Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Summary

Crystallization-driven self-assembly (CDSA) displays the unique ability to fabricate cylindrical nanostructures of narrow length distributions. The organocatalyzed ring-opening polymerization of ε-caprolactone and subsequent chain extensions of methyl methacrylate and N,N-dimethyl acrylamide are demonstrated. A living CDSA protocol that produces monodisperse cylinders up to 500 nm in length is outlined.

Abstract

The production of monodisperse cylindrical micelles is a significant challenge in polymer chemistry. Most cylindrical constructs formed from diblock copolymers are produced by one of three techniques: thin film rehydration, solvent switching or polymerization-induced self-assembly, and produce only flexible, polydisperse cylinders. Crystallization-driven self-assembly (CDSA) is a method which can produce cylinders with these properties, by stabilizing structures of a lower curvature due to the formation of a crystalline core. However, the living polymerization techniques by which most core-forming blocks are formed are not trivial processes and the CDSA process may yield unsatisfactory results if carried out incorrectly. Here, the synthesis of cylindrical nanoparticles from simple reagents is shown. The drying and purification of reagents prior to a ring-opening polymerization of ε-caprolactone catalyzed by diphenyl phosphate is described. This polymer is then chain extended by methyl methacrylate (MMA) followed by N,N-dimethyl acrylamide (DMA) using reversible addition−fragmentation chain-transfer (RAFT) polymerization, affording a triblock copolymer that can undergo CDSA in ethanol. The living CDSA process is outlined, the results of which yield cylindrical nanoparticles up to 500 nm in length and a length dispersity as low as 1.05. It is anticipated that these protocols will allow others to produce cylindrical nanostructures and elevate the field of CDSA in the future.

Introduction

One-dimensional (1D) nanostructures, such as cylinders, fibers and tubes, have garnered increasing attention in a variety of fields. Amongst these, their popularity in polymer science is owed to their rich variety of properties. For example, Geng et al. demonstrated that filomicelles exhibit a tenfold increase in residence time in the bloodstream of a rodent model compared to their spherical counterparts, and Won et al. revealed that polybutadiene-b-poly(ethylene oxide) fiber dispersions display an increase in storage modulus by two orders of magnitude upon crosslinking of the core during rheological measurements^1,2. Interestingly, many of these systems are synthesized via the self-assembly of block copolymers, whether this be through more traditional methods of solvent switching and thin-film rehydration³, or more advanced methods such as polymerization-induced self-assembly and crystallization-driven self-assembly (CDSA)^4,5. Each technique holds their own advantages, however, only CDSA can produce rigid particles with a uniform and controllable length distribution.

Pioneering work by Gilroy et al. formed long polyferrocenylsilane-b-polydimethylsiloxane (PFS-PDMS) cylinders in hexanes and, when using mild sonication, very short cylinders with a low contour length dispersity (L_n). Upon the addition of a predetermined mass of diblock copolymer chains in a common solvent, cylinders of varying lengths with an L_n as low as 1.03 were synthesised^5,6. Further work by the Manners group highlighted the high degree of control possible with the PFS system, which may be used to form remarkably complex and hierarchal structures: block-co-micelles, scarf shaped and dumbbell micelles to name a few^7,8. Following these demonstrations, researchers investigated other, more functional systems for CDSA including: semi-crystalline commodity polymers (polyethylene, poly(ε-caprolactone), polylactide)^{9,10,11,12,13} and conducting polymers (poly(3-hexylthiophene), polyselenophene)^14,15. Armed with this toolbox of diblock copolymer systems that can be assembled quickly and efficiently, researchers have carried out more application-driven research in recent years¹⁶.  Jin et al. have demonstrated exciton diffusion lengths in the hundreds of nanometers in polythiophene block copolymers and our group demonstrated the formation of gels from poly(ε-caprolactone) (PCL) containing cylindrical constructs^10,17.

Although it is a powerful technique, CDSA does have its limitations. The block copolymers must have a semi-crystalline component, as well as low dispersity values and high end group fidelities; lower order block contaminants may cause particle aggregation or induce morphology changes^18,19. Due to these restrictions, living polymerizations are used. However, significant reagent purification, drying procedures and water/oxygen free environments are required in order to achieve polymers with the aforementioned properties. Attempts have been made to design systems that overcome this. For example, PFS block copolymers have been formed using click chemistry to couple polymer chains together²⁰. Although the resulting cylindrical nanoparticles have demonstrated exemplary properties, the block copolymers are typically purified by preparative size exclusion chromatography and the synthesis of PFS still requires the use of living anionic polymerizations. Our group recently realized the living CDSA of PCL, the success of which revolved around using both living organobase-catalyzed ring-opening polymerizations (ROP) and reversible addition-fragmentation chain transfer (RAFT) polymerizations¹⁰. Although this method is simpler, living polymerizations are still required.

As the field is moving towards more application-driven research, and due to the problems associated with living polymerizations, it is believed that an outline of the polymer synthesis and self-assembly protocols will be advantageous to future scientific work. Thus, in this manuscript, the complete synthesis and self-assembly of a PCL-b-PMMA-b-PDMA copolymer is outlined. Drying techniques will be highlighted in the context of an organocatalyzed ROP of ε-caprolactone and the subsequent RAFT polymerizations of MMA and DMA will be outlined. Finally, a living CDSA protocol for this polymer in ethanol will be presented and common errors in characterization data due to poor experimental technique will be critiqued.

Protocol

1. Drying of toluene

NOTE: If you have access to dry solvent towers, collect the toluene and degas by five freeze-pump-thaw cycles.

1. Dry 3 Å molecular sieves in a 250 mL Schlenk flask at 250-300 °C under vacuum for 48 h and transfer into a glovebox.
2. Dry two ampoules in the oven at 150 °C overnight and transfer them into the glovebox.
3. Transfer the activated molecular sieves into the two ampoules and remove from the glovebox.
4. Dry a two-neck round-bottom flask (RBF) and add 100 mL of toluene, the volume of which equals to, at most, half of the ampoule volume. Add 1.0 g of CaH₂ to the toluene and stir.
   CAUTION: Be careful of H₂ release at this point. Always add CaH₂ under a steady flow of nitrogen to remove any H₂ build up in the flask.
5. Transfer the toluene into one of the ampoules containing the molecular sieves with a filter cannula and rest overnight.
6. Transfer the toluene into the last ampoule containing sieves with a filter cannula. Freeze-pump-thaw (5 cycles) the toluene and transfer into a glovebox.

2. Drying of the CTA-initiator/DPP

1. Add the chain transfer agent/initiator to a vial, securing with tissue paper.
2. Add 10 g of P₂O₅ into a desiccator. Place the vial above the powder.
3. Place the desiccator under dynamic vacuum for 8 h and static vacuum overnight.
4. Open the desiccator to agitate the P₂O₅. Resume the vacuum cycles for 5 days.
   NOTE: The P₂O₅ may discolor or become clumpy if excess solvent/water is present. Replace the P₂O₅ if this is observed.
5. Backfill the desiccator with nitrogen and transfer to a glovebox.

3. Drying/Purification of ε-caprolactone

NOTE: For this section, all glassware and stirrer bars must have been dried in a 150 °C oven overnight prior to use. This will remove all water from the surfaces of the glass.

1. Add 100 mL of ε-caprolactone to a two-neck 250 mL RBF equipped with a stirrer bar and tap on the small neck.
2. Add 1.0 g of calcium hydride into the RBF, under a steady flow of nitrogen. Fit with a glass stopper and stir overnight at room temperature under a nitrogen atmosphere.
3. Dry the vacuum distillation equipment.
4. Attach the two-neck flask to a Schlenk line and purge by evacuating and filling with nitrogen three times. After purging, open the line to a steady flow of nitrogen.
5. Assemble the vacuum distillation equipment from the ε-caprolactone RBF, maintaining a steady flow of nitrogen to prevent water from entering the system. Attach the thermometer and seal in place.
6. Attach the adaptor to the Schlenk line. Remove the nitrogen flow and place the system under vacuum under this new connection.
7. Heat the ε-caprolactone at 60-80 °C, collecting the first 5.0 mL in the small RBFs and the rest in the two-neck RBF. Place the flasks in liquid nitrogen to condense the caprolactone effectively. Wrap the distillation equipment in cotton wool and foil to speed up the process.
8. Attach the Schlenk line to the collection flask and purge the line three times. Turn the line to nitrogen and open the tap. Add 1.0 g of calcium hydride to the flask, and a stopper, then leave under a nitrogen atmosphere stirring overnight.
9. Meanwhile, dispose of the excess calcium hydride by the dropwise addition of isopropanol, followed by 5.0 mL of methanol and then an excess of water once bubbling ceases. Rinse the glassware with acetone and place in the oven overnight.
10. Repeat the vacuum distillation again, without adding CaH₂ to the monomer once finished. Instead, transfer the caprolactone via cannula into an ampoule and transfer to the glovebox.

4. Ring opening polymerization of ε-caprolactone

1. Prepare stock solutions of initiator, catalyst and monomer. Weigh 0.10 g of diphenyl phosphate, 0.011 g of CTA-OH and 0.25 g of caprolactone into three separate vials. Add 0.5 mL of toluene to each of the initiator and catalyst vials and gently agitate until the reagents are dissolved.
2. Mix the initiator and diphenyl phosphate stock solutions into one vial and add a stir bar.
3. Under moderate stirring, add the monomer into the initiator/catalyst vial. Fit the vial with a lid and stir for 8 h at room temperature.
4. After 8 h, remove the vial from the glovebox and immediately precipitate into an excess of cold diethyl ether dropwise.
5. Filter the white solid, dry and dissolve in 1 mL of tetrahydrofuran (THF). Precipitate twice more and dry thoroughly.

5. RAFT polymerization of methyl methacrylate and N,N-dimethylacrylamide

1. To remove the stabilizers from the dioxane and MMA, prepare several basic alumina plugs in Pasteur pipettes and filter the liquids into separate vials.
2. Weigh 0.5 g of PCL synthesized previously, 0.424 g of methyl methacrylate and measure 2 mL of dioxane into a vial and allow to dissolve.
3. Prepare a stock solution of pure azobisisobutyronitrile (AIBN, 10 mg in 1.0 mL) and pipette in 139 μL into the reaction mixture. Transfer to an ampoule equipped with a stir bar and seal.
4. Freeze-pump-thaw the solution three times. Backfill with nitrogen and place the ampoule in a preheated oil bath at 65 °C for 4 h.
   NOTE: Do not heat the container with anything more than 30 °C before the freeze-pump-thaw cycles are complete, as this can cause the initiator to decompose.
5. To monitor conversion, remove the ampoule from the oil bath. Switch the cap for a suba seal under a flow of nitrogen, remove two drops and mix with deuterated chloroform. Run a proton spectrum on an NMR instrument.
6. Place the ampoule in liquid nitrogen until frozen and open the ampoule to air to quench the polymerization.
7. Precipitate the mixture dropwise into a vast excess of cold diethyl ether. Isolate by Buchner filtration and dry.
8. Take the polymer up in THF and precipitate twice more. Dry the polymer thoroughly and analyze by ¹H NMR spectroscopy and gel permeation chromatography (GPC).
9. Follow this procedure again, but with 0.5 g of PCL-PMMA, 1.406 g of DMA, 2.0 mL of dioxane and 111 μL of 10 mg.mL^-1 AIBN in dioxane. Heat the polymerization at 70 °C for 1 h and precipitate the reaction mixture into cold diethyl ether three times.

6. Self-nucleation, seed generation and living crystallization-driven self-assembly

1. Place 5.0 mg of triblock copolymer into a vial and add 1.0 mL of ethanol. Seal the vial with a lid and parafilm and heat at 70 °C for 3 h.
2. Leave the vial to cool slowly to room temperature. Leave the solution to age at room temperature for two weeks. The solution will turn cloudy and will form a distinct layer at the bottom when fully assembled.
3. Dilute the 5.0 mg.mL^-1 dispersion to 1.0 mg.mL^-1.
4. Place the dispersion in a sonication proof tube and place in an ice bath.
5. Insert the tip of the sonication probe into the middle area of the dispersion.
6. Sonicate the solution for fifteen cycles of 2 min at the lowest intensity, allowing to cool for 15 min before the next cycle.
7. Take an aliquot of the 1.0 mg.mL^-1 seed dispersion and dilute to 0.18 mg.mL^-1.
8. Prepare a solution of unimer in THF at 25 mg.mL^-1. Add 32.8 μL into the seed dispersion and gently shake to allow full dissolution.
9. Leave the dispersion to age for three days with the lid slightly ajar so the THF can evaporate. This will produce cylinders of 500 nm in length if the starting seeds were 90 nm in length.

Results

PCL was analyzed by ¹H NMR spectroscopy and gel permeation chromatography (GPC). The ¹H NMR spectrum yielded a degree of polymerization (DP) of 50, by comparison of resonances at 3.36 ppm and 4.08 ppm, which correspond to the end group ethyl protons and the in-chain ester α-protons respectively (Figure 1b). This provided validation of the molecular weight values obtained by GPC where a single peak, with a dispersity value of 1.07, was ob...

Discussion

The synthesis and living CDSA of the triblock copolymer PCL₅₀-PMMA₁₀-PDMA₂₀₀ has been outlined. Although stringent conditions are required, the ring-opening polymerization of ε-caprolactone gave polymers with excellent properties that enabled the successful chain extensions of MMA and DMA. These polymers were successful in their self-seeding, obtaining a pure phase of cylindrical micelles, which were sonicated into seed particles of L_N 98 nm. Through simple additi...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
2,2'-azobisisobutyrnitrile	Sigma Aldrich
250 mL ampoule
250 mL two neck RBF
Ampoule (25 mL)
B19 tap
B24 stopper
Basic Alumina	Fluka
Buchner Flask
Buchner Funnel
Caclium Hydride
Cannulae
caprolactone	Arcos Organics
Chain Transfer Agent	Made in House
Conical Flask (multiple sizes)
Dessicator
Diethyl Ether	Merck
Dioxane	Fisher
diphenylphosphate	Sigma Aldrich
Distillation Condenser
Ethanol	Fisher
Filter Paper (multiple sizes)
Gel Permeation Chrmoatography Instrument	Agilent Technologies Infinity 1260 II		Running DMF at 50 °C
Glovebox	Mbraun, Unilab
Hotplate	IKA, RCT basic
Mercury Thermometer
Methyl Methacrylate	Sigma Aldrich
Molecular seives	Fisher	MS/1030/53
N,N-dimethyl acrylamide	Sigma Aldrich
NMR spectrometer	Bruker 400 MHz
Phosphorus pentoxide	Sigma Aldrich
RBF (multiple sizes)
Schlenk Cap (B24)
Schlenk Flask (250 mL)
Schlenk Line
Sonication Probe	Bandelin Sonoplus
Suba Seal (multiple sizes)
TEM grids	EmResolutions, Formvar/carbon film 300 mesh copper
THF	Merck
three neck adaptor
Toluene	Fisher
Transmission Electron Microscope	Jeol 2100