Gas-phase reactivity of the O=P(OCH3)2+ phosphonium ion with aliphatic esters in a quadrupole ion trap. Spontaneous elimination of ketenes |
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Authors: | Leclerc Eric Taphanel Marie-Hélène Morizur Jean-Pierre |
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Affiliation: | Laboratoire Analyse et Environnement, CNRS UMR 8587, Université d'Evry Val d'Essonne, Bd Fran?ois Mitterrand, 91025 Evry Cedex, France. |
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Abstract: | Ion-molecule reactions between the O=P(OCH(3))(2) (+) phosphonium ions and five aliphatic esters (methyl acetate, methyl propionate, methyl 2-methylpropionate, methyl butyrate and ethyl acetate) were performed in a quadrupole ion trap mass spectrometer. The O=P(OCH(3))(2) (+) phosphonium ions, formed by electron ionization from neutral trimethyl phosphite, were found to react with aliphatic esters to give an adduct ion [RR'CHCOOR", O=P(OCH(3))(2)](+), which loses spontaneously a molecule of ketene CH(2)=CO or substituted ketenes RR'C=CO. Isotope-labeled methyl acetate was used to elucidate fragmentation mechanisms. The potential energy surface obtained from B3LYP/6-31G(d,p) calculations for the reaction between O=P(OCH(3))(2) (+) and methyl acetate is described. |
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Keywords: | ion–molecule reactions phosphonium ion quadrupole ion trap ab initio calculations |
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