Studies on the formation of N-methylperfluoroalkylnitrile cations from perfluoroacylphenethylamines in electron ionisation mass spectrometry: unique marker ion fragments in methamphetamine analysis.
Eur J Mass Spectrom (Chichester)
; 18(3): 287-99, 2012.
Article
in En
| MEDLINE
| ID: mdl-22837439
ABSTRACT
The mass spectra of the perfluoroacyl derivatives of methamphetamine show a unique and characteristic fragment ion identified as the N-methylperfluoroalkylnitrile cation (C(n)F(2n+1)CNCH(3))(+). This ion appears at various m/z values depending on the nature of the perfluoroacyl species and is generated via rearrangement of the perfluoroacyl immonium fragment formed by loss of the benzyl-radical from the molecular ion. Analogous ions have been described in the mass spectra of other methamphetamine-like side chain substances regardless of the aromatic ring substitution pattern. The scope and limitation of this rearrangement pathway were evaluated in this study by preparing a set of substituted phenethylamines and related compounds of varying structure. The perfluoroacyl moiety leads to the formation of the highest abundance of the N-methyl nitrile cation fragment while hydrocarbon acyl groups do not show the N-methylnitrile cation as a significant peak. The N-methyl group is required for the formation of the N-methyl nitrile cation and higher N-alkyl homologues eliminate the corresponding alkene species from the acyl immonium fragment. The loss of benzaldehyde and acetone from the perfluoroacylimmonium species produces the highest relative abundance of the unique N- methylperfluoroalkylnitrile cation.
Full text:
1
Database:
MEDLINE
Main subject:
Cations
/
Substance Abuse Detection
/
Forensic Toxicology
/
Gas Chromatography-Mass Spectrometry
/
Methamphetamine
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Year:
2012
Type:
Article