O−and OH−chemical ionization of some fatty acid methyl esters and triacylglycerols

✍ Scribed by Mary Cheung; Alex.B. Young; Alex G. Harrison

• Publisher: Elsevier Science
• Year: 1994
• Tongue: English
• Weight: 449 KB
• Volume: 5
• Category: Article
• ISSN: 1044-0305
• DOI: 10.1016/1044-0305(94)90004-3

✦ Synopsis

0--and OH-react with fatty acid methyl esters (FAMES) under chemical ionization conditions both as Br$nsted bases to form [M -HI-and as nucleophiles to form the carboxylate ion RCOW. O-' shows a much greater tendency to react as a nucleophile than does OH-. The [M -H]-ions fragment by elimination of CH,OH, with unsaturation in certain positions in the fatty acid hydrocarbon chain promoting this elimination for unknown reasons. The reaction of O-' and OH-with triacylglycerols leads to [M -HI-, characteristic of the molecular mass, and to carboxylate ions characteristic of the fatty acid(s) present in the lipid. The presence of the three ester functions in the lipids greatly enhances the formation of carboxylate ions compared to the FAMES. (I