Beilstein Journal of Organic Chemistry (Apr 2019)

Halogen bonding and host–guest chemistry between N-alkylammonium resorcinarene halides, diiodoperfluorobutane and neutral guests

  • Fangfang Pan,
  • Mohadeseh Dashti,
  • Michael R. Reynolds,
  • Kari Rissanen,
  • John F. Trant,
  • Ngong Kodiah Beyeh

DOI
https://doi.org/10.3762/bjoc.15.91
Journal volume & issue
Vol. 15, no. 1
pp. 947 – 954

Abstract

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Single crystal X-ray structures of halogen-bonded assemblies formed between host N-hexylammonium resorcinarene bromide (1) or N-cyclohexylammonium resorcinarene chloride (2), and 1,4-diiodooctafluorobutane and accompanying small solvent guests (methanol, acetonitrile and water) are presented. The guests’ inclusion affects the geometry of the cavity of the receptors 1 and 2, while the divalent halogen bond donor 1,4-diiodooctafluorobutane determines the overall nature of the halogen bond assembly. The crystal lattice of 1 contains two structurally different dimeric assemblies A and B, formally resulting in the mixture of a capsular dimer and a dimeric pseudo-capsule. 1H and 19F NMR analyses supports the existence of these halogen-bonded complexes and enhanced guest inclusion in solution.

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