Issue 26, 2015

Energy level tuning of blue emitting and electron transporting vinylene bis(vinyl quinolinyl)benzene derivatives: synthesis, characterisation, thin film characterisation and performance in OLEDs

Abstract

A number of thermally stable, conjugated, blue-emitting vinylene bis(vinyl quinolinyl)benzene derivatives were prepared and three of them were characterised by single crystal X-ray crystallography. They exhibit blue to bluish-green emission (fluorescence and electroluminescence) depending on the substituents. Their effectiveness as electron transporters in red and green organic light emitting diodes (OLEDs) has been explored. The phenyl and naphthyl substituted compounds were found to be superior to Alq3 in OLEDs as electron transporters. The electron mobility of the parent molecule, phenyl, thienyl and naphthyl substituted compounds were determined to be 8.0 × 10−7, 3.3 × 10−6, 5.5 × 10−6 and 8.0 × 10−6 cm2 V−1 s−1 respectively. Lifetime measurements were carried out for the red and green fluorescent devices and compared with Alq3 as an electron transporter. Some vinylene bis(vinyl quinolinyl)benzene derivatives show significantly longer lifetimes than analogous devices made with Alq3 as the electron transport layer. Purple to dark blue emitting devices were achieved from two of the derivatives.

Graphical abstract: Energy level tuning of blue emitting and electron transporting vinylene bis(vinyl quinolinyl)benzene derivatives: synthesis, characterisation, thin film characterisation and performance in OLEDs

Supplementary files

Article information

Article type
Paper
Submitted
02 Сәу. 2015
Accepted
19 Мам. 2015
First published
20 Мам. 2015

J. Mater. Chem. C, 2015,3, 6652-6667

Author version available

Energy level tuning of blue emitting and electron transporting vinylene bis(vinyl quinolinyl)benzene derivatives: synthesis, characterisation, thin film characterisation and performance in OLEDs

P. Kathirgamanathan, S. Surendrakumar, S. Ravichandran, M. Kumaraverl, J. Antipan Lara, S. Ganeshamurugan, L. M. Bushby, J. P. Tidey and A. J. Blake, J. Mater. Chem. C, 2015, 3, 6652 DOI: 10.1039/C5TC00932D

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