Erno Karjalainen

Diblock copolymers consisting of a polymerized ionic liquid and poly(N-isopropylacrylamide). Effects of PNIPAM block length and counter ion on self-assembling and thermal properties

Amphiphilic diblock copolymers composed of a polymeric ionic liquid, PIL, and poly(N-isopropylacrylamide), PNIPAM, have been synthesized using RAFT reactions. The length of the PIL block was kept constant while the molecular mass of the PNIPAM block was varied. The PIL was poly(2-(1-butylimidazolium-3-yl)ethyl methacrylate tetrafluoroborate) which is insoluble in water owing to the bulky hydrophobic counterion. When the PNIPAM block was long enough, the polymers formed spherical micelles in water, which showed thermally responsive behaviour. Colloidally stable particles could be prepared also from the homopolymeric PIL. PNIPAM affects noticeably the properties of the PIL, and also the polycation has a strong effect on the thermal properties of PNIPAM in aqueous dispersions. As a reference, a polymer where bromide was the counter ion instead of the tetrafluoroborate ion was synthesized, providing a water soluble PIL block. The core–shell micelles formed by amphiphilic block copolymers in pure water and those by double-hydrophilic polymers in aqueous NaBF4 undergo partial structural inversion upon the thermal collapse of PNIPAM.

Imidazolium‐Based Poly(ionic liquid)s as New Alternatives for CO2 Capture

Solid imidazolium-based poly(ionic liquid)s with variable molecular weights that contain the poly[2-(1-butylimidazolium-3-yl)ethyl methacrylate] (BIEMA) cation and different counter anions were evaluated in terms of CO2 capture and compared with classical ionic liquids with similar counter anions. In addition to poly(ionic liquid)s with often-applied ions such as BF4 (-) , PF6 (-) , NTf2 (-) , trifluoromethanesulfonate (OTf(-) ) and Br(-) , for the first time [BIEMA][acetate] was synthesised, which revealed a remarkably high CO2 sorption performance that exceeded the poly(ionic liquid)s studied previously on average by a factor of four (12.46 mg gPIL (-1) ). This study provides an understanding of the factors that affect CO2 sorption and a comparison of the CO2 capture efficiency with the frequently used sorbents. Moreover, all the studied sorbents were reusable if regenerated under carefully selected conditions and can be considered as suitable candidates for CO2 sorption.

An enzymatic biomimetic system: enhancement of catalytic efficiency with new polymeric chiral ionic liquids synthesised by controlled radical polymerisation

The controlled radical polymerization of monomeric units containing chiral ionic liquids (CILs) allows the synthesis of intrinsically chiral polymers through a bottom-up design. These polymeric chiral ionic liquids (PCILs) show a well-defined three dimensional structure organized as the result of a complex non-covalent network of hydrogen-bonding contacts driven by the C2 hydrogen atoms of the imidazolium aromatic rings and the OH moieties present in the side functionalities of the main polymeric chain. The exchange of the chloride counter ion by the L-prolinate anion leads to new types of polymeric catalysts, which behave as efficient artificial aldolase biomimetic systems, being highly active and selective for the aldol reaction in water. These new polymeric catalysts are significantly more active than the corresponding monomeric counterpart when the reaction is performed either in water or in the presence of water. The increase in catalytic efficiency can be related to their 3D structure, displaying helical chirality in the polymeric chain as a function of their preparation methodology. Under suitable experimental conditions, these polymers are able to catalyse the consecutive aldol-dehydration process, behaving as synthetic mimics of the aldolase-dehydrogenase enzymatic system. Moderate enantioselectivities can be achieved under suitable conditions.

Advanced reactor engineering with 3D printing for the continuous-flow synthesis of silver nanoparticles

The implementation of advanced reactor engineering concepts employing additive manufacturing is demonstrated. The design and manufacturing of miniaturised continuous flow oscillatory baffled reactors (mCOBR) employing low cost stereolithography based 3D printing is reported for the first time. Residence time distribution experiments have been employed to demonstrate that these small scale reactors offer improved mixing conditions at a millimetre scale, when compared to tubular reactors. Nearly monodisperse silver nanoparticles have been synthesised employing mCOBR, showing higher temporal stability and superior control over particle size distribution than tubular flow reactors.

Surface initiated polymerization of a cationic monomer on inner surfaces of silica capillaries: Analyte separation by capillary electrophoresis versus polyelectrolyte behavior

[2-(Methacryloyl)oxyethyl]trimethylammonium chloride was successfully polymerized by surface-initiated atom transfer radical polymerization method on the inner surface of fused-silica capillaries resulting in a covalently bound poly([2-(methacryloyl)oxyethyl]trimethylammonium chloride) coating. The coated capillaries provided in capillary electrophoresis an excellent run-to-run repeatability, capillary-to-capillary and day-to-day reproducibility. The capillaries worked reliably over 1 month with EOF repeatability below 0.5%. The positively charged coated capillaries were successfully applied to the capillary electrophoretic separation of three standard proteins and five β-blockers with the separation efficiencies ranging from 132,000 to 303,000 plates/m, and from 82,000 to 189,000 plates/m, respectively. In addition, challenging high- and low-density lipoprotein particles could be separated. The hydrodynamic sizes of free polymer chains in buffers used in the capillary electrophoretic experiments were measured for the characterization of the coatings.

Phase separation of aqueous poly(2-dimethylaminoethyl methacrylate-block-N-vinylcaprolactams).

Details of the phase separation of the poly(N-vinylcaprolactam) (PVCL) homopolymers and block copolymers of PVCL and poly(2-dimethylaminoethyl methacrylate) (PDMAEMA) were studied in aqueous buffer solutions. Phase separation occurred at either one or two temperatures depending on pH. The lower critical solution temperature of PVCL can be fine-tuned by varying the molecular weight of the block, whereas the phase separation temperature of the PDMAEMA block is strongly dependent on pH. The enthalpies of the collapse of the PVCL homopolymer and PVCL-b-PDMAEMA block copolymers were measured and show that the blocks phase separate independently upon heating. PVCL is known to bind amphiphilic cations, and correspondingly, according to light scattering, the block copolymers dissolve as single molecules but also form aggregates at room temperature. At temperatures above the cloud points of both blocks, only homogeneous large aggregates were observed. Zeta potential measurements confirmed that, upon heating, PDMAEMA blocks turn out from the collapsed PVCL globule toward the aqueous phase.

Redox-active organic–inorganic hybrid polyoxometalate micelles

A redox-active hybrid organic–inorganic polyoxometalate surfactant showed solvent-dependent self-assembly to form nano-scale architectures. The supramolecular assemblies exhibited contrasting electronic structure and redox activity to their molecular building units, and were found to be stable under electrochemical reduction and re-oxidation.

3D printable photochromic molecular materials for reversible information storage

The formulation of advanced molecular materials with bespoke polymeric ionic-liquid matrices that stabilize and solubilize hybrid organic-inorganic polyoxometalates and allow their processing by additive manufacturing, is effectively demonstrated. The unique photo and redox properties of nanostructured polyoxometalates are translated across the scales (from molecular design to functional materials) to yield macroscopic functional devices with reversible photochromism. These properties open a range of potential applications including reversible information storage based on controlled topological and temporal reduction/oxidation of pre-formed printed devices. This approach pushes the boundaries of 3D printing to the molecular limits, allowing the freedom of design enabled by 3D printing to be coupled with the molecular tuneability of polymerizable ionic liquids and the photoactivity and orbital engineering possible with hybrid polyoxometalates.

Novel cationic polyelectrolyte coatings for capillary electrophoresis

The use of bare fused silica capillary in CE can sometimes be inconvenient due to undesirable effects including adsorption of sample or instability of the EOF. This can often be avoided by coating the inner surface of the capillary. In this work, we present and characterize two novel polyelectrolyte coatings (PECs) poly(2‐(methacryloyloxy)ethyl trimethylammonium iodide) (PMOTAI) and poly(3‐methyl‐1‐(4‐vinylbenzyl)‐imidazolium chloride) (PIL‐1) for CE. The coated capillaries were studied using a series of aqueous buffers of varying pH, ionic strength, and composition. Our results show that the investigated polyelectrolytes are usable as semi‐permanent (physically adsorbed) coatings with at least five runs stability before a short coating regeneration is necessary. Both PECs showed a considerably decreased stability at pH 11.0. The EOF was higher using Goods buffers than with sodium phosphate buffer at the same pH and ionic strength. The thickness of the PEC layers studied by quartz crystal microbalance was 0.83 and 0.52 nm for PMOTAI and PIL‐1, respectively. The hydrophobicity of the PEC layers was determined by analysis of a homologous series of alkyl benzoates and expressed as the distribution constants. Our result demonstrates that both PECs had comparable hydrophobicity, which enabled separation of compounds with log Po/w > 2. The ability to separate cationic drugs was shown with β‐blockers, compounds often misused in doping. Both coatings were also able to separate hydrolysis products of the ionic liquid 1,5‐diazabicyclo[4.3.0]non‐5‐ene acetate at highly acidic conditions, where bare fused silica capillaries failed to accomplish the separation.

Water-Dispersible Silica-Polyelectrolyte Nanocomposites Prepared via Acid-Triggered Polycondensation of Silicic Acid and Directed by Polycations

The present work describes the acid-triggered condensation of silicic acid, Si(OH)4, as directed by selected polycations in aqueous solution in the pH range of 6.5–8.0 at room temperature, without the use of additional solvents or surfactants. This process results in the formation of silica-polyelectrolyte (S-PE) nanocomposites in the form of precipitate or water-dispersible particles. The mean hydrodynamic diameter (dh) of size distributions of the prepared water-dispersible S-PE composites is presented as a function of the solution pH at which the composite formation was achieved. Poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) and block copolymers of DMAEMA and oligo(ethylene glycol) methyl ether methacrylate (OEGMA) were used as weak polyelectrolytes in S-PE composite formation. The activity of the strong polyelectrolytes poly(methacryloxyethyl trimethylammonium iodide) (PMOTAI) and PMOTAI-b-POEGMA in S-PE formation is also examined. The effect of polyelectrolyte strength and the OEGMA block on the formation of the S-PE composites is assessed with respect to the S-PE composites prepared using the PDMAEMA homopolymer. In the presence of the PDMAEMA60 homopolymer (Mw = 9400 g/mol), the size of the dispersible S-PE composites increases with solution pH in the range pH 6.6–8.1, from dh = 30 nm to dh = 800 nm. S-PDMAEMA60 prepared at pH 7.8 contained 66% silica by mass (TGA). The increase in dispersible S-PE particle size is diminished when directed by PDMAEMA300 (Mw = 47,000 g/mol), reaching a maximum of dh = 75 nm. S-PE composites formed using PDMAEMA-b-POEGMA remain in the range dh = 20–30 nm across this same pH regime. Precipitated S-PE composites were obtained as spheres of up to 200 nm in diameter (SEM) and up to 65% mass content of silica (TGA). The conditions of pH for the preparation of dispersible and precipitate S-PE nanocomposites, as directed by the five selected polyelectrolytes PDMAEMA60, PDMAEMA300, PMOTAI60, PDMAEMA60-b-POEGMA38 and PMOTAI60-b-POEGMA38 is summarized.