Issue 9, 2015

Triphenylamine-based π-conjugated dendrimers: convenient synthesis, easy solution processability, and good hole-transporting properties

Abstract

Two, third-generation triphenylamine-based dendrimers (DT1 and DT2) were prepared through a simple convergent approach by using a combination of versatile carbon–carbon formation reactions. It is found that the π-linkages connecting the periphery into the core have a pronounced effect on the properties of the material. The introduction of C[triple bond, length as m-dash]C bonds in the periphery improves the photophysical behavior and optical qualities of the films in comparison with their introduction in the core of the dendrimer. Both dendrimers exhibit high Tgs (above 240 °C) and high-lying HOMO energy levels of ∼5.2 eV. As the hole-transporting layer fabricated through a facile solution process, DT2 can endow an Alq3 based multi-layer OLED device with a maximum brightness of 5020 cd m−2, and a maximum current efficiency of 2.36 cd A−1.

Graphical abstract: Triphenylamine-based π-conjugated dendrimers: convenient synthesis, easy solution processability, and good hole-transporting properties

Supplementary files

Article information

Article type
Paper
Submitted
27 Aug 2014
Accepted
01 Dec 2014
First published
22 Dec 2014

J. Mater. Chem. C, 2015,3, 2016-2023

Triphenylamine-based π-conjugated dendrimers: convenient synthesis, easy solution processability, and good hole-transporting properties

Z. Li, T. Ye, S. Tang, C. Wang, D. Ma and Z. Li, J. Mater. Chem. C, 2015, 3, 2016 DOI: 10.1039/C4TC01923G

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