Chiromers: conformation-driven mirror-image supramolecular chirality isomerism identified in a new class of helical rosette nanotubes

Nanoscale. 2014 Aug 21;6(16):9421-7. doi: 10.1039/c4nr00340c. Epub 2014 Apr 28.

Abstract

Rosette nanotubes are biologically inspired nanostructures, formed through the hierarchical organization of a hybrid DNA base analogue (G∧C), which features hydrogen-bonding arrays of guanine and cytosine. Several twin-G∧C motifs functionalized with chiral moieties, which undergo a self-assembly process under methanolic and aqueous conditions to produce helical rosette nanotubes (RNTs), were synthesized and characterized. The built-in molecular chirality in the twin-G∧C building blocks led to the supramolecular chirality exhibited by the RNTs, as evidenced by the CD activity. Depending on the motifs and environmental conditions, mirror-image supramolecular chirality due to absolute molecular chirality, solvent-induced and structure-dependent supramolecular chirality inversion, and pH-controlled chiroptical switching were observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Isomerism
  • Models, Molecular
  • Molecular Conformation
  • Nanotechnology / methods*
  • Nanotubes / chemistry*
  • Nanotubes / ultrastructure*
  • Stereoisomerism