4.8 Article

C-I•••π Halogen Bonding Driven Supramolecular Helix of Bilateral N-Amidothioureas Bearing β-Turns

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 139, Issue 19, Pages 6605-6610

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b13171

Keywords

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Funding

  1. NSF of China [21275121, 21435003, 91427304, 21521004, J1310024]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT13036]

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We report the first example of C-I center dot center dot center dot pi halogen bonding driven supramolecular helix in highly dilute solution of micromolar concentration, using alanine based bilateral I-substituted N-amidothioureas that contain helical fragments, the beta-turn structures. The halogen bonding interactions afford head-to-tail linkages that help to propagate the helicity of the helical fragments. In support of this action of the halogen bonding, chiral amplification was observed in the supra molecular helix formed in acetonitrile solution. The present finding provides alternative tools in the design of self-assembling macromolecules.

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