The mass spectrometric behaviour of six Schiff bases derived from the condensation in acetonitrile or methanol of ferrocenecarboxaldehyde with polyamines H,N-R-NHz (R =-H,C-CHz-9-CHz-CHr, -HzC-CH,-, -HzC--CHrN[(CH2 ),,-CH3]-CHZ-CHz-, -(HzC)&,H8Nr(CHz)~) has been investigated by fast atom bombardment
Fast-atom Bombardment Mass Spectrometry of New Polydentate Schiff Bases. 5. The Case of Bis-aldimines Containing Oxamide Groups
โ Scribed by Patrizia Tomasin; Sergio Tamburini; Pietro Alessandro Vigato; Martina D 'Alpaos; Pietro Traldi
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 131 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0951-4198
No coin nor oath required. For personal study only.
โฆ Synopsis
Four macrocyclic tetraimine Schiff bases containing oxamidic groups were synthesized by [2 + 2] condensation of N,N'-bis(2-aminoethyl)oxamide or N,N'-bis(2-amino-1,1-dimethylethyl)oxamide with 2,6-diformyl-4chlorophenol or 2,6-diformyl-4-methylphenol and characterized by elemental analyses and IR and NMR spectrometry; their [2 + 2] cyclic nature was inferred (especially) by fast-atom bombardment (FAB) mass spectrometry. The FAB-induced fragmentation patterns of the protonated molecules, investigated with the aid of metastable ion studies, evidence characteristic behaviours related to the presence of oxamidic groups or of 1,1-dimethylethyl species.
๐ SIMILAR VOLUMES