NMR determination of EPR hyperfine coupling constants of some 5-(n-alkyl)-1,1,3,3-tetrakis(trideuteriomethyl)isoindolin-2-yloxyls

Abstract
2D 1H–13C chemical shift correlation spectroscopy has been used to determine some small 1H and 13C EPR hyperfine interaction constants in some 5-(n-alkyl)isoindolin-2-yloxyl radicals. In the methodology used, it was necessary to measure the chemical shifts of both the isoindolines and of the cognate isoindolin-2-yloxyl radicals. The latter n-alkyl-substituted radicals have considerable potential as EPR spin probes in lipid systems.

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