Abstract
Carbonyl azides are important precursors to isocyanates and are used as energetic compounds. However, the further development of these compounds is limited by their inherently poor stability. In this study, we present a new family of carbonyl azides, 5-nitro-1H-1,2,4-triazol-3-yl-carbamoyl-azide (NTCA), which was synthesized through in situ oxidation cleavage of amino-tetrazole. Compared with its precursor (nitrocarbamoyl azide, HNCA), X-ray data and quantum calculations indicate that NTCA has much stronger conjugation (dihedral angle decreased from 13.39° to 1.35°) and more H-bonds (increase from 2 to 7 pairs). As a result, NTCA exhibits the highest thermal stability (decomposition temperature of 212 °C) and highest density (1.820 g cm-3) among all known carbonyl azides. In addition, a series of Curtius rearrangements were performed to generate substituted ionic derivatives, which also exhibit high stability and energy. This study provides an effective strategy for synthesizing carbonyl azides with high stability and energy, paving the way for future practical applications.
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