TY - JOUR
T1 - Assembly of three oxadiazole isomers toward versatile energetics
AU - Sun, Qi
AU - Jiang, Zhiyi
AU - Ding, Ning
AU - Zhao, Chaofeng
AU - Tian, Baojing
AU - Li, Shenghua
AU - Pang, Siping
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/10/17
Y1 - 2023/10/17
N2 - Three stable oxadiazole isomers, viz. 1,2,5-oxadiazole, 1,2,4-oxadiazole and 1,3,4-oxadiazole, were combined to obtain a new tricyclic skeleton, which was then controllably functionalized to generate versatile energetic materials: nitro/nitroamino 6, azide/nitroamino 8, nitroamino/nitroamino 10, and ionic salts 11 and 12. All these oxadiazoles were structurally confirmed and exhibit good energetic performance. In addition, a comparative study with existing isomers was carried out.
AB - Three stable oxadiazole isomers, viz. 1,2,5-oxadiazole, 1,2,4-oxadiazole and 1,3,4-oxadiazole, were combined to obtain a new tricyclic skeleton, which was then controllably functionalized to generate versatile energetic materials: nitro/nitroamino 6, azide/nitroamino 8, nitroamino/nitroamino 10, and ionic salts 11 and 12. All these oxadiazoles were structurally confirmed and exhibit good energetic performance. In addition, a comparative study with existing isomers was carried out.
UR - http://www.scopus.com/inward/record.url?scp=85175538649&partnerID=8YFLogxK
U2 - 10.1039/d3ta04193j
DO - 10.1039/d3ta04193j
M3 - Article
AN - SCOPUS:85175538649
SN - 2050-7488
VL - 11
SP - 23228
EP - 23232
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 43
ER -
