4.6 Article

Photochromic Nanostructures Based on Diarylethenes with Perylene Diimide

Journal

LANGMUIR
Volume 26, Issue 9, Pages 6702-6707

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la9040387

Keywords

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Funding

  1. Nature Science Foundation of Shandong Province [Y2006B14]
  2. Ph.D. Programs Foundation of the Ministry of Education of China

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A bisthienylethene-functionalized perylene diimide (3TE-PDI) photochromic dyad was synthesized for self-assembly into 1-D nanotubes by a reprecipitation method. SEM and TEM observations showed that the nanotubes were formed from their 0-D precursors of hollow nanospheres. HR-TEM images revealed that both the nanospheres and the nanotubes have highly ordered lamellar structure, indicating the hierarchical process during assembly. The IR and XRD results revealed that DAE-PDI molecules were connected through intermolecular hydrogen bonds to form building blocks that self-assembled into nanostructures. Electronic absorption and fluorescence spectroscopic results indicated the H-aggregate nature of the self-assembled nanostructures. Competition and cooperation between the dipole dipole in in pi-pi stacking, and hydrophilic/hydrophobic in arc suggested to result in nanostructures. Reconstruction was found to happen during the morphology transition progress from the 0-D nanospheres to the 1-D nanotubes, which was driven by donor-acceptor-dipole-dipole interactions. Green emission at 520 nm originating from the DAE subunit was observed for the aggregates of vesicles and nanotubes, which could be regulated by photoirradiation with 365 mu light, suggesting the nanoagaregates to be photochromic switches.

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