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Crystal Engineering through Halogen Bonding:  Complexes of Nitrogen Heterocycles with Organic Iodides

Crystal Growth & Design · 2001 · Vol. 1(2) · pp. 165–175
Rosa Bailey WalshClifford W. PadgettPierangelo MetrangoloGiuseppe ResnatiTimothy W. HanksWilliam T. Pennington

Abstract

X-ray analysis has revealed that 4,4‘-bipyridine, 1,2-bis(4-pyridyl)ethylene, and hexamethylenetetramine form donor−acceptor complexes with 1,4-diiodobenzene, 1,4-diiodotetrafluorobenzene, and tetraiodoethylene in which the N···I distance is longer than that for the corresponding I2 complexes. As opposed to the corresponding I2 complexes that are molecular adducts, these complexes have extended structures and longer N···I distances. Steric and electronic effects influence the strength of the N···I interaction and the crystal packing. An additional complex of 1,2-bis(4-pyridyl)ethane and 1,4-dibromotetrafluorobenzene has also been investigated for comparison of N···I and N···Br interactions.

Crystallography and molecular interactionsCrystal structures of chemical compoundsOrganic and Molecular Conductors ResearchHexamethylenetetramineChemistrySteric effectsHalogen bondCrystal engineeringCrystal (programming language)HalogenAdductAcceptorEthylene

Funding

  • Division of Chemistry
Citations
341
FWCI
15.70
field-weighted impact
References
33
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100%
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Cited by
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References
van der Waals Volumes and Radii
The Journal of Physical Chemistry · 1964 · 19,102 citations
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