication-title: Adv. Mater. – volume: 4 start-page: 9998 year: 2016 publication-title: J. Mater. Chem. C – volume: 5 start-page: 7341 year: 2013 publication-title: ACS Appl. Mater. Interfaces – volume: 65 start-page: 170 year: 2019 publication-title: Org. Electron. – volume: 55 128 start-page: 3017 3069 year: 2016 2016 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 26 start-page: 7931 year: 2014 publication-title: Adv. Mater. – volume: 8 start-page: 032104 year: 2018 publication-title: J. Photonics Energy – volume: 7 start-page: 199 year: 2019 publication-title: Front. Chem. – volume: 11 start-page: 10758 year: 2019 publication-title: ACS Appl. Mater. Interfaces – volume: 6 start-page: 1800568 year: 2018 publication-title: Adv. Opt. Mater. – volume: 3 start-page: 18020 year: 2018 publication-title: Nat. Rev. Mater. – volume: 5 start-page: 1600749 year: 2017 publication-title: Adv. Opt. Mater. – volume: 62 start-page: 10967 year: 2000 publication-title: Phys. Rev. B – volume: 22 start-page: 2327 year: 2012 publication-title: Adv. Funct. Mater. – volume: 29 start-page: 1605444 year: 2017 publication-title: Adv. Mater. – volume: 25 start-page: 3038 year: 2013 publication-title: Chem. Mater. – volume: 134 start-page: 562 year: 2016 publication-title: Dyes Pigm. – volume: 163 start-page: 145 year: 2019 publication-title: Dyes Pigm. – volume: 10 start-page: 2915 year: 2019 publication-title: Chem. Sci. – volume: 11 start-page: 28096 year: 2019 publication-title: ACS Appl. Mater. Interfaces – volume: 63 start-page: 166 year: 2018 publication-title: Org. Electron. – volume: 24 start-page: 9581 year: 2018 publication-title: Chem. Eur. J. – volume: 25 start-page: 5623 year: 2019 publication-title: Chem. Eur. J. – volume: 12 start-page: 216 year: 2017 publication-title: Chem. Asian J. – volume: 137 start-page: 480 year: 2017 publication-title: Dyes Pigm. – ident: e_1_2_7_20_1 doi: 10.1016/j.orgel.2018.11.018 – ident: e_1_2_7_48_2 doi: 10.1002/ange.201709125 – ident: e_1_2_7_16_1 doi: 10.1016/j.dyepig.2016.08.023 – ident: e_1_2_7_41_1 doi: 10.1002/adma.201301603 – ident: e_1_2_7_36_1 doi: 10.1063/1.3558906 – ident: e_1_2_7_12_1 doi: 10.1021/cm4011597 – ident: e_1_2_7_52_1 doi: 10.1002/adma.201807388 – ident: e_1_2_7_3_1 doi: 10.1039/C6CS00368K – ident: e_1_2_7_13_1 doi: 10.1002/adom.201600749 – ident: e_1_2_7_5_1 doi: 10.1002/adma.201605444 – ident: e_1_2_7_9_1 doi: 10.1002/adom.201800568 – ident: e_1_2_7_8_1 doi: 10.1039/C8TC01139G – ident: e_1_2_7_33_1 doi: 10.1002/adfm.201300547 – ident: e_1_2_7_40_1 doi: 10.1103/PhysRevB.62.10967 – ident: e_1_2_7_2_1 doi: 10.1002/adma.201402532 – ident: e_1_2_7_28_1 doi: 10.1021/acsami.7b08258 – ident: e_1_2_7_49_1 doi: 10.1021/acs.chemmater.7b03371 – ident: e_1_2_7_46_1 doi: 10.1002/asia.201601384 – ident: e_1_2_7_48_1 doi: 10.1002/anie.201709125 – ident: e_1_2_7_35_1 doi: 10.1063/1.1751232 – ident: e_1_2_7_23_1 doi: 10.1016/j.dyepig.2018.11.042 – ident: e_1_2_7_53_1 doi: 10.1002/adfm.201802031 – ident: e_1_2_7_22_1 doi: 10.1002/anie.201509231 – ident: e_1_2_7_21_1 doi: 10.3389/fchem.2019.00199 – ident: e_1_2_7_25_1 doi: 10.1016/j.orgel.2018.09.023 – ident: e_1_2_7_44_1 doi: 10.1021/acsomega.8b03296 – ident: e_1_2_7_4_1 doi: 10.1021/acs.chemmater.6b05324 – ident: e_1_2_7_22_2 doi: 10.1002/ange.201509231 – ident: e_1_2_7_31_1 doi: 10.1021/acsami.8b00053 – ident: e_1_2_7_51_1 doi: 10.1021/acsami.9b07820 – ident: e_1_2_7_45_1 doi: 10.1039/C7TC00119C – ident: e_1_2_7_47_1 doi: 10.1002/chem.201800822 – ident: e_1_2_7_19_1 doi: 10.1039/C8SC04991B – ident: e_1_2_7_15_1 doi: 10.1016/j.dyepig.2015.02.014 – ident: e_1_2_7_38_1 doi: 10.1002/adfm.201101907 – ident: e_1_2_7_6_1 doi: 10.1002/jsid.598 – ident: e_1_2_7_39_1 doi: 10.1039/C4TC00865K – ident: e_1_2_7_43_1 doi: 10.1016/j.orgel.2017.06.029 – ident: e_1_2_7_30_1 doi: 10.1039/C9TC02491C – ident: e_1_2_7_29_1 doi: 10.1021/acsami.8b20699 – ident: e_1_2_7_17_1 doi: 10.1039/C6TC02702D – ident: e_1_2_7_24_1 doi: 10.1117/1.JPE.8.032104 – ident: e_1_2_7_11_1 doi: 10.1002/adma.201803524 – ident: e_1_2_7_18_1 doi: 10.1021/jacs.7b00873 – ident: e_1_2_7_50_1 doi: 10.1002/adfm.201705813 – ident: e_1_2_7_26_1 doi: 10.1016/j.cap.2003.11.091 – ident: e_1_2_7_32_1 doi: 10.1021/am401694s – ident: e_1_2_7_42_1 doi: 10.1016/j.dyepig.2016.10.029 – ident: e_1_2_7_7_1 doi: 10.1038/natrevmats.2018.20 – ident: e_1_2_7_10_1 doi: 10.1002/chem.201805952 – ident: e_1_2_7_27_1 doi: 10.1021/cm703682q – ident: e_1_2_7_1_1 doi: 10.1038/nature11687 – ident: e_1_2_7_37_1 doi: 10.1002/adma.200701730 – ident: e_1_2_7_14_1 doi: 10.1039/c3cp52255e – ident: e_1_2_7_34_1 doi: 10.1063/1.1568146 – volume: 4 start-page: 1861 year: 2019 ident: WOS:000460214700204 article-title: Achieving Deep-Blue Thermally Activated Delayed Fluorescence in Nondoped Organic Light-Emitting Diodes through a Spiro-Blocking Strategy publication-title: ACS OMEGA doi: 10.1021/acsomega.8b03296 – volume: 5 start-page: 7341 year: 2013 ident: WOS:000323241100079 article-title: A New Class of Sky-Blue-Emitting Ir(III) Phosphors Assembled Using Fluorine-Free Pyridyl Pyrimidine Cyclometalates: Application toward High-Performance Sky-Blue- and White-Emitting OLEDs publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/am401694s – volume: 20 start-page: 2125 year: 2008 ident: WOS:000257044600018 article-title: Pyridine-containing triphenylbenzene derivatives with high electron mobility for highly efficient phosphorescent OLEDs publication-title: ADVANCED MATERIALS doi: 10.1002/adma.200701730 – volume: 48 start-page: 262 year: 2017 ident: WOS:000405458400037 article-title: Carbazole-dendrite-encapsulated electron acceptor core for constructing thermally activated delayed fluorescence emitters used in nondoped solution-processed organic light-emitting diodes publication-title: ORGANIC ELECTRONICS doi: 10.1016/j.orgel.2017.06.029 – volume: 25 start-page: 5623 year: 2019 ident: WOS:000467079100003 article-title: Thermally Activated Delayed Fluorescence Materials: Towards Realization of High Efficiency through Strategic Small Molecular Design publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201805952 – volume: 5 year: 2017 ident: WOS:000398950500007 article-title: Tuning the twist angle of thermally activated delayed fluorescence molecules via a dendronization strategy: high-efficiency solution-processed non-doped OLEDs publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c7tc00119c – volume: 20 start-page: 1691 year: 2008 ident: WOS:000253727400011 article-title: Pyridine-containing bipolar host materials for highly efficient blue phosphorescent OLEDs publication-title: CHEMISTRY OF MATERIALS doi: 10.1021/cm703682q – volume: 10 start-page: 12886 year: 2018 ident: WOS:000430642100083 article-title: Optically Triggered Planarization of Boryl-Substituted Phenoxazine: Another Horizon of TADF Molecules and High-Performance OLEDs publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.8b00053 – volume: 7 start-page: ARTN 199 year: 2019 ident: WOS:000463468900001 article-title: New Aggregation-Induced Delayed Fluorescence Luminogens With Through-Space Charge Transfer for Efficient Non-doped OLEDs publication-title: FRONTIERS IN CHEMISTRY doi: 10.3389/fchem.2019.00199 – volume: 5 start-page: ARTN 1600749 year: 2017 ident: WOS:000393209600007 article-title: Harnessing Triplet Excited States by Fluorescent Dopant Utilizing Codoped Phosphorescent Dopant in Exciplex Host for Efficient Fluorescent Organic Light Emitting Diodes publication-title: ADVANCED OPTICAL MATERIALS doi: 10.1002/adom.201600749 – volume: 26 start-page: 7931 year: 2014 ident: WOS:000346263100001 article-title: Thermally Activated Delayed Fluorescence Materials Towards the Breakthrough of Organoelectronics publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201402532 – volume: 25 start-page: 3038 year: 2013 ident: WOS:000323193000018 article-title: Suppression of Efficiency Roll-Off Characteristics in Thermally Activated Delayed Fluorescence Based Organic Light-Emitting Diodes Using Randomly Oriented Host Molecules publication-title: CHEMISTRY OF MATERIALS doi: 10.1021/cm4011597 – volume: 23 start-page: 4914 year: 2013 ident: WOS:000327480000009 article-title: Exciplex-Forming Co-host for Organic Light-Emitting Diodes with Ultimate Efficiency publication-title: ADVANCED FUNCTIONAL MATERIALS doi: 10.1002/adfm.201300547 – volume: 137 start-page: 480 year: 2017 ident: WOS:000390182700055 article-title: Linkage modes on phthaloyl/triphenylamine hybrid compounds: Multi-functional AIE luminogens, non-doped emitters and organic hosts for highly efficient solution-processed delayed fluorescence OLEDs publication-title: DYES AND PIGMENTS doi: 10.1016/j.dyepig.2016.10.029 – volume: 56 start-page: 15006 year: 2017 ident: WOS:000445812900038 article-title: Combining Charge-Transfer Pathways to Achieve Unique Thermally Activated Delayed Fluorescence Emitters for High-Performance Solution-Processed, Non-doped Blue OLEDs publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201709125 – volume: 12 start-page: 216 year: 2017 ident: WOS:000393434200009 article-title: Constructing a Novel Dendron for a Self-Host Blue Emitter with Thermally Activated Delayed Fluorescence: Solution-Processed Nondoped Organic Light-Emitting Diodes with Bipolar Charge Transfer and Stable Color Purity publication-title: CHEMISTRY-AN ASIAN JOURNAL doi: 10.1002/asia.201601384 – volume: 492 start-page: 234 year: 2012 ident: WOS:000312259300038 article-title: Highly efficient organic light-emitting diodes from delayed fluorescence publication-title: NATURE doi: 10.1038/nature11687 – volume: 25 start-page: 480 year: 2017 ident: WOS:000413667400003 article-title: Solution-processable thermally activated delayed fluorescence emitters for application in organic light emitting diodes publication-title: JOURNAL OF THE SOCIETY FOR INFORMATION DISPLAY doi: 10.1002/jsid.598 – volume: 29 start-page: 1946 year: 2017 ident: WOS:000396639400006 article-title: Molecular Design Strategy of Organic Thermally Activated Delayed Fluorescence Emitters publication-title: CHEMISTRY OF MATERIALS doi: 10.1021/acs.chemmater.6b05324 – volume: 98 start-page: ARTN 083302 year: 2011 ident: WOS:000287764300088 article-title: Efficient up-conversion of triplet excitons into a singlet state and its application for organic light emitting diodes publication-title: APPLIED PHYSICS LETTERS doi: 10.1063/1.3558906 – volume: 7 start-page: 7672 year: 2019 ident: WOS:000475453000018 article-title: High efficiency green TADF emitters of acridine donor and triazine acceptor D-A-D structures publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c9tc02491c – volume: 55 start-page: 3017 year: 2016 ident: WOS:000370656200004 article-title: Pyridyl Pyrrolide Boron Complexes: The Facile Generation of Thermally Activated Delayed Fluorescence and Preparation of Organic Light-Emitting Diodes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201509231 – volume: 95 start-page: 7798 year: 2004 ident: WOS:000221843400037 article-title: Triplet exciton confinement and unconfinement by adjacent hole-transport layers publication-title: JOURNAL OF APPLIED PHYSICS doi: 10.1063/1.1751232 – volume: 129 start-page: 15202 year: 2017 ident: WOS:000501147800001.9 publication-title: ANGEW CHEM – volume: 11 start-page: 28096 year: 2019 ident: WOS:000480498600067 article-title: Achieving Efficient Blue Delayed Electrofluorescence by Shielding Acceptors with Carbazole Units publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.9b07820 – volume: 134 start-page: 562 year: 2016 ident: WOS:000383526000069 article-title: Design of ortho-linkage carbazole-triazine structure for high-efficiency blue thermally activated delayed fluorescent emitters publication-title: DYES AND PIGMENTS doi: 10.1016/j.dyepig.2016.08.023 – volume: 4 start-page: 9998 year: 2016 ident: WOS:000387229000011 article-title: Asymmetric-triazine-cored triads as thermally activated delayed fluorescence emitters for high-efficiency yellow OLEDs with slow efficiency roll-off publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c6tc02702d – volume: 63 start-page: 166 year: 2018 ident: WOS:000449270700024 article-title: Efficient donor-acceptor-donor borylated compounds with extremely small ΔEST for thermally activated delayed fluorescence OLEDs publication-title: ORGANIC ELECTRONICS doi: 10.1016/j.orgel.2018.09.023 – volume: 8 start-page: ARTN 032104 year: 2018 ident: WOS:000456697900005 article-title: Emission properties of thermally activated delayed fluorescence emitters: analysis based on a four-level model considering a higher triplet excited state publication-title: JOURNAL OF PHOTONICS FOR ENERGY doi: 10.1117/1.JPE.8.032104 – volume: 117 start-page: 141 year: 2015 ident: WOS:000352664900018 article-title: Thermally activated delayed fluorescence of N-phenylcarbazole and triphenylamine functionalised tris(aryl)triazines publication-title: DYES AND PIGMENTS doi: 10.1016/j.dyepig.2015.02.014 – volume: 11 start-page: 10758 year: 2019 ident: WOS:000462260000035 article-title: Blue TADF Emitters Based on Indenocarbazole Derivatives with High Photoluminescence and Electroluminescence Efficiencies publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.8b20699 – volume: 46 start-page: 915 year: 2017 ident: WOS:000395629200010 article-title: Recent advances in organic thermally activated delayed fluorescence materials publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c6cs00368k – volume: 24 start-page: 9581 year: 2018 ident: WOS:000437730300021 article-title: Aggregation-Enhanced Emission and Thermally Activated Delayed Fluorescence of Derivatives of 9-Phenyl-9H-Carbazole: Effects of Methoxy and tert-Butyl Substituents publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201800822 – volume: 82 start-page: 2422 year: 2003 ident: WOS:000182104900018 article-title: Blue organic electrophosphorescence using exothermic host-guest energy transfer publication-title: APPLIED PHYSICS LETTERS doi: 10.1063/1.1568146 – volume: 163 start-page: 145 year: 2019 ident: WOS:000457666300017 article-title: Triarylboryl-substituted carbazoles as bipolar host materials for efficient green phosphorescent organic light-emitting devices publication-title: DYES AND PIGMENTS doi: 10.1016/j.dyepig.2018.11.042 – volume: 15 start-page: 15850 year: 2013 ident: WOS:000324412300020 article-title: Enhanced electroluminescence based on thermally activated delayed fluorescence from a carbazole-triazine derivative publication-title: PHYSICAL CHEMISTRY CHEMICAL PHYSICS doi: 10.1039/c3cp52255e – volume: 29 start-page: 8012 year: 2017 ident: WOS:000411918900044 article-title: Isobenzofuranone- and Chromone-Based Blue Delayed Fluorescence Emitters with Low Efficiency Roll-Off in Organic Light-Emitting Diodes publication-title: CHEMISTRY OF MATERIALS doi: 10.1021/acs.chemmater.7b03371 – volume: 22 start-page: 2327 year: 2012 ident: WOS:000304749600013 article-title: Triplet Exciton Confinement in Green Organic Light-Emitting Diodes Containing Luminescent Charge-Transfer Cu(I) Complexes publication-title: ADVANCED FUNCTIONAL MATERIALS doi: 10.1002/adfm.201101907 – volume: 9 start-page: 27090 year: 2017 ident: WOS:000408178400049 article-title: First N-Borylated Emitters Displaying Highly Efficient Thermally Activated Delayed Fluorescence and High-Performance OLEDs publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.7b08258 – volume: 2 start-page: 6269 year: 2014 ident: WOS:000340353700005 article-title: Os(II) metal phosphors bearing tridentate 2,6-di(pyrazol-3-yl)pyridine chelate: synthetic design, characterization and application in OLED fabrication publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c4tc00865k – volume: 139 start-page: 4894 year: 2017 ident: WOS:000398764000044 article-title: Thermally Activated Delayed Fluorescence and Aggregation Induced Emission with Through-Space Charge Transfer publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.7b00873 – volume: 25 start-page: 6801 year: 2013 ident: WOS:000328424600002 article-title: Efficiency Roll-Off in Organic Light-Emitting Diodes publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201301603 – volume: 5 start-page: 305 year: 2005 ident: WOS:000227690700003 article-title: Organic electrophosphorescent devices with mixed hole transport material as emission layer publication-title: CURRENT APPLIED PHYSICS doi: 10.1016/j.cap.2003.11.091 – volume: 6 start-page: ARTN 1800568 year: 2018 ident: WOS:000453512700001 article-title: Design Strategy for Solution-Processable Thermally Activated Delayed Fluorescence Emitters and Their Applications in Organic Light-Emitting Diodes publication-title: ADVANCED OPTICAL MATERIALS doi: 10.1002/adom.201800568 – volume: 31 start-page: ARTN 1807388 year: 2019 ident: WOS:000462619000015 article-title: Highly Efficient Blue Fluorescent OLEDs Based on Upper Level Triplet-Singlet Intersystem Crossing publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201807388 – volume: 10 start-page: 2915 year: 2019 ident: WOS:000461509800003 article-title: Through-space charge transfer hexaarylbenzene dendrimers with thermally activated delayed fluorescence and aggregation-induced emission for efficient solution-processed OLEDs publication-title: CHEMICAL SCIENCE doi: 10.1039/c8sc04991b – volume: 29 start-page: ARTN 1605444 year: 2017 ident: WOS:000402963400023 article-title: Purely Organic Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201605444 – volume: 28 start-page: ARTN 1705813 year: 2018 ident: WOS:000427110100016 article-title: Efficient Nondoped Blue Fluorescent Organic Light-Emitting Diodes (OLEDs) with a High External Quantum Efficiency of 9.4% @ 1000 cd m-2 Based on Phenanthroimidazole-Anthracene Derivative publication-title: ADVANCED FUNCTIONAL MATERIALS doi: 10.1002/adfm.201705813 – volume: 62 start-page: 10967 year: 2000 ident: WOS:000165058600057 article-title: Transient analysis of organic electrophosphorescence. II. Transient analysis of triplet-triplet annihilation publication-title: PHYSICAL REVIEW B – volume: 31 start-page: ARTN 1803524 year: 2019 ident: WOS:000481877300012 article-title: Recent Progress of the Lifetime of Organic Light-Emitting Diodes Based on Thermally Activated Delayed Fluorescent Material publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201803524 – volume: 28 start-page: ARTN 1802031 year: 2018 ident: WOS:000442205200010 article-title: High-Performance Dibenzoheteraborin-Based Thermally Activated Delayed Fluorescence Emitters: Molecular Architectonics for Concurrently Achieving Narrowband Emission and Efficient Triplet-Singlet Spin Conversion publication-title: ADVANCED FUNCTIONAL MATERIALS doi: 10.1002/adfm.201802031 – volume: 128 start-page: 3069 year: 2016 ident: WOS:000501147800001.36 publication-title: ANGEW CHEM – volume: 6 start-page: 5577 year: 2018 ident: WOS:000434260700001 article-title: Recent progress in solution processable TADF materials for organic light-emitting diodes publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c8tc01139g – volume: 65 start-page: 170 year: 2019 ident: WOS:000453572400026 article-title: Solution-processed aggregation-induced delayed fluorescence (AIDF) emitters based on strong π-accepting triazine cores for highly efficient nondoped OLEDs with low efficiency roll-off publication-title: ORGANIC ELECTRONICS doi: 10.1016/j.orgel.2018.11.018 – volume: 3 start-page: ARTN 18020 year: 2018 ident: WOS:000430173500006 article-title: All-organic thermally activated delayed fluorescence materials for organic light-emitting diodes publication-title: NATURE REVIEWS MATERIALS doi: 10.1038/natrevmats.2018.20 |
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Snippet | A series of donor–acceptor–donor triazine‐based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly... A series of donor-acceptor-donor triazine-based molecules with thermally activated delayed fluorescence (TADF) properties were synthesized to obtain highly... |
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SubjectTerms | Benzene blue-emitting OLEDs Charge transfer Chemistry Chemistry, Multidisciplinary donor–acceptor systems Electroluminescence Electrons Emission Emissions Emitters Emitters (electron) Energy gap Energy levels Fabrication Fluorescence Molecular structure Organic light emitting diodes Physical Sciences Quantum efficiency Science & Technology Triazine triazines |
Title | Facile Generation of Thermally Activated Delayed Fluorescence and Fabrication of Highly Efficient Non‐Doped OLEDs Based on Triazine Derivatives |
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