Szczegóły publikacji
Opis bibliograficzny
4-vinyl guaiacol acetate as a sustainable lignin-derivable alternative to styrene: renewable monomer synthesis and its atom transfer radical polymerization / Nicola Porcelli, Izabela Zaborniak, Niccolò Braidi, Małgorzata Klamut, Kinga PIELICHOWSKA, Francesca Parenti, Fabrizio Roncaglia, Paweł Chmielarz // European Polymer Journal ; ISSN 0014-3057 . — 2026 — vol. 249 art. no. 114611, s. 1–11. — Bibliogr. s. 9–11, Abstr. — Publikacja dostępna online od: 2026-02-28
Autorzy (8)
- Porcelli Nicola
- Zaborniak Izabela
- Braidi Niccolò
- Klamut Małgorzata
- AGHPielichowska Kinga
- Parenti Francesca
- Roncaglia Fabrizio
- Chmielarz Paweł
Słowa kluczowe
Dane bibliometryczne
| ID BaDAP | 166731 |
|---|---|
| Data dodania do BaDAP | 2026-03-25 |
| Tekst źródłowy | URL |
| DOI | 10.1016/j.eurpolymj.2026.114611 |
| Rok publikacji | 2026 |
| Typ publikacji | artykuł w czasopiśmie |
| Otwarty dostęp | |
| Czasopismo/seria | European Polymer Journal |
Abstract
4-Vinyl guaiacol acetate (4-VGA) is a renewable 4-vinylphenol-type monomer featuring a pendant protecting group suitable for post-functionalization. Herein, we report a more sustainable, telescoping synthesis route from vanillin, involving a Knoevenagel-Doebner condensation followed by acetylation, affording satisfactory yields through a single, straightforward purification step. The monomer was then tested in Atom Transfer Radical Polymerization (ATRP), achieving good control in the Supplementary Activator and Reducing Agent (SARA) variant. Optimization required evaluating reaction parameters and their effect on the polymerization system, leading to the optimal choice of solvent, catalytic system, and initiator. Notably, the use of highly active chloride-based initiators and CuCl2/TPMA catalytic system played a major role in establishing control over the polymerization. The polymers produced by SARA ATRP exhibit decent control over molecular weight and dispersity, and high initiation efficiency values. However, early termination due to dehydrohalogenation poses a severe limitation to the reaction system, allowing satisfactory monomer conversion values only at low target degrees of polymerization.