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Volumn 118, Issue 9, 2014, Pages 1576-1594

8-HaloBODIPYs and Their 8-(C, N, O, S) substituted analogues: Solvent dependent UV-Vis spectroscopy, variable temperature NMR, crystal structure determination, and quantum chemical calculations

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION AND EMISSIONS; CRYSTAL STRUCTURE DETERMINATION; FLUORESCENCE LIFETIMES; FLUORESCENCE QUANTUM YIELD; QUANTUM CHEMICAL CALCULATIONS; QUANTUM-CHEMICAL CALCULATION; SPECTROSCOPIC PROPERTY; VARIABLE-TEMPERATURE NMR;

EID: 84897744998     PISSN: 10895639     EISSN: 15205215     Source Type: Journal    
DOI: 10.1021/jp412132y     Document Type: Article
Times cited : (60)

References (92)
  • 1
    • 84982338521 scopus 로고
    • Difluorboryl-Komplexe von Di- und Tripyrrylmethenen
    • Treibs, A.; Kreuzer, F.-H. Difluorboryl-Komplexe von Di- und Tripyrrylmethenen Liebigs Ann. Chem. 1968, 718, 208-223
    • (1968) Liebigs Ann. Chem. , vol.718 , pp. 208-223
    • Treibs, A.1    Kreuzer, F.-H.2
  • 2
    • 36849053388 scopus 로고    scopus 로고
    • BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties
    • Loudet, A.; Burgess, K. BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties Chem. Rev. 2007, 107, 4891-4932
    • (2007) Chem. Rev. , vol.107 , pp. 4891-4932
    • Loudet, A.1    Burgess, K.2
  • 3
    • 40849107127 scopus 로고    scopus 로고
    • The Chemistry of Fluorescent BODIPY Dyes: Versatility Unsurpassed
    • Ulrich, G.; Ziessel, R.; Harriman, A. The Chemistry of Fluorescent BODIPY Dyes: Versatility Unsurpassed Angew. Chem., Int. Ed. 2008, 47, 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
    • Boens, N.; Leen, V.; Dehaen, W. Fluorescent Indicators Based on BODIPY Chem. Soc. Rev. 2012, 41, 1130-1172
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 1130-1172
    • Boens, N.1    Leen, V.2    Dehaen, W.3
  • 6
    • 80052834503 scopus 로고    scopus 로고
    • Rational Design and Spectroscopic Properties of a Visible Light Excitable, Ratiometric, Brightly Fluorescent, Near-Neutral pH Indicator Based on the BODIPY Fluorophore
    • Boens, N.; Qin, W.; Baruah, M.; De Borggraeve, W. M.; Filarowski, A.; Smisdom, N.; Ameloot, M.; Crovetto, L.; Talavera, E. M.; Alvarez-Pez, J. M. Rational Design and Spectroscopic Properties of a Visible Light Excitable, Ratiometric, Brightly Fluorescent, Near-Neutral pH Indicator Based on the BODIPY Fluorophore Chem.-Eur. J. 2011, 17, 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    Ameloot, M.7    Crovetto, L.8    Talavera, E.M.9    Alvarez-Pez, J.M.10
  • 9
    • 79955522955 scopus 로고    scopus 로고
    • 4,4′-Difluoro-4-bora-3a,4a-diaza- s -indacenes (BODIPYs) as Components of Novel Light Active Materials
    • Benstead, M.; Mehl, G. H.; Boyle, R. W. 4,4′-Difluoro-4-bora-3a,4a- diaza- s -indacenes (BODIPYs) as Components of Novel Light Active Materials Tetrahedron 2011, 67, 3573-3601
    • (2011) Tetrahedron , vol.67 , pp. 3573-3601
    • Benstead, M.1    Mehl, G.H.2    Boyle, R.W.3
  • 13
    • 33746175423 scopus 로고    scopus 로고
    • Light Harvesting and Efficient Energy Transfer in a Boron-dipyrrin (BODIPY) Functionalized Perylenediimide Derivative
    • Yilmaz, M. D.; Bozdemir, O. A.; Akkaya, E. U. Light Harvesting and Efficient Energy Transfer in a Boron-dipyrrin (BODIPY) Functionalized Perylenediimide Derivative Org. Lett. 2006, 8, 2871-2873
    • (2006) Org. Lett. , vol.8 , pp. 2871-2873
    • Yilmaz, M.D.1    Bozdemir, O.A.2    Akkaya, E.U.3
  • 14
    • 33747752533 scopus 로고    scopus 로고
    • Rapid Energy Transfer in Cascade-Type BODIPY Dyes
    • Harriman, A.; Izzet, G.; Ziessel, R. Rapid Energy Transfer in Cascade-Type BODIPY Dyes J. Am. Chem. Soc. 2006, 128, 10868-10875
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 10868-10875
    • Harriman, A.1    Izzet, G.2    Ziessel, R.3
  • 15
    • 61349140603 scopus 로고    scopus 로고
    • Highly Efficient Energy Transfer in Subphthalocyanine-BODIPY Conjugates
    • Liu, J.-Y.; Yeung, H.-S.; Xu, W.; Li, X.; Ng, D. K. P. Highly Efficient Energy Transfer in Subphthalocyanine-BODIPY Conjugates Org. Lett. 2008, 10, 5421-5424
    • (2008) Org. Lett. , vol.10 , pp. 5421-5424
    • Liu, J.-Y.1    Yeung, H.-S.2    Xu, W.3    Li, X.4    Ng, D.K.P.5
  • 16
    • 66749164879 scopus 로고    scopus 로고
    • Electronic Energy Transfer in Molecular Dyads Built Around Boron-Ethyne-Substituted Subphthalocyanines
    • Ziessel, R.; Ulrich, G.; Elliott, K. J.; Harriman, A. Electronic Energy Transfer in Molecular Dyads Built Around Boron-Ethyne-Substituted Subphthalocyanines Chem.-Eur. J. 2009, 15, 4980-4984
    • (2009) Chem. - Eur. J. , vol.15 , pp. 4980-4984
    • Ziessel, R.1    Ulrich, G.2    Elliott, K.J.3    Harriman, A.4
  • 17
    • 60649102072 scopus 로고    scopus 로고
    • Boradiazaindacene (BODIPY)-based building blocks for the construction of energy transfer cassettes
    • Barin, G.; Yilmaz, M. D.; Akkaya, E. U. Boradiazaindacene (BODIPY)-based building blocks for the construction of energy transfer cassettes Tetrahedron Lett. 2009, 50, 1738-1740
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1738-1740
    • Barin, G.1    Yilmaz, M.D.2    Akkaya, E.U.3
  • 20
    • 79952126048 scopus 로고    scopus 로고
    • Convenient and Efficient FRET Platform Featuring a Rigid Biphenyl Spacer between Rhodamine and BODIPY: Transformation of 'Turn-On' Sensors into Ratiometric Ones with Dual Emission
    • Yu, H.; Xiao, Y.; Guo, H.; Qian, X. Convenient and Efficient FRET Platform Featuring a Rigid Biphenyl Spacer between Rhodamine and BODIPY: Transformation of 'Turn-On' Sensors into Ratiometric Ones with Dual Emission Chem.-Eur. J. 2011, 17, 3179-3191
    • (2011) Chem. - Eur. J. , vol.17 , pp. 3179-3191
    • Yu, H.1    Xiao, Y.2    Guo, H.3    Qian, X.4
  • 22
    • 84055187718 scopus 로고    scopus 로고
    • Synthesis and photophysical properties of covalently linked boron dipyrromethene dyads
    • Khan, T. K.; Shaikh, M. S.; Ravikanth, M. Synthesis and photophysical properties of covalently linked boron dipyrromethene dyads Dyes Pigm. 2012, 94, 66-73
    • (2012) Dyes Pigm. , vol.94 , pp. 66-73
    • Khan, T.K.1    Shaikh, M.S.2    Ravikanth, M.3
  • 23
    • 24344476979 scopus 로고    scopus 로고
    • Charge Separation in a Nonfluorescent Donor-Acceptor Dyad Derived from Boron Dipyrromethene Dye, Leading to Photocurrent Generation
    • Hattori, S.; Ohkubo, K.; Urano, Y.; Sunahara, H.; Nagano, T.; Wada, Y.; Tkachenko, N. V.; Lemmetyinen, H.; Fukuzumi, S. Charge Separation in a Nonfluorescent Donor-Acceptor Dyad Derived from Boron Dipyrromethene Dye, Leading to Photocurrent Generation J. Phys. Chem. B. 2005, 109, 15368-15375
    • (2005) J. Phys. Chem. B. , vol.109 , pp. 15368-15375
    • Hattori, S.1    Ohkubo, K.2    Urano, Y.3    Sunahara, H.4    Nagano, T.5    Wada, Y.6    Tkachenko, N.V.7    Lemmetyinen, H.8    Fukuzumi, S.9
  • 24
    • 59949105338 scopus 로고    scopus 로고
    • A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells
    • Erten-Ela, S.; Yilmaz, M. D.; Icli, B.; Dede, Y.; Icli, S.; Akkaya, E. U. A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells Org. Lett. 2008, 10, 3299-3302
    • (2008) Org. Lett. , vol.10 , pp. 3299-3302
    • Erten-Ela, S.1    Yilmaz, M.D.2    Icli, B.3    Dede, Y.4    Icli, S.5    Akkaya, E.U.6
  • 25
    • 67649577252 scopus 로고    scopus 로고
    • Color Tuning in New Metal-Free Organic Sensitizers (BODIPYs) for Dye-Sensitized Solar Cells
    • Kumaresan, D.; Thummel, R. P.; Bura, T.; Ulrich, G.; Ziessel, R. Color Tuning in New Metal-Free Organic Sensitizers (BODIPYs) for Dye-Sensitized Solar Cells Chem.-Eur. J. 2009, 15, 6335-6339
    • (2009) Chem. - Eur. J. , vol.15 , pp. 6335-6339
    • Kumaresan, D.1    Thummel, R.P.2    Bura, T.3    Ulrich, G.4    Ziessel, R.5
  • 26
    • 77749274609 scopus 로고    scopus 로고
    • 2 Sensitization with a BODIPY-Porphyrin Antenna System
    • 2 Sensitization with a BODIPY-Porphyrin Antenna System Langmuir 2010, 26, 3760-3765
    • (2010) Langmuir , vol.26 , pp. 3760-3765
    • Lee, C.Y.1    Hupp, J.T.2
  • 28
    • 79961051691 scopus 로고    scopus 로고
    • Panchromatic Trichromophoric Sensitizer for Dye-Sensitized Solar Cells Using Antenna Effect
    • Warnan, J.; Buchet, F.; Pellegrin, Y.; Blart, E.; Odobel, F. Panchromatic Trichromophoric Sensitizer for Dye-Sensitized Solar Cells Using Antenna Effect Org. Lett. 2011, 13, 3944-3947
    • (2011) Org. Lett. , vol.13 , pp. 3944-3947
    • Warnan, J.1    Buchet, F.2    Pellegrin, Y.3    Blart, E.4    Odobel, F.5
  • 29
    • 80855144822 scopus 로고    scopus 로고
    • Towards Unimolecular Luminescent Solar Concentrators: BODIPY-Based Dendritic Energy-Transfer Cascade with Panchromatic Absorption and Monochromatized Emission
    • Bozdemir, O. A.; Erbas-Cakmak, S.; Ekiz, O. O.; Dana, A.; Akkaya, E. U. Towards Unimolecular Luminescent Solar Concentrators: BODIPY-Based Dendritic Energy-Transfer Cascade with Panchromatic Absorption and Monochromatized Emission Angew. Chem., Int. Ed. 2011, 50, 10907-10912
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 10907-10912
    • Bozdemir, O.A.1    Erbas-Cakmak, S.2    Ekiz, O.O.3    Dana, A.4    Akkaya, E.U.5
  • 30
    • 84871548948 scopus 로고    scopus 로고
    • Synthesis of Meso -Halogenated BODIPYs and Access to Meso -Substituted Analogues
    • Leen, V.; Yuan, P.; Wang, L.; Boens, N.; Dehaen, W. Synthesis of Meso -Halogenated BODIPYs and Access to Meso -Substituted Analogues Org. Lett. 2012, 14, 6150-6153
    • (2012) Org. Lett. , vol.14 , pp. 6150-6153
    • Leen, V.1    Yuan, P.2    Wang, L.3    Boens, N.4    Dehaen, W.5
  • 31
    • 66349095435 scopus 로고    scopus 로고
    • Toward a Generalized Treatment of the Solvent Effect Based on Four Empirical Scales: Dipolarity (SdP, a New Scale), Polarizability (SP), Acidity (SA), and Basicity (SB) of the Medium
    • Catalán, J. Toward a Generalized Treatment of the Solvent Effect Based on Four Empirical Scales: Dipolarity (SdP, a New Scale), Polarizability (SP), Acidity (SA), and Basicity (SB) of the Medium J. Phys. Chem. B 2009, 113, 5951-5960
    • (2009) J. Phys. Chem. B , vol.113 , pp. 5951-5960
    • Catalán, J.1
  • 33
    • 27844573003 scopus 로고    scopus 로고
    • Photophysical Properties of BODIPY-Derived Hydroxyaryl Fluorescent pH Probes in Solution
    • Qin, W.; Baruah, M.; Stefan, A.; Van der Auweraer, M.; Boens, N. Photophysical Properties of BODIPY-Derived Hydroxyaryl Fluorescent pH Probes in Solution ChemPhysChem 2005, 6, 2343-2351
    • (2005) ChemPhysChem , vol.6 , pp. 2343-2351
    • Qin, W.1    Baruah, M.2    Stefan, A.3    Van Der Auweraer, M.4    Boens, N.5
  • 35
    • 34548850885 scopus 로고    scopus 로고
    • Boron Dipyrromethene Analogs with Phenyl, Styryl, and Ethynylphenyl Substituents: Synthesis, Photophysics, Electrochemistry, and Quantum-Chemical Calculations
    • Qin, W.; Rohand, T.; Dehaen, W.; Clifford, J. N.; Driesen, K.; Beljonne, D.; Van Averbeke, B.; Van der Auweraer, M.; Boens, N. Boron Dipyrromethene Analogs with Phenyl, Styryl, and Ethynylphenyl Substituents: Synthesis, Photophysics, Electrochemistry, and Quantum-Chemical Calculations J. Phys. Chem. A 2007, 111, 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    Van Averbeke, B.7    Van Der Auweraer, M.8    Boens, N.9
  • 37
    • 77956482245 scopus 로고    scopus 로고
    • Synthesis, Spectroscopy, Crystal Structure Determination, and Quantum Chemical Calculations of BODIPY Dyes with Increasing Conformational Restriction and Concomitant Red-Shifted Visible Absorption and Fluorescence Spectra
    • Leen, V.; Qin, W.; Yang, W.; Cui, J.; Xu, C.; Tang, X.; Liu, W.; Robeyns, K.; Van Meervelt, L.; Beljonne, D. Synthesis, Spectroscopy, Crystal Structure Determination, and Quantum Chemical Calculations of BODIPY Dyes with Increasing Conformational Restriction and Concomitant Red-Shifted Visible Absorption and Fluorescence Spectra Chem. Asian J. 2010, 5, 2016-2026
    • (2010) Chem. Asian J. , vol.5 , pp. 2016-2026
    • Leen, V.1    Qin, W.2    Yang, W.3    Cui, J.4    Xu, C.5    Tang, X.6    Liu, W.7    Robeyns, K.8    Van Meervelt, L.9    Beljonne, D.10
  • 39
    • 79961139992 scopus 로고    scopus 로고
    • 2- and 3-Monohalogenated BODIPY Dyes and Their Functionalized Analogues: Synthesis and Spectroscopy
    • Leen, V.; Leemans, T.; Boens, N.; Dehaen, W. 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
  • 43
    • 0001203111 scopus 로고
    • Fluorescence and Absorption Spectroscopic Properties of Dipyrrometheneboron Difluoride (BODIPY) Derivatives in Liquids, Lipid Membranes, and Proteins
    • Karolin, J.; Johansson, L. B.-Å.; Strandberg, L.; Ny, T. Fluorescence and Absorption Spectroscopic Properties of Dipyrrometheneboron Difluoride (BODIPY) Derivatives in Liquids, Lipid Membranes, and Proteins J. Am. Chem. Soc. 1994, 116, 7801-7806
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 7801-7806
    • Karolin, J.1    Johansson, L.B.-Å.2    Strandberg, L.3    Ny, T.4
  • 44
    • 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
    • Kollmannsberger, M.; Rurack, K.; Resch-Genger, U.; Daub, J. 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 1998, 102, 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
  • 45
    • 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
    • Rurack, K.; Kollmannsberger, M.; Daub, J. A Highly Efficient Sensor Molecule Emitting in the Near Infrared (NIR): 3,5-distyryl-8-(p -dimethylaminophenyl)difluoroboradiaza- s -indacene New. J. Chem. 2001, 25, 289-292
    • (2001) New. J. Chem. , vol.25 , pp. 289-292
    • Rurack, K.1    Kollmannsberger, M.2    Daub, J.3
  • 46
    • 0035910598 scopus 로고    scopus 로고
    • Molecular Switching in the Near Infrared (NIR) with a Functionalized Boron-Dipyrromethene Dye
    • Rurack, K.; Kollmannsberger, M.; Daub, J. Molecular Switching in the Near Infrared (NIR) with a Functionalized Boron-Dipyrromethene Dye Angew. Chem., Int. Ed. 2001, 40, 385-387
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 385-387
    • Rurack, K.1    Kollmannsberger, M.2    Daub, J.3
  • 47
    • 0037116520 scopus 로고    scopus 로고
    • Dimers of Dipyrrometheneboron Difluoride (BODIPY) with Light Spectroscopic Applications in Chemistry and Biology
    • Bergström, F.; Mikhalyov, I.; Hägglöf, P.; Wortmann, R.; Ny, T.; Johansson, L. B.-Å. Dimers of Dipyrrometheneboron Difluoride (BODIPY) with Light Spectroscopic Applications in Chemistry and Biology J. Am. Chem. Soc. 2002, 124, 196-204
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 196-204
    • Bergström, F.1    Mikhalyov, I.2    Hägglöf, P.3    Wortmann, R.4    Ny, T.5    Johansson, L.B.-Å.6
  • 50
    • 33746298183 scopus 로고    scopus 로고
    • Distyryl-boradiazaindacenes: Facile synthesis of novel near IR emitting fluorophores
    • Dost, Z.; Atilgan, S.; Akkaya, E. U. Distyryl-boradiazaindacenes: facile synthesis of novel near IR emitting fluorophores Tetrahedron 2006, 62, 8484-8488
    • (2006) Tetrahedron , vol.62 , pp. 8484-8488
    • Dost, Z.1    Atilgan, S.2    Akkaya, E.U.3
  • 51
    • 35548939515 scopus 로고    scopus 로고
    • Synthesis and Spectral Properties of Cholesterol- and FTY720-Containing Boron Dipyrromethene Dyes
    • Li, Z.; Bittman, R. Synthesis and Spectral Properties of Cholesterol- and FTY720-Containing Boron Dipyrromethene Dyes J. Org. Chem. 2007, 72, 8376-8382
    • (2007) J. Org. Chem. , vol.72 , pp. 8376-8382
    • Li, Z.1    Bittman, R.2
  • 52
    • 39049119009 scopus 로고    scopus 로고
    • A Monostyryl-boradiazaindacene (BODIPY) Derivative as Colorimetric and Fluorescent Probe for Cyanide Ions
    • Ekmekci, Z.; Yilmaz, M. D.; Akkaya, E. U. A Monostyryl-boradiazaindacene (BODIPY) Derivative as Colorimetric and Fluorescent Probe for Cyanide Ions Org. Lett. 2008, 10, 461-464
    • (2008) Org. Lett. , vol.10 , pp. 461-464
    • Ekmekci, Z.1    Yilmaz, M.D.2    Akkaya, E.U.3
  • 53
    • 41149110285 scopus 로고    scopus 로고
    • Syntheses and Spectral Properties of Functionalized, Water-Soluble BODIPY Derivatives
    • Li, L.; Han, J.; Nguyen, B.; Burgess, K. Syntheses and Spectral Properties of Functionalized, Water-Soluble BODIPY Derivatives J. Org. Chem. 2008, 73, 1963-1970
    • (2008) J. Org. Chem. , vol.73 , pp. 1963-1970
    • Li, L.1    Han, J.2    Nguyen, B.3    Burgess, K.4
  • 54
    • 70349459754 scopus 로고    scopus 로고
    • β-Formyl-BODIPYs from the Vilsmeier-Haack Reaction
    • Jiao, L.; Yu, C.; Li, J.; Wang, Z.; Wu, M.; Hao, E. β-Formyl-BODIPYs from the Vilsmeier-Haack Reaction J. Org. Chem. 2009, 74, 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
  • 55
    • 84055217260 scopus 로고    scopus 로고
    • Regioselective Stepwise Bromination of Boron Dipyrromethene (BODIPY) Dyes
    • Jiao, L.; Pang, W.; Zhou, J.; Wei, Y.; Mu, X.; Bai, G.; Hao, E. Regioselective Stepwise Bromination of Boron Dipyrromethene (BODIPY) Dyes J. Org. Chem. 2011, 76, 9988-9996
    • (2011) J. Org. Chem. , vol.76 , pp. 9988-9996
    • Jiao, L.1    Pang, W.2    Zhou, J.3    Wei, Y.4    Mu, X.5    Bai, G.6    Hao, E.7
  • 56
    • 64849115797 scopus 로고    scopus 로고
    • The Synthesis and Crystal Structure of Unsubstituted 4,4-difluoro-4-bora- 3a,4a-diaza- s -indacene (BODIPY)
    • Tram, K.; Yan, H.; Jenkins, H. A.; Vassiliev, S.; Bruce, D. The Synthesis and Crystal Structure of Unsubstituted 4,4-difluoro-4-bora-3a,4a-diaza- s -indacene (BODIPY) Dyes Pigm. 2009, 82, 392-395
    • (2009) Dyes Pigm. , vol.82 , pp. 392-395
    • Tram, K.1    Yan, H.2    Jenkins, H.A.3    Vassiliev, S.4    Bruce, D.5
  • 57
    • 70349252287 scopus 로고    scopus 로고
    • Synthesis of the Core Compound of the BODIPY Dye Class: 4,4′-Difluoro-4-bora-(3a,4a)-diaza- s -indacene
    • Schmitt, A.; Hinkeldey, B.; Wild, M.; Jung, G. Synthesis of the Core Compound of the BODIPY Dye Class: 4,4′-Difluoro-4-bora-(3a,4a)-diaza- s -indacene J. Fluoresc. 2009, 19, 755-758
    • (2009) J. Fluoresc. , vol.19 , pp. 755-758
    • Schmitt, A.1    Hinkeldey, B.2    Wild, M.3    Jung, G.4
  • 58
    • 33646099627 scopus 로고    scopus 로고
    • Synthesis of 8-heteroatom-substituted 4,4-difluoro-4-bora-3a,4a-diaza- s -indacene Dyes (BODIPY)
    • Goud, T. V.; Tutar, A.; Biellmann, J.-F. Synthesis of 8-heteroatom-substituted 4,4-difluoro-4-bora-3a,4a-diaza- s -indacene Dyes (BODIPY) Tetrahedron 2006, 62, 5084-5091
    • (2006) Tetrahedron , vol.62 , pp. 5084-5091
    • Goud, T.V.1    Tutar, A.2    Biellmann, J.-F.3
  • 63
    • 84897697591 scopus 로고    scopus 로고
    • Ultrafast Emission Quenching in Perylene Diimides by Structure Rearrangement Induced Electron Transfer from their Substituents
    • In; Roeffaers, M. Hofkens, J. Department of Chemistry, Faculty of Science, KU Leuven: Leuven, Belgium
    • Kölle, P. Ultrafast Emission Quenching in Perylene Diimides by Structure Rearrangement Induced Electron Transfer from their Substituents. In Book of Abstracts ICP; Roeffaers, M.; Hofkens, J., Eds.; Department of Chemistry, Faculty of Science, KU Leuven: Leuven, Belgium, 2013; p 185.
    • (2013) Book of Abstracts ICP , pp. 185
    • Kölle, P.1
  • 64
    • 84862798438 scopus 로고    scopus 로고
    • A BODIPY-Based Reactive Probe for Ratiometric Fluorescence Sensing of Mercury Ions
    • Kim, D.; Yamamoto, K.; Ahn, K. H. A BODIPY-Based Reactive Probe for Ratiometric Fluorescence Sensing of Mercury Ions Tetrahedron 2012, 68, 5279-5282
    • (2012) Tetrahedron , vol.68 , pp. 5279-5282
    • Kim, D.1    Yamamoto, K.2    Ahn, K.H.3
  • 65
    • 84872695870 scopus 로고    scopus 로고
    • Meso -Alkoxy BODIPYs with a Good Balance between Larger Stokes Shifts and Higher Fluorescence Quantum Yields
    • Wang, L.; Zhang, Y.; Xiao, Y. meso -Alkoxy BODIPYs with a Good Balance between Larger Stokes Shifts and Higher Fluorescence Quantum Yields RSC Adv. 2013, 3, 2203-2206
    • (2013) RSC Adv. , vol.3 , pp. 2203-2206
    • Wang, L.1    Zhang, Y.2    Xiao, Y.3
  • 67
    • 84875334188 scopus 로고    scopus 로고
    • Meso -Alkynyl BODIPYs: Structure, Photoproperties, π-Extension, and Manipulation of Frontier Orbitals
    • Kusaka, S.; Sakamoto, R.; Kitagawa, Y.; Okumura, M.; Nishihara, H. meso -Alkynyl BODIPYs: Structure, Photoproperties, π-Extension, and Manipulation of Frontier Orbitals Chem. Asian. J. 2013, 8, 723-727
    • (2013) Chem. Asian. J. , vol.8 , pp. 723-727
    • Kusaka, S.1    Sakamoto, R.2    Kitagawa, Y.3    Okumura, M.4    Nishihara, H.5
  • 68
    • 84883512184 scopus 로고    scopus 로고
    • Donor-Acceptor meso -Alkynylated Ferrocenyl BODIPYs: Synthesis, Structure, and Properties
    • Misra, R.; Dhokale, B.; Jadhav, T.; Mobin, S. M. Donor-Acceptor meso -Alkynylated Ferrocenyl BODIPYs: Synthesis, Structure, and Properties Dalton Trans. 2013, 42, 13658-13666
    • (2013) Dalton Trans. , vol.42 , pp. 13658-13666
    • Misra, R.1    Dhokale, B.2    Jadhav, T.3    Mobin, S.M.4
  • 69
    • 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
    • Bonardi, L.; Ulrich, G.; Ziessel, R. Tailoring the Properties of Boron-Dipyrromethene Dyes with Acetylenic Functions at the 2,6,8 and 4-B Substitution Positions Org. Lett. 2008, 10, 2183-2186
    • (2008) Org. Lett. , vol.10 , pp. 2183-2186
    • Bonardi, L.1    Ulrich, G.2    Ziessel, R.3
  • 70
    • 84876731111 scopus 로고    scopus 로고
    • Synthesis of Donor-Substituted meso -Phenyl and meso -Ethynylphenyl BODIPYs with Broad Absorption
    • Gräf, K.; Körzdörfer, T.; Kümmel, S.; Thelakkat, M. Synthesis of Donor-Substituted meso -Phenyl and meso -Ethynylphenyl BODIPYs with Broad Absorption New J. Chem. 2013, 37, 1417-1426
    • (2013) New J. Chem. , vol.37 , pp. 1417-1426
    • Gräf, K.1    Körzdörfer, T.2    Kümmel, S.3    Thelakkat, M.4
  • 72
    • 34147166057 scopus 로고    scopus 로고
    • Glossary of Terms Used in Photochemistry, 3rd ed.; IUPAC Recommendations 2006
    • Braslavsky, S. E. Glossary of Terms Used in Photochemistry, 3rd ed.; IUPAC Recommendations 2006 Pure Appl. Chem. 2007, 79, 293-465
    • (2007) Pure Appl. Chem. , vol.79 , pp. 293-465
    • Braslavsky, S.E.1
  • 73
    • 42449100481 scopus 로고    scopus 로고
    • Bright Ideas for Chemical Biology
    • Lavis, L. D.; Raines, R. T. Bright Ideas for Chemical Biology ACS Chem. Biol. 2008, 3, 142-155
    • (2008) ACS Chem. Biol. , vol.3 , pp. 142-155
    • Lavis, L.D.1    Raines, R.T.2
  • 75
    • 21844433172 scopus 로고    scopus 로고
    • Pitfalls and Their Remedies in Time-Resolved Fluorescence Spectroscopy and Microscopy
    • vandeVen, M.; Ameloot, M.; Valeur, B.; Boens, N. Pitfalls and Their Remedies in Time-Resolved Fluorescence Spectroscopy and Microscopy J. Fluoresc. 2005, 15, 377-413
    • (2005) J. Fluoresc. , vol.15 , pp. 377-413
    • Vandeven, M.1    Ameloot, M.2    Valeur, B.3    Boens, N.4
  • 77
    • 12344315145 scopus 로고    scopus 로고
    • Empirical Treatment of the Inductive and Dispersive Components of Solute-Solvent Interactions: The Solvent Polarizability (SP) Scale
    • Catalán, J.; Hopf, H. Empirical Treatment of the Inductive and Dispersive Components of Solute-Solvent Interactions: The Solvent Polarizability (SP) Scale Eur. J. Org. Chem. 2004, 4694-4702
    • (2004) Eur. J. Org. Chem. , pp. 4694-4702
    • Catalán, J.1    Hopf, H.2
  • 78
    • 0003443809 scopus 로고    scopus 로고
    • In; Wypych, G. ChemTec Publishing: Toronto - 616
    • Catalán, J. In Handbook of solvents; Wypych, G., Ed.; ChemTec Publishing: Toronto, 2001; pp 583-616.
    • (2001) Handbook of Solvents , pp. 583
    • Catalán, J.1
  • 79
    • 33748732072 scopus 로고    scopus 로고
    • A Generalized Solvent Acidity Scale: The Solvatochromism of o-tert -Butylstilbazolium Betaine Dye and Its Homomorph o, o ′-Di- tert -butylstilbazolium Betaine Dye
    • Catalán, J.; Díaz, C. A Generalized Solvent Acidity Scale: The Solvatochromism of o-tert -Butylstilbazolium Betaine Dye and Its Homomorph o, o ′-Di- tert -butylstilbazolium Betaine Dye Liebigs Ann. 1997, 1941-1949
    • (1997) Liebigs Ann. , pp. 1941-1949
    • Catalán, J.1    Díaz, C.2
  • 80
    • 1642549118 scopus 로고    scopus 로고
    • A Generalized Solvent Basicity Scale: The Solvatochromism of 5-Nitroindoline and Its Homomorph 1-Methyl-5-nitroindoline
    • Catalán, J.; Díaz, C.; López, V.; Pérez, P.; de Paz, J. L. G.; Rodriguez, J. G. A Generalized Solvent Basicity Scale: The Solvatochromism of 5-Nitroindoline and Its Homomorph 1-Methyl-5-nitroindoline Liebigs Ann. 1996, 1785-1794
    • (1996) Liebigs Ann. , pp. 1785-1794
    • Catalán, J.1    Díaz, C.2    López, V.3    Pérez, P.4    De Paz, J.L.G.5    Rodriguez, J.G.6
  • 81
    • 0042860391 scopus 로고
    • Nature of the Free Electron Model. The Simple Case of the Symmetric Polymethines
    • Kuhn, H.; Huber, W.; Handschig, G.; Martin, H.; Schäfer, F.; Bär, F. Nature of the Free Electron Model. The Simple Case of the Symmetric Polymethines J. Chem. Phys. 1960, 32, 467-469
    • (1960) J. Chem. Phys. , vol.32 , pp. 467-469
    • Kuhn, H.1    Huber, W.2    Handschig, G.3    Martin, H.4    Schäfer, F.5    Bär, F.6
  • 82
    • 84981781268 scopus 로고
    • Elektronengasmodell zur quantitativen Deutung der Lichtabsorption von organischen Farbstoffen II. Teil B. Störung des Elektronengases durch Heteroatome
    • Kuhn, H. Elektronengasmodell zur quantitativen Deutung der Lichtabsorption von organischen Farbstoffen II. Teil B. Störung des Elektronengases durch Heteroatome Helv. Chim. Acta 1951, 34, 2371-2402
    • (1951) Helv. Chim. Acta , vol.34 , pp. 2371-2402
    • Kuhn, H.1
  • 84
    • 33947440147 scopus 로고
    • Color and Constitution. II. Absorptions of Some Related Vinylene-Homologous Series
    • Brooker, L. G. S.; White, F. L.; Keyes, G. H. J.; Smyth, C. P.; Oesper, P. F. Color and Constitution. II. Absorptions of Some Related Vinylene-Homologous Series J. Am. Chem. Soc. 1941, 63, 3192-3203
    • (1941) J. Am. Chem. Soc. , vol.63 , pp. 3192-3203
    • Brooker, L.G.S.1    White, F.L.2    Keyes, G.H.J.3    Smyth, C.P.4    Oesper, P.F.5
  • 85
    • 33947435425 scopus 로고
    • Color and Constitution. V. The Absorption of Unsymmetrical Cyanines. Resonance as a Basis for a Classification of Dyes
    • Brooker, L. G. S.; Keyes, G. H. J.; Williams, W. W. Color and Constitution. V. The Absorption of Unsymmetrical Cyanines. Resonance as a Basis for a Classification of Dyes J. Am. Chem. Soc. 1942, 64, 199-210
    • (1942) J. Am. Chem. Soc. , vol.64 , pp. 199-210
    • Brooker, L.G.S.1    Keyes, G.H.J.2    Williams, W.W.3
  • 90
    • 0000238999 scopus 로고
    • Completely Numerical Calculations on Diatomic Molecules in the Local-Density Approximation
    • Becke, A. D. Completely Numerical Calculations on Diatomic Molecules in the Local-Density Approximation Phys. Rev. A 1986, 33, 2786-2788
    • (1986) Phys. Rev. A , vol.33 , pp. 2786-2788
    • Becke, A.D.1
  • 91
    • 0031553301 scopus 로고    scopus 로고
    • Evaluation of Solvent Effects in Isotropic and Anisotropic Dielectrics and in Ionic Solutions with a Unified Integral Equation Method: Theoretical Bases, Computational Implementation, and Numerical Applications
    • Mennucci, B.; Cancès, E.; Tomasi, J. Evaluation of Solvent Effects in Isotropic and Anisotropic Dielectrics and in Ionic Solutions with a Unified Integral Equation Method: Theoretical Bases, Computational Implementation, and Numerical Applications J. Phys. Chem. B 1997, 101, 10506-10517
    • (1997) J. Phys. Chem. B , vol.101 , pp. 10506-10517
    • Mennucci, B.1    Cancès, E.2    Tomasi, J.3
  • 92
    • 84875704143 scopus 로고    scopus 로고
    • QM/MM Excited State Molecular Dynamics and Fluorescence Spectroscopy of BODIPY
    • Briggs, E. A.; Besley, N. A.; Robinson, D. QM/MM Excited State Molecular Dynamics and Fluorescence Spectroscopy of BODIPY J. Phys. Chem. A 2013, 117, 2644-2650
    • (2013) J. Phys. Chem. A , vol.117 , pp. 2644-2650
    • Briggs, E.A.1    Besley, N.A.2    Robinson, D.3


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