Bernard Desmazieres
Centre national de la recherche scientifique
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Featured researches published by Bernard Desmazieres.
Mass Spectrometry Reviews | 2011
Peran Terrier; Bernard Desmazieres; Jeanine Tortajada; William Buchmann
Modern mass spectrometry of synthetic polymers involves soft ionization techniques. Whereas matrix-assisted laser desorption/ionization (MALDI) and electrospray (ESI) are employed routinely, atmospheric pressure chemical ionization (APCI) and more recently atmospheric pressure photoionization (APPI) are used to a lesser extent. However, these latter ionization methods coupled to liquid-phase separation techniques create new opportunities for the characterization of polymers, especially for low molecular weight compounds or for the polymers that are poorly ionizable by the usual methods. After a part devoted to the description of classical MS methods employed for polymer analysis (MALDI, ESI, and their use with chromatography), APCI and APPI techniques will be described, discussed, and selected examples will present the interest of these ionization sources (or interfaces for LC/MS) in the field of polymer analysis.
Rapid Communications in Mass Spectrometry | 2008
Cédric Schneider; Michel Sablier; Bernard Desmazieres
For a complete understanding of the raw material used for cosmetic surgery under uncontrolled medical conditions, an unknown sample of polydimethylsiloxanes has been investigated utilizing a combination of analytical techniques: pyrolysis/gas chromatography/mass spectrometry (Py/GC/MS), electrospray ionization (ESI)-MS, matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF)MS, and liquid chromatography (LC)/MS. Among these techniques, the LC/APCI-MS coupling allowed the fastest and more effective analysis. In addition, the complexity of the mass spectra deduced from these LC/MS experiments was simplified compared to the mass spectra obtained by MALDI-TOF. In this work, we have demonstrated how the LC/APCI-MS coupling applied to polydimethylsiloxane samples permits the full characterization of samples where end groups of different nature can be present in very small quantities.
Analytica Chimica Acta | 2014
Bernard Desmazieres; Véronique Legros; Alexandre Giuliani; William Buchmann
Atmospheric pressure photoionization (APPI) followed by mass spectrometric detection was used to ionize a variety of polymers: polyethylene glycol, polymethyl methacrylate, polystyrene, and polysiloxane. In most cases, whatever the polymer or the solvent used (dichloromethane, tetrahydrofuran, hexane, acetone or toluene), only negative ion mode produced intact ions such as chlorinated adducts, with no or few fragmentations, in contrast to the positive ion mode that frequently led to important in-source fragmentations. In addition, it was shown that optimal detection of polymer distributions require a fine tuning of other source parameters such as temperature and ion transfer voltage. Series of mass spectra were recorded in the negative mode, in various solvents (dichloromethane, tetrahydrofuran, hexane, toluene, and acetone), by varying the photon energy from 8eV up to 10.6eV using synchrotron radiation. To these solvents, addition of a classical APPI dopant (toluene or acetone) was not necessary. Courtesy of the synchrotron radiation, it was demonstrated that the photon energy required for an efficient ionization of the polymer was correlated to the ionization energy of the solvent. As commercial APPI sources typically use krypton lamps with energy fixed at 10eV and 10.6eV, the study of the ionization of polymers over a wavelength range allowed to confirm and refine the previously proposed ionization mechanisms. Moreover, the APPI source can efficiently be used as an interface between size exclusion chromatography or reverse phase liquid chromatography and MS for the study of synthetic oligomers. However, the photoionization at fixed wavelength of polymer standards with different molecular weights showed that it was difficult to obtain intact ionized oligomers with molecular weights above a few thousands.
Chromatographia | 2002
William Buchmann; Hung Anh Nguyen; Hervé Cheradame; Jean-Pierre Morizur; Bernard Desmazieres
SummaryAn analytical strategy has been developed for analysis of polyisobutylenes partially functionalized with isothiocyanate groups (
Analytical Chemistry | 2005
Peran Terrier; William Buchmann; Ghislain Cheguillaume; Bernard Desmazieres; Jeanine Tortajada
Analytical Chemistry | 2008
Bernard Desmazieres; William Buchmann; Peran Terrier; Jeanine Tortajada
\bar M_n< 2000g mol^{ - 1}
Analytical Chemistry | 2006
Peran Terrier; William Buchmann; Bernard Desmazieres; Jeanine Tortajada
Polymer International | 2010
Véronique Bennevault-Celton; Olek Maciejak; Bernard Desmazieres; Hervé Cheradame
) by capillary supercritical-fluid chromatography (CSFC), size- exclusion chromatography (SEC), and reversed-phase liquid chromatography (RPLC). Fractions collected from semi-preparative RPLC and SEC were further characterized by capillary GC-MS (gas chromatography coupled with mass spectrometry). Complete characterization of the polymer was achieved by comparing the results obtained from the different techniques. The degree of polymerization and the relative quantity of the different series of macromolecular chains of polyisobutylene were estimated.
Polymer International | 2010
Véronique Bennevault-Celton; Olek Maciejak; Bernard Desmazieres; Hervé Cheradame
Chromatographia | 2004
Ghislain Cheguillaume; William Buchmann; Bernard Desmazieres; Jeanine Tortajada