Issue 20, 2008

A tetra-substituted chrysene: orientation of multiple electrophilic substitution and use of a tetra-substituted chrysene as a blue emitter for OLEDs

Abstract

The first tetra-substituted non-fused chrysene, 3,6,9,12-tetrakis(4-tert-butylphenyl)chrysene7 with blue electroluminescence at 450 nm, and with a radiance of 500 cd m−2, was synthesized by a two-step procedure: direct bromination of chrysene in trimethyl phosphate, followed by palladium-catalyzed cross-coupling of tetrabromochrysene 2 and tert-butylphenylboronic acid 3.

Graphical abstract: A tetra-substituted chrysene: orientation of multiple electrophilic substitution and use of a tetra-substituted chrysene as a blue emitter for OLEDs

Supplementary files

Article information

Article type
Communication
Submitted
08 Oct 2007
Accepted
08 Mar 2008
First published
09 Apr 2008

Chem. Commun., 2008, 2319-2321

A tetra-substituted chrysene: orientation of multiple electrophilic substitution and use of a tetra-substituted chrysene as a blue emitter for OLEDs

A. S. Ionkin, W. J. Marshall, B. M. Fish, L. M. Bryman and Y. Wang, Chem. Commun., 2008, 2319 DOI: 10.1039/B715386D

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