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Unimolecular dissociation of anions derived from succinic acid (H2Su) in the gas phase: HSu- and ClMgSu-. Relationship to CO2 fixation.

Joakim S JestiläEinar Uggerud
Published in: European journal of mass spectrometry (Chichester, England) (2017)
Electrospray ionization of mixtures of succinic acid (here denoted H2Su) and magnesium chloride in water/methanol give rise to ions of the type ESu- (E = H or ClMg). The unimolecular dissociation of these ions was studied by collisionally induced dissociation mass spectrometry and interpreted by quantum chemical calculations (density functional theory and the composite Gaussian-4 method) of relevant parts of the potential energy surfaces. The major dissociation pathways from HSu- were seen to be dehydration and decarboxylation, while ClMgSu- mainly undergoes decarboxylation. The latter reaction proceeds without barrier for the reverse reaction; addition of CO2 to a Grignard type structure ClMg(CH2CH2CO2)-. In contrast, addition of CO2 to the analogous H(CH2CH2CO2)- ion has a substantial barrier. Dehydration of HSu- gives rise to deprotonated succinic anhydride via a transition state for the key intramolecular proton transfer having an entropically favorable seven-member ring structure. The succinate systems studied here are compared to the previously reported analogous maleate systems, providing further insight to the structure-reactivity relationship.
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