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Volumn 116, Issue , 2015, Pages 52-57

Ratiometric glyco-probe for transient determination of thiophenol in full aqueous solution and river water

Author keywords

Full aqueous; Glycodye; Naphthalimide; Ratiometric; River water; Thiophenol

Indexed keywords

FLUORESCENCE; PROBES; SOLUBILITY; SOLUTIONS; SPECTROSCOPIC ANALYSIS; SYNTHESIS (CHEMICAL);

EID: 84922391018     PISSN: 01437208     EISSN: 18733743     Source Type: Journal    
DOI: 10.1016/j.dyepig.2015.01.013     Document Type: Article
Times cited : (46)

References (40)
  • 1
    • 18044398972 scopus 로고    scopus 로고
    • Self-assembled monolayers of thiolates on metals as a form of nanotechnology
    • Love JC, Estroff LA, Kriebel JK, Nuzzo RG, Whitesides GM. Self-assembled monolayers of thiolates on metals as a form of nanotechnology. Chem Rev 2005;105:1103-70.
    • (2005) Chem Rev , vol.105 , pp. 1103-1170
    • Love, J.C.1    Estroff, L.A.2    Kriebel, J.K.3    Nuzzo, R.G.4    Whitesides, G.M.5
  • 2
    • 0034583438 scopus 로고    scopus 로고
    • Chemistry and photophysics of thiol-stabilized II-VI semiconductor nanocrystals
    • EychmKller A, Rogach AL. Chemistry and photophysics of thiol-stabilized II-VI semiconductor nanocrystals. Pure Appl Chem 2000;72:179-88.
    • (2000) Pure Appl Chem , vol.72 , pp. 179-188
    • EychmKller, A.1    Rogach, A.L.2
  • 3
    • 84906877853 scopus 로고    scopus 로고
    • Near-infrared fluorescent probe for detection of thiolphenols in water samples and living cells
    • Yu D, Huang F, Ding S, Feng G. Near-infrared fluorescent probe for detection of thiolphenols in water samples and living cells. Anal Chem 2014;86:8835-41.
    • (2014) Anal Chem , vol.86 , pp. 8835-8841
    • Yu, D.1    Huang, F.2    Ding, S.3    Feng, G.4
  • 4
    • 0024426719 scopus 로고
    • Toxicological properties of thiols and alkylphenols causing flavor tainting in fish from the upper Wisconsin river
    • Heil TP, Lindsay RC. Toxicological properties of thiols and alkylphenols causing flavor tainting in fish from the upper Wisconsin river. J Environ Sci Health B 1989;24:349-60.
    • (1989) J Environ Sci Health B , vol.24 , pp. 349-360
    • Heil, T.P.1    Lindsay, R.C.2
  • 6
    • 84880091003 scopus 로고    scopus 로고
    • Disulfide-cleavagetriggered chemosensors and their biological applications
    • Lee MH, Yang Z, Lim CW, Lee YH, Sun D, Kang C, et al. Disulfide-cleavagetriggered chemosensors and their biological applications. Chem Rev 2013;113:5071-109.
    • (2013) Chem Rev , vol.113 , pp. 5071-5109
    • Lee, M.H.1    Yang, Z.2    Lim, C.W.3    Lee, Y.H.4    Sun, D.5    Kang, C.6
  • 7
    • 84864666324 scopus 로고    scopus 로고
    • Combinatorial strategies in fluorescent probe development
    • Vendrell M, Zhai D, Er JC, Chang YT. Combinatorial strategies in fluorescent probe development. Chem Rev 2012;112:4391-420.
    • (2012) Chem Rev , vol.112 , pp. 4391-4420
    • Vendrell, M.1    Zhai, D.2    Er, J.C.3    Chang, Y.T.4
  • 8
    • 84889050211 scopus 로고    scopus 로고
    • Recent progress in the development of nearinfrared fluorescent probes for bioimaging applications
    • Guo Z, Park S, Yoon J, Shin I. Recent progress in the development of nearinfrared fluorescent probes for bioimaging applications. Chem Soc Rev 2014;3:16-29.
    • (2014) Chem Soc Rev , vol.3 , pp. 16-29
    • Guo, Z.1    Park, S.2    Yoon, J.3    Shin, I.4
  • 9
    • 84886791136 scopus 로고    scopus 로고
    • Revisit of a dipropargyl rhodamine probe reveals its alternative ion sensitivity in both a solution and live cells
    • Li KB, Wei XL, Zang Y, He XP, Chen GR, Li J, et al. Revisit of a dipropargyl rhodamine probe reveals its alternative ion sensitivity in both a solution and live cells. Analyst 2013;138:7087-9.
    • (2013) Analyst , vol.138 , pp. 7087-7089
    • Li, K.B.1    Wei, X.L.2    Zang, Y.3    He, X.P.4    Chen, G.R.5    Li, J.6
  • 10
    • 84876737783 scopus 로고    scopus 로고
    • Bis-triazolyl indoleamines as unique "off-approach-on" chemosensors for copper and fluorine
    • Shi DT, Zhang B, Yang YX, Guan CC, He XP, Li YC, et al. Bis-triazolyl indoleamines as unique "off-approach-on" chemosensors for copper and fluorine. Analyst 2013;138:2808-11.
    • (2013) Analyst , vol.138 , pp. 2808-2811
    • Shi, D.T.1    Zhang, B.2    Yang, Y.X.3    Guan, C.C.4    He, X.P.5    Li, Y.C.6
  • 11
    • 84871973480 scopus 로고    scopus 로고
    • Pyrene excimer-based bis-triazolyl pyranoglycoligands as specific mercury sensors
    • He X, Xie J, Chen G, Chen K. Pyrene excimer-based bis-triazolyl pyranoglycoligands as specific mercury sensors. Chin J Chem 2012;30:2874-8.
    • (2012) Chin J Chem , vol.30 , pp. 2874-2878
    • He, X.1    Xie, J.2    Chen, G.3    Chen, K.4
  • 12
    • 77957853197 scopus 로고    scopus 로고
    • Highly optically selective and electrochemically active chemosensor for copper (II) based on triazole-linked glucosyl anthraquinone
    • Zhang YJ, He XP, Hu M, Li Z, Shi XX, Chen GR. Highly optically selective and electrochemically active chemosensor for copper (II) based on triazole-linked glucosyl anthraquinone. Dyes Pigments 2011;88:391-5.
    • (2011) Dyes Pigments , vol.88 , pp. 391-395
    • Zhang, Y.J.1    He, X.P.2    Hu, M.3    Li, Z.4    Shi, X.X.5    Chen, G.R.6
  • 13
    • 84055181331 scopus 로고    scopus 로고
    • Discovery of a sensitive Cu(II)-cyanide "off-on " sensor based on new C-glycosyl triazolyl bis-amino acid scaffold
    • Tang YH, Qu Y, Song Z, He XP, Xie J, Hua JL, et al. Discovery of a sensitive Cu(II)-cyanide "off-on " sensor based on new C-glycosyl triazolyl bis-amino acid scaffold. Org Biomol Chem 2012;10:555-60.
    • (2012) Org Biomol Chem , vol.10 , pp. 555-560
    • Tang, Y.H.1    Qu, Y.2    Song, Z.3    He, X.P.4    Xie, J.5    Hua, J.L.6
  • 14
    • 84897639621 scopus 로고    scopus 로고
    • Substitution pattern reverses the fluorescence response of coumarin glycoligands upon coordination with silver (I)
    • Shi DT, Wei XL, Sheng Y, Zang Y, He XP, Xie J, et al. Substitution pattern reverses the fluorescence response of coumarin glycoligands upon coordination with silver (I). Sci Rep 2014;4:4252.
    • (2014) Sci Rep , vol.4 , pp. 4252
    • Shi, D.T.1    Wei, X.L.2    Sheng, Y.3    Zang, Y.4    He, X.P.5    Xie, J.6
  • 15
    • 79954987831 scopus 로고    scopus 로고
    • Creation of 3,4-bis-triazolocoumarinesugar conjugates via flourogenic dual click chemistry and their quenching specificity with silver(I) in aqueous media
    • He XP, Song Z, Wang ZZ, Shi XX, Chen KX, Chen GR. Creation of 3,4-bis-triazolocoumarinesugar conjugates via flourogenic dual click chemistry and their quenching specificity with silver(I) in aqueous media. Tetrahedron 2011;67:3343-7.
    • (2011) Tetrahedron , vol.67 , pp. 3343-3347
    • He, X.P.1    Song, Z.2    Wang, Z.Z.3    Shi, X.X.4    Chen, K.X.5    Chen, G.R.6
  • 16
    • 78751569549 scopus 로고    scopus 로고
    • 'Click' to bidentate bistriazolyl sugar derivatives with promising biological and optical features
    • Song Z, He XP, Jin XP, Gao LX, Li S, Zhou YB, et al. 'Click' to bidentate bistriazolyl sugar derivatives with promising biological and optical features. Tetrahedron Lett 2011;52:894-8.
    • (2011) Tetrahedron Lett , vol.52 , pp. 894-898
    • Song, Z.1    He, X.P.2    Jin, X.P.3    Gao, L.X.4    Li, S.5    Zhou, Y.B.6
  • 17
    • 77952824313 scopus 로고    scopus 로고
    • Fluorescent and colorimetric probes for detection of thiols
    • Chen X, Zhou Y, Peng X, Yoon J. Fluorescent and colorimetric probes for detection of thiols. Chem Soc Rev 2010;39:2120-35.
    • (2010) Chem Soc Rev , vol.39 , pp. 2120-2135
    • Chen, X.1    Zhou, Y.2    Peng, X.3    Yoon, J.4
  • 18
    • 36148962893 scopus 로고    scopus 로고
    • A highly selective fluorescent probe for thiophenols
    • Jiang W, Fu Q, Fan H, Ho J, Wang W. A highly selective fluorescent probe for thiophenols. Angew Chem Int Ed 2007;46:8445-8.
    • (2007) Angew Chem Int Ed , vol.46 , pp. 8445-8448
    • Jiang, W.1    Fu, Q.2    Fan, H.3    Ho, J.4    Wang, W.5
  • 19
    • 84861896256 scopus 로고    scopus 로고
    • Reaction-based fluorescent probe for selective discrimination of thiophenols over aliphaticthiols and its application in water samples
    • Wang Z, Han DM, Jia WP, Zhou QZ, Deng WP. Reaction-based fluorescent probe for selective discrimination of thiophenols over aliphaticthiols and its application in water samples. Anal Chem 2012;84:4915-20.
    • (2012) Anal Chem , vol.84 , pp. 4915-4920
    • Wang, Z.1    Han, D.M.2    Jia, W.P.3    Zhou, Q.Z.4    Deng, W.P.5
  • 20
    • 84864459067 scopus 로고    scopus 로고
    • BODIPY based colorimetric fluorescent probe for selective thiophenol detection: Theoretical and experimental studies
    • Kand D, Mishra PK, Saha T, Lahiri M, Talukdar P. BODIPY based colorimetric fluorescent probe for selective thiophenol detection: theoretical and experimental studies. Analyst 2012;137:3921-4.
    • (2012) Analyst , vol.137 , pp. 3921-3924
    • Kand, D.1    Mishra, P.K.2    Saha, T.3    Lahiri, M.4    Talukdar, P.5
  • 21
    • 76949101068 scopus 로고    scopus 로고
    • A highly sensitive fluorescent probe for detection of benzenethiols in environmental samples and living cells
    • Lin W, Long L, Tan W. A highly sensitive fluorescent probe for detection of benzenethiols in environmental samples and living cells. Chem Commun 2010;46:1503-5.
    • (2010) Chem Commun , vol.46 , pp. 1503-1505
    • Lin, W.1    Long, L.2    Tan, W.3
  • 22
    • 77949378021 scopus 로고    scopus 로고
    • Rational design of a highly selective and sensitive fluorescent PET probe for discrimination of thiophenols and aliphatic thiols
    • Jiang W, Cao Y, Liu Y, Wang W. Rational design of a highly selective and sensitive fluorescent PET probe for discrimination of thiophenols and aliphatic thiols. Chem Commun 2010;46:1944-6.
    • (2010) Chem Commun , vol.46 , pp. 1944-1946
    • Jiang, W.1    Cao, Y.2    Liu, Y.3    Wang, W.4
  • 23
    • 84867464839 scopus 로고    scopus 로고
    • Quinolinium-based fluorescent probes for the detection of thiophenols in environmental samples and living cells
    • Liu XL, Duan XY, Du XJ, Song QH. Quinolinium-based fluorescent probes for the detection of thiophenols in environmental samples and living cells. Chem Asian J 2012;7:2696-702.
    • (2012) Chem Asian J , vol.7 , pp. 2696-2702
    • Liu, X.L.1    Duan, X.Y.2    Du, X.J.3    Song, Q.H.4
  • 24
    • 84896520902 scopus 로고    scopus 로고
    • A coumarin-based fluorescent probe for selective and sensitive detection of thiophenols and its application
    • Li J, Zhang CF, Yang SH, Yang WC, Yang GF. A coumarin-based fluorescent probe for selective and sensitive detection of thiophenols and its application. Anal Chem 2014;86:3037-43.
    • (2014) Anal Chem , vol.86 , pp. 3037-3043
    • Li, J.1    Zhang, C.F.2    Yang, S.H.3    Yang, W.C.4    Yang, G.F.5
  • 25
    • 84862270950 scopus 로고    scopus 로고
    • Design of a ratiometric fluorescent probe for benzenethiols based on a thiol-sulfoxide reaction
    • Wang X, Cao J, Zhao C. Design of a ratiometric fluorescent probe for benzenethiols based on a thiol-sulfoxide reaction. Org Biomol Chem 2012;10:4689-91.
    • (2012) Org Biomol Chem , vol.10 , pp. 4689-4691
    • Wang, X.1    Cao, J.2    Zhao, C.3
  • 26
    • 78649304681 scopus 로고    scopus 로고
    • Colorimetric and fluorescent anion sensors: An overview of recent developments in the use of 1,8-naphthalimide-based chemosensors
    • Duke RM, Veale EB, Pfeffer FM, Kruger PE, Gunnlaugsson T. Colorimetric and fluorescent anion sensors: an overview of recent developments in the use of 1,8-naphthalimide-based chemosensors. Chem Soc Rev 2010;39:3936-53.
    • (2010) Chem Soc Rev , vol.39 , pp. 3936-3953
    • Duke, R.M.1    Veale, E.B.2    Pfeffer, F.M.3    Kruger, P.E.4    Gunnlaugsson, T.5
  • 27
    • 24644469501 scopus 로고    scopus 로고
    • Copper complexes for fluorescence-based NO detection in aqueous solution
    • Lim MH, Lippard SJ. Copper complexes for fluorescence-based NO detection in aqueous solution. J Am Chem Soc 2005;127:12170-1.
    • (2005) J Am Chem Soc , vol.127 , pp. 12170-12171
    • Lim, M.H.1    Lippard, S.J.2
  • 28
    • 67651213457 scopus 로고    scopus 로고
    • Thiol-selective fluorogenic probes for labeling and release
    • Hong V, Kislukhin AA, Finn MG. Thiol-selective fluorogenic probes for labeling and release. J Am Chem Soc 2009;131:9986-94.
    • (2009) J Am Chem Soc , vol.131 , pp. 9986-9994
    • Hong, V.1    Kislukhin, A.A.2    Finn, M.G.3
  • 29
    • 84897997736 scopus 로고    scopus 로고
    • Cyanine-based fluorescent probe for highly selective detection of glutathione in cell cultures and live mouse tissues
    • Yin J, Kwon Y, Kim D, Lee D, Kim G, Hu Y, et al. Cyanine-based fluorescent probe for highly selective detection of glutathione in cell cultures and live mouse tissues. J Am Chem Soc 2014;136:5351-8.
    • (2014) J Am Chem Soc , vol.136 , pp. 5351-5358
    • Yin, J.1    Kwon, Y.2    Kim, D.3    Lee, D.4    Kim, G.5    Hu, Y.6
  • 30
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective ligation of azides and terminal alkynes
    • Rostovtsev VV, Green LG, Fokin VV, Sharpless KB. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective ligation of azides and terminal alkynes. Angew Chem Int Ed 2002;41:2596-9.
    • (2002) Angew Chem Int Ed , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 31
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on solid phase: [1,2,3]- triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
    • Tornøe CW, Christensen C, Meldal M. Peptidotriazoles on solid phase: [1,2,3]- triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J Org Chem 2002;67:3057-64.
    • (2002) J Org Chem , vol.67 , pp. 3057-3064
    • Tornøe, C.W.1    Christensen, C.2    Meldal, M.3
  • 32
    • 84880290938 scopus 로고    scopus 로고
    • FRET-based small-molecule fluorescent probes: Rational design and bioimaging applications
    • Yuan L, Lin W, Zheng K, Zhu S. FRET-based small-molecule fluorescent probes: rational design and bioimaging applications. Acc Chem Res 2013;46:1462-73.
    • (2013) Acc Chem Res , vol.46 , pp. 1462-1473
    • Yuan, L.1    Lin, W.2    Zheng, K.3    Zhu, S.4
  • 33
    • 84888241427 scopus 로고    scopus 로고
    • A per-acetyl glycosyl rhodamine as a novel fluorescent ratiometric probe for mercury (II)
    • Li KB, Zhang HL, Zhu B, He XP, Xie J, Chen GR. A per-acetyl glycosyl rhodamine as a novel fluorescent ratiometric probe for mercury (II). Dyes Pigments 2014;102:273-7.
    • (2014) Dyes Pigments , vol.102 , pp. 273-277
    • Li, K.B.1    Zhang, H.L.2    Zhu, B.3    He, X.P.4    Xie, J.5    Chen, G.R.6
  • 34
    • 84864411271 scopus 로고    scopus 로고
    • Probing bacterial-toxin inhibition with synthetic glycopolymers prepared by tandem post-polymerization modification: Role of linker length and carbohydrate density
    • Richards SJ, Jones MW, Hunaban M, Haddleton DM, Gibson MI. Probing bacterial-toxin inhibition with synthetic glycopolymers prepared by tandem post-polymerization modification: role of linker length and carbohydrate density. Angew Chem Int Ed 2012;51:7812-6.
    • (2012) Angew Chem Int Ed , vol.51 , pp. 7812-7816
    • Richards, S.J.1    Jones, M.W.2    Hunaban, M.3    Haddleton, D.M.4    Gibson, M.I.5
  • 35
    • 77955147884 scopus 로고    scopus 로고
    • Clicking fluoroionophores onto mesoporous silicas: A universal strategy toward efficient fluorescent surface sensors for metal ions
    • Jin Z, Zhang XB, Xie DX, Gong YJ, Zhang J, Chen X, et al. Clicking fluoroionophores onto mesoporous silicas: a universal strategy toward efficient fluorescent surface sensors for metal ions. Anal Chem 2010;82:6343-6.
    • (2010) Anal Chem , vol.82 , pp. 6343-6346
    • Jin, Z.1    Zhang, X.B.2    Xie, D.X.3    Gong, Y.J.4    Zhang, J.5    Chen, X.6
  • 36
    • 84908423283 scopus 로고    scopus 로고
    • Hepatoma-selective imaging of heavy metal ions using a 'clicked' galactosylrhodamine probe
    • Li KB, Zang Y, Wang H, Li J, Chen GR, James TD, et al. Hepatoma-selective imaging of heavy metal ions using a 'clicked' galactosylrhodamine probe. Chem Commun 2014;50:11735-7.
    • (2014) Chem Commun , vol.50 , pp. 11735-11737
    • Li, K.B.1    Zang, Y.2    Wang, H.3    Li, J.4    Chen, G.R.5    James, T.D.6
  • 37
    • 84908347164 scopus 로고    scopus 로고
    • Fluorogenic supramolecular complexes formed between pyrenyl-β-cyclodextrin and glycorhodamine for the selective detection of lectins
    • He XP, Li RH, Maisonneuve S, Ruan Y, Chen GR, Xie J. Fluorogenic supramolecular complexes formed between pyrenyl-β-cyclodextrin and glycorhodamine for the selective detection of lectins. Chem Commun 2014;50:14141-4.
    • (2014) Chem Commun , vol.50 , pp. 14141-14144
    • He, X.P.1    Li, R.H.2    Maisonneuve, S.3    Ruan, Y.4    Chen, G.R.5    Xie, J.6
  • 38
    • 84903735944 scopus 로고    scopus 로고
    • A 'clicked' tetrameric hydroxamic acid glycopeptidomimetic antagonizes sugar-lectin interactions on the cellular level
    • Zhang HL, Zang Y, Xie J, Li J, Chen GR, He XP, et al. A 'clicked' tetrameric hydroxamic acid glycopeptidomimetic antagonizes sugar-lectin interactions on the cellular level. Sci Rep 2014;4:5513.
    • (2014) Sci Rep , vol.4 , pp. 5513
    • Zhang, H.L.1    Zang, Y.2    Xie, J.3    Li, J.4    Chen, G.R.5    He, X.P.6
  • 39
    • 84882455057 scopus 로고    scopus 로고
    • Fluorogenic probing of specific recognitions between sugar ligands and glycoprotein receptors on cancer cells by an economic graphene nanocomposite
    • Zhang HL, Wei XL, Zang Y, Cao JY, Liu S, He XP, et al. Fluorogenic probing of specific recognitions between sugar ligands and glycoprotein receptors on cancer cells by an economic graphene nanocomposite. Adv Mater 2013;25:4097-101.
    • (2013) Adv Mater , vol.25 , pp. 4097-4101
    • Zhang, H.L.1    Wei, X.L.2    Zang, Y.3    Cao, J.Y.4    Liu, S.5    He, X.P.6
  • 40
    • 84931289185 scopus 로고    scopus 로고
    • Probing disease-related proteins with fluorogenic composite materials
    • He XP, Zang Y, James TD, Li J, Chen GR. Probing disease-related proteins with fluorogenic composite materials. Chem Soc Rev 2015. http://dx.doi.org/10.1039/c4cs00252k.
    • (2015) Chem Soc Rev
    • He, X.P.1    Zang, Y.2    James, T.D.3    Li, J.4    Chen, G.R.5


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