Issue 15, 2016

The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides

Abstract

In two recent articles (Org. Biomol. Chem., 2015 and 2016), we showed that changes in the phosphorus hyperfine coupling constant aP at position β in β-phosphorylated nitroxides can be dramatic. Such changes were applied to the titration of water in organic solvents and conversely of organic solvents in water. One of the molecules tested was a non-cyclic nitroxide meaning that a thorough investigation of the solvent effect on the EPR hyperfine coupling constant is timely due. In this article, we show that the aP of persistent non-cyclic β-phosphorylated nitroxides decrease with the normalized polarity Reichardt's constant ENT. The Koppel–Palm and Kalmet–Abboud–Taft relationships were applied to gain deeper insight into the effects influencing aN and aP: polarity/polarizability, hydrogen bond donor properties, and the structuredness of the cybotactic region.

Graphical abstract: The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2016
Accepted
09 Mar 2016
First published
17 Mar 2016

Org. Biomol. Chem., 2016,14, 3729-3743

Author version available

The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides

G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Brémond, T. Butscher and S. R. A. Marque, Org. Biomol. Chem., 2016, 14, 3729 DOI: 10.1039/C6OB00359A

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