J Am Soc Mass Spectrom. 1996 Jun;7(6):565-72. doi: 10.1016/1044-0305(96)00016-5.

Effects of functional group interactions on the gas-phase methylation and dissociation of acids and esters.

Journal of the American Society for Mass Spectrometry

J J Isbell, J S Brodbelt

PMID: 24203429 DOI: 10.1016/1044-0305(96)00016-5

Abstract

Functional group interactions have been observed to affect gas-phase ion-molecule chemistry in a quadrupole ion trap mass spectrometer. Gas-phase methylation and collisionactivated dissociation reactions of a series of related acids and esters allows an evaluation of the structural factors that influence reactivity and functional group interactions of these compounds. Examination of the [M+H](+) or [M+15](+) product ions by collision-activated dissociation has provided insight into the conformations from which diacids and diesters undergo electrophilic addition. Collision-activated dissociation has provided not only more detailed information on the structures of the ions, but also the data necessary for confident mechanistic interpretation. Labeling studies were done to probe fragmentation pathways. Upon activation of the [M+CD3](+) products of dimethyl maleate and dimethyl succinate, formed from reaction of the neutrals with CD3OCD 2 (+) ions, a rapid interfunctional group methyl transfer causes scrambling of the methyls prior to elimination of dimethyl ether or methanol. The [M+15](+) ions of dimethyl maleate are believed to lose dimethyl ether through a rate-determining 1,6-methyl transfer, whereas the [M+15](+) ions of dimethyl succinate eliminate methanol through a rate-determining 1,5-proton transfer.

References

1. J Am Soc Mass Spectrom. 1993 Mar;4(3):230-41 - PubMed

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• Journal Article