Diversification of Self-Organized Architectures in Supramolecular Dye Assemblies.

Upon complexation with bismelamine receptors (BMn) featuring different alkyl linker lengths (number of methylene groups (n) = 5-12), a barbituric acid merocyanine dye (1) can be loaded into diverse self-organized superstructures through multiple hydrogen-bonding interactions. UV/vis, dynamic light s...

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Publicado en:Journal of the American Chemical Society Vol. 129; no. 43; pp. 13277 - 13288
Autores principales: Yagai, Shiki, Kinoshita, Tetsuro, Higashi, Masatsugu, Kishikawa, Keiki, Nakanishi, Takashi, Karatsu, Takashi, Kitamura, Akihide
Formato: Artículo
Publicado: American Chemical Society 10/31/2007
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Acceso en línea:Ver este registro en EBSCOhost
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      dt: 10/31/2007
      vid: 129
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      pub: American Chemical Society
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        10.1021/ja075257c
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        atl: Diversification of Self-Organized Architectures in Supramolecular Dye Assemblies.
      aug:
        au:
          Yagai, Shiki
          Kinoshita, Tetsuro
          Higashi, Masatsugu
          Kishikawa, Keiki
          Nakanishi, Takashi
          Karatsu, Takashi
          Kitamura, Akihide
        affil:
          Department of Applied Chemistry and Biotechnology, Faculty of Engineering, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
          PRESTO, Japan Science and Technology Agency (JST), 4-1-8 Honcho Kawaguchi, Saitama, Japan.
          National Institute for Materials Science (NIMS), 1-2-1 Sengen, Tsukuba 305-0047, Japan.
          Max Planck Institute of Colloids and Interfaces, Research Campus Golm, Potsdam 14424, Germany.
      su:
        Dyes & dyeing
        Hydrogen
        Chemical bonds
        Microscopy
        Solvents
      sug:
        subj:
          Dyes & dyeing
          Hydrogen
          Chemical bonds
          Microscopy
          Solvents
      ab: Upon complexation with bismelamine receptors (BMn) featuring different alkyl linker lengths (number of methylene groups (n) = 5-12), a barbituric acid merocyanine dye (1) can be loaded into diverse self-organized superstructures through multiple hydrogen-bonding interactions. UV/vis, dynamic light scattering, and NMR studies in cyclohexane demonstrate that the diversification of the primarily formed hydrogen-bonded species in solution occurs by varying the linker length of BMn. Hierarchical organization of the hydrogen-bonded species is achieved by slow evaporation of the solvent (forming solvent-free films), and the resulting superstructures are evaluated by polarized optical microscopy, X-ray diffraction, SEM, and AFM techniques. The formation of columnar structures with and without two-dimensional ordering are revealed for shorter (n = 5-7) and longer (n = 11, 12) linker bis(melamines), respectively. On the contrary, in the cases of n = 8-10, the formation of lamellar structures is unveiled. Several assemblies (n = 5, 7, 11) indicate the formation of a liquid crystalline mesophase in POM and DSC analyses. Hierarchical organization is also achieved in solution by prolonged aging, affording phase-separated crystalline nanotibers (n 5, 7) and soft nanofibrils agglomerating into wormlike objects (n = 8), gel-forming continuous globular networks (n = 10), and nanofibers (n = 11, 12). These superstructural and morphological diversifications are an outcome of the variation in the primarily formed hydrogen-bonded supramolecular architectures. Using this strategy, diverse self-assembled materials will be obtained from a single dye component.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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