메뉴 건너뛰기




Volumn 117, Issue 49, 2013, Pages 26316-26323

Tuning solvatochromism of Azo dyes with intramolecular hydrogen bonding in solution and on titanium dioxide nanoparticles

Author keywords

[No Author keywords available]

Indexed keywords

AZO DYES; DESIGN FOR TESTABILITY; ISOMERIZATION; NANOPARTICLES; OPTICAL PROPERTIES; OXIDES; SOLAR CELLS; SOLVENTS; TITANIUM DIOXIDE;

EID: 84890478863     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/jp4088783     Document Type: Article
Times cited : (41)

References (53)
  • 2
    • 84865682944 scopus 로고    scopus 로고
    • Azo-Hydrazone Tautomerism Observed from UV-Vis Spectra by pH Control and Metal-Ion Complexation for Two Heterocyclic Disperse Yellow Dyes
    • Chen, X.-C.; Tao, T.; Wang, Y.-G.; Peng, Y.-X.; Huang, W.; Qian, H.-F. Azo-Hydrazone Tautomerism Observed from UV-Vis Spectra by pH Control and Metal-Ion Complexation for Two Heterocyclic Disperse Yellow Dyes Dalton Trans. 2012, 41, 11107-11115
    • (2012) Dalton Trans. , vol.41 , pp. 11107-11115
    • Chen, X.-C.1    Tao, T.2    Wang, Y.-G.3    Peng, Y.-X.4    Huang, W.5    Qian, H.-F.6
  • 3
    • 0001700196 scopus 로고    scopus 로고
    • Linear and Nonlinear Optical Properties of Photochromic Molecules and Materials
    • Delaire, J. A.; Nakatani, K. Linear and Nonlinear Optical Properties of Photochromic Molecules and Materials Chem. Rev. 2000, 100, 1817-1846
    • (2000) Chem. Rev. , vol.100 , pp. 1817-1846
    • Delaire, J.A.1    Nakatani, K.2
  • 4
    • 79751526343 scopus 로고    scopus 로고
    • Low Band Gap Dyes Based on 2-Styryl-5-Phenylazo-Pyrrole: Synthesis and Application for Efficient Dye-Sensitized Solar Cells
    • Mikroyannidis, J. A.; Tsagkournos, D. V.; Balraju, P.; Sharma, G. D. Low Band Gap Dyes Based on 2-Styryl-5-Phenylazo-Pyrrole: Synthesis and Application for Efficient Dye-Sensitized Solar Cells J. Power Sources 2011, 196, 4152-4161
    • (2011) J. Power Sources , vol.196 , pp. 4152-4161
    • Mikroyannidis, J.A.1    Tsagkournos, D.V.2    Balraju, P.3    Sharma, G.D.4
  • 5
    • 0035891138 scopus 로고    scopus 로고
    • Photoelectrochemical Cells
    • Grätzel, M. Photoelectrochemical Cells Nature 2001, 414, 338-344
    • (2001) Nature , vol.414 , pp. 338-344
    • Grätzel, M.1
  • 7
    • 0032747009 scopus 로고    scopus 로고
    • The Influence of Intramolecular Hydrogen Bonding on the Order Parameter and Photostability Properties of Dichroic Azo Dyes in a Nematic Liquid Crystal Host
    • Griffiths, J.; Feng, K. The Influence of Intramolecular Hydrogen Bonding on the Order Parameter and Photostability Properties of Dichroic Azo Dyes in a Nematic Liquid Crystal Host J. Mater. Chem. 1999, 9, 2333-2338
    • (1999) J. Mater. Chem. , vol.9 , pp. 2333-2338
    • Griffiths, J.1    Feng, K.2
  • 8
    • 68049084766 scopus 로고    scopus 로고
    • Near-Infrared Absorbing Azo Dyes: Synthesis and X-Ray Crystallographic and Spectral Characterization of Monoazopyrroles, Bisazopyrroles, and a Boron-Azopyrrole Complex
    • Yan, L.; O'Brian, P.; David, D. Near-Infrared Absorbing Azo Dyes: Synthesis and X-Ray Crystallographic and Spectral Characterization of Monoazopyrroles, Bisazopyrroles, and a Boron-Azopyrrole Complex J. Org. Chem. 2009, 5237-5243
    • (2009) J. Org. Chem. , pp. 5237-5243
    • Yan, L.1    O'Brian, P.2    David, D.3
  • 9
    • 77956087801 scopus 로고    scopus 로고
    • Torsionally Responsive C3-Symmetric Azo Dyes: Azo-Hydrazone Tautomerism, Conformational Switching, and Application for Chemical Sensing
    • Lee, H. Y.; Song, X.; Park, H.; Baik, M.-H.; Lee, D. Torsionally Responsive C3-Symmetric Azo Dyes: Azo-Hydrazone Tautomerism, Conformational Switching, and Application for Chemical Sensing J. Am. Chem. Soc. 2010, 132, 12133-12144
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 12133-12144
    • Lee, H.Y.1    Song, X.2    Park, H.3    Baik, M.-H.4    Lee, D.5
  • 10
    • 84859094072 scopus 로고    scopus 로고
    • Rationalizing the Molecular Origins of Ru- and Fe-Based Dyes for Dye-Sensitized Solar Cells
    • Low, K. S.; Cole, J. M.; Zhou, X.; Yufa, N. Rationalizing the Molecular Origins of Ru- and Fe-Based Dyes for Dye-Sensitized Solar Cells Acta Crystallogr., Sect. B 2012, 68, 137-149
    • (2012) Acta Crystallogr., Sect. B , vol.68 , pp. 137-149
    • Low, K.S.1    Cole, J.M.2    Zhou, X.3    Yufa, N.4
  • 12
    • 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, 7, 5648-5652
    • (1993) J. Chem. Phys. , vol.7 , pp. 5648-5652
    • Becke, A.D.1
  • 14
    • 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
    • Miertuš, 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
    • Miertuš, S.1    Scrocco, E.2    Tomasi, J.3
  • 15
    • 84880155503 scopus 로고    scopus 로고
    • Solvent Effects on the UV-Vis Absorption and Emission of Optoelectronic Coumarins: A Comparison of Three Empirical Solvatochromic Models
    • 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, 14731-14741
    • (2013) J. Phys. Chem. C , vol.117 , pp. 14731-14741
    • Liu, X.1    Cole, J.M.2    Low, K.S.3
  • 17
    • 84962426609 scopus 로고    scopus 로고
    • Relating Electron Donor and Carboxylic Acid Anchoring Substitution Effects in Azo Dyes to Dye-Sensitized Solar Cell Performance
    • Zhang, L.; Cole, J. M.; Waddell, P. G.; Low, K. S.; Liu, X. Relating Electron Donor and Carboxylic Acid Anchoring Substitution Effects in Azo Dyes to Dye-Sensitized Solar Cell Performance ACS Sustainable Chem. Eng. 2013, 1, 1440-1452
    • (2013) ACS Sustainable Chem. Eng. , vol.1 , pp. 1440-1452
    • Zhang, L.1    Cole, J.M.2    Waddell, P.G.3    Low, K.S.4    Liu, X.5
  • 18
    • 84871871509 scopus 로고    scopus 로고
    • Synthesis, Structure and Tautomerism of Two Benzothiazolyl Azo Derivatives of 2-Naphthol: A Crystallographic, NMR and Computational Study
    • Racané, L.; Mihalić, Z.; Cerić, H.; Popović, J.; Tralić-Kulenović, V. Synthesis, Structure and Tautomerism of Two Benzothiazolyl Azo Derivatives of 2-Naphthol: A Crystallographic, NMR and Computational Study Dyes Pigm. 2013, 96, 672-678
    • (2013) Dyes Pigm. , vol.96 , pp. 672-678
    • Racané, L.1    Mihalić, Z.2    Cerić, H.3    Popović, J.4    Tralić-Kulenović, V.5
  • 19
    • 79960653922 scopus 로고    scopus 로고
    • Spectrophotometric Investigations and Computational Calculations of Prototropic Tautomerism and Acid-Base Properties of Some New Azo Dyes
    • Ebead, Y. H. Spectrophotometric Investigations and Computational Calculations of Prototropic Tautomerism and Acid-Base Properties of Some New Azo Dyes Dyes Pigm. 2012, 92, 705-713
    • (2012) Dyes Pigm. , vol.92 , pp. 705-713
    • Ebead, Y.H.1
  • 20
    • 53349163960 scopus 로고    scopus 로고
    • Azo-Hydrazone Tautomerism in Protonated Aminoazobenzenes: Resonance Raman Spectroscopy and Quantum-Chemical Calculations
    • Matazo, D. R. C.; Ando, R. A.; Borin, A. C.; Santos, P. S. Azo-Hydrazone Tautomerism in Protonated Aminoazobenzenes: Resonance Raman Spectroscopy and Quantum-Chemical Calculations J. Phys. Chem. A 2008, 112, 4437-4443
    • (2008) J. Phys. Chem. A , vol.112 , pp. 4437-4443
    • Matazo, D.R.C.1    Ando, R.A.2    Borin, A.C.3    Santos, P.S.4
  • 21
    • 79960654858 scopus 로고    scopus 로고
    • Tautomerism in 1-Phenylazo-4-Naphthols: Experimental Results Vs Quantum-Chemical Predictions
    • Antonov, L.; Kurteva, V.; Crochet, A.; Mirolo, L.; Fromm, K. M.; Angelova, S. Tautomerism in 1-Phenylazo-4-Naphthols: Experimental Results Vs Quantum-Chemical Predictions Dyes Pigm. 2012, 92, 714-723
    • (2012) Dyes Pigm. , vol.92 , pp. 714-723
    • Antonov, L.1    Kurteva, V.2    Crochet, A.3    Mirolo, L.4    Fromm, K.M.5    Angelova, S.6
  • 22
    • 17144368401 scopus 로고    scopus 로고
    • Experimental and Computational Studies of Structure and Bonding in Parent and Reduced Forms of the Azo Dye Orange II
    • Abbott, L. C.; Batchelor, S. N.; Oakes, J.; Gilbert, B. C.; Whitwood, A. C.; Lindsay Smith, J. R.; Moore, J. N. Experimental and Computational Studies of Structure and Bonding in Parent and Reduced Forms of the Azo Dye Orange II J. Phys. Chem. A 2005, 109, 2894-2905
    • (2005) J. Phys. Chem. A , vol.109 , pp. 2894-2905
    • Abbott, L.C.1    Batchelor, S.N.2    Oakes, J.3    Gilbert, B.C.4    Whitwood, A.C.5    Lindsay Smith, J.R.6    Moore, J.N.7
  • 23
    • 84855463497 scopus 로고    scopus 로고
    • Photoisomerization in Different Classes of Azobenzene
    • Bandara, H. M. D.; Burdette, S. C. Photoisomerization in Different Classes of Azobenzene Chem. Soc. Rev. 2012, 41, 1809-1825
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 1809-1825
    • Bandara, H.M.D.1    Burdette, S.C.2
  • 24
    • 70350637502 scopus 로고    scopus 로고
    • Highly Efficient Reversible Z-E Photoisomerization of a Bridged Azobenzene with Visible Light through Resolved S1(nπ) Absorption Bands
    • Siewertsen, R.; Neumann, H.; Buchheim-Stehn, B.; Herges, R.; Näther, C.; Renth, F.; Temps, F. Highly Efficient Reversible Z-E Photoisomerization of a Bridged Azobenzene with Visible Light through Resolved S1(nπ) Absorption Bands J. Am. Chem. Soc. 2009, 131, 15594-15595
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 15594-15595
    • Siewertsen, R.1    Neumann, H.2    Buchheim-Stehn, B.3    Herges, R.4    Näther, C.5    Renth, F.6    Temps, F.7
  • 26
    • 84962418539 scopus 로고    scopus 로고
    • Photoisomerization of Disperse Red 1 Studied with Transient Absorption Spectroscopy and Quantum Chemical Calculations
    • Poprawa-Smoluch, M.; Baggerman, J.; Zhang, H.; Maas, H. P.; De Cola, L.; Brouwer, A. M. Photoisomerization of Disperse Red 1 Studied with Transient Absorption Spectroscopy and Quantum Chemical Calculations J. Phys. Chem. A 2006, 110, 11926-11937
    • (2006) J. Phys. Chem. A , vol.110 , pp. 11926-11937
    • Poprawa-Smoluch, M.1    Baggerman, J.2    Zhang, H.3    Maas, H.P.4    De Cola, L.5    Brouwer, A.M.6
  • 27
    • 26244464026 scopus 로고    scopus 로고
    • Organic-Inorganic Hybrid Materials for Non-Linear Optics
    • Innocenzi, P.; Lebeau, B. Organic-Inorganic Hybrid Materials for Non-Linear Optics J. Mater. Chem. 2005, 15, 3821-3831
    • (2005) J. Mater. Chem. , vol.15 , pp. 3821-3831
    • Innocenzi, P.1    Lebeau, B.2
  • 28
    • 0036856343 scopus 로고    scopus 로고
    • Photoinduced Motions in Azo-Containing Polymers
    • Natansohn, A.; Rochon, P. Photoinduced Motions in Azo-Containing Polymers Chem. Rev. 2002, 102, 4139-4176
    • (2002) Chem. Rev. , vol.102 , pp. 4139-4176
    • Natansohn, A.1    Rochon, P.2
  • 29
    • 33746271910 scopus 로고    scopus 로고
    • Optimizing Dyes for Dye-Sensitized Solar Cells
    • Robertson, N. Optimizing Dyes for Dye-Sensitized Solar Cells Angew. Chem., Int. Ed. 2006, 45, 2338-2345
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 2338-2345
    • Robertson, N.1
  • 32
    • 84880178963 scopus 로고    scopus 로고
    • Molecular Origins of Optoelectronic Properties in Coumarins 343, 314T, 445, and 522B
    • Liu, X.; Cole, J. M.; Waddell, P. G.; Lin, T.-C.; McKechnie, S. Molecular Origins of Optoelectronic Properties in Coumarins 343, 314T, 445, and 522B J. Phys. Chem. C 2013, 117, 14130-14141
    • (2013) J. Phys. Chem. C , vol.117 , pp. 14130-14141
    • Liu, X.1    Cole, J.M.2    Waddell, P.G.3    Lin, T.-C.4    McKechnie, S.5
  • 33
    • 49149095798 scopus 로고    scopus 로고
    • Effect of Different Dye Baths and Dye-Structures on the Performance of Dye-Sensitized Solar Cells Based on Triphenylamine Dyes
    • Tian, H.; Yang, X.; Chen, R.; Zhang, R.; Hagfeldt, A.; Sun, L. Effect of Different Dye Baths and Dye-Structures on the Performance of Dye-Sensitized Solar Cells Based on Triphenylamine Dyes J. Phys. Chem. C 2008, 112, 11023-11033
    • (2008) J. Phys. Chem. C , vol.112 , pp. 11023-11033
    • Tian, H.1    Yang, X.2    Chen, R.3    Zhang, R.4    Hagfeldt, A.5    Sun, L.6
  • 36
    • 78751674922 scopus 로고    scopus 로고
    • Conformational Properties of Methyl β-Maltoside and Methyl α- And β-Cellobioside Disaccharides
    • Hatcher, E.; Säwén, E.; Widmalm, G.; MacKerell, A. D. Conformational Properties of Methyl β-Maltoside and Methyl α- and β-Cellobioside Disaccharides J. Phys. Chem. B 2011, 115, 597-608
    • (2011) J. Phys. Chem. B , vol.115 , pp. 597-608
    • Hatcher, E.1    Säwén, E.2    Widmalm, G.3    MacKerell, A.D.4
  • 37
    • 0034715461 scopus 로고    scopus 로고
    • Evidence for Intramolecular N-H···O Resonance-Assisted Hydrogen Bonding in β-Enaminones and Related Heterodienes. A Combined Crystal-Structural, IR and NMR Spectroscopic, and Quantum-Mechanical Investigation
    • Gilli, P.; Bertolasi, V.; Ferretti, V.; Gilli, G. Evidence for Intramolecular N-H···O Resonance-Assisted Hydrogen Bonding in β-Enaminones and Related Heterodienes. A Combined Crystal-Structural, IR and NMR Spectroscopic, and Quantum-Mechanical Investigation J. Am. Chem. Soc. 2000, 122, 10405-10417
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10405-10417
    • Gilli, P.1    Bertolasi, V.2    Ferretti, V.3    Gilli, G.4
  • 38
    • 77953121260 scopus 로고    scopus 로고
    • 15N NMR Spectroscopic and GIAO DFT Study of Ethyl 5-Oxo-2-Phenyl-4-(2-Phenylhydrazono)-4,5-Dihydro-1 H -Pyrrole-3-Carboxylate
    • 15N NMR Spectroscopic and GIAO DFT Study of Ethyl 5-Oxo-2-Phenyl-4-(2-Phenylhydrazono)-4,5-Dihydro-1 H -Pyrrole-3-Carboxylate Tetrahedron Lett. 2010, 51, 3149-3151
    • (2010) Tetrahedron Lett. , vol.51 , pp. 3149-3151
    • Lyčka, A.1    Luňák, S.2    Aysha, T.3    Holuša, R.4    Hrdina, R.5
  • 39
    • 72449120388 scopus 로고    scopus 로고
    • Intra- and Intermolecular N-H.O Hydrogen Bonds in Pyrrolyl Derivatives of Indane-1,3-Dione-Experimental and Theoretical Study
    • Sigalov, M.; Shainyan, B.; Chipanina, N.; Ushakov, I.; Shulunova, A. Intra- and Intermolecular N-H...O Hydrogen Bonds in Pyrrolyl Derivatives of Indane-1,3-Dione-Experimental and Theoretical Study J. Phys. Org. Chem. 2009, 22, 1178-1187
    • (2009) J. Phys. Org. Chem. , vol.22 , pp. 1178-1187
    • Sigalov, M.1    Shainyan, B.2    Chipanina, N.3    Ushakov, I.4    Shulunova, A.5
  • 41
    • 77954452495 scopus 로고    scopus 로고
    • Role of the Medium on the C343 Inter/intramolecular Hydrogen Bond Interactions. An Absorption, Emission, and H NMR Investigation of C343 in Benzene/ n -Heptane Mixtures
    • Gutierrez, J. A.; Falcone, R. D.; Silber, J. J.; Correa, N. M. Role of the Medium on the C343 Inter/intramolecular Hydrogen Bond Interactions. An Absorption, Emission, and H NMR Investigation of C343 in Benzene/ n -Heptane Mixtures J. Phys. Chem. A 2010, 114, 7326-7330
    • (2010) J. Phys. Chem. A , vol.114 , pp. 7326-7330
    • Gutierrez, J.A.1    Falcone, R.D.2    Silber, J.J.3    Correa, N.M.4
  • 44
    • 0001752768 scopus 로고    scopus 로고
    • The Cambridge Structural Database: A Quarter of A Million Crystal Structures and Rising
    • Allen, F. H. The Cambridge Structural Database: A Quarter of A Million Crystal Structures and Rising Acta Crystallogr., Sect. B 2002, 58, 380-388
    • (2002) Acta Crystallogr., Sect. B , vol.58 , pp. 380-388
    • Allen, F.H.1
  • 45
    • 84977289173 scopus 로고
    • Crystallographic Studies and Physicochemical Properties of π-Electron Compounds. III. Stabilization Energy and the Kekulé Structure Contributions Derived from Experimental Bond Lengths
    • Tadeusz, B. Y.; Krygowski, M.; Kruszewski, J. Crystallographic Studies and Physicochemical Properties of π-Electron Compounds. III. Stabilization Energy and the Kekulé Structure Contributions Derived from Experimental Bond Lengths Acta Crystallogr., Sect. B 1983, 39, 732-739
    • (1983) Acta Crystallogr., Sect. B , vol.39 , pp. 732-739
    • Tadeusz, B.Y.1    Krygowski, M.2    Kruszewski, J.3
  • 46
    • 81855193636 scopus 로고    scopus 로고
    • Molecular Origins of Commercial Laser Dye Functionality in Azacoumarins and 2-Quinolones: LD 425, LD 489 and LD 473
    • Liu, X.; Cole, J. M.; Waddell, P. G.; Lin, T.-C. Molecular Origins of Commercial Laser Dye Functionality in Azacoumarins and 2-Quinolones: LD 425, LD 489 and LD 473 Acta Crystallogr., Sect. B 2011, 67, 1-9
    • (2011) Acta Crystallogr., Sect. B , vol.67 , pp. 1-9
    • Liu, X.1    Cole, J.M.2    Waddell, P.G.3    Lin, T.-C.4
  • 47
    • 84862967139 scopus 로고    scopus 로고
    • Molecular Origins of Optoelectronic Properties in Coumarin Dyes: Toward Designer Solar Cell and Laser Applications
    • Liu, X.; Cole, J. M.; Waddell, P. G.; Lin, T.-C.; Radia, J.; Zeidler, A. Molecular Origins of Optoelectronic Properties in Coumarin Dyes: Toward Designer Solar Cell and Laser Applications J. Phys. Chem. A 2012, 116, 727-737
    • (2012) J. Phys. Chem. A , vol.116 , pp. 727-737
    • Liu, X.1    Cole, J.M.2    Waddell, P.G.3    Lin, T.-C.4    Radia, J.5    Zeidler, A.6
  • 48
    • 0005607369 scopus 로고    scopus 로고
    • Second-Order Nonlinear Optical Materials: Recent Advances in Chromophore Design
    • Verbiest, T.; Houbrechts, S.; Kauranen, M.; Clays, K.; Persoons, A. Second-Order Nonlinear Optical Materials: Recent Advances in Chromophore Design J. Mater. Chem. 1997, 7, 2175-2189
    • (1997) J. Mater. Chem. , vol.7 , pp. 2175-2189
    • Verbiest, T.1    Houbrechts, S.2    Kauranen, M.3    Clays, K.4    Persoons, A.5
  • 49
    • 0346342987 scopus 로고    scopus 로고
    • Organic Materials for Second-Harmonic Generation: Advances in Relating Structure to Function
    • Cole, J. M. Organic Materials for Second-Harmonic Generation: Advances in Relating Structure to Function Philos. Trans. R. Soc., A 2003, 361, 2751-2770
    • (2003) Philos. Trans. R. Soc., A , vol.361 , pp. 2751-2770
    • Cole, J.M.1
  • 51
    • 84860469467 scopus 로고    scopus 로고
    • Solid-State Dilution of Dihydroxybenzophenones with 4,13-Diaza-18-Crown-6 for Photocrystallographic Studies
    • Cole, J. M.; Waddell, P. G.; Jayatilaka, D. Solid-State Dilution of Dihydroxybenzophenones with 4,13-Diaza-18-Crown-6 for Photocrystallographic Studies Cryst. Growth Des. 2012, 12, 2277-2287
    • (2012) Cryst. Growth Des. , vol.12 , pp. 2277-2287
    • Cole, J.M.1    Waddell, P.G.2    Jayatilaka, D.3
  • 52
    • 0346010653 scopus 로고    scopus 로고
    • Exploiting Structure/Property Relationships in Organic Non-Linear Optical Materials: Developing Strategies to Realize the Potential of TCNQ Derivatives
    • Cole, J. M.; Kreiling, S. Exploiting Structure/Property Relationships in Organic Non-Linear Optical Materials: Developing Strategies to Realize the Potential of TCNQ Derivatives CrystEngComm 2002, 4, 232-238
    • (2002) CrystEngComm , vol.4 , pp. 232-238
    • Cole, J.M.1    Kreiling, S.2
  • 53


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.