Related Experiment Video
Updated: Dec 18, 2025

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
A mechanism for two-step thermal decomposition of 2,6-diamino-3,5-dinitropyrazine-1-oxide (LLM-105)
Qian Yu1, Chuande Zhao1, Longyu Liao1
1Institute of Chemical Materials, China Academy of Engineering Physics (CAEP), P. O. Box 919-311, Mianyang, 621900, P. R. China. ljs915@263.net.
Abstract:
2,6-Diamino-3,5-dinitropyrazine-1-oxide (LLM-105) is a representative of the new generation of low-sensitivity energetic materials and has been applied extensively in formulations as an insensitive high-energetic ingredient. Although the initial thermal decomposition mechanism of LLM-105 has been studied based on quantum chemical calculations, the internal mechanism of the two-step thermal decomposition still lacks experimental research. Thus, this study involves a detailed experimental study to reveal the mechanism of the two-step thermal decomposition of LLM-105. The results showed that LLM-105 decay was a consecutive reaction. The first-step reaction dominated the early stage of the LLM-105 decomposition, and its products participated in the reaction of the second step. The cleavage of NO2 and NH2 groups of LLM-105 mainly occurred in the first step, while gaseous products NO and C2N2 were released during the second reaction step. The first-step reaction had a higher oxygen consumption rate and a lower carbon consumption rate, producing more heat due to more extensive oxidation of the carbon backbone. The difference in the oxidative ability and reaction rate between the two steps resulted in a two-step exothermic and mass loss behavior. This study provides further insights into the entire reaction process of LLM-105 and would be helpful for its better application and for the design of new explosives.
More Related Videos
Related Concept Videos
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Cycloaddition Reactions: MO Requirements for Thermal Activation
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Rate-Determining Steps
In a multistep reaction mechanism, one of the elementary steps progresses significantly slower than the others. This slowest step is called the rate-limiting step (or rate-determining step). A reaction cannot proceed faster than its slowest step, and hence, the rate-determining step limits the overall reaction rate.
The concept of rate-determining step can be understood from the analogy of a 4-lane freeway with a short-stretch of traffic-bottleneck caused due to...
Radical Formation: Elimination
Radical Formation: Homolysis

