Issue 1, 2015

Synthesis and use of “clickable” bay-region tetrasubstituted perylene tetracarboxylic tetraesters and a perylene monoimide diester as energy acceptors

Abstract

Two novel bay-region chlorine- or phenoxy-substituted perylene tetracarboxylic tetrapropargylesters (PTTEs) and a phenoxy-substituted perylene monoimide dipropargylester (PMIDE) were synthesized, photophysically characterized, and decorated with energy donating coumarin chromophores by means of microwave-assisted Cu(I)-catalyzed 1,3-dipolar cycloaddition reactions.

Graphical abstract: Synthesis and use of “clickable” bay-region tetrasubstituted perylene tetracarboxylic tetraesters and a perylene monoimide diester as energy acceptors

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2014
Accepted
21 Oct 2014
First published
22 Oct 2014

New J. Chem., 2015,39, 548-554

Author version available

Synthesis and use of “clickable” bay-region tetrasubstituted perylene tetracarboxylic tetraesters and a perylene monoimide diester as energy acceptors

E. Aydin, B. Nisanci, M. Acar, A. Dastan and Ö. A. Bozdemir, New J. Chem., 2015, 39, 548 DOI: 10.1039/C4NJ01565G

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