Abstract
Triptycene-derived vinyl sulfide polymers 4a-d were synthesized from a versatile catalyst-free thiol-yne click reaction using 1,4-diethynyl triptycene 1 with various aryl dithiol building blocks 3a-d. The resulting triptycene-bearing poly(vinylene sulfide)s 4a-d display excellent solubility and chemical stability allowing for their structural, thermal, and photophysical characterization by various instrumental analysis techniques. The thioether groups in polymers 4a-d were selectively oxidized into their respective sulfone derivatives via mild reaction conditions affording the corresponding triptycene-based poly(vinylene sulfone)s 5a-d in quantitative yield.
| Original language | English |
|---|---|
| Pages (from-to) | 233-240 |
| Number of pages | 8 |
| Journal | Polymer |
| Volume | 154 |
| DOIs | |
| State | Published - 10 Oct 2018 |
Keywords
- Catalyst-free polymerization
- Click-chemistry
- C–S bond formation
- Poly(thioethers)
- Polysulfones
Funding Agency
- Kuwait Foundation for the Advancement of Sciences
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