Issue 36, 2016

Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism

Abstract

Tetraruthenium macrocycles with 1,4-divinylphenylene and diarylamine-substituted isophthalic acids as the sides display up to eight one-electron redox steps and rich electrochromic behaviour with strong absorptions of the dications in the near infrared and of the tetra- and hexacations at low energies in the visible.

Graphical abstract: Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism

Supplementary files

Article information

Article type
Communication
Submitted
29 Jan 2016
Accepted
24 Mar 2016
First published
12 Apr 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 6103-6106

Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism

D. Fink, B. Weibert and R. F. Winter, Chem. Commun., 2016, 52, 6103 DOI: 10.1039/C6CC00936K

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