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Original Articles

Synthesis, reactivity, and sulfide quenching of helical viologens

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Pages 222-226 | Received 20 Oct 2016, Accepted 20 Oct 2016, Published online: 01 Nov 2016
 

GRAPHICAL ABSTRACT

ABSTRACT

The first examples of chiral helical viologens are reported. These novel compounds have sufficiently long singlet lifetimes to support bimolecular photochemical reactions. They are quenched with diffusion-controlled rates with dialkyl-, diaryl-, and alkyl-aryl sulfides presumably by a charge transfer/electron transfer mechanism.

Funding

We thank the National Science Foundation (CHE-1147542) for their generous support of this research.

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