Issue 44, 2009
From the journal:

Chemical Communications

Redox rich dicobalt macrocycles as templates for multi-electron transformations†

Nathaniel K. Szymczak,a   Louise A. Berbena  and  Jonas C. Peters*a  

* Corresponding authors

a Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
E-mail: jcpeters@mit.edu

Abstract

Pyridazine-templated dicobalt macrocycles reversibly support five oxidation states with unusually positive CoII/CoI redox couples, and are also active proton reduction electrocatalysts.

Graphical abstract: Redox rich dicobalt macrocycles as templates for multi-electron transformations

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B913946J
Article type
Communication
Submitted
13 júl. 2009
Accepted
17 sep. 2009
First published
06 okt. 2009

Chem. Commun., 2009, 6729-6731

Permissions

Request permissions

Redox rich dicobalt macrocycles as templates for multi-electron transformations

N. K. Szymczak, L. A. Berben and J. C. Peters, Chem. Commun., 2009, 6729 DOI: 10.1039/B913946J

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