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Spontaneous assembly of a hinged coordination network

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Abstract

THE field of supramolecular chemistry has advanced to a stage at which it is possible to select building blocks that will self-assemble into structures with specific network topologies1–3. This makes possible the rational design and synthesis of molecular solids with potentially interesting properties. Here we report the construction of open, hinged networks from molecular building blocks. This class of materials has been predicted to exhibit unusual mechanical properties, including auxetic behaviour (negative Poisson's ratio) and negative coefficients of thermal expansion4–6. Our approach relies on the notion that rigid organic molecules of high symmetry will adopt one of only a few possible structures when linked via hydrogen bonds or coordination to metals7–9. We use trigonal lig-ands to make networks joined at the vertices by metal ions; the resulting networks are homeotypic10 with the honeycomb-like A1B2 and the hinge-like ThSi2 phases. The hinge-like network has channels of inner diameter 15 Å, within which included molecules can be exchanged while the framework remains intact. We have not yet determined whether this material is auxetic.

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Authors and Affiliations

  1. Department of Chemistry, University of Michigan, Ann Arbor, Michigan, 48109, USA

    Geoffrey B. Gardner & Stephen Lee

  2. Departments of Chemistry, and Materials Science and Engineering, University of Illinois, Urbana, Illinois, 61801, USA

    D. Venkataraman & Jeffrey S. Moore

Authors
  1. Geoffrey B. Gardner
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  2. D. Venkataraman
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  3. Jeffrey S. Moore
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  4. Stephen Lee
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Gardner, G., Venkataraman, D., Moore, J. et al. Spontaneous assembly of a hinged coordination network. Nature 374, 792–795 (1995). https://doi.org/10.1038/374792a0

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