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      Dissymmetrical U-Shaped π-Stacked Supramolecular Assemblies by Using a Dinuclear CuIClip with Organophosphorus Ligands and Monotopic Fully π-Conjugated Ligands

      , , , ,   ,
      Chemistry - A European Journal
      Wiley-Blackwell

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          Abstract

          Reactions between the U-shaped binuclear Cu(I) complex A that bears short metal-metal distances and the cyano-capped monotopic π-conjugated ligands 1-5 that carry gradually bulkier polyaromatic terminal fragments lead to the formation of π-stacked supramolecular assemblies 6-10, respectively, in yields of 50-80 %. These derivatives have been characterized by multinuclear NMR spectroscopic analysis and X-ray diffraction studies. Their solid-state structures show the selective formation of U-shaped supramolecular assemblies in which two monotopic π-conjugated systems present large (6, 7, and 9) or medium (8 and 10) intramolecular π overlap, thus revealing π-π interactions. These assemblies self-organize into head-to-tail π-stacked dimers that in turn self-assemble to afford infinite columnar π stacks. The nature, extent, and complexity of the intermolecular contacts within the head-to-tail π-stacked dimer depend on the nature of the terminal polyaromatic fragment carried by the cyano-capped monotopic ligand, but it does not alter the result of the self-assembling process. These results demonstrate that the dinuclear molecular clip A that bears short metal-metal distances allows selective supramolecular assembly processes driven by the formation of intra- and intermolecular short π-π interactions in the resulting self-assembled structures; thus, demonstrating that their shape is not only dictated by the symmetry of the building blocks. This approach opens perspectives toward the formation of extended π-stacked columns based on dissymmetrical and functional π-conjugated systems.

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          Author and article information

          Journal
          Chemistry - A European Journal
          Chem. Eur. J.
          Wiley-Blackwell
          09476539
          November 03 2014
          November 03 2014
          : 20
          : 45
          : 14853-14867
          Article
          10.1002/chem.201403758
          25234637
          dd54489c-81f3-42f0-abbd-6520e0f29542
          © 2014
          History

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