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Novel Soluble N-Phenyl-Carbazole-Containing PPVs for Light-Emitting Devices: Synthesis, Electrochemical, Optical, and Electroluminescent Properties

✍ Scribed by Hongchao Li; Yanguang Zhang; Yufeng Hu; Dongge Ma; Lixiang Wang; Xiabin Jing; Fosong Wang


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
157 KB
Volume
205
Category
Article
ISSN
1022-1352

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✦ Synopsis


Abstract

Summary: Novel PPV derivatives (PCA8‐PV and PCA8‐MEHPV) containing N‐phenyl‐carbazole units on the backbone were successfully synthesized by the Wittig polycondensation of 3,6‐bisformyl‐N‐(4‐octyloxy‐phenyl)carbazole with the corresponding tributyl phosphonium salts in good yields. The newly formed and dominant trans vinylene double bonds were confirmed by FT‐IR and NMR spectroscopy. The polymers (with $\overline M _{\rm w}$ of 6 289 for PCA8‐PV and 7 387 for PCA8‐MEHPV) were soluble in common organic solvents and displayed high thermal stability (T~g~s are 110.7 °C for PCA8‐PV and 92.2 °C for PCA8‐MEHPV, respectively) because of the incorporation of the N‐phenyl‐carbazole units. Cyclic voltammetry investigations (onsets: 0.8 V for PCA8‐PV and 0.7 V for PCA8‐MEHPV) suggested that the polymers possess enhanced hole injection/transport properties, which can be also attributed to the N‐phenyl‐carbazole units on the backbone. Both the single‐layer and the double‐layer light‐emitting diodes (LEDs) that used the polymers as the active layer emitted a greenish‐blue or bluish‐green light (the maximum emissions located 494 nm for PCA8‐PV and 507 nm for PCA8‐MEHPV, respectively). Compared with those of the single‐layer devices, the emission efficiencies of the double‐layer devices, in which an electron‐transporting layer (Alq~3~) was added, were enhanced by a factor of 10, implying that the better hole‐electron balance is achieved because of the incorporation of the electron‐transporting layer.

The N‐phenyl‐carbazole‐containing polymers synthesized.

imageThe N‐phenyl‐carbazole‐containing polymers synthesized.