Kinzelmann M, Fröhlich N, Vogel A, Kivala M, Drewello T (2024)
Publication Type: Journal article
Publication year: 2024
Book Volume: 59
Article Number: e5079
Journal Issue: 9
DOI: 10.1002/jms.5079
Triphenylamine (TPA) and N-heterotriangulene (N-HTA) scaffolds with up to three oligophenyl extensions are investigated by electrospray ionization (tandem) mass spectrometry (ESI-[MS/]MS). Due to their low oxidation potentials, all molecules readily form radical cations in the electrospray process. The energy-resolved collision-induced dissociation behaviour of the molecular ions is contrasted to that of the silver(I) adducts. Complexation with Ag(I) leads to the expected [1:1] and [2:1] complexes (MAg+ and M
APA:
Kinzelmann, M., Fröhlich, N., Vogel, A., Kivala, M., & Drewello, T. (2024). Tandem mass spectrometry of π-expanded triphenylamine and N-heterotriangulene scaffolds: Radical cation versus silver(I) adduct. Journal of Mass Spectrometry, 59(9). https://doi.org/10.1002/jms.5079
MLA:
Kinzelmann, Marina, et al. "Tandem mass spectrometry of π-expanded triphenylamine and N-heterotriangulene scaffolds: Radical cation versus silver(I) adduct." Journal of Mass Spectrometry 59.9 (2024).
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