Application and evaluation of solvent-free matrix-assisted laser desorption/ionization mass spectrometry for the analysis of derivatized fullerenes
Date
2006Author
Hungerbühler, H.Kotsiris, Sotirios G.
Vasil'ev, Y. V.
Streletskii, A. V.
Hart, M.
Mark, L. P.
Boltalina, O. V.


Drewello, T.
ISSN
1469-0667Source
European Journal of Mass SpectrometryVolume
12Issue
6Pages
397-408Google Scholar check
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Metadata
Show full item recordAbstract
A variety of derivatized fullerenes have been studied by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry. Of particular emphasis has been the evaluation of a recently introduced solvent-free sample/target preparation method. Solventfree MALDI is particularly valuable in overcoming adverse solvent-related effects, such as insolubility and/or degradation of the sample. The method was applied to fullerene derivatives susceptible to decomposition under insufficiently "soft" MALDI conditions. Analytes included the hydrofullerene: C60H36, fluorofullerenes: C60Fx where x=18, 36, 46, 48 and C70F x, where x = 54,56, methanobridged amphiphilic ligand adducts to C60 and the [4+2] cycloadduct of tetracene to C60. The new solvent-free sample preparation is established as an exceedingly valuable addition to the repertoire of preparation protocols within MALDI. The MALDI mass spectra were of very high quality throughout, providing a testimony that "soft" MALDI conditions could be achieved. Using the [4+2] cycloadduct of tetracene to C60 as the model analyte for direct comparison with solvent-based MALDI, the solvent-free approach led to less fragmentation and more abundant analyte ions. Applying solvent-free sample preparation, different matrix compounds have been examined for use in the MALDI of derivatized fullerenes, including sulfur, tetracyanoquinodimethane (TCNQ), 9-nitroanthracene (9-NA) and trans-2-[3-(4-tert-butylpheny1)-2-methyl-2-propenylidene] malononitrile (DCTB). DCTB was confirmed as the best performing matrix, reducing unwanted decomposition and suppression effects. © IM Publications 2006.