Synthesis and derivatization of epoxy-functional sterically-stabilized diblock copolymer spheres in non-polar media: does the spatial location of the epoxy groups matter?. Issue 24 (10th June 2022)

• Record Type: Journal Article
• Authors: György, Csilla; Smith, Timothy; Growney, David J.; Armes, Steven P.
• Is Part Of: Polymer chemistry. Volume 13:Issue 24(2022)
• Page Start: 3619
• Page End: 3630
• Publication Date: 2022-06-10
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/d2py00559j
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : Epoxy-functional sterically-stabilized diblock copolymer nanoparticles are prepared via PISA in mineral oil and then derivatized using various reagents and reaction conditions. Abstract : Epoxy-functional sterically-stabilized diblock copolymer spherical nanoparticles were synthesized via polymerization-induced self-assembly (PISA) in mineral oil. Epoxy groups were located either (i) in the nanoparticle cores or (ii) within the steric stabilizer chains. For the first system, reversible addition–fragmentation chain transfer (RAFT) dispersion polymerization of glycidyl methacrylate (GlyMA) was conducted using a poly(lauryl methacrylate) (PLMA63 ) precursor. The second system involved statistical copolymerization of GlyMA with lauryl methacrylate to produce a P(LMA50 - stat -GlyMA9 ) precursor followed by chain extension using methyl methacrylate (MMA). 1 H NMR studies and THF GPC analysis indicated that high monomer conversions (≥ 95%) and narrow molecular weight distributions ( M w / M n ≤ 1.17) were obtained for both formulations. Dynamic light scattering indicated hydrodynamic diameters of 26 nm and 28 nm for P(LMA50 - stat -GlyMA9 )-PMMA67 and PLMA63 -PGlyMA89 spheres, respectively. Transmission electron microscopy studies confirmed a well-defined spherical morphology in each case. Post-polymerization modification of these spherical nanoparticles was examined by reacting the epoxy groups with benzylamine. For the PLMA63 -PGlyMA89 spheres, an [amine]/[epoxy] molar ratio of unity was sufficient to react all the epoxy groups. In contrast, the P(LMA50 - stat -GlyMA9 )-PMMA67 spheres required a fifty-fold excess of benzylamine for complete reaction. Furthermore, epoxy ring-opening reactions were conducted using either a trace amount of water or 50% v/v aqueous acetic acid at 110 °C. The extent of reaction was assessed using 1 H NMR spectroscopy and THF GPC for the P(LMA50 - stat -GlyMA9 )-PMMA67 spheres and by FT-IR spectroscopy for the core-crosslinked PLMA63 -PGlyMA89 spheres.