Selective Synthesis of Molecular Borromean Rings: Engineering of Supramolecular Topology via Coordination-Driven Self-Assembly.

Molecular Borromean rings (BRs) is one of the rare topology among interlocked molecules. Template-free synthesis of BRs via coordination-driven self-assembly of tetracene-based Ru(II) acceptor and ditopic pyridyl donors is reported. NMR and single-crystal XRD analysis observed sequential transformat...

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Publicado en:Journal of the American Chemical Society Vol. 138; no. 27; pp. 8368 - 8372
Autores principales: Taegeun Kim, Nem Singh, Jihun Oh, Eun-Hee Kim, Jaehoon Jung, Hyunuk Kim, Ki-Whan Chi
Formato: Artículo
Publicado: American Chemical Society 7/13/2016
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Acceso en línea:Ver este registro en EBSCOhost
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      dt: 7/13/2016
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      pub: American Chemical Society
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        10.1021/jacs.6b04545
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        atl: Selective Synthesis of Molecular Borromean Rings: Engineering of Supramolecular Topology via Coordination-Driven Self-Assembly.
      aug:
        au:
          Taegeun Kim
          Nem Singh
          Jihun Oh
          Eun-Hee Kim
          Jaehoon Jung
          Hyunuk Kim
          Ki-Whan Chi
        affil:
          Department of Chemistry, University of Ulsan, Ulsan 44610, Republic of Korea
          Protein Structure Group, Korea Basic Science Institute, Ochang, Chungbuk 28119, Republic of Korea
          Energy Materials and Convergence Research Department, Korea Institute of Energy Research, Daejeon 34129, Republic of Korea
      su:
        Molecular dynamics
        X-ray diffraction
        Topology
        Crystal structure
        Density functional theory
        Intermolecular interactions
      sug:
        subj:
          Molecular dynamics
          X-ray diffraction
          Topology
          Crystal structure
          Density functional theory
          Intermolecular interactions
      ab: Molecular Borromean rings (BRs) is one of the rare topology among interlocked molecules. Template-free synthesis of BRs via coordination-driven self-assembly of tetracene-based Ru(II) acceptor and ditopic pyridyl donors is reported. NMR and single-crystal XRD analysis observed sequential transformation of a fully characterized monomeric rectangle to molecular BRs and vice versa. Crystal structure of BRs revealed that the particular topology was enforced by the appropriate geometry of the metallacycle and multiple parallel-displaced π–π interactions between the donor and tetracene moiety of the acceptor. Computational studies based on density functional theory also supported the formation of BRs through dispersive intermolecular interactions in solution.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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          year: 2016
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