355-41-9Relevant articles and documents
PERFLUORO DIACYL PEROXIDE, SOLUTION, POLYMERIZATION INITIATOR, POLYMER PREPARATION METHOD, AND PERFLUORO ACYL CHLORIDE
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Paragraph 0091-0092, (2021/02/05)
A perfluorodiacyl peroxide represented by the following formula (1): [in-line-formulae](C5F11COO)2 ??(1).[/in-line-formulae] Also disclosed is a solution containing the perfluorodiacyl peroxide, a polymerization initiator containing the perfluorodiacyl peroxide, a method for producing a polymer which includes polymerizing a radically polymerizable monomer with the perfluorodiacyl peroxide, and a perfluoroacyl chloride represent by the following formula (2): [in-line-formulae]C5F11COCl (2).[/in-line-formulae]
PYROLYTIC REACTIONS OF PERFLUORINATED CARBOXYLIC ACID HALIDES
Podsevalov, P. V.,Bil'dinov, I. K.,Rychkov, M. L.,Deev, L. E.,Igumnov, S. M.
, p. 1269 - 1273 (2007/10/02)
Unlike other acyl halides, perfluoroacyl fluorides only enter into reaction with polar reagents.Perfluoroacyl fluorides, perfluoroacyl bromides, and perfluoroacyl iodides are smoothly decarbonylated at active carbon at elevated temperatures.In the absence of the active carbon the perfluoroacyl fluorides react with halogens, polyhalogenoalkanes, and iodoperfluoroalkanes with the formation of the corresponding halogenoperfluoroalkanes or their mixtures with perfluoroacyl halides; the low yields of the iodoperfluoroalkanes in the reaction of perfluoroacyl fluorides withiodine are explained by their ability to act themselves as reagents in these processes.The catalytic properties of active carbon are due to its ability to transfer electrons to the molecules of the adsorbed reagent and to hold the reaction particles on the surface; graphite and nickel also have specific catalytic activity.