Volume 46, Issue 30 pp. 5728-5730
Communication

Generation of a RuII–Semiquinone–Anilino-Radical Complex through the Deprotonation of a RuIII–Semiquinone–Anilido Complex

Yuji Miyazato Dr.

Yuji Miyazato Dr.

Institute for Molecular Science, 5-1 Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan, Fax: (+81) 564-59-5582

Search for more papers by this author
Tohru Wada Dr.

Tohru Wada Dr.

Institute for Molecular Science, 5-1 Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan, Fax: (+81) 564-59-5582

Search for more papers by this author
James T. Muckerman Dr.

James T. Muckerman Dr.

Brookhaven National Laboratory, Upton, NY 11973-5000, USA

Search for more papers by this author
Etsuko Fujita Dr.

Etsuko Fujita Dr.

Brookhaven National Laboratory, Upton, NY 11973-5000, USA

Search for more papers by this author
Koji Tanaka Prof.

Koji Tanaka Prof.

Institute for Molecular Science, 5-1 Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan, Fax: (+81) 564-59-5582

Search for more papers by this author
First published: 13 July 2007
Citations: 70

We thank Prof. T. Yokoyama and Dr. T. Nakagawa at the Institute for Molecular Science for measuring the X-ray photoelectron spectra (XPS) and the Research Center for Molecular-Scale Nanoscience at the Institute for Molecular Science for measurements with the SQUID magnetometer. This research was supported financially by a Grant-in-Aid for Scientific Research on Priority Areas (No. 18033057). Research carried out at the Brookhaven National Laboratory was funded by the Division of Chemical Sciences, Geosciences, & Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy under the contract DE-AC02-98CH10886.

Graphical Abstract

Calming the radicals: Aminyl radicals may one day be useful oxidation catalysts if their thermodynamic instability can be overcome, for example, through complexation with a metal. The semiquinone–anilino-radical and catechol–anilino-radical complexes 1 and 2 have now been prepared and the anilino-radical character of the tetradentate amine ligand proved by electron paramagentic resonance and resonance Raman spectroscopy, as well as DFT calculations.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.