Related Experiment Video
Updated: Jul 26, 2025
Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange
Published on: June 23, 2023
Triazole-induced planarization of a twisted tetrazole-based molecule towards energetic materials with improved
Zhaoyang Yin1, Lijincao Hu1, Wei Huang1
1School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China. huang_wei@njust.edu.cn.
Abstract:
Pursuing the structural planarization of energetic materials is an efficient method for achieving improved performance. Although many planar energetic molecules have been prepared so far, the innovation of advanced planar explosives still relies on the scientific intuition, experience and trial-and-error of researchers. Now, a triazole-induced planarization strategy is proposed based on the regulation of aromaticity, charge distribution, and hydrogen bonds. The incorporation of a triazole ring into the non-planar molecule 5-amino-1-nitriminotetrazole (VII) results in a planar energetic material named N-[5-amino-1-(1H-tetrazol-5-yl)-1H-1,2,4-triazol-3-yl]nitramide (3). Compared with VII (Td = 85 °C; IS < 0.25 J; FS < 5 N), 3 shows remarkably improved thermal stability (Td = 145 °C) and reduced sensitivities (IS = 20 J; FS > 360 N). The variation of thermal stability and mechanical sensitivity from VII to 3 reflects the effectiveness and superiority of the planarization strategy. Benefiting from the properties of 3, its energetic salt 5 exhibits excellent overall performance (Dv = 9342 m s-1; P = 31.6 GPa; Td = 201 °C; IS = 20 J; FS = 360 N), which is comparable to that of HMX. Moreover, the triazole-induced planarization strategy may serve as a guide for exploring advanced energetic materials.
More Related Videos
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
06:34Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides CHIPS
Published on: June 20, 2014
Related Concept Videos
01:18Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
02:46Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
01:28Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
02:11Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal...
01:26Thermal and Photochemical Electrocyclic Reactions: Overview
01:17Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.