Licht, H. H. published the artcileTautomerism in nitrotriazoles: structure investigation by combined 1H, 13C and 15N NMR spectroscopy, Application of 5-Nitro-1H-1,2,3-triazole, the publication is Magnetic Resonance in Chemistry (1998), 36(5), 343-350, database is CAplus.
The tautomerism and isomerism of triazoles make the structure anal. of such compounds a difficult problem, and in the case of several nitrotriazoles a detailed structure assignment had been lacking up to now. Supported by selected compounds, a definite structure determination of ten nitrotriazoles was achieved by combined application of 15N NMR spectroscopy and increment calculations This method also succeeded in cases where equilibrium of tautomers were present. An evaluation of the shift data and coupling modes gave systematic references to structure and substituent influences.
Magnetic Resonance in Chemistry published new progress about 14544-45-7. 14544-45-7 belongs to triazoles, auxiliary class Triazoles, name is 5-Nitro-1H-1,2,3-triazole, and the molecular formula is C2H2N4O2, Application of 5-Nitro-1H-1,2,3-triazole.
Referemce:
https://en.wikipedia.org/wiki/1,2,3-Triazole,
Triazoles – an overview | ScienceDirect Topics