Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2016Bridged bisnitramide-substituted furazan-based energetic materials47citations

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Shreeve, Jeanne M.
1 / 3 shared
Zhang, Jiaheng
1 / 2 shared
Parrish, Damon A.
1 / 3 shared
Chart of publication period
2016

Co-Authors (by relevance)

  • Shreeve, Jeanne M.
  • Zhang, Jiaheng
  • Parrish, Damon A.
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article

Bridged bisnitramide-substituted furazan-based energetic materials

  • Dharavath, Srinivas
  • Shreeve, Jeanne M.
  • Zhang, Jiaheng
  • Parrish, Damon A.
Abstract

<p>A series of bridged bisnitramide energetic compounds was designed and synthesized based on amino/nitro-functionalized furazans with methyl-NNO-azoxy, 1,2,4-oxadiazole and 3-hydrazino(imino)methyl side-chain groups. For comparison, 4-(methyl-azoxy)-3-nitraminofurazan as a direct nitration product and the corresponding ammonium salt were also prepared. All new compounds were thoroughly characterized by IR, NMR, elemental analyses, and differential scanning calorimetry (DSC). Two of them were further confirmed by single-crystal X-ray diffraction analysis. Heats of formation and detonation properties were calculated by using Gaussian 03 and EXPLO 5 programs, respectively. Energetic evaluation indicates that these compounds have potential to compete with the traditional explosive TNT and in some cases approach high explosive PETN. In addition, these results show that the combination of alkyl-bridging moiety and furazan ring expand the options for the design of new energetic materials with varying sensitivities.</p>

Topics
  • compound
  • x-ray diffraction
  • differential scanning calorimetry
  • Nuclear Magnetic Resonance spectroscopy