Issue 34, 2015

Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes

Abstract

A series of oligofluorenes bearing two 3,6-dipyrenylcarbazole units as the terminal substituents, namely BPCFn (n = 1–3), were successfully synthesized and characterized as non-doped hole-transporting blue emitters. These molecules showed strong blue emission with good solubility, and thermally stable amorphous and excellent film-forming properties. OLEDs using these materials as the emissive layers were fabricated by a simple solution spin-coating process. The blue OLED with excellent device performance (brightness of 6085 cd m−2, luminance efficiency of 4.13 cd A−1 and turn-on voltage of 3.4 V) was attained from BPCF3.

Graphical abstract: Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes

Supplementary files

Article information

Article type
Paper
Submitted
07 Feb 2015
Accepted
05 Mar 2015
First published
05 Mar 2015

RSC Adv., 2015,5, 26569-26579

Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes

T. Sangchart, A. Niroram, T. Kaewpuang, N. Prachumrak, S. Namuangruk, T. Sudyoadsuk, T. Keawin, S. Saengsuwan, S. Jungsuttiwong, S. Maensiri, N. Kungwan and V. Promarak, RSC Adv., 2015, 5, 26569 DOI: 10.1039/C5RA02382C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements