Noncovalent Helicene Structure between Nucleic Acids and Cyanuric Acid

Asem Alenaizan, Kévin Fauché, Ramanarayanan Krishnamurthy, C. David Sherrill*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Cyanuric acid (CA), a triazine heterocycle, is extensively utilized for noncovalent self-assembly. The association between poly(adenine) and CA into micron-length fibers was a remarkable observation made by Sleiman and co-workers, who proposed that adenine and CA adopt a hexameric rosette configuration in analogy with previously reported structures for CA assemblies. However, recent experimental observations from the Krishnamurthy group led to a reevaluation of the hexameric rosette model, wherein they have proposed a hydrogen-bonded helicene model as an alternative. Our molecular dynamics simulations show that the hexad model is indeed unlikely and that this novel noncovalent helicene geometry, where the adenine and CA bases form an extended helical hydrogen-bond network across the system, is a more probable structural motif. The existence of noncovalent helicene compounds may have wide-ranging applications in DNA nanotechnology and helicene chemistry.

Original languageEnglish
Pages (from-to)4043-4052
Number of pages10
JournalChemistry - A European Journal
Volume27
Issue number12
DOIs
StatePublished - 24 Feb 2021
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2020 Wiley-VCH GmbH

Keywords

  • molecular dynamics
  • noncovalent helicenes
  • nucleic acids
  • self-assembly

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Organic Chemistry

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