Addition of the nitroxyl radical TEMPO to 1-naphthylketene: formation of an unusual adduct

Abstract

1-Naphthylketene (2), generated by thermal Wolff-rearrangement, is trapped in situ by 2,2,6,6-tetramethylpiridinyloxy radical (TEMPO, TO·) to form the adduct 1-naphthCH(OT)CO 2 T (4), whose structure is confirmed by an X-ray determination. The 1 H NMR spectrum of 4 displays three CH 3 groups with very high field chemical shifts (δ 0.10-0.47), and this is attributed to the location of these groups in the shielding region above the π system of the naphthyl ring. At -40°C, doubling of most of the 1 H NMR signals occurs, and this is attributed to a freezing out of two conformations differing by rotation around the naphthyl—CH bond.Key words: ketene, TEMPO, restricted rotation, 1 H NMR, conformational analysis, free radicals.