A Dislocated Twin‐Locking Acceptor‐Donor‐Acceptor Configuration for Efficient Delayed Fluorescence with Multiple Through‐Space Charge Transfer

Organic materials featuring intramolecular through‐space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three‐dimensional disl...

Full description

Saved in:
Bibliographic Details
Published inAngewandte Chemie International Edition Vol. 61; no. 49; pp. e202213823 - n/a
Main Authors Xie, Feng‐Ming, Li, Hao‐Ze, Zhang, Kai, Shen, Yang, Zhao, Xin, Li, Yan‐Qing, Tang, Jian‐Xin
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 05.12.2022
Wiley Subscription Services, Inc
EditionInternational ed. in English
Subjects
Charge materials
Charge transfer
Chemistry
Chemistry, Multidisciplinary
Configurations
Fluorene
Fluorescence
Locking
Multiple Through-Space Charge Transfer
Organic Light-Emitting Diodes
Organic materials
Photoluminescence
Photons
Physical Sciences
Polycyclic Aromatic Hydrocarbons
Quantum efficiency
Science & Technology
Space charge
Thermally Activated Delayed Fluorescence
Triazine
Twin-Locking Configuration
Thermally Activated Delayed Fluorescence
Polycyclic Aromatic Hydrocarbons
Organic Light-Emitting Diodes
CRYSTALLIZATION-INDUCED EMISSION
Multiple Through-Space Charge Transfer
AGGREGATION
Twin-Locking Configuration
Online AccessGet full text

Cover

Abstract Organic materials featuring intramolecular through‐space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three‐dimensional dislocated sandwich acceptor‐donor‐acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6‐triphenyl‐1,3,5‐triazine (TRZ) acceptor through the twin‐locking of two spiro‐fluorene bridges. The twin‐locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ‐2TRZ, leading to a small singlet‐triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield. This material simultaneously possesses the capabilities of TADF and aggregation‐induced emission. The device employing 2PXZ‐2TRZ as a dopant displays an optimal external quantum efficiency of 27.1 % and a low efficiency roll‐off. Locking a large polycyclic aromatic hydrocarbon (PAH) by two spirofluorene groups has led to a rigid dislocated sandwich acceptor‐donor‐acceptor (A‐D‐A) configuration that exhibits multiple through‐space charge transfer (TSCT). This emitter shows both efficient thermally activated delayed fluorescence (TADF) and aggregation‐induced emission (AIE).
AbstractList Organic materials featuring intramolecular through‐space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three‐dimensional dislocated sandwich acceptor‐donor‐acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6‐triphenyl‐1,3,5‐triazine (TRZ) acceptor through the twin‐locking of two spiro‐fluorene bridges. The twin‐locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ‐2TRZ, leading to a small singlet‐triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield. This material simultaneously possesses the capabilities of TADF and aggregation‐induced emission. The device employing 2PXZ‐2TRZ as a dopant displays an optimal external quantum efficiency of 27.1 % and a low efficiency roll‐off.
Organic materials featuring intramolecular through‐space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three‐dimensional dislocated sandwich acceptor‐donor‐acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6‐triphenyl‐1,3,5‐triazine (TRZ) acceptor through the twin‐locking of two spiro‐fluorene bridges. The twin‐locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ‐2TRZ, leading to a small singlet‐triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield. This material simultaneously possesses the capabilities of TADF and aggregation‐induced emission. The device employing 2PXZ‐2TRZ as a dopant displays an optimal external quantum efficiency of 27.1 % and a low efficiency roll‐off. Locking a large polycyclic aromatic hydrocarbon (PAH) by two spirofluorene groups has led to a rigid dislocated sandwich acceptor‐donor‐acceptor (A‐D‐A) configuration that exhibits multiple through‐space charge transfer (TSCT). This emitter shows both efficient thermally activated delayed fluorescence (TADF) and aggregation‐induced emission (AIE).
Organic materials featuring intramolecular through-space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three-dimensional dislocated sandwich acceptor-donor-acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6-triphenyl-1,3,5-triazine (TRZ) acceptor through the twin-locking of two spiro-fluorene bridges. The twin-locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ-2TRZ, leading to a small singlet-triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield. This material simultaneously possesses the capabilities of TADF and aggregation-induced emission. The device employing 2PXZ-2TRZ as a dopant displays an optimal external quantum efficiency of 27.1 % and a low efficiency roll-off.Organic materials featuring intramolecular through-space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three-dimensional dislocated sandwich acceptor-donor-acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6-triphenyl-1,3,5-triazine (TRZ) acceptor through the twin-locking of two spiro-fluorene bridges. The twin-locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ-2TRZ, leading to a small singlet-triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield. This material simultaneously possesses the capabilities of TADF and aggregation-induced emission. The device employing 2PXZ-2TRZ as a dopant displays an optimal external quantum efficiency of 27.1 % and a low efficiency roll-off.
Author Shen, Yang
Xie, Feng‐Ming
Li, Yan‐Qing
Zhao, Xin
Tang, Jian‐Xin
Li, Hao‐Ze
Zhang, Kai
Author_xml – sequence: 1
  givenname: Feng‐Ming
  surname: Xie
  fullname: Xie, Feng‐Ming
  organization: Soochow University
– sequence: 2
  givenname: Hao‐Ze
  surname: Li
  fullname: Li, Hao‐Ze
  organization: East China Normal University
– sequence: 3
  givenname: Kai
  surname: Zhang
  fullname: Zhang, Kai
  organization: Macau University of Science and Technology
– sequence: 4
  givenname: Yang
  surname: Shen
  fullname: Shen, Yang
  organization: Soochow University
– sequence: 5
  givenname: Xin
  surname: Zhao
  fullname: Zhao, Xin
  organization: Suzhou University of Science and Technology
– sequence: 6
  givenname: Yan‐Qing
  surname: Li
  fullname: Li, Yan‐Qing
  email: yqli@phy.ecnu.edu.cn
  organization: East China Normal University
– sequence: 7
  givenname: Jian‐Xin
  orcidid: 0000-0002-6813-0448
  surname: Tang
  fullname: Tang, Jian‐Xin
  email: jxtang@suda.edu.cn
  organization: Macau University of Science and Technology
BookMark eNqNks1uEzEQx1eoiH7AlfNKXJCqDf5Ye51jtElLpQAHwnnlOOPEZWsv9q6i3HgETn1AnoRJk4JUCYFk2aOZ3388Hs95duKDhyx7TcmIEsLeae9gxAhjlCvGn2VnVDBa8KriJ2iXnBeVEvQ0O0_pFnmliHyRnXLJiORSnGX3k3zqUhuM7mGVL7bO__z-Yx7MV-fX-cQY6PoQ0TUN_uF8dOV18Nath6h7F3xu0TOz1hkHvs-n0OodprtqhxAhGfAG8q3rN_mHoe1d10K-2MQwrDeY8XOnMVpvdFyjO2qfLMSX2XOr2wSvjudF9uVqtqjfF_NP1zf1ZF4YLggvlLJjKVfMUKY4lCWUurJ2KbgpicZNlMtSK44LXy4MBUmE4Utqq1U15lLzi-ztIW8Xw7cBUt_cOay3bbWHMKSGVYxTIVQlEX3zBL0NQ_RYHVIlkVVFxBipywO1hWWwad8PA00X3Z2Ou4YQgj9QKi7RIhRp9f907fqHZtdh8D1Ky4PUxJBSBNuYY7yP2rUNJc1-QJr9gDS_BwRloyeyx9v-KhgfS3Qt7P5BN5OPN7M_2l9vItFo
CitedBy_id crossref_primary_10_1016_j_cej_2023_148314
crossref_primary_10_1002_ange_202402704
crossref_primary_10_1002_anie_202414488
crossref_primary_10_1002_adma_202304103
crossref_primary_10_1002_asia_202400679
crossref_primary_10_1002_ange_202401833
crossref_primary_10_1002_chem_202500644
crossref_primary_10_1039_D2CP05848K
crossref_primary_10_1039_D3QM01125A
crossref_primary_10_1002_asia_202401488
crossref_primary_10_1002_smll_202407220
crossref_primary_10_1021_acsaom_3c00370
crossref_primary_10_1039_D3SC04264B
crossref_primary_10_1002_adom_202300432
crossref_primary_10_1021_acsami_2c21533
crossref_primary_10_1002_chem_202404238
crossref_primary_10_1016_j_cej_2024_153511
crossref_primary_10_1002_adfm_202412267
crossref_primary_10_1002_adom_202400860
crossref_primary_10_1016_j_dyepig_2023_111572
crossref_primary_10_1002_ange_202414488
crossref_primary_10_1002_anie_202301896
crossref_primary_10_1016_j_matt_2024_07_017
crossref_primary_10_1002_adom_202402464
crossref_primary_10_1002_adfm_202411957
crossref_primary_10_1021_acs_chemrev_3c00755
crossref_primary_10_1039_D4SC08094G
crossref_primary_10_1002_adma_202307725
crossref_primary_10_1002_adma_202415951
crossref_primary_10_1039_D3CP05495K
crossref_primary_10_1002_smo_20240055
crossref_primary_10_1038_s41467_024_55569_0
crossref_primary_10_1039_D4MH00400K
crossref_primary_10_1021_acsmaterialslett_4c02232
crossref_primary_10_1002_adfm_202306574
crossref_primary_10_1016_j_jcis_2024_01_050
crossref_primary_10_1002_adfm_202422927
crossref_primary_10_1002_ange_202301896
crossref_primary_10_1002_ajoc_202400284
crossref_primary_10_1039_D4TC01525H
crossref_primary_10_1002_anie_202402704
crossref_primary_10_1002_anie_202401833
Cites_doi 10.1002/adma.201505491
10.1002/anie.202207293
10.1002/anie.202200337
10.1002/aelm.202101114
10.1021/ja501977a
10.1002/anie.202206916
10.1002/ange.202207293
10.1002/adma.202202464
10.1021/acs.jpcc.5b06088
10.1021/jacs.0c08980
10.1002/ange.202206916
10.1002/anie.202206861
10.1002/ange.202109335
10.1002/anie.202201588
10.1002/adom.202102092
10.1002/anie.201603232
10.1002/ange.202011384
10.1038/s41566-020-0667-0
10.1021/jacs.7b10578
10.1039/D1SC02042K
10.1038/s41566-020-0668-z
10.1002/ange.202117181
10.1002/anie.202200059
10.1016/j.cej.2021.129366
10.1002/ange.202201588
10.1002/adom.201902142
10.1021/jacs.7b00873
10.1002/ange.201603232
10.1021/acsami.1c17707
10.1021/jacs.0c10081
10.1038/s41566-019-0476-5
10.1039/D0MH00952K
10.1002/anie.202011384
10.1002/ange.202008264
10.1021/jacs.1c01826
10.1002/ange.201911266
10.1002/anie.202117181
10.1038/s41563-020-0710-z
10.1002/adfm.201908677
10.1021/jacs.9b04893
10.1002/ange.202200337
10.1002/ange.202200059
10.1021/jacs.1c10038
10.1002/adma.202003885
10.1002/anie.202008264
10.1021/ja510144h
10.1002/adma.202106954
10.1016/j.cclet.2022.06.057
10.1002/anie.202013051
10.1002/anie.201911266
10.1002/ange.202206861
10.1002/anie.202109335
10.34133/2022/9892802
10.1039/d1sc02042k
10.1039/d0mh00952k
ContentType Journal Article
Copyright 2022 Wiley‐VCH GmbH
2022 Wiley-VCH GmbH.
Copyright_xml – notice: 2022 Wiley‐VCH GmbH
– notice: 2022 Wiley-VCH GmbH.
DBID AAYXX
CITATION
17B
1KM
AHQBO
BLEPL
DTL
EGQ
7TM
K9.
7X8
DOI 10.1002/anie.202213823
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Web of Science - Science Citation Index Expanded - 2022
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Nucleic Acids Abstracts
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitle CrossRef
Web of Science
ProQuest Health & Medical Complete (Alumni)
Nucleic Acids Abstracts
MEDLINE - Academic
DatabaseTitleList CrossRef

Web of Science
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
Database_xml – sequence: 1
  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 1521-3773
Edition International ed. in English
EndPage n/a
ExternalDocumentID 000880483600001
10_1002_anie_202213823
ANIE202213823
Genre shortCommunication
GrantInformation_xml – fundername: National Key R&D Program of China
  funderid: 2022YFE0108900
– fundername: Fundo para o Desenvolvimento das Ciências e da Tecnologia
  funderid: 0008/2022/AMJ
– fundername: National Natural Science Foundation of China
  funderid: 51873138; 62075061; 62274117
– fundername: Collaborative Innovation Center of Suzhou Nano Science Technology
– fundername: National Natural Science Foundation of China; National Natural Science Foundation of China (NSFC)
  grantid: 62274117; 62075061; 51873138
– fundername: Science and Technology Innovation Plan Of Shanghai Science and Technology Commission
  grantid: 22520760600
– fundername: Jiangsu Provincial department of Science and Technology
  grantid: BZ2022054
– fundername: Science and Technology Development Fund (FDCT), Macau SAR
  grantid: 0008/2022/AMJ
– fundername: National Key R&D Program of China
  grantid: 2022YFE0108900
GroupedDBID ---
-DZ
-~X
.3N
.GA
05W
0R~
10A
1L6
1OB
1OC
1ZS
23M
33P
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5RE
5VS
66C
6TJ
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AAHQN
AAMNL
AANLZ
AAONW
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABLJU
ABPPZ
ABPVW
ACAHQ
ACCFJ
ACCZN
ACFBH
ACGFS
ACIWK
ACNCT
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AHMBA
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ATUGU
AUFTA
AZBYB
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BTSUX
BY8
CS3
D-E
D-F
D0L
DCZOG
DPXWK
DR1
DR2
DRFUL
DRSTM
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
M53
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
P2P
P2W
P2X
P4D
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RNS
ROL
RWI
RX1
RYL
SUPJJ
TN5
UB1
UPT
UQL
V2E
VQA
W8V
W99
WBFHL
WBKPD
WH7
WIB
WIH
WIK
WJL
WOHZO
WQJ
WRC
WXSBR
WYISQ
XG1
XPP
XSW
XV2
YZZ
ZZTAW
~IA
~KM
~WT
AAYXX
ABDBF
ABJNI
AEYWJ
AGHNM
AGYGG
CITATION
17B
1KM
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
7TM
K9.
7X8
ID FETCH-LOGICAL-c3503-88f966d2c1283e44e4a7ffb53c40a3c454b4a83a832885c1e605c3b1f7d7936a3
IEDL.DBID DR2
ISICitedReferencesCount 45
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000880483600001
ISSN 1433-7851
1521-3773
IngestDate Fri Jul 11 09:53:34 EDT 2025
Fri Jul 25 10:33:00 EDT 2025
Fri Aug 29 16:26:02 EDT 2025
Wed Jul 09 18:31:58 EDT 2025
Tue Jul 01 01:18:30 EDT 2025
Thu Apr 24 23:00:04 EDT 2025
Wed Jan 22 16:22:49 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 49
Keywords Thermally Activated Delayed Fluorescence
Polycyclic Aromatic Hydrocarbons
Organic Light-Emitting Diodes
CRYSTALLIZATION-INDUCED EMISSION
Multiple Through-Space Charge Transfer
AGGREGATION
Twin-Locking Configuration
Language English
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c3503-88f966d2c1283e44e4a7ffb53c40a3c454b4a83a832885c1e605c3b1f7d7936a3
Notes These authors contributed equally to this work.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-6813-0448
0000-0001-7988-3755
0009-0004-1764-0570
PMID 36206365
PQID 2740677059
PQPubID 946352
PageCount 6
ParticipantIDs crossref_citationtrail_10_1002_anie_202213823
webofscience_primary_000880483600001CitationCount
proquest_miscellaneous_2723155876
proquest_journals_2740677059
webofscience_primary_000880483600001
crossref_primary_10_1002_anie_202213823
wiley_primary_10_1002_anie_202213823_ANIE202213823
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate December 5, 2022
PublicationDateYYYYMMDD 2022-12-05
PublicationDate_xml – month: 12
  year: 2022
  text: December 5, 2022
  day: 05
PublicationDecade 2020
PublicationPlace WEINHEIM
PublicationPlace_xml – name: WEINHEIM
– name: Weinheim
PublicationTitle Angewandte Chemie International Edition
PublicationTitleAbbrev ANGEW CHEM INT EDIT
PublicationYear 2022
Publisher Wiley
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley
– name: Wiley Subscription Services, Inc
References 2018; 140
2020; 142
2019; 13
2020 2020; 59 132
2020; 14
2021; 143
2020; 32
2019; 141
2014; 136
2019 2019; 58 131
2017; 139
2020; 19
2020; 8
2021; 418
2021; 13
2020; 7
2022 2022; 61 134
2016 2016; 55 128
2021; 12
2022; 2022
2020; 30
2022
2022; 8
2022; 34
2021 2021; 60 133
2015; 119
2022; 10
2016; 28
Jiang C. (e_1_2_3_30_1) 2022; 2022
e_1_2_3_2_1
e_1_2_3_6_1
e_1_2_3_16_1
e_1_2_3_39_1
e_1_2_3_4_1
e_1_2_3_18_1
e_1_2_3_18_2
e_1_2_3_12_1
e_1_2_3_35_1
e_1_2_3_33_2
e_1_2_3_8_1
e_1_2_3_14_1
e_1_2_3_37_1
e_1_2_3_31_1
e_1_2_3_10_1
e_1_2_3_33_1
(e_1_2_3_24_2) 2022; 134
(e_1_2_3_12_2) 2022; 134
e_1_2_3_28_1
e_1_2_3_24_1
e_1_2_3_26_1
e_1_2_3_20_1
e_1_2_3_41_1
e_1_2_3_22_1
e_1_2_3_1_1
e_1_2_3_5_2
e_1_2_3_5_1
e_1_2_3_17_1
e_1_2_3_38_1
e_1_2_3_17_2
e_1_2_3_3_1
e_1_2_3_19_1
e_1_2_3_9_1
e_1_2_3_13_1
e_1_2_3_34_1
e_1_2_3_7_2
e_1_2_3_13_2
e_1_2_3_7_1
e_1_2_3_15_1
e_1_2_3_36_1
e_1_2_3_11_1
e_1_2_3_32_1
(e_1_2_3_2_2) 2022; 134
e_1_2_3_40_1
(e_1_2_3_8_2) 2022; 134
e_1_2_3_27_1
e_1_2_3_27_2
e_1_2_3_29_1
e_1_2_3_23_1
e_1_2_3_25_1
e_1_2_3_42_1
e_1_2_3_21_1
(e_1_2_3_25_2) 2021; 133
e_1_2_3_42_2
Zeng (000880483600001.3) 2022; 134
Peng, CC (WOS:000582779800001) 2020; 32
Yang, ML (WOS:000696247200001) 2021; 60
(000880483600001.25) 2019; 131
Lv, XL (WOS:000803622700001) 2022; 61
Wang (000880483600001.16) 2022; 134
Zhang, YW (WOS:000492218500001) 2019; 58
Cai, XL (WOS:000778033200001) 2022; 61
Tsujimoto, H (WOS:000398764000044) 2017; 139
Kondo, Y (WOS:000487333400005) 2019; 13
(000880483600001.37) 2021; 133
Lee, HL (WOS:000826194200001) 2022; 34
Cui, LS (WOS:000555386900001) 2020; 14
Zeng, X (WOS:000755169600001) 2022; 61
(000880483600001.18) 2021; 133
Song, YJ (WOS:000731031800001) 2021; 13
Huang (000880483600001.32) 2022; 134
Zhang, YW (WOS:000557993900001) 2020; 59
Wada, Y (WOS:000555386900002) 2020; 14
Hatakeyama, T (WOS:000373839600014) 2016; 28
Liu, Y (WOS:000662326300001) 2021; 12
(000880483600001.53) 2016; 128
Wu, C (WOS:000602612900001) 2021; 60
Crocker, RD (WOS:000750743100039) 2021; 143
Suresh, SM (WOS:000535648400001) 2020; 30
Shi, YZ (WOS:000575959700017) 2020; 7
Ye, ZW (WOS:000487180200004) 2019; 141
Yang, ML (WOS:000592911000007) 2020; 142
Wang, XQ (WOS:000606866600001) 2021; 60
Matsui, K (WOS:000424313000002) 2018; 140
Furue, R (WOS:000382790600025) 2016; 55
Wang, X (WOS:000838145300001) 2022; 61
Yang, SY (WOS:000655663700002) 2021; 418
Jiang, PC (WOS:000720785100001) 2022; 34
Liu, PC (WOS:000641160700005) 2021; 143
Han, JM (WOS:000729435600001) 2022; 10
Wu, C. (000880483600001.34) 2021; 133
Jiang, CL (WOS:000818653100001) 2022; 2022
Huang, TY (WOS:000749622600001) 2022; 61
Zhang, QS (WOS:000347438300030) 2014; 136
Liu, JF (WOS:000986018200001) 2023; 34
Tong, JQ (WOS:000361921600014) 2015; 119
Yang, SY (WOS:000579400400063) 2020; 142
Naveen, KR (WOS:000721829700001) 2022; 8
Yang, SY (WOS:000822728200001) 2022; 61
Meng (000880483600001.11) 2022; 134
(000880483600001.23) 2020; 132
Meng, GY (WOS:000829907700001) 2022; 61
Tang, X (WOS:000540412500004) 2020; 19
Xu, YC (WOS:000531416200016) 2020; 8
Galer, P (WOS:000336416600033) 2014; 136
References_xml – volume: 13
  start-page: 678
  year: 2019
  end-page: 682
  publication-title: Nat. Photonics
– volume: 140
  start-page: 1195
  year: 2018
  end-page: 1198
  publication-title: J. Am. Chem. Soc.
– volume: 7
  start-page: 2734
  year: 2020
  end-page: 2740
  publication-title: Mater. Horiz.
– volume: 418
  year: 2021
  publication-title: Chem. Eng. J.
– volume: 8
  year: 2022
  publication-title: Adv. Electron. Mater.
– volume: 8
  year: 2020
  publication-title: Adv. Opt. Mater.
– volume: 10
  year: 2022
  publication-title: Adv. Opt. Mater.
– volume: 136
  start-page: 7383
  year: 2014
  publication-title: J. Am. Chem. Soc.
– volume: 55 128
  start-page: 7171 7287
  year: 2016 2016
  end-page: 7175 7291
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 34
  year: 2022
  publication-title: Adv. Mater.
– volume: 19
  start-page: 1332
  year: 2020
  end-page: 1338
  publication-title: Nat. Mater.
– volume: 14
  start-page: 636
  year: 2020
  end-page: 642
  publication-title: Nat. Photonics
– volume: 142
  start-page: 19468
  year: 2020
  end-page: 19472
  publication-title: J. Am. Chem. Soc.
– volume: 30
  year: 2020
  publication-title: Adv. Funct. Mater.
– volume: 12
  start-page: 9408
  year: 2021
  end-page: 9412
  publication-title: Chem. Sci.
– volume: 119
  start-page: 21875
  year: 2015
  end-page: 21881
  publication-title: J. Phys. Chem. C
– volume: 142
  start-page: 17756
  year: 2020
  end-page: 17765
  publication-title: J. Am. Chem. Soc.
– volume: 139
  start-page: 4894
  year: 2017
  end-page: 4900
  publication-title: J. Am. Chem. Soc.
– volume: 60 133
  start-page: 23142 23326
  year: 2021 2021
  end-page: 23147 23331
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 32
  year: 2020
  publication-title: Adv. Mater.
– volume: 60 133
  start-page: 3994 4023
  year: 2021 2021
  end-page: 3998 4028
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 2022
  year: 2022
  publication-title: Research
– volume: 136
  start-page: 18070
  year: 2014
  end-page: 18081
  publication-title: J. Am. Chem. Soc.
– volume: 143
  start-page: 5314
  year: 2021
  end-page: 5318
  publication-title: J. Am. Chem. Soc.
– volume: 141
  start-page: 14491
  year: 2019
  end-page: 14495
  publication-title: J. Am. Chem. Soc.
– volume: 14
  start-page: 643
  year: 2020
  end-page: 649
  publication-title: Nat. Photonics
– volume: 28
  start-page: 2777
  year: 2016
  end-page: 2781
  publication-title: Adv. Mater.
– volume: 59 132
  start-page: 17499 17652
  year: 2020 2020
  end-page: 17503 17656
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– year: 2022
  publication-title: Chin. Chem. Lett.
– volume: 61 134
  year: 2022 2022
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 143
  start-page: 20384
  year: 2021
  end-page: 20394
  publication-title: J. Am. Chem. Soc.
– volume: 58 131
  start-page: 16912 17068
  year: 2019 2019
  end-page: 16917 17073
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 13
  start-page: 60269
  year: 2021
  end-page: 60278
  publication-title: ACS Appl. Mater. Interfaces
– volume: 60 133
  start-page: 5213 5273
  year: 2021 2021
  end-page: 5219 5279
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– ident: e_1_2_3_6_1
  doi: 10.1002/adma.201505491
– ident: e_1_2_3_8_1
  doi: 10.1002/anie.202207293
– ident: e_1_2_3_5_1
  doi: 10.1002/anie.202200337
– ident: e_1_2_3_16_1
  doi: 10.1002/aelm.202101114
– ident: e_1_2_3_32_1
  doi: 10.1021/ja501977a
– ident: e_1_2_3_12_1
  doi: 10.1002/anie.202206916
– volume: 134
  year: 2022
  ident: e_1_2_3_8_2
  publication-title: Angew. Chem.
  doi: 10.1002/ange.202207293
– ident: e_1_2_3_9_1
  doi: 10.1002/adma.202202464
– ident: e_1_2_3_34_1
  doi: 10.1021/acs.jpcc.5b06088
– ident: e_1_2_3_26_1
  doi: 10.1021/jacs.0c08980
– volume: 134
  year: 2022
  ident: e_1_2_3_12_2
  publication-title: Angew. Chem.
  doi: 10.1002/ange.202206916
– ident: e_1_2_3_33_1
  doi: 10.1002/anie.202206861
– ident: e_1_2_3_13_2
  doi: 10.1002/ange.202109335
– ident: e_1_2_3_7_1
  doi: 10.1002/anie.202201588
– ident: e_1_2_3_20_1
  doi: 10.1002/adom.202102092
– ident: e_1_2_3_42_1
  doi: 10.1002/anie.201603232
– ident: e_1_2_3_27_2
  doi: 10.1002/ange.202011384
– ident: e_1_2_3_36_1
  doi: 10.1038/s41566-020-0667-0
– ident: e_1_2_3_10_1
  doi: 10.1021/jacs.7b10578
– ident: e_1_2_3_14_1
  doi: 10.1039/D1SC02042K
– ident: e_1_2_3_40_1
  doi: 10.1038/s41566-020-0668-z
– volume: 134
  year: 2022
  ident: e_1_2_3_2_2
  publication-title: Angew. Chem.
  doi: 10.1002/ange.202117181
– ident: e_1_2_3_24_1
  doi: 10.1002/anie.202200059
– ident: e_1_2_3_37_1
  doi: 10.1016/j.cej.2021.129366
– ident: e_1_2_3_7_2
  doi: 10.1002/ange.202201588
– ident: e_1_2_3_19_1
  doi: 10.1002/adom.201902142
– ident: e_1_2_3_21_1
  doi: 10.1021/jacs.7b00873
– ident: e_1_2_3_42_2
  doi: 10.1002/ange.201603232
– ident: e_1_2_3_28_1
  doi: 10.1021/acsami.1c17707
– ident: e_1_2_3_1_1
  doi: 10.1021/jacs.0c10081
– ident: e_1_2_3_11_1
  doi: 10.1038/s41566-019-0476-5
– ident: e_1_2_3_41_1
  doi: 10.1039/D0MH00952K
– volume: 133
  start-page: 4023
  year: 2021
  ident: e_1_2_3_25_2
  publication-title: Angew. Chem.
– ident: e_1_2_3_27_1
  doi: 10.1002/anie.202011384
– ident: e_1_2_3_17_2
  doi: 10.1002/ange.202008264
– ident: e_1_2_3_31_1
– ident: e_1_2_3_3_1
  doi: 10.1021/jacs.1c01826
– ident: e_1_2_3_18_2
  doi: 10.1002/ange.201911266
– ident: e_1_2_3_2_1
  doi: 10.1002/anie.202117181
– ident: e_1_2_3_22_1
  doi: 10.1038/s41563-020-0710-z
– ident: e_1_2_3_4_1
  doi: 10.1002/adfm.201908677
– volume: 2022
  year: 2022
  ident: e_1_2_3_30_1
  publication-title: Research
– ident: e_1_2_3_38_1
  doi: 10.1021/jacs.9b04893
– ident: e_1_2_3_5_2
  doi: 10.1002/ange.202200337
– volume: 134
  year: 2022
  ident: e_1_2_3_24_2
  publication-title: Angew. Chem.
  doi: 10.1002/ange.202200059
– ident: e_1_2_3_35_1
  doi: 10.1021/jacs.1c10038
– ident: e_1_2_3_23_1
  doi: 10.1002/adma.202003885
– ident: e_1_2_3_17_1
  doi: 10.1002/anie.202008264
– ident: e_1_2_3_39_1
  doi: 10.1021/ja510144h
– ident: e_1_2_3_15_1
  doi: 10.1002/adma.202106954
– ident: e_1_2_3_29_1
  doi: 10.1016/j.cclet.2022.06.057
– ident: e_1_2_3_25_1
  doi: 10.1002/anie.202013051
– ident: e_1_2_3_18_1
  doi: 10.1002/anie.201911266
– ident: e_1_2_3_33_2
  doi: 10.1002/ange.202206861
– ident: e_1_2_3_13_1
  doi: 10.1002/anie.202109335
– volume: 34
  start-page: ARTN 2106954
  year: 2022
  ident: WOS:000720785100001
  article-title: Quenching-Resistant Multiresonance TADF Emitter Realizes 40% External Quantum Efficiency in Narrowband Electroluminescence at High Doping Level
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.202106954
– volume: 14
  start-page: 643
  year: 2020
  ident: WOS:000555386900002
  article-title: Organic light emitters exhibiting very fast reverse intersystem crossing
  publication-title: NATURE PHOTONICS
  doi: 10.1038/s41566-020-0667-0
– volume: 13
  start-page: 60269
  year: 2021
  ident: WOS:000731031800001
  article-title: Through-Space Charge-Transfer Emitters Developed by Fixing the Acceptor for High-Efficiency Thermally Activated Delayed Fluorescence
  publication-title: ACS APPLIED MATERIALS & INTERFACES
  doi: 10.1021/acsami.1c17707
– volume: 133
  start-page: 5273
  year: 2021
  ident: 000880483600001.37
  publication-title: Angew. Chem
– volume: 134
  year: 2022
  ident: 000880483600001.11
  publication-title: Angew. Chem
– volume: 58
  start-page: 16912
  year: 2019
  ident: WOS:000492218500001
  article-title: Multi-Resonance Induced Thermally Activated Delayed Fluorophores for Narrowband Green OLEDs
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201911266
– volume: 59
  start-page: 17499
  year: 2020
  ident: WOS:000557993900001
  article-title: Achieving Pure Green Electroluminescence with CIEy of 0.69 and EQE of 28.2% from an Aza-Fused Multi-Resonance Emitter
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202008264
– volume: 14
  start-page: 636
  year: 2020
  ident: WOS:000555386900001
  article-title: Fast spin-flip enables efficient and stable organic electroluminescence from charge-transfer states
  publication-title: NATURE PHOTONICS
  doi: 10.1038/s41566-020-0668-z
– volume: 28
  start-page: 2777
  year: 2016
  ident: WOS:000373839600014
  article-title: Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO-LUMO Separation by the Multiple Resonance Effect
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.201505491
– volume: 30
  start-page: ARTN 1908677
  year: 2020
  ident: WOS:000535648400001
  article-title: Multiresonant Thermally Activated Delayed Fluorescence Emitters Based on Heteroatom-Doped Nanographenes: Recent Advances and Prospects for Organic Light-Emitting Diodes
  publication-title: ADVANCED FUNCTIONAL MATERIALS
  doi: 10.1002/adfm.201908677
– volume: 61
  start-page: ARTN e202207293
  year: 2022
  ident: WOS:000829907700001
  article-title: Amine-Directed Formation of B-N Bonds for BN-Fused Polycyclic Aromatic Multiple Resonance Emitters with Narrowband Emission
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202207293
– volume: 60
  start-page: 23142
  year: 2021
  ident: WOS:000696247200001
  article-title: Wide-Range Color Tuning of Narrowband Emission in Multi-resonance Organoboron Delayed Fluorescence Materials through Rational Imine/Amine Functionalization
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202109335
– volume: 61
  start-page: ARTN e202206916
  year: 2022
  ident: WOS:000838145300001
  article-title: Mesityl-Functionalized Multi-Resonance Organoboron Delayed Fluorescent Frameworks with Wide-Range Color Tunability for Narrowband OLEDs
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202206916
– volume: 418
  start-page: ARTN 129366
  year: 2021
  ident: WOS:000655663700002
  article-title: π-stacked donor-acceptor molecule to realize hybridized local and charge-transfer excited state emission with multi-stimulus response
  publication-title: CHEMICAL ENGINEERING JOURNAL
  doi: 10.1016/j.cej.2021.129366
– volume: 10
  start-page: ARTN 2102092
  year: 2022
  ident: WOS:000729435600001
  article-title: Simple Molecular Design Strategy for Multiresonance Induced TADF Emitter: Highly Efficient Deep Blue to Blue Electroluminescence with High Color Purity
  publication-title: ADVANCED OPTICAL MATERIALS
  doi: 10.1002/adom.202102092
– volume: 13
  start-page: 678
  year: 2019
  ident: WOS:000487333400005
  article-title: Narrowband deep-blue organic light-emitting diode featuring an organoboron-based emitter
  publication-title: NATURE PHOTONICS
  doi: 10.1038/s41566-019-0476-5
– volume: 131
  start-page: 17068
  year: 2019
  ident: 000880483600001.25
  publication-title: Angew. Chem
– volume: 61
  start-page: ARTN e202206861
  year: 2022
  ident: WOS:000822728200001
  article-title: Highly Efficient Sky-Blue π-Stacked Thermally Activated Delayed Fluorescence Emitter with Multi-Stimulus Response Properties
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202206861
– volume: 2022
  start-page: ARTN 9892802
  year: 2022
  ident: WOS:000818653100001
  article-title: Acceptor-Donor-Acceptor π-Stacking Boosts Intramolecular Through-Space Charge Transfer towards Efficient Red TADF and High-Performance OLEDs
  publication-title: RESEARCH
  doi: 10.34133/2022/9892802
– volume: 140
  start-page: 1195
  year: 2018
  ident: WOS:000424313000002
  article-title: One-Shot Multiple Borylation toward BN-Doped Nanographenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.7b10578
– volume: 136
  start-page: 7383
  year: 2014
  ident: WOS:000336416600033
  article-title: Crystal Structures and Emission Properties of the BF2 Complex 1-Phenyl-3-(3,5-dimethoxyphenyl)-propane-1,3-dione: Multiple Chromisms, Aggregation- or Crystallization-Induced Emission, and the Self-Assembly Effect
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja501977a
– volume: 34
  start-page: ARTN 107634
  year: 2023
  ident: WOS:000986018200001
  article-title: Acceptor modulation for improving thermally activated delayed fluorescence emitter in through-space charge transfer on spiroskeletons
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2022.06.057
– volume: 61
  start-page: ARTN e202201588
  year: 2022
  ident: WOS:000803622700001
  article-title: Extending the π-Skeleton of Multi-Resonance TADF Materials towards High-Efficiency Narrowband Deep-Blue Emission
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202201588
– volume: 134
  year: 2022
  ident: 000880483600001.32
  publication-title: Angew. Chem
– volume: 60
  start-page: 3994
  year: 2021
  ident: WOS:000602612900001
  article-title: Face-to-Face Orientation of Quasiplanar Donor and Acceptor Enables Highly Efficient Intramolecular Exciplex Fluorescence
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202013051
– volume: 141
  start-page: 14491
  year: 2019
  ident: WOS:000487180200004
  article-title: Quaternary Piperazine-Substituted Rhodamines with Enhanced Brightness for Super-Resolution Imaging
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b04893
– volume: 128
  start-page: 7287
  year: 2016
  ident: 000880483600001.53
  publication-title: Angew. Chem
– volume: 143
  start-page: 20384
  year: 2021
  ident: WOS:000750743100039
  article-title: Unusual Alternating Crystallization-Induced Emission Enhancement Behavior in Nonconjugated ω-Phenylalkyl Tropylium Salts
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.1c10038
– volume: 8
  start-page: ARTN 1902142
  year: 2020
  ident: WOS:000531416200016
  article-title: Molecular-Structure and Device-Configuration Optimizations toward Highly Efficient Green Electroluminescence with Narrowband Emission and High Color Purity
  publication-title: ADVANCED OPTICAL MATERIALS
  doi: 10.1002/adom.201902142
– volume: 61
  start-page: ARTN e202200337
  year: 2022
  ident: WOS:000778033200001
  article-title: Achieving 37.1% Green Electroluminescent Efficiency and 0.09 eV Full Width at Half Maximum Based on a Ternary Boron-Oxygen-Nitrogen Embedded Polycyclic Aromatic System
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202200337
– volume: 136
  start-page: 18070
  year: 2014
  ident: WOS:000347438300030
  article-title: Anthraquinone-Based Intramolecular Charge-Transfer Compounds: Computational Molecular Design, Thermally Activated Delayed Fluorescence, and Highly Efficient Red Electroluminescence
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja510144h
– volume: 12
  start-page: 9408
  year: 2021
  ident: WOS:000662326300001
  article-title: Molecular design of thermally activated delayed fluorescent emitters for narrowband orange-red OLEDs boosted by a cyano-functionalization strategy
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/d1sc02042k
– volume: 61
  start-page: ARTN e202200059
  year: 2022
  ident: WOS:000749622600001
  article-title: Accelerating Radiative Decay in Blue Through-Space Charge Transfer Emitters by Minimizing the Face-to-Face Donor-Acceptor Distances
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202200059
– volume: 55
  start-page: 7171
  year: 2016
  ident: WOS:000382790600025
  article-title: Aggregation-Induced Delayed Fluorescence Based on Donor/Acceptor-Tethered Janus Carborane Triads: Unique Photophysical Properties of Nondoped OLEDs
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201603232
– 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: 133
  start-page: 4023
  year: 2021
  ident: 000880483600001.34
  publication-title: Angew. Chem
– volume: 142
  start-page: 17756
  year: 2020
  ident: WOS:000579400400063
  article-title: Circularly Polarized Thermally Activated Delayed Fluorescence Emitters in Through-Space Charge Transfer on Asymmetric Spiro Skeletons
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.0c08980
– volume: 32
  start-page: ARTN 2003885
  year: 2020
  ident: WOS:000582779800001
  article-title: Highly Efficient Thermally Activated Delayed Fluorescence via an Unconjugated Donor-Acceptor System Realizing EQE of Over 30%
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.202003885
– volume: 8
  start-page: ARTN 2101114
  year: 2022
  ident: WOS:000721829700001
  article-title: Narrow Band Red Emission Fluorophore with Reasonable Multiple Resonance Effect
  publication-title: ADVANCED ELECTRONIC MATERIALS
  doi: 10.1002/aelm.202101114
– volume: 19
  start-page: 1332
  year: 2020
  ident: WOS:000540412500004
  article-title: Highly efficient luminescence from space-confined charge-transfer emitters
  publication-title: NATURE MATERIALS
  doi: 10.1038/s41563-020-0710-z
– volume: 60
  start-page: 5213
  year: 2021
  ident: WOS:000606866600001
  article-title: Multi-Layer π-Stacked Molecules as Efficient Thermally Activated Delayed Fluorescence Emitters
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202011384
– volume: 61
  start-page: ARTN e202117181
  year: 2022
  ident: WOS:000755169600001
  article-title: Nitrogen-Embedded Multi-Resonance Heteroaromatics with Prolonged Homogeneous Hexatomic Rings
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202117181
– volume: 143
  start-page: 5314
  year: 2021
  ident: WOS:000641160700005
  article-title: Revisiting Acepleiadylene: Two-Step Synthesis and p-Extension toward Nonbenzenoid Nanographene
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.1c01826
– volume: 132
  start-page: 17652
  year: 2020
  ident: 000880483600001.23
  publication-title: Angew. Chem
– volume: 134
  year: 2022
  ident: 000880483600001.16
  publication-title: Angew. Chem
– volume: 119
  start-page: 21875
  year: 2015
  ident: WOS:000361921600014
  article-title: Crystallization-Induced Emission Enhancement of a Simple Tolane-Based Mesogenic Luminogen
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY C
  doi: 10.1021/acs.jpcc.5b06088
– volume: 142
  start-page: 19468
  year: 2020
  ident: WOS:000592911000007
  article-title: Full-Color, Narrowband, and High-Efficiency Electroluminescence from Boron and Carbazole Embedded Polycyclic Heteroaromatics
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.0c10081
– volume: 7
  start-page: 2734
  year: 2020
  ident: WOS:000575959700017
  article-title: Hydrogen bond-modulated molecular packing and its applications in high-performance non-doped organic electroluminescence
  publication-title: MATERIALS HORIZONS
  doi: 10.1039/d0mh00952k
– volume: 134
  year: 2022
  ident: 000880483600001.3
  publication-title: Angew. Chem
– volume: 133
  start-page: 23326
  year: 2021
  ident: 000880483600001.18
  publication-title: Angew. Chem
– volume: 34
  start-page: ARTN 2202464
  year: 2022
  ident: WOS:000826194200001
  article-title: Multiple-Resonance Extension and Spin-Vibronic-Coupling-Based Narrowband Blue Organic Fluorescence Emitters with Over 30% Quantum Efficiency
  publication-title: ADVANCED MATERIALS
  doi: 10.1002/adma.202202464
SSID ssj0028806
Score 2.5705745
Snippet Organic materials featuring intramolecular through‐space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed...
Organic materials featuring intramolecular through-space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed...
Source Web of Science
SourceID proquest
webofscience
crossref
wiley
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage e202213823
SubjectTerms Charge materials
Charge transfer
Chemistry
Chemistry, Multidisciplinary
Configurations
Fluorene
Fluorescence
Locking
Multiple Through-Space Charge Transfer
Organic Light-Emitting Diodes
Organic materials
Photoluminescence
Photons
Physical Sciences
Polycyclic Aromatic Hydrocarbons
Quantum efficiency
Science & Technology
Space charge
Thermally Activated Delayed Fluorescence
Triazine
Twin-Locking Configuration
Title A Dislocated Twin‐Locking Acceptor‐Donor‐Acceptor Configuration for Efficient Delayed Fluorescence with Multiple Through‐Space Charge Transfer
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202213823
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000880483600001
https://www.proquest.com/docview/2740677059
https://www.proquest.com/docview/2723155876
Volume 61
WOS 000880483600001
WOSCitedRecordID wos000880483600001
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB6hXuDCGxEoyEiVOLlN_MjmutqHCqI9wFbqLbIdp1qxSqrdjVB74idw4gfyS5hxHu0iIRBIUbJxnGwcjz3fJDPfABxYmQmXesNHJlUc8X_BMxsbbr0qbJm4pNAUO3xymh6fqffn-vxWFH_LDzG8cKOREeZrGuDGbo5uSEMpAhvtOyGIRY_oPslhi1DRx4E_SqBwtuFFUnLKQt-zNsbiaPf0Xa10AzV3lNEufg0KaP4ATH_rrd_J58Nmaw_d9S-sjv_Ttodwv0OnbNyK0yO446vHcHfSJ4V7At_HbLrckAJEpMoWX5bVj6_fPuCcihqQjR35yNRrLJrWVdj2RYwiC5cXTStvDJEymwXyCtR5bOpX5govN1819TrQSznP6AUxO-ncHdmiTSeEV_yERr5n5CVwgcUBdvv1UzibzxaTY96lduBO6ljyLCvRziqEQ_UovVJemVFZWi2dig2utLLKZBIX7EPtEo9Wl5M2KUcFTiipkc9gr6or_xyYLgsX29ghjpHKpCIrrSjlSJci9j4VLgLed23uOt5zSr-xylvGZpHT086Hpx3B26H-Zcv48dua-72k5N3I3-Ro5RMpH6LWCN4Mh7GX6EOMqXzdUB1E1VqjIorg4LaEDX9I0Cwjtv80fH6JIPmbapOueURnsI1ABBH7QyPy8em72bD34l9Oegn36Hdw8tH7sLddN_4VQrWtfR2G408gkTqV
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lj9MwEB7BclguvBGBBYy0EqfsJn6kuVZ9qAttD9CVuEW246wqqgR1GyE48RM48QP5Jcw4j6VICARS1Ciundbx2PONM_MNwLERKbeJ0-FAJzJE_J-HqYl0aJzMTRHbOFcUO7xYJrNz-eqd6rwJKRam4YfoN9xoZvj1miY4bUifXrGGUgg2GnicE42euA43KK23t6re9AxSHMWzCTASIqQ89B1vY8RP99vv66UrsLmnjvYRrFdB09tguj_feJ68P6l35sR-_oXX8b96dwdutQCVDRuJugvXXHkPDkddXrj78G3IxutL0oEIVtnq47r8_uXrHJdVVIJsaMlNptpi0bgq_bkrYhRcuL6oG5FjCJbZxPNXoNpjY7fRn_B2001dbT3DlHWM9ojZovV4ZKsmoxDe8S3a-Y6Ro8AFFnvk7bYP4Hw6WY1mYZvdIbRCRSJM0wJNrZxb1JDCSemkHhSFUcLKSOOHkkbqVOCBg6hs7NDwssLExSDHNSXR4iEclFXpHgFTRW4jE1mEMkLqhKeF4YUYqIJHziXcBhB2Y5vZlvqcMnBssoa0mWf0tLP-aQfwsq__oSH9-G3No05UsnbyX2Zo6BMvHwLXAF70X-Mo0bsYXbqqpjoIrJVCXRTA8c8i1v8gobOUCP8T_wYmgPhvqo3a7hGjwS4A7mXsD53IhsuzSX_1-F8aPYfD2Woxz-Zny9dP4CaVe58fdQQHu23tniJy25lnfm7-AKJKPrA
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1ba9RAFD5oBfXFuxitOkLBp7TJXLJ5XTa7tNouolvoW5iZzJTFJSnbXUp98if45A_0l3hObu0KoiiEhEwml8mcmfOd5JzvAOwYkXKbOB0OdCJDxP9FmJpIh8bJwvjYxoWi2OGjabJ_LN-dqJNrUfwNP0T_wY1GRj1f0wA_K_zeFWkoRWCjfcc5seiJm3BLJlFKcp197AmkOEpnE18kREhp6DvaxojvbZ6_qZausOaGNtoEsLUGmtwH3T1743jyeXe9Mrv2yy-0jv_TuAdwr4WnbNjI00O44cpHcGfUZYV7DN-HLJufkwZEqMpmF_Pyx9dvhzipogpkQ0tOMtUSi7KqrLddEaPQwvnpuhE4hlCZjWv2ClR6LHMLfYmXmyzW1bLml7KO0RdidtT6O7JZk08Ir_gJrXzHyE3gFItr3O2WT-B4Mp6N9sM2t0NohYpEmKYeDa2CW9SPwknppB54b5SwMtK4UtJInQpcsA-VjR2aXVaY2A8KnFESLZ7CVlmV7hkw5QsbmcgikBFSJzz1hnsxUJ5HziXcBhB2XZvblvic8m8s8oaymef0tvP-bQfwtq9_1lB-_LbmdicpeTv0z3M084mVD2FrAG_6w9hL9CdGl65aUx2E1UqhJgpg57qE9TckbJYS3X9S_38JIP6baqO2ecRnsAqA1yL2h0bkw-nBuN97_i8nvYbbH7JJfngwff8C7lJx7fCjtmFrtVy7lwjbVuZVPTJ_AtmaPWg
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=A+Dislocated+Twin-Locking+Acceptor-Donor-Acceptor+Configuration+for+Efficient+Delayed+Fluorescence+with+Multiple+Through-Space+Charge+Transfer&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Xie%2C+Feng-Ming&rft.au=Li%2C+Hao-Ze&rft.au=Zhang%2C+Kai&rft.au=Shen%2C+Yang&rft.date=2022-12-05&rft.issn=1521-3773&rft.eissn=1521-3773&rft.volume=61&rft.issue=49&rft.spage=e202213823&rft_id=info:doi/10.1002%2Fanie.202213823&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon