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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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)

  • 2019Reactive intermediates in the reaction of hydrazinecarbothioamides with 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate3citations

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Chart of shared publication
Nieger, Martin
1 / 21 shared
Aly, Ashraf A.
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El-Shaieb, Kamal M.
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Mohamed, Nasr K.
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Makhlouf, Maysa M.
1 / 1 shared
Bräse, Stefan
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2019

Co-Authors (by relevance)

  • Nieger, Martin
  • Aly, Ashraf A.
  • El-Shaieb, Kamal M.
  • Mohamed, Nasr K.
  • Makhlouf, Maysa M.
  • Bräse, Stefan
OrganizationsLocationPeople

article

Reactive intermediates in the reaction of hydrazinecarbothioamides with 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate

  • Nieger, Martin
  • Aly, Ashraf A.
  • El-Shaieb, Kamal M.
  • Mohamed, Nasr K.
  • Makhlouf, Maysa M.
  • Hassan, Alaa A.
  • Bräse, Stefan
Abstract

<p>The reaction of N-substituted hydrazinecarbothioamides with both 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate afforded various heterocyclic rings such as 5-amino-4-cyano-3-(methylthio)-N-phenyl-1H-pyrazole-1-carbothioamide, 5-amino-3-(methylthio)-1H-pyrazole-4-carbonitrile, 4-substituted-3-(substituted amino)-1H-1,2,4-triazole-5(4H)-thione, ethyl 5-amino-3-(methylthio)-1-(substituted carbamothioyl)-1H-pyrazole-4-carboxylate, and (Z)-ethyl 2-cyano-2-(5-(substituted amino)-1,3,4-thiadiazol-2(3H)-ylidene)acetate. However, under gentle heating, the reaction of the same starting substances behaved differently. The structure of the obtained products was fully characterized using different spectral techniques including infrared (IR), nuclear magnetic resonance (NMR), and mass spectrometry (MS) together with elemental analyses as well as single-crystal X-ray diffraction analysis.</p><p>[GRAPHICS]</p><p>.</p>

Topics
  • x-ray diffraction
  • reactive
  • mass spectrometry
  • Nuclear Magnetic Resonance spectroscopy
  • spectrometry