4.8 Article

Nitrotetrazolate-2N-oxides and the Strategy of N-Oxide Introduction

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 48, Pages 17216-17226

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja106892a

Keywords

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Funding

  1. Ludwig-Maximilian University of Munich (LMU)
  2. U.S. Army Research Laboratory (ARL)
  3. Armament Research, Development and Engineering Center (ARDEC)
  4. Strategic Environmental Research and Development Program (SERDP)
  5. Office of Naval Research (ONR) [W911NF-09-2-0018, W911NF-09-1-0120, W011NF-09-1-0056, 10 WP-SEED01-002/WP-1765]

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The first anionic tetrazole-2N-oxide has been prepared by mild aqueous oxidation of easily prepared 5-nitrotetrazole with commercially available oxone in high yields. The result of protonating 5-nitrotetrazolate-2N-oxide has been identified as a hydroxytetrazole, and the nitrogen-rich salts including ammonium, hydroxylammonium, guanidinium, aminoguanidinum, diaminoguanidinium, and triaminoguanidinium have been prepared and characterized. When compared to the nitrogen-rich salts of nitrotetrazole, the nitrogen-rich salts of nitrotetrazole-2N-oxide show superior energetic performance as calculated by the EXPLO5 computer code, using heats of formation calculated using the CBS-4M level of quantum mechanical theory. The impact, friction, and electrical spark sensitivities of the nitrogen-rich nitrotetrazolate-2N-oxides were measured and cover the whole range from sensitive to insensitive energetic materials.

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