A novel amorphous oligo(phenylenevinylene) dimer with a biphenyl linkage center and fluorene end groups for electroluminescent devices

Journal of Materials Chemistry

Volumn 14, Issue 18, 2004, Pages 2735-2740

  He, Feng ^a   Xia, Hong ^a   Tang, Shi ^a   Duan, Yu ^a   Zeng, Ming ^a   Liu, Linlin ^a   Li, Mao ^a   Zhang, Haiquan ^a   Yang, Bing ^a   Ma, Yuguang ^a   Liu, Shiyong ^a   Shen, Jiacong ^a  

^a JILIN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; DIMERS; ELECTROLUMINESCENCE; ELECTROOPTICAL DEVICES; MULTILAYERS; SYNTHESIS (CHEMICAL);

ELECTROLUMINSCENT DEVICES; FLUORENE; LIGHT EMITTING DEVICES (LED); WITTIG REACTION;

OLIGOMERS;

2,5,2',5' TETRAKIS(9,9' DIHEXYLFLUORENYL)BIPHENYL; BIPHENYL DERIVATIVE; DIMER; FLUORENE DERIVATIVE; OLIGO(PHENYLENEVINYLENE) DIMER; OLIGOMER; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CROSS LINKING; DEVICE; DISSOLUTION; EVAPORATION; FILM; FLUORESCENCE; LIGHT EMITTING DIODE; LUMINESCENCE; MATERIAL COATING; OPTICAL ROTATION; SYNTHESIS; WITTIG REACTION;

EID: 5044221190     PISSN: 09599428     EISSN: None     Source Type: Journal    
DOI: 10.1039/b407262f     Document Type: Article

References (23)

1. J. H. Burroughes, D. D. C. Bradley, A. R. Brown, R. N. Marks, K. Mackay, R. H. Friend, P. L. Burn and A. B. Holmes, Nature, 1990, 347, 539.
2. G. Gustafsson, Y. Cao, G. M. Treacy, F. Klavetter, N. Colaneri and A. J. Heeger, Nature, 1992, 357, 447.
3. A. B. Holmes, D. D. C. Bradley, A. R. Brown, P. L. Burn, J. H. Burroughes, R. H. Friend, N. C. Greenham, R. W. Gymer, D. A. Halliday, R. W. Jackson, A. Kraft, J. H. F. Martens, K. Pichler and I. D. W. Samuel, Synth. Met., 1993, 55-57, 4031.
4. A. Kraft, A. C. Grimsdale and A. B. Holmes, Angew. Chem., Int. Ed, 1998, 37, 402.
5. G. Yu, J. Wang, J. McElvain and A. J. Heeger, Adv. Mater., 1998. 10, 1431.
6. P. M. Ruiz, B. Behnisch, K. H. Schweikart, M. Hanack, L. Ler and D. Oelkrug, Chem. Eur. J., 2000, 6, 1294.
7. H. K. Ryu, W. Y. Kim, K. S. Nahm, Y. B. Hahn, Y. S. Lee and C. Lee, Synth. Met., 2002, 128, 21.
8. F. J. Lange, M. Leuze and M. Hanack, J. Phys. Org. Chem., 2001, 14, 474.
9. F. Wurthner, C. Thalacker, S. Dieke and C. Tschierske, Chem. Eur. J., 2001, 7, 2245.
10. D. Oelkrug, A. Tompert, H. J. Egelhaaf, M. Hanack, E. Steinhuber, M. Hohloch, H. Meier and U. Stalmach, Synth. Met., 1996, 83, 231.
11. D. Oelkrug, A. Tompert, J. Gierschner, H. J. Egelhaaf, M. Hanack, M. Hohloch and E. Steinhuber, J. Phys. Chem. B, 1998, 102, 1902.
12. F. T. Luo, Y. T. Tao, S. L. Ko, C. H. Chuen and H. Chen, J. Mater. Chem., 2002, 12, 47.
13. S. Wang, W. J. Oldham, R. A. Hudack and G. C. Bazan. J. Am. Chem. Soc., 2000, 122, 5695.
14. T. Gu, G. Accorsi, N. Armaroli, D. Guillon and J. F. Nierengarten, Tetrahedron Lett., 2001, 42, 2309.
15. M. R. Robinson, S. Wang, G. C. Bazan and Y. Cao, Adv. Mater., 2000, 12, 1701.
16. F. He, G. Cheng, H. Q. Zhang, Y. Zheng, Z. Q. Xie, B. Yang, Y. G. Ma, S. Y. Liu and J. C. Shen, Chem. Commun., 2003, 2206.
17. A. J. Heeger and D. Braun, UNIAX, Patent No. WO-B 92/16023, 1992; A. J. Heeger and D. Braun, Chem. Abstr., 1993, 118, 157401j.
18. A. J. Heeger and D. Braun, UNIAX, Patent No. WO-B 92/16023, 1992; A. J. Heeger and D. Braun, Chem. Abstr., 1993, 118, 157401j.
19. S. H. Jin, S. Y. Kang, I. S. Yeom, J. Y. Kim, S. H. Park and K. Lee, Chem. Mater., 2002, 14, 5090.
20. A. M. John, Chem. Mater., 2003, 15, 1865.
21. R. M. Silverstein, G. C. Bassler and T. C. Morrill, Spectrometric Identification of Organic Compounds, Wiley, New York, 1974.
22. Y. Ito Y. Uozu, T. Dote, M. Ueda and T. Matsuura, J. Am. Chem. Soc., 1988, 110, 189.
23. Y. Geng, A. Trajkovska, D. Katsis, J. J. Ou, S. W. Culligan and S. H. Chen, J. Am. Chem. Soc., 2002, 124, 8337.