Differential detection of strong acids in weak acids: a combination of a benzimidazole-carbazole backbone with AIE luminophores as highly sensitive and selective turn-on fluorescent probes

o -BzcDPE and p -BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AIEgens) that are incorporated with a benzimidazole-carbazole backbone. Both probes show turn-on green fluorescence with a good contrast in the pres...

Full description

Saved in:
Bibliographic Details
Published inNew journal of chemistry Vol. 46; no. 21; pp. 1317 - 1327
Main Authors Lin, Pei-Chi, Lin, Yu-Ting, Liu, Kuan-Ting, Chen, Meng-Sin, Zhang, Yong-Yun, Li, Jie-Cheng, Leung, Man-kit
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 30.05.2022
Royal Society of Chemistry
Subjects
Online AccessGet full text

Cover

Loading…
Abstract o -BzcDPE and p -BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AIEgens) that are incorporated with a benzimidazole-carbazole backbone. Both probes show turn-on green fluorescence with a good contrast in the presence of trace amounts of strong acids in a weak acid environment. These probes are not only suitable for visual detection of strong acids, but also exhibit high selectivity, excellent sensitivity, and short response time and are capable of quantitative detection of strong acids with a good linear relationship. A concentration of H 2 SO 4 as low as 1 mol% in acetic acid can be differentiated. The fluorescence-turn-on mechanisms are due to protonation on the benzimidazole moiety that have been proved by X-ray crystallographic analysis and NMR spectroscopy. With the combination of a benzimidazole-carbazole backbone and AIE luminophores, highly sensitive and selective turn-on fluorescent probes are achieved and applicable for differential detection of strong acids in weak acids.
AbstractList o-BzcDPE and p-BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AIEgens) that are incorporated with a benzimidazole-carbazole backbone. Both probes show turn-on green fluorescence with a good contrast in the presence of trace amounts of strong acids in a weak acid environment. These probes are not only suitable for visual detection of strong acids, but also exhibit high selectivity, excellent sensitivity, and short response time and are capable of quantitative detection of strong acids with a good linear relationship. A concentration of H 2 SO 4 as low as 1 mol% in acetic acid can be differentiated. The fluorescence-turn-on mechanisms are due to protonation on the benzimidazole moiety that have been proved by X-ray crystallographic analysis and NMR spectroscopy.
o -BzcDPE and p -BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AIEgens) that are incorporated with a benzimidazole-carbazole backbone. Both probes show turn-on green fluorescence with a good contrast in the presence of trace amounts of strong acids in a weak acid environment. These probes are not only suitable for visual detection of strong acids, but also exhibit high selectivity, excellent sensitivity, and short response time and are capable of quantitative detection of strong acids with a good linear relationship. A concentration of H 2 SO 4 as low as 1 mol% in acetic acid can be differentiated. The fluorescence-turn-on mechanisms are due to protonation on the benzimidazole moiety that have been proved by X-ray crystallographic analysis and NMR spectroscopy. With the combination of a benzimidazole-carbazole backbone and AIE luminophores, highly sensitive and selective turn-on fluorescent probes are achieved and applicable for differential detection of strong acids in weak acids.
o-BzcDPE and p-BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AIEgens) that are incorporated with a benzimidazole-carbazole backbone. Both probes show turn-on green fluorescence with a good contrast in the presence of trace amounts of strong acids in a weak acid environment. These probes are not only suitable for visual detection of strong acids, but also exhibit high selectivity, excellent sensitivity, and short response time and are capable of quantitative detection of strong acids with a good linear relationship. A concentration of H2SO4 as low as 1 mol% in acetic acid can be differentiated. The fluorescence-turn-on mechanisms are due to protonation on the benzimidazole moiety that have been proved by X-ray crystallographic analysis and NMR spectroscopy.
o-BzcDPE and p-BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AlEgens) that are incorporated with a benzimidazole-carbazole backbone. Both probes show turn-on green fluorescence with a good contrast in the presence of trace amounts of strong acids in a weak acid environment. These probes are not only suitable for visual detection of strong acids, but also exhibit high selectivity, excellent sensitivity, and short response time and are capable of quantitative detection of strong acids with a good linear relationship. A concentration of H2SO4 as low as 1 mol% in acetic acid can be differentiated. The fluorescence-turn-on mechanisms are due to protonation on the benzimidazole moiety that have been proved by X-ray crystallographic analysis and NMR spectroscopy.
Author Li, Jie-Cheng
Liu, Kuan-Ting
Leung, Man-kit
Chen, Meng-Sin
Lin, Pei-Chi
Lin, Yu-Ting
Zhang, Yong-Yun
AuthorAffiliation Chang Chun Plastics Co., Ltd. Kaohsiung Factory
National Taiwan University
Department of Chemistry and Advanced Research Center for Green Materials Science and Technology
AuthorAffiliation_xml – name: National Taiwan University
– name: Department of Chemistry and Advanced Research Center for Green Materials Science and Technology
– name: Chang Chun Plastics Co., Ltd. Kaohsiung Factory
Author_xml – sequence: 1
  givenname: Pei-Chi
  surname: Lin
  fullname: Lin, Pei-Chi
– sequence: 2
  givenname: Yu-Ting
  surname: Lin
  fullname: Lin, Yu-Ting
– sequence: 3
  givenname: Kuan-Ting
  surname: Liu
  fullname: Liu, Kuan-Ting
– sequence: 4
  givenname: Meng-Sin
  surname: Chen
  fullname: Chen, Meng-Sin
– sequence: 5
  givenname: Yong-Yun
  surname: Zhang
  fullname: Zhang, Yong-Yun
– sequence: 6
  givenname: Jie-Cheng
  surname: Li
  fullname: Li, Jie-Cheng
– sequence: 7
  givenname: Man-kit
  surname: Leung
  fullname: Leung, Man-kit
BookMark eNqNkkFv1DAQhS1UJNrChTuSJW6ggMdJnIRbtS2lVdVe4BzZzrjrbdZebIdV-9v4cfVu2nLl5DfS9zxPM3NEDpx3SMh7YF-Ald3XgbsVA87F6hU5hFJ0RccFHGQNVVWwuhJvyFGMK8YAGgGH5O-pNQYDumTlSAdMqJP1jnpDYwre3VKp7RCpdXSL8m6uvlFJtV8r6-QzLKlC92DXdpAPfsRCy6D2iiqp71ROSbc2LenJxRkdp7V1frP0ASOVkS7t7XK8pxFdtMn-QSrdkKtxFyVXaQquyF3MOO0cOmelm-AVxrfktZFjxHdP7zH59f3s5-JHcXVzfrE4uSo0r1gqhEaoTWcEYxK5GKRsGiMUM4Bc1qIWvK6g6xQIXQMXrWmHhrXQ5JnVoq1UeUw-zv_mtr8njKlf-Rwqt-y5aKCrKw6QqU8zpYOPMaDpN8GuZbjvgfW77fSn_Ppyv53LDLczvEXlTdQWncYXA2Os6YRgXZkVg4VN-0Ev_ORStn7-f2umP8x0iPoF-ncm5SMMkrH4
Cites_doi 10.1002/adfm.202105452
10.1039/d0ra00107d
10.1039/c7qm00298j
10.1002/anie.202000940
10.1021/acsami.8b15084
10.1039/c3ra45329d
10.1016/j.tet.2018.11.018
10.1021/acs.analchem.8b01455
10.1021/acs.jafc.0c04275
10.1002/jhet.1058
10.1016/j.aca.2017.04.020
10.1039/c3ra41329b
10.1016/j.cplett.2007.08.030
10.1016/j.dyepig.2016.01.029
10.1016/j.synthmet.2008.03.020
10.1039/c5tc03933a
10.1038/srep15189
10.1039/c9an01778j
10.1021/ja068551y
10.1038/s41467-020-14477-9
10.1039/c2cc35188a
10.1039/c6nj00063k
10.1063/1.2753723
10.1021/ja808611d
10.1021/ja409971k
10.1021/cr940745l
10.1016/j.jhazmat.2021.126243
10.3390/polym10111259
10.1039/c5tc02865e
10.1016/j.aca.2007.01.070
10.1039/c0jm04100a
10.1021/m902432m
10.1039/c3cc46008h
10.1002/marc.200900794
10.1016/j.dyepig.2017.09.043
10.1016/j.talanta.2021.123111
10.1039/c7nj02086d
10.1016/j.snb.2014.09.107
10.1039/c9cs00495e
10.1021/acs.chemmater.9b01278
10.1021/acs.joc.5b02051
10.1002/anie.202005785
10.1016/j.snb.2011.06.047
10.1021/acsomega.8b01706
10.1016/j.ab.2019.113403
10.1016/j.jphotochem.2020.112542
10.1021/jp022549l
10.1021/ja0269082
10.1021/jf501113j
10.1039/c6cp02778d
10.1016/j.tet.2011.01.093
10.1021/es702192c
10.1021/jp8111167
10.1039/c9nj01972c
10.1039/b608425g
10.1016/j.ccr.2020.213693
10.1002/chem.200902505
10.1016/j.orgel.2019.06.017
10.1021/ac1018028
10.1039/c3tc32551b
10.1016/j.dyepig.2017.03.021
10.1021/acsami.7b13444
10.1039/c1cs15113d
10.1039/c2jm16510d
10.1039/d0an01141j
10.1021/ja044421i
10.1021/am506322h
10.1002/anie.200900963
10.1038/s41467-019-13993-7
10.1039/C6NJ00063K
10.1039/C6CP02778D
10.1039/C3TC32551B
10.1039/C5TC03933A
10.1039/C9NJ01972C
10.1039/C7QM00298J
10.1039/C3RA45329D
10.1039/C9CS00495E
10.1039/D0RA00107D
10.1016/0003-2697(72)90182-0
10.1039/b105159h
10.1021/jp9905023
10.1039/C7NJ02086D
10.1039/C9AN01778J
10.1021/ma902432m
10.1039/C5TC02865E
10.1039/D0AN01141J
10.1002/anie.199422071
ContentType Journal Article
Copyright Copyright Royal Society of Chemistry 2022
Copyright_xml – notice: Copyright Royal Society of Chemistry 2022
DBID 17B
1KM
AHQBO
BLEPL
DTL
EGQ
AAYXX
CITATION
7SR
8BQ
8FD
H9R
JG9
KA0
DOI 10.1039/d2nj01226j
DatabaseName 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)
CrossRef
Engineered Materials Abstracts
METADEX
Technology Research Database
Illustrata: Natural Sciences
Materials Research Database
ProQuest Illustrata: Technology Collection
DatabaseTitle Web of Science
CrossRef
Materials Research Database
ProQuest Illustrata: Natural Sciences
Engineered Materials Abstracts
ProQuest Illustrata: Technology Collection
Technology Research Database
METADEX
DatabaseTitleList CrossRef

Materials Research Database
Web of Science
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 1369-9261
EndPage 1327
ExternalDocumentID 10_1039_D2NJ01226J
000796609300001
d2nj01226j
GrantInformation_xml – fundername: "Advanced Research Center for Green Materials Science and Technology" from The Featured Area Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education
  grantid: MOE 111L9006
– fundername: Ministry of Science and Technology, Republic of China (Taiwan)
– fundername: Chang Chun Plastics Company
  grantid: MOST 111-2622-8-007-011; MOST 110-2113-M-002-009; MOST 111-2634-F-002-016; MOST 110-2622-8-007-015; MOST 110-2622-E-155-010
GroupedDBID -
0-7
0R
123
1TJ
29N
4.4
70
705
70J
7~J
AAEMU
AAGNR
AAIWI
AAJAE
AALRV
AANOJ
AAXPP
ABASK
ABDVN
ABFLS
ABGFH
ABPTK
ABRYZ
ACGFS
ACIWK
ACLDK
ACNCT
ADMRA
ADSRN
AENEX
AFVBQ
AGKEF
AGRSR
AGSTE
AGSWI
ALMA_UNASSIGNED_HOLDINGS
ANUXI
ASKNT
AUDPV
AZFZN
BLAPV
BSQNT
C6K
CS3
D0L
DU5
DZ
EBS
ECGLT
EE0
EF-
F5P
GNO
H13
HZ
H~N
IDZ
J3I
JG
L7B
M4U
N9A
O9-
OK1
P2P
R7B
R7C
R7D
RCNCU
RIG
RNS
RPMJG
RRA
RRC
RSCEA
SKA
SKF
SKH
SLH
TN5
TWZ
VH6
X
YNT
YQT
---
-DZ
-~X
0R~
17B
1KM
2WC
70~
AAMEH
AAWGC
AAXHV
ABCQX
ABEMK
ABJNI
ABPDG
ABXOH
AEFDR
AENGV
AESAV
AETIL
AFLYV
AFOGI
AFRDS
AFRZK
AGEGJ
AHGCF
AKMSF
ALUYA
APEMP
BLEPL
DTL
GGIMP
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
HZ~
R56
RAOCF
AAYXX
CITATION
7SR
8BQ
8FD
H9R
JG9
KA0
ID FETCH-LOGICAL-c240t-6ce15f9f600ae26daa77f6b0f1e2a5656254199b16c51268f8d708171145684b3
ISICitedReferencesCount 0
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000796609300001
ISSN 1144-0546
IngestDate Mon Jun 30 09:53:56 EDT 2025
Tue Jul 01 02:51:13 EDT 2025
Wed Jul 09 18:10:35 EDT 2025
Fri Aug 29 16:16:34 EDT 2025
Thu Jun 02 04:21:16 EDT 2022
IsPeerReviewed true
IsScholarly true
Issue 21
Keywords BODIPY
ELECTRON-TRANSFER
FLUOROPHORES
AGGREGATION-INDUCED EMISSION
DONOR
PH
ENHANCED EMISSION
TETRAPHENYLETHYLENE
DERIVATIVES
INTRAMOLECULAR CHARGE-TRANSFER
Language English
LinkModel OpenURL
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c240t-6ce15f9f600ae26daa77f6b0f1e2a5656254199b16c51268f8d708171145684b3
Notes Electronic supplementary information (ESI) available. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
https://doi.org/10.1039/d2nj01226j
2153889-2153891
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ORCID 0000-0001-5100-7227
0000-0002-3297-9087
PQID 2671954211
PQPubID 2048886
PageCount 11
ParticipantIDs webofscience_primary_000796609300001CitationCount
rsc_primary_d2nj01226j
crossref_primary_10_1039_D2NJ01226J
proquest_journals_2671954211
webofscience_primary_000796609300001
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-05-30
PublicationDateYYYYMMDD 2022-05-30
PublicationDate_xml – month: 05
  year: 2022
  text: 2022-05-30
  day: 30
PublicationDecade 2020
PublicationPlace CAMBRIDGE
PublicationPlace_xml – name: CAMBRIDGE
– name: Cambridge
PublicationTitle New journal of chemistry
PublicationTitleAbbrev NEW J CHEM
PublicationYear 2022
Publisher Royal Soc Chemistry
Royal Society of Chemistry
Publisher_xml – name: Royal Soc Chemistry
– name: Royal Society of Chemistry
References Liu, JZ (WOS:000278109700013) 2010; 43
ROGERS, KS (WOS:A1972M988800019) 1972; 48
Gao, HC (WOS:000431723400079) 2018; 10
Hu, RR (WOS:000308827600006) 2012; 48
Lu, PP (WOS:000729414400006) 2022; 239
Yuan, CX (WOS:000265383300065) 2009; 113
Wang, XR (WOS:000302367500062) 2012; 22
Moreno-Yruela, C (WOS:000366877900022) 2015; 80
Gao, Y (WOS:000382766300004) 2016; 18
Chen, B (WOS:000325642400026) 2013; 49
Horak, E (WOS:000401393100014) 2017; 142
Cao, YL (WOS:000335000300003) 2014; 2
(000796609300001.64) 1000
An, BK (WOS:000179510800034) 2002; 124
Sunahara, H (WOS:000245946400066) 2007; 129
Derinkuyu, S (WOS:000245500900007) 2007; 588
Dong, YQ (WOS:000247819700011) 2007; 91
Li, ZS (WOS:000373547300022) 2016; 128
Li, J (WOS:000515511500002) 2020; 49
Jung, HS (WOS:000264792100069) 2009; 131
Qiao, WG (WOS:000682483800001) 2021; 31
Chen, BY (WOS:000454456800081) 2018; 10
Chen, W (WOS:000498558200011) 2019; 144
Chao, JB (WOS:000402250300006) 2017; 975
Jana, P (WOS:000474646200022) 2019; 43
Helal, A (WOS:000289330000008) 2011; 67
Secci, D (WOS:000310562600032) 2012; 49
Xu, CG (WOS:000689358300006) 2021; 418
Zhang, G (WOS:000462418900013) 2019; 75
Hopper, TR (WOS:000485830300055) 2019; 31
Suzuki, S (WOS:000533322900001) 2020; 59
Grabowski, ZR (WOS:000185910900003) 2003; 103
Dong, YQ (WOS:000250194400023) 2007; 446
Wang, J (WOS:000288220600006) 2011; 21
Ma, WW (WOS:000474343300029) 2019; 73
Lin, Z (WOS:000543984200012) 2020; 11
Yang, XD (WOS:000367255100020) 2016; 4
Yamada, A (WOS:000339694300036) 2014; 62
Matoliukstyte, A (WOS:000258011100005) 2008; 158
Sumalekshmy, S (WOS:000220323500006) 2004; 108
He, LW (WOS:000347139400068) 2014; 6
Hong, YN (WOS:000280758400039) 2010; 82
Zhang, X (WOS:000345234200086) 2015; 206
Shimizu, M (WOS:000266174200019) 2009; 48
Zhu, ZF (WOS:000362819100001) 2015; 5
Zhang, X (WOS:000413892500011) 2017; 1
Badugu, R (WOS:000227627800072) 2005; 127
Wang, DW (WOS:000580512000026) 2020; 68
Sasaki, S (WOS:000373611700008) 2016; 4
Wu, YC (WOS:000423246900001) 2018; 149
Li, YY (WOS:000537579200001) 2020; 59
Tong, H (WOS:000240109400012) 2006
Hong, YN (WOS:000295921500012) 2011; 40
Zhang, MX (WOS:000528740900007) 2020; 10
Yin, ZY (WOS:000532679200018) 2020; 396
Kim, HJ (WOS:000328099400049) 2013; 135
Alam, P (WOS:000606806800031) 2021; 429
JAMES, TD (WOS:A1994PT87700019) 1994; 33
Chen, HY (WOS:000434893200098) 2018; 90
Lu, P (WOS:000278436300007) 2010; 31
Das, P (WOS:000449026500155) 2018; 3
Liu, Y (WOS:000280819100027) 2010; 16
Long, LL (WOS:000321623200037) 2013; 3
Xue, ZW (WOS:000327547000050) 2014; 4
Luo, JD (WOS:000171287300017) 2001
Goss, KU (WOS:000252317700025) 2008; 42
Lv, X (WOS:000295500200059) 2011; 158
Chang, SY (WOS:000453488900096) 2018; 10
Wang, XD (WOS:000582413100025) 2020; 145
Yuan, YL (WOS:000518175200006) 2019; 585
Aich, K (WOS:000381717500052) 2016; 40
Maus, M (WOS:000080304200008) 1999; 103
Liu, AK (WOS:000411767400059) 2017; 41
Jung (D2NJ01226J/cit8/1) 2009; 131
Lu (D2NJ01226J/cit11/1) 2022; 239
Cao (D2NJ01226J/cit54/1) 2014; 2
An (D2NJ01226J/cit4/1) 2002; 124
Li (D2NJ01226J/cit45/1) 2020; 49
Chen (D2NJ01226J/cit16/1) 2013; 49
Zhang (D2NJ01226J/cit24/1) 2017; 1
Lv (D2NJ01226J/cit2/1) 2011; 158
Li (D2NJ01226J/cit33/1) 2016; 128
Hong (D2NJ01226J/cit38/1) 2011; 40
Hu (D2NJ01226J/cit39/1) 2012; 48
Badugu (D2NJ01226J/cit17/1) 2005; 127
Goss (D2NJ01226J/cit65/1) 2008; 42
Yamada (D2NJ01226J/cit66/1) 2014; 62
Helal (D2NJ01226J/cit20/1) 2011; 67
Dong (D2NJ01226J/cit41/1) 2007; 446
Maus (D2NJ01226J/cit50/1) 1999; 103
Wang (D2NJ01226J/cit13/1) 2020; 68
Qiao (D2NJ01226J/cit12/1) 2021; 31
Chen (D2NJ01226J/cit14/1) 2018; 10
Liu (D2NJ01226J/cit47/1) 2010; 16
Tong (D2NJ01226J/cit5/1) 2006
Chao (D2NJ01226J/cit22/1) 2017; 975
Chen (D2NJ01226J/cit25/1) 2018; 90
Luo (D2NJ01226J/cit36/1) 2001
Xue (D2NJ01226J/cit72/1) 2014; 4
Lin (D2NJ01226J/cit61/1) 2020; 11
Zhang (D2NJ01226J/cit59/1) 2019; 75
Alam (D2NJ01226J/cit10/1) 2021; 429
Zhang (D2NJ01226J/cit58/1) 2020; 10
Moreno-Yruela (D2NJ01226J/cit51/1) 2015; 80
Lu (D2NJ01226J/cit43/1) 2010; 31
Zhang (D2NJ01226J/cit21/1) 2015; 206
He (D2NJ01226J/cit35/1) 2014; 6
Shimizu (D2NJ01226J/cit6/1) 2009; 48
Wang (D2NJ01226J/cit9/1) 2012; 22
Hopper (D2NJ01226J/cit57/1) 2019; 31
D2NJ01226J/cit64/1
Long (D2NJ01226J/cit29/1) 2013; 3
Yuan (D2NJ01226J/cit34/1) 2009; 113
Hong (D2NJ01226J/cit42/1) 2010; 82
Suzuki (D2NJ01226J/cit40/1) 2020; 59
Chen (D2NJ01226J/cit55/1) 2019; 144
Jana (D2NJ01226J/cit32/1) 2019; 43
Gao (D2NJ01226J/cit62/1) 2016; 18
Wang (D2NJ01226J/cit26/1) 2020; 145
Rogers (D2NJ01226J/cit71/1) 1972; 48
Yin (D2NJ01226J/cit69/1) 2020; 396
Kim (D2NJ01226J/cit73/1) 2013; 135
Derinkuyu (D2NJ01226J/cit31/1) 2007; 588
Das (D2NJ01226J/cit56/1) 2018; 3
Gao (D2NJ01226J/cit1/1) 2018; 10
Sumalekshmy (D2NJ01226J/cit53/1) 2004; 108
Aich (D2NJ01226J/cit27/1) 2016; 40
Ma (D2NJ01226J/cit48/1) 2019; 73
James (D2NJ01226J/cit7/1) 1994; 33
Yang (D2NJ01226J/cit15/1) 2016; 4
Zhu (D2NJ01226J/cit44/1) 2015; 5
Secci (D2NJ01226J/cit67/1) 2012; 49
Matoliukstyte (D2NJ01226J/cit68/1) 2008; 158
Horak (D2NJ01226J/cit23/1) 2017; 142
Li (D2NJ01226J/cit46/1) 2020; 59
Grabowski (D2NJ01226J/cit49/1) 2003; 103
Wu (D2NJ01226J/cit30/1) 2018; 149
Liu (D2NJ01226J/cit28/1) 2017; 41
Dong (D2NJ01226J/cit37/1) 2007; 91
Liu (D2NJ01226J/cit18/1) 2010; 43
Chang (D2NJ01226J/cit60/1) 2018; 10
Sasaki (D2NJ01226J/cit52/1) 2016; 4
Xu (D2NJ01226J/cit63/1) 2021; 418
Sunahara (D2NJ01226J/cit3/1) 2007; 129
Yuan (D2NJ01226J/cit70/1) 2019; 585
Wang (D2NJ01226J/cit19/1) 2011; 21
References_xml – volume: 31
  start-page: ARTN 2105452
  year: 2021
  ident: WOS:000682483800001
  article-title: Designing Squaraine Dyes with Bright Deep-Red Aggregation-Induced Emission for Specific and Ratiometric Fluorescent Detection of Hypochlorite
  publication-title: ADVANCED FUNCTIONAL MATERIALS
  doi: 10.1002/adfm.202105452
– volume: 10
  start-page: 14520
  year: 2020
  ident: WOS:000528740900007
  article-title: Tuning the fluorescence based on the combination of TICT and AIE emission of a tetraphenylethylene with D-π-A structure
  publication-title: RSC ADVANCES
  doi: 10.1039/d0ra00107d
– volume: 1
  start-page: 2292
  year: 2017
  ident: WOS:000413892500011
  article-title: A pH-sensitive multifunctional fluorescent probe based on N-annulated perylene for the sensitive and selective detection of hypochlorous acid
  publication-title: MATERIALS CHEMISTRY FRONTIERS
  doi: 10.1039/c7qm00298j
– volume: 59
  start-page: 9856
  year: 2020
  ident: WOS:000533322900001
  article-title: Principles of Aggregation-Induced Emission: Design of Deactivation Pathways for Advanced AIEgens and Applications
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202000940
– volume: 10
  start-page: 42723
  year: 2018
  ident: WOS:000453488900096
  article-title: Construction of Highly Efficient Carbazol-9-yl-Substituted Benzimidazole Bipolar Hosts for Blue Phosphorescent Light-Emitting Diodes: Isomer and Device Performance Relationships
  publication-title: ACS APPLIED MATERIALS & INTERFACES
  doi: 10.1021/acsami.8b15084
– volume: 4
  start-page: 374
  year: 2014
  ident: WOS:000327547000050
  article-title: A rhodamine-benzimidazole based sensor for selective imaging of acidic pH
  publication-title: RSC ADVANCES
  doi: 10.1039/c3ra45329d
– volume: 75
  start-page: 1658
  year: 2019
  ident: WOS:000462418900013
  article-title: Halogenation of 1,1-diarylethylenes by N-halosuccinimides
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2018.11.018
– volume: 90
  start-page: 7056
  year: 2018
  ident: WOS:000434893200098
  article-title: Dual-Emitting Fluorescent Metal-Organic Framework Nanocomposites as a Broad-Range pH Sensor for Fluorescence Imaging
  publication-title: ANALYTICAL CHEMISTRY
  doi: 10.1021/acs.analchem.8b01455
– volume: 68
  start-page: 11301
  year: 2020
  ident: WOS:000580512000026
  article-title: Functionalized Copper Nanoclusters-Based Fluorescent Probe with Aggregation-Induced Emission Property for Selective Detection of Sulfide Ions in Food Additives
  publication-title: JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
  doi: 10.1021/acs.jafc.0c04275
– volume: 49
  start-page: 1187
  year: 2012
  ident: WOS:000310562600032
  article-title: Conventional and Microwave-Assisted Synthesis of Benzimidazole Derivatives and Their In Vitro Inhibition of Human Cyclooxygenase
  publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY
  doi: 10.1002/jhet.1058
– volume: 975
  start-page: 52
  year: 2017
  ident: WOS:000402250300006
  article-title: A single pH fluorescent probe for biosensing and imaging of extreme acidity and extreme alkalinity
  publication-title: ANALYTICA CHIMICA ACTA
  doi: 10.1016/j.aca.2017.04.020
– volume: 3
  start-page: 12204
  year: 2013
  ident: WOS:000321623200037
  article-title: Amino-coumarin based fluorescence ratiometric sensors for acidic pH and their application for living cells imaging
  publication-title: RSC ADVANCES
  doi: 10.1039/c3ra41329b
– volume: 446
  start-page: 124
  year: 2007
  ident: WOS:000250194400023
  article-title: Endowing hexaphenylsilole with chemical sensory and biological probing properties by attaching amino pendants to the silolyl core
  publication-title: CHEMICAL PHYSICS LETTERS
  doi: 10.1016/j.cplett.2007.08.030
– volume: 128
  start-page: 165
  year: 2016
  ident: WOS:000373547300022
  article-title: Benzimidazole-BODIPY as optical and fluorometric pH sensor
  publication-title: DYES AND PIGMENTS
  doi: 10.1016/j.dyepig.2016.01.029
– volume: 158
  start-page: 462
  year: 2008
  ident: WOS:000258011100005
  article-title: Carbazole-containing enamines as charge transport materials for electrophotography
  publication-title: SYNTHETIC METALS
  doi: 10.1016/j.synthmet.2008.03.020
– volume: 4
  start-page: 2731
  year: 2016
  ident: WOS:000373611700008
  article-title: Recent advances in twisted intramolecular charge transfer (TICT) fluorescence and related phenomena in materials chemistry
  publication-title: JOURNAL OF MATERIALS CHEMISTRY C
  doi: 10.1039/c5tc03933a
– volume: 5
  start-page: ARTN 15189
  year: 2015
  ident: WOS:000362819100001
  article-title: Using AIE Luminogen for Longterm and Low-background Three-Photon Microscopic Functional Bioimaging
  publication-title: SCIENTIFIC REPORTS
  doi: 10.1038/srep15189
– volume: 144
  start-page: 6922
  year: 2019
  ident: WOS:000498558200011
  article-title: An intramolecular charge transfer and excited state intramolecular proton transfer based fluorescent probe for highly selective detection and imaging of formaldehyde in living cells
  publication-title: ANALYST
  doi: 10.1039/c9an01778j
– volume: 129
  start-page: 5597
  year: 2007
  ident: WOS:000245946400066
  article-title: Design and synthesis of a library of BODIPY-based environmental polarity sensors utilizing photoinduced electron-transfer-controlled fluorescence ON/OFF switching
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja068551y
– volume: 11
  year: 2020
  ident: WOS:000543984200012
  article-title: A RAF-SnRK2 kinase cascade mediates early osmotic stress signaling in higher plants
  publication-title: NATURE COMMUNICATIONS
  doi: 10.1038/s41467-020-14477-9
– volume: 48
  start-page: 10099
  year: 2012
  ident: WOS:000308827600006
  article-title: Synthesis, solvatochromism, aggregation-induced emission and cell imaging of tetraphenylethene-containing BODIPY derivatives with large Stokes shifts
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c2cc35188a
– volume: 40
  start-page: 6907
  year: 2016
  ident: WOS:000381717500052
  article-title: Carbazole-benzimidazole based dyes for acid responsive ratiometric emissive switches
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c6nj00063k
– volume: 91
  start-page: ARTN 011111
  year: 2007
  ident: WOS:000247819700011
  article-title: Aggregation-induced emissions of tetraphenylethene derivatives and their utilities as chemical vapor sensors and in organic light-emitting diodes
  publication-title: APPLIED PHYSICS LETTERS
  doi: 10.1063/1.2753723
– volume: 131
  start-page: 2008
  year: 2009
  ident: WOS:000264792100069
  article-title: Coumarin-Derived Cu2+-Selective Fluorescence Sensor: Synthesis, Mechanisms, and Applications in Living Cells
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja808611d
– volume: 135
  start-page: 17969
  year: 2013
  ident: WOS:000328099400049
  article-title: Benzimidazole-Based Ratiometric Two-Photon Fluorescent Probes for Acidic pH in Live Cells and Tissues
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja409971k
– volume: 103
  start-page: 3899
  year: 2003
  ident: WOS:000185910900003
  article-title: Structural changes accompanying intramolecular electron transfer: Focus on twisted intramolecular charge-transfer states and structures
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr940745l
– volume: 418
  start-page: ARTN 126243
  year: 2021
  ident: WOS:000689358300006
  article-title: Rational design of AIE-based fluorescent probes for hypochlorite detection in real water samples and live cell imaging
  publication-title: JOURNAL OF HAZARDOUS MATERIALS
  doi: 10.1016/j.jhazmat.2021.126243
– volume: 10
  start-page: ARTN 1259
  year: 2018
  ident: WOS:000454456800081
  article-title: Novel Multifunctional Luminescent Electrospun Fluorescent Nanofiber Chemosensor-Filters and Their Versatile Sensing of pH, Temperature, and Metal Ions
  publication-title: POLYMERS
  doi: 10.3390/polym10111259
– volume: 4
  start-page: 383
  year: 2016
  ident: WOS:000367255100020
  article-title: A highly selective and sensitive fluorescent chemosensor for detection of CN-, SO32- and Fe3+ based on aggregation-induced emission
  publication-title: JOURNAL OF MATERIALS CHEMISTRY C
  doi: 10.1039/c5tc02865e
– volume: 588
  start-page: 42
  year: 2007
  ident: WOS:000245500900007
  article-title: Fiber optic pH sensing with long wavelength excitable Schiff bases in the pH range of 7.0-12.0
  publication-title: ANALYTICA CHIMICA ACTA
  doi: 10.1016/j.aca.2007.01.070
– volume: 21
  start-page: 4056
  year: 2011
  ident: WOS:000288220600006
  article-title: Hyperbranched polytriazoles with high molecular compressibility: aggregation-induced emission and superamplified explosive detection
  publication-title: JOURNAL OF MATERIALS CHEMISTRY
  doi: 10.1039/c0jm04100a
– volume: 43
  start-page: 4921
  year: 2010
  ident: WOS:000278109700013
  article-title: Hyperbranched Conjugated Polysiloles: Synthesis, Structure, Aggregation-Enhanced Emission, Multicolor Fluorescent Photopatterning, and Superamplified Detection of Explosives
  publication-title: MACROMOLECULES
  doi: 10.1021/m902432m
– volume: 49
  start-page: 10136
  year: 2013
  ident: WOS:000325642400026
  article-title: Steric hindrance-enforced distortion as a general strategy for the design of fluorescence "turn-on" cyanide probes
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c3cc46008h
– volume: 31
  start-page: 834
  year: 2010
  ident: WOS:000278436300007
  article-title: Aggregation-Induced Emission in a Hyperbranched Poly(silylenevinylene) and Superamplification in Its Emission Quenching by Explosives
  publication-title: MACROMOLECULAR RAPID COMMUNICATIONS
  doi: 10.1002/marc.200900794
– volume: 149
  start-page: 1
  year: 2018
  ident: WOS:000423246900001
  article-title: Novel benzimidazole-based ratiometric fluorescent probes for acidic pH
  publication-title: DYES AND PIGMENTS
  doi: 10.1016/j.dyepig.2017.09.043
– volume: 239
  start-page: ARTN 123111
  year: 2022
  ident: WOS:000729414400006
  article-title: An aggregation-induced emission fluorescence probe for evaluating the effect of CYP450 changes under tumor chemotherapy
  publication-title: TALANTA
  doi: 10.1016/j.talanta.2021.123111
– start-page: 1740
  year: 2001
  ident: WOS:000171287300017
  article-title: Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole
  publication-title: CHEMICAL COMMUNICATIONS
– volume: 41
  start-page: 10096
  year: 2017
  ident: WOS:000411767400059
  article-title: A ratiometric fluorescent probe for sensing sulfite based on a pyrido[1,2-a] benzimidazole fluorophore
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c7nj02086d
– volume: 206
  start-page: 663
  year: 2015
  ident: WOS:000345234200086
  article-title: New fluorescent pH probes for acid conditions
  publication-title: SENSORS AND ACTUATORS B-CHEMICAL
  doi: 10.1016/j.snb.2014.09.107
– volume: 49
  start-page: 1144
  year: 2020
  ident: WOS:000515511500002
  article-title: Supramolecular materials based on AIE luminogens (AIEgens): construction and applications
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c9cs00495e
– volume: 31
  start-page: 6860
  year: 2019
  ident: WOS:000485830300055
  article-title: Control of Donor-Acceptor Photophysics through Structural Modification of a "Twisting" Push-Pull Molecule
  publication-title: CHEMISTRY OF MATERIALS
  doi: 10.1021/acs.chemmater.9b01278
– volume: 80
  start-page: 12115
  year: 2015
  ident: WOS:000366877900022
  article-title: D-π-A Compounds with Tunable Intramolecular Charge Transfer Achieved by Incorporation of Butenolide Nitriles as Acceptor Moieties
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.5b02051
– volume: 59
  start-page: 12822
  year: 2020
  ident: WOS:000537579200001
  article-title: ACQ-to-AIE Transformation: Tuning Molecular Packing by Regioisomerization for Two-Photon NIR Bioimaging
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202005785
– volume: 48
  start-page: 199
  year: 1972
  ident: WOS:A1972M988800019
  article-title: EFFECTS OF PH ON BENZIMIDAZOLE FLUORESCENCE
  publication-title: ANALYTICAL BIOCHEMISTRY
– volume: 158
  start-page: 405
  year: 2011
  ident: WOS:000295500200059
  article-title: Rhodafluor-based chromo- and fluorogenic probe for cyanide anion
  publication-title: SENSORS AND ACTUATORS B-CHEMICAL
  doi: 10.1016/j.snb.2011.06.047
– volume: 33
  start-page: 2207
  year: 1994
  ident: WOS:A1994PT87700019
  article-title: A GLUCOSE-SELECTIVE MOLECULAR FLUORESCENCE SENSOR
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH
– volume: 3
  start-page: 13757
  year: 2018
  ident: WOS:000449026500155
  article-title: Aggregation-Induced Emission and White Luminescence from a Combination of π-Conjugated Donor-Acceptor Organic Luminogens
  publication-title: ACS OMEGA
  doi: 10.1021/acsomega.8b01706
– volume: 585
  start-page: ARTN 113403
  year: 2019
  ident: WOS:000518175200006
  article-title: New switch on fluorescent probe with AIE characteristics for selective and reversible detection of mercury ion in aqueous solution
  publication-title: ANALYTICAL BIOCHEMISTRY
  doi: 10.1016/j.ab.2019.113403
– volume: 396
  start-page: ARTN 112542
  year: 2020
  ident: WOS:000532679200018
  article-title: AIE based colorimetric and "turn-on" fluorescence Schiff base sensor for detecting Fe3+in an aqueous media and its application
  publication-title: JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
  doi: 10.1016/j.jphotochem.2020.112542
– volume: 108
  start-page: 3705
  year: 2004
  ident: WOS:000220323500006
  article-title: Photoinduced intramolecular charge transfer in donor-acceptor substituted tetrahydropyrenes
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY B
  doi: 10.1021/jp022549l
– volume: 124
  start-page: 14410
  year: 2002
  ident: WOS:000179510800034
  article-title: Enhanced emission and its switching in fluorescent organic nanoparticles
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0269082
– volume: 103
  start-page: 3388
  year: 1999
  ident: WOS:000080304200008
  article-title: Photoinduced intramolecular charge transfer in a series of differently twisted donor - Acceptor biphenyls as revealed by fluorescence
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY A
– volume: 62
  start-page: 7593
  year: 2014
  ident: WOS:000339694300036
  article-title: Perfluoroalkyl Acid Contamination and Polyunsaturated Fatty Acid Composition of French Freshwater and Marine Fishes
  publication-title: JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
  doi: 10.1021/jf501113j
– volume: 18
  start-page: 24176
  year: 2016
  ident: WOS:000382766300004
  article-title: Hybridization and de-hybridization between the locally-excited (LE) state and the charge-transfer (CT) state: a combined experimental and theoretical study
  publication-title: PHYSICAL CHEMISTRY CHEMICAL PHYSICS
  doi: 10.1039/c6cp02778d
– volume: 67
  start-page: 2794
  year: 2011
  ident: WOS:000289330000008
  article-title: Chromogenic and fluorogenic sensing of Cu2+ based on coumarin
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2011.01.093
– volume: 42
  start-page: 456
  year: 2008
  ident: WOS:000252317700025
  article-title: The pKa values of PFOA and other highly fluorinated carboxylic acids
  publication-title: ENVIRONMENTAL SCIENCE & TECHNOLOGY
  doi: 10.1021/es702192c
– volume: 113
  start-page: 6809
  year: 2009
  ident: WOS:000265383300065
  article-title: Fluorescent Turn-On Detection and Assay of Protein Based on Lambda (Λ)-Shaped Pyridinium Salts with Aggregation-Induced Emission Characteristics
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY C
  doi: 10.1021/jp8111167
– volume: 43
  start-page: 10859
  year: 2019
  ident: WOS:000474646200022
  article-title: A "turn-on" Michler's ketone-benzimidazole fluorescent probe for selective detection of serum albumins
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c9nj01972c
– start-page: 3705
  year: 2006
  ident: WOS:000240109400012
  article-title: Fluorescent "light-up" bioprobes based on tetraphenylethylene derivatives with aggregation-induced emission characteristics
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b608425g
– year: 1000
  ident: 000796609300001.64
  publication-title: What is Acid Rain?
– volume: 429
  start-page: ARTN 213693
  year: 2021
  ident: WOS:000606806800031
  article-title: AIE-based luminescence probes for metal ion detection
  publication-title: COORDINATION CHEMISTRY REVIEWS
  doi: 10.1016/j.ccr.2020.213693
– volume: 16
  start-page: 8433
  year: 2010
  ident: WOS:000280819100027
  article-title: Simple Biosensor with High Selectivity and Sensitivity: Thiol-Specific Biomolecular Probing and Intracellular Imaging by AIE Fluorogen on a TLC Plate through a Thiol-Ene Click Mechanism
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200902505
– volume: 73
  start-page: 226
  year: 2019
  ident: WOS:000474343300029
  article-title: Large Stokes-shift AIE fluorescent materials for high-performance luminescent solar concentrators
  publication-title: ORGANIC ELECTRONICS
  doi: 10.1016/j.orgel.2019.06.017
– volume: 82
  start-page: 7035
  year: 2010
  ident: WOS:000280758400039
  article-title: Quantitation, Visualization, and Monitoring of Conformational Transitions of Human Serum Albumin by a Tetraphenylethene Derivative with Aggregation-Induced Emission Characteristics
  publication-title: ANALYTICAL CHEMISTRY
  doi: 10.1021/ac1018028
– volume: 2
  start-page: 3686
  year: 2014
  ident: WOS:000335000300003
  article-title: Aggregation-induced and crystallization-enhanced emissions with time-dependence of a new Schiff-base family based on benzimidazole
  publication-title: JOURNAL OF MATERIALS CHEMISTRY C
  doi: 10.1039/c3tc32551b
– volume: 142
  start-page: 108
  year: 2017
  ident: WOS:000401393100014
  article-title: Reversible pH switchable aggregation-induced emission of self assembled benzimidazole-based acrylonitrile dye in aqueous solution
  publication-title: DYES AND PIGMENTS
  doi: 10.1016/j.dyepig.2017.03.021
– volume: 10
  start-page: 14956
  year: 2018
  ident: WOS:000431723400079
  article-title: Anomalous Effect of Intramolecular Charge Transfer on the Light Emitting Properties of BODIPY
  publication-title: ACS APPLIED MATERIALS & INTERFACES
  doi: 10.1021/acsami.7b13444
– volume: 40
  start-page: 5361
  year: 2011
  ident: WOS:000295921500012
  article-title: Aggregation-induced emission
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c1cs15113d
– volume: 22
  start-page: 8622
  year: 2012
  ident: WOS:000302367500062
  article-title: Highly sensitive and selective fluorometric off-on K+ probe constructed via host-guest molecular recognition and aggregation-induced emission
  publication-title: JOURNAL OF MATERIALS CHEMISTRY
  doi: 10.1039/c2jm16510d
– volume: 145
  start-page: 7018
  year: 2020
  ident: WOS:000582413100025
  article-title: A red-emission fluorescent probe for visual monitoring of lysosomal pH changes during mitophagy and cell apoptosis
  publication-title: ANALYST
  doi: 10.1039/d0an01141j
– volume: 127
  start-page: 3635
  year: 2005
  ident: WOS:000227627800072
  article-title: Enhanced fluorescence cyanide detection at physiologically lethal levels: Reduced ICT-based signal transduction
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja044421i
– volume: 6
  start-page: 22326
  year: 2014
  ident: WOS:000347139400068
  article-title: A Unique Type of Pyrrole-Based Cyanine Fluorophores with Turn-on and Ratiometric Fluorescence Signals at Different pH Regions for Sensing pH in Enzymes and Living Cells
  publication-title: ACS APPLIED MATERIALS & INTERFACES
  doi: 10.1021/am506322h
– volume: 48
  start-page: 3653
  year: 2009
  ident: WOS:000266174200019
  article-title: 1,4-Bis(alkenyl)-2,5-dipiperidinobenzenes: Minimal Fluorophores Exhibiting Highly Efficient Emission in the Solid State
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200900963
– volume: 11
  start-page: 1
  year: 2020
  ident: D2NJ01226J/cit61/1
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-019-13993-7
– volume: 10
  start-page: 1259
  year: 2018
  ident: D2NJ01226J/cit14/1
  publication-title: Polymers
  doi: 10.3390/polym10111259
– volume: 91
  start-page: 011111
  year: 2007
  ident: D2NJ01226J/cit37/1
  publication-title: Appl. Phys. Lett.
  doi: 10.1063/1.2753723
– volume: 3
  start-page: 13757
  year: 2018
  ident: D2NJ01226J/cit56/1
  publication-title: ACS Omega
  doi: 10.1021/acsomega.8b01706
– volume: 48
  start-page: 3653
  year: 2009
  ident: D2NJ01226J/cit6/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200900963
– volume: 103
  start-page: 3899
  year: 2003
  ident: D2NJ01226J/cit49/1
  publication-title: Chem. Rev.
  doi: 10.1021/cr940745l
– volume: 108
  start-page: 3705
  year: 2004
  ident: D2NJ01226J/cit53/1
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp022549l
– volume: 418
  start-page: 126243
  year: 2021
  ident: D2NJ01226J/cit63/1
  publication-title: J. Hazard. Mater.
  doi: 10.1016/j.jhazmat.2021.126243
– volume: 40
  start-page: 6907
  year: 2016
  ident: D2NJ01226J/cit27/1
  publication-title: New J. Chem.
  doi: 10.1039/C6NJ00063K
– volume: 40
  start-page: 5361
  year: 2011
  ident: D2NJ01226J/cit38/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c1cs15113d
– volume: 6
  start-page: 22326
  year: 2014
  ident: D2NJ01226J/cit35/1
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/am506322h
– volume: 18
  start-page: 24176
  year: 2016
  ident: D2NJ01226J/cit62/1
  publication-title: Phys. Chem. Chem. Phys.
  doi: 10.1039/C6CP02778D
– volume: 67
  start-page: 2794
  year: 2011
  ident: D2NJ01226J/cit20/1
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2011.01.093
– volume: 2
  start-page: 3686
  year: 2014
  ident: D2NJ01226J/cit54/1
  publication-title: J. Mater. Chem. C
  doi: 10.1039/C3TC32551B
– volume: 21
  start-page: 4056
  year: 2011
  ident: D2NJ01226J/cit19/1
  publication-title: J. Mater. Chem.
  doi: 10.1039/c0jm04100a
– volume: 124
  start-page: 14410
  year: 2002
  ident: D2NJ01226J/cit4/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja0269082
– volume: 158
  start-page: 405
  year: 2011
  ident: D2NJ01226J/cit2/1
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2011.06.047
– volume: 22
  start-page: 8622
  year: 2012
  ident: D2NJ01226J/cit9/1
  publication-title: J. Mater. Chem.
  doi: 10.1039/c2jm16510d
– volume: 975
  start-page: 52
  year: 2017
  ident: D2NJ01226J/cit22/1
  publication-title: Anal. Chim. Acta
  doi: 10.1016/j.aca.2017.04.020
– volume: 113
  start-page: 6809
  year: 2009
  ident: D2NJ01226J/cit34/1
  publication-title: J. Phys. Chem. C
  doi: 10.1021/jp8111167
– volume: 129
  start-page: 5597
  year: 2007
  ident: D2NJ01226J/cit3/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja068551y
– volume: 4
  start-page: 2731
  year: 2016
  ident: D2NJ01226J/cit52/1
  publication-title: J. Mater. Chem. C
  doi: 10.1039/C5TC03933A
– volume: 90
  start-page: 7056
  year: 2018
  ident: D2NJ01226J/cit25/1
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.8b01455
– volume: 3
  start-page: 12204
  year: 2013
  ident: D2NJ01226J/cit29/1
  publication-title: RSC Adv.
  doi: 10.1039/c3ra41329b
– volume: 43
  start-page: 10859
  year: 2019
  ident: D2NJ01226J/cit32/1
  publication-title: New J. Chem.
  doi: 10.1039/C9NJ01972C
– volume: 59
  start-page: 9856
  year: 2020
  ident: D2NJ01226J/cit40/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.202000940
– volume: 1
  start-page: 2292
  year: 2017
  ident: D2NJ01226J/cit24/1
  publication-title: Mater. Chem. Front.
  doi: 10.1039/C7QM00298J
– volume: 75
  start-page: 1658
  year: 2019
  ident: D2NJ01226J/cit59/1
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2018.11.018
– volume: 4
  start-page: 374
  year: 2014
  ident: D2NJ01226J/cit72/1
  publication-title: RSC Adv.
  doi: 10.1039/C3RA45329D
– volume: 42
  start-page: 456
  year: 2008
  ident: D2NJ01226J/cit65/1
  publication-title: Environ. Sci. Technol.
  doi: 10.1021/es702192c
– volume: 62
  start-page: 7593
  year: 2014
  ident: D2NJ01226J/cit66/1
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/jf501113j
– volume: 82
  start-page: 7035
  year: 2010
  ident: D2NJ01226J/cit42/1
  publication-title: Anal. Chem.
  doi: 10.1021/ac1018028
– volume: 49
  start-page: 1144
  year: 2020
  ident: D2NJ01226J/cit45/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00495E
– volume: 127
  start-page: 3635
  year: 2005
  ident: D2NJ01226J/cit17/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja044421i
– ident: D2NJ01226J/cit64/1
– volume: 80
  start-page: 12115
  year: 2015
  ident: D2NJ01226J/cit51/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.5b02051
– volume: 10
  start-page: 14520
  year: 2020
  ident: D2NJ01226J/cit58/1
  publication-title: RSC Adv.
  doi: 10.1039/D0RA00107D
– volume: 49
  start-page: 1187
  year: 2012
  ident: D2NJ01226J/cit67/1
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.1058
– volume: 48
  start-page: 199
  year: 1972
  ident: D2NJ01226J/cit71/1
  publication-title: Anal. Biochem.
  doi: 10.1016/0003-2697(72)90182-0
– volume: 239
  start-page: 123111
  year: 2022
  ident: D2NJ01226J/cit11/1
  publication-title: Talanta
  doi: 10.1016/j.talanta.2021.123111
– volume: 16
  start-page: 8433
  year: 2010
  ident: D2NJ01226J/cit47/1
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.200902505
– volume: 446
  start-page: 124
  year: 2007
  ident: D2NJ01226J/cit41/1
  publication-title: Chem. Phys. Lett.
  doi: 10.1016/j.cplett.2007.08.030
– volume: 73
  start-page: 226
  year: 2019
  ident: D2NJ01226J/cit48/1
  publication-title: Org. Electron.
  doi: 10.1016/j.orgel.2019.06.017
– volume: 585
  start-page: 113403
  year: 2019
  ident: D2NJ01226J/cit70/1
  publication-title: Anal. Biochem.
  doi: 10.1016/j.ab.2019.113403
– volume: 68
  start-page: 11301
  year: 2020
  ident: D2NJ01226J/cit13/1
  publication-title: J. Agric. Food Chem.
  doi: 10.1021/acs.jafc.0c04275
– volume: 31
  start-page: 2105452
  year: 2021
  ident: D2NJ01226J/cit12/1
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.202105452
– start-page: 1740
  year: 2001
  ident: D2NJ01226J/cit36/1
  publication-title: Chem. Commun.
  doi: 10.1039/b105159h
– volume: 5
  start-page: 15189
  year: 2015
  ident: D2NJ01226J/cit44/1
  publication-title: Sci. Rep.
  doi: 10.1038/srep15189
– volume: 31
  start-page: 6860
  year: 2019
  ident: D2NJ01226J/cit57/1
  publication-title: Chem. Mater.
  doi: 10.1021/acs.chemmater.9b01278
– volume: 128
  start-page: 165
  year: 2016
  ident: D2NJ01226J/cit33/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2016.01.029
– volume: 10
  start-page: 14956
  year: 2018
  ident: D2NJ01226J/cit1/1
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.7b13444
– start-page: 3705
  year: 2006
  ident: D2NJ01226J/cit5/1
  publication-title: Chem. Commun.
  doi: 10.1039/b608425g
– volume: 429
  start-page: 213693
  year: 2021
  ident: D2NJ01226J/cit10/1
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2020.213693
– volume: 103
  start-page: 3388
  year: 1999
  ident: D2NJ01226J/cit50/1
  publication-title: J. Phys. Chem. A
  doi: 10.1021/jp9905023
– volume: 149
  start-page: 1
  year: 2018
  ident: D2NJ01226J/cit30/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2017.09.043
– volume: 41
  start-page: 10096
  year: 2017
  ident: D2NJ01226J/cit28/1
  publication-title: New J. Chem.
  doi: 10.1039/C7NJ02086D
– volume: 49
  start-page: 10136
  year: 2013
  ident: D2NJ01226J/cit16/1
  publication-title: Chem. Commun.
  doi: 10.1039/c3cc46008h
– volume: 396
  start-page: 112542
  year: 2020
  ident: D2NJ01226J/cit69/1
  publication-title: J. Photochem. Photobiol., A
  doi: 10.1016/j.jphotochem.2020.112542
– volume: 144
  start-page: 6922
  year: 2019
  ident: D2NJ01226J/cit55/1
  publication-title: Analyst
  doi: 10.1039/C9AN01778J
– volume: 10
  start-page: 42723
  year: 2018
  ident: D2NJ01226J/cit60/1
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.8b15084
– volume: 43
  start-page: 4921
  year: 2010
  ident: D2NJ01226J/cit18/1
  publication-title: Macromolecules
  doi: 10.1021/ma902432m
– volume: 158
  start-page: 462
  year: 2008
  ident: D2NJ01226J/cit68/1
  publication-title: Synth. Met.
  doi: 10.1016/j.synthmet.2008.03.020
– volume: 4
  start-page: 383
  year: 2016
  ident: D2NJ01226J/cit15/1
  publication-title: J. Mater. Chem. C
  doi: 10.1039/C5TC02865E
– volume: 135
  start-page: 17969
  year: 2013
  ident: D2NJ01226J/cit73/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja409971k
– volume: 588
  start-page: 42
  year: 2007
  ident: D2NJ01226J/cit31/1
  publication-title: Anal. Chim. Acta
  doi: 10.1016/j.aca.2007.01.070
– volume: 142
  start-page: 108
  year: 2017
  ident: D2NJ01226J/cit23/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2017.03.021
– volume: 145
  start-page: 7018
  year: 2020
  ident: D2NJ01226J/cit26/1
  publication-title: Analyst
  doi: 10.1039/D0AN01141J
– volume: 33
  start-page: 2207
  year: 1994
  ident: D2NJ01226J/cit7/1
  publication-title: Angew. Chem., Int. Ed. Engl.
  doi: 10.1002/anie.199422071
– volume: 59
  start-page: 12822
  year: 2020
  ident: D2NJ01226J/cit46/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.202005785
– volume: 131
  start-page: 2008
  year: 2009
  ident: D2NJ01226J/cit8/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja808611d
– volume: 206
  start-page: 663
  year: 2015
  ident: D2NJ01226J/cit21/1
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2014.09.107
– volume: 48
  start-page: 10099
  year: 2012
  ident: D2NJ01226J/cit39/1
  publication-title: Chem. Commun.
  doi: 10.1039/c2cc35188a
– volume: 31
  start-page: 834
  year: 2010
  ident: D2NJ01226J/cit43/1
  publication-title: Macromol. Rapid Commun.
  doi: 10.1002/marc.200900794
SSID ssj0011761
Score 2.3552158
Snippet o -BzcDPE and p -BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens...
o-BzcDPE and p-BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AlEgens)...
o-BzcDPE and p-BzcDPE have been synthesized and used as probes for strong acid detection. The probes contain aggregation-induced emission luminogens (AIEgens)...
Source Web of Science
SourceID proquest
crossref
webofscience
rsc
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1317
SubjectTerms Acetic acid
Acids
Backbone
Carbazoles
Chemistry
Chemistry, Multidisciplinary
Crystallography
Fluorescent indicators
NMR spectroscopy
Physical Sciences
Protonation
Response time
Science & Technology
Selectivity
Sulfuric acid
Title Differential detection of strong acids in weak acids: a combination of a benzimidazole-carbazole backbone with AIE luminophores as highly sensitive and selective turn-on fluorescent probes
URI http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000796609300001
https://www.proquest.com/docview/2671954211
Volume 46
WOS 000796609300001
WOSCitedRecordID wos000796609300001
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLa67QFeELeJwkCW2FtlaOJceau6oq2CCYlOGk-V7ThbupJOayJEfxtv_DHOiZ3LUCcNXqLk1EkjfV-Oz7GPPxNyyFUq0ijhbKggRfGUHzLo9HwWpF4kOUTkUSWl9Pk0OD7zpuf-ea_3u1O1VBbyndpsXVfyP6iCDXDFVbL_gGzzUDDAOeALR0AYjvfC-MjublLgsHeiC63q-G-NI9wXA6EyU_D6Q4src2VWN8PbQErchItiIHW-yb5nidislpopnIXAs4EU6kquIBKtBmxHJ5MBeLMsX11friBRx11qUPB4-XOwxkr4qg6pGoqvttfBK-jScobljMsS78BiUCwKk7Z2cdGqR3VELFS9DV1TL2SkDr7ojI0vs7-s30o2q3vgylpW7qsU-S372C5EwUJe9tUqjtsBD8iVca5-2PHRkAOCzY5camPjQcxi1-i6147dtjAENuuwrZt2uFkwart8yMjDrd3JkKMaa-LmC5yBDBZtp9mUMrY_7pA9F3IVcLZ7o8ns5FMzmeWERra3fu9aJZfH79u7b8dFbbKzc7NWW4OiKgCaPSaPbOZCR4aGT0hP50_Jg3GN1DPyq0tH2tCRrlJq6EgrAtIsp0hHc_WBCtohIzYW9A4y0pqMFMlIgYy0S0Yq1tSQkTZkpEBG2pCRWjLSDhmpIeNzcvZxMhsfM7s5CFMQhBYsUNrx0ziFgF1oN0iECMM0kMPU0a7ALMX1PSeOpRMoiGmDCBxSCOFvCCj4QeRJvk92c3jjF4RKTwuuh1HqptLjSSq09mOJNQMiTGPX7ZO3NTTza6MBM69qN3g8P3JPpxWA0z45qFGb2w9mPXeDECUVXcfpk31Asrm_Bb5PDrvgNi0wekfp3JhXM3B94tyn2dgq-6OiRfHyrv98RR62X9YB2S1uSv0agutCvrHk_QNtG9e9
linkProvider Royal Society of Chemistry
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=Differential+detection+of+strong+acids+in+weak+acids%3A+a+combination+of+a+benzimidazole-carbazole+backbone+with+AIE+luminophores+as+highly+sensitive+and+selective+turn-on+fluorescent+probes&rft.jtitle=New+journal+of+chemistry&rft.au=Lin%2C+Pei-Chi&rft.au=Lin%2C+Yu-Ting&rft.au=Liu%2C+Kuan-Ting&rft.au=Chen%2C+Meng-Sin&rft.date=2022-05-30&rft.issn=1144-0546&rft.eissn=1369-9261&rft.volume=46&rft.issue=21&rft.spage=1317&rft.epage=1327&rft_id=info:doi/10.1039%2Fd2nj01226j&rft.externalDocID=d2nj01226j
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1144-0546&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1144-0546&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1144-0546&client=summon