Abstract

The influence of substitution pattern and electronic structure on the N=N stretching frequencies of compounds containing three to six linearly connected nitrogen atoms has been investigated by FT-IR and Raman spectroscopy. For a series of 1-phenyl-3,3-dialkyl-triazenes, Phe-N¹=N²-N³ R₂, shifts in the two valence vibrations of the triazeno group are studied with respect to the type and position of substituents at the aromatic ring, and for various alkyl substituents at N³. The N¹=N² stretching frequency is lowered by electron-withdrawing substituents at the aromatic ring; this effect is most pronounced for para-positioned substituents. A decrease in the N¹=N² bond order, and of the associated valence vibration, is also observed upon introduction of heavier N³-alkyl substituents, due to an inductive effect. Changes in vibrational frequencies are correlated with characteristic fragmentation patterns in the mass spectra of these compounds, where two degradation routes subsequent to ionization at the nitrogen atoms N¹ and N² have been observed. For the investigated pentazadiene derivatives, a weaker dependence of the N=N vibrational frequencies on the substituents is found. Mass spectra are interpreted in terms of two typical fragmentation pathways, involving a McLafferty rearrangement.

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