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Hydrogen bond-Driven Self-Assembly between Amidinium Cations and Carboxylate Anions: A Combined Molecular Dynamics, NMR Spectroscopy, and Single Crystal X-ray Diffraction Study.

Michael ThomasThomas Anglim LagonesMartyna JuddMahbod MorshediMegan L O'MaraNicholas G White
Published in: Chemistry, an Asian journal (2017)
A combination of molecular dynamics (MD), NMR spectroscopy, and single crystal X-ray diffraction (SCXRD) techniques was used to probe the self-assembly of para- and meta-bis(amidinium) compounds with para-, meta-, and ortho-dicarboxylates. Good concordance was observed between the MD and experimental results. In DMSO solution, the systems form several rapidly exchanging assemblies, in part because a range of hydrogen bonding interactions is possible between the amidinium and carboxylate moieties. Upon crystallization, the majority of the systems form 1D supramolecular polymers, which are held together by short N-H⋅⋅⋅O hydrogen bonds.
Keyphrases
  • molecular dynamics
  • ionic liquid
  • electron microscopy
  • density functional theory
  • high resolution
  • dual energy
  • solid state
  • crystal structure
  • computed tomography
  • water soluble