The extent of counterion dissociation at the interface of cationic diblock copolymer nanoparticles in non-polar solvents

Gregory N Smith; Sandra van Meurs; Steven P Armes

doi:10.1016/j.jcis.2020.04.102

The extent of counterion dissociation at the interface of cationic diblock copolymer nanoparticles in non-polar solvents

J Colloid Interface Sci. 2020 Oct 1:577:523-529. doi: 10.1016/j.jcis.2020.04.102. Epub 2020 May 8.

Authors

Gregory N Smith¹, Sandra van Meurs², Steven P Armes²

Affiliations

¹ Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, South Yorkshire S3 7HF, United Kingdom; Niels Bohr Institute, University of Copenhagen, H. C. Ørsted Institute, Universitetsparken 5, 2100 Copenhagen Ø, Denmark. Electronic address: gregory.smith@nbi.ku.dk.
² Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, South Yorkshire S3 7HF, United Kingdom.

PMID: 32534191
DOI: 10.1016/j.jcis.2020.04.102

Abstract

Hypothesis: Diblock copolymer nanoparticles prepared in non-polar solvents that are sterically stabilized but possess ionic functionality from the inclusion of cationic comonomers in the stabilizer shell are known to exhibit complex electrokinetic behavior (Chem. Sci. 9 (2018) 922-934). For example, core-shell nanoparticles with cationic comonomers located solely within the shell layer have lower magnitude electrophoretic mobilities than nanoparticles containing the same cationic comonomers located within the core, whereas nanoparticles prepared using a minor fraction of steric stabilizer chains containing cationic comonomer repeat units have comparable electrophoretic mobilities to nanoparticles prepared with this cationic comonomer solely located within the core. We hypothesize that these observations can be explained in terms of the strength of the Coulombic interaction between counterions and the nanoparticle interface.

Experiments: The highly-fluorinated anionic counterion associated with these cationic nanoparticles is studied by ¹⁹F nuclear magnetic resonance (NMR) spectroscopy in n-dodecane. This revealed only one type of ¹⁹F environment for a soluble macromolecular cation (the oil-soluble steric stabilizer chains used to prepare the nanoparticles), whereas two distinct environments were observed for the sterically-stabilized cationic nanoparticles. Both ¹⁹F diffusion NMR and ¹⁹F-¹³C heteronuclear single quantum correlation (HSQC) measurements support the existence of two environments for this counterion.

Findings: The existence of two distinct ¹⁹F environments for the highly-fluorinated anion associated with the sterically-stabilized nanoparticles demonstrates the presence of spectroscopically distinguishable populations of ion pairs and of fully dissociated free anions. ¹⁹F NMR spectra recorded for sterically-stabilized nanoparticles with a fully ionic shell (all stabilizer chains containing the cationic comonomer) and those with a partly ionic shell (10% of stabilizer chains containing the cationic comonomer) reveal a higher proportion of dissociated anions in the partly ionic case. This suggests a stronger Coulombic interaction between counterions and the cationic interface when the shell is fully ionic, which accounts for the observed reduction in the magnitude of the electrophoretic mobility.

Keywords: Block copolymer self-assembly; Charged colloids; Diffusion; Nuclear magnetic resonance.