A PARAMAGNETIC RESONANCE STUDY OF HINDERED DIARYLMETHYL RADICALS AND RELATED COMPOUNDS: I. ANALYSIS OF THE SPECTRA

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Abstract
Several ortho-substituted radicals of the benzhydryl type and a variety of diaryl ketyls have been studied through the nuclear hyperfine structure of their electron spin resonance spectra. A strong similarity is found between the spectra of a given ketyl and its hydrocarbon analogue. This suggests that when ketones are reduced, a very tight ion pair is formed between the ketyl anion and its cation. Although the coupling constants of the protons vary with different reducing agents, larger variations are observed when bulky groups are substituted into ortho positions. These larger changes are attributed to a forced internal rotation of the phenyl rings. The distortion results from the steric repulsion between the ortho groups. The effect of 'buttressing' of ortho methyl groups is also studied. Deuterium and13C substitutions have been effected in some of the compounds.

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