Issue 24, 2022

Synthesis and derivatization of epoxy-functional sterically-stabilized diblock copolymer spheres in non-polar media: does the spatial location of the epoxy groups matter?

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). 1H NMR studies and THF GPC analysis indicated that high monomer conversions (≥ 95%) and narrow molecular weight distributions (Mw/Mn ≤ 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 1H 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.

Graphical abstract: Synthesis and derivatization of epoxy-functional sterically-stabilized diblock copolymer spheres in non-polar media: does the spatial location of the epoxy groups matter?

Supplementary files

Article information

Article type
Paper
Submitted
29 4 2022
Accepted
01 6 2022
First published
10 6 2022
This article is Open Access
Creative Commons BY license

Polym. Chem., 2022,13, 3619-3630

Synthesis and derivatization of epoxy-functional sterically-stabilized diblock copolymer spheres in non-polar media: does the spatial location of the epoxy groups matter?

C. György, T. Smith, D. J. Growney and S. P. Armes, Polym. Chem., 2022, 13, 3619 DOI: 10.1039/D2PY00559J

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