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Volumn 98, Issue 2, 2013, Pages 304-315

Photophysical properties of 2-phenylanthracene and its conformationally- stabilized derivatives

Author keywords

2 Phenylanthracene; Anthracene derivatives; Carrier mobility; Concentration quenching; Fluorescence; Heteroatoms

Indexed keywords

2-PHENYLANTHRACENE; ANTHRACENE DERIVATIVES; CONCENTRATION QUENCHING; CONJUGATED ELECTRON SYSTEMS; ELECTRON-VIBRATIONAL COUPLING; FLUORESCENCE QUANTUM EFFICIENCY; HETEROATOMS; OPTICAL AND ELECTRICAL PROPERTIES;

EID: 84876401676     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2013.02.018     Document Type: Article
Times cited : (20)

References (54)
  • 1
    • 0026776299 scopus 로고
    • Anthracene-9,10-diones as potential anticancer agents. Synthesis, DNA-binding, and biological studies on a series of 2,6-disubstituted derivatives
    • M. Agbandje, T.C. Jenkins, R. McKenna, A.P. Reszka, and S. Neidle Anthracene-9,10-diones as potential anticancer agents. Synthesis, DNA-binding, and biological studies on a series of 2,6-disubstituted derivatives J Med Chem 35 1992 1418 1429
    • (1992) J Med Chem , vol.35 , pp. 1418-1429
    • Agbandje, M.1    Jenkins, T.C.2    McKenna, R.3    Reszka, A.P.4    Neidle, S.5
  • 3
    • 39149101463 scopus 로고    scopus 로고
    • Novel anthracene-core molecule for the development of efficient PCBM-based solar cells
    • L. Valentini, D. Bagnis, A. Marrocchi, M. Seri, A. Taticchi, and J.M. Kenny Novel anthracene-core molecule for the development of efficient PCBM-based solar cells Chem Mater 20 2008 32 34
    • (2008) Chem Mater , vol.20 , pp. 32-34
    • Valentini, L.1    Bagnis, D.2    Marrocchi, A.3    Seri, M.4    Taticchi, A.5    Kenny, J.M.6
  • 4
    • 84861307326 scopus 로고    scopus 로고
    • The development of anthracene derivatives for organic light-emitting diodes
    • J. Huang, J.H. Su, and H. Tian The development of anthracene derivatives for organic light-emitting diodes J Mat Chem 22 2012 10977 10989
    • (2012) J Mat Chem , vol.22 , pp. 10977-10989
    • Huang, J.1    Su, J.H.2    Tian, H.3
  • 5
    • 27144437222 scopus 로고
    • Electroluminescence in organic crystals
    • M. Pope, H.P. Kallmann, and P.J. Magnante Electroluminescence in organic crystals Chem Phys 38 1963 2042 2043
    • (1963) Chem Phys , vol.38 , pp. 2042-2043
    • Pope, M.1    Kallmann, H.P.2    Magnante, P.J.3
  • 7
    • 65249145305 scopus 로고    scopus 로고
    • Fluorescence quantum yield of aromatic hydrocarbon crystals
    • R. Katoh, K. Suzuki, A. Furube, M. Kotani, and K. Tokumaru Fluorescence quantum yield of aromatic hydrocarbon crystals J Phys Chem C 113 2009 2961 2965
    • (2009) J Phys Chem C , vol.113 , pp. 2961-2965
    • Katoh, R.1    Suzuki, K.2    Furube, A.3    Kotani, M.4    Tokumaru, K.5
  • 8
    • 0034743731 scopus 로고    scopus 로고
    • The influence of molecular symmetry and topological factors on the internal heavy atom effect in aromatic and heteroaromatic compounds
    • N. Nijegorodov, and R. Mabbs The influence of molecular symmetry and topological factors on the internal heavy atom effect in aromatic and heteroaromatic compounds Spectrochim Acta A 57 2001 1449 1462
    • (2001) Spectrochim Acta A , vol.57 , pp. 1449-1462
    • Nijegorodov, N.1    Mabbs, R.2
  • 9
    • 0346569869 scopus 로고
    • Fluorescence quantum yield determinations. 9,10-Diphenylanthracene as a reference standard in different solvents
    • J.V. Morris, M.A. Mahaney, and J.R. Huber Fluorescence quantum yield determinations. 9,10-Diphenylanthracene as a reference standard in different solvents J Phys Chem 80 1976 969 974
    • (1976) J Phys Chem , vol.80 , pp. 969-974
    • Morris, J.V.1    Mahaney, M.A.2    Huber, J.R.3
  • 10
    • 8644265990 scopus 로고    scopus 로고
    • Stable styrylamine-doped blue organic electroluminescent device based on 2-methyl-9,10-di(2-naphthyl)anthracene
    • M.T. Lee, H.H. Chen, C.H. Liao, C.H. Tsai, and C.H. Chen Stable styrylamine-doped blue organic electroluminescent device based on 2-methyl-9,10-di(2-naphthyl)anthracene Appl Phys Lett 85 2004 3301 3303
    • (2004) Appl Phys Lett , vol.85 , pp. 3301-3303
    • Lee, M.T.1    Chen, H.H.2    Liao, C.H.3    Tsai, C.H.4    Chen, C.H.5
  • 11
    • 77956095080 scopus 로고    scopus 로고
    • Synthesis and electroluminescent properties of blue-emitting t-butylated bis(diarylaminoaryl)anthracenes for OLEDs
    • K.H. Lee, J.N. You, S. Kang, J.Y. Lee, H.J. Kwon, and Y.K. Kim Synthesis and electroluminescent properties of blue-emitting t-butylated bis(diarylaminoaryl)anthracenes for OLEDs Thin Solid Films 518 2012 6253 6258
    • (2012) Thin Solid Films , vol.518 , pp. 6253-6258
    • Lee, K.H.1    You, J.N.2    Kang, S.3    Lee, J.Y.4    Kwon, H.J.5    Kim, Y.K.6
  • 12
    • 23844498766 scopus 로고    scopus 로고
    • Electronic spectroscopy and methyl internal rotation dynamics of 9,10-dimethylanthracene
    • Y. Stepanenko, A.L. Sobolewski, and A. Mordzinsky Electronic spectroscopy and methyl internal rotation dynamics of 9,10-dimethylanthracene J Mol Spectrosc 233 2005 15 22
    • (2005) J Mol Spectrosc , vol.233 , pp. 15-22
    • Stepanenko, Y.1    Sobolewski, A.L.2    Mordzinsky, A.3
  • 13
    • 78651382174 scopus 로고    scopus 로고
    • Asymmetric anthracene-based blue host materials: Synthesis and electroluminescence properties of 9-(2-naphthyl)-10 arylanthracenes
    • K.R. Wee, W.S. Han, J.E. Kim, A.L. Kim, S. Kwon, and S.O. Kang Asymmetric anthracene-based blue host materials: synthesis and electroluminescence properties of 9-(2-naphthyl)-10 arylanthracenes J Mat Chem 21 2011 1115 1123
    • (2011) J Mat Chem , vol.21 , pp. 1115-1123
    • Wee, K.R.1    Han, W.S.2    Kim, J.E.3    Kim, A.L.4    Kwon, S.5    Kang, S.O.6
  • 14
    • 61349144404 scopus 로고    scopus 로고
    • Efficient non-doped blue-light-emitting diodes incorporating an anthracene derivative end-capped with fluorene groups
    • C.H. Wu, C.H. Chien, F.M. Hsu, P.I. Shih, and C.F. Shu Efficient non-doped blue-light-emitting diodes incorporating an anthracene derivative end-capped with fluorene groups J Mat Chem 19 2009 1464 1470
    • (2009) J Mat Chem , vol.19 , pp. 1464-1470
    • Wu, C.H.1    Chien, C.H.2    Hsu, F.M.3    Shih, P.I.4    Shu, C.F.5
  • 15
    • 78649464412 scopus 로고    scopus 로고
    • Unsymmetrically amorphous 9,10-disubstituted anthracene derivatives for high-efficiency blue organic electroluminescence devices
    • J. Huang, B. Xu, M.K. Lam, K.W. Cheah, C.H. Chen, and J.H. Su Unsymmetrically amorphous 9,10-disubstituted anthracene derivatives for high-efficiency blue organic electroluminescence devices Dyes Pigm 89 2011 155 161
    • (2011) Dyes Pigm , vol.89 , pp. 155-161
    • Huang, J.1    Xu, B.2    Lam, M.K.3    Cheah, K.W.4    Chen, C.H.5    Su, J.H.6
  • 16
    • 84987341318 scopus 로고
    • Planar and nonplanar unsaturation. Preparation, properties and molecular-orbital characterization of some fluoro-derivatives of anthracene and anthraquinone
    • A.Y. Meyer, and A. Goldblum Planar and nonplanar unsaturation. Preparation, properties and molecular-orbital characterization of some fluoro-derivatives of anthracene and anthraquinone Isr J Chem 11 1973 791 804
    • (1973) Isr J Chem , vol.11 , pp. 791-804
    • Meyer, A.Y.1    Goldblum, A.2
  • 17
    • 0141643992 scopus 로고
    • Blue light-emitting organic electroluminescent devices
    • Ch Adachi, T. Tsutsui, and S. Saito Blue light-emitting organic electroluminescent devices Appl Phys Lett 58 1990 799 801
    • (1990) Appl Phys Lett , vol.58 , pp. 799-801
    • Adachi, C.1    Tsutsui, T.2    Saito, S.3
  • 18
    • 79956010183 scopus 로고    scopus 로고
    • Anthracene derivatives for stable blue-emitting organic electroluminescence devices
    • J. Shia, and C.W. Tang Anthracene derivatives for stable blue-emitting organic electroluminescence devices Appl Phys Lett 80 2002 3201 3203
    • (2002) Appl Phys Lett , vol.80 , pp. 3201-3203
    • Shia, J.1    Tang, C.W.2
  • 19
    • 47049115105 scopus 로고    scopus 로고
    • Exceedingly efficient deep-blue electroluminescence from new anthracenes obtained using rational molecular design
    • S.K. Kim, B. Yang, Y. Ma, J.Y. Lee, and J. Park Exceedingly efficient deep-blue electroluminescence from new anthracenes obtained using rational molecular design J Mater Chem 18 2008 3376 3384
    • (2008) J Mater Chem , vol.18 , pp. 3376-3384
    • Kim, S.K.1    Yang, B.2    Ma, Y.3    Lee, J.Y.4    Park, J.5
  • 20
    • 79751525820 scopus 로고    scopus 로고
    • New blue host materials based on anthracene-containing dibenzothiophene
    • L. Wang, ZhY. Wu, W.Y. Wong, K.W. Cheah, H. Huang, and ChH. Chen New blue host materials based on anthracene-containing dibenzothiophene Org Electron 12 2011 595 601
    • (2011) Org Electron , vol.12 , pp. 595-601
    • Wang, L.1    Wu, ZhY.2    Wong, W.Y.3    Cheah, K.W.4    Huang, H.5    Chen, ChH.6
  • 21
    • 79952555220 scopus 로고    scopus 로고
    • Efficient blue organic light-emitting diode using anthracene-derived emitters based on polycyclic aromatic hydrocarbons
    • J.K. Bin, and J.I. Hong Efficient blue organic light-emitting diode using anthracene-derived emitters based on polycyclic aromatic hydrocarbons Org Electron 12 2011 802 808
    • (2011) Org Electron , vol.12 , pp. 802-808
    • Bin, J.K.1    Hong, J.I.2
  • 22
    • 84980144440 scopus 로고
    • The photo-dimerization and excimer fluorescence of 9-methyl anthracene
    • J.B. Birks, and J.B. Aladekomo The photo-dimerization and excimer fluorescence of 9-methyl anthracene Photochem Photobiol 2 1963 415 418
    • (1963) Photochem Photobiol , vol.2 , pp. 415-418
    • Birks, J.B.1    Aladekomo, J.B.2
  • 23
    • 0038166559 scopus 로고    scopus 로고
    • Synthesis of t-butylated diphenylanthracene derivatives as blue host materials for OLED applications
    • B. Balaganesan, W.J. Shen, and ChH. Chen Synthesis of t-butylated diphenylanthracene derivatives as blue host materials for OLED applications Tetrahedron Lett 44 2003 5747 5750
    • (2003) Tetrahedron Lett , vol.44 , pp. 5747-5750
    • Balaganesan, B.1    Shen, W.J.2    Chen, ChH.3
  • 24
    • 67649083658 scopus 로고    scopus 로고
    • High efficient organic light emitting diodes using new 9,10-diphenylanthracene derivatives containing bulky substituents on 2,6-position
    • W.J. Jo, K.H. Kim, D.Y. Shin, S.J. Oh, J.H. Son, and Y.H. Kim High efficient organic light emitting diodes using new 9,10-diphenylanthracene derivatives containing bulky substituents on 2,6-position Synth Met 159 2009 1359 1364
    • (2009) Synth Met , vol.159 , pp. 1359-1364
    • Jo, W.J.1    Kim, K.H.2    Shin, D.Y.3    Oh, S.J.4    Son, J.H.5    Kim, Y.H.6
  • 25
    • 84880125944 scopus 로고    scopus 로고
    • Doosan Corporation United States patent US2012/0161615 A1
    • Doosan Corporation. Inventor. United States patent US2012/0161615 A1. 2012.
    • (2012) Inventor
  • 26
    • 0009244255 scopus 로고
    • J. Synthesis of furano compounds. XXVIII Synthesis of γ-brazan and naphtho[2':3':1,2]dibenzofuran
    • J.N. Chatterjea, and V.N. Mehrotra J. Synthesis of furano compounds. XXVIII Synthesis of γ-brazan and naphtho[2':3':1,2]dibenzofuran J Indian Chem Soc 42 1965 205 210
    • (1965) J Indian Chem Soc , vol.42 , pp. 205-210
    • Chatterjea, J.N.1    Mehrotra, V.N.2
  • 27
    • 84970580260 scopus 로고
    • The base-catalysed skeletal rearrangement of a thianaphthofluorene derivative
    • W.H. Cherry, W. Davies, B.C. Ennis, and Q.N. Porter The base-catalysed skeletal rearrangement of a thianaphthofluorene derivative Aust J Chem 20 1967 313 320
    • (1967) Aust J Chem , vol.20 , pp. 313-320
    • Cherry, W.H.1    Davies, W.2    Ennis, B.C.3    Porter, Q.N.4
  • 29
    • 21844439601 scopus 로고
    • Synthese einiger naphthocarbazole
    • [German]
    • M. Zander, and W. Franke Synthese einiger naphthocarbazole Chemische Berichte 96 1963 699 706 [German]
    • (1963) Chemische Berichte , vol.96 , pp. 699-706
    • Zander, M.1    Franke, W.2
  • 30
    • 84876385150 scopus 로고    scopus 로고
    • Idemitsu Kosan Co (Ltd) European patent EP2218706 A1
    • Idemitsu Kosan Co (Ltd). Inventor. European patent EP2218706 A1. 2010.
    • (2010) Inventor
  • 31
    • 33847088401 scopus 로고
    • Determination of absolute fluorescence quantum efficiency of quinine bisulfate in aqueous medium by optoacoustic spectrometry
    • M.J. Adams, J.G. Highfield, and G.F. Kirkbright Determination of absolute fluorescence quantum efficiency of quinine bisulfate in aqueous medium by optoacoustic spectrometry Anal Chem 49 1977 1850 1852
    • (1977) Anal Chem , vol.49 , pp. 1850-1852
    • Adams, M.J.1    Highfield, J.G.2    Kirkbright, G.F.3
  • 32
    • 0031069035 scopus 로고    scopus 로고
    • An improved experimental determination of external photoluminescence quantum efficiency
    • J.C. de Mello, H.F. Wittmann, and R.H. Friend An improved experimental determination of external photoluminescence quantum efficiency Adv Mater 9 1997 230 232
    • (1997) Adv Mater , vol.9 , pp. 230-232
    • De Mello, J.C.1    Wittmann, H.F.2    Friend, R.H.3
  • 33
    • 0011180578 scopus 로고
    • The discharge kinetics of negatively charged selenium electrophotographic layers
    • E. Montrimas, V. Gaidelis, and A. Pazera The discharge kinetics of negatively charged selenium electrophotographic layers Lith J Phys 6 1966 569 576
    • (1966) Lith J Phys , vol.6 , pp. 569-576
    • Montrimas, E.1    Gaidelis, V.2    Pazera, A.3
  • 34
    • 0037511140 scopus 로고    scopus 로고
    • Extraction current transients: New method of study of charge transport in microcrystalline silicon
    • G. Juška, K. Arlauskas, and M. Viliūnas Extraction current transients: new method of study of charge transport in microcrystalline silicon Phys Rew Lett 84 2000 4946 4949
    • (2000) Phys Rew Lett , vol.84 , pp. 4946-4949
    • Juška, G.1    Arlauskas, K.2    Viliunas, M.3
  • 35
    • 43049170499 scopus 로고    scopus 로고
    • Triindolylmethane-based high triplet energy glass-forming electroactive molecular materials
    • M. Kirkus, R. Lygaitis, M.H. Tsai, J.V. Grazulevicius, and C.C. Wu Triindolylmethane-based high triplet energy glass-forming electroactive molecular materials Synth Met 158 2008 226 232
    • (2008) Synth Met , vol.158 , pp. 226-232
    • Kirkus, M.1    Lygaitis, R.2    Tsai, M.H.3    Grazulevicius, J.V.4    Wu, C.C.5
  • 37
    • 21644480454 scopus 로고    scopus 로고
    • Intramolecular heavy-atom effect in the photophysics of organic molecules
    • K.N. Solov'ev, and E.A. Borisevich Intramolecular heavy-atom effect in the photophysics of organic molecules Physics-Uspekhi 48 2005 231 253
    • (2005) Physics-Uspekhi , vol.48 , pp. 231-253
    • Solov'Ev, K.N.1    Borisevich, E.A.2
  • 38
    • 58149279606 scopus 로고    scopus 로고
    • DFT study of the electronic structure of anthracene derivatives in their neutral, anion and cation forms
    • A.V. Kukhta, I.N. Kukhta, N.A. Kukhta, O.L. Neyra, and E. Meza DFT study of the electronic structure of anthracene derivatives in their neutral, anion and cation forms J Phys B-At Mol Opt 41 2008 205701
    • (2008) J Phys B-At Mol Opt , vol.41 , pp. 205701
    • Kukhta, A.V.1    Kukhta, I.N.2    Kukhta, N.A.3    Neyra, O.L.4    Meza, E.5
  • 39
    • 0000346849 scopus 로고
    • Vapor absorption spectra and oscillator strenghts of napthtalene, anthracene, and pyrene
    • J. Ferguson, L.W. Reeves, and W.G. Schneider Vapor absorption spectra and oscillator strenghts of napthtalene, anthracene, and pyrene Can J Chem 35 1957 1117 1136
    • (1957) Can J Chem , vol.35 , pp. 1117-1136
    • Ferguson, J.1    Reeves, L.W.2    Schneider, W.G.3
  • 40
    • 28144435668 scopus 로고
    • Structure, absorption et comportement chimique dans la serie du phenanthrene
    • [French]
    • M. Ramart-Lucas, M.J. Matti, and T. Guilmart Structure, absorption et comportement chimique dans la serie du phenanthrene Bull Soc Chim Fr 15 1948 1215 1225 [French]
    • (1948) Bull Soc Chim Fr , vol.15 , pp. 1215-1225
    • Ramart-Lucas, M.1    Matti, M.J.2    Guilmart, T.3
  • 42
    • 0042360967 scopus 로고
    • The absorption spectra of some N-substituted p-aminotriphenylmethyl ions
    • H. Walba, and G.E.K. Branch The absorption spectra of some N-substituted p-aminotriphenylmethyl ions J Am Chem Soc 73 1951 3341 3348
    • (1951) J Am Chem Soc , vol.73 , pp. 3341-3348
    • Walba, H.1    Branch, G.E.K.2
  • 43
    • 84982345300 scopus 로고
    • Synthesis of benzothiophenes
    • E.G.G. Werner Synthesis of benzothiophenes Recl Trav Chim Pays Bas 68 1949 509 519
    • (1949) Recl Trav Chim Pays Bas , vol.68 , pp. 509-519
    • Werner, E.G.G.1
  • 46
    • 0000044134 scopus 로고
    • Unimolecular photochemistry of anthracenes
    • H.D. Becker Unimolecular photochemistry of anthracenes Chem Rev 93 1993 145 172
    • (1993) Chem Rev , vol.93 , pp. 145-172
    • Becker, H.D.1
  • 47
    • 36849126497 scopus 로고
    • Relationship between absorption intensity and fluorescence lifetime of molecules
    • R.S. Strickler, and R.A. Berg Relationship between absorption intensity and fluorescence lifetime of molecules J Chem Phys 37 1962 814 822
    • (1962) J Chem Phys , vol.37 , pp. 814-822
    • Strickler, R.S.1    Berg, R.A.2
  • 48
    • 0038508532 scopus 로고    scopus 로고
    • Femtosecond site-selective probing of energy relaxing excitons in poly(phenylenevinylene): Luminescence dynamics and lifetime spectra
    • R. Kersting, B. Mollay, M. Rusch, J. Wenisch, G. Leising, and H.F. Kauffmann Femtosecond site-selective probing of energy relaxing excitons in poly(phenylenevinylene): luminescence dynamics and lifetime spectra J Chem Phys 106 1997 2850 2864
    • (1997) J Chem Phys , vol.106 , pp. 2850-2864
    • Kersting, R.1    Mollay, B.2    Rusch, M.3    Wenisch, J.4    Leising, G.5    Kauffmann, H.F.6
  • 49
    • 79958152749 scopus 로고    scopus 로고
    • Impact of intramolecular twisting and exciton migration on emission efficiency of multifunctional fluorene-benzothiadiazole-carbazole compounds
    • R. Karpicz, S. Puzinas, S. Krotkus, K. Kazlauskas, S. Jursenas, and J.V. Grazulevicius Impact of intramolecular twisting and exciton migration on emission efficiency of multifunctional fluorene-benzothiadiazole-carbazole compounds J Chem Phys 134 2011 204508
    • (2011) J Chem Phys , vol.134 , pp. 204508
    • Karpicz, R.1    Puzinas, S.2    Krotkus, S.3    Kazlauskas, K.4    Jursenas, S.5    Grazulevicius, J.V.6
  • 50
    • 14544269324 scopus 로고    scopus 로고
    • Dendronized perylene diimide Emitters: Synthesis, luminescence, and electron and energy transfer studies
    • J. Qu, J. Zhang, A.C. Grimsdale, K. Müllen, F. Jaiser, and X. Yang Dendronized perylene diimide Emitters: synthesis, luminescence, and electron and energy transfer studies Macromolecules 37 2004 8297 8306
    • (2004) Macromolecules , vol.37 , pp. 8297-8306
    • Qu, J.1    Zhang, J.2    Grimsdale, A.C.3    Müllen, K.4    Jaiser, F.5    Yang, X.6
  • 54
    • 84987058072 scopus 로고
    • Charge transport in disordered organic photoconductors a Monte Carlo simulation study
    • H. Baessler Charge transport in disordered organic photoconductors a Monte Carlo simulation study Phys Status Solidi B 175 1993 15 56
    • (1993) Phys Status Solidi B , vol.175 , pp. 15-56
    • Baessler, H.1


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