4.7 Article

Chiral Amplification during Asymmetric-Induced Copolymerization of Phenylacetylenes with Tight Cis-Cisoidal Main Chains

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume 34, Issue 14, Pages 1140-1144

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.201300318

Keywords

asymmetric-induced (co) polymerization; chiral; hydrogen bonding; main-chain conformation; polyphenylacetylene

Funding

  1. National Science Foundation of China [21204014]
  2. Fundamental Research Funds for the Central Universities, China [HEUCFR1227, HEUCFT1009, HEUCF201310003, HEUCF201310009]
  3. [19350054]
  4. Grants-in-Aid for Scientific Research [23655100] Funding Source: KAKEN

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A novel phenylacetylene (1) having two hydroxyl groups and a chiral pinanyl group together with the other three related phenylacetylenes has been synthesized and (co)polymerized by using an achiral catalytic system. Among the four monomers, only 1 is suitable to the asymmetric-induced polymerization (AIP). Chiral amplification phenomenon is only observed in the copolymerization of 1 with an achiral phenylacetylene having two hydroxyl groups (3). The tight helical cis-cisoidal main chain formed by making intramolecular hydrogen bonds between the hydroxyl groups in the copoly(1/3) enhances the efficiency of chiral induction and as a result chiral amplification phenomenon is observed during the copolymerization.

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