Issue 13, 2002
From the journal:

Chemical Communications

Electronic coupling in 6,6″-donor-substituted terpyridines: tuning of the mixed valence state by proton and metal ion complexation†

Michael Büschel,a   Markus Helldoblera  and  Jörg Daub*a  

* Corresponding authors

a Institut für Organische Chemie, Universität Regensburg, D-93040 Regensburg, Germany
E-mail: joerg.daub@chemie.uni-regensburg.de

Abstract

6,6″-Terpyridyl-bishydroquinone conjugates are synthesised by Pd-catalyzed cross-coupling and their conformational switching, triggered by protons, zinc(II) or cobalt(II), is studied by cyclovoltammetry and in situ UV/Vis/NIR and FT-IR spectroelectrochemistry.

Graphical abstract: Electronic coupling in 6,6″-donor-substituted terpyridines: tuning of the mixed valence state by proton and metal ion complexation

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B110289C
Article type
Communication
Submitted
12 Nov 2001
Accepted
30 Apr 2002
First published
22 May 2002

Chem. Commun., 2002, 1338-1339

Permissions

Request permissions

Electronic coupling in 6,6″-donor-substituted terpyridines: tuning of the mixed valence state by proton and metal ion complexation

M. Büschel, M. Helldobler and J. Daub, Chem. Commun., 2002, 1338 DOI: 10.1039/B110289C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements