Ultralong-Chain-Spaced Crystalline Poly(H-phosphonate)s and Poly(phenylphosphonate)s
| Autor: | Eva Schiebel, Annika Sickinger, Hanna Busch, Stefan Mecking |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
chemistry.chemical_classification
Polymers and Plastics Molecular mass 010405 organic chemistry Chemistry Organic Chemistry Minimal extent Polymer 010402 general chemistry 01 natural sciences Phosphonate 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound Yield (chemistry) Polymer chemistry Materials Chemistry Melting point Degradation (geology) Methylene |
| Zdroj: | Macromolecules. 50:7901-7910 |
| ISSN: | 1520-5835 0024-9297 |
| DOI: | 10.1021/acs.macromol.7b01368 |
| Popis: | Aliphatic poly(H-phosphonate)s were obtained by polyesterification of dimethyl H-phosphonate with bio-based long-chain diols. Nonadecane-1,19-diol, tricosane-1,23-diol, and octatetracontane-1,48-diol with dimethyl H-phosphonate yield the corresponding polyphosphoesters (PPE19H, PPE23H, and PPE48H) with molecular weights (Mn) up to 4.3 × 104 g mol–1. Postfunctionalization of these polymers via Hirao cross-coupling yields the selectively functionalized poly(H-phosphonate)s PPE19Ph, PPE23Ph, and PPE48Ph. DSC analysis revealed significantly enhanced crystallinities and melting points (up to Tm = 110 °C) with increasing methylene sequence lengths. Hydrolytic degradation of polymer powder of poly-(H-phosphonate) occurred up to 95% in 2 days. The degradation rates decreased with increasing methylene sequence length. After postfunctionalization, degradation occurred only to a minimal extent over 3 months in basic and in acidic media. |
| Databáze: | OpenAIRE |
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