RAFT dispersion polymerization of N,N-dimethylacrylamide in a series of n-alkanes using a thermoresponsive poly(tert-octyl acrylamide) steric stabilizer

Abstract

Herein we report the reversible addition–fragmentation chain transfer (RAFT) solution polymerization of tert-octyl acrylamide (OAA) in 1,4-dioxane using a trithiocarbonate-based RAFT agent. POAA homopolymers were synthesized with good control (M_w/M_n < 1.22) within 1 h at 70 °C when targeting mean degrees of polymerization (DP) of up to 100. Differential scanning calorimetry studies conducted on a series of five POAA homopolymers indicated a weak molecular weight dependence for the glass transition temperature (T_g), which varied from 67 to 83 °C for POAA DPs ranging from 22 to 99. High blocking efficiencies were observed when chain-extending such homopolymers with OAA, suggesting that most of the RAFT end-groups remain intact. Subsequently, we employed POAA as a steric stabilizer block for the PISA syntheses of spherical nanoparticles in n-heptane via RAFT dispersion polymerization of N,N-dimethylacrylamide (DMAC) at 70 °C. Targeting PDMAC DPs between 50 and 250 resulted in reasonably good control (M_w/M_n ≤ 1.42) and produced well-defined spherical diblock copolymer nanoparticles (z-average diameters ranging from 23 nm to 91 nm, with DLS polydispersities remaining below 0.10) within 5 h. A facile one-pot synthesis route to near-monodisperse 36 nm diameter POAA₈₂-PDMAC₁₀₀ nanoparticles was developed in n-heptane that provided similar control over the molecular weight distribution (M_w/M_n = 1.19). Unfortunately, POAA₈₅-PDMAC_x diblock copolymer nanoparticles tended to deform and undergo film formation prior to transmission electron microscopy (TEM) studies. To overcome this problem, ethylene glycol diacrylate (EGDA) was introduced towards the end of the DMAC polymerization. The resulting core-crosslinked POAA₈₅-PDMAC₁₉₅-PEGDA₂₀ triblock copolymer nano-objects exhibited a relatively well-defined spherical morphology. Interestingly, the colloidal stability of POAA₈₅-PDMAC_x diblock copolymer dispersions depends on the type of n-alkane. Spherical nanoparticles produced in n-heptane or n-octane remained colloidally stable on cooling to 20 °C. However, the colloidally stable POAA-PDMAC nanoparticles prepared at 70 °C in higher n-alkanes became flocculated on cooling. This is because the POAA steric stabilizer chains exhibit upper critical solution temperature (UCST)-type behavior in such solvents. Nanoparticle aggregation was characterized by variable temperature turbidimetry and dynamic light scattering experiments.