Chiral molecules preferentially form one-handed supramolecular assemblies that reflect the absolute configuration of the molecules. Under specific conditions, however, the opposite-handed supramolecular assemblies are also obtained because of flexibility in the bond length and reversibility of non-covalent interactions. The mechanism of the handedness selectivity or switching phenomenon remains ambiguous, and most phenomena are observed by chance. Here we demonstrate the construction of chiral hydrogen-bonded twofold helical assemblies with controlled handedness in the crystalline state based on crystallographic studies. Detailed investigation of the obtained crystal structures enabled us to clarify the mechanism, and the handedness of the supramolecular chirality was successfully controlled by exploiting achiral factors. This study clearly reveals a connection between molecular chirality and supramolecular chirality in the crystalline state. © 2013 Macmillan Publishers Limited. All rights reserved.
CITATION STYLE
Sasaki, T., Hisaki, I., Miyano, T., Tohnai, N., Morimoto, K., Sato, H., … Miyata, M. (2013). Linkage control between molecular and supramolecular chirality in 2 1 -helical hydrogen-bonded networks using achiral components. Nature Communications, 4. https://doi.org/10.1038/ncomms2756
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