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Acenaphthylene

Acenaphthylene is a polycyclic aromatic hydrocarbon. The molecule resembles naphthalene with positions 1 and 8 connected by a C2H2 unit. It is a yellow solid. Unlike many polycyclic aromatic hydrocarbons, it has no fluorescence. Acenaphthylene is a polycyclic aromatic hydrocarbon. The molecule resembles naphthalene with positions 1 and 8 connected by a C2H2 unit. It is a yellow solid. Unlike many polycyclic aromatic hydrocarbons, it has no fluorescence. Acenaphthylene occurs as about 2% of coal tar. It is produced industrially by dehydrogenation of acenaphthene. Hydrogenation gives the more saturated compound acenaphthene. It functions as a ligand for some organometallic compounds. Chemical reduction affords the radical anion sodium or potassium acenaphthalenide, which is used as a strong reductant (E = -2.26 V vs FC). The no-observed-effect-level of acenaphthylene after repeated 28-day oral administration to both male and female rats was found to be 4 mg/kg/day.

[ "Phenanthrene", "Pyrene", "Naphthalene" ]
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