Issue 7, 2014

Dramatic synergistic effects between hydroquinone and resorcinol derivatives for the organocatalyzed reduction of dioxygen by diethylhydroxylamine

Abstract

Diethylhydroxylamine reduces dioxygen in the presence of catalytic amounts of hydroquinone. A great improvement is achieved by adding resorcinol derivatives as co-catalysts. Though the formation of heterodimers does not seem to be the sole cause of the synergy, such products constitute a new class of powerful organocatalysts for dioxygen scavenging.

Graphical abstract: Dramatic synergistic effects between hydroquinone and resorcinol derivatives for the organocatalyzed reduction of dioxygen by diethylhydroxylamine

Supplementary files

Article information

Article type
Communication
Submitted
23 Sep 2013
Accepted
12 Nov 2013
First published
12 Nov 2013

Chem. Commun., 2014,50, 866-868

Dramatic synergistic effects between hydroquinone and resorcinol derivatives for the organocatalyzed reduction of dioxygen by diethylhydroxylamine

R. Lebeuf, V. Nardello-Rataj and J. Aubry, Chem. Commun., 2014, 50, 866 DOI: 10.1039/C3CC47261B

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