6533b7d5fe1ef96bd1264fbb
RESEARCH PRODUCT
Chemical recycling of polyenaminones by transamination reaction via amino–enaminone polymerisation/depolymerisation
Urša ŠTanfelAleš RučigajAnja KristlTomaž KotnikDavid PahovnikFranc PožganEma ŽAgarJurij SveteBogdan ŠTefaneLev MatohHelena Brodnik ŽUgeljTill OpatzAnže ZupancUroš Grošeljsubject
chemistry.chemical_classificationLight absorbanceEthanolPolymers and PlasticsTransaminationOrganic ChemistryGeneral Physics and Astronomy02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymerizationMaterials Chemistry0210 nano-technologyDimethylaminedescription
Abstract Novel oligo- and polyenaminones with Mw ∼ 3000 Da were prepared in excellent yields by amino–enaminone ‘click’ polymerisation of 1,3- and 1,4-bis[3-(dimethylamino)acryloyl]arenes with 1,3- and 1,4-phenylenediamine. The obtained oligomers and polymers were depolymerised quantitatively to the starting bis-enaminones and diamines by treatment with excess dimethylamine in ethanol at 50 °C. This simple polymerisation/depolymerisation method allows for a closed-loop recycling of polyenaminone-based materials. UV light absorbance at wavelengths below 470 nm indicates promising optical properties of these polymers.
year | journal | country | edition | language |
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2019-12-01 | European Polymer Journal |