Pentazoles: proton and carbon-13 NMR spectra of some 1-arylpentazoles: kinetics and mechanism of degradation of the arylpentazole system

Abstract
The proton and carbon-13 NMR spectra of a range of 1-(p-substituted-phenyl)pentazoles are reported. The influence of the –N5 group on the aryl shifts is compared with that of the –NO2 and –N3 groups. Direct kinetic measurements of the degradation of 1-arylpentazoles in CD3OD–CD2Cl2(1:1, v/v) gave a Hammett p value of + 1.25. For 1-(p-chlorophenyl)pentazole values of ΔE, 88.6 kJ mol–1, ΔH 86.3 kJ mol–1 and ΔS+ 19.9 J mol–1 K–1 are obtained at –10–0 °C. These data suggest a polar two-step mechanism with rate-determining cleavage of the 1–2 bond giving an unstable azido–azo (pentazene) intermediate, the nitrogen analogue of the azido–azomethine species of tetrazole ring-opening.

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