Mass spectra of aliphatic dicarboxylic acids and their dimethyl esters: Cyclic structures for the [M − H 2 O] +˙ ions from the diacids and [M − MeOH] +˙ ions from the dimethyl esters

1988; Wiley; Volume: 23; Issue: 10 Linguagem: Inglês

10.1002/oms.1210231009

ISSN

2376-3884

Autores

Alex G. Harrison, R. Krishna Mohan Rao Kallury, Ulrich J. Krull, Michael Thompson,

Tópico(s)

Various Chemistry Research Topics

Resumo

Abstract Methyl 2‐oxocycIoalkane carboxylate structures are proposed lor the [M − MeOH] +˙ ions from dimethyl adipate, pimelate, suberate and azelate. This proposal is based on a comparison of the metastable ion mass spectra and the kinetic energy releases for the major fragmentation reaction of these species with the same data for the molecular ions of authentic cyclic β‐keto esters. The mass spectra of α,α,α′,α′‐d 4 ‐pimelic acid and its dimethyl ester indicate that the α‐hydrogens are involved only to a minor extent in the formation of [M − ROH] +˙ and [M − 2ROH] +˙ ions, while these α‐hydrogens are involved almost exclusively in the loss of ROH from the [M − RO˙] + ions (R = H or CH 3 ). The molecules XCO(CH 2 ) 7 COOMe (X = OH, Cl) form abundant ions in their mass spectra with the same structure as the [M − 2MeOH] +˙ ions from dimethyl azelate.

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