SCOPUS 정보 검색 플랫폼

Volumn 1, Issue 3, 2013, Pages 432-440

Synthesis and electroluminescence properties of highly efficient blue fluorescence emitters using dual core chromophores

Author keywords

[No Author keywords available]

Indexed keywords

BLUE EMISSION; BLUE FLUORESCENCE; CORE MATERIAL; EL DEVICES; ELECTROLUMINESCENCE PROPERTIES; HIGH LUMINANCES; SUZUKI COUPLING REACTION; TERPHENYLS;

ANTHRACENE; COREMAKING; ELECTROLUMINESCENCE; LUMINANCE; PYRENE;

CHROMOPHORES;

EID: 84876930694 PISSN: 20507534 EISSN: 20507526 Source Type: Journal
DOI: 10.1039/c2tc00185c Document Type: Article

Times cited : (103)

References (23)

1
- 21544459113
- C. W. Tang S. A. Van Slyke Appl. Phys. Lett. 1987 51 913
- (1987) Appl. Phys. Lett. , vol.51 , pp. 913
- Tang, C.W.¹ Van Slyke, S.A.²

2
- 33645881353
- Y. R. Sun N. Giebink C. Kanno B. Ma M. E. Thompson S. R. Forrest Nature 2006 440 908
- (2006) Nature , vol.440 , pp. 908
- Sun, Y.R.¹ Giebink, N.² Kanno, C.³ Ma, B.⁴ Thompson, M.E.⁵ Forrest, S.R.⁶

3
- 36148961148
- S. K. Kim Y. I. Park I. N. Kang J. H. Lee J. W. Park J. Mater. Chem. 2007 17 4670
- (2007) J. Mater. Chem. , vol.17 , pp. 4670
- Kim, S.K.¹ Park, Y.I.² Kang, I.N.³ Lee, J.H.⁴ Park, J.W.⁵

4
- 47049115105
- S. K. Kim B. Yang Y. Ma J. H. Lee J. W. Park J. Mater. Chem. 2008 18 3376
- (2008) J. Mater. Chem. , vol.18 , pp. 3376
- Kim, S.K.¹ Yang, B.² Ma, Y.³ Lee, J.H.⁴ Park, J.W.⁵

5
- 42649142918
- Y. I. Park J. H. Son J. S. Kang S. K. Kim J. H. Lee J. W. Park Chem. Commun. 2008 2143
- (2008) Chem. Commun. , pp. 2143
- Park, Y.I.¹ Son, J.H.² Kang, J.S.³ Kim, S.K.⁴ Lee, J.H.⁵ Park, J.W.⁶

6
- 77954577844
- Y. Park J. H. Lee D. H. Jung S. H. Liu Y. H. Lin L. Y. Chen C. C. Wu J. W. Park J. Mater. Chem. 2010 20 5930
- (2010) J. Mater. Chem. , vol.20 , pp. 5930
- Park, Y.¹ Lee, J.H.² Jung, D.H.³ Liu, S.H.⁴ Lin, Y.H.⁵ Chen, L.Y.⁶ Wu, C.C.⁷ Park, J.W.⁸

7
- 77950690667
- Y. Park S. Kim J. H. Lee D. H. Jung C. C. Wu J. Park Org. Electron. 2010 11 864
- (2010) Org. Electron. , vol.11 , pp. 864
- Park, Y.¹ Kim, S.² Lee, J.H.³ Jung, D.H.⁴ Wu, C.C.⁵ Park, J.⁶

8
- 84876896838
- R. Ma P. A. Levermore A. Dyatkin Z. Elshenawy V. Adamovich H. Pang R. C. Kwong M. S. Weaver M. Hack J. J. Brown IMID Dig. 2011 60
- (2011) IMID Dig. , pp. 60
- Ma, R.¹ Levermore, P.A.² Dyatkin, A.³ Elshenawy, Z.⁴ Adamovich, V.⁵ Pang, H.⁶ Kwong, R.C.⁷ Weaver, M.S.⁸ Hack, M.⁹ Brown, J.J.¹⁰

9
- 84863190105
- Y. Kawamura H. Kuma M. Funahashi M. Kawamura Y. Mizuki H. Saito R. Naraoka K. Nishimura Y. Jinde T. Iwakuma C. Hosokawa SID Dig. 2011 829
- (2011) SID Dig. , pp. 829
- Kawamura, Y.¹ Kuma, H.² Funahashi, M.³ Kawamura, M.⁴ Mizuki, Y.⁵ Saito, H.⁶ Naraoka, R.⁷ Nishimura, K.⁸ Jinde, Y.⁹ Iwakuma, T.¹⁰ Hosokawa, C.¹¹

10
- 84862908521
- H. Park J. Lee I. Kang H. Y. Chu J. I. Lee S. K. Kwon Y. H. Kim J. Mater. Chem. 2012 22 2695
- (2012) J. Mater. Chem. , vol.22 , pp. 2695
- Park, H.¹ Lee, J.² Kang, I.³ Chu, H.Y.⁴ Lee, J.I.⁵ Kwon, S.K.⁶ Kim, Y.H.⁷

11
- 84863115616
- Z. Q. Wang C. Xu W. Z. Wang L. M. Duan Z. Li B. T. Zhao B. M. Ji New J. Chem. 2012 36 662
- (2012) New J. Chem. , vol.36 , pp. 662
- Wang, Z.Q.¹ Xu, C.² Wang, W.Z.³ Duan, L.M.⁴ Li, Z.⁵ Zhao, B.T.⁶ Ji, B.M.⁷

12
- 78649353359
- M. S. Gong H. S. Lee Y. M. Jeon J. Mater. Chem. 2010 20 10735
- (2010) J. Mater. Chem. , vol.20 , pp. 10735
- Gong, M.S.¹ Lee, H.S.² Jeon, Y.M.³

13
- 61349144404
- C. H. Wu C. H. Chien F. M. Hsu P. I. Shih C. F. Shu J. Mater. Chem. 2009 19 1464
- (2009) J. Mater. Chem. , vol.19 , pp. 1464
- Wu, C.H.¹ Chien, C.H.² Hsu, F.M.³ Shih, P.I.⁴ Shu, C.F.⁵

14
- 78651410816
- S. L. Lai Q. X. Tong M. Y. Chan T. W. Ng M. F. Lo S. T. Lee C. S. Lee J. Mater. Chem. 2011 21 1206
- (2011) J. Mater. Chem. , vol.21 , pp. 1206
- Lai, S.L.¹ Tong, Q.X.² Chan, M.Y.³ Ng, T.W.⁴ Lo, M.F.⁵ Lee, S.T.⁶ Lee, C.S.⁷

15
- 77649224711
- T. M. Figueira-Duarte P. G. D. Rosso R. Trattnig S. Sax E. J. W. List K. Mullen Adv. Mater. 2010 22 990
- (2010) Adv. Mater. , vol.22 , pp. 990
- Figueira-Duarte, T.M.¹ Rosso, P.G.D.² Trattnig, R.³ Sax, S.⁴ List, E.J.W.⁵ Mullen, K.⁶

16
- 0038166559
- B. Balaganesan W. J. Shen C. H. Chem Tetrahedron Lett. 2003 44 5747
- (2003) Tetrahedron Lett. , vol.44 , pp. 5747
- Balaganesan, B.¹ Shen, W.J.² Chem, C.H.³

17
- 54949123049
- D. Mansell N. Rattray L. L. Etchells C. H. Schwalbe A. J. Blake E. V. Bichenkova R. A. Bryce C. J. Barker A. Diaz C. Kremer S. Freeman Chem. Commun. 2008 5161
- (2008) Chem. Commun. , pp. 5161
- Mansell, D.¹ Rattray, N.² Etchells, L.L.³ Schwalbe, C.H.⁴ Blake, A.J.⁵ Bichenkova, E.V.⁶ Bryce, R.A.⁷ Barker, C.J.⁸ Diaz, A.⁹ Kremer, C.¹⁰ Freeman, S.¹¹

18
- 0031552545
- J. Cornil A. J. Heeger J. L. Bredas Chem. Phys. Lett. 1997 272 463
- (1997) Chem. Phys. Lett. , vol.272 , pp. 463
- Cornil, J.¹ Heeger, A.J.² Bredas, J.L.³

19
- 79952848552
- PL and EL emissions seem to follow what is observed for the anthracene moiety more than for the pyrene moiety. Further studies on this issue are under way
- Y. Park B. Kim C. Lee A. Hyun S. Jang J. H. Lee Y. S. Gal T. H. Kim K. S. Kim J. Park J. Phys. Chem. C 2011 115 4843
- (2011) J. Phys. Chem. C , vol.115 , pp. 4843
- Park, Y.¹ Kim, B.² Lee, C.³ Hyun, A.⁴ Jang, S.⁵ Lee, J.H.⁶ Gal, Y.S.⁷ Kim, T.H.⁸ Kim, K.S.⁹ Park, J.¹⁰

20
- 80053418623
- D. Yokoyama Y. Park B. Kim S. Kim Y. J. Pu J. Kido J. Park Appl. Phys. Lett. 2011 99 123303
- (2011) Appl. Phys. Lett. , vol.99 , pp. 123303
- Yokoyama, D.¹ Park, Y.² Kim, B.³ Kim, S.⁴ Pu, Y.J.⁵ Kido, J.⁶ Park, J.⁷

21
- 58049182462
- D. Yokoyama A. Sakaguchi M. Suzuki C. Adachi Org. Electron. 2009 10 127
- (2009) Org. Electron. , vol.10 , pp. 127
- Yokoyama, D.¹ Sakaguchi, A.² Suzuki, M.³ Adachi, C.⁴

22
- 82455174319
- When transition dipole moments of emitting molecules are oriented in the horizontal direction, the outcoupling efficiency of the OLED becomes higher than that with randomly oriented transition dipole moments. This is because vertically oriented transition dipole moments are excluded from the emitting layer. Because the vertically oriented transition dipole moments emit light mainly in the horizontal direction, the light emitted from them cannot be extracted from the device due to the total reflection. If it is ideally assumed that transition dipole moments of all emitting molecules are oriented completely in the horizontal direction, the increasing rate compared to random orientation is around 1.5. Thus, the outcoupling efficiency of OLEDs can be enhanced by designing emitting molecules so that their transition dipole moments are horizontally oriented well in the film
- D. Yokoyama J. Mater. Chem. 2011 21 19187
- (2011) J. Mater. Chem. , vol.21 , pp. 19187
- Yokoyama, D.¹

23
- 84859145750
- Y. J. Pu G. Nakata F. Satoh H. Sasabe D. Yokoyama J. Kido Adv. Mater. 2012 24 1765
- (2012) Adv. Mater. , vol.24 , pp. 1765
- Pu, Y.J.¹ Nakata, G.² Satoh, F.³ Sasabe, H.⁴ Yokoyama, D.⁵ Kido, J.⁶

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