Experimental and Theoretical Investigations of the Existence of CuII, CuIII, and CuIV in Copper Corrolato Complexes

1. Woormileela Sinha^1,†, 
2. Michael G. Sommer^2,†, 
3. Naina Deibel^2,3, 
4. Fabian Ehret³, 
5. Prof. Dr. Matthias Bauer⁴, 
6. Prof. Dr. Biprajit Sarkar^2,* and
7. Dr. Sanjib Kar^1,*

Article first published online: 25 SEP 2015

DOI: 10.1002/anie.201507330

© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

http://onlinelibrary.wiley.com/doi/10.1002/anie.201507330/abstract

• Abstract

Keywords:

• copper corroles;
• EPR spectroscopy;
• higher oxidation states;
• spectroelectrochemistry;
• XANES measurements

Abstract

The most common oxidation states of copper in stable complexes are +I and +II. Cu^III complexes are often considered as intermediates in biological and homogeneous catalysis. More recently, Cu^IV species have been postulated as possible intermediates in oxidation catalysis. Despite the importance of these higher oxidation states of copper, spectroscopic data for these oxidation states remain scarce, with such information on Cu^IV complexes being non-existent. We herein present the synthesis and characterization of three copper corrolato complexes. A combination of electrochemistry, UV/Vis/NIR/EPR spectroelectrochemistry, XANES measurements, and DFT calculations points to existence of three distinct redox states in these molecules for which the oxidation states +II, +III, and +IV can be invoked for the copper centers. The present results thus represent the first spectroscopic and theoretical investigation of a Cu^IV species, and describe a redox series where Cu^II, Cu^III, and Cu^IV are discussed within the same molecular platform.