A Highly Stable Organic Radical Cation

Org Lett. 2018 Dec 21;20(24):8004-8008. doi: 10.1021/acs.orglett.8b03579. Epub 2018 Dec 11.

Abstract

Functionalization of a methylviologen with four methyl ester substituents significantly facilitates the first two reduction steps. The easily generated radical cation shows markedly improved air stability compared to the parent methylviologen, making this derivative of interest in organic electronic applications.

Publication types

  • Research Support, Non-U.S. Gov't