6533b874fe1ef96bd12d6135
RESEARCH PRODUCT
Temperature Variation Enables the Design of Biobased Block Copolymers via One‐Step Anionic Copolymerization
Markus GalleiJennifer BareutherMartina PlankTobias KrausBjörn KuttichHolger Freysubject
Materials sciencePolymers and PlasticsPolymers02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationStyrenechemistry.chemical_compoundMaterials ChemistryCopolymerMolar massOrganic ChemistryTemperature021001 nanoscience & nanotechnology0104 chemical sciencesMolecular WeightMonomerAnionic addition polymerizationchemistryChemical engineeringPolymerizationPolystyrenesSelf-assemblyPolystyrene0210 nano-technologydescription
A one-pot approach for the preparation of diblock copolymers consisting of polystyrene and polymyrcene blocks is described via a temperature-induced block copolymer (BCP) formation strategy. A monomer mixture of styrene and myrcene is employed. The unreactive nature of myrcene in a polar solvent (tetrahydrofuran) at -78 °C enables the sole formation of active polystyrene macroinitiators, while an increase of the temperature (-38 °C to room temperature) leads to poly(styrene-block-myrcene) formation due to polymerization of myrcene. Well-defined BCPs featuring molar masses in the range of 44-117.2 kg mol-1 with dispersities, Ð, of 1.09-1.21, and polymyrcene volume fractions of 30-64% are accessible. Matrix assisted laser desorption ionization-time of flight mass spectrometry measurements reveal the temperature-controlled polymyrcene block formation, while both transmission electron microscopy and small-angle X-ray scattering measurements prove the presence of clearly microphase-separated, long range-ordered domains in the block copolymers. The temperature-controlled one-pot anionic block copolymerization approach may be general for other terpene-diene monomers.
year | journal | country | edition | language |
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2021-04-01 | Macromolecular Rapid Communications |