Abstract
Observable changes in the pattern of polarization of n.m.r. spectra of products (XC6H4)(YC6H4)CH·CHFPh from insertion of diarylmethylenes into the benzylic C–H bond of benzyl fluoride occur with different substituents X and Y and hence different g-values of the intermediate diarylmethyl radicals for 1H and 19F nuclei.
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