Engineering Helical Chirality in Metal-Coordinated Cyclodextrin Nanochannels

Helicates are a defining element of DNAs and proteins, with functions that are critical to a variety of biological processes. Cyclodextrins are promising candidates for forging multiple-stranded helicates with well-defined helicity, but a lack of available tools has precluded the construction of artificial helical nanochannels with a controllable geometry and helicity from these widely available chiral building blocks. Herein, we disclose a family of Ag<sub>6</sub>L<sub>2</sub> helical nanochannels that can be readily assembled from α-cyclodextrin-derived ligands through coordination between pyridinyl groups and Ag<sup>+</sup> cations. We discovered that the nanochannels exhibit either an <i>M</i> or a <i>P</i> helicity when the Ag<sup>+</sup> cations adopt a tetrahedral coordination geometry while losing most of their helicity when the Ag<sup>+</sup> cations are linearly coordinated. Both the geometry and helicity of the nanochannels can be precisely controlled by simply changing the number of methyl groups at the <i>ortho</i> positions of the pyridinyl ligands. The tetracoordinated Ag<sup>+</sup> cations interconnect the helical nanochannels into an infinite two-dimensional coordinative network characterized by hexagonal tessellation. Theoretical calculations, which reveal lower energies of the helical conformations observed in crystals compared with those of their inverted counterparts, support the experimental results.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-02-18
DOI
https://doi.org/10.1021/jacs.4c14123
Citations
13
Primary Topic
Advanced NMR Techniques and Applications
Type
article
Field-Weighted Citation Impact
9.83

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article

Engineering Helical Chirality in Metal-Coordinated Cyclodextrin Nanochannels

Xiujun Yu, Shuai Lu, Zhiyuan Jiang, Weitao Xu et al.
13 citations
Journal of the American Chemical Society
Advanced NMR Techniques and Applications
9.83
article

Engineering Helical Chirality in Metal-Coordinated Cyclodextrin Nanochannels

Xiujun Yu, Shuai Lu, Zhiyuan Jiang, Weitao Xu, Dengke Shen, Charlotte L. Stern, Ye‐Qiang Han, Zhi Chen, Xiao‐Yang Chen, Kaikai Ma, Yue Zhao, Kang Cai, Xiaopeng Li, Shuyi Li, Bo Yu, Xinzhi Liu, Shuqi Chen
article en
13 citations

Abstract

Helicates are a defining element of DNAs and proteins, with functions that are critical to a variety of biological processes. Cyclodextrins are promising candidates for forging multiple-stranded helicates with well-defined helicity, but a lack of available tools has precluded the construction of artificial helical nanochannels with a controllable geometry and helicity from these widely available chiral building blocks. Herein, we disclose a family of Ag<sub>6</sub>L<sub>2</sub> helical nanochannels that can be readily assembled from α-cyclodextrin-derived ligands through coordination between pyridinyl groups and Ag<sup>+</sup> cations. We discovered that the nanochannels exhibit either an <i>M</i> or a <i>P</i> helicity when the Ag<sup>+</sup> cations adopt a tetrahedral coordination geometry while losing most of their helicity when the Ag<sup>+</sup> cations are linearly coordinated. Both the geometry and helicity of the nanochannels can be precisely controlled by simply changing the number of methyl groups at the <i>ortho</i> positions of the pyridinyl ligands. The tetracoordinated Ag<sup>+</sup> cations interconnect the helical nanochannels into an infinite two-dimensional coordinative network characterized by hexagonal tessellation. Theoretical calculations, which reveal lower energies of the helical conformations observed in crystals compared with those of their inverted counterparts, support the experimental results.

Journal of the American Chemical SocietyVol. 147(9)
Northwestern University (US), Hong Kong Polytechnic University (HK), Anhui University (CN), Shenzhen University (CN), Nankai University (CN), Hefei Institutes of Physical Science (CN), University of Hong Kong (HK)
Chinese Academy of Sciences, Research Grants Council, University Grants Committee, University of Hong Kong, Hong Kong Polytechnic University
Openalex Percentile: Top 1%
Advanced NMR Techniques and Applications
9.83
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