메뉴 건너뛰기




Volumn 117, Issue 28, 2013, Pages 14723-14730

Molecular origins of dye aggregation and complex formation effects in coumarin 343

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGEN; HYDROGEN BONDS; KNOWLEDGE BASED SYSTEMS; ORGANIC SOLVENTS; SOLAR CELLS; SOLVENTS;

EID: 84962339705     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/jp4024266     Document Type: Article
Times cited : (59)

References (45)
  • 1
    • 33746330437 scopus 로고    scopus 로고
    • What Can You Learn from a Molecular Probe? New Insights on the Behavior of C343 in Homogeneous Solutions and AOT Reverse Micelles
    • Correa, N. M.; Levinger, N. E. What Can You Learn from a Molecular Probe? New Insights on the Behavior of C343 in Homogeneous Solutions and AOT Reverse Micelles J. Phys. Chem. B 2006, 110, 13050-13061
    • (2006) J. Phys. Chem. B , vol.110 , pp. 13050-13061
    • Correa, N.M.1    Levinger, N.E.2
  • 4
    • 0037473596 scopus 로고    scopus 로고
    • 2 Solar Cells Based on Novel Coumarin Dyes
    • 2 Solar Cells Based on Novel Coumarin Dyes Sol. Energy Mater. Sol. Cells 2003, 77, 89-103
    • (2003) Sol. Energy Mater. Sol. Cells , vol.77 , pp. 89-103
    • Hara, K.1
  • 7
    • 0037015760 scopus 로고    scopus 로고
    • Effect of Trap States on Interfacial Electron Transfer between Molecular Absorbates and Semiconductor Nanoparticles
    • Hao, E.; Anderson, N. A.; Asbury, J. B.; Lian, T. Effect of Trap States on Interfacial Electron Transfer between Molecular Absorbates and Semiconductor Nanoparticles J. Phys. Chem. B 2002, 106, 10191-10198
    • (2002) J. Phys. Chem. B , vol.106 , pp. 10191-10198
    • Hao, E.1    Anderson, N.A.2    Asbury, J.B.3    Lian, T.4
  • 8
    • 0038697807 scopus 로고    scopus 로고
    • Design of New Coumarin Dyes Having Thiophene Moieties for Highly Efficient Organic-dye-sensitized Solar Cells
    • Hara, K.; Kurashige, M.; Dan-oh, Y.; Kasada, C.; Shinpo, A.; Suga, S.; Sayama, K.; Arakawa, H. Design of New Coumarin Dyes Having Thiophene Moieties for Highly Efficient Organic-dye-sensitized Solar Cells New J. Chem. 2003, 27, 783-785
    • (2003) New J. Chem. , vol.27 , pp. 783-785
    • Hara, K.1    Kurashige, M.2    Dan-Oh, Y.3    Kasada, C.4    Shinpo, A.5    Suga, S.6    Sayama, K.7    Arakawa, H.8
  • 9
    • 0016484758 scopus 로고
    • New Coumarin Dyes with Rigidized Structure for Flashlamp-pumped Dye Lasers
    • Reynolds, G. A.; Drexhage, K. H. New Coumarin Dyes with Rigidized Structure for Flashlamp-pumped Dye Lasers Opt. Commun. 1975, 13, 222-225
    • (1975) Opt. Commun. , vol.13 , pp. 222-225
    • Reynolds, G.A.1    Drexhage, K.H.2
  • 10
    • 0141731326 scopus 로고    scopus 로고
    • Enhanced Förster Resonance Energy Transfer in Electrostatically Self-Assembled Multilayer Films Made from New Fluorescently Labeled Polycations
    • Baussard, J.-F.; Habib-Jiwan, J.-L.; Laschewsky, A. Enhanced Förster Resonance Energy Transfer in Electrostatically Self-Assembled Multilayer Films Made from New Fluorescently Labeled Polycations Langmuir 2003, 19, 7963-7969
    • (2003) Langmuir , vol.19 , pp. 7963-7969
    • Baussard, J.-F.1    Habib-Jiwan, J.-L.2    Laschewsky, A.3
  • 11
    • 84962436409 scopus 로고    scopus 로고
    • Time-dependent Density Functional Theory Investigation of the Ground and Excited States of Coumarins 102, 152, 153, and 343
    • Cave, R. J.; Castner, E. W., Jr. Time-dependent Density Functional Theory Investigation of the Ground and Excited States of Coumarins 102, 152, 153, and 343 J. Phys. Chem. A 2002, 106, 12117-12123
    • (2002) J. Phys. Chem. A , vol.106 , pp. 12117-12123
    • Cave, R.J.1    Castner Jr., E.W.2
  • 12
    • 84859226503 scopus 로고    scopus 로고
    • Theoretical Studies on Absorption, Emission, and Resonance Raman Spectra of Coumarin 343 Isomers
    • Wu, W.; Cao, Z.; Zhao, Y. Theoretical Studies on Absorption, Emission, and Resonance Raman Spectra of Coumarin 343 Isomers J. Chem. Phys. 2012, 136, 114305
    • (2012) J. Chem. Phys. , vol.136 , pp. 114305
    • Wu, W.1    Cao, Z.2    Zhao, Y.3
  • 14
    • 0037058081 scopus 로고    scopus 로고
    • Theoretical Investigation of the Ground and Excited States of Coumarin 151 and Coumarin 120
    • Cave, R. J.; Burke, K.; Castner, E. W., Jr Theoretical Investigation of the Ground and Excited States of Coumarin 151 and Coumarin 120 J. Phys. Chem. A 2002, 106, 9294-9305
    • (2002) J. Phys. Chem. A , vol.106 , pp. 9294-9305
    • Cave, R.J.1    Burke, K.2    Jr., W.C.E.3
  • 17
    • 84880155503 scopus 로고    scopus 로고
    • Solvent Effects on the UV-vis Absorption and Emission of Optoelectronic Coumarins: A Comparison of Three Empirical Solvatochromic Models
    • 10.1021/jp310397z
    • Liu, X.; Cole, J. M.; Low, K. S. Solvent Effects on the UV-vis Absorption and Emission of Optoelectronic Coumarins: a Comparison of Three Empirical Solvatochromic Models. J. Phys. Chem. C 2013, 117, 10.1021/jp310397z.
    • (2013) J. Phys. Chem. C , vol.117
    • Liu, X.1    Cole, J.M.2    Low, K.S.3
  • 18
    • 0001273546 scopus 로고    scopus 로고
    • Solvent Effects on Electronic Transitions in Several Coumarins
    • Moog, R. S.; Davis, W. W.; Ostrowski, S. G.; Wilson, G. L. Solvent Effects on Electronic Transitions in Several Coumarins Chem. Phys. Lett. 1999, 299, 265-271
    • (1999) Chem. Phys. Lett. , vol.299 , pp. 265-271
    • Moog, R.S.1    Davis, W.W.2    Ostrowski, S.G.3    Wilson, G.L.4
  • 19
    • 7444270887 scopus 로고    scopus 로고
    • Solvent Effects on Electronic Transitions of Highly Dipolar Dyes: A Comparison of Three Approaches
    • Moog, R. S.; Kim, D. D.; Oberle, J. J.; Ostrowski, S. G. Solvent Effects on Electronic Transitions of Highly Dipolar Dyes: a Comparison of Three Approaches J. Phys. Chem. A 2004, 108, 9294-9301
    • (2004) J. Phys. Chem. A , vol.108 , pp. 9294-9301
    • Moog, R.S.1    Kim, D.D.2    Oberle, J.J.3    Ostrowski, S.G.4
  • 20
    • 70450206724 scopus 로고    scopus 로고
    • Gaussian Inc. Wallingford, CT
    • Frisch, M. J.; Gaussian 09; Gaussian Inc.: Wallingford, CT, 2009.
    • (2009) Gaussian 09
    • Frisch, M.J.1
  • 21
    • 33751157732 scopus 로고
    • Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Fields
    • Stephens, P. J.; Devlin, F. J.; Chabalowski, C. F.; Frisch, M. J. Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Fields J. Phys. Chem. 1994, 98, 11623-11627
    • (1994) J. Phys. Chem. , vol.98 , pp. 11623-11627
    • Stephens, P.J.1    Devlin, F.J.2    Chabalowski, C.F.3    Frisch, M.J.4
  • 22
    • 0000189651 scopus 로고
    • Density-functional Thermochemistry. III. the Role of Exact Exchange
    • Becke, A. D. Density-functional Thermochemistry. III. the Role of Exact Exchange J. Chem. Phys. 1993, 98, 5648-5652
    • (1993) J. Chem. Phys. , vol.98 , pp. 5648-5652
    • Becke, A.D.1
  • 23
    • 0345491105 scopus 로고
    • Development of the Colle-salvetti Correlation-energy Formula into a Functional of the Electron Density
    • Lee, C.; Yang, W.; Parr, R. G. Development of the Colle-salvetti Correlation-energy Formula into a Functional of the Electron Density Phys. Rev. B 1988, 37, 785-789
    • (1988) Phys. Rev. B , vol.37 , pp. 785-789
    • Lee, C.1    Yang, W.2    Parr, R.G.3
  • 24
    • 26844534384 scopus 로고
    • Self-consistent Molecular-orbital Methods. XX. Basis Set for Correlated Wave-functions
    • Krishnan, R.; Binkley, J. S.; Seeger, R.; Pople, J. A. Self-consistent Molecular-orbital Methods. XX. Basis Set for Correlated Wave-functions J. Chem. Phys. 1980, 72, 650-654
    • (1980) J. Chem. Phys. , vol.72 , pp. 650-654
    • Krishnan, R.1    Binkley, J.S.2    Seeger, R.3    Pople, J.A.4
  • 25
    • 0141509423 scopus 로고
    • Contracted Gaussian Basis Sets for Molecular Calculations. I. Second Row Atoms, Z= 11-18
    • McLean, A. D.; Chandler, G. S. Contracted Gaussian Basis Sets for Molecular Calculations. I. Second Row Atoms, Z= 11-18 J. Chem. Phys. 1980, 72, 5639-5648
    • (1980) J. Chem. Phys. , vol.72 , pp. 5639-5648
    • McLean, A.D.1    Chandler, G.S.2
  • 26
    • 84890021933 scopus 로고
    • The Calculation of Small Molecular Interactions by the Differences of Separate Total Energies. Some Procedures with Reduced Errors
    • Boys, S. F.; Bernardi, F. The Calculation of Small Molecular Interactions by the Differences of Separate Total Energies. Some Procedures with Reduced Errors Mol. Phys. 1970, 19, 553-566
    • (1970) Mol. Phys. , vol.19 , pp. 553-566
    • Boys, S.F.1    Bernardi, F.2
  • 27
    • 30244527819 scopus 로고    scopus 로고
    • How Does Basis Set Superposition Error Change the Potential Surfaces for Hydrogen-bonded Dimers?
    • Simon, S.; Duran, M.; Dannenberg, J. J. How Does Basis Set Superposition Error Change the Potential Surfaces for Hydrogen-bonded Dimers? J. Chem. Phys. 1996, 105, 11024-11031
    • (1996) J. Chem. Phys. , vol.105 , pp. 11024-11031
    • Simon, S.1    Duran, M.2    Dannenberg, J.J.3
  • 29
    • 0000262725 scopus 로고    scopus 로고
    • Reaction Field Treatment of Charge Penetration
    • Chipman, D. M. Reaction Field Treatment of Charge Penetration J. Chem. Phys. 2000, 112, 5558-5565
    • (2000) J. Chem. Phys. , vol.112 , pp. 5558-5565
    • Chipman, D.M.1
  • 30
    • 84946893847 scopus 로고
    • Electrostatic Interaction of a Solute with a Continuum. A Direct Utilizaion of Ab Initio Molecular Potentials for the Prevision of Solvent Effects
    • Miertus, S.; Scrocco, E.; Tomasi, J. Electrostatic Interaction of a Solute with a Continuum. A Direct Utilizaion of Ab Initio Molecular Potentials for the Prevision of Solvent Effects Chem. Phys. 1981, 55, 117-129
    • (1981) Chem. Phys. , vol.55 , pp. 117-129
    • Miertus, S.1    Scrocco, E.2    Tomasi, J.3
  • 31
    • 79953237097 scopus 로고    scopus 로고
    • J-Aggregates: From Serendipitous Discovery to Supramolecular Engineering of Functional Dye Materials
    • Würthner, F.; Kaiser, T. E.; Saha-Möller, C. R. J-Aggregates: from Serendipitous Discovery to Supramolecular Engineering of Functional Dye Materials Angew. Chem., Int. Ed. 2011, 50, 3376-3410
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 3376-3410
    • Würthner, F.1    Kaiser, T.E.2    Saha-Möller, C.R.3
  • 32
    • 84880178963 scopus 로고    scopus 로고
    • The Molecular Origins of Optoelectronic Properties in Coumarins 343, 314T, 445 and 522B
    • DOI: 10.1021/jp400614e
    • Liu, X.; Cole, J. M.; Waddell, P. G.; Lin, T.-C.; McKechnie, S. The Molecular Origins of Optoelectronic Properties in Coumarins 343, 314T, 445 and 522B. J. Phys. Chem. C 2013, DOI: 10.1021/jp400614e.
    • (2013) J. Phys. Chem. C
    • Liu, X.1    Cole, J.M.2    Waddell, P.G.3    Lin, T.-C.4    McKechnie, S.5
  • 33
    • 33847800055 scopus 로고
    • The Solvatochromic Comparison Method. I. the β-Scale of Solvent Hydrogen-bond Acceptor (HBA) Basicities
    • Kamlet, M. J.; Taft, R. The Solvatochromic Comparison Method. I. The β-Scale of Solvent Hydrogen-bond Acceptor (HBA) Basicities J. Am. Chem. Soc. 1976, 98, 377-383
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 377-383
    • Kamlet, M.J.1    Taft, R.2
  • 34
    • 33847797571 scopus 로고
    • The Solvatochromic Comparison Method. 2. the α-Scale of Solvent Hydrogen-bond Donor (HBD) Acidities
    • Taft, R.; Kamlet, M. J. The Solvatochromic Comparison Method. 2. The α-Scale of Solvent Hydrogen-bond Donor (HBD) Acidities J. Am. Chem. Soc. 1976, 98, 2886-2894
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2886-2894
    • Taft, R.1    Kamlet, M.J.2
  • 35
    • 0039726458 scopus 로고
    • The Solvatochromic Comparison Method. 6. the π* Scale of Solvent Polarities
    • Kamlet, M. J.; Abboud, J. L.; Taft, R. The Solvatochromic Comparison Method. 6. The π* Scale of Solvent Polarities J. Am. Chem. Soc. 1977, 99, 6027-6038
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 6027-6038
    • Kamlet, M.J.1    Abboud, J.L.2    Taft, R.3
  • 36
    • 0041573625 scopus 로고
    • Linear Solvation Energy Relationships. 23. A Comprehensive Collection of the Solvatochromic Parameters π*, α, and β, and Some Methods for Simplifying the Generalized Solvatochromic Equation
    • Kamlet, M. J.; Abboud, J. L. M.; Abraham, M. H.; Taft, R. Linear Solvation Energy Relationships. 23. A Comprehensive Collection of the Solvatochromic Parameters π*, α, and β, and Some Methods for Simplifying the Generalized Solvatochromic Equation J. Org. Chem. 1983, 48, 2877-2887
    • (1983) J. Org. Chem. , vol.48 , pp. 2877-2887
    • Kamlet, M.J.1    Abboud, J.L.M.2    Abraham, M.H.3    Taft, R.4
  • 37
    • 84962406372 scopus 로고    scopus 로고
    • Department of Chemistry, National University of Rio Cuarto, Argentina
    • June
    • Correa, M. Department of Chemistry, National University of Rio Cuarto, Argentina. Personal communication, June 2012.
    • (2012) Personal Communication
    • Correa, M.1
  • 39
    • 0006469110 scopus 로고
    • The Properties of Organic Liquids That Are Relevant to Their Use as Solvating Solvents
    • Marcus, Y. The Properties of Organic Liquids That Are Relevant to Their Use as Solvating Solvents Chem. Soc. Rev. 1993, 22, 409-416
    • (1993) Chem. Soc. Rev. , vol.22 , pp. 409-416
    • Marcus, Y.1
  • 40
  • 41
    • 0000106306 scopus 로고
    • Nuclear Magnetic Resonance of Hydroxyl and Amido, Protons of Oligosaccharides in Aqueous Solution: Evidence for a Strong Intramolecular Hydrogen Bond in Sialic Acid Residues
    • Poppe, L.; Van Halbeek, H. Nuclear Magnetic Resonance of Hydroxyl and Amido, Protons of Oligosaccharides in Aqueous Solution: Evidence for a Strong Intramolecular Hydrogen Bond in Sialic Acid Residues J. Am. Chem. Soc. 1991, 113, 363-365
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 363-365
    • Poppe, L.1    Van Halbeek, H.2
  • 42
    • 0026839242 scopus 로고
    • The Solution Conformation of Sialyl-α(2→6)-lactose Studied by Modern NMR Techniques and Monte Carlo Simulations
    • Poppe, L.; Stuike-Prill, R.; Meyer, B.; Van Halbeek, H. The Solution Conformation of Sialyl-α(2→6)-lactose Studied by Modern NMR Techniques and Monte Carlo Simulations J. Biomol. NMR 1992, 2, 109-136
    • (1992) J. Biomol. NMR , vol.2 , pp. 109-136
    • Poppe, L.1    Stuike-Prill, R.2    Meyer, B.3    Van Halbeek, H.4
  • 43
    • 3042567738 scopus 로고    scopus 로고
    • Conformational Study of a Guaiacyl β-o-4 Lignin Model Compound by NMR. Examination of Intramolecular Hydrogen Bonding Interactions and Conformational Flexibility in Solution
    • Besombes, S.; Utille, J. P.; Mazeau, K.; Robert, D.; Taravel, F. R. Conformational Study of a Guaiacyl β-o-4 Lignin Model Compound by NMR. Examination of Intramolecular Hydrogen Bonding Interactions and Conformational Flexibility in Solution Magn. Reson. Chem. 2004, 42, 337-347
    • (2004) Magn. Reson. Chem. , vol.42 , pp. 337-347
    • Besombes, S.1    Utille, J.P.2    Mazeau, K.3    Robert, D.4    Taravel, F.R.5
  • 44
    • 0030835189 scopus 로고    scopus 로고
    • DMSO Solvent Induced Photochemistry in Highly Photostable Compounds. the Role of Intermolecular Hydrogen Bonding
    • McGarry, P. F.; Jockusch, S.; Fujiwara, Y.; Kaprinidis, N. A.; Turro, N. J. DMSO Solvent Induced Photochemistry in Highly Photostable Compounds. the Role of Intermolecular Hydrogen Bonding J. Phys. Chem. A 1997, 101, 764-767
    • (1997) J. Phys. Chem. A , vol.101 , pp. 764-767
    • McGarry, P.F.1    Jockusch, S.2    Fujiwara, Y.3    Kaprinidis, N.A.4    Turro, N.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.