Differentiation of Isomeric Hydroxypyridine N-Oxides Using Metal Complexation and Electrospray Ionization Mass Spectrometry

• Published in: Journal of the American Society for Mass Spectrometry 2011-03, Vol.22 (3), p.545-556
• Main Authors: Butler, Matias, Arroyo Mañez, Pau, Cabrera, Gabriela M.
• Format: Article
• Language: English
• Subjects: Adducts; Aluminum; Analytical Chemistry; Bioinformatics; Biotechnology; Chemistry; Chemistry and Materials Science; Cobalt; Complex formation; Complexation; Differentiation; Divalent cations; Electrospraying; Exact sciences and technology; Ionization; Ions; Iron; Isomers; Ligands; Mass spectra; Mass spectrometry; Mass spectroscopy; Mathematical analysis; Nickel; Organic Chemistry; Proteomics; Quantum chemistry; Research Article; Scandium; Spectrometric and optical methods; Trivalent ions
• ISSN: 1044-0305; 1879-1123
• DOI: 10.1007/s13361-010-0059-7

Differentiation between two isomers of hydroxypyridine N -oxide according to the metal cation adducts generated by electrospray ionization (ESI) was investigated for different metal cations, namely Mg (II), Al (III), Ca (II), Sc (III), Fe (III), Co (II), Ni (II), Cu (II), Zn (II), Ga (III), besides the diatomic cation VO(IV). Protonated molecules of the isomeric hydroxypyridine N -oxides as well as the singly/doubly charged adducts formed from neutral or deprotonated ligands and a doubly/triply charged cation were produced in the gas phase using ESI, recording mass spectra with different metal ions for each isomer. While complex formation was successful for 2-hydroxypyridine N -oxide with trivalent ions, in the case of 3-hydroxypyridine N -oxide, only peaks related to the protonated molecule were present. On the other hand, divalent cations formed specific species for each isomer, giving characteristic spectra in every case. Hence, differentiation was possible irrespective of the metal cation utilized. In addition, quantum chemical calculations at the B3LYP/6-31 + G(d,p) level of theory were performed in order to gain insight into the different complexation of calcium(II) with the isomers of hydroxypyridine N -oxide. The relative stability in the gas phase of the neutral complexes of calcium made up of two ligands, as well as the singly charged and doubly charged complexes, was investigated. The results of these calculations improved the understanding of the differences observed in the mass spectra obtained for each isomer.