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Volumn 99, Issue 1, 2013, Pages 240-249

Synthesis, photophysical and electrochemical properties of aza-boron-diquinomethene complexes

Author keywords

Boron fluorine complexes; DFT calculations; Electrochemical properties; Fluorescence; Optical properties; Synthesis

Indexed keywords

BORON-FLUORINE COMPLEXES; DFT CALCULATION; EMISSION QUANTUM YIELD; INTRA-MOLECULAR CHARGE TRANSFER; PHOTOLUMINESCENCE QUANTUM YIELDS; PHOTOPHYSICAL PROPERTIES; THEORETICAL CALCULATIONS; VISIBLE SPECTRAL REGIONS;

EID: 84884869575     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2013.05.009     Document Type: Article
Times cited : (39)

References (55)
  • 1
    • 36849053388 scopus 로고    scopus 로고
    • BODIPY dyes and their derivatives: Syntheses and spectroscopic properties
    • DOI 10.1021/cr078381n
    • A. Loudet, and K. Burgess BODIPY dyes and their derivatives: syntheses and spectroscopic properties Chem Rev 107 2007 4891 4932 (Pubitemid 350225866)
    • (2007) Chemical Reviews , vol.107 , Issue.11 , pp. 4891-4932
    • Loudet, A.1    Burgess, K.2
  • 2
    • 80054104219 scopus 로고    scopus 로고
    • Fluorescent indicators based on BODIPY
    • N. Boens, V. Leen, and W. Dehaen Fluorescent indicators based on BODIPY Chem Soc Rev 41 2012 1130 1172
    • (2012) Chem Soc Rev , vol.41 , pp. 1130-1172
    • Boens, N.1    Leen, V.2    Dehaen, W.3
  • 4
    • 82455192763 scopus 로고    scopus 로고
    • Color-tunable solid-state emission of 2,2′-biindenyl-based fluorophores
    • Z.Y. Zhang, B. Xu, J.H. Su, L.P. Shen, Y.S. Xie, and H. Tian Color-tunable solid-state emission of 2,2′-biindenyl-based fluorophores Angew Chem Int Ed 50 2011 11654 11657
    • (2011) Angew Chem Int Ed , vol.50 , pp. 11654-11657
    • Zhang, Z.Y.1    Xu, B.2    Su, J.H.3    Shen, L.P.4    Xie, Y.S.5    Tian, H.6
  • 5
    • 39749128941 scopus 로고    scopus 로고
    • Isomeric boron-fluorine complexes with donor-acceptor architecture: Strong solid/liquid fluorescence and large stokes shift
    • Y. Zhou, Y. Xiao, S.M. Chi, and X.H. Qian Isomeric boron-fluorine complexes with donor-acceptor architecture: strong solid/liquid fluorescence and large stokes shift Org Lett 10 2008 633 636
    • (2008) Org Lett , vol.10 , pp. 633-636
    • Zhou, Y.1    Xiao, Y.2    Chi, S.M.3    Qian, X.H.4
  • 6
    • 40849107127 scopus 로고    scopus 로고
    • The chemistry of fluorescent BODIPY dyes: Versatility unsurpassed
    • G. Ulrich, R. Ziessel, and A. Harriman The chemistry of fluorescent BODIPY dyes: versatility unsurpassed Angew Chem Int Ed 47 2008 1184 1201
    • (2008) Angew Chem Int Ed , vol.47 , pp. 1184-1201
    • Ulrich, G.1    Ziessel, R.2    Harriman, A.3
  • 7
    • 34147111647 scopus 로고    scopus 로고
    • The chemistry of Bodipy: A new El Dorado for fluorescence tools
    • DOI 10.1039/b617972j
    • R. Ziessel, G. Ulrich, and A. Harriman The chemistry of BODIPY: a new El Dorado for fluorescence tools New J Chem 31 2007 496 501 (Pubitemid 46558017)
    • (2007) New Journal of Chemistry , vol.31 , Issue.4 , pp. 496-501
    • Ziessel, R.1    Ulrich, G.2    Harriman, A.3
  • 8
    • 39349105765 scopus 로고    scopus 로고
    • Novel fluorescent fluorine-boron complexes: Synthesis, crystal structure, photoluminescence, and electrochemistry properties
    • DOI 10.1021/jo702265x
    • Y. Zhou, Y. Xiao, D. Li, M.Y. Fu, and X.H. Qian Novel fluorescent fluorine-boron complexes: synthesis, crystal structure, photoluminescence, and electrochemistry properties J Org Chem 73 2008 1571 1574 (Pubitemid 351263676)
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.4 , pp. 1571-1574
    • Zhou, Y.1    Xiao, Y.2    Li, D.3    Fu, M.4    Qian, X.5
  • 9
    • 84869200753 scopus 로고    scopus 로고
    • Oligothienyl-BODIPYs: Red and near-infrared emitters
    • A. Poirel, A.D. Nicola, and R. Ziessel Oligothienyl-BODIPYs: red and near-infrared emitters Org Lett 14 2012 5696 5699
    • (2012) Org Lett , vol.14 , pp. 5696-5699
    • Poirel, A.1    Nicola, A.D.2    Ziessel, R.3
  • 10
    • 84961985395 scopus 로고    scopus 로고
    • Gold(I) complexes of brominated azadipyrromethene ligands
    • L. Gao, N. Deligonul, and T.G. Gray Gold(I) complexes of brominated azadipyrromethene ligands Inorg Chem 51 2012 7682 7688
    • (2012) Inorg Chem , vol.51 , pp. 7682-7688
    • Gao, L.1    Deligonul, N.2    Gray, T.G.3
  • 13
    • 72449131878 scopus 로고    scopus 로고
    • Azide conjugatable and pH responsive near-infrared fluorescent imaging probes
    • J. Murtagh, D.O. Frimannsson, and D.F. O'Shea Azide conjugatable and pH responsive near-infrared fluorescent imaging probes Org Lett 11 2009 5386 5389
    • (2009) Org Lett , vol.11 , pp. 5386-5389
    • Murtagh, J.1    Frimannsson, D.O.2    O'Shea, D.F.3
  • 14
    • 78650347651 scopus 로고    scopus 로고
    • Tuning photosensitized singlet oxygen generation efficiency of novel aza-BODIPY dyes
    • N. Adarsh, R.R. Avirah, and D. Ramaiah Tuning photosensitized singlet oxygen generation efficiency of novel aza-BODIPY dyes Org Lett 12 2010 5720 5723
    • (2010) Org Lett , vol.12 , pp. 5720-5723
    • Adarsh, N.1    Avirah, R.R.2    Ramaiah, D.3
  • 16
    • 79951885628 scopus 로고    scopus 로고
    • Multifunctional materials in high-performance OLEDs: Challenges for solid-state lighting
    • H. Sasabe, and J. Kido Multifunctional materials in high-performance OLEDs: challenges for solid-state lighting Chem Mater 23 2011 621 630
    • (2011) Chem Mater , vol.23 , pp. 621-630
    • Sasabe, H.1    Kido, J.2
  • 18
    • 73049113368 scopus 로고    scopus 로고
    • 2 complex of indol-2-yl-isoindol-1-ylidene- amine: A fully conjugated azadipyrromethene
    • 2 complex of indol-2-yl-isoindol-1-ylidene-amine: a fully conjugated azadipyrromethene Tetrahedron Lett 51 2010 811 814
    • (2010) Tetrahedron Lett , vol.51 , pp. 811-814
    • Li, Y.1    Dolphin, D.2    Patrick, B.O.3
  • 19
    • 66149087346 scopus 로고    scopus 로고
    • New redox stable low band gap conjugated polymer based on an EDOT-BODIPY-EDOT repeat unit
    • J.C. Forgie, P.J. Skabara, I. Stibor, F. Vilela, and Z. Vobecka New redox stable low band gap conjugated polymer based on an EDOT-BODIPY-EDOT repeat unit Chem Mater 21 2009 1784 1786
    • (2009) Chem Mater , vol.21 , pp. 1784-1786
    • Forgie, J.C.1    Skabara, P.J.2    Stibor, I.3    Vilela, F.4    Vobecka, Z.5
  • 20
    • 4544239239 scopus 로고    scopus 로고
    • Highly efficient energy transfer to a novel organic dye in OLED devices
    • A. Hepp, G. Uirich, R. Schmechel, H. von Seggern, and R. Ziessel Highly efficient energy transfer to a novel organic dye in OLED devices Synth Met 146 2004 11 15
    • (2004) Synth Met , vol.146 , pp. 11-15
    • Hepp, A.1    Uirich, G.2    Schmechel, R.3    Von Seggern, H.4    Ziessel, R.5
  • 21
    • 27744559789 scopus 로고    scopus 로고
    • Recent development of blue fluorescent OLED materials and devices
    • DOI 10.1109/JDT.2005.852802
    • S.W. Wen, M.T. Lee, and C.H. Chen Recent development of blue fluorescent OLED materials and devices J Disp Technol 1 2005 90 99 (Pubitemid 41584126)
    • (2005) IEEE/OSA Journal of Display Technology , vol.1 , Issue.1 , pp. 90-99
    • Wen, S.-W.1    Lee, M.-T.2    Chen, C.H.3
  • 22
    • 84861307326 scopus 로고    scopus 로고
    • The development of anthracene derivatives for organic light-emitting diodes
    • J.H. Huang, J.H. Su, and H. Tian The development of anthracene derivatives for organic light-emitting diodes J Mater Chem 22 2012 10977 10989
    • (2012) J Mater Chem , vol.22 , pp. 10977-10989
    • Huang, J.H.1    Su, J.H.2    Tian, H.3
  • 23
    • 14644411755 scopus 로고    scopus 로고
    • New dopant and host materials for blue-light-emitting phosphorescent organic electroluminescent devices
    • DOI 10.1002/adma.200401373
    • S.J. Yeh, M.F. Wu, C.T. Chen, Y.H. Song, Y. Chi, and M.H. Ho New dopant and host materials for blue-light-emitting phosphorescent organic electroluminescent devices Adv Mater 17 2005 285 289 (Pubitemid 40320144)
    • (2005) Advanced Materials , vol.17 , Issue.3 , pp. 285-289
    • Yeh, S.-J.1    Wu, M.-F.2    Chen, C.-T.3    Song, Y.-H.4    Chi, Y.5    Ho, M.-H.6    Hsu, S.-F.7    Chen, C.H.8
  • 25
    • 79951504485 scopus 로고    scopus 로고
    • Difluoro-boron-triaza-anthracene: A laser dye in the blue region. Theoretical simulation of alternative difluoro-boron-diaza-aromatic systems
    • J. Bañuelos, F.L. Arbeloa, V. Martinez, M. Liras, A. Costela, and I.G. Moreno Difluoro-boron-triaza-anthracene: a laser dye in the blue region. Theoretical simulation of alternative difluoro-boron-diaza-aromatic systems Phys Chem Chem Phys 13 2011 3437 3445
    • (2011) Phys Chem Chem Phys , vol.13 , pp. 3437-3445
    • Bañuelos, J.1    Arbeloa, F.L.2    Martinez, V.3    Liras, M.4    Costela, A.5    Moreno, I.G.6
  • 26
    • 80054820649 scopus 로고    scopus 로고
    • New solution-processable electron transport materials for highly efficient blue phosphorescent OLEDs
    • E. Ahmed, T. Earmme, and S.A. Jenekhe New solution-processable electron transport materials for highly efficient blue phosphorescent OLEDs Adv Funct Mater 21 2011 3889 3899
    • (2011) Adv Funct Mater , vol.21 , pp. 3889-3899
    • Ahmed, E.1    Earmme, T.2    Jenekhe, S.A.3
  • 27
    • 34248572498 scopus 로고    scopus 로고
    • Blue-light-emitting oligoquinolines: Synthesis, properties, and high-efficiency blue-light-emitting diodes
    • DOI 10.1002/adfm.200600542
    • C.J. Tonzola, A.P. Kulkarni, A.P. Gifford, W. Kaminsky, and S.A. Jenekhe Blue-light-emitting oligoquinolines: synthesis, properties, and high-efficiency blue-light-emitting diodes Adv Funct Mater 17 2007 863 874 (Pubitemid 46750860)
    • (2007) Advanced Functional Materials , vol.17 , Issue.6 , pp. 863-874
    • Tonzola, C.J.1    Kulkarni, A.P.2    Gifford, A.P.3    Kaminsky, W.4    Jenekhe, S.A.5
  • 28
    • 2542633612 scopus 로고    scopus 로고
    • New soluble n-type conjugated polymers for use as electron transport materials in light-emitting diodes
    • C.J. Tonzola, M.M. Alam, B.A. Bean, and S.A. Jenekhe New soluble n-type conjugated polymers for use as electron transport materials in light-emitting diodes Macromolecules 37 2004 3554 3563
    • (2004) Macromolecules , vol.37 , pp. 3554-3563
    • Tonzola, C.J.1    Alam, M.M.2    Bean, B.A.3    Jenekhe, S.A.4
  • 29
    • 28144437155 scopus 로고    scopus 로고
    • A new synthetic route to soluble polyquinolines with tunable photophysical, redox, and electroluminescent properties
    • DOI 10.1021/ma051280b
    • C.J. Tonzola, M.M. Alam, B.A. Bean, and S.A. Jenekhe A new synthetic route to soluble polyquinolines with tunable photophysical, redox, and electroluminescent properties Macromolecules 38 2005 9539 9547 (Pubitemid 41698406)
    • (2005) Macromolecules , vol.38 , Issue.23 , pp. 9539-9547
    • Tonzola, C.J.1    Alam, M.M.2    Jenekhe, S.A.3
  • 30
    • 75649094888 scopus 로고    scopus 로고
    • Highly efficient fluorescent-phosphorescent triplet-harvesting hybrid organic light-emitting diodes
    • M.E. Kondakova, J.C. Deaton, T.D. Pawlik, D.J. Giesen, D.Y. Kondakov, and R.H. Young Highly efficient fluorescent-phosphorescent triplet-harvesting hybrid organic light-emitting diodes J Appl Phys 107 2010 014515-1 014515-13
    • (2010) J Appl Phys , vol.107 , pp. 0145151-01451513
    • Kondakova, M.E.1    Deaton, J.C.2    Pawlik, T.D.3    Giesen, D.J.4    Kondakov, D.Y.5    Young, R.H.6
  • 31
    • 84864577729 scopus 로고    scopus 로고
    • Novel multifunctional organic semiconductor materials based on 4,8-substituted 1,5-naphthyridine: Synthesis, single crystal structures, opto-electrical properties and quantum chemistry calculation
    • K.Y. Wang, C. Chen, J.F. Liu, Q. Wang, J. Chang, and H.J. Zhu Novel multifunctional organic semiconductor materials based on 4,8-substituted 1,5-naphthyridine: synthesis, single crystal structures, opto-electrical properties and quantum chemistry calculation Biomol Chem 10 2012 6693 6704
    • (2012) Biomol Chem , vol.10 , pp. 6693-6704
    • Wang, K.Y.1    Chen, C.2    Liu, J.F.3    Wang, Q.4    Chang, J.5    Zhu, H.J.6
  • 32
    • 84864236637 scopus 로고    scopus 로고
    • The synthesis, photophysical and electrochemical properties of a series of novel 3,8,13-substituted triindole derivatives
    • T.H. Zhu, G.K. He, J. Chang, D.D. Zhao, X.L. Zhu, and H.J. Zhu The synthesis, photophysical and electrochemical properties of a series of novel 3,8,13-substituted triindole derivatives Dyes Pigm 95 2012 679 688
    • (2012) Dyes Pigm , vol.95 , pp. 679-688
    • Zhu, T.H.1    He, G.K.2    Chang, J.3    Zhao, D.D.4    Zhu, X.L.5    Zhu, H.J.6
  • 33
    • 0000189651 scopus 로고
    • Density-functional thermochemistry. III. The role of exact exchange
    • D.B. Axel Density-functional thermochemistry. III. The role of exact exchange J Chem Phys 98 1993 5648 5652
    • (1993) J Chem Phys , vol.98 , pp. 5648-5652
    • Axel, D.B.1
  • 34
    • 0345491105 scopus 로고
    • Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
    • C. Lee, W. Yang, and R.G. Parr Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density Phys Rev B 37 1988 785 789
    • (1988) Phys Rev B , vol.37 , pp. 785-789
    • Lee, C.1    Yang, W.2    Parr, R.G.3
  • 35
    • 84986468715 scopus 로고
    • Efficient diffuse function-augmented basis sets for anion calculations. III. The 3-21 + G basis set for first-row elements, lithium to fluorine
    • T. Clark, J. Chandrasekhar, G.W. Spitznagel, and P.V.R. Schleyer Efficient diffuse function-augmented basis sets for anion calculations. III. The 3-21 + G basis set for first-row elements, lithium to fluorine J Comput Chem 4 1983 294 301
    • (1983) J Comput Chem , vol.4 , pp. 294-301
    • Clark, T.1    Chandrasekhar, J.2    Spitznagel, G.W.3    Schleyer, P.V.R.4
  • 36
    • 33645949559 scopus 로고
    • Self-consistent molecular orbital methods. XXIII. A polarization type basis set for second-row elements
    • M.M. Francl, W.J. Pietro, W.J. Hehre, J.S. Binkley, M.S. Gordon, and D.J. DeFrees Self-consistent molecular orbital methods. XXIII. A polarization type basis set for second-row elements J Chem Phys 77 1982 3654 3665
    • (1982) J Chem Phys , vol.77 , pp. 3654-3665
    • Francl, M.M.1    Pietro, W.J.2    Hehre, W.J.3    Binkley, J.S.4    Gordon, M.S.5    Defrees, D.J.6
  • 37
    • 0000712790 scopus 로고
    • The performance of the Becke-Lee-Yang-Parr (B-LYP) density-functional theory with various basis sets
    • P.M.W. Gill, B.G. Johnson, J.A. Pople, and M.J. Frisch The performance of the Becke-Lee-Yang-Parr (B-LYP) density-functional theory with various basis sets Chem Phys Lett 197 1992 499 505
    • (1992) Chem Phys Lett , vol.197 , pp. 499-505
    • Gill, P.M.W.1    Johnson, B.G.2    Pople, J.A.3    Frisch, M.J.4
  • 38
    • 26844534384 scopus 로고
    • Self-consistent molecular orbital methods. A basis set for correlated wave functions
    • R. Krishnan, J.S. Binkley, R. Seeger, and J.A. Pople Self-consistent molecular orbital methods. A basis set for correlated wave functions J Chem Phys 72 1980 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
  • 40
    • 33947478760 scopus 로고
    • Aza-aromatic substitution. I. The selective bromination of the quinoline nucleus1
    • J.J. Eisch Aza-aromatic substitution. I. The selective bromination of the quinoline nucleus1 J Org Chem 27 1962 1318 1323
    • (1962) J Org Chem , vol.27 , pp. 1318-1323
    • Eisch, J.J.1
  • 41
    • 84886600249 scopus 로고
    • Polarization of aromatic heterocyclic compounds. LXXV. Nitration of quinoline 1-oxide having substituents in their benzene ring
    • T. Naito Polarization of aromatic heterocyclic compounds. LXXV. Nitration of quinoline 1-oxide having substituents in their benzene ring Yakugaku Zasshi 68 1948 209 210
    • (1948) Yakugaku Zasshi , vol.68 , pp. 209-210
    • Naito, T.1
  • 42
    • 34447643979 scopus 로고    scopus 로고
    • Synthesis of pyrido[2′,1′:2,3]imidazo[4,5-b]quinoline and pyrido[1′,2′:1,2]imidazo[4,5-b]quinoline and their benzo and aza analogs via tandem catalysis
    • DOI 10.1016/j.tet.2007.06.011, PII S0040402007010381
    • K.T. Loones, B.U. Maes, and R.A. Dommisse Synthesis of pyrido[2',1':2,3] imidazo[4,5-b]quinoline and pyrido[1',2':1,2]imidazo[4,5-b]quinoline and their benzo and aza analogs via tandem catalysis Tetrahedron 63 2007 8954 8961 (Pubitemid 47087860)
    • (2007) Tetrahedron , vol.63 , Issue.36 , pp. 8954-8961
    • Loones, K.T.J.1    Maes, B.U.W.2    Dommisse, R.A.3
  • 44
    • 47849107520 scopus 로고    scopus 로고
    • Synthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues
    • DOI 10.1039/b804106g
    • J.K. Klosterman, A. Linden, and J.S. Siegel Synthesis of aryl-substitute 2-pyridyl-1,10-phenanthrolines; a series of oriented terpyridine analogues Org Biomol Chem 6 2008 2755 2764 (Pubitemid 352035437)
    • (2008) Organic and Biomolecular Chemistry , vol.6 , Issue.15 , pp. 2755-2764
    • Klosterman, J.K.1    Linden, A.2    Siegel, J.S.3
  • 46
    • 77949794863 scopus 로고    scopus 로고
    • Two-step total syntheses of canthin-6-one alkaloids: New one-pot sequential Pd-catalyzed Suzuki-Miyaura coupling and Cu-catalyzed amidation reaction
    • A. Gollner, and P.A. Koutentis Two-step total syntheses of canthin-6-one alkaloids: new one-pot sequential Pd-catalyzed Suzuki-Miyaura coupling and Cu-catalyzed amidation reaction Org Lett 12 2010 1352 1355
    • (2010) Org Lett , vol.12 , pp. 1352-1355
    • Gollner, A.1    Koutentis, P.A.2
  • 47
    • 33745747321 scopus 로고    scopus 로고
    • Safe and practical large-scale synthesis of 2-aminoquinoline-6-carboxylic acid benzyl ester
    • DOI 10.1021/op060044d
    • M. Couturier, and T. Le Safe and practical large-scale synthesis of 2-aminoquinoline-6-carboxylic acid benzyl ester Org Process Res Dev 10 2006 534 538 (Pubitemid 44012694)
    • (2006) Organic Process Research and Development , vol.10 , Issue.3 , pp. 534-538
    • Couturier, M.1    Le, T.2
  • 48
    • 84055223624 scopus 로고    scopus 로고
    • Synthesis and fluorescence properties of novel pyrazine-boron complexes bearing a β-iminoketone ligand
    • Y. Kubota, H. Hara, S. Tanaka, K. Funabiki, and M. Matsui Synthesis and fluorescence properties of novel pyrazine-boron complexes bearing a β-iminoketone ligand Org Lett 24 2011 6545 6547
    • (2011) Org Lett , vol.24 , pp. 6545-6547
    • Kubota, Y.1    Hara, H.2    Tanaka, S.3    Funabiki, K.4    Matsui, M.5
  • 49
    • 84867421133 scopus 로고    scopus 로고
    • A BODIPY fluorescence probe modulated by selenoxide spirocyclization reaction for peroxynitrite detection and imaging in living cells
    • B. Wang, F.B. Yu, P. Li, X.F. Sun, and K.L. Han A BODIPY fluorescence probe modulated by selenoxide spirocyclization reaction for peroxynitrite detection and imaging in living cells Dyes Pigm 96 2013 383 390
    • (2013) Dyes Pigm , vol.96 , pp. 383-390
    • Wang, B.1    Yu, F.B.2    Li, P.3    Sun, X.F.4    Han, K.L.5
  • 52
    • 70350504861 scopus 로고    scopus 로고
    • Reevaluation of absolute luminescence quantum yields of standard solutions using a spectrometer with an integrating sphere and a back-thinned CCD detector
    • K. Suzuki, A. Kobayashi, S. Kaneko, K. Takehira, T. Yoshihara, and H. Ishida Reevaluation of absolute luminescence quantum yields of standard solutions using a spectrometer with an integrating sphere and a back-thinned CCD detector Phys Chem Chem Phys 11 2009 9850 9860
    • (2009) Phys Chem Chem Phys , vol.11 , pp. 9850-9860
    • Suzuki, K.1    Kobayashi, A.2    Kaneko, S.3    Takehira, K.4    Yoshihara, T.5    Ishida, H.6
  • 53
    • 5444249877 scopus 로고    scopus 로고
    • Spectroscopic and electrochemical characterization of di-tert-butylated sterically hindered Schiff bases and their phenoxyl radicals
    • V.T. Kasumov, A.A. Medjidov, N. Yayli, and Y. Zeren Spectroscopic and electrochemical characterization of di-tert-butylated sterically hindered Schiff bases and their phenoxyl radicals Spectrochimica Acta Part A 60 2004 3037 3047
    • (2004) Spectrochimica Acta Part A , vol.60 , pp. 3037-3047
    • Kasumov, V.T.1    Medjidov, A.A.2    Yayli, N.3    Zeren, Y.4
  • 54
    • 84860615840 scopus 로고    scopus 로고
    • A general synthetic route to 3,5-substituted boron dipyrromethenes: Applications and properties
    • G. Ulrich, R. Ziessel, and A. Haefele A general synthetic route to 3,5-substituted boron dipyrromethenes: applications and properties J Org Chem 77 2012 4298 4311
    • (2012) J Org Chem , vol.77 , pp. 4298-4311
    • Ulrich, G.1    Ziessel, R.2    Haefele, A.3
  • 55
    • 33646132027 scopus 로고    scopus 로고
    • Electronic structures and electron-injection mechanisms of cesium-carbonate-incorporated cathode structures for organic light-emitting devices
    • C.I. Wu, C.T. Lin, Y.H. Chen, and M.H. Chen Electronic structures and electron-injection mechanisms of cesium-carbonate-incorporated cathode structures for organic light-emitting devices Appl Phys Lett 88 2006 152104
    • (2006) Appl Phys Lett , vol.88 , pp. 152104
    • Wu, C.I.1    Lin, C.T.2    Chen, Y.H.3    Chen, M.H.4


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