4.6 Article

Chemically Responsive Supramolecular Assemblies of Pyrene-β-Cyclodextrin Dimer

Journal

LANGMUIR
Volume 26, Issue 5, Pages 3169-3173

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la903103w

Keywords

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Funding

  1. Ishikawa Foundation for Carbon Science Technology
  2. Ministry of Education, Culture, Sports, Science and Technology, Japan [KIBAN C-20550120, WAKATE B-21750140]

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We report supramolecular assemblies of a beta-cyclodextrin dimer linked at both ends of a fluorescent phenylethynylpyrene moiety (Py-beta-CD dimer). The Py-beta-CD dimer formed supramolecular associations in aqueous media due to the pi-pi stacking of the hydrophobic phenylethynylpyrene moiety. From tapping mode atomic force microscopy measurements, the Py-beta-CD dimer Formed wire-shaped assemblies in aqueous media. By adding sodium adamantane carboxylate to the supramolecular assemblies. the structural change to J-type assemblies was observed. In contrast, upon addition of the electron-deficient guest, the electron transfer from the electron rich Phenylethynylpyrene moiety of the supramolecular assemblies to the electron-deficient guest, took place.

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