Atmospheric oxidation of polyfluorinated amides: historical source of perfluorinated carboxylic acids to the
Derek A Jackson1, Timothy J Wallington, Scott A Mabury
1Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON, Canada M5S 3H6.
Abstract:
Polyfluorinated amides (PFAMs) are a class of fluorinated compounds which were produced as unintentional byproducts in the electrochemical fluorination process used for polyfluorinated sulfonamide synthesis in 1947-2002. To investigate the historical potential of PFAMs as an atmospheric perfluorinated acid (PFCA) source we studied N-ethylperfluorobutyramide (EtFBA) as a surrogate for longer chained PFAMs. Smog chamber relative rate techniques were used to measure bimolecular rate coefficients for reactions of EtFBA with chlorine atoms and hydroxyl radicals. It was found kCl = (2.08 ± 0.15) × 10(-11) cm(3) molecule(-1) s(-1) and kOH = (2.65 ± 0.50) × 10(-12) cm(3) molecule(-1) s(-1) and the atmospheric lifetime of EtFBA with respect to reaction with OH was estimated to be approximately 4.4 days. Offline sampling with both GC-MS and LC-MS/MS techniques was used to determine the products and hence a plausible pathway of atmospheric oxidation of EtFBA. Three primary oxidation products were observed by GC-MS, the N-dealkylation product C3F7C(O)NH2 and two carbonyl products, probably C3F7C(O)N(H)C(O)CH3 and C3F7C(O)N(H)CH2CHO. These primary products react further to give perfluorocarboxylic acids (PFCAs) as detected by LC-MS/MS, suggesting that eight carbon PFAMs were a historical source of PFCAs to remote regions, including the Canadian Arctic.
Related Concept Videos
Radical Autoxidation
Autoxidation of Ethers to Peroxides and Hydroperoxides
α-Halogenation of Carboxylic Acid Derivatives: Overview
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Carboxylic Acids to Acid Chlorides
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...


