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...

Full description

Saved in:
Bibliographic Details
Published inChemistry : a European journal Vol. 25; no. 72; pp. 16699 - 16711
Main Authors Chih, Hsin‐Yun, Chen, Ying‐Wei, Hsieh, Yi‐Chun, Li, Wei‐Cheng, Liao, Chia‐Wei, Lin, Chun‐Han, Chiu, Ting‐Ya, Tsai, Wei‐Wen, Lu, Chin‐Wei, Chang, Chih‐Hao
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 20.12.2019
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text
ISSN0947-6539
1521-3765
1521-3765
DOI10.1002/chem.201904411

Cover

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.
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
BookMark eNqNks1uEzEQgC1URNPClSNaiQsSSvDPem0fS34apEAv4bzyOmPiamMHe7conHgEeEWeBIekQaqE4OSR9X0z4_FcoDMfPCD0nOARwZi-MWvYjCgmCpclIY_QgHBKhkxU_AwNsCrFsOJMnaOLlG4xxqpi7Ak6Z6Rikko5QD9m2rgWimvwEHXngi-CLZZriBvdtrviynTuTnewKibQ6l0-Z20fIiQD3kChfb7QTXTm5M7dp3UWp9Y648B3xYfgf377PgnbLN8sppNUvNUpxxlfRqe_Og85edyXcXeQnqLHVrcJnh3PS_RxNl2O58PFzfW78dViaEqCyZAqha1luBElFlSCFCC4krahSnBBhZAKM2GbPAMo2YoJyldWscpwy61dYXaJXh3ybmP43EPq6o3Lr2pb7SH0qaYMC8FkyVlGXz5Ab0Mffe4uU1RyXgpeZerFkeqbDazqbXQbHXf1_bAzIA_AF2iCTfvpGDhh-Xc4JqQUMkeYjF33e6Tj0Psuq6__X810eaBNDClFsLU5Zuuidm1NcL1fnnq_PPVpebI2eqDdF_iroI5d5RXa_YOux_Pp-z_uLwL31KY
CitedBy_id crossref_primary_10_1039_D2TC05554F
crossref_primary_10_1016_j_orgel_2022_106571
crossref_primary_10_1016_j_cej_2024_148567
crossref_primary_10_1021_acs_jpcc_0c05731
crossref_primary_10_1021_acsaom_3c00156
crossref_primary_10_1039_D0AN00997K
crossref_primary_10_1021_acsami_0c18245
crossref_primary_10_1002_chem_202101807
crossref_primary_10_1039_D1SC07180G
crossref_primary_10_1039_D1TC01629F
crossref_primary_10_1016_j_dyepig_2020_108781
crossref_primary_10_1016_j_molliq_2021_117879
crossref_primary_10_1016_j_dyepig_2021_109892
crossref_primary_10_1016_j_dyepig_2022_110346
crossref_primary_10_1016_j_optmat_2024_116513
crossref_primary_10_1021_acs_chemmater_1c03870
crossref_primary_10_1021_acs_jpcc_0c05418
crossref_primary_10_1002_chem_202004719
crossref_primary_10_1016_j_tet_2021_132175
crossref_primary_10_1016_j_cej_2023_145023
crossref_primary_10_1016_j_orgel_2024_107005
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
ContentType Journal Article
Copyright 2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Copyright_xml – notice: 2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
– notice: 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
DBID AAYXX
CITATION
17B
1KM
AAWJD
BLEPL
DTL
EGQ
NPM
7SR
8BQ
8FD
JG9
K9.
7X8
DOI 10.1002/chem.201904411
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Web of Science - Science Citation Index Expanded - 2019
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
PubMed
Engineered Materials Abstracts
METADEX
Technology Research Database
Materials Research Database
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitle CrossRef
Web of Science
PubMed
Materials Research Database
ProQuest Health & Medical Complete (Alumni)
Engineered Materials Abstracts
Technology Research Database
METADEX
MEDLINE - Academic
DatabaseTitleList PubMed
MEDLINE - Academic
CrossRef
Materials Research Database

Web of Science
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 1KM
  name: Index Chemicus
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.IC
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1521-3765
EndPage 16711
ExternalDocumentID 31638288
000501147800001
10_1002_chem_201904411
CHEM201904411
Genre article
Journal Article
GrantInformation_xml – fundername: Ministry of Science and Technology, Taiwan
  funderid: 107-2113-M-126-004-MY2; 107-2221-E-155-028
– fundername: Ministry of Science and Technology of Taiwan; Ministry of Science and Technology, Taiwan
  grantid: MOST 107-2113-M-126-004-MY2; MOST 107-2221-E-155-028
– fundername: Ministry of Science and Technology, Taiwan
  grantid: 107-2113-M-126-004-MY2
– fundername: Ministry of Science and Technology, Taiwan
  grantid: 107-2221-E-155-028
GroupedDBID ---
-DZ
-~X
.3N
.GA
05W
0R~
10A
1L6
1OB
1OC
1ZS
29B
33P
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
6J9
702
77Q
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AAHQN
AAMNL
AANLZ
AAONW
AASGY
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABDBF
ABIJN
ABJNI
ABLJU
ABPVW
ACAHQ
ACCFJ
ACCZN
ACGFS
ACIWK
ACNCT
ACPOU
ACUHS
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AEIMD
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AHMBA
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALVPJ
AMBMR
AMYDB
ATUGU
AUFTA
AZBYB
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BY8
CS3
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRSTM
EBD
EBS
F00
F01
F04
F5P
G-S
G.N
GNP
GODZA
H.T
H.X
HBH
HGLYW
HHY
HHZ
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LYRES
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
P2W
P2X
P4D
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RGC
RNS
ROL
RWI
RX1
RYL
SUPJJ
TN5
TWZ
UB1
UPT
V2E
V8K
W8V
W99
WBFHL
WBKPD
WH7
WIB
WIH
WIK
WJL
WOHZO
WQJ
WRC
WXSBR
WYISQ
XG1
XPP
XV2
YZZ
ZZTAW
~IA
~WT
AAYXX
AEYWJ
AGHNM
AGYGG
CITATION
17B
1KM
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
NPM
7SR
8BQ
8FD
JG9
K9.
7X8
ID FETCH-LOGICAL-c4101-2990ff30b740728e87e7598fb2975727789037fb094e43d3725df936c5f5ffd03
IEDL.DBID DR2
ISICitedReferencesCount 22
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000501147800001
ISSN 0947-6539
1521-3765
IngestDate Fri Jul 11 09:53:23 EDT 2025
Fri Jul 25 12:10:21 EDT 2025
Wed Feb 19 02:25:45 EST 2025
Tue Jul 29 09:25:30 EDT 2025
Fri Sep 26 20:41:06 EDT 2025
Thu Apr 24 22:53:14 EDT 2025
Tue Jul 01 01:30:01 EDT 2025
Wed Jan 22 16:36:10 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 72
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
Language English
License 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c4101-2990ff30b740728e87e7598fb2975727789037fb094e43d3725df936c5f5ffd03
Notes OLED=organic light emitting diode.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-5586-9526
0000-0003-1516-8685
PMID 31638288
PQID 2328554756
PQPubID 986340
PageCount 13
ParticipantIDs crossref_citationtrail_10_1002_chem_201904411
crossref_primary_10_1002_chem_201904411
proquest_journals_2328554756
wiley_primary_10_1002_chem_201904411_CHEM201904411
webofscience_primary_000501147800001CitationCount
proquest_miscellaneous_2307738453
pubmed_primary_31638288
webofscience_primary_000501147800001
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate December 20, 2019
PublicationDateYYYYMMDD 2019-12-20
PublicationDate_xml – month: 12
  year: 2019
  text: December 20, 2019
  day: 20
PublicationDecade 2010
PublicationPlace WEINHEIM
PublicationPlace_xml – name: WEINHEIM
– name: Germany
– name: Weinheim
PublicationSubtitle A European Journal
PublicationTitle Chemistry : a European journal
PublicationTitleAbbrev CHEM-EUR J
PublicationTitleAlternate Chemistry
PublicationYear 2019
Publisher Wiley
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley
– name: Wiley Subscription Services, Inc
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
SSID ssj0009633
Score 2.42769
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...
Source Web of Science
SourceID proquest
pubmed
webofscience
crossref
wiley
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 16699
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fchem.201904411
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000501147800001
https://www.ncbi.nlm.nih.gov/pubmed/31638288
https://www.proquest.com/docview/2328554756
https://www.proquest.com/docview/2307738453
Volume 25
WOS 000501147800001
WOSCitedRecordID wos000501147800001
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVEBS
  databaseName: EBSCOhost Academic Search Ultimate
  customDbUrl: https://search.ebscohost.com/login.aspx?authtype=ip,shib&custid=s3936755&profile=ehost&defaultdb=asn
  eissn: 1521-3765
  dateEnd: 20241001
  omitProxy: true
  ssIdentifier: ssj0009633
  issn: 0947-6539
  databaseCode: ABDBF
  dateStart: 20120604
  isFulltext: true
  titleUrlDefault: https://search.ebscohost.com/direct.asp?db=asn
  providerName: EBSCOhost
– providerCode: PRVWIB
  databaseName: Wiley Online Library - Core collection (SURFmarket)
  issn: 0947-6539
  databaseCode: DR2
  dateStart: 19980101
  customDbUrl:
  isFulltext: true
  eissn: 1521-3765
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0009633
  providerName: Wiley-Blackwell
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Jb9UwEB6hXuDCvgQKMlIlTmnzbCfOO5a3qEJQJNRKvUVeLzwl1VsqlRM_Af4iv4QZZ2lfEQLBKdtMkolnPOPY8w3AnjUF4bj5tHBeplIKkxpeuFQXbsQdVyMbE4U_HBdHp_LdWX52LYu_xYcYfriRZcT-mgxcm9XBFWgoykSZ5OjQ0KPT-Gck8jhP--kKPwq1q60lL1VKGKw9amPGD7bZt73SL6HmDa-0HchGTzS_B7qXoV2A8nl_szb79ssNeMf_EfI-3O3CVHbY6tUDuOXrh3B70leHewTf59riHVkLW02ty5rAUOmwo18sLtmhjXXTvGNTv9CXuJ0vNs0ygkdZz3SNJ7RZdn8MiZdWnCDjLGJaoCtkx0394-u3aXOOzB_fz6Yr9hZdrmNIfoJmQ7DYePNlLM924VeP4XQ-O5kcpV15h9RK7AhScoQhiMwoAmkrfam8ysdlMJTsi2EVpegKFQy2npfCCcVzF8aisHnIQ3CZeAI7dVP7Z8ByQ71JcLLE0aW20hTOjLkrZa69V9YkkPbNW9kO-5xKcCyqFrWZV_Shq-FDJ_BmoD9vUT9-S7nba0vVWf-qwiiVVv-pvEjg9XAZG4gmY3Ttmw3RZEoJfEORwNNWy4ZHCQqSeVkmsHdd7YbrEbUHB7KqjJMzCYz-hmzSCU5gB-sEeNS7P4hXETDHcPT8X5hewB3apyVAPNuFnfVy419iILc2r6Kx_gSgbj51
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9NAEB6hcigX3g9DgUWqxMmts2t7nWPJQwHSIKFU4mZ5Xxcsu8oDqZz4CfAX-SXMrB8lRQgEpyj2jJPxzmt3Z78BONQqJRw3G6bGxmEcCxUqnpqwSM2AGy4H2h8UPl2ks7P4zYekqyakszANPkS_4EaW4f01GTgtSB9fooaiUHSUHCMahnScAF2nTTqyzfH7SwQp1K-mm3wsQ0Jh7XAbI368y78bl35JNq_Epd1U1sei6S1QnRRNCcrHo-1GHenPVwAe_0vM23CzzVTZSaNad-Care7C_qhrEHcPvk0LjY9kDXI1DTCrHUO9Q19flhfsRPvWadawsS2LC_ycltt65fGjtGVFhRcKtWoXDYmXik6QceJhLTAaskVdff_ydVyfI_O7-WS8Zq8w6hqG5Eu0HELGxoevfIe2T3Z9H86mk-VoFrYdHkIdoy8IKRY6JyIlCacts5m0MhlmTtF5X8ys6JSukE7h8NlYGCF5YtxQpDpxiXMmEg9gr6or-whYosihOBNnOMEsdKxSo4bcZHFSWCu1CiDsxjfXLfw5deEo8wa4mef0ovP-RQfwsqc_b4A_fkt50KlL3jqAdY6JKhUAyiQN4EV_GweI9mOKytZboomkFPgPRQAPGzXrf0pQnsyzLIDDn_Wuv--Be3AuKzO_PxPA4G_IRq3ghHewCYB7xfuDeDlhc_TfHv8L03PYny1P5_n89eLtE7hB16kiiEcHsLdZbe1TzOs26pm33B90oUKR
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6hIgEX3o9AASNV4pQ2Gztx9lj2oQJlQaiVeovi14UoWe2jUnviJ8Bf5Jcw4zzaLUIgOEVJZpKMPeMZx55vAHa0SgnHzYapsSIUgqtQxakJi9QMYhPLgfaJwh9m6cGxeHeSnFzK4m_wIfofbmQZfrwmA58bt3cBGooyUSY5OjT06Dj_uS5SnGJRWPT5AkAK1aspJi9kSCCsHWxjFO9t8m-6pV9izStuaTOS9a5oegeKTohmB8qX3fVK7erzK_iO_yPlXbjdxqlsv1Gse3DNVvfh5qgrD_cAvk8LjU9kDW41dS-rHUOtw5G-LM_YvvaF06xhY1sWZ3iclut64dGjtGVFhRcKtWh_GRIvbTlBxokHtUBfyGZ19ePrt3E9R-aPh5Pxkr1Bn2sYkh-h3RAuNj584euzndrlQzieTo5GB2Fb3yHUAkeCkDyhczxSklDaMptJK5Nh5hRl-2JcRTm6XDqFvWcFN1zGiXFDnurEJc6ZiD-Craqu7BNgiaLhxBmR4fSy0EKlRg1jk4mksFZqFUDYdW-uW_BzqsFR5g1sc5xTQ-d9QwfwuqefN7Afv6Xc7rQlb81_mWOYStv_ZJIG8Kq_jR1EqzFFZes10URScvxCHsDjRsv6V3GKkuMsC2Dnstr19z1sD85kZeZXZwIY_A3ZqBWc0A5WAcRe7_4gXk7IHP3Z039hegk3Po2n-eHb2ftncIsu03agONqGrdVibZ9jULdSL7zd_gRtcUFA
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Facile+Generation+of+Thermally+Activated+Delayed+Fluorescence+and+Fabrication+of+Highly+Efficient+Non-Doped+OLEDs+Based+on+Triazine+Derivatives&rft.jtitle=Chemistry+%3A+a+European+journal&rft.au=Chih%2C+Hsin-Yun&rft.au=Chen%2C+Ying-Wei&rft.au=Hsieh%2C+Yi-Chun&rft.au=Li%2C+Wei-Cheng&rft.date=2019-12-20&rft.eissn=1521-3765&rft.volume=25&rft.issue=72&rft.spage=16699&rft_id=info:doi/10.1002%2Fchem.201904411&rft_id=info%3Apmid%2F31638288&rft.externalDocID=31638288
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0947-6539&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0947-6539&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0947-6539&client=summon