A Highly Stable Organic Radical Cation.
Mathilde BervilleJimmy RichardMonika StolarSylvie ChouaNolwenn Le BretonChristophe GourlaouenCorinne BoudonLaurent RuhlmannThomas BaumgartnerJennifer A WytkoJean WeissPublished in: Organic letters (2018)
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.
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