93343-13-6Relevant articles and documents
OXIDATION OF OCTAFLUORONAPHTHALENE AND HEPTAFLUORONAPHTHOLS WITH HYDROGEN PEROXIDE
Bogachev, A. A.,Kobrina, L. S.,Yakobson, G. G.
, p. 2307 - 2313 (2007/10/02)
Derivatives of 1-oxodihydronaphthalenes and 1,4-naphthoquinone are formed preferentially during the thermal decomposition of hydrogen peroxide in an excess of octafluoronaphthalene or heptafluoro-1- and heptafluoro-2-naphthols.The oxidation of these substrates with an excess of hydrogen peroxide leads to destruction of the aromatic ring.Possible paths to the formation of the main products, including the generation of heptafluoronaphthoxyl radicals both as a result of reaction of the octafluoronaphthalene with the hydroxyl radicals and as a result of oxidation of the heptafluoronaphthols, are considered.