Abstract 17 O NMR has been applied to the study of urea over a wide pH range, in fluorosulfonic acid and in magic acid (HFSO 3 SbF 5 ). A 96 ppm diamagnetic chemical shift was observed on modifying the medium from an aqueous solution at pH 3 to a fluorosulfonic acid solvent. We attributed this shift to a protonation reaction at the urea oxygen having a p K a of 0.1. A 36 ppm paramagnetic shift was observed in magic acid relative to the resonance position in fluorosulfonic acid, which is consistent with the formation of a diprotonated form of urea. Values of transverse and longitudinal relaxation rates were found to be equal as a function of pH and to double on lowering the pH from 2 to −1.
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Valentine et al. (1984) studied this question.
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