Electron-nuclear double resonance bonding

Electron nuclear double resonance of transition metal complexes with organic ligands. A. Schweiger, Struct. Bonding (Berlin), 1982, 51, 1-119 (294). 

S. Sinnecker, E. Reijerse, F. Neese and W. Lubitz, Hydrogen bond geometries from paramagnetic resonance and electron-nuclear double resonance parameters Density functional study of quinone radical anion-solvent interactions, J. Am. Chem. Soc., 2004, 126, 3280. 

As most of the nitroxyl spin-labelled synthetic derivatives of conjugated polyenes are light yellow crystals, the bond lengths were determined by X-ray crystallography38. The spectroscopic method used to measure the conformation is electron nuclear double resonance (ENDOR). It is beyond the scope of the present review to explain the method38 but the authors of the pertinent paper conclude that ENDOR is an accurate non-crystallographic method to determine polyene structures in solution. 

The role of compound I rather than its Fe(III)-OOH precursor (Fig. 4.1g) in oxidation of C-H bonds is consistent with cryogenic electron-nuclear double resonance (ENDOR) studies of the hydroxylation of camphor by CYPlOl (P450 3 ) [86], Hoffman and colleagues prepared the P450 3 ferric hydroperoxide complex at 77 K by... 

ESR can equally be used for detection of radicals in masticated rubber their identification in relation to the chemical structure might be approached with specific techniques such as electron nuclear double resonance (ENDOR). ESR studies also contribute to the understanding of the char forming process of various polymers [815], to the study of mechanical fracture, which produces free radicals, grafting reactions, etc. Pedulli et al. [816,817] have determined the bond dissociation enthalpies of a-tocopherol and other phenolic AOs by means of ESR. The determination of the O—H bond dissociation enthalpies of phenolic molecules is of considerable practical interest since this class of chemical compounds includes most of the synthetic and naturally occurring antioxidants which exert their action via an initial hydrogen transfer reaction whose rate constant depends on the strength of the O—H bond. 

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