Thiophenol detection using an AIE fluorescent probe through self-assembly with TPE-based glycoclusters
We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4 H -pyran (TPE-DCM) based fluorescent probe ( TD-1 ). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solu...
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| Published in | Organic & biomolecular chemistry Vol. 17; no. 41; pp. 9251 - 9256 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
CAMBRIDGE
Royal Soc Chemistry
23.10.2019
Royal Society of Chemistry |
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| Abstract | We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4
H
-pyran (TPE-DCM) based fluorescent probe (
TD-1
). Conjugating TPE and DCM moieties allowed
TD-1
to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solubility of the hydrophobic structure resulted in a weak and unstable emission intensity. The non-covalent self-assembly of
TD-1
with a TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could sensitively detect exogenous thiophenol concentrations in PBS buffer or environmental water samples.
While the original probe (
TD-1
) was not efficient enough, supramolecular self-assembly with a glycocluster (
TPE2S
or
TPE4S
) could restore and enhance its fluorescence detection properties. |
|---|---|
| AbstractList | We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4H-pyran (TPE-DCM) based fluorescent probe (TD-1). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solubility of the hydrophobic structure resulted in a weak and unstable emission intensity. The non-covalent self-assembly of TD-1 with a TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could sensitively detect exogenous thiophenol concentrations in PBS buffer or environmental water samples.We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4H-pyran (TPE-DCM) based fluorescent probe (TD-1). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solubility of the hydrophobic structure resulted in a weak and unstable emission intensity. The non-covalent self-assembly of TD-1 with a TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could sensitively detect exogenous thiophenol concentrations in PBS buffer or environmental water samples. We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4 H -pyran (TPE-DCM) based fluorescent probe ( TD-1 ). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solubility of the hydrophobic structure resulted in a weak and unstable emission intensity. The non-covalent self-assembly of TD-1 with a TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could sensitively detect exogenous thiophenol concentrations in PBS buffer or environmental water samples. While the original probe ( TD-1 ) was not efficient enough, supramolecular self-assembly with a glycocluster ( TPE2S or TPE4S ) could restore and enhance its fluorescence detection properties. We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4H-pyran (TPE-DCM) based fluorescent probe (TD-1). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water-solubility from the hydrophobic structure resulted in the weak and unstable emission intensity. Non-covalent self-assembly of TD-1 with TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could detect sensitively exogenous thiophenol concentrations in PBS buffer or environmental water samples. We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4H-pyran (TPE-DCM) based fluorescent probe (TD-1). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solubility of the hydrophobic structure resulted in a weak and unstable emission intensity. The non-covalent self-assembly of TD-1 with a TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could sensitively detect exogenous thiophenol concentrations in PBS buffer or environmental water samples. We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4 H -pyran (TPE-DCM) based fluorescent probe ( TD-1 ). Conjugating TPE and DCM moieties allowed TD-1 to display high selectivity for thiophenol with excellent AIE properties in aqueous solution. Nevertheless, the poor water solubility of the hydrophobic structure resulted in a weak and unstable emission intensity. The non-covalent self-assembly of TD-1 with a TPE glycocluster (TPE2S) led to a largely improved water solubility producing a reliable and stable sensing system. The corresponding glyco-probe could sensitively detect exogenous thiophenol concentrations in PBS buffer or environmental water samples. |
| Author | Chen, Guo-Rong Dong, Lei Vidal, Sébastien He, Xiao-Peng |
| AuthorAffiliation | Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering Feringa Nobel Prize Scientist Joint Research Center Université de Lyon School of Chemistry and Molecular Engineering East China University of Science and Technology Institut de Chimie et Biochimie Moléculaires et Supramoléculaires UMR 5246 Laboratoire de Chimie Organique 2-Glycochimie CNRS and Université Claude Bernard Lyon 1 |
| AuthorAffiliation_xml | – name: Université de Lyon – name: UMR 5246 – name: Institut de Chimie et Biochimie Moléculaires et Supramoléculaires – name: CNRS and Université Claude Bernard Lyon 1 – name: Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering – name: East China University of Science and Technology – name: Laboratoire de Chimie Organique 2-Glycochimie – name: School of Chemistry and Molecular Engineering – name: Feringa Nobel Prize Scientist Joint Research Center |
| Author_xml | – sequence: 1 givenname: Lei surname: Dong fullname: Dong, Lei – sequence: 2 givenname: Guo-Rong surname: Chen fullname: Chen, Guo-Rong – sequence: 3 givenname: Xiao-Peng surname: He fullname: He, Xiao-Peng – sequence: 4 givenname: Sébastien surname: Vidal fullname: Vidal, Sébastien |
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| Cites_doi | 10.1021/acssensors.7b00151 10.1002/jat.2550090208 10.1039/C7RA08707A 10.1016/0891-5849(89)90147-0 10.1039/b105159h 10.1039/C7AN01994G 10.1080/03067310902874889 10.1039/c2cc33749e 10.1039/C6RA07046A 10.1039/C6PY01109H 10.1021/acssensors.8b00685 10.1248/cpb.50.1233 10.1002/anie.200702271 10.1039/C7NJ03692B 10.1021/acs.analchem.6b04608 10.1039/C4RA09042J 10.1039/C6CC00100A 10.1021/acsami.7b14548 10.1039/C5TC03977K 10.1039/b926070f 10.1039/C5TC03369A 10.1021/cr0300789 10.1039/c2an35524h 10.1039/C7CC07666E 10.1039/C5OB01564B 10.1021/acs.langmuir.8b01036 10.1039/C4CS00044G 10.1351/pac200072010179 10.1021/ac403885n 10.1021/acs.analchem.5b02021 10.1002/adma.201602748 10.1039/c0ob00910e 10.1039/C8OB02035C 10.1039/C5AY01672J 10.1021/acs.analchem.6b02520 10.1080/03601238909372654 10.1021/acs.chemrev.5b00263 10.1021/acsami.7b14845 10.1039/c7ra08707a 10.1039/c6ra07046a 10.1039/c8ob02035c 10.1039/c5tc03977k 10.1039/c7an01994g 10.1039/c7nj03692b 10.1039/c6py01109h 10.1039/c5ob01564b 10.1039/c5ay01672j 10.1039/c4ra09042j 10.1039/c5tc03369a 10.1039/c4cs00044g 10.1039/c6cc00100a 10.1039/c7cc07666e |
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| Keywords | TURN-ON PROBE THIOLS TOXICITY SENSITIVE DETECTION SELECTIVE DETECTION AGGREGATION-INDUCED EMISSION |
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| References | Yu (C9OB01937E-(cit22)/*[position()=1]) 2015; 7 Hu (C9OB01937E-(cit29)/*[position()=1]) 2014; 43 Rahman (C9OB01937E-(cit3)/*[position()=1]) 1999; 277 He (C9OB01937E-(cit8)/*[position()=1]) 2002; 50 Kand (C9OB01937E-(cit13)/*[position()=1]) 2012; 137 Liu (C9OB01937E-(cit18)/*[position()=1]) 2015; 87 Amrolia (C9OB01937E-(cit7)/*[position()=1]) 1989; 9 Khandare (C9OB01937E-(cit21)/*[position()=1]) 2016; 6 Jiang (C9OB01937E-(cit23)/*[position()=1]) 2010; 46 Zhang (C9OB01937E-(cit4a)/*[position()=1]) 2012; 48 Xie (C9OB01937E-(cit11)/*[position()=1]) 2017; 89 Liu (C9OB01937E-(cit34)/*[position()=1]) 2017; 53 Kand (C9OB01937E-(cit17)/*[position()=1]) 2014; 4 Luo (C9OB01937E-(cit28)/*[position()=1]) 2001 Zhang (C9OB01937E-(cit24)/*[position()=1]) 2018; 143 Donnier-Marechal (C9OB01937E-(cit37)/*[position()=1]) 2018; 16 Xiong (C9OB01937E-(cit19)/*[position()=1]) 2017; 2 Yin (C9OB01937E-(cit12)/*[position()=1]) 2017; 7 Dou (C9OB01937E-(cit32)/*[position()=1]) 2016; 52 Ji (C9OB01937E-(cit33)/*[position()=1]) 2016; 28 Zhao (C9OB01937E-(cit36)/*[position()=1]) 2018; 42 Guo (C9OB01937E-(cit25)/*[position()=1]) 2016; 4 Munday (C9OB01937E-(cit5)/*[position()=1]) 1989; 7 Yue (C9OB01937E-(cit14)/*[position()=1]) 2016; 88 Yang (C9OB01937E-(cit4b)/*[position()=1]) 2018; 3 Hell (C9OB01937E-(cit6)/*[position()=1]) 1989; 24 Liu (C9OB01937E-(cit10)/*[position()=1]) 2016; 4 Mei (C9OB01937E-(cit27)/*[position()=1]) 2015; 115 Li (C9OB01937E-(cit15)/*[position()=1]) 2014; 86 Jana (C9OB01937E-(cit35)/*[position()=1]) 2015; 13 Lin (C9OB01937E-(cit31)/*[position()=1]) 2018; 10 Pagidi (C9OB01937E-(cit16)/*[position()=1]) 2018; 34 Jiang (C9OB01937E-(cit20a)/*[position()=1]) 2007; 46 Eychmüller (C9OB01937E-(cit1)/*[position()=1]) 2000; 72 Li (C9OB01937E-(cit30)/*[position()=1]) 2018; 10 Love (C9OB01937E-(cit2)/*[position()=1]) 2005; 105 Wang (C9OB01937E-(cit26)/*[position()=1]) 2016; 7 Wang (C9OB01937E-(cit9)/*[position()=1]) 2010; 90 Guo (C9OB01937E-(cit20b)/*[position()=1]) 2011; 9 Xie, XL (WOS:000395964400049) 2017; 89 Li, J (WOS:000333235700030) 2014; 86 Dou, WT (WOS:000371477100019) 2016; 52 Eychmuller, A (WOS:000087833100020) 2000; 72 Li, J (WOS:000430642100008) 2018; 10 HEIL, TP (WOS:A1989AQ28600005) 1989; 24 MUNDAY, R (WOS:A1989CF76400009) 1989; 7 Mei, J (WOS:000364727100004) 2015; 115 AMROLIA, P (WOS:A1989U246400007) 1989; 9 Wang, X (WOS:000382143400002) 2016; 7 Wang, TW (WOS:000281321800004) 2010; 90 Donnier-Marechal, M (WOS:000451074500019) 2018; 16 Kand, D (WOS:000345652300087) 2014; 4 Yue, YK (WOS:000386991200025) 2016; 88 Rahman, I (WOS:000084234800001) 1999; 277 Khandare, DG (WOS:000378563200035) 2016; 6 Ji, DK (WOS:000391174600012) 2016; 28 Yu, DH (WOS:000360929200018) 2015; 7 He, JX (WOS:000177740100016) 2002; 50 Liu, HW (WOS:000360773100042) 2015; 87 Pagidi, S (WOS:000439398100005) 2018; 34 Zhao, G (WOS:000418369000060) 2018; 42 Yin, GX (WOS:000412211300033) 2017; 7 Jiang, W (WOS:000275099600043) 2010; 46 Jana, D (WOS:000364074300010) 2015; 13 Lin, H (WOS:000430642100011) 2018; 10 Luo, JD (WOS:000171287300017) 2001 Guo, ZQ (WOS:000373611700002) 2016; 4 Liu, Y (WOS:000414146300019) 2017; 53 Zhang, M (WOS:000307300900017) 2012; 48 Jiang, W (WOS:000250990000025) 2007; 46 Love, JC (WOS:000228412800003) 2005; 105 Yang, L (WOS:000446276300035) 2018; 3 Hu, R (WOS:000337131200013) 2014; 43 Xiong, L (WOS:000400541500020) 2017; 2 Liu, XJ (WOS:000376041700026) 2016; 4 Zhang, MZ (WOS:000423680700021) 2018; 143 Guo, HM (WOS:000289897200033) 2011; 9 Kand, D (WOS:000306932400006) 2012; 137 |
| References_xml | – volume: 2 start-page: 599 year: 2017 ident: C9OB01937E-(cit19)/*[position()=1] publication-title: ACS Sens. doi: 10.1021/acssensors.7b00151 – volume: 9 start-page: 113 year: 1989 ident: C9OB01937E-(cit7)/*[position()=1] publication-title: J. Appl. Toxicol. doi: 10.1002/jat.2550090208 – volume: 7 start-page: 46148 year: 2017 ident: C9OB01937E-(cit12)/*[position()=1] publication-title: RSC Adv. doi: 10.1039/C7RA08707A – volume: 7 start-page: 659 year: 1989 ident: C9OB01937E-(cit5)/*[position()=1] publication-title: Free Radical Biol. Med. doi: 10.1016/0891-5849(89)90147-0 – start-page: 1740 year: 2001 ident: C9OB01937E-(cit28)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/b105159h – volume: 143 start-page: 756 year: 2018 ident: C9OB01937E-(cit24)/*[position()=1] publication-title: Analyst doi: 10.1039/C7AN01994G – volume: 90 start-page: 948 year: 2010 ident: C9OB01937E-(cit9)/*[position()=1] publication-title: Int. J. Environ. Anal. Chem. doi: 10.1080/03067310902874889 – volume: 48 start-page: 8925 year: 2012 ident: C9OB01937E-(cit4a)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/c2cc33749e – volume: 6 start-page: 52790 year: 2016 ident: C9OB01937E-(cit21)/*[position()=1] publication-title: RSC Adv. doi: 10.1039/C6RA07046A – volume: 7 start-page: 5217 year: 2016 ident: C9OB01937E-(cit26)/*[position()=1] publication-title: Polym. Chem. doi: 10.1039/C6PY01109H – volume: 3 start-page: 1863 year: 2018 ident: C9OB01937E-(cit4b)/*[position()=1] publication-title: ACS Sens. doi: 10.1021/acssensors.8b00685 – volume: 50 start-page: 1233 year: 2002 ident: C9OB01937E-(cit8)/*[position()=1] publication-title: Chem. Pharm. Bull. doi: 10.1248/cpb.50.1233 – volume: 277 start-page: L1067 year: 1999 ident: C9OB01937E-(cit3)/*[position()=1] publication-title: Am. J. Physiol.: Lung Cell. Mol. Physiol. – volume: 46 start-page: 8445 year: 2007 ident: C9OB01937E-(cit20a)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200702271 – volume: 42 start-page: 555 year: 2018 ident: C9OB01937E-(cit36)/*[position()=1] publication-title: New J. Chem. doi: 10.1039/C7NJ03692B – volume: 89 start-page: 3015 year: 2017 ident: C9OB01937E-(cit11)/*[position()=1] publication-title: Anal. Chem. doi: 10.1021/acs.analchem.6b04608 – volume: 4 start-page: 59579 year: 2014 ident: C9OB01937E-(cit17)/*[position()=1] publication-title: RSC Adv. doi: 10.1039/C4RA09042J – volume: 52 start-page: 3821 year: 2016 ident: C9OB01937E-(cit32)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C6CC00100A – volume: 10 start-page: 12150 year: 2018 ident: C9OB01937E-(cit30)/*[position()=1] publication-title: ACS Appl. Mater. Interfaces doi: 10.1021/acsami.7b14548 – volume: 4 start-page: 4320 year: 2016 ident: C9OB01937E-(cit10)/*[position()=1] publication-title: J. Mater. Chem. C doi: 10.1039/C5TC03977K – volume: 46 start-page: 1944 year: 2010 ident: C9OB01937E-(cit23)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/b926070f – volume: 4 start-page: 2640 year: 2016 ident: C9OB01937E-(cit25)/*[position()=1] publication-title: J. Mater. Chem. C doi: 10.1039/C5TC03369A – volume: 105 start-page: 1103 year: 2005 ident: C9OB01937E-(cit2)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr0300789 – volume: 137 start-page: 3921 year: 2012 ident: C9OB01937E-(cit13)/*[position()=1] publication-title: Analyst doi: 10.1039/c2an35524h – volume: 53 start-page: 11937 year: 2017 ident: C9OB01937E-(cit34)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C7CC07666E – volume: 13 start-page: 10663 year: 2015 ident: C9OB01937E-(cit35)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/C5OB01564B – volume: 34 start-page: 8170 year: 2018 ident: C9OB01937E-(cit16)/*[position()=1] publication-title: Langmuir doi: 10.1021/acs.langmuir.8b01036 – volume: 43 start-page: 4494 year: 2014 ident: C9OB01937E-(cit29)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/C4CS00044G – volume: 72 start-page: 179 year: 2000 ident: C9OB01937E-(cit1)/*[position()=1] publication-title: Pure Appl. Chem. doi: 10.1351/pac200072010179 – volume: 86 start-page: 3037 year: 2014 ident: C9OB01937E-(cit15)/*[position()=1] publication-title: Anal. Chem. doi: 10.1021/ac403885n – volume: 87 start-page: 8896 year: 2015 ident: C9OB01937E-(cit18)/*[position()=1] publication-title: Anal. Chem. doi: 10.1021/acs.analchem.5b02021 – volume: 28 start-page: 9356 year: 2016 ident: C9OB01937E-(cit33)/*[position()=1] publication-title: Adv. Mater. doi: 10.1002/adma.201602748 – volume: 9 start-page: 3844 year: 2011 ident: C9OB01937E-(cit20b)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/c0ob00910e – volume: 16 start-page: 8804 year: 2018 ident: C9OB01937E-(cit37)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/C8OB02035C – volume: 7 start-page: 7534 year: 2015 ident: C9OB01937E-(cit22)/*[position()=1] publication-title: Anal. Methods doi: 10.1039/C5AY01672J – volume: 88 start-page: 10499 year: 2016 ident: C9OB01937E-(cit14)/*[position()=1] publication-title: Anal. Chem. doi: 10.1021/acs.analchem.6b02520 – volume: 24 start-page: 349 year: 1989 ident: C9OB01937E-(cit6)/*[position()=1] publication-title: J. Environ. Sci. Health, Part B doi: 10.1080/03601238909372654 – volume: 115 start-page: 11718 year: 2015 ident: C9OB01937E-(cit27)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.5b00263 – volume: 10 start-page: 12173 year: 2018 ident: C9OB01937E-(cit31)/*[position()=1] publication-title: ACS Appl. Mater. Interfaces doi: 10.1021/acsami.7b14845 – volume: 7 start-page: 46148 year: 2017 ident: WOS:000412211300033 article-title: A novel fluorescence turn-on probe for the selective detection of thiophenols by caged benzooxazolidinoindocyanine publication-title: RSC ADVANCES doi: 10.1039/c7ra08707a – volume: 7 start-page: 659 year: 1989 ident: WOS:A1989CF76400009 article-title: TOXICITY OF THIOLS AND DISULFIDES - INVOLVEMENT OF FREE-RADICAL SPECIES publication-title: FREE RADICAL BIOLOGY AND MEDICINE – volume: 46 start-page: 8445 year: 2007 ident: WOS:000250990000025 article-title: A highly selective fluorescent probe for thiophenols publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200702271 – volume: 50 start-page: 1233 year: 2002 ident: WOS:000177740100016 article-title: Development of a simple HPLC method for determination of paeoniflorin-metabolizing activity of intestinal bacteria in rat feces publication-title: CHEMICAL & PHARMACEUTICAL BULLETIN – volume: 34 start-page: 8170 year: 2018 ident: WOS:000439398100005 article-title: Triarylboron Anchored Luminescent Probes: Selective Detection and Imaging of Thiophenols in the Intracellular Environment publication-title: LANGMUIR doi: 10.1021/acs.langmuir.8b01036 – 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: 89 start-page: 3015 year: 2017 ident: WOS:000395964400049 article-title: Combinatorial Strategy to Identify Fluorescent Probes for Biothiol and Thiophenol Based on Diversified Pyrimidine Moieties and Their Biological Applications publication-title: ANALYTICAL CHEMISTRY doi: 10.1021/acs.analchem.6b04608 – volume: 3 start-page: 1863 year: 2018 ident: WOS:000446276300035 article-title: A Triple-Emission Fluorescent Probe for Discriminatory Detection of Cysteine/Homocysteine, Glutathione/Hydrogen Sulfide, and Thiophenol in Living Cells publication-title: ACS SENSORS doi: 10.1021/acssensors.8b00685 – volume: 72 start-page: 179 year: 2000 ident: WOS:000087833100020 article-title: Chemistry and photophysics of thiol-stabilized II-VI semiconductor nanocrystals publication-title: PURE AND APPLIED CHEMISTRY – volume: 115 start-page: 11718 year: 2015 ident: WOS:000364727100004 article-title: Aggregation-Induced Emission: Together We Shine, United We Soar! publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.5b00263 – volume: 87 start-page: 8896 year: 2015 ident: WOS:000360773100042 article-title: Efficient Two-Photon Fluorescent Probe with Red Emission for Imaging of Thiophenols in Living Cells and Tissues publication-title: ANALYTICAL CHEMISTRY doi: 10.1021/acs.analchem.5b02021 – volume: 277 start-page: L1067 year: 1999 ident: WOS:000084234800001 article-title: Lung glutathione and oxidative stress: implications in cigarette smoke-induced airway disease publication-title: AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY – volume: 6 start-page: 52790 year: 2016 ident: WOS:000378563200035 article-title: Green synthesis of a benzothiazole based 'turn-on' type fluorimetric probe and its use for the selective detection of thiophenols in environmental samples and living cells publication-title: RSC ADVANCES doi: 10.1039/c6ra07046a – volume: 16 start-page: 8804 year: 2018 ident: WOS:000451074500019 article-title: Tetraphenylethylene- based glycoclusters with aggregation- induced emission ( AIE) properties as high- affinity ligands of bacterial lectins publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c8ob02035c – volume: 4 start-page: 4320 year: 2016 ident: WOS:000376041700026 article-title: A red emitting fluorescent probe for instantaneous sensing of thiophenol in both aqueous medium and living cells with a large Stokes shift publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c5tc03977k – volume: 24 start-page: 349 year: 1989 ident: WOS:A1989AQ28600005 article-title: TOXICOLOGICAL PROPERTIES OF THIO-PHENOLS AND ALKYLPHENOLS CAUSING FLAVOR TAINTING IN FISH FROM THE UPPER WISCONSIN RIVER publication-title: JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART B-PESTICIDES FOOD CONTAMINANTS AND AGRICULTURAL WASTES – volume: 143 start-page: 756 year: 2018 ident: WOS:000423680700021 article-title: Reaction-based fluorescent probe for the selective and sensitive detection of thiophenols with a large Stokes shift and its application in water samples publication-title: ANALYST doi: 10.1039/c7an01994g – volume: 90 start-page: 948 year: 2010 ident: WOS:000281321800004 article-title: Identification of hydrolytic metabolites of dyfonate in alkaline aqueous solutions by using high performance liquid chromatography - UV detection and gas chromatography-mass spectrometry publication-title: INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY doi: 10.1080/03067310902874889 – volume: 28 start-page: 9356 year: 2016 ident: WOS:000391174600012 article-title: Targeted Intracellular Production of Reactive Oxygen Species by a 2D Molybdenum Disulfide Glycosheet publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201602748 – volume: 42 start-page: 555 year: 2018 ident: WOS:000418369000060 article-title: Facile preparation and investigation of the properties of single molecular POSS-based white-light-emitting hybrid materials using click chemistry publication-title: NEW JOURNAL OF CHEMISTRY doi: 10.1039/c7nj03692b – volume: 137 start-page: 3921 year: 2012 ident: WOS:000306932400006 article-title: BODIPY based colorimetric fluorescent probe for selective thiophenol detection: theoretical and experimental studies publication-title: ANALYST doi: 10.1039/c2an35524h – volume: 7 start-page: 5217 year: 2016 ident: WOS:000382143400002 article-title: Aggregation induced emission of a cyanostilbene amphiphile as a novel platform for FRET-based ratiometric sensing of mercury ions in water publication-title: POLYMER CHEMISTRY doi: 10.1039/c6py01109h – volume: 13 start-page: 10663 year: 2015 ident: WOS:000364074300010 article-title: Planar-rotor architecture based pyrene-vinyl-tetraphenylethylene conjugated systems: photophysical properties and aggregation behavior publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c5ob01564b – volume: 88 start-page: 10499 year: 2016 ident: WOS:000386991200025 article-title: Curcumin-Based "Enhanced SNAr" Promoted Ultrafast Fluorescent Probe for Thiophenols Detection in Aqueous Solution and in Living Cells publication-title: ANALYTICAL CHEMISTRY doi: 10.1021/acs.analchem.6b02520 – volume: 48 start-page: 8925 year: 2012 ident: WOS:000307300900017 article-title: A nitroolefin functionalized BODIPY chemodosimeter for biothiols driven by an unexpected conjugated addition mechanism publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc33749e – volume: 7 start-page: 7534 year: 2015 ident: WOS:000360929200018 article-title: A colorimetric and near-infrared fluorescent turn-on probe for in vitro and in vivo detection of thiophenols publication-title: ANALYTICAL METHODS doi: 10.1039/c5ay01672j – volume: 105 start-page: 1103 year: 2005 ident: WOS:000228412800003 article-title: Self-assembled monolayers of thiolates on metals as a form of nanotechnology publication-title: CHEMICAL REVIEWS doi: 10.1021/cr0300789 – volume: 4 start-page: 59579 year: 2014 ident: WOS:000345652300087 article-title: Structural imposition on the off-on response of naphthalimide based probes for selective thiophenol sensing publication-title: RSC ADVANCES doi: 10.1039/c4ra09042j – volume: 9 start-page: 3844 year: 2011 ident: WOS:000289897200033 article-title: Highly selective fluorescent OFF-ON thiol probes based on dyads of BODIPY and potent intramolecular electron sink 2,4-dinitrobenzenesulfonyl subunits publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c0ob00910e – volume: 4 start-page: 2640 year: 2016 ident: WOS:000373611700002 article-title: Long wavelength AIEgen of quinoline-malononitrile publication-title: JOURNAL OF MATERIALS CHEMISTRY C doi: 10.1039/c5tc03369a – volume: 2 start-page: 599 year: 2017 ident: WOS:000400541500020 article-title: Highly Sensitive Squaraine-Based Water-Soluble Far-Red/Near-Infrared Chromofluorogenic Thiophenol Probe publication-title: ACS SENSORS doi: 10.1021/acssensors.7b00151 – volume: 86 start-page: 3037 year: 2014 ident: WOS:000333235700030 article-title: A Coumarin-Based Fluorescent Probe for Selective and Sensitive Detection of Thiophenols and Its Application publication-title: ANALYTICAL CHEMISTRY doi: 10.1021/ac403885n – volume: 46 start-page: 1944 year: 2010 ident: WOS:000275099600043 article-title: Rational design of a highly selective and sensitive fluorescent PET probe for discrimination of thiophenols and aliphatic thiols publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/b926070f – volume: 10 start-page: 12173 year: 2018 ident: WOS:000430642100011 article-title: Caspase-1 Specific Light-Up Probe with Aggregation-Induced Emission Characteristics for Inhibitor Screening of Coumarin-Originated Natural Products publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.7b14845 – volume: 43 start-page: 4494 year: 2014 ident: WOS:000337131200013 article-title: AIE macromolecules: syntheses, structures and functionalities publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c4cs00044g – volume: 10 start-page: 12150 year: 2018 ident: WOS:000430642100008 article-title: Aggregation-Induced Fluorescence Probe for Monitoring Membrane Potential Changes in Mitochondria publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.7b14548 – volume: 52 start-page: 3821 year: 2016 ident: WOS:000371477100019 article-title: Interlocked supramolecular glycoconjugated polymers for receptor-targeting theranostics publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c6cc00100a – volume: 9 start-page: 113 year: 1989 ident: WOS:A1989U246400007 article-title: TOXICITY OF AROMATIC THIOLS IN THE HUMAN RED BLOOD-CELL publication-title: JOURNAL OF APPLIED TOXICOLOGY – volume: 53 start-page: 11937 year: 2017 ident: WOS:000414146300019 article-title: Supramolecular assembly of fluorogenic glyco-dots from perylenediimide-based glycoclusters for targeted imaging of cancer cells publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c7cc07666e |
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| Snippet | We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4
H
-pyran (TPE-DCM) based fluorescent probe (
TD-1
). Conjugating TPE and DCM moieties... We describe a novel green-emitting tetraphenylethylene-dicyanomethylene-4H-pyran (TPE-DCM) based fluorescent probe (TD-1). Conjugating TPE and DCM moieties... |
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| SubjectTerms | Analytical chemistry Aqueous solutions Chemical Sciences Chemistry Chemistry, Organic Fluorescent indicators Hydrophobicity Physical Sciences Science & Technology Selectivity Self-assembly Solubility Thiophenol Water analysis Water sampling |
| Title | Thiophenol detection using an AIE fluorescent probe through self-assembly with TPE-based glycoclusters |
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