# Effect of Different Substituents on the Properties of 4-R-1,5-Diaminotetrazolium Pentazolate Salts

**Authors:** Xiaofeng Yuan, Ze Xu, Ming Lu, Yuangang Xu

PMC · DOI: 10.3390/ma18051077 · Materials · 2025-02-27

## TL;DR

This study examines how different chemical groups affect the stability and performance of 4-R-1,5-diaminotetrazolium pentazolate salts.

## Contribution

The paper introduces a systematic comparison of substituent effects on the properties of pentazolate salts using quantum chemical methods.

## Key findings

- The hydroxy-substituted salt showed the lowest interaction energy and highest stability.
- The azido-substituted salt exhibited the best detonation performance with high velocity and pressure.
- Hydrogen bonding and van der Waals interactions were identified as key factors in interionic stability.

## Abstract

To explore the impact of different substituents (R) in 4-R-1,5-diaminotetrazolium cations on the performance of their pentazolate salts, five types of pentazolate salts with different groups were designed: -H, -OH, -NH2, -NH-NH2, and -N3. Quantum chemical methods were employed to deeply study the interionic interactions and detonation properties of these 4-R-1,5-diaminotetrazolium pentazolate salts. Among these five ionic compounds, the 1,5-diamino-4-hydroxytetrazolium pentazolate ([DAT-OH+] [N5−]) system exhibited the lowest interaction energy and highest stability, while the 1,5-diamino-1H-1,2,3,4-tetrazolium pentazolate ([DAT-H+] [N5−]) system was the least stable. Symmetry-adapted perturbation theory (SAPT) analysis indicated that electrostatic and dispersion effects predominantly contributed to these interactions. An independent gradient model based on Hirshfeld partition (IGMH) analysis further highlighted the interionic interaction regions, revealing extensive van der Waals interactions and the formation of N-H…N type hydrogen bonds. The hydrogen bond formed by the cyclo-N5− and hydroxyl groups was relatively strong, while other hydrogen bonds were weaker. Benefiting from a higher enthalpy of formation, the 1,5-diamino-4-azidotetrazolium pentazolate ([DAT-N3+] [N5−]) compound exhibited the highest detonation performance (D: 9295.77 m·s−1; P: 32.13 GPa), while [DAT-OH+] [N5−] also demonstrated good performance and stability (D: 8924.96 m·s−1; P: 28.85 GPa).

## Full-text entities

- **Chemicals:** P (MESH:D010758), N5- (MESH:C031785), 1,5-diamino-4-azidotetrazolium pentazolate (-), hydrogen (MESH:D006859)

## Full text

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## Figures

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## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC11901200/full.md

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Source: https://tomesphere.com/paper/PMC11901200