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Makale Tam Makale Uluslararası 2022

Aromatic stacking and the self-assembly of perylene monoimide diester homodimers

Demet Gültekin

Journal Of Photochemistry And Photobiology A-Chemistry Cilt 426 · Makale no 113769 · 01.04.2022
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Özet

The self-assembly properties of two novel perylene monoimide diester homodimers have been investigated by concentration-dependent UV-Vis and H-1 NMR titration experiments and steady-state fluorescence and SEM techniques. It was found that, as a result of different positioning of the perylene monoimide diester subunits in these structures, the cooperativity and binding-models for their chain growth processes differ significantly in dichloromethane (DCM) and dimethyl sulfoxide (DMSO) due to a change in efficiency of the pi-pi stacking. The mechanism of aggregation in each case was determined by the application of Goldstein-Stryer nucleation - elongation model to the concentration-dependent data. Because of different aggregation propensities of the respective monomers in DCM, scanning electron microscopy revealed different morphologies for the assemblies.

Anahtar kelimeler

DERIVATIVES Supramolecular polymerization Nucleation-elongation model Self-assembly PI-STACKS COMPLEXES PROGRESS EFFICIENT SYNTHESIS SUPRAMOLECULAR POLYMERS Perylene monoimide diester Fluorescent compounds LIQUID-CRYSTALS TETRAESTERS MORPHOLOGIES

Atıf için künye

Gültekin, D. (2022). Aromatic stacking and the self-assembly of perylene monoimide diester homodimers. Journal Of Photochemistry And Photobiology A-Chemistry, 426, 113769. https://doi.org/10.1016/j.jphotochem.2022.113769

BibTeX
@article{gultekin2022-329818,
  author = {Gültekin, Demet},
  title = {Aromatic stacking and the self-assembly of perylene monoimide diester homodimers},
  journal = {Journal Of Photochemistry And Photobiology A-Chemistry},
  year = {2022},
  volume = {426},
  issn = {1010-6030},
  doi = {10.1016/j.jphotochem.2022.113769},
  url = {https://akademik.atauni.edu.tr/yayinlar/329818-aromatic-stacking-and-the-self-assembly-of-perylene-monoimide-diester-homodimers}
}