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Theoretical Study of Mechanisms, Thermodynamics, and Kinetics of the Decomposition of Gas-Phase α-HMX (Octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine)

✍ Scribed by Zhang, Shaowen; Nguyen, Hung N.; Truong, Thanh N.

Book ID
121421532
Publisher
American Chemical Society
Year
2003
Tongue
English
Weight
183 KB
Volume
107
Category
Article
ISSN
1089-5639

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New adducts of octahydro-1,3,5,7-tetrani
New adducts of octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)
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## Abstract A new series of relatively stable adducts of octahydro‐1,3,5,7‐tetranitro‐1,3,5,7‐tetrazocine (HMX) with derivatives of pyridine‐N‐oxide were prepared. In addition, relative stable new adducts of HMX were prepared with 5‐membered, 6‐membered, and condensed‐ring heterocyclic compounds. M

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A Combined Experimental and Theoretical Study of HMX (Octogen, Octahydro-1,3,5,7-Tetranitro-1,3,5,7-Tetrazocine) in the Gas Phase
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The \({ }^{14} \mathrm{C}\)-uniformly labeled (UL) explosive, octahydro-1,3,5,7-tetranitro-1,3,5,7tetrazocine (HMX) was synthesized in \(40 \%\) yield by nitrolysis of \({ }^{14} \mathrm{C}\)-labeled hexamethylenetetramine (hexamine) in the presence of boron trifluoride diethyl etherate as catalyst.