Control over the emerging chirality in supramolecular gels and solutions by chiral microvortices in milliseconds

The origin of homochirality in life is a fundamental mystery. Symmetry breaking and subsequent amplification of chiral bias are regarded as one of the underlying mechanisms. However, the selection and control of initial chiral bias in a spontaneous mirror symmetry breaking process remains a great ch...

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Veröffentlicht in:Nature communications 2018-07, Vol.9 (1), p.2599-8, Article 2599
Hauptverfasser: Sun, Jiashu, Li, Yike, Yan, Fusheng, Liu, Chao, Sang, Yutao, Tian, Fei, Feng, Qiang, Duan, Pengfei, Zhang, Li, Shi, Xinghua, Ding, Baoquan, Liu, Minghua
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Sprache:eng
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Zusammenfassung:The origin of homochirality in life is a fundamental mystery. Symmetry breaking and subsequent amplification of chiral bias are regarded as one of the underlying mechanisms. However, the selection and control of initial chiral bias in a spontaneous mirror symmetry breaking process remains a great challenge. Here we show experimental evidences that laminar chiral microvortices generated within asymmetric microchambers can lead to a hydrodynamic selection of initial chiral bias of supramolecular systems composed of exclusively achiral molecules within milliseconds. The self-assembled nuclei with the chirality sign affected by the shear force of enantiomorphic microvortices are subsequently amplified into almost absolutely chirality-controlled supramolecular gels or nanotubes. In contrast, turbulent vortices in stirring cuvettes fail to select the chirality of supramolecular gels. This study reveals that a laminar chiral microflow can induce enantioselection far from equilibrium, and provides an insight on the origin of natural homochirality. Symmetry breaking and chiral amplification are fundamental principles in chemistry and biology but the control of initial chiral bias remains a great challenge. Here the authors show that chiral microvortices can lead to a selection of initial chiral bias of supramolecular systems composed of achiral molecules.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-018-05017-7