Issue 4, 2006

Supramolecular stabilization of hydroxylamine TEMPOH by complexation with an amphiphilic calixarene

Abstract

In an ethanol/water mixture, the nitroxyl radical TEMPO abstracts a hydrogen atom from a phenolic OH group of the amphiphilic para-hexanoylcalix[4]arene, and the hydroxylamine TEMPOH formed yields a stable inclusion complex with another molecule of the calixarene.

Graphical abstract: Supramolecular stabilization of hydroxylamine TEMPOH by complexation with an amphiphilic calixarene

Supplementary files

Article information

Article type
Communication
Submitted
18 Aug 2005
Accepted
03 Nov 2005
First published
07 Dec 2005

Chem. Commun., 2006, 386-388

Supramolecular stabilization of hydroxylamine TEMPOH by complexation with an amphiphilic calixarene

G. S. Ananchenko, M. Pojarova, K. A. Udachin, D. M. Leek, A. W. Coleman and J. A. Ripmeester, Chem. Commun., 2006, 386 DOI: 10.1039/B511810G

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