Helical Polyacetylenes Induced via Noncovalent Chiral Interactions and Their Applications as Chiral Materials

Top Curr Chem (Cham). 2017 Aug;375(4):72. doi: 10.1007/s41061-017-0161-4. Epub 2017 Jul 20.

Abstract

Construction of predominantly one-handed helical polyacetylenes with a desired helix sense utilizing noncovalent chiral interactions with nonracemic chiral guest compounds based on a supramolecular approach is described. As with the conventional dynamic helical polymers possessing optically active pendant groups covalently bonded to the polymer chains, this noncovalent helicity induction system can show significant chiral amplification phenomena, in which the chiral information of the nonracemic guests can transfer with high cooperativity through noncovalent bonding interactions to induce an almost single-handed helical conformation in the polymer backbone. An intriguing "memory effect" of the induced macromolecular helicity is observed for some polyacetylenes, which means that the helical conformations induced in dynamic helical polyacetylene can be transformed into metastable static ones by tuning their helix-inversion barriers. Potential applications of helical polyacetylenes with controlled helix sense constructed by the "noncovalent helicity induction and/or memory effect" as chiral materials are also described.

Keywords: Chiral amplification; Chiral recognition ability; Chiral stationary phase; Helicity induction; Helix; Memory; Noncovalent chiral interaction; Polyacetylene.

Publication types

  • Review

MeSH terms

  • Fullerenes / chemistry
  • Macromolecular Substances / chemistry
  • Molecular Conformation
  • Polyacetylene Polymer / chemistry*
  • Stereoisomerism
  • Tryptophan / chemistry

Substances

  • Fullerenes
  • Macromolecular Substances
  • Polyacetylene Polymer
  • Tryptophan
  • fullerene C60