메뉴 건너뛰기




Volumn 96, Issue 2, 2013, Pages 328-332

BODIPY-based sulfoxide: Synthesis, photophysical characterization and response to benzenethiols

Author keywords

Benzenethiols; BODIPY based sulfoxide; Chemodosimeter; Chemospecific reduction; Hypsochromic shifts; Ratiometric fluorescence response

Indexed keywords

BENZENETHIOLS; BODIPY-BASED SULFOXIDE; CHEMODOSIMETERS; HYPSOCHROMIC SHIFTS; RATIOMETRIC FLUORESCENCE;

EID: 84867424548     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2012.08.026     Document Type: Article
Times cited : (35)

References (60)
  • 1
    • 84871042796 scopus 로고    scopus 로고
    • For recent reviews see
    • For recent reviews see
  • 2
    • 34147111647 scopus 로고    scopus 로고
    • The chemistry of BODIPY: A new El Dorado for fluorescence tools
    • R. Ziessel, G. Ulrich, and A. Harriman The chemistry of BODIPY: a new El Dorado for fluorescence tools New J Chem 31 2007 496 501
    • (2007) New J Chem , vol.31 , pp. 496-501
    • Ziessel, R.1    Ulrich, G.2    Harriman, A.3
  • 3
    • 36849053388 scopus 로고    scopus 로고
    • BODIPY dyes and their derivatives: Syntheses and spectroscopic properties
    • A. Loudet, and K. Burgess BODIPY dyes and their derivatives: syntheses and spectroscopic properties Chem Rev 107 2007 4891 4932
    • (2007) Chem Rev , vol.107 , pp. 4891-4932
    • Loudet, A.1    Burgess, K.2
  • 4
    • 40849107127 scopus 로고    scopus 로고
    • The chemistry of fluorescent BODIPY dyes: Versatility unsurpassed
    • G. Ulrich, R. Ziessel, and A. Harriman The chemistry of fluorescent BODIPY dyes: versatility unsurpassed Angew Chem Int Ed 47 2008 1184 1201
    • (2008) Angew Chem Int Ed , vol.47 , pp. 1184-1201
    • Ulrich, G.1    Ziessel, R.2    Harriman, A.3
  • 5
    • 80054104219 scopus 로고    scopus 로고
    • Fluorescent indicators based on BODIPY
    • N. Boens, V. Leen, and W. Dehaen Fluorescent indicators based on BODIPY Chem Soc Rev 41 2012 1130 1172
    • (2012) Chem Soc Rev , vol.41 , pp. 1130-1172
    • Boens, N.1    Leen, V.2    Dehaen, W.3
  • 6
    • 79961139992 scopus 로고    scopus 로고
    • 2- and 3-Monohalogenated BODIPY dyes and their functionalized analogues: Synthesis and spectroscopy
    • V. Leen, T. Leemans, N. Boens, and W. Dehaen 2- and 3-Monohalogenated BODIPY dyes and their functionalized analogues: synthesis and spectroscopy Eur J Org Chem 2011 4386 4396
    • (2011) Eur J Org Chem , pp. 4386-4396
    • Leen, V.1    Leemans, T.2    Boens, N.3    Dehaen, W.4
  • 7
    • 33644698915 scopus 로고    scopus 로고
    • Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution
    • T. Rohand, M. Baruah, W. Qin, N. Boens, and W. Dehaen Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution Chem Commun 3 2006 266 268
    • (2006) Chem Commun , vol.3 , pp. 266-268
    • Rohand, T.1    Baruah, M.2    Qin, W.3    Boens, N.4    Dehaen, W.5
  • 9
    • 61749088367 scopus 로고    scopus 로고
    • Synthesis, spectroscopy, crystal structure, electrochemistry, and quantum chemical and molecular dynamics calculations of a 3-Anilino difluoroboron dipyrromethene dye
    • W. Qin, V. Leen, T. Rohand, W. Dehaen, P. Dedecker, and M. Van der Auweraer Synthesis, spectroscopy, crystal structure, electrochemistry, and quantum chemical and molecular dynamics calculations of a 3-Anilino difluoroboron dipyrromethene dye J Phys Chem A 113 2009 439 447
    • (2009) J Phys Chem A , vol.113 , pp. 439-447
    • Qin, W.1    Leen, V.2    Rohand, T.3    Dehaen, W.4    Dedecker, P.5    Van Der Auweraer, M.6
  • 10
    • 84555196199 scopus 로고    scopus 로고
    • 2+ fluorescent probe: Solvent effects on modulation sensing ability
    • 2+ fluorescent probe: solvent effects on modulation sensing ability Dalton Trans 41 2012 831 838
    • (2012) Dalton Trans , vol.41 , pp. 831-838
    • Zhao, C.1    Zhang, Y.2    Feng, P.3    Cao, J.4
  • 11
    • 80054746217 scopus 로고    scopus 로고
    • Regioselective synthesis of 5-Monostyryl and 2-Tetracyanobutadiene BODIPY dyes
    • S. Niu, G. Ulrich, P. Retailleau, and R. Ziessel Regioselective synthesis of 5-Monostyryl and 2-Tetracyanobutadiene BODIPY dyes Org Lett 13 2011 4996 4999
    • (2011) Org Lett , vol.13 , pp. 4996-4999
    • Niu, S.1    Ulrich, G.2    Retailleau, P.3    Ziessel, R.4
  • 13
    • 0035127109 scopus 로고    scopus 로고
    • A highly efficient sensor molecule emitting in the near infrared (NIR): 3,5-distyryl-8-(p-dimethylaminophenyl)difluoroboradiaza-s-indacene
    • K. Rurack, M. Kollmannsberger, and J. Daub A highly efficient sensor molecule emitting in the near infrared (NIR): 3,5-distyryl-8-(p- dimethylaminophenyl)difluoroboradiaza-s-indacene New J Chem 25 2001 289 292
    • (2001) New J Chem , vol.25 , pp. 289-292
    • Rurack, K.1    Kollmannsberger, M.2    Daub, J.3
  • 14
    • 2942552704 scopus 로고    scopus 로고
    • Difluorobora-s-diazaindacene dyes as highly selective dosimetric reagents for fluoride anions
    • A. Coskun, and E. Akkaya Difluorobora-s-diazaindacene dyes as highly selective dosimetric reagents for fluoride anions Tetrahedron Lett 45 2004 4947 4949
    • (2004) Tetrahedron Lett , vol.45 , pp. 4947-4949
    • Coskun, A.1    Akkaya, E.2
  • 15
    • 33744781284 scopus 로고    scopus 로고
    • Solvent and pH dependent fluorescent properties of a dimethylaminostyryl borondipyrromethene dye in solution
    • M. Baruah, W. Qin, C. Flors, J. Hofkens, R.A.L. Vallée, and D. Beljonne Solvent and pH dependent fluorescent properties of a dimethylaminostyryl borondipyrromethene dye in solution J Phys Chem A 110 2006 5998 6009
    • (2006) J Phys Chem A , vol.110 , pp. 5998-6009
    • Baruah, M.1    Qin, W.2    Flors, C.3    Hofkens, J.4    Vallée, R.A.L.5    Beljonne, D.6
  • 16
    • 33747761914 scopus 로고    scopus 로고
    • Photophysical properties of an on/off fluorescent pH indicator excitable with visible light based on a borondipyrromethene-linked phenol
    • W. Qin, M. Baruah, W.M. De Borggraeve, and N. Boens Photophysical properties of an on/off fluorescent pH indicator excitable with visible light based on a borondipyrromethene-linked phenol J Photochem Photobiol A: Chem 183 2006 190 197
    • (2006) J Photochem Photobiol A: Chem , vol.183 , pp. 190-197
    • Qin, W.1    Baruah, M.2    De Borggraeve, W.M.3    Boens, N.4
  • 17
    • 80052834503 scopus 로고    scopus 로고
    • Rational design, synthesis, and spectroscopic and photophysical properties of a visible-light-excitable, ratiometric, fluorescent near-neutral pH indicator based on BODIPY
    • N. Boens, W. Qin, M. Baruah, W.M. De Borggraeve, A. Filarowski, and N. Smisdom Rational design, synthesis, and spectroscopic and photophysical properties of a visible-light-excitable, ratiometric, fluorescent near-neutral pH indicator based on BODIPY Chem Eur J 17 2011 10924 10934
    • (2011) Chem Eur J , vol.17 , pp. 10924-10934
    • Boens, N.1    Qin, W.2    Baruah, M.3    De Borggraeve, W.M.4    Filarowski, A.5    Smisdom, N.6
  • 18
    • 33846114719 scopus 로고    scopus 로고
    • Convenient method to access new 4,4-Dialkoxy- and 4,4-Diaryloxy-diaza-s- indacene dyes: Synthesis and spectroscopic evaluation
    • C. Tahtaoui, C. Thomas, F. Rohmer, P. Klotz, G. Duportail, and Y. Mely Convenient method to access new 4,4-Dialkoxy- and 4,4-Diaryloxy-diaza-s-indacene dyes: synthesis and spectroscopic evaluation J Org Chem 72 2007 269 272
    • (2007) J Org Chem , vol.72 , pp. 269-272
    • Tahtaoui, C.1    Thomas, C.2    Rohmer, F.3    Klotz, P.4    Duportail, G.5    Mely, Y.6
  • 19
    • 33746903538 scopus 로고    scopus 로고
    • Synthesis and photophysical properties of borondipyrromethene dyes bearing aryl substituents at the boron center
    • C. Goze, G. Ulrich, L. Mallon, B. Allen, A. Harriman, and R. Ziessel Synthesis and photophysical properties of borondipyrromethene dyes bearing aryl substituents at the boron center J Am Chem Soc 128 2006 10231 10239
    • (2006) J Am Chem Soc , vol.128 , pp. 10231-10239
    • Goze, C.1    Ulrich, G.2    Mallon, L.3    Allen, B.4    Harriman, A.5    Ziessel, R.6
  • 20
    • 79958776438 scopus 로고    scopus 로고
    • Water-Soluble phosphonate-substituted BODIPY derivatives with tunable emission channels
    • T. Bura, and R. Ziessel Water-Soluble phosphonate-substituted BODIPY derivatives with tunable emission channels Org Lett 13 2011 3072 3075
    • (2011) Org Lett , vol.13 , pp. 3072-3075
    • Bura, T.1    Ziessel, R.2
  • 22
    • 75749111320 scopus 로고    scopus 로고
    • Borondipyrromethene dyes with pentane-2,4-dione anchors
    • J.-H. Olivier, A. Haefele, P. Retailleau, and R. Ziessel Borondipyrromethene dyes with pentane-2,4-dione anchors Org Lett 12 2010 408 411
    • (2010) Org Lett , vol.12 , pp. 408-411
    • Olivier, J.-H.1    Haefele, A.2    Retailleau, P.3    Ziessel, R.4
  • 23
    • 52649090831 scopus 로고    scopus 로고
    • Tailoring the properties of Boron-Dipyrromethene dyes with acetylenic functions at the 2,6,8 and 4-B substitution positions
    • L. Bonardi, G. Ulrich, and R. Ziessel Tailoring the properties of Boron-Dipyrromethene dyes with acetylenic functions at the 2,6,8 and 4-B substitution positions Org Lett 10 2008 2183 2186
    • (2008) Org Lett , vol.10 , pp. 2183-2186
    • Bonardi, L.1    Ulrich, G.2    Ziessel, R.3
  • 24
    • 33947160119 scopus 로고    scopus 로고
    • Convenient synthesis of green Diisoindolodithienylpyrromethene-Dialkynyl borane dyes
    • S. Goeb, and R. Ziessel Convenient synthesis of green Diisoindolodithienylpyrromethene-Dialkynyl borane dyes Org Lett 9 2007 737 740
    • (2007) Org Lett , vol.9 , pp. 737-740
    • Goeb, S.1    Ziessel, R.2
  • 25
    • 33750040001 scopus 로고    scopus 로고
    • Unusual fluorescent monomeric and dimeric dialkynyl dipyrromethene-borane complexes
    • C. Goze, G. Ulrich, and R. Ziessel Unusual fluorescent monomeric and dimeric dialkynyl dipyrromethene-borane complexes Org Lett 8 2006 4445 4448
    • (2006) Org Lett , vol.8 , pp. 4445-4448
    • Goze, C.1    Ulrich, G.2    Ziessel, R.3
  • 26
    • 70349467631 scopus 로고    scopus 로고
    • Length dependence for intramolecular energy transfer in three- and four-color donor-spacer-Acceptor arrays
    • A. Harriman, L.J. Mallon, K.J. Elliot, A. Haefele, G. Ulrich, and R. Ziessel Length dependence for intramolecular energy transfer in three- and four-color donor-spacer-Acceptor arrays J Am Chem Soc 131 2009 13375 13386
    • (2009) J Am Chem Soc , vol.131 , pp. 13375-13386
    • Harriman, A.1    Mallon, L.J.2    Elliot, K.J.3    Haefele, A.4    Ulrich, G.5    Ziessel, R.6
  • 27
    • 33747752533 scopus 로고    scopus 로고
    • Rapid energy transfer in cascade-type BODIPY dyes
    • A. Harriman, G. Izzet, and R. Ziessel Rapid energy transfer in cascade-type BODIPY dyes J Am Chem Soc 128 2006 10868 10875
    • (2006) J Am Chem Soc , vol.128 , pp. 10868-10875
    • Harriman, A.1    Izzet, G.2    Ziessel, R.3
  • 28
    • 33750392902 scopus 로고    scopus 로고
    • Palladium-catalyzed coupling reactions for the functionalization of BODIPY dyes with fluorescence spanning the visible spectrum
    • T. Rohand, W. Qin, N. Boens, and W. Dehaen Palladium-catalyzed coupling reactions for the functionalization of BODIPY dyes with fluorescence spanning the visible spectrum Eur J Org Chem 20 2006 4658 4663
    • (2006) Eur J Org Chem , vol.20 , pp. 4658-4663
    • Rohand, T.1    Qin, W.2    Boens, N.3    Dehaen, W.4
  • 29
    • 80054107166 scopus 로고    scopus 로고
    • 1,7-Disubstituted boron dipyrromethene (BODIPY) dyes: Synthesis and spectroscopic properties
    • V. Leen, D. Miscoria, S. Yin, A. Filarowski, J.M. Ngongo, and M. Van der Auweraer 1,7-Disubstituted boron dipyrromethene (BODIPY) dyes: synthesis and spectroscopic properties J Org Chem 76 2011 8168 8176
    • (2011) J Org Chem , vol.76 , pp. 8168-8176
    • Leen, V.1    Miscoria, D.2    Yin, S.3    Filarowski, A.4    Ngongo, J.M.5    Van Der Auweraer, M.6
  • 30
    • 31344478344 scopus 로고    scopus 로고
    • Time-resolved infrared dynamics of C-F bond activation by a tungsten metal-carbonyl
    • T. Kim, J. Castro, A. Loudet, J. Jiao, R. Hochstrasser, and K. Burgess Time-resolved infrared dynamics of C-F bond activation by a tungsten metal-carbonyl J Phys Chem B 110 2006 20 27
    • (2006) J Phys Chem B , vol.110 , pp. 20-27
    • Kim, T.1    Castro, J.2    Loudet, A.3    Jiao, J.4    Hochstrasser, R.5    Burgess, K.6
  • 32
    • 34548850885 scopus 로고    scopus 로고
    • Boron dipyrromethene analogs with phenyl, styryl, and ethynylphenyl substituents:synthesis, photophysics, electrochemistry, and quantum-chemical calculations
    • W. Qin, T. Rohand, W. Dehaen, J.N. Clifford, K. Driesen, and D. Beljonne Boron dipyrromethene analogs with phenyl, styryl, and ethynylphenyl substituents:synthesis, photophysics, electrochemistry, and quantum-chemical calculations J Phys Chem A 111 2007 8588 8597
    • (2007) J Phys Chem A , vol.111 , pp. 8588-8597
    • Qin, W.1    Rohand, T.2    Dehaen, W.3    Clifford, J.N.4    Driesen, K.5    Beljonne, D.6
  • 33
    • 70349459754 scopus 로고    scopus 로고
    • β-Formyl-BODIPYs from the Vilsmeier-Haack reaction
    • L. Jiao, C. Yu, J. Li, Z. Wang, M. Wu, and E. Hao β-Formyl-BODIPYs from the Vilsmeier-Haack reaction J Org Chem 74 2009 7525 7528
    • (2009) J Org Chem , vol.74 , pp. 7525-7528
    • Jiao, L.1    Yu, C.2    Li, J.3    Wang, Z.4    Wu, M.5    Hao, E.6
  • 34
    • 41149110285 scopus 로고    scopus 로고
    • Syntheses and spectral properties of functionalized, water-soluble BODIPY derivatives
    • L. Li, J. Han, B. Nguyen, and K. Burgess Syntheses and spectral properties of functionalized, water-soluble BODIPY derivatives J Org Chem 73 2008 1963 1970
    • (2008) J Org Chem , vol.73 , pp. 1963-1970
    • Li, L.1    Han, J.2    Nguyen, B.3    Burgess, K.4
  • 35
    • 24644451949 scopus 로고    scopus 로고
    • Highly efficient and photostable photosensitizer based on BODIPY chromophore
    • T. Yogo, Y. Urano, Y. Ishitsuka, F. Maniwa, and T. Nagano Highly efficient and photostable photosensitizer based on BODIPY chromophore J Am Chem Soc 127 2005 12162 12163
    • (2005) J Am Chem Soc , vol.127 , pp. 12162-12163
    • Yogo, T.1    Urano, Y.2    Ishitsuka, Y.3    Maniwa, F.4    Nagano, T.5
  • 36
    • 79958002791 scopus 로고    scopus 로고
    • A targetable fluorescent sensor reveals that copper-deficient SCO1 and SCO2 patient cells prioritize mitochondrial copper homeostasis
    • S.C. Dodani, S.C. Leary, P.A. Cobine, D.R. Winge, and C.J. Chang A targetable fluorescent sensor reveals that copper-deficient SCO1 and SCO2 patient cells prioritize mitochondrial copper homeostasis J Am Chem Soc 133 2011 8606 8616
    • (2011) J Am Chem Soc , vol.133 , pp. 8606-8616
    • Dodani, S.C.1    Leary, S.C.2    Cobine, P.A.3    Winge, D.R.4    Chang, C.J.5
  • 37
    • 77950394708 scopus 로고    scopus 로고
    • Visualizing ascorbate-triggered release of labile copper within living cells using a ratiometric fluorescent sensor
    • D.W. Domaille, L. Zeng, and C.J. Chang Visualizing ascorbate-triggered release of labile copper within living cells using a ratiometric fluorescent sensor J Am Chem Soc 132 2010 1194 1195
    • (2010) J Am Chem Soc , vol.132 , pp. 1194-1195
    • Domaille, D.W.1    Zeng, L.2    Chang, C.J.3
  • 38
    • 26644452991 scopus 로고    scopus 로고
    • A highly potassium-selective ratiometric fluorescent indicator based on BODIPY Azacrown ether excitable with visible light
    • M. Baruah, W. Qin, R.A.L. Vallée, D. Beljonne, T. Rohand, and W. Dehaen A highly potassium-selective ratiometric fluorescent indicator based on BODIPY Azacrown ether excitable with visible light Org Lett 7 2005 4377 4380
    • (2005) Org Lett , vol.7 , pp. 4377-4380
    • Baruah, M.1    Qin, W.2    Vallée, R.A.L.3    Beljonne, D.4    Rohand, T.5    Dehaen, W.6
  • 39
    • 77953119120 scopus 로고    scopus 로고
    • Conjugated polymers that respond to oxidation with increased emission
    • E.L. Dane, S.B. King, and T.M. Swager Conjugated polymers that respond to oxidation with increased emission J Am Chem Soc 132 2010 7758 7768
    • (2010) J Am Chem Soc , vol.132 , pp. 7758-7768
    • Dane, E.L.1    King, S.B.2    Swager, T.M.3
  • 40
    • 67650292728 scopus 로고    scopus 로고
    • Fluorescent signaling based on sulfoxide profluorophores: Application to the visual detection of the explosive TATP
    • S. Malashikhin, and N.S. Finney Fluorescent signaling based on sulfoxide profluorophores: application to the visual detection of the explosive TATP J Am Chem Soc 130 2008 12846 12847
    • (2008) J Am Chem Soc , vol.130 , pp. 12846-12847
    • Malashikhin, S.1    Finney, N.S.2
  • 41
    • 79960216043 scopus 로고    scopus 로고
    • Multistimuli responsive micelles formed by a Tetrathiafulvalene- functionalized amphiphile
    • X.J. Wang, L.B. Xing, F. Wang, G.X. Wang, B. Chen, and C.H. Tung multistimuli responsive micelles formed by a Tetrathiafulvalene-functionalized amphiphile Langmuir 27 2011 8665 8671
    • (2011) Langmuir , vol.27 , pp. 8665-8671
    • Wang, X.J.1    Xing, L.B.2    Wang, F.3    Wang, G.X.4    Chen, B.5    Tung, C.H.6
  • 43
    • 12044255356 scopus 로고
    • Disulfide bond formation in peptides by dimethyl sulfoxide. Scope and applications
    • J.P. Tam, C.R. Wu, W. Liu, and J.W. Zhang Disulfide bond formation in peptides by dimethyl sulfoxide. Scope and applications J Am Chem Soc 113 1991 6657 6662
    • (1991) J Am Chem Soc , vol.113 , pp. 6657-6662
    • Tam, J.P.1    Wu, C.R.2    Liu, W.3    Zhang, J.W.4
  • 44
    • 0141508049 scopus 로고    scopus 로고
    • Recent developments in the synthesis and utilization of chiral sulfoxides
    • I. Fernández, and N. Khiar Recent developments in the synthesis and utilization of chiral sulfoxides Chem Rev 103 2003 3651 3706
    • (2003) Chem Rev , vol.103 , pp. 3651-3706
    • Fernández, I.1    Khiar, N.2
  • 45
    • 11944251609 scopus 로고
    • Applications of sulfoxides to asymmetric synthesis of biologically active compounds
    • M.C. Carreno Applications of sulfoxides to asymmetric synthesis of biologically active compounds Chem Rev 95 1995 1717 1760
    • (1995) Chem Rev , vol.95 , pp. 1717-1760
    • Carreno, M.C.1
  • 46
    • 0011242466 scopus 로고
    • Dimethyl sulfoxide oxidations
    • W.W. Epstein, and F.W. Sweat Dimethyl sulfoxide oxidations Chem Rev 67 1967 247 260
    • (1967) Chem Rev , vol.67 , pp. 247-260
    • Epstein, W.W.1    Sweat, F.W.2
  • 47
    • 0009398516 scopus 로고
    • Oxidation of 2-chloroethyl sulfides to sulfoxides by dimethyl sulfoxide
    • F.L. Hsu, L.L. Szafraniec, W.T. Beaudry, and Y.C. Yang Oxidation of 2-chloroethyl sulfides to sulfoxides by dimethyl sulfoxide J Org Chem 55 1990 4153 4155
    • (1990) J Org Chem , vol.55 , pp. 4153-4155
    • Hsu, F.L.1    Szafraniec, L.L.2    Beaudry, W.T.3    Yang, Y.C.4
  • 48
    • 0001110135 scopus 로고
    • Reactions of thiols with sulfoxides. I. Scope of the reaction and synthetic applications
    • T.J. Wallace Reactions of thiols with sulfoxides. I. Scope of the reaction and synthetic applications J Am Chem Soc 86 1964 2018 2021
    • (1964) J Am Chem Soc , vol.86 , pp. 2018-2021
    • Wallace, T.J.1
  • 49
    • 0000443850 scopus 로고
    • Reactions of thiols with sulfoxides. II. Kinetics and mechanistic implications
    • T.J. Wallace, and J.J. Mahon Reactions of thiols with sulfoxides. II. Kinetics and mechanistic implications J Am Chem Soc 86 1964 4099 4103
    • (1964) J Am Chem Soc , vol.86 , pp. 4099-4103
    • Wallace, T.J.1    Mahon, J.J.2
  • 50
    • 0001644418 scopus 로고
    • Reactions of thiols with sulfoxides. III. Catalysis by acids and bases
    • T.J. Wallace, and J.J. Mahon Reactions of thiols with sulfoxides. III. Catalysis by acids and bases J Org Chem 30 1965 1502 1506
    • (1965) J Org Chem , vol.30 , pp. 1502-1506
    • Wallace, T.J.1    Mahon, J.J.2
  • 51
    • 36148962893 scopus 로고    scopus 로고
    • A highly selective fluorescent probe for thiophenols
    • W. Jiang, Q. Fu, H. Fan, J. Ho, and W. Wang A highly selective fluorescent probe for thiophenols Angew Chem Int Ed 46 2007 8445 8448
    • (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
  • 52
    • 77949378021 scopus 로고    scopus 로고
    • Rational design of a highly selective and sensitive fluorescent PET probe for discrimination of thiophenols and aliphatic thiols
    • W. Jiang, Y. Cao, Y. Liu, and W. Wang Rational design of a highly selective and sensitive fluorescent PET probe for discrimination of thiophenols and aliphatic thiols Chem Commun 46 2010 1944 1946
    • (2010) Chem Commun , vol.46 , pp. 1944-1946
    • Jiang, W.1    Cao, Y.2    Liu, Y.3    Wang, W.4
  • 53
    • 76949101068 scopus 로고    scopus 로고
    • A highly sensitive fluorescent probe for detection of benzenethiols in environmental samples and living cells
    • W. Lin, L. Long, and W. Tan A highly sensitive fluorescent probe for detection of benzenethiols in environmental samples and living cells Chem Commun 46 2010 1503 1505
    • (2010) Chem Commun , vol.46 , pp. 1503-1505
    • Lin, W.1    Long, L.2    Tan, W.3
  • 54
    • 79952099827 scopus 로고    scopus 로고
    • Development of an Indole-based boron-dipyrromethene fluorescent probe for benzenethiols
    • C. Zhao, Y. Zhou, Q. Lin, L. Zhu, P. Feng, and Y. Zhang Development of an Indole-based boron-dipyrromethene fluorescent probe for benzenethiols J Phys Chem B 115 2011 642 647
    • (2011) J Phys Chem B , vol.115 , pp. 642-647
    • Zhao, C.1    Zhou, Y.2    Lin, Q.3    Zhu, L.4    Feng, P.5    Zhang, Y.6
  • 56
    • 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
    • (1998) J Phys Chem A , vol.102 , pp. 10211-10220
    • Kollmannsberger, M.1    Rurack, K.2    Resch-Genger, U.3    Daub, J.4
  • 57
    • 77954189093 scopus 로고    scopus 로고
    • Generalized solvent scales as a tool for investigating solventdependence of spectroscopic and kinetic parameters. Application to fluorescent BODIPY dyes
    • A. Filarowski, M. Kluba, K. Cieslik-Boczula, A. Koll, A. Kochel, and L. Pandey Generalized solvent scales as a tool for investigating solventdependence of spectroscopic and kinetic parameters. Application to fluorescent BODIPY dyes Photochem Photobiol Sci 9 2010 996 1008
    • (2010) Photochem Photobiol Sci , vol.9 , pp. 996-1008
    • Filarowski, A.1    Kluba, M.2    Cieslik-Boczula, K.3    Koll, A.4    Kochel, A.5    Pandey, L.6
  • 58
    • 0035936236 scopus 로고    scopus 로고
    • 2SO: Relevance to photostereomutation
    • 2SO: relevance to photostereomutation J Phys Chem A 105 2001 10588 10595
    • (2001) J Phys Chem A , vol.105 , pp. 10588-10595
    • Cubbage, J.W.1    Jenks, W.S.2
  • 59
    • 0035951587 scopus 로고    scopus 로고
    • Photophysics and photostereomutation of aryl methyl sulfoxides
    • W. Lee, and W.S. Jencks Photophysics and photostereomutation of aryl methyl sulfoxides J Org Chem 66 2001 474 480
    • (2001) J Org Chem , vol.66 , pp. 474-480
    • Lee, W.1    Jencks, W.S.2
  • 60
    • 0037139536 scopus 로고    scopus 로고
    • Evidence for a nonradical pathway in the photoracemization of aryl sulfoxides
    • B.W. Vos, and W.S. Jencks Evidence for a nonradical pathway in the photoracemization of aryl sulfoxides J Am Chem Soc 124 2002 2544 2547
    • (2002) J Am Chem Soc , vol.124 , pp. 2544-2547
    • Vos, B.W.1    Jencks, W.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.