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Redox mediators in visible light photocatalysis: photocatalytic radical thiol-ene additions.


ABSTRACT: Synthetically useful radical thiol-ene reactions can be initiated by visible light irradiation in the presence of transition metal polypyridyl photocatalysts. The success of this method relies upon the use of p-toluidine as an essential additive. Using these conditions, high-yielding thiol-ene reactions of cysteine-containing biomolecules can be accomplished using biocompatibile wavelengths of visible light, under aqueous conditions, and with the thiol component as the limiting reagent. We present evidence that p-toluidine serves as a redox mediator that is capable of catalyzing the otherwise inefficient photooxidation of thiols to the key thiyl radical intermediate. Thus, we show that co-catalytic oxidants can be important in the design of synthetic reactions involving visible light photoredox catalysis.

SUBMITTER: Tyson EL 

PROVIDER: S-EPMC3985841 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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Redox mediators in visible light photocatalysis: photocatalytic radical thiol-ene additions.

Tyson Elizabeth L EL   Niemeyer Zachary L ZL   Yoon Tehshik P TP  

The Journal of organic chemistry 20140127 3


Synthetically useful radical thiol-ene reactions can be initiated by visible light irradiation in the presence of transition metal polypyridyl photocatalysts. The success of this method relies upon the use of p-toluidine as an essential additive. Using these conditions, high-yielding thiol-ene reactions of cysteine-containing biomolecules can be accomplished using biocompatibile wavelengths of visible light, under aqueous conditions, and with the thiol component as the limiting reagent. We prese  ...[more]

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