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Published on: June 2, 2017
Tunable emission from H-type supramolecular polymers in optical nanocavities
Giulia Lavarda1, Anton M Berghuis2, Kripa Joseph1
1Institute for Complex Molecular Systems and Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, Eindhoven 5600 MB, The Netherlands. g.lavarda@tue.nl.
Chiral tetraphenylene monomers self-assemble into H-type supramolecular polymers. These polymers exhibit efficient emission and controlled helicity, with their fluorescence reshaped by nanoparticle arrays.
Area of Science:
- Supramolecular chemistry
- Materials science
- Optoelectronics
Background:
- Chiral molecules are crucial for creating materials with specific optical properties.
- Supramolecular polymers offer tunable characteristics through self-assembly.
- Controlling polymer structure influences their photophysical behavior.
Purpose of the Study:
- To synthesize H-type supramolecular polymers from chiral tetraphenylene monomers.
- To investigate the influence of self-assembly on polymer helicity and emission efficiency.
- To explore the effect of integrating these polymers into dielectric nanoparticle arrays on their fluorescence.
Main Methods:
- Self-assembly of chiral tetraphenylene-based monomers.
- Characterization of the resulting supramolecular polymers (e.g., structure, helicity, emission).
- Fabrication of dielectric nanoparticle arrays incorporating the one-dimensional polymer fibers.
Main Results:
- Successful preparation of H-type supramolecular polymers with defined helical structures.
- Demonstration of highly efficient fluorescence emission from the polymers.
- Observation of significant fluorescence reshaping when polymers are integrated into nanoparticle arrays due to weak light-matter coupling.
Conclusions:
- Chiral tetraphenylene monomers are effective building blocks for helical supramolecular polymers.
- The self-assembly process allows for control over polymer structure and optical properties.
- Integration with nanoparticle arrays provides a method to modulate polymer fluorescence through light-matter interactions.
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