Hydroxyl radical naphthalene, reaction, products

The transformation of arenes in the troposphere has been discussed in detail (Arey 1998). Their destruction can be mediated by reaction with hydroxyl radicals, and from naphthalene a wide range of compounds is produced, including 1- and 2-naphthols, 2-formylcinnamaldehyde, phthalic anhydride, and with less certainty 1,4-naphthoquinone and 2,3-epoxynaphthoquinone. Both 1- and 2-nitronaphthalene were formed through the intervention of NO2 (Bunce et al. 1997). Attention has also been directed to the composition of secondary organic aerosols from the photooxidation of monocyclic aromatic hydrocarbons in the presence of NO (Eorstner et al. 1997) the main products from a range of alkylated aromatics were 2,5-furandione and the 3-methyl and 3-ethyl congeners. 

When the hydroxylation reaction of naphthalene was carried out with Fe3+ and H202 (the Fenton reaction), which produce the OH radical, the main products... 

The nature of the reactions of hydroxyl radicals with polynuclear aromatic hydrocarbons is illustrated by studies of products observed with naphthalene (Fig. 6.25)." Addition of the hydroxyl radical to the aromatic ring produces ring opening with the... 

Photocatalysis by semiconductor powders, most usually titanium dioxide, has been applied to the oxidation of several aromatics. In many such photocatalytic reactions, the key intermediates are hydroxyl radicals formed by oxidation of water. With rather good donors such as aromatic compounds, hole transfer on the excited semiconductor surface is a viable alternative in this case, the reaction of the radical cation of the substrate or further intermediates arising from it with oxygen or superoxide anion may have a role. Photocatalyzed oxidation of naphthalene yields 2-formyldrmamaldehyde and 1,4-naphthoquinone as the primary products (Eq. (45.16)), similarly to what occurs upon direct irradiation of naphthalene in water ... 

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