One‐Handed Helical Tubular Ladder Polymers for Chromatographic Enantioseparation **

Abstract: Defect‐free one‐handed contracted helical tubular ladder polymers with a π‐electron‐rich cylindrical helical cavity were synthesized by alkyne benzannulations of the random‐coil precursor polymers containing 6,6′‐linked‐1,1′‐spirobiindane‐7,7′‐diol‐based chiral monomer units. The resulting tightly‐twisted helical tubular ladder polymers showed remarkably high enantioseparation abilities toward a variety of chiral hydrophobic aromatics with point, axial, and planar chiralities. The random‐coil precursor polymer and analogous rigid‐rod extended helical ribbon‐like ladder polymer with no internal helical cavity exhibited no resolution abilities. The molecular dynamics simulations suggested that the π‐electron‐rich cylindrical helical cavity formed in the tightly‐twisted tubular helical ladder structures is of key importance for producing the highly‐enantioseparation ability, by which chiral aromatics can be enantioselectively encapsulated by specific π‐π and/or hydrophobic interactions.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
One‐Handed Helical Tubular Ladder Polymers for Chromatographic Enantioseparation ** ; day:06 ; month:02 ; year:2023 ; extent:10
Angewandte Chemie ; (06.02.2023) (gesamt 10)

Urheber
Zheng, Wei
Oki, Kosuke
Saha, Ranajit
Hijikata, Yuh
Yashima, Eiji
Ikai, Tomoyuki

DOI
10.1002/ange.202218297
URN
urn:nbn:de:101:1-2023020714110411206907
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:55 MESZ

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Beteiligte

  • Zheng, Wei
  • Oki, Kosuke
  • Saha, Ranajit
  • Hijikata, Yuh
  • Yashima, Eiji
  • Ikai, Tomoyuki

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