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Related Experiment Videos

Hexamethylenetetraminium 2,4,6-trinitrophenolate.

Anwar Usman1, Suchada Chantrapromma, Hoong-Kun Fun

  • 1X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia.

Acta Crystallographica. Section C, Crystal Structure Communications
|January 10, 2002
PubMed
Summary
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The crystal structure of hexamethylenetetraminium 2,4,6-trinitrophenolate reveals bifurcated hydrogen bonds. These interactions, along with C-H...O and C-H...pi bonds, stabilize the sheet-like arrangement of ions.

Area of Science:

  • Crystal Engineering
  • Supramolecular Chemistry
  • Materials Science

Background:

  • Understanding intermolecular interactions is crucial for designing novel materials.
  • The study of ionic adducts provides insights into crystal packing and stability.
  • Hexamethylenetetramine derivatives and picrate anions are common motifs in crystal engineering.

Purpose of the Study:

  • To characterize the crystal structure of the 1:1 ionic adduct of hexamethylenetetraminium and 2,4,6-trinitrophenolate.
  • To investigate the role of hydrogen bonding and other non-covalent interactions in stabilizing the crystal lattice.
  • To elucidate the supramolecular assembly of cations and anions in the solid state.

Main Methods:

  • Single-crystal X-ray diffraction was employed to determine the molecular and crystal structure.

Related Experiment Videos

  • Analysis of hydrogen bonding (C-H...O) and pi-pi interactions was performed.
  • Intermolecular interactions were visualized and quantified using crystallographic software.
  • Main Results:

    • The 1:1 ionic adduct, C6H13N4+*C6H2N3O7-, was successfully synthesized and characterized.
    • The hexamethylenetetraminium cation acts as a hydrogen bond donor.
    • Bifurcated hydrogen bonds were observed between the cation and the oxygen atoms of the phenolate and nitro groups of the anion.
    • The crystal structure is organized into sheets of alternating cations and anions.
    • Intermolecular C-H...O and C-H...pi interactions contribute to the overall crystal stability.

    Conclusions:

    • The crystal structure is stabilized by a combination of hydrogen bonding and C-H...pi interactions.
    • The observed bifurcated hydrogen bonding pattern influences the packing arrangement of the ions.
    • This study provides a detailed understanding of the supramolecular architecture in this ionic complex.