Chemo-enzymatic synthesis of a levoglucosenone-derived bi-functional monomer and its ring-opening metathesis polymerization in the green solvent Cyrene™ - Archive ouverte HAL Access content directly
Journal Articles Polymer Chemistry Year : 2020

Chemo-enzymatic synthesis of a levoglucosenone-derived bi-functional monomer and its ring-opening metathesis polymerization in the green solvent Cyrene™

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Abstract

The quite recent, yet quickly expanding, norbornene-levoglucosenone-based monomer family was extended to include a novel bi-functional methacrylate monomer that can be readily synthesized through a chemo-enzymatic pathway. The norbornene moiety was selectively polymerized via ring-opening metathesis polymerization (ROMP) under ambient conditions where Cyrene™ was explored for the first time as a green bio-alternative organic solvent for ROMP reactions. The activity of the metathesis catalysts was finely tuned in Cyrene™, versus common and toxic solvents such as dichloromethane, resulting in highly thermostable functional polymers with a Td5% up to 401 °C and a Tg of −16.8 °C.
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Dates and versions

hal-03630782 , version 1 (05-04-2022)

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Sami Fadlallah, Aurélien Peru, Lionel Longé, Florent Allais. Chemo-enzymatic synthesis of a levoglucosenone-derived bi-functional monomer and its ring-opening metathesis polymerization in the green solvent Cyrene™. Polymer Chemistry, 2020, 11 (47), pp.7471-7475. ⟨10.1039/D0PY01471K⟩. ⟨hal-03630782⟩

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