1. Enzymatic catalysis as a versatile tool for the synthesis of multifunctional, bio-based oligoester resins
- Author
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Mats Johansson, Stefan Semlitsch, Susana Torron, and Mats Martinelle
- Subjects
Polymers ,Polyesters ,Ethylene glycol dimethacrylate ,02 engineering and technology ,010402 general chemistry ,Methacrylate ,Oxetane ,01 natural sciences ,Oligomer ,Bark ,chemistry.chemical_compound ,Oligoester ,Polymerkemi ,Environmental Chemistry ,Organic chemistry ,Maleimide ,biology ,Route ,Lipase ,Polymer Chemistry ,021001 nanoscience & nanotechnology ,biology.organism_classification ,Pollution ,0104 chemical sciences ,Ring-Opening Polymerization ,Chemistry ,Monomer ,chemistry ,Candida antarctica ,0210 nano-technology ,Acids ,Suberin Monomer - Abstract
The use of enzymes as selective catalysts for processing renewable monomers into added value polymers and materials has received increased attention during the last decade. In the present work Candida antarctica lipase B (CalB) was used as catalyst in one-pot routes to synthesise multifunctional oligoester resins based on an epoxy-functional omega-hydroxy-fatty acid (EFA) extracted from birch bark. The chemoselective enzymatic process resulted in three different EFA-based telechelic oligomers with targeted molecular weights; containing maleimide, methacrylate or oxetane as end-groups, respectively. The enzyme catalysed synthesis of the maleimide and the oxetane telechelic oligomers reached full conversion of monomers (>95%) after 2 h. In the case of methacrylate functional oligomer the EFA monomer reached full conversion (>98%) after 2 h but the integration of the methacrylate moiety took more than 10 h. This was due to a rate limiting reaction path using ethylene glycol dimethacrylate as substrate. The oligomer products were characterised by NMR, MALDI-TOF-MS and SEC. QC 20160426
- Published
- 2016
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