Browse > Article
http://dx.doi.org/10.5012/jkcs.2010.54.6.711

Synthesis and Properties about Color Stability of m-SiP-PPDFV with Difluoro Groups in Vinylene Units  

Jin, Young-Eup (Department of Industrial Chemistry, Pukyong National University)
Suh, Hong-Suk (Department of Chemistry, Pusan National University)
Publication Information
Abstract
New electroluminescent polymers with fluoro groups in vinylene units, poly(m-silylphenyl-p-phenylene-difluorovinylene) (m-SiP-PPDFV) have been synthesized by GILCH polymerization. These polymers have been used as the electroluminescent (EL) layers in single layer light-emitting diodes (LEDs) (ITO/PEDOT/polymer/Ca:Al). m-SiP-PPDFV shows PL around $\lambda_{max}$ = 452 nm and green EL around $\lambda_{max}$ = 497 nm. The current-voltage-luminance (I-V-L) characteristics of the polymers show turn-on voltages of 4.0 V approximately. Two fluoro groups were introduced on every vinylene units of m-SiP-PPV to give m-SiP-PPDFV in an attempt to increase the electron affinity of the parent polymer, and the devices show an increased color stability even with vinylene units. The color stability is attributed to the electron-withdrawing effect of the fluoro groups, which protect vinylene units from oxidation in PPV derivatives. We believe that fluoro groups can be introduced in vinylene units in order to attain excellent stability of PPV derivatives.
Keywords
Electroluminescence; Polymer light-emitting diodes; Color stability; PPVs;
Citations & Related Records

Times Cited By SCOPUS : 0
연도 인용수 순위
  • Reference
1 Ramsdale, C. M.; Greenham, N. C. Adv. Mater. 2002, 14, 212.   DOI
2 Morgado, J.; Thomas, D. S.; Friend, R. H.; Cacialli, F. Synth. Met. 2000, 111-112, 549.   DOI
3 Janssen, F. J. J.; van IJzendoorn, L. J.; Schoo, H. F. M.; Sturm, J. M.; Andersson, G. G.; Denier van Der Gon, A. W.; Brongersma, H. H.; De Voigt, M. J. A. Synth. Met. 2002, 131, 167.   DOI
4 Papadimitrakopoulos, F.; Konstadinidis, K.; Miller, T. M.; Opila, R.; Chandross, E. A.; Galvin, M. E. Chem. Mater. 1994, 6, 1563.   DOI
5 Zyung, T.; Kim, J. J. Appl. Phys. Lett. 1995, 67, 3420.   DOI
6 Ke, L.; Chen, P.; Chua, S. J. Appl. Phys. Lett. 2002, 80, 697.   DOI
7 Rothberg, L. J.; Yan, M.; Son, S.; Galvin, M. E.; Kwock, E. W.; Miller, T. M.; Katz, H. E.; Haddon, R. C.; Papadimitrakopoulos, F. Synth. Met. 1996, 78, 231.   DOI
8 Cumpston, B. H.; Jensen, K. F. Synth. Met. 1995, 73, 195.   DOI
9 Scurlock, R. D.; Wang, B.; Ogilby, P. R.; Sheats, J. R.; Clough, R. L. J. Am. Chem. Soc. 1995, 117, 10194.   DOI
10 Losurdo, M.; Giangregorio, M. M.; Capezzuto, P.; Cardone, A.; Martinelli, C.; Farinola, G. M.; Babudri, F.; Naso, F.; Buchel, M.; Bruno, G. Adv. Mater. 2009, 21, 1115.   DOI
11 Losurdo, M.; Giangregorio, M. M.; Capezzuto, P.; Bruno, G.; Babudri, F.; Cardone, A.; Martinelli, C.; Farinola, G. M.; Naso, F.; Buchel, M. Polymer 2008, 49, 4133.   DOI
12 Jin, Y.; Kim, K.; Park, S. H.; Song, S.; Kim, J.; Jung, J.; Lee, K.; Suh, H. Macromolecules 2007, 40, 6799.   DOI
13 Jin, Y.; Kim, J.; Lee, S.; Kim, J. Y.; Park, S. H.; Lee, K.; Suh, H. Macromolecules 2004, 37, 6711.   DOI
14 Park, S. H.; Cho, S.; Lee, J. K.; Lee, K.; Heeger, A. J. Org. Electron. 2009, 10, 426.   DOI
15 Bernius, M. T.; Inbasekaran, M.; O’Brien, J.; Wu, W. Adv. Mater. 2000, 12, 1737.   DOI
16 Zhang, L.; Di, C.; Yu, G.; Liu, Y. J. Mater. Chem. 2010, 20, 7059.   DOI
17 Lee, T. W.; Chung, Y.; Kwon, O.; Park, J. J. Adv. Funct. Mater. 2007, 17, 390.   DOI
18 Song, S.; Jin, Y.; Kim, S. H.; Shim, J. Y.; Son, S.; Kim, I.; Lee, K.; Suh, H. J. Polym. Sci. Pol. Chem. 2009, 47, 6540.   DOI
19 Song, S.; Jin, Y.; Kim, S. H.; Moon, J.; Kim, K.; Kim, J. Y.; Park, S. H.; Lee, K.; Suh, H. Macromolecules 2008, 41, 7296.   DOI
20 Kim, H. J.; Kim, M. J.; Park, H. D.; Lee, J. H.; Noh, S. T.; Lee, Y. C.; Kim, J. J. Synth. Met. 2010, 160, 1994.   DOI
21 Wang, X.; Wang, H.; Yang, Y.; He, Y.; Zhang, L.; Li, Y.; Li, X. Macromolecules 2010, 43, 709.   DOI
22 Park, Y.; Lee, J. H.; Jung, D. H.; Liu, S. H.; Lin, Y. H.; Chen, L. Y.; Wu, C. C.; Park, J. J. Mater. Chem. 2010, 20, 5930.   DOI