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Laser desorption/ionization and laser ablation synthesis of new selenium oxide compounds from selenium(IV) dioxide

Authors

  • Zbyněk Špalt,

    1. Department of Analytical Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
    2. Laboratory of Plasma Physics and Plasma Sources, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
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  • Eladia María Peña-Méndez,

    1. Department of Analytical Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
    2. Laboratory of Plasma Physics and Plasma Sources, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
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    • On leave from: Department of Analytical Chemistry, Nutrition and Food Science, University of La Laguna, 38071 La Laguna, Tenerife, Spain.

  • Milan Alberti,

    1. Laboratory of Plasma Physics and Plasma Sources, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
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  • Josef Havel

    Corresponding author
    1. Department of Analytical Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
    2. Laboratory of Plasma Physics and Plasma Sources, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
    • Department of Analytical Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic.
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Abstract

Laser desorption/ionization (LDI) and/or laser ablation (LA) of selenium dioxide crystals or its mixtures with sodium peroxide were studied using a commercial matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometer. It was found that LDI and LA of selenium (IV) dioxide not only ionizes SeO2, but also leads to the formation of several positively and negatively singly charged species: SeOmath image (n = 0–2), Semath image, SeOmath image (n = 0–4), Se2Omath image (n = 3–7), Se3Omath image (n = 4–9), Se4Omath image (n = 8–10). A rather high yield of selenium species in the positive ion mode, Semath image (m = 1–8) and SemOH+ (m = 3–7), was obtained by using the MALDI approach while the species detected in the negative ion mode, SeOmath image (n = 0–4), Se2Omath image (n = 3–7), Se3Omath image (n = 4–9), and Se4Omath image (n = 9, 10), were the same as those observed during LDI/LA of selenium dioxide. The addition of sodium peroxide to selenium dioxide with the aim of enhancing its oxidation and thus increasing the production of SeO4 product resulted in extensive cationization of the species with sodium or potassium. The following positively and negatively charged species were identified: Se+, Semath image, Se2OH+, Se2ONa+, SeOmath image (n = 0–3), and Se2Omath image (n = 0, 1, 4). Also observed in mass spectra of such mixtures, various mixed sodium and/or potassium adducts with selenium oxide species, e.g. Se2O4K2Na, were identified. In all, 26 totally new species, Se2Omath image (n = 3–6), Se3Omath image (n = 4–9), Se4Omath image (n = 8–10), Se4O11Hmath image, Se4O12Hmath image, Se2O4Na, Se2O5HNa, Se2O5HNamath image, Se3O6K2Na, Se3O6K2Namath image, Se2ONa+, and SemOH+ (m = 3–7), were described for the first time. Also, for the first time, the formation of selenium(IV) diperoxide, O-O-Se-O-O or O2SeO2, is described. The stoichiometries of the compounds generated were confirmed using isotopic pattern modeling. Copyright © 2006 John Wiley & Sons, Ltd.

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