Synthesis and Light-Emitting Properties of Solution-Processable Oligothiophenes Containing Triazole Moiety

Abstract:

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The aromatic triazole is an interesting electron-injection/transport chromophore because it possesses high electron affinity and thermal stability. In organic lighting-emitting diodes (OLEDs), highly electron-deficient triazole (Tz) derivates have been demonstrated to have more efficient electron-transport and hole-blocking characteristics and have a higher stability to high current density than the oxadiazole derivates. In this study, we have successfully synthesized a star-shaped soluble oligomer,4-(4-butylphenyl)-3,5-bis(4-(5'-hexyl-2,2'-bithiophen-5-yl)phenyl)-4H-1,2,4-triazole(Tz-2T-Hex) via Suzuki coupling reaction. The Tz-2T-Hex shows a red-shifted UV-vis absorption spectrum than Tz-Br with a maximum at 380 nm, due to the introduction of two bithiophene units at both ends. As film, Tz-2T-Hex showed the PL maximum at 530 nm. Tz-2T-Hex emitted light of a white color with the CIE coordinates (0.32 and 0.34).

Info:

Periodical:

Materials Science Forum (Volumes 663-665)

Edited by:

Yuan Ming Huang

Pages:

12-15

DOI:

10.4028/www.scientific.net/MSF.663-665.12

Citation:

B. E. Kim et al., "Synthesis and Light-Emitting Properties of Solution-Processable Oligothiophenes Containing Triazole Moiety", Materials Science Forum, Vols. 663-665, pp. 12-15, 2011

Online since:

November 2010

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$35.00

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