Issue 4, 2009

Synthesis, spectroscopy, photophysics and thermal behaviour of stilbene-based triarylamines with dehydroabietic acid methyl ester moieties

Abstract

Novel stilbene-based triarylamines with dehydroabietic acid methyl ester moieties have been synthesised by palladium catalysed C–N coupling reactions. The presence of the bulky dehydroabietic acid group increases solubility, hinders crystallisation and permits their sublimation while preserving their electronic and optical characteristics. This makes them good candidates for various molecular electronic applications. We report a detailed characterisation of their electrochemical, spectroscopic and photophysical properties. In addition, the thermal stability and behaviour is discussed with reference to the potential for preparation of stable thin films.

Graphical abstract: Synthesis, spectroscopy, photophysics and thermal behaviour of stilbene-based triarylamines with dehydroabietic acid methyl ester moieties

Supplementary files

Article information

Article type
Paper
Submitted
09 Sep 2008
Accepted
14 Jan 2009
First published
05 Feb 2009

New J. Chem., 2009,33, 877-885

Synthesis, spectroscopy, photophysics and thermal behaviour of stilbene-based triarylamines with dehydroabietic acid methyl ester moieties

B. Gigante, M. A. Esteves, N. Pires, M. L. Davies, P. Douglas, S. M. Fonseca, H. D. Burrows, R. A. E. Castro, J. Pina and J. Seixas de Melo, New J. Chem., 2009, 33, 877 DOI: 10.1039/B815711A

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