Abstract
By optimizing and adapting the synthesis of double dissymmetric functionalized phenylene Building blocks, a library of nine anthracene-containing poly(arylene ethynylene)-alt-poly(phenylene vinylene)s
(AnE-PVs) with diverse successions of octyloxy and 2-ethylhexyloxy side chains was realized. Despite the structural resemblance of the regioisomeric omonomers and the polymers, their 1H NMR spectra were
found to feature perceptible side chain configuration-specific patterns. The differentiation of the photophysical
characteristics of the polymers induced by the various defined, semi-defined and random side chain sequences has been thoroughly investigated by UV-vis absorption and photoluminescence spectroscopy in solution and in thin film. The gained insights allowed the specification of the notions on the
complex structure–property relationships in AnE-PV systems. In particular, the side chain assignment in direct proximity to the anthracene moieties distinctly affects the optical properties. This systematic study presents an illustrative example for the versatile but also intricate capabilities of side chain engineering.
| Original language | English |
|---|---|
| Pages (from-to) | 5339-5347 |
| Number of pages | 9 |
| Journal | Polymer Chemistry |
| Volume | 10 |
| Issue number | 39 |
| DOIs | |
| Publication status | Published - 21 Oct 2019 |
Fields of science
- 304007 Tissue engineering
- 204002 Chemical reaction engineering
- 210004 Nanomaterials
- 104 Chemistry
- 104002 Analytical chemistry
- 104011 Materials chemistry
- 104014 Surface chemistry
- 104016 Photochemistry
- 104018 Polymer chemistry
- 104008 Catalysis
- 104010 Macromolecular chemistry
- 104015 Organic chemistry
- 104019 Polymer sciences
- 106002 Biochemistry
- 107002 Bionics
- 301305 Medical chemistry
- 301207 Pharmaceutical chemistry
- 301904 Cancer research
- 302009 Chemotherapy
JKU Focus areas
- Sustainable Development: Responsible Technologies and Management
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