Volume 56, Issue 12 pp. 3360-3363
Communication

A Stable Hexakis(guanidino)benzene: Realization of the Strongest Neutral Organic Four-Electron Donor

Benjamin Eberle

Benjamin Eberle

Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany

Search for more papers by this author
Dr. Elisabeth Kaifer

Dr. Elisabeth Kaifer

Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany

Search for more papers by this author
Prof. Dr. Hans-Jörg Himmel

Corresponding Author

Prof. Dr. Hans-Jörg Himmel

Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany

Search for more papers by this author
First published: 17 February 2017
Citations: 42

Graphical Abstract

Multistage electron donor: The first hexakis(guanidino)benzene derivative donates four electrons at a record low potential.

Abstract

The growing demand for efficient batteries has stimulated the search for redox-active organic compounds with multistage redox behavior, as materials with large charge capacity. Herein we report the synthesis and properties of the first hexakis(guanidino)benzene derivative: a strong neutral organic electron donor with reversible multistage redox behavior and a record low redox potential for donation of four electrons. Detailed structural and spectroscopic characterization of three redox states (0, +2, and +4) reveal its unique electronic features. Despite its nitrogen richness, the compound is thermally robust and can be readily purified by sublimation.

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