Abstract
Dialkoxy- and dialkyl-substituted phenylene benzothiadiazole paracyclophane-1,9-diene monomers undergo living ring-opening metathesis polymerization using ruthenium carbene initiators (G3) to give regularly alternating cis,trans-poly(p-phenylenevinylene) benzothiadiazole copolymers. These polymers can be readily isomerized in dilute solution using visible light to the all-trans polymers. The influence of the polymer microstructure and the phenylene substituents on the optical and electrochemical properties of these polymers is examined.
| Original language | English |
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| Journal | Macromolecules |
| DOIs | |
| Publication status | Published - 24 Sept 2019 |
Research Beacons, Institutes and Platforms
- Henry Royce Institute