Issue 3, 2012
From the journal:

New Journal of Chemistry

Tetraazaarenes by the ceramidonine approach†

Parantap Sarkar,a   Ie-Rang Jeon,a   Fabien Durolaa  and  Harald Bock*a  

* Corresponding authors

a Centre de Recherche Paul Pascal, CNRS UPR8641 and Université de Bordeaux, 115 av. Schweitzer, 33600 Pessac, France
E-mail: bock@crpp-bordeaux.cnrs.fr
Fax: +33-556845600
Tel: +33-556845673

Abstract

The synthesis of extended heteroarenesvia the acid-promoted dehydrocyclisation of arylamino-anthraquinones is examined as an approach to highly conjugated electron-acceptor materials and eventually to heterographene nanoribbons. Whilst the latter perspective is found to remain challenging, the former is exemplified by the synthesis of extended tetraazaheterocycles bearing solubilising alkyl substituents.

Graphical abstract: Tetraazaarenes by the ceramidonine approach

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Article information

DOI
https://doi.org/10.1039/C2NJ21033A
Article type
Letter
Submitted
12 Dec 2011
Accepted
06 Jan 2012
First published
25 Jan 2012

New J. Chem., 2012,36, 570-574

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Tetraazaarenes by the ceramidonine approach

P. Sarkar, I. Jeon, F. Durola and H. Bock, New J. Chem., 2012, 36, 570 DOI: 10.1039/C2NJ21033A

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