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A comparative study of crystal structures and inclusion properties of fluorinated triazines

Auteur(s)
Reichenbaecher, Katharina
Stoeckli-Evans, Helen 
Institut de physique 
Weber, Edwin
Hulliger, Jürg
Date de parution
2006
In
Journal of Fluorine Chemistry, Elsevier, 2006/127/2/270-276
Mots-clés
  • Fluorine compounds
  • Triazines
  • Inclusions
  • Host–guest compounds
  • Fluorine interactions
  • Fluorine compounds

  • Triazines

  • Inclusions

  • Host–guest compounds

  • Fluorine interactions...

Résumé
Three perfluorinated host compounds of the triazine type, namely 2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine (<b>1</b>), 2,4,6-tris(pentafluorothiophenoxy)-1,3,5-triazine (<b>2</b>) and 2,4,6-tris(pentafluorophenamin)-1,3,5-triazine (<b>3</b>), were synthesized differing only in the linking heteroatom (O, S and NH) between the triazine core and the pentafluorophenyl groups. The crystal structures involving compounds <b>1</b>, <b>2</b> and their inclusion compounds are dominated by a variety of fluorine interactions (phenyl-perfluorophenyl, C–HF, FF, C–FπF). However, in the structure of <b>3</b>, possessing additional hydrogen atoms of the linkage NH-groups, the formation of hydrogen bonds is favoured, whereas fluorine contacts are less apparent. Investigations by powder X-ray diffraction and thermogravimetric analysis revealed substantial differences in the host–guest interactions of the inclusion compounds.
Identifiants
https://libra.unine.ch/handle/123456789/15427
_
10.1016/j.jfluchem.2005.12.003
Type de publication
journal article
Dossier(s) à télécharger
 main article: Reinbacher_Katharina_-_A_comparative_study_of_crystal_20090504.pdf (526.83 KB)
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