Issue 23, 2012
From the journal:

Chemical Communications

Triply ferrocene-bridged boroxine cyclophane†‡

Teng-Hao Chen,a   Watchareeya Kaveevivitchai,a   Nghia Buia  and  Ognjen Š. Miljanić*a  

* Corresponding authors

a University of Houston, Department of Chemistry, 136 Fleming Building, Houston, USA
E-mail: miljanic@uh.edu
Fax: +1 713 743-2709
Tel: +1 832 842-8827

Abstract

Mild solvothermal dehydration of 1,1′-ferrocenediboronic acid produces a triply ferrocene-bridged boroxine cyclophane. Its crystal structure reveals a rigid trigonal prism that presents a minimal boroxine-based covalent organic polyhedron (COP).

Graphical abstract: Triply ferrocene-bridged boroxine cyclophane

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

DOI
https://doi.org/10.1039/C2CC17744G
Article type
Communication
Submitted
10 Tsh 2011
Accepted
17 Phe 2012
First published
18 Phe 2012

Chem. Commun., 2012,48, 2855-2857

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Triply ferrocene-bridged boroxine cyclophane

T. Chen, W. Kaveevivitchai, N. Bui and O. Š. Miljanić, Chem. Commun., 2012, 48, 2855 DOI: 10.1039/C2CC17744G

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