J. Krause et al., STUDIES ON THE SELECTION OF NEW MATRICES FOR ULTRAVIOLET MATRIX-ASSISTED LASER DESORPTION IONIZATION TIME-OF-FLIGHT MASS-SPECTROMETRY/, Rapid communications in mass spectrometry, 10(15), 1996, pp. 1927-1933
A new group of compounds has been successfully tested as matrices for
ultraviolet matrix-assisted laser desorption/ionization mass spectrome
try (UV-MALDI MS). Several new matrices for UV-MALDI MS have been foun
d by choosing, as potential matrices, compounds that perform an intram
olecular proton transfer along an intramolecular H-bond under UV irrad
iation. Compounds of this type are, for example, salicylamide, salicyl
anilide, several ortho-hydroxyacetophenones and ortho-hydroxybenzophen
ones. The matrix activity of these compounds is compared to the corres
ponding meta- and para-isomers and to the matrix activity of such well
known matrices as 2,5-dihydroxybenzoic acid and 2,4,6-trihydroxyaceto
phenone. It was found that meta- and para-substituted hydroxycarbonyl
compounds show either a significantly lower or no matrix activity comp
ared with the ortho isomers.