Abstract
Furazanopyrazine-based energetic compounds were developed through a substitution–nitration strategy combining flexible biogenic amine side chains with nitramine modification. Structural and thermal analyses revealed that side-chain flexibility effectively tunes crystal packing and phase behavior. Among compounds I–VII·H2O, compound II exhibited the most favorable melt-cast characteristics, with a melting point of 89 °C, competitive detonation performance, and acceptable sensitivities. These results offer a useful design strategy for fused-ring melt-cast energetic materials.
| Original language | English |
|---|---|
| Pages (from-to) | 7004-7008 |
| Number of pages | 5 |
| Journal | Organic Letters |
| Volume | 28 |
| Issue number | 22 |
| DOIs | |
| State | Published - 5 Jun 2026 |
| Externally published | Yes |
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