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Volumn 199, Issue , 2014, Pages 93-100

TICT based fluorescence "turn-on" hydrazine probes

Author keywords

Crystal structure; DFT; Fluorescence probes; Hydrazine

Indexed keywords

ALDEHYDES; CRYSTAL STRUCTURE; HYDRAZINE; PROBES;

EID: 84898988225     PISSN: 09254005     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.snb.2014.03.087     Document Type: Article
Times cited : (77)

References (51)
  • 1
    • 0030949577 scopus 로고    scopus 로고
    • Peroxidase substrates stimulate the oxidation of hydralazine to metabolites which cause single-strand breaks in DNA
    • DOI 10.1021/tx960189l
    • C.A. Reilly, and S.D. Aust Peroxidase substrates stimulate the oxidation of hydralazine to metabolites which cause single-strand breaks in DNA Chem. Res. Toxicol. 10 1997 328 334 (Pubitemid 27137144)
    • (1997) Chemical Research in Toxicology , vol.10 , Issue.3 , pp. 328-334
    • Reilly, C.A.1    Aust, S.D.2
  • 2
    • 57249083928 scopus 로고    scopus 로고
    • Synthetic methodology for alkyl substituted hydrazines
    • DOI 10.1039/b010091a
    • U. Ragnarsson Synthetic methodology for alkyl substituted hydrazines Chem. Soc. Rev. 30 2001 205 213 (Pubitemid 33303574)
    • (2001) Chemical Society Reviews , vol.30 , Issue.4 , pp. 205-213
    • Ragnarsson, U.1
  • 4
    • 0001353683 scopus 로고
    • Hydrazine detection using a tyrosinase-based inhibition biosensor
    • J. Wang, and L. Chen Hydrazine detection using a tyrosinase-based inhibition biosensor Anal. Chem. 67 1995 3824 3827
    • (1995) Anal. Chem. , vol.67 , pp. 3824-3827
    • Wang, J.1    Chen, L.2
  • 5
    • 37349019340 scopus 로고    scopus 로고
    • Zinc oxide nanonail based chemical sensor for hydrazine detection
    • DOI 10.1039/b711215g
    • A. Umar, M.M. Rahman, S.H. Kim, and Y.B. Hahn Zinc oxide nanonail based chemical sensor for hydrazine detection Chem. Commun. 2008 166 168 (Pubitemid 350294088)
    • (2008) Chemical Communications , Issue.2 , pp. 166-168
    • Umar, A.1    Rahman, M.M.2    Kim, S.H.3    Hahn, Y.-B.4
  • 6
    • 82255195933 scopus 로고    scopus 로고
    • A novel detection technique of hydrazine hydrate: Modality change of hydrogen bonding-induced rapid and ultrasensitive colorimetric assay
    • Z.L. Zhao, G. Zhang, Y. Gao, X.Y. Yang, and Y.H. Li A novel detection technique of hydrazine hydrate: modality change of hydrogen bonding-induced rapid and ultrasensitive colorimetric assay Chem. Commun. 47 2011 12816 12818
    • (2011) Chem. Commun. , vol.47 , pp. 12816-12818
    • Zhao, Z.L.1    Zhang, G.2    Gao, Y.3    Yang, X.Y.4    Li, Y.H.5
  • 7
    • 77956461000 scopus 로고    scopus 로고
    • C@ZnO nanorod array-based hydrazine electrochemical sensor with improved sensitivity and stability
    • J.P. Liu, Y.Y. Li, J. Jiang, and X.T. Huang C@ZnO nanorod array-based hydrazine electrochemical sensor with improved sensitivity and stability Dalton Trans. 39 2010 8693 8697
    • (2010) Dalton Trans. , vol.39 , pp. 8693-8697
    • Liu, J.P.1    Li, Y.Y.2    Jiang, J.3    Huang, X.T.4
  • 8
    • 14844325773 scopus 로고    scopus 로고
    • Hydrazine detection by polyaniline using fluorinated alcohol additives
    • DOI 10.1021/cm0484091
    • S. Virji, R.B. Kaner, and B.H. Weiller Hydrazine detection by polyaniline using fluorinated alcohol additives Chem. Mater. 17 2005 1256 1260 (Pubitemid 40344050)
    • (2005) Chemistry of Materials , vol.17 , Issue.5 , pp. 1256-1260
    • Virji, S.1    Kaner, R.B.2    Weiller, B.H.3
  • 9
    • 34249089998 scopus 로고    scopus 로고
    • Ultrasensitive nanostructured platform for the electrochemical sensing of hydrazine
    • DOI 10.1021/jp0700837
    • B.K. Jena, and C.R. Raj Ultrasensitive nanostructured platform for the electrochemical sensing of hydrazine J. Phys. Chem. C 111 2007 6228 6232 (Pubitemid 46787838)
    • (2007) Journal of Physical Chemistry C , vol.111 , Issue.17 , pp. 6228-6232
    • Jena, B.K.1    Retna Raj, C.2
  • 10
    • 37049087358 scopus 로고
    • Fluorescent detection of hydrazine, monomethylhydrazine, and 1,1-dimethylhydrazine by derivatization with aromatic dicarbaldehydes
    • G.E. Collins, and S.L. Rose-Pehrsson Fluorescent detection of hydrazine, monomethylhydrazine, and 1,1-dimethylhydrazine by derivatization with aromatic dicarbaldehydes Analyst 119 1994 1907 1913
    • (1994) Analyst , vol.119 , pp. 1907-1913
    • Collins, G.E.1    Rose-Pehrsson, S.L.2
  • 12
    • 33646574950 scopus 로고    scopus 로고
    • Trace hydrazine detection with fluorescent conjugated polymers: A turn-on sensory mechanism
    • S.W. Thomas III, and T.M. Swager Trace hydrazine detection with fluorescent conjugated polymers: a turn-on sensory mechanism Adv. Mater. 18 2006 1047 1050
    • (2006) Adv. Mater. , vol.18 , pp. 1047-1050
    • Thomas III, S.W.1    Swager, T.M.2
  • 13
    • 80054735403 scopus 로고    scopus 로고
    • Hydrazine-selective chromogenic and fluorogenic probe based on levulinated coumarin
    • M.G. Choi, J.Y. Hwang, J.O. Moon, J.Y. Sung, and S.K. Chang Hydrazine-selective chromogenic and fluorogenic probe based on levulinated coumarin Org. Lett. 13 2011 5260 5263
    • (2011) Org. Lett. , vol.13 , pp. 5260-5263
    • Choi, M.G.1    Hwang, J.Y.2    Moon, J.O.3    Sung, J.Y.4    Chang, S.K.5
  • 14
    • 23144451167 scopus 로고    scopus 로고
    • Fluorescence-enhancement sensing of ammonia and hydrazines via disruption of the internal hydrogen bond in a carbazolopyridinophane
    • DOI 10.1016/j.snb.2005.01.007, PII S092540050500095X
    • A.B. Brown, T.L. Gibson, J.C. Baum, T. Ren, and T.M. Smith Fluorescence-enhancement sensing of ammonia and hydrazines via disruption of the internal hydrogen bond in a carbazolopyridinophane Sens. Actuators, B: Chem. 110 2005 8 12 (Pubitemid 41085199)
    • (2005) Sensors and Actuators, B: Chemical , vol.110 , Issue.1 , pp. 8-12
    • Brown, A.B.1    Gibson, T.L.2    Baum, J.C.3    Ren, T.4    Smith, T.M.5
  • 15
    • 49449091258 scopus 로고    scopus 로고
    • Sensitive and selective fluorescence determination of trace hydrazine in aqueous solution utilizing 5-chlorosalicylaldehyde
    • X.T. Chen, Y. Xiang, Z.F. Li, and A.J. Tong Sensitive and selective fluorescence determination of trace hydrazine in aqueous solution utilizing 5-chlorosalicylaldehyde Anal. Chim. Acta 625 2008 41 46
    • (2008) Anal. Chim. Acta , vol.625 , pp. 41-46
    • Chen, X.T.1    Xiang, Y.2    Li, Z.F.3    Tong, A.J.4
  • 16
    • 78751705994 scopus 로고    scopus 로고
    • Control and analysis of hydrazine, hydrazides and hydrazones-genotoxic impurities pharmaceutical ingredients (APIs) and drug products
    • D.P. Elder, D. Snodin, and A. Teasdale Control and analysis of hydrazine, hydrazides and hydrazones-genotoxic impurities pharmaceutical ingredients (APIs) and drug products J. Pharm. Biomed. Anal. 54 2011 900 910
    • (2011) J. Pharm. Biomed. Anal. , vol.54 , pp. 900-910
    • Elder, D.P.1    Snodin, D.2    Teasdale, A.3
  • 17
    • 30944439620 scopus 로고    scopus 로고
    • The electroanalytical detection of hydrazine: A comparison of the use of palladium nanoparticles supported on boron-doped diamond and palladium plated BDD microdisc array
    • DOI 10.1039/b513751a
    • C. Batchelor-McAuley, C.E. Banks, A.O. Simm, T.G.J. Jones, and R.G. Compton The electroanalytical detection of hydrazine: a comparison of the use of palladium nanoparticles supported on boron-doped diamond and palladium plated BDD microdisc array Analyst 131 2006 106 110 (Pubitemid 43117129)
    • (2006) Analyst , vol.131 , Issue.1 , pp. 106-110
    • Batchelor-McAuley, C.1    Banks, C.E.2    Simm, A.O.3    Jones, T.G.J.4    Compton, R.G.5
  • 19
    • 84861898197 scopus 로고    scopus 로고
    • Highly selective colorimetric sensing of cyanide based on formation of dipyrrin adducts
    • Y.B. Ding, T. Li, W.H. Zhu, and Y.S. Xie Highly selective colorimetric sensing of cyanide based on formation of dipyrrin adducts Org. Biomol. Chem. 10 2012 4201 4207
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 4201-4207
    • Ding, Y.B.1    Li, T.2    Zhu, W.H.3    Xie, Y.S.4
  • 20
    • 80053301640 scopus 로고    scopus 로고
    • Iridium(III) complex-coated nanosystem for ratiometric upconversion luminescence bioimaging of cyanide anions
    • J.L. Liu, Y. Liu, Q. Liu, C.Y. Li, L.N. Sun, and F.Y. Li Iridium(III) complex-coated nanosystem for ratiometric upconversion luminescence bioimaging of cyanide anions J. Am. Chem. Soc. 133 2011 15276 15279
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15276-15279
    • Liu, J.L.1    Liu, Y.2    Liu, Q.3    Li, C.Y.4    Sun, L.N.5    Li, F.Y.6
  • 21
    • 33750484988 scopus 로고    scopus 로고
    • IV complexes of N-confused porphyrins and oxoporphyrins - Unique fluorescence "switch-on" halide receptors
    • DOI 10.1002/anie.200602481
    • IV complexes of N-confused porphyrins and oxoporphyrins-unique fluorescence "switch- on" halide receptors Angew. Chem. Int. Ed. 45 2006 6907 6910 (Pubitemid 44654491)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.41 , pp. 6907-6910
    • Xie, Y.1    Morimoto, T.2    Furuta, H.3
  • 22
    • 80054879885 scopus 로고    scopus 로고
    • Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species
    • X.Q. Chen, X.Z. Tian, I. Shin, and J.Y. Yoon Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species Chem. Soc. Rev. 40 2011 4783 4804
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4783-4804
    • Chen, X.Q.1    Tian, X.Z.2    Shin, I.3    Yoon, J.Y.4
  • 23
    • 79955143096 scopus 로고    scopus 로고
    • Selective and sensitive "turn-on" fluorescent Zn2+ sensors based on di- and tripyrrins with readily modulated emission wavelengths
    • Y.B. Ding, Y.S. Xie, X. Li, J.P. Hill, W.B. Zhang, and W.H. Zhu Selective and sensitive "turn-on" fluorescent Zn2+ sensors based on di- and tripyrrins with readily modulated emission wavelengths Chem. Commun. 47 2011 5431 5433
    • (2011) Chem. Commun. , vol.47 , pp. 5431-5433
    • Ding, Y.B.1    Xie, Y.S.2    Li, X.3    Hill, J.P.4    Zhang, W.B.5    Zhu, W.H.6
  • 24
    • 78649263333 scopus 로고    scopus 로고
    • Boron based anion receptors as sensors
    • E. Galbraith, and T.D. James Boron based anion receptors as sensors Chem. Sov. Rev. 39 2010 3831 3842
    • (2010) Chem. Sov. Rev. , vol.39 , pp. 3831-3842
    • Galbraith, E.1    James, T.D.2
  • 25
    • 84863659866 scopus 로고    scopus 로고
    • Iridium- complex-modified upconversion nanophosphors for effective LRET detection of cyanide anions in pure water
    • L.M. Yao, J. Zhou, J.L. Liu, W. Feng, and F.Y. Li Iridium- complex-modified upconversion nanophosphors for effective LRET detection of cyanide anions in pure water Adv. Funct. Mater. 22 2012 2667 2672
    • (2012) Adv. Funct. Mater. , vol.22 , pp. 2667-2672
    • Yao, L.M.1    Zhou, J.2    Liu, J.L.3    Feng, W.4    Li, F.Y.5
  • 26
    • 84879282973 scopus 로고    scopus 로고
    • α-Monoacylated and α, α′- And α, β′-diacylated dipyrrins as highly sensitive fluorescence "turn-on" Zn2+ probes
    • Y.B. Ding, X. Li, T. Li, Y.S. Xie, and W.H. Zhu α-Monoacylated and α, α′- and α, β′-diacylated dipyrrins as highly sensitive fluorescence "turn-on" Zn2+ probes J. Org. Chem. 78 2013 5328 5338
    • (2013) J. Org. Chem. , vol.78 , pp. 5328-5338
    • Ding, Y.B.1    Li, X.2    Li, T.3    Xie, Y.S.4    Zhu, W.H.5
  • 27
    • 84876972137 scopus 로고    scopus 로고
    • From nonconjugation to conjugation: Novel meso-OH substituted dipyrromethanes as fluorescence turn-on Zn2+ probes
    • Y.B. Ding, T. Li, X. Li, W.H. Zhu, and Y.S. Xie From nonconjugation to conjugation: novel meso-OH substituted dipyrromethanes as fluorescence turn-on Zn2+ probes Org. Biomol. Chem. 11 2013 2685 2692
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 2685-2692
    • Ding, Y.B.1    Li, T.2    Li, X.3    Zhu, W.H.4    Xie, Y.S.5
  • 28
    • 79959420418 scopus 로고    scopus 로고
    • Recent progress in fluorescent and colorimetric chemosensors for detection of precious metal ions (silver, gold and platinum ions)
    • J.F. Zhang, Y. Zhou, J.Y. Yoon, and J.S. Kim Recent progress in fluorescent and colorimetric chemosensors for detection of precious metal ions (silver, gold and platinum ions) Chem. Soc. Rev. 40 2011 3416 3429
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 3416-3429
    • Zhang, J.F.1    Zhou, Y.2    Yoon, J.Y.3    Kim, J.S.4
  • 29
    • 84868359335 scopus 로고    scopus 로고
    • Selective, sensitive and reversible "turn-on" fluorescent cyanide probes based on 2,2′-dipyridylaminoanthracene-Cu2+ ensembles
    • Y.S. Xie, Y.B. Ding, C. Wang, J.P. Hill, K. Ariga, W.B. Zhang, and W.H. Zhu Selective, sensitive and reversible "turn-on" fluorescent cyanide probes based on 2,2′-dipyridylaminoanthracene-Cu2+ ensembles Chem. Commun. 48 2012 11513 11515
    • (2012) Chem. Commun. , vol.48 , pp. 11513-11515
    • Xie, Y.S.1    Ding, Y.B.2    Wang, C.3    Hill, J.P.4    Ariga, K.5    Zhang, W.B.6    Zhu, W.H.7
  • 30
    • 84871289375 scopus 로고    scopus 로고
    • A simple visual sensor with the potential for determining the concentration of fluoride in water at environmentally significant levels
    • T. Nishimura, S.Y. Xu, Y.B. Jiang, J.S. Fossy, K. Sakurai, S.D. Bull, and T.D. James A simple visual sensor with the potential for determining the concentration of fluoride in water at environmentally significant levels Chem. Commun. 49 2013 478 480
    • (2013) Chem. Commun. , vol.49 , pp. 478-480
    • Nishimura, T.1    Xu, S.Y.2    Jiang, Y.B.3    Fossy, J.S.4    Sakurai, K.5    Bull, S.D.6    James, T.D.7
  • 32
    • 84864666324 scopus 로고    scopus 로고
    • Combinatorial strategies in fluorescent probe development
    • M. Vendrell, D.T. Zhai, J.C. Er, and Y.T. Chang Combinatorial strategies in fluorescent probe development Chem. Rev. 112 2012 4391 4420
    • (2012) Chem. Rev. , vol.112 , pp. 4391-4420
    • Vendrell, M.1    Zhai, D.T.2    Er, J.C.3    Chang, Y.T.4
  • 35
    • 84885109338 scopus 로고    scopus 로고
    • Steric hindrance-enforced distortion as a general strategy for the design of fluorescence "turn-on" cyanide probes
    • B. Chen, Y.B. Ding, X. Li, W.H. Zhu, J.P. Hill, K. Ariga, and Y.S. Xie Steric hindrance-enforced distortion as a general strategy for the design of fluorescence "turn-on" cyanide probes Chem. Commun. 49 2013 10136 10138
    • (2013) Chem. Commun. , vol.49 , pp. 10136-10138
    • Chen, B.1    Ding, Y.B.2    Li, X.3    Zhu, W.H.4    Hill, J.P.5    Ariga, K.6    Xie, Y.S.7
  • 37
    • 16244386901 scopus 로고    scopus 로고
    • Study on synthesis of organic light emitting diode materials of aminoanthrancenes and their light emitting property
    • M.X. Yu, X.H. Chen, and C.H. Cheng Study on synthesis of organic light emitting diode materials of aminoanthrancenes and their light emitting property Chin. J. Org. Chem. 25 2005 218 221
    • (2005) Chin. J. Org. Chem. , vol.25 , pp. 218-221
    • Yu, M.X.1    Chen, X.H.2    Cheng, C.H.3
  • 38
    • 0008662621 scopus 로고
    • The measurement of photoluminescence quantum yields. A review
    • J.N. Demas, and G.A. Crosby The measurement of photoluminescence quantum yields. A review J. Phys. Chem. 75 1971 991 1024
    • (1971) J. Phys. Chem. , vol.75 , pp. 991-1024
    • Demas, J.N.1    Crosby, G.A.2
  • 39
    • 0020954536 scopus 로고
    • Fluorescence quantum yields of some rhodamine dyes
    • DOI 10.1016/0022-2313(82)90045-X
    • R.F. Kubin, and A.N. Fletcher Fluorescence quantum yields of some rhodamine dyes J. Lumin. 27 1982 455 462 (Pubitemid 13505734)
    • (1983) Journal of Luminescence , vol.27 , Issue.4 , pp. 455-462
    • Kubin, R.F.1    Fletcher, A.N.2
  • 40
    • 4344577294 scopus 로고    scopus 로고
    • Hybrid meta density functional theory methods for thermochemistry, thermochemical kinetics, and noncovalent interactions: The MPW1B95 and MPWB1K models and comparative assessments for hydrogen bonding and van der Waals interactions
    • Y. Zhao, and D.G. Truhlar Hybrid meta density functional theory methods for thermochemistry, thermochemical kinetics, and noncovalent interactions: the MPW1B95 and MPWB1K models and comparative assessments for hydrogen bonding and van der Waals interactions J. Phys. Chem. A 108 2004 6908 6918
    • (2004) J. Phys. Chem. A , vol.108 , pp. 6908-6918
    • Zhao, Y.1    Truhlar, D.G.2
  • 41
    • 0000189651 scopus 로고
    • Density-functional thermochemistry. III. The role of exact exchange
    • A.D. Becke Density-functional thermochemistry. III. The role of exact exchange J. Chem. Phys. 98 1993 5648 5652
    • (1993) J. Chem. Phys. , vol.98 , pp. 5648-5652
    • Becke, A.D.1
  • 42
    • 84961980477 scopus 로고    scopus 로고
    • Quantum mechanical continuum solvation models
    • DOI 10.1021/cr9904009
    • J. Tomasi, B. Mennucci, and R. Cammi Quantum mechanical continuum solvation models Chem. Rev. 105 2005 2999 3093 (Pubitemid 41222791)
    • (2005) Chemical Reviews , vol.105 , Issue.8 , pp. 2999-3093
    • Tomasi, J.1    Mennucci, B.2    Cammi, R.3
  • 43
    • 0142231517 scopus 로고    scopus 로고
    • Structural changes accompanying intramolecular electron transfer: Focus on twisted intramolecular charge-transfer states and structures
    • Z.R. Grabowski, and K. Rotkiewicz Structural changes accompanying intramolecular electron transfer: focus on twisted intramolecular charge-transfer states and structures Chem. Rev. 103 2003 3899 4031
    • (2003) Chem. Rev. , vol.103 , pp. 3899-4031
    • Grabowski, Z.R.1    Rotkiewicz, K.2
  • 44
    • 84985609328 scopus 로고
    • Charge separation in excited states of decoupled systems-TICT compounds and implications regarding the development of new laser dyes and the primary processes of vision and photosynthesis
    • W. Rettig Charge separation in excited states of decoupled systems-TICT compounds and implications regarding the development of new laser dyes and the primary processes of vision and photosynthesis Angew. Chem. Int. Ed. Engl. 25 1986 971 988
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 971-988
    • Rettig, W.1
  • 45
    • 77954571759 scopus 로고    scopus 로고
    • Planar vs. Twisted intramolecular charge transfer mechanism in Nile Red: New hints from theory
    • C.A. Guido, B. Mennucci, D. Jacquemin, and C. Adamo Planar vs. twisted intramolecular charge transfer mechanism in Nile Red: new hints from theory Phys. Chem. Chem. Phys. 12 2010 8016 8023
    • (2010) Phys. Chem. Chem. Phys. , vol.12 , pp. 8016-8023
    • Guido, C.A.1    Mennucci, B.2    Jacquemin, D.3    Adamo, C.4
  • 46
    • 84859369750 scopus 로고    scopus 로고
    • What is the "best" atomic charge model to describe through-space charge-transfer excitations?
    • D. Jacquemin, T.L. Bahers, C. Adamo, and I. Ciofini What is the "best" atomic charge model to describe through-space charge-transfer excitations? Phys. Chem. Chem. Phys. 14 2012 5383 5388
    • (2012) Phys. Chem. Chem. Phys. , vol.14 , pp. 5383-5388
    • Jacquemin, D.1    Bahers, T.L.2    Adamo, C.3    Ciofini, I.4
  • 47
    • 84961978276 scopus 로고    scopus 로고
    • The excited states of π-stacked 9-methyladenine oligomers: A TD-DFT study in aqueous solution
    • R. Improta The excited states of π-stacked 9-methyladenine oligomers: a TD-DFT study in aqueous solution Phys. Chem. Chem. Phys. 10 2008 2656 2664
    • (2008) Phys. Chem. Chem. Phys. , vol.10 , pp. 2656-2664
    • Improta, R.1
  • 48
    • 84884195801 scopus 로고    scopus 로고
    • Role of solvent on charge transfer in 7-aminocoumarin dyes: New hints from TD-CAM-B3LYP and state specic PCM calculations
    • A. Pedone Role of solvent on charge transfer in 7-aminocoumarin dyes: new hints from TD-CAM-B3LYP and state specic PCM calculations J. Chem. Theory Comput. 9 2013 4087 4096
    • (2013) J. Chem. Theory Comput. , vol.9 , pp. 4087-4096
    • Pedone, A.1
  • 49
    • 84860157346 scopus 로고    scopus 로고
    • A new "turn-on" naphthalenedimide-based chemosensor for mercury ions with high selectivity: Successful utilization of the mechanism of twisted intramolecular charge transfer, near-IR fluorescence, and cell images
    • Q.Q. Li, M. Peng, H.Y. Li, C. Zhong, L. Zhang, X.H. Cheng, X.N. Peng, Q.Q. Wang, J.G. Qin, and Z. Li A new "turn-on" naphthalenedimide-based chemosensor for mercury ions with high selectivity: successful utilization of the mechanism of twisted intramolecular charge transfer, near-IR fluorescence, and cell images Org. Lett. 14 2012 2094 2097
    • (2012) Org. Lett. , vol.14 , pp. 2094-2097
    • Li, Q.Q.1    Peng, M.2    Li, H.Y.3    Zhong, C.4    Zhang, L.5    Cheng, X.H.6    Peng, X.N.7    Wang, Q.Q.8    Qin, J.G.9    Li, Z.10
  • 50
    • 51649130452 scopus 로고    scopus 로고
    • A proton-triggered ON-OFF-ON fluorescent chemosensor for Mg(II) via twisted intramolecular charge transfer
    • Y. Liu, M. Han, H.Y. Zhang, L.X. Yang, and W. Jiang A proton-triggered ON-OFF-ON fluorescent chemosensor for Mg(II) via twisted intramolecular charge transfer Org. Lett. 10 2008 2873 2876
    • (2008) Org. Lett. , vol.10 , pp. 2873-2876
    • Liu, Y.1    Han, M.2    Zhang, H.Y.3    Yang, L.X.4    Jiang, W.5
  • 51
    • 0001323770 scopus 로고    scopus 로고
    • Ultrafast charge transfer in amino-substituted boron dipyrromethene dyes and its inhibition by cation complexation: A new design concept for highly sensitive fluorescent probes
    • M. Kollmannsberger, K. Rurack, U. Resch-Genger, and J. Daub Ultrafast charge transfer in amino-substituted boron dipyrromethene dyes and its inhibition by cation complexation: a new design concept for highly sensitive fluorescent probes J. Phys. Chem. A 102 1998 10211 10220 (Pubitemid 128604969)
    • (1998) Journal of Physical Chemistry A , vol.102 , Issue.50 , pp. 10211-10220
    • Kollmannsberger, M.1    Rurack, K.2    Resch-Genger, U.3    Daub, J.4


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