Intermolecular interactions in solution, such as the formation of donor-acceptor complexes, can be readily studied by 1H-NMR spectroscopy by means of a trick in the case of chiral compounds. Reaction of the donor, e.g. (RS)-(1), with an optically active acceptor, e.g. (R)-(2), gives the two diastereomeric complexes [(R)-(1) + (R)-(2)] and [(S)-(1) + (R)-(2)], whose NMR spectra differ: a signal splitting is observed.
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Mannschreck et al. (1978) studied this question.
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