“…5‐N ‐ Substituted tetrazoles,30 for example, 5‐aminotetrazoles,31 5,5′‐azotetrazolates,32 bis(1 H ‐tetrazol‐5‐yl)amine (H 2 BTA),4, 33 5,5′‐bis(1 H ‐tetrazolyl)hydrazine (BTH),34 and 5‐azido‐1 H ‐tetrazole6 have nitrogen contents greater than 82 %, and many of their derivatives that bear tetrazole group(s) are weakly acidic and thus have constituted anionic moieties in energetic salts 4. 31, 35, 36 Our recent communications4, 37 about dianionic salts of N , N ‐bis(1 H ‐tetrazol‐5‐yl)amine (Scheme ) have aroused wide interest in many applications, such as high‐energetic materials,31, 33, 35, 36, 38–61 metallic coordination compounds62–65 and polymers,66, 67 theoretical calculations and physical predictions,68–72 functional ionic liquids,73–77 and so on 78. 79…”