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Left-handed helical polymer resin nanotubes prepared by using N-palmitoyl glucosamine.

Jiangang LiYi LiBaozong LiYonggang Yang
Published in: Chirality (2017)
Although the preparation of single-handed helical inorganic and hybrid organic-inorganic nanotubes is well developed, approaches to the formation of single-handed organopolymeric nanotubes are limited. Here, left-handed helical m-phenylenediamine-formaldehyde resin and 3-aminophenol-formaldehyde resin nanotubes were prepared by using N-palmitoyl glucosamine that can self-assemble into left-handed twisted nanoribbons in a mixture of methanol and water. In the reaction mixture, the helical pitch of the nanoribbons decreased with increasing reaction time. The resin nanotubes were obtained after removing the N-palmitoyl glucosamine template, and circular dichroism spectroscopy indicated that the organopolymeric nanotubes had optical activity. Carbonaceous nanotubes were then prepared by carbonization of the 3-aminophenol-formaldehyde resin nanotubes.
Keyphrases
  • high resolution
  • room temperature
  • mass spectrometry
  • computed tomography
  • single molecule
  • water soluble
  • liquid chromatography
  • tandem mass spectrometry