Studies on the synthesis and properties of nitramino compounds based on tetrazine backbones
Shiyu Zhang1, Guangbin Cheng, Hongwei Yang
1School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China. hyang@mail.njust.edu.cn.
Abstract:
In this paper, a series of novel energetic compounds based on the backbone of the tetrazine-triazole structure were successfully synthesized. N,N'-((1,2,4,5-Tetrazine-3,6-diyl)bis(1,2-dihydro-3H-1,2,4-triazole-5-yl-3-ylidene))dinitramino (4) was prepared by the nitration of 5,5'-(1,4-dihydro-1,2,4,5-tetrazine-3,6-diyl)bis(1H-1,2,4-triazol-3-amine) (3) with 100% nitric acid and its energetic salts (6-14) were also prepared. All the compounds were fully characterized. The structures of 4 and 5 were further confirmed by single crystal X-ray diffraction analysis. The results show that these compounds have high heats of formation ranging from 2.09 to 3.95 kJ g-1, good detonation pressures and detonation velocities and acceptable sensitivities. Among them, compound 4, with low sensitivities (IS: 20 J and FS: 270 N) and excellent detonation properties (vD = 9100 m s-1; P = 34.1 GPa) shows potential for application in the field of highly energetic and insensitive explosives. The hydroxylammonium salt (7) exhibits promising energetic properties, which, in some cases, are superior to those of octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX).
More Related Videos
07:56Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
Published on: August 12, 2019
10:42Preparation of N-2-alkoxyvinylsulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
Related Concept Videos
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
2° Amines to N-Nitrosamines: Reaction with NaNO2
Diazonium Group Substitution: –OH and –H
Structure of Amines
Electrophilic Aromatic Substitution: Nitration of Benzene
