The stereochemistry in solution of spirocyclophosphazenes 1–3 containing 2,2′-dioxybiphenyl groups, tris(2,2′-dioxybiphenyl)cyclotriphosphazene [N3P3(O2C12H8)3] (1) and the chloro derivatives [N3P3Cl2(O2C12H8)2] (2) and [N3P3Cl4(O2C12H8)] (3), was studied using high field 1H, 13C and 31P NMR spectroscopy (variable temperature experiments) combined with molecular dynamics (MD) simulations. The ambient temperature spectra, after full assignments, showed a unique set of signals (four and six for hydrogens and carbons, respectively) for the corresponding
nuclei of all the biphenoxy systems. This isochrony was compatible with symmetry equivalence as well as with fast interconversions on the NMR time scale between the stereoisomers RRR, SSS, RRS, SSR (1), RR, SS, RS, SR (2) and R, S (3). Dynamic NMR studies evidenced that atropoisomers of 1–3 are populated at low temperature (≤ 183 K) bearing out fast racemization of the NP(O2C12H8) units in solution at ambient temperature. The MD trajectories, which were long enough (50 ns) to monitor time-averaged processes on the NMR scale, were selectively compatible with DNMR results, and provided insights into the motional properties of 1–3.
They significantly complemented the experimental information on the exchange process of 3, due to the inherent limitation of the single use of the NMR technique when NMR active diastereotopic nuclei are absent in the investigated system.