Electron-Transfer Ionization in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry
Terthiophene and anthracene, both of which in positive mode form only molecular radical cations (M+·) upon laser irradiation (λ = 337 nm) at near-threshold laser powers, were used as matrices for matrix-assisted laser desorption/electron-transfer ionization of metallocenes (1,2-diferrocenylethane, ferrocene, and decamethylferrocene) and a methylene-bridged bisphenol, 2,2′-methylenebis-(6-tert-butyl-4-methylphenol). In the mass spectra of these matrix/analyte combinations, the formation of protonated molecules was not observed. Instead, each analyte formed a molecular radical cation (A+·) when either matrix was used. Experiments utilizing anthracene-d10 as the matrix confirmed the formation of only the analyte molecular radical cation. In addition, the molecular radical cation of ferrocene - not the protonated molecule-was produced when 2,5-dihydroxybenzoic acid was used as the matrix, indicating that a matrix commonly used to form protonated polar analytes can, in addition, function as an electron-transfer MALDI matrix.
Publication Source (Journal or Book title)
McCarley, T., McCarley, R., & Limbach, P. (1998). Electron-Transfer Ionization in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry. Analytical Chemistry, 70 (20), 4376-4379. https://doi.org/10.1021/ac980527i