Hexaferrocenylbenzene

Yong Yu; Andrew D. Bond; Philip W. Leonard; Ulrich J. Lorenz; Tatiana V. Timofeeva; K. Peter C. Vollhardt; Glenn D. Whitener; Andrey A. Yakovenko

doi:10.1039/B604844G

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Hexaferrocenylbenzene†

Yong Yu,^a Andrew D. Bond,^b Philip W. Leonard,^a Ulrich J. Lorenz,^a Tatiana V. Timofeeva,^c K. Peter C. Vollhardt,*^a Glenn D. Whitener^a and Andrey A. Yakovenko^c

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* Corresponding authors

^a Department of Chemistry, University of California at Berkeley, and the Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
E-mail: kpcv@berkeley.edu
Fax: ++1 510 643 5208
Tel: ++1 510 642 0286

^b Department of Chemistry, University of Southern Denmark, Campusvej 55, Denmark

^c Department of Natural Sciences, New Mexico Highlands University, Las Vegas, USA

Abstract

Hexaferrocenylbenzene has been synthesized by six-fold Negishi type ferrocenylation of hexabromo- or hexaiodobenzene.

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DOI: https://doi.org/10.1039/B604844G
Article type: Communication
Submitted: 04 Apr 2006
Accepted: 05 May 2006
First published: 23 May 2006

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Chem. Commun., 2006, 2572-2574

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Hexaferrocenylbenzene

Y. Yu, A. D. Bond, P. W. Leonard, U. J. Lorenz, T. V. Timofeeva, K. P. C. Vollhardt, G. D. Whitener and A. A. Yakovenko, Chem. Commun., 2006, 2572 DOI: 10.1039/B604844G

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Chemical Communications

Hexaferrocenylbenzene†

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Hexaferrocenylbenzene

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