REACTION MECHANISM OF MONOACYL- AND BISACYLPHOSPHINE OXIDE PHOTOINITIATORS STUDIED BY P-31-, C-13-, AND H-1-CIDNP AND ESR

摘要

P-31-NMR-CIDNP (CIDNP = chemically induced dynamic nuclear polarization) spectroscopy was applied for the first time to investigate the formation and reaction of phosphorus-centered radicals obtained from phosphorus-containing photoinitiators. C-13-NMR- and H-1-NMR-CIDNP and ESR spectroscopies were used as complementary experimental techniques for the elucidation of the photochemistry of these compounds. The large hyperfine coupling constants of the P-31-nucleus results in a violation of Kaptein's rules, which is the only observation of this kind in C-13-NMR-CIDNP spectra reported so far. Interpretation of the CIDNP spectra, using a modification of Kaptein's rules for the C-13-NMR- and H-1-NMR-CIDNP, consistently shows that all compounds investigated undergo a photoinduced cleavage of the carbonyl-phosphinoyl bond from a triplet state. The fate of the primary radicals is discussed, and it is unambiguously shown by trapping experiments that the novel bisacylphosphine oxide photoinitiators give four radicals in a stepwise process.