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Volumn 119, Issue 51, 2015, Pages 28335-28346

Effect of Ethynyl Linkages on the Properties of the Derivatives of Triphenylamine and 1,8-Naphthalimide

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; CYCLIC VOLTAMMETRY; FLUORESCENCE; GLASS; GLASS TRANSITION; IONIZATION POTENTIAL;

EID: 84952950514     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/acs.jpcc.5b10163     Document Type: Article
Times cited : (53)

References (57)
  • 4
    • 34248326379 scopus 로고    scopus 로고
    • Organic Electronics and Optoelectronics
    • Forrest, S. R.; Thompson, M. E. Organic Electronics and Optoelectronics Chem. Rev. 2007, 107, 923-1386 10.1021/cr0501590
    • (2007) Chem. Rev. , vol.107 , pp. 923-1386
    • Forrest, S.R.1    Thompson, M.E.2
  • 5
    • 10344259627 scopus 로고    scopus 로고
    • Molecular Materials Across Fields: TTFs, Fullerenes and Acenes
    • Bendikov, M.; Wudl, F.; Perepichka, D. F. Molecular Materials Across Fields: TTFs, Fullerenes and Acenes Chem. Rev. 2004, 104, 4891-4945 10.1021/cr030666m
    • (2004) Chem. Rev. , vol.104 , pp. 4891-4945
    • Bendikov, M.1    Wudl, F.2    Perepichka, D.F.3
  • 6
    • 34248578376 scopus 로고    scopus 로고
    • Charge Carrier Transporting Molecular Materials and Their Applications in Devices
    • Shirota, Y.; Kageyama, H. Charge Carrier Transporting Molecular Materials and Their Applications in Devices Chem. Rev. 2007, 107, 953-1010 10.1021/cr050143+
    • (2007) Chem. Rev. , vol.107 , pp. 953-1010
    • Shirota, Y.1    Kageyama, H.2
  • 7
    • 77951529148 scopus 로고    scopus 로고
    • Conjugated Molecules with Fused Rings for Organic Field-Effect Transistors: Design, Synthesis and Applications
    • Wu, W.; Liu, Y.; Zhu, D. Conjugated Molecules with Fused Rings for Organic Field-Effect Transistors: Design, Synthesis and Applications Chem. Soc. Rev. 2010, 39, 1489-1502 10.1039/B813123F
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1489-1502
    • Wu, W.1    Liu, Y.2    Zhu, D.3
  • 8
    • 84860149992 scopus 로고    scopus 로고
    • Pyrene-Fluorene Hybrids Containing Acetylene Linkage as Color-Tunable Emitting Materials for Organic Light-Emitting Diodes
    • Thomas, K. R. J.; Kapoor, N.; Bolisetty, M. N. K. P.; Jou, J. H.; Chen, Y. L.; Jou, Y. C. Pyrene-Fluorene Hybrids Containing Acetylene Linkage as Color-Tunable Emitting Materials for Organic Light-Emitting Diodes J. Org. Chem. 2012, 77, 3921-3932 10.1021/jo300285v
    • (2012) J. Org. Chem. , vol.77 , pp. 3921-3932
    • Thomas, K.R.J.1    Kapoor, N.2    Bolisetty, M.N.K.P.3    Jou, J.H.4    Chen, Y.L.5    Jou, Y.C.6
  • 9
    • 0034512975 scopus 로고    scopus 로고
    • Progress with Light-Emitting Polymers
    • Bernius, M. T.; Inbasekaran, M.; O'Brien, J.; Wu, W. S. Progress with Light-Emitting Polymers Adv. Mater. 2000, 12, 1737-1750 10.1002/1521-4095(200012)12:23<1737::AID-ADMA1737>3.0.CO;2-N
    • (2000) Adv. Mater. , vol.12 , pp. 1737-1750
    • Bernius, M.T.1    Inbasekaran, M.2    O'Brien, J.3    Wu, W.S.4
  • 10
    • 84856888739 scopus 로고    scopus 로고
    • Processable Star-Shaped Molecules with Triphenylamine Core as Hole-Transporting Materials: Experimental and Theoretical Approach
    • Metri, N.; Sallenave, X.; Plesse, C.; Beouch, L.; Aubert, P. H.; Goubard, F.; Chevrot, C.; Sini, G. Processable Star-Shaped Molecules with Triphenylamine Core as Hole-Transporting Materials: Experimental and Theoretical Approach J. Phys. Chem. C 2012, 116, 3765-3772 10.1021/jp2098872
    • (2012) J. Phys. Chem. C , vol.116 , pp. 3765-3772
    • Metri, N.1    Sallenave, X.2    Plesse, C.3    Beouch, L.4    Aubert, P.H.5    Goubard, F.6    Chevrot, C.7    Sini, G.8
  • 11
    • 84874440641 scopus 로고    scopus 로고
    • Photophysical Properties of Isoelectronic Oligomers with Vinylene, Imine, Azine and Ethynylene Spacers Bearing Triphenylamine and Carbazole End-Groups
    • Grigoras, M.; Vacareanu, L.; Ivan, T.; Catargiu, A. M. Photophysical Properties of Isoelectronic Oligomers with Vinylene, Imine, Azine and Ethynylene Spacers Bearing Triphenylamine and Carbazole End-Groups Dyes Pigm. 2013, 98, 71-81 10.1016/j.dyepig.2013.01.025
    • (2013) Dyes Pigm. , vol.98 , pp. 71-81
    • Grigoras, M.1    Vacareanu, L.2    Ivan, T.3    Catargiu, A.M.4
  • 12
    • 84874165088 scopus 로고    scopus 로고
    • Red Emitting Solid State Fluorescent Triphenylamine Dyes: Synthesis, Photo-Physical Property and DFT Study
    • Gupta, V. D.; Tathe, A. B.; Padalkar, V. S.; Umape, P. G.; Sekar, N. Red Emitting Solid State Fluorescent Triphenylamine Dyes: Synthesis, Photo-Physical Property and DFT Study Dyes Pigm. 2013, 97, 429-439 10.1016/j.dyepig.2012.12.024
    • (2013) Dyes Pigm. , vol.97 , pp. 429-439
    • Gupta, V.D.1    Tathe, A.B.2    Padalkar, V.S.3    Umape, P.G.4    Sekar, N.5
  • 13
    • 77952377611 scopus 로고    scopus 로고
    • Molecular Design of Anthracene-Bridged Metal-Free Organic Dyes for Efficient Dye-Sensitized Solar Cells
    • Teng, C.; Yang, X. C.; Yang, C.; Li, S. F.; Cheng, M.; Hagfeldt, A.; Sun, L. C. Molecular Design of Anthracene-Bridged Metal-Free Organic Dyes for Efficient Dye-Sensitized Solar Cells J. Phys. Chem. C 2010, 114, 9101-9110 10.1021/jp101238k
    • (2010) J. Phys. Chem. C , vol.114 , pp. 9101-9110
    • Teng, C.1    Yang, X.C.2    Yang, C.3    Li, S.F.4    Cheng, M.5    Hagfeldt, A.6    Sun, L.C.7
  • 15
    • 84896959795 scopus 로고    scopus 로고
    • New Derivatives of Triphenylamine and Naphthalimide as Ambipolar Organic Semiconductors: Experimental and Theoretical Approach
    • Gudeika, D.; Grazulevicius, J. V.; Sini, G.; Bucinskas, A.; Jankauskas, V.; Miasojedovas, A.; Jursenas, S. New Derivatives of Triphenylamine and Naphthalimide as Ambipolar Organic Semiconductors: Experimental and Theoretical Approach Dyes Pigm. 2014, 106, 58-70 10.1016/j.dyepig.2014.02.023
    • (2014) Dyes Pigm. , vol.106 , pp. 58-70
    • Gudeika, D.1    Grazulevicius, J.V.2    Sini, G.3    Bucinskas, A.4    Jankauskas, V.5    Miasojedovas, A.6    Jursenas, S.7
  • 16
    • 0031069035 scopus 로고    scopus 로고
    • An Improved Experimental Determination of External Photoluminescence Quantum Efficiency
    • de Mello, J. C.; Wittmann, H. F.; Friend, R. H. An Improved Experimental Determination of External Photoluminescence Quantum Efficiency Adv. Mater. 1997, 9, 230-232 10.1002/adma.19970090308
    • (1997) Adv. Mater. , vol.9 , pp. 230-232
    • De Mello, J.C.1    Wittmann, H.F.2    Friend, R.H.3
  • 17
    • 0021410857 scopus 로고
    • Recommendations on Reporting Electrode Potentials in Nonaqueous Solvents (Recommendations 1983)
    • Gritzner, G.; Kuta, J. Recommendations on Reporting Electrode Potentials in Nonaqueous Solvents (Recommendations 1983) Pure Appl. Chem. 1984, 56, 461-466 10.1351/pac198456040461
    • (1984) Pure Appl. Chem. , vol.56 , pp. 461-466
    • Gritzner, G.1    Kuta, J.2
  • 18
    • 0001211694 scopus 로고
    • Ionization Potential of Organic Pigment Film by Atmospheric Photoelectron Emission Analysis
    • Miyamoto, E.; Yamaguchi, Y.; Yokoyama, M. Ionization Potential of Organic Pigment Film by Atmospheric Photoelectron Emission Analysis Electrophotography 1989, 28, 364-370
    • (1989) Electrophotography , vol.28 , pp. 364-370
    • Miyamoto, E.1    Yamaguchi, Y.2    Yokoyama, M.3
  • 19
    • 42349116897 scopus 로고    scopus 로고
    • Photoemission Measurement of Extremely Insulating Materials: Capacitive Photocurrent Detection in Photoelectron Yield Spectroscopy
    • Nakayama, Y.; Machida, S.; Tsunami, D.; Kimura, Y.; Niwano, M.; Noguchi, Y.; Ishii, H. Photoemission Measurement of Extremely Insulating Materials: Capacitive Photocurrent Detection in Photoelectron Yield Spectroscopy Appl. Phys. Lett. 2008, 92, 153306-153308 10.1063/1.2908888
    • (2008) Appl. Phys. Lett. , vol.92 , pp. 153306-153308
    • Nakayama, Y.1    Machida, S.2    Tsunami, D.3    Kimura, Y.4    Niwano, M.5    Noguchi, Y.6    Ishii, H.7
  • 20
    • 0011180578 scopus 로고    scopus 로고
    • The Discharge Kinetics of Negatively Charge Se Electrophotographic Layers
    • Montrimas, E.; Gaidelis, V.; Pazera, A. The Discharge Kinetics of Negatively Charge Se Electrophotographic Layers Lithuanian J. Phys. 1996, 6, 569-576
    • (1996) Lithuanian J. Phys. , vol.6 , pp. 569-576
    • Montrimas, E.1    Gaidelis, V.2    Pazera, A.3
  • 23
    • 70349789520 scopus 로고    scopus 로고
    • Symmetric and Unsymmetric Donor Functionalization Comparing Structural and Spectral Benefits of Chromophores for Dye-Sensitized Solar Cells
    • Hagberg, D. P.; Jiang, X.; Gabrielsson, E.; Linder, M.; Marinado, T.; Brinck, T.; Hagfeldt, A.; Sun, L. Symmetric and Unsymmetric Donor Functionalization Comparing Structural and Spectral Benefits of Chromophores for Dye-Sensitized Solar Cells J. Mater. Chem. 2009, 19, 7232-7238 10.1039/b911397p
    • (2009) J. Mater. Chem. , vol.19 , pp. 7232-7238
    • Hagberg, D.P.1    Jiang, X.2    Gabrielsson, E.3    Linder, M.4    Marinado, T.5    Brinck, T.6    Hagfeldt, A.7    Sun, L.8
  • 24
    • 0035366043 scopus 로고    scopus 로고
    • Synthesis and Properties of Novel Triphenylamine Polymers Containing Ethynyl and Aromatic Moieties
    • Kim, S. W.; Shim, S. C.; Kim, D. Y.; Kim, C. Y. Synthesis and Properties of Novel Triphenylamine Polymers Containing Ethynyl and Aromatic Moieties Synth. Met. 2001, 122, 363-368 10.1016/S0379-6779(00)00398-2
    • (2001) Synth. Met. , vol.122 , pp. 363-368
    • Kim, S.W.1    Shim, S.C.2    Kim, D.Y.3    Kim, C.Y.4
  • 25
    • 79955163647 scopus 로고    scopus 로고
    • Organic Dyes Incorporating Low-Band-Gap Chromophores Based on π-Extended Benzothiadiazole for Dye-Sensitized Solar Cells
    • Lee, D. H.; Lee, M. J.; Song, H. M.; Song, B. J.; Seo, K. D.; Pastore, M.; Anselmi, C.; Fantacci, S.; De Angelis, F.; Nazeeruddin, M. K. et al. Organic Dyes Incorporating Low-Band-Gap Chromophores Based on π-Extended Benzothiadiazole for Dye-Sensitized Solar Cells Dyes Pigm. 2011, 91, 192-198 10.1016/j.dyepig.2011.03.015
    • (2011) Dyes Pigm. , vol.91 , pp. 192-198
    • Lee, D.H.1    Lee, M.J.2    Song, H.M.3    Song, B.J.4    Seo, K.D.5    Pastore, M.6    Anselmi, C.7    Fantacci, S.8    De Angelis, F.9    Nazeeruddin, M.K.10
  • 26
    • 84864423758 scopus 로고    scopus 로고
    • Triphenylamine Derivatized Phenylacetylene Macrocycle with Large Two-Photon Absorption Cross-Section
    • Fang, Z.; Samoc, M.; Webster, R. D.; Samoc, A.; Lai, Y. H. Triphenylamine Derivatized Phenylacetylene Macrocycle with Large Two-Photon Absorption Cross-Section Tetrahedron Lett. 2012, 53, 4885-4888 10.1016/j.tetlet.2012.07.003
    • (2012) Tetrahedron Lett. , vol.53 , pp. 4885-4888
    • Fang, Z.1    Samoc, M.2    Webster, R.D.3    Samoc, A.4    Lai, Y.H.5
  • 27
    • 84871724798 scopus 로고    scopus 로고
    • Tunable Star-Shaped Triphenylamine Fluorophores for Fluorescence Quenching Detection and Identification of Nitro-Aromatic Explosives
    • Niamnont, N.; Kimpitak, N.; Wongravee, K.; Rashatasakhon, P.; Baldridge, K. K.; Siegel, J. S.; Sukwattanasinitt, M. Tunable Star-Shaped Triphenylamine Fluorophores for Fluorescence Quenching Detection and Identification of Nitro-Aromatic Explosives Chem. Commun. 2013, 49, 780-782 10.1039/C2CC34008A
    • (2013) Chem. Commun. , vol.49 , pp. 780-782
    • Niamnont, N.1    Kimpitak, N.2    Wongravee, K.3    Rashatasakhon, P.4    Baldridge, K.K.5    Siegel, J.S.6    Sukwattanasinitt, M.7
  • 28
    • 0042113153 scopus 로고
    • Self-Consistent Equations Including Exchange and Correlation Effects
    • Kohn, W.; Sham, L. Self-Consistent Equations Including Exchange and Correlation Effects Phys. Rev. 1965, 140, A1133-A1138 10.1103/PhysRev.140.A1133
    • (1965) Phys. Rev. , vol.140 , pp. A1133-A1138
    • Kohn, W.1    Sham, L.2
  • 29
    • 0345491105 scopus 로고
    • Development of the Colle-Salvetti Correlation-Energy Formula into a Functional of the Electron Density
    • Lee, C. T.; Yang, W. T.; Parr, R. G. Development of the Colle-Salvetti Correlation-Energy Formula into a Functional of the Electron Density Phys. Rev. B: Condens. Matter Mater. Phys. 1988, 37, 785-789 10.1103/PhysRevB.37.785
    • (1988) Phys. Rev. B: Condens. Matter Mater. Phys. , vol.37 , pp. 785-789
    • Lee, C.T.1    Yang, W.T.2    Parr, R.G.3
  • 30
    • 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 10.1063/1.464913
    • (1993) J. Chem. Phys. , vol.98 , pp. 5648-5652
    • Becke, A.D.1
  • 31
    • 55849117399 scopus 로고    scopus 로고
    • Long-Range Corrected Hybrid Density Functionals with Damped Atom-Atom Dispersion Corrections
    • Chai, J. D.; Head-Gordon, M. Long-Range Corrected Hybrid Density Functionals with Damped Atom-Atom Dispersion Corrections Phys. Chem. Chem. Phys. 2008, 10, 6615-6620 10.1039/b810189b
    • (2008) Phys. Chem. Chem. Phys. , vol.10 , pp. 6615-6620
    • Chai, J.D.1    Head-Gordon, M.2
  • 33
    • 33645944934 scopus 로고
    • Local Density-Functional Theory of Frequency-Dependent Linear Response
    • Gross, E. K. U.; Kohn, W. Local Density-Functional Theory of Frequency-Dependent Linear Response Phys. Rev. Lett. 1985, 55, 2850-2852 10.1103/PhysRevLett.55.2850
    • (1985) Phys. Rev. Lett. , vol.55 , pp. 2850-2852
    • Gross, E.K.U.1    Kohn, W.2
  • 34
    • 0012597289 scopus 로고
    • Density-Functional Theory for Time-Dependent Systems
    • Runge, E.; Gross, E. K. U. Density-Functional Theory for Time-Dependent Systems Phys. Rev. Lett. 1984, 52, 997-1000 10.1103/PhysRevLett.52.997
    • (1984) Phys. Rev. Lett. , vol.52 , pp. 997-1000
    • Runge, E.1    Gross, E.K.U.2
  • 35
    • 1542595937 scopus 로고
    • Time-Dependent Density Functional Theory
    • Gross, E. K. U.; Kohn, W. Time-Dependent Density Functional Theory Adv. Quantum Chem. 1990, 21, 255-291 10.1016/S0065-3276(08)60600-0
    • (1990) Adv. Quantum Chem. , vol.21 , pp. 255-291
    • Gross, E.K.U.1    Kohn, W.2
  • 36
    • 0030570285 scopus 로고    scopus 로고
    • Treatment of Electronic Excitations Within the Adiabatic Approximation of Time Dependent Density Functional Theory
    • Bauernschmitt, R.; Ahlrichs, R. Treatment of Electronic Excitations Within the Adiabatic Approximation of Time Dependent Density Functional Theory Chem. Phys. Lett. 1996, 256, 454-464 10.1016/0009-2614(96)00440-X
    • (1996) Chem. Phys. Lett. , vol.256 , pp. 454-464
    • Bauernschmitt, R.1    Ahlrichs, R.2
  • 37
    • 0000287603 scopus 로고    scopus 로고
    • Molecular Excitation Energies to High-Lying Bound States from Time-Dependent Density-Functional Response Theory: Characterization and Correction of the Time-Dependent Local Density Approximation Ionization Threshold
    • Casida, M. E.; Jamorski, C.; Casida, K. C.; Salahub, D. R. Molecular Excitation Energies to High-Lying Bound States from Time-Dependent Density-Functional Response Theory: Characterization and Correction of the Time-Dependent Local Density Approximation Ionization Threshold J. Chem. Phys. 1998, 108, 4439-4449 10.1063/1.475855
    • (1998) J. Chem. Phys. , vol.108 , pp. 4439-4449
    • Casida, M.E.1    Jamorski, C.2    Casida, K.C.3    Salahub, D.R.4
  • 39
    • 10244229148 scopus 로고    scopus 로고
    • Charge-Transfer and Energy-Transfer Processes in π-Conjugated Oligomers and Polymers: A Molecular Picture
    • Bredas, J. L.; Beljonne, D.; Coropceanu, V.; Cornil, J. Charge-Transfer and Energy-Transfer Processes in π-Conjugated Oligomers and Polymers: A Molecular Picture Chem. Rev. 2004, 104, 4971-5004 10.1021/cr040084k
    • (2004) Chem. Rev. , vol.104 , pp. 4971-5004
    • Bredas, J.L.1    Beljonne, D.2    Coropceanu, V.3    Cornil, J.4
  • 40
    • 79952584870 scopus 로고    scopus 로고
    • Evaluating the Performance of DFT Functionals in Assessing the Interaction Energy and Ground-State Charge Transfer of Donor/Acceptor Complexes: Tetrathiafulvalene-Tetracyanoquinodimethane (TTF-TCNQ) as a Model Case
    • Sini, G.; Sears, J. S.; Bredas, J. L. Evaluating the Performance of DFT Functionals in Assessing the Interaction Energy and Ground-State Charge Transfer of Donor/Acceptor Complexes: Tetrathiafulvalene-Tetracyanoquinodimethane (TTF-TCNQ) as a Model Case J. Chem. Theory Comput. 2011, 7, 602-609 10.1021/ct1005517
    • (2011) J. Chem. Theory Comput. , vol.7 , pp. 602-609
    • Sini, G.1    Sears, J.S.2    Bredas, J.L.3
  • 41
    • 84860779059 scopus 로고    scopus 로고
    • Why are the Interaction Energies of Charge-Transfer Complexes Challenging for DFT?
    • Steinmann, N. S.; Piemontesi, C.; Delachat, A.; Corminboeuf, C. Why are the Interaction Energies of Charge-Transfer Complexes Challenging for DFT? J. Chem. Theory Comput. 2012, 8, 1629-1640 10.1021/ct200930x
    • (2012) J. Chem. Theory Comput. , vol.8 , pp. 1629-1640
    • Steinmann, N.S.1    Piemontesi, C.2    Delachat, A.3    Corminboeuf, C.4
  • 42
    • 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 10.1080/00268977000101561
    • (1970) Mol. Phys. , vol.19 , pp. 553-566
    • Boys, S.F.1    Bernardi, F.2
  • 43
    • 33746658076 scopus 로고    scopus 로고
    • Effect of Electronic Polarization on Charge-Transport Parameters in Molecular Organic Semiconductors
    • Valeev, E. F.; Coropceanu, V.; da Silva Filho, D. A.; Salman, S.; Bredas, J. L. Effect of Electronic Polarization on Charge-Transport Parameters in Molecular Organic Semiconductors J. Am. Chem. Soc. 2006, 128, 9882-9886 10.1021/ja061827h
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9882-9886
    • Valeev, E.F.1    Coropceanu, V.2    Da Silva Filho, D.A.3    Salman, S.4    Bredas, J.L.5
  • 44
    • 0042166074 scopus 로고    scopus 로고
    • Participation of Chromophore Pairs in Photoinduced Intramolecular Electron Transfer for a Naphthalimide Spermine Conjugate
    • Jones, G., II; Kumar, S. Participation of Chromophore Pairs in Photoinduced Intramolecular Electron Transfer for a Naphthalimide Spermine Conjugate J. Photochem. Photobiol., A 2003, 160, 139-149 10.1016/S1010-6030(03)00207-7
    • (2003) J. Photochem. Photobiol., A , vol.160 , pp. 139-149
    • Jones, G.I.I.1    Kumar, S.2
  • 46
    • 82355170423 scopus 로고    scopus 로고
    • Photophysical Property of Photoactive Molecules with Multibranched Push-Pull Structures
    • Wang, Y. Y.; Ma, X. N.; Vdovic, S.; Yan, L. Y.; Wang, X. F.; Guo, Q. J.; Xia, A. D. Photophysical Property of Photoactive Molecules with Multibranched Push-Pull Structures Chin. J. Chem. Phys. 2011, 24, 563-571 10.1088/1674-0068/24/05/563-571
    • (2011) Chin. J. Chem. Phys. , vol.24 , pp. 563-571
    • Wang, Y.Y.1    Ma, X.N.2    Vdovic, S.3    Yan, L.Y.4    Wang, X.F.5    Guo, Q.J.6    Xia, A.D.7
  • 47
    • 0002196663 scopus 로고    scopus 로고
    • Excited State Photodynamics of 4-N, N Dimethylamino Cinnamaldehyde: A Solvent Dependent Competition of TICT and Intermolecular Hydrogen Bonding
    • Bangal, P. R.; Panja, S.; Chakravorti, S. Excited State Photodynamics of 4-N, N Dimethylamino Cinnamaldehyde: A Solvent Dependent Competition of TICT and Intermolecular Hydrogen Bonding J. Photochem. Photobiol., A 2001, 139, 5-16 10.1016/S1010-6030(00)00423-8
    • (2001) J. Photochem. Photobiol., A , vol.139 , pp. 5-16
    • Bangal, P.R.1    Panja, S.2    Chakravorti, S.3
  • 48
    • 84879815538 scopus 로고    scopus 로고
    • Asymmetric Perylene Bisimide Dyes with Strong Solvatofluorism
    • Luo, M. H.; Chen, K. Y. Asymmetric Perylene Bisimide Dyes with Strong Solvatofluorism Dyes Pigm. 2013, 99, 456-464 10.1016/j.dyepig.2013.05.033
    • (2013) Dyes Pigm. , vol.99 , pp. 456-464
    • Luo, M.H.1    Chen, K.Y.2
  • 49
    • 79953769950 scopus 로고    scopus 로고
    • Characterization of Ultrafast Intramolecular Charge Transfer Dynamics in Pyrenyl Derivatives: Systematic Change of the Number of Peripheral N,N-Dimethyaniline Substituents
    • Sung, J.; Kim, P.; Lee, Y. O.; Kim, J. S.; Kim, D. Characterization of Ultrafast Intramolecular Charge Transfer Dynamics in Pyrenyl Derivatives: Systematic Change of the Number of Peripheral N,N-Dimethyaniline Substituents J. Phys. Chem. Lett. 2011, 2, 818-823 10.1021/jz200042s
    • (2011) J. Phys. Chem. Lett. , vol.2 , pp. 818-823
    • Sung, J.1    Kim, P.2    Lee, Y.O.3    Kim, J.S.4    Kim, D.5
  • 50
    • 84884839521 scopus 로고    scopus 로고
    • Twisted Intramolecular Charge Transfer State for Long-Wavelength Thermally Activated Delayed Fluorescence
    • Tanaka, H.; Shizu, K.; Nakanotani, H.; Adachi, C. Twisted Intramolecular Charge Transfer State for Long-Wavelength Thermally Activated Delayed Fluorescence Chem. Mater. 2013, 25, 3766-3771 10.1021/cm402428a
    • (2013) Chem. Mater. , vol.25 , pp. 3766-3771
    • Tanaka, H.1    Shizu, K.2    Nakanotani, H.3    Adachi, C.4
  • 51
    • 79952079869 scopus 로고    scopus 로고
    • Efficient Up-Conversion of Triplet Excitons into a Singlet State and Its Application to Organic Light Emitting Diodes
    • Endo, A.; Sato, K.; Yoshimura, K.; Kai, T.; Kawada, A.; Miyazaki, H.; Adachi, C. Efficient Up-Conversion of Triplet Excitons into a Singlet State and Its Application to Organic Light Emitting Diodes Appl. Phys. Lett. 2011, 98, 083302-3 10.1063/1.3558906
    • (2011) Appl. Phys. Lett. , vol.98 , pp. 083302-083303
    • Endo, A.1    Sato, K.2    Yoshimura, K.3    Kai, T.4    Kawada, A.5    Miyazaki, H.6    Adachi, C.7
  • 52
    • 84871027786 scopus 로고    scopus 로고
    • Highly Efficient Organic Light-Emitting Diodes from Delayed Fluorescence
    • Uoyama, H.; Goushi, K.; Shizu, K.; Nomura, H.; Adachi, C. Highly Efficient Organic Light-Emitting Diodes from Delayed Fluorescence Nature 2012, 492, 234-238 10.1038/nature11687
    • (2012) Nature , vol.492 , pp. 234-238
    • Uoyama, H.1    Goushi, K.2    Shizu, K.3    Nomura, H.4    Adachi, C.5
  • 53
    • 21144473420 scopus 로고
    • Electron Transfer Reactions in Chemistry. Theory and Experiment
    • Marcus, R. A. Electron Transfer Reactions in Chemistry. Theory and Experiment Rev. Mod. Phys. 1993, 65, 599-610 10.1103/RevModPhys.65.599
    • (1993) Rev. Mod. Phys. , vol.65 , pp. 599-610
    • Marcus, R.A.1
  • 54
    • 0003030312 scopus 로고
    • Present State of the Theory of Oxidation and Reduction in Solution (Bulk and Electrode Reactions)
    • Levich, V. G. Present State of the Theory of Oxidation and Reduction in Solution (Bulk and Electrode Reactions) Adv. Electrochem. Electrochem. Eng. 1966, 4, 249-271
    • (1966) Adv. Electrochem. Electrochem. Eng. , vol.4 , pp. 249-271
    • Levich, V.G.1
  • 55
    • 0010884753 scopus 로고
    • On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer i
    • Marcus, R. A. On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer I J. Chem. Phys. 1956, 24, 966-978 10.1063/1.1742723
    • (1956) J. Chem. Phys. , vol.24 , pp. 966-978
    • Marcus, R.A.1
  • 56
    • 0022004980 scopus 로고
    • Electron Transfers in Chemistry and Biology
    • Marcus, R. A.; Sutin, N. Electron Transfers in Chemistry and Biology Biochim. Biophys. Acta, Rev. Bioenerg. 1985, 811, 265-322 10.1016/0304-4173(85)90014-X
    • (1985) Biochim. Biophys. Acta, Rev. Bioenerg. , vol.811 , pp. 265-322
    • Marcus, R.A.1    Sutin, N.2
  • 57
    • 84946565391 scopus 로고    scopus 로고
    • Can Hydrogen Bonds Improve the Hole-Mobility in Amorphous Organic Semiconductors? Experimental and Theoretical Insights
    • Mimaite, V.; Grazulevicius, J. V.; Laurinaviciute, R.; Volyniuk, D.; Jankauskas, V.; Sini, G. Can Hydrogen Bonds Improve the Hole-Mobility in Amorphous Organic Semiconductors? Experimental and Theoretical Insights J. Mater. Chem. C 2015, 3, 11660-11674 10.1039/C5TC02534F
    • (2015) J. Mater. Chem. C , vol.3 , pp. 11660-11674
    • Mimaite, V.1    Grazulevicius, J.V.2    Laurinaviciute, R.3    Volyniuk, D.4    Jankauskas, V.5    Sini, G.6


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