Issue 70, 2012
From the journal:

Chemical Communications

Highly π electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references†‡

Arnaud Rives,ab   Iaroslav Baglai,abc   Volodymyr Malytskyi,abc   Valérie Maraval,*ab   Nathalie Saffon-Merceron,b   Zoia Voitenkoc  and  Remi Chauvin*ab  

* Corresponding authors

a CNRS, LCC (Laboratoire de Chimie de Coordination), 205 route de Narbonne, F-31077 Toulouse Cedex 4, France
E-mail: vmaraval@lcc-toulouse.fr, chauvin@lcc-toulouse.fr
Fax: +33 (0)5 61 55 30 03
Tel: +33 (0)5 61 33 31 13

b Université de Toulouse, UPS, ICT-FR2599, F-31077 Toulouse, France

c Kiev National Taras Shevchenko University, 60 Volodymlyrska St, 01033 Kiev, Ukraine

Abstract

A series of stable quadrupolar bis(p-aminophenyl)-carbo-benzenes, featuring both donor–donor–donor π-frustration and central macro-aromaticity, is described and compared to the acyclic dibutatrienylacetylene (DBA) reference series.

Graphical abstract: Highly π electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references

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

DOI
https://doi.org/10.1039/C2CC34176J
Article type
Communication
Submitted
11 jun 2012
Accepted
02 jul 2012
First published
03 jul 2012

Chem. Commun., 2012,48, 8763-8765

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Highly π electron-rich macro-aromatics: bis(p-aminophenyl)-carbo-benzenes and their DBA acyclic references

A. Rives, I. Baglai, V. Malytskyi, V. Maraval, N. Saffon-Merceron, Z. Voitenko and R. Chauvin, Chem. Commun., 2012, 48, 8763 DOI: 10.1039/C2CC34176J

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