Issue 50, 2012
From the journal:

Chemical Communications

Meta-B-entacenes: new polycyclic aromatics incorporating two fused borepin rings†‡

David R. Levine,a   Anthony Caruso, Jr.,a   Maxime A. Sieglera  and  John D. Tovar*a  

* Corresponding authors

a Department of Chemistry, Department of Materials Science and Engineering, Johns Hopkins University, 3400 North Charles Street (NCB 316), Baltimore, USA
E-mail: tovar@jhu.edu
Fax: (+1)410-516-7044

Abstract

The synthesis of new boron-containing acenes (meta-B-entacenes) is reported. These compounds exhibit slightly non-planar core geometries with blue-shifted spectral properties and more negative electrochemical reduction potentials relative to known para isomers. Polarizable π-extended architectures were realized via cross-coupling procedures with chloro-functionalized precursors.

Graphical abstract: Meta-B-entacenes: new polycyclic aromatics incorporating two fused borepin rings

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

DOI
https://doi.org/10.1039/C2CC32500D
Article type
Communication
Submitted
06 4 2012
Accepted
23 4 2012
First published
24 4 2012

Chem. Commun., 2012,48, 6256-6258

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Meta-B-entacenes: new polycyclic aromatics incorporating two fused borepin rings

D. R. Levine, A. Caruso, M. A. Siegler and J. D. Tovar, Chem. Commun., 2012, 48, 6256 DOI: 10.1039/C2CC32500D

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