Issue 5, 2000
From the journal:

Chemical Communications

Ferrocenylsilylation of dendrons: a fast convergent route to redox-stable ferrocene dendrimers

Sylvain Nlate,a   Jaime Ruiz,a   Jean-Claude Blaisb  and  Didier Astruc*a  

* Corresponding authors

a Groupe de Chimie Supramoléculaire des Métaux de Transition, LCOO, UMR CNRS No 5802, Université Bordeaux I, Talence Cédex, France.
E-mail: d.astruc@lcoo.u-bordeaux.fr

b Laboratoire de Chimie Structurale Organique et Biologique, E, P CNRS No 103, Université Paris VI, 4 Place Jussieu, Paris, France

Abstract

A 54-ferrocene dendrimer is synthesized by a convergent route and can be used to modify a Pt electrode in CH2Cl2; it can be reversibly oxidized in DMF in a single 54-electron wave (and with NO+).

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Article information

DOI
https://doi.org/10.1039/A908791E
Article type
Communication
Submitted
04 Nov 1999
Accepted
04 Feb 2000
First published
23 Feb 2000

Chem. Commun., 2000, 417-418

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Ferrocenylsilylation of dendrons: a fast convergent route to redox-stable ferrocene dendrimers

S. Nlate, J. Ruiz, J. Blais and D. Astruc, Chem. Commun., 2000, 417 DOI: 10.1039/A908791E

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