Issue 42, 2012
From the journal:

Chemical Communications

Diazaheterocycle analogues of tetracene: synthesis and properties of a naphtho-fused cinnoline and a naphtho-fused isoindazole†‡

Brian S. Young,a   Jonathan L. Marshall,a   Ellen MacDonald,a   Chris L. Vonneguta  and  Michael M. Haley*a  

* Corresponding authors

a Department of Chemistry and the Materials Science Institute, 1253 University of Oregon, Eugene, USA
E-mail: haley@uoregon.edu
Fax: +1-541-346-0487
Tel: +1-541-346-0456

Abstract

The synthesis and characterization of a diethynyl naphtho-fused cinnoline and isoindazole are described. The results show that both electron-accepting and electron-donating molecules can be prepared from a common intermediate.

Graphical abstract: Diazaheterocycle analogues of tetracene: synthesis and properties of a naphtho-fused cinnoline and a naphtho-fused isoindazole

  • This article is part of the themed collection: Aromaticity
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Article information

DOI
https://doi.org/10.1039/C2CC31613G
Article type
Communication
Submitted
03 Mac 2012
Accepted
23 Mac 2012
First published
19 Apr 2012

Chem. Commun., 2012,48, 5166-5168

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Diazaheterocycle analogues of tetracene: synthesis and properties of a naphtho-fused cinnoline and a naphtho-fused isoindazole

B. S. Young, J. L. Marshall, E. MacDonald, C. L. Vonnegut and M. M. Haley, Chem. Commun., 2012, 48, 5166 DOI: 10.1039/C2CC31613G

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