The speciation of vanadyl (VO2+) porphyrins in crude oil (vanadyl petroporphyrins) is an area of ongoing interest in petroleomics. In this paper, we describe a method for the speciation of vanadyl porphyrins that uses electron nuclear double resonance (ENDOR), a high-resolution electron paramagnetic resonance (EPR) spectroscopic technique. We use 1H ENDOR to measure hyperfine couplings between ligand protons and the paramagnetic vanadyl ion as small as about 0.15 MHz. From the measured hyperfine couplings, we directly determine all vanadium–ligand proton distances up to 8 Å. This information differentiates porphyrin ligands by their ring substitution pattern and substituent nature. We demonstrate this using a series of vanadyl porphyrin model compounds. Additionally, we demonstrate that the composition of binary vanadyl porphyrins mixtures can be determined. The ability of ENDOR to differentiate types of ligand protons in vanadyl porphyrin mixtures provides a basis for analyzing more complex mixtures of vanadyl petroporphyrins.

Tyrosine hydroxylase is a mononuclear non-heme iron monooxygenase found in the central nervous system that catalyzes the hydroxylation of tyrosine to yield L-3,4-dihydroxyphenylalanine, the rate-limiting step in the biosynthesis of catecholamine neurotransmitters. Catalysis requires the binding of tyrosine, a tetrahydropterin, and O₂ at an active site that consists of a ferrous ion coordinated facially by the side chains of two histidines and a glutamate. We used nitric oxide as a surrogate for O₂ to poise the active site iron in an S = ³/₂ {FeNO}⁷ form that is amenable to electron paramagnetic resonance (EPR) spectroscopy. The pulsed EPR method of hyperfine sublevel correlation (HYSCORE) spectroscopy was then used to probe the ligands at the remaining labile coordination sites on iron. For the complex formed by the addition of tyrosine and nitric oxide, TyrH/NO/Tyr, orientation-selective HYSCORE studies provided evidence of the coordination of one H₂O molecule characterized by proton isotropic hyperfine couplings (A(iso) = 0.0 ± 0.3 MHz) and dipolar couplings (T = 4.4 and 4.5 ± 0.2 MHz). These data show complex HYSCORE cross peak contours that required the addition of a third coupled proton, characterized by an A(iso) of 2.0 MHz and a T of 3.8 MHz, to the analysis. This proton hyperfine coupling differed from those measured previously for H₂O bound to {FeNO}⁷ model complexes and was assigned to a hydroxide ligand. For the complex formed by the addition of tyrosine, 6-methyltetrahydropterin, and NO, TyrH/NO/Tyr/6-MPH₄, the HYSCORE cross peaks attributed to H₂O and OH⁻ for the TyrH/NO/Tyr complex were replaced by a cross peak due to a single proton characterized by an A(iso) of 0.0 MHz and a dipolar coupling (T = 3.8 MHz). This interaction was assigned to the N₅ proton of the reduced pterin.

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The hyperfine coupling between an electron spin and a nuclear spin depends on the Fermi contact coupling aiso and, through dipolar coupling, the distance r between the electron and the...