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Multi-level chirality in liquid crystals formed by achiral molecules

Author

Listed:
  • Mirosław Salamończyk

    (University of Warsaw
    Lawrence Berkeley National Laboratory)

  • Nataša Vaupotič

    (University of Maribor
    Jozef Stefan Institute)

  • Damian Pociecha

    (University of Warsaw)

  • Rebecca Walker

    (University of Aberdeen)

  • John M. D. Storey

    (University of Aberdeen)

  • Corrie T. Imrie

    (University of Aberdeen)

  • Cheng Wang

    (Lawrence Berkeley National Laboratory)

  • Chenhui Zhu

    (Lawrence Berkeley National Laboratory)

  • Ewa Gorecka

    (University of Warsaw)

Abstract

Complex materials often exhibit a hierarchical structure with an intriguing mechanism responsible for the ‘propagation’ of order from the molecular to the nano- or micro-scale level. In particular, the chirality of biological molecules such as nucleic acids and amino acids is responsible for the helical structure of DNA and proteins, which in turn leads to the lack of mirror symmetry of macro-bio-objects. To fully understand mechanisms of cross-level order transfer there is an intensive search for simpler artificial structures exhibiting hierarchical arrangement. Here we present complex systems built of achiral molecules that show four levels of structural chirality: layer chirality, helicity of a basic repeating unit, mesoscopic helix and helical filaments. The structures are identified by a combination of hard and soft x-ray diffraction measurements, optical studies and theoretical modelling. Similarly to many biological systems, the studied materials exhibit a coupling between chirality at different levels.

Suggested Citation

  • Mirosław Salamończyk & Nataša Vaupotič & Damian Pociecha & Rebecca Walker & John M. D. Storey & Corrie T. Imrie & Cheng Wang & Chenhui Zhu & Ewa Gorecka, 2019. "Multi-level chirality in liquid crystals formed by achiral molecules," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09862-y
    DOI: 10.1038/s41467-019-09862-y
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