CHARACTERIZATION OF MODEL NITROSYLHEME PIGMENTS WITH VISIBLE, INFRARED AND 15N FOURIER TRANSFORM NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY

Synthetic pigments that model the organic-soluble pigment in heat-processed cured ham were characterized with infrared (IR) and ¹⁵N nuclear magnetic resonance (NMR) spectroscopy. The two pigments synthesized were ¹⁵N nitrosyl (protoporphyrinato- IX) iron (II), or Fe^II PP¹⁵ NO, and ¹⁵N dinitrosyl (protoporphyrinato-IX), or Fe^II PP(¹⁵NO)₂. An NMR spectrum was obtained only for the Fe^II PP¹⁵ NO. The NMR spectrum consisted of a single peak + 1.78 ppm from the Na¹⁵ NO³ and –6.8 from the CH₃NO₂ reference. The IR spectrum included a single NO symmetric stretch at 1801 cm^?1. The visible spectrum of Fe^II PPNO did not match the visible spectrum of ham extracts, while it did with FE^II PP(¹⁵NO)₂. An unequivocal structural assignment of Fe^II PP¹⁵ NO was made, but longer NMR runs may be necessary to obtain a spectrum and unequivocal structural assignment of Fe^II PP(¹⁵ NO)₂.