Polycyclic aromatic hydrocarbons hydrogenation

Naphthalene and other polycyclic aromatic hydrocarbons show many of the chemical properties associated with aromaticity. Thus, measurement of its heat of hydrogenation shows an aromatic stabilization energy of approximately 250 kj/mol (60 kcal/mol). Furthermore, naphthalene reacts slowly with electrophiles such as Br2 to give substitution products rather than double-bond addition products. 

Major unknowns in the mechanism by which a hydrocarbon fuel bums concern the pyrosynthesis reactions that lead to the formation of polycyclic aromatic hydrocarbons (PAHs) and soot and the oxidation chemistry of atoms other than carbon and hydrogen (heteroatoms) in the fuel, particularly nitrogen, sulfur, and halogens. 

Jacinto, M.J., Santos, O., Landers, R., Kiyohara, P.K. and Rossi, L.M. (2009) On the catalytic hydrogenation of polycyclic aromatic hydrocarbons into less toxic compounds by a facile recoverable catalyst. Applied Catalysis B Environmental, 90 (3-4), 688-692. 

Ortiz Leon, M. Velasco, L., and Vazquez-Duhalt, R., Biocatalytic Oxidation of Polycyclic Aromatic-Hydrocarbons by Hemoglobin and Hydrogen-Peroxide. Biochemical and Biophysical Research Communications, 1995. 215(3) pp. 968-973. 

Peroxyoxalate-based CL reactions are related to the hydrogen peroxide oxidation of an aryl oxalate ester, producing a high-energy intermediate. This intermediate (l,2-dioxetane-3,4-dione) forms, in the presence of a fluorophore, a charge transfer complex that dissociates to yield an excited-state fluorophore, which then emits. This type of CL reaction can be used to determine hydrogen peroxide or fluorophores including polycyclic aromatic hydrocarbons, dansyl- or fluores-camine-labeled analytes, or, indirectly, nonfluorescers that are easily oxidized (e.g., sulfite, nitrite) and quench the emission. The most widely used oxalate... 

Pure substance RMs pesticides with quoted purities, polycyclic aromatic hydrocarbons with quoted purities and potassium hydrogen phthalate with a quoted purity. 

All 60 C-atoms of Cjq are incorporated in the CgoHjo polycyclic aromatic hydrocarbon (PAH) 6, for which an efficient synthesis was developed [153], Laser irradiation of 6 at 337 nm induces hydrogen loss and the formation of CgQ, as detected by mass spectrometry (Scheme 1.6). Control experiments with C-labeled material and with the C48H24 homologue of 6 verified that the C50 is formed by a molecular transformation directly from the C50H30 PAH and not by fragmentation and recombination in the gas phase. 

Carbonaceous material (Fig. 12.8b) is intimately mixed with silicates and is very abundant (carbon abundance averages 13% and varies up to 50%) in CP IDPs. Some carbon is elemental (graphite), but C-H stretching resonances in infrared spectra show that aliphatic hydrocarbons are also present. Polycyclic aromatic hydrocarbons (PAHs) also occur. Nanodiamonds have been identified in cluster IDPs, but not in smaller CP IDPs. Enormous D/H and 15N/14N anomalies have been measured in bulk IDPs, and the hydrogen isotopic anomalies are correlated with organic-rich domains. Ratios of D/H as high as 25 times the solar ratio suggest the presence of molecular cloud materials. 

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