Jay A.
Syrett
a,
Giuseppe
Mantovani
b,
William R. S.
Barton
c,
David
Price
c and
David M.
Haddleton
*a
aDepartment of Chemistry, University of Warwick, Coventry, UK CV4 7AL. E-mail: d.m.haddleton@warwick.ac.uk
bSchool of Pharmacy, University of Nottingham, Nottingham, UK NG7 24D. E-mail: giuseppe.mantovani@nottingham.ac.uk
cLubrizol Corporation, Hazelwood Research Centre, Derby, UK DE56 1QN
First published on 15th January 2010
Diels–Alder chemistry has been used to synthesise polymerisation initiators and a dimethacrylic cross-linker that leads to efficient cleavage and reformation; self-healing. The initiators were prepared using 1-(2-hydroxyethyl)-1H-pyrrole-2,5-dione (3) as an intermediate, and reacting this with furfuryl alcohol to afford 2-bromo-2-methyl-propionic acid 2-[1-(2-bromo-2-methyl-propionyloxymethyl)-3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.02,6]dec-8-en-4-yl]-ethyl ester (7) and 9-anthracenemethanol to yield initiator (8). The former exhibited polymers with excellent cleavage properties (Mn 12000 g mol−1 to 6500 g mol−1) with reformation at efficiency of 50% (Mn 8900 g mol−1). The initiator from the anthracene derivative initially indicated that retro-Diels–Alder was not occurring with no change in the NMR or GPC data. An excess of a rhodamine-based dienophile was added to capture any cleaved anthracene-terminated polymer, with results indicating that the polymer is cleaving and reforming upon the cooling cycle. Similar results were observed with arm first stars, made using a Diels–Alder based dimethacrylate cross-linker. Little cleavage was observed initially, however, addition of the tag gave a significant reduction in Mw (7080 g mol−1 to 5300 g mol−1) and Mw/Mn (1.78 to 1.26).
Diels–Alder (DA) cycloaddition is a convenient route for the formation of carbon–carbon bonds via a facile reaction under undemanding conditions that fulfills the requirements of a “click” reaction.4–8 Diels–Alder cycloadditions are thermoreversible reactions9 and this feature has been exploited in the preparation of self-healing polymers carrying functionalities, either as the polymer chain-end or in the repeating units.3 Furthermore, the reverse DA reaction does not involve free radicals, thus avoiding many side reactions that might prevent reformation.10 Diels–Alder moieties were first incorporated into polymers by Stevens and Jenkins.11 Subsequently, Saegusa and co-workers developed a thermally “mendable” polymeric DA network.12 A Diels–Alder cross-linked polymer synthesised for the specific use of self-healing was prepared by Wudl et al. in 2003, using furan- and maleimide-based monomers cross-linking along the polymer backbone.9 In this study it was shown that fractured polymer materials, heated to 120 °C, exhibited 83% recovery of the polymers original strength. Crucially, this fracture/repair cycle could also be repeated, making this the first real DA polymeric system exhibiting a thermally responsive self-healing behaviour.
This route to self-healing polymers is applicable to composite materials and large cross-linked networks. Advances in controlled radical polymerisation (CRP) allow for the synthesis of functional polymers with excellent control over molecular weight, molecular weight distribution, architecture and incorporation of functionality. The introduction of a range of techniques, ATRP,13–15 RAFT16–18 and NMRP,19 gives the polymer chemist a great deal of control of polymer properties. Herein, we report the use of a living radical polymerisation to synthesise a self-healing polymer. The chemistry employed is efficient and relatively simple and has allowed for the design of cleavable linkers that contain polymerisation initiators. Additionally, a DA based cross-linker that can be employed in the synthesis of arm first stars is reported.
In this present study we report the synthesis of novel well-defined linear and star methyl methacrylate (MMA) polymers bearing DA adducts within their macromolecular backbone and a preliminary evaluation of their ability to cleave and reform under external thermal stimuli.
Scheme 1 Reagents and conditions: (i) toluene, 80 °C; (ii) ethanolamine, Et3N, MeOH, 0 °C to 70 °C; (iii) toluene, reflux, 24 h; (iv) furfuryl alcohol, benzene, reflux; (v) anthracenemethanol, toluene, reflux; (vi) acryloyl chloride, dichloromethane, 0–25 °C; (vii and viii) 2-bromo isobutyl bromide, Et3N, 0–25 °C, THF. |
Fig. 1 (i) Comparison of rates for polymers 10 (50 °C) and 12 (70 °C). (ii) Mnvs. conversion for the polymers 10 and 12. [Cu(I)Br]–[ligand]–[initiator]0–[MMA]0 2 : 4 : 1 : 100. |
The ability of polymers 9–12 to respond to thermal stimuli was investigated. The 1H NMR signals for the Diels–Alder derived polymer feature a very distinctive pattern of signals, which can be easily distinguished from the dissociated polymer (Fig. 2).
Fig. 2 1H NMR of polymer 10 (i) prior to heating, (ii) cleaved polymer following heating, and (iii) reformed polymer. |
Following thermal treatment of polymers 9–11 under reflux in toluene over 24 h a completely different pattern of peaks in the 1H NMR was observed and each signal was easily identified, indicating that a retro-Diels–Alder process occurred efficiently under these conditions, to give N-maleimide (6.89 ppm) and furfuryl ester (6.36 and 6.39 ppm)-terminated polymers. After removal of the solvent under reduced pressure, the reaction mixture was heated at 60 °C for 24 h. NMR analysis of the resulting reaction mixture revealed that approximately 50% of the Diels–Alder linker had reformed under these conditions (5.22, 6.45 and 6.57 ppm). This value is comparable to the 59% yield observed for the analogous cycloaddition in which the maleimide alcohol (3) and furfuryl alcohol were converted into the adduct (4). It is noted that previous reports have often reported healing efficiencies of <50%, which were found to be sufficient for significant recovery of mechanical properties.22 In the 1H NMR spectrum two new signals at 6.49 and 5.3 ppm, not previously seen either in the spectra of the DA polymers (9–11) or in the maleimide- and furan-terminated polymers, were observed after the retro-Diels–Alder process (Fig. 2). NMR investigation and comparison with data reported in the literature23 indicated that the reformed polymer was a mixture of endo and exo isomeric Diels–Alder linkers.
GPC traces confirmed a significant proportion of polymer reformation (Fig. 3), although a quantitative assessment of the yields for this Diels–Alder process was not extrapolated from these data due to partial overlapping of the peaks of the cleaved and non-cleaved polymers. As expected, the molecular weight of the former was found to be approximately half that of the original polymer, whilst, upon reformation, the molecular weight increases, as expected. The PDI's also increased upon Diels–Alder linker reformation, which was due to partial peak overlap, Tables 1 and 2.
Polymer | M n/kDaa | M w/kDaa | M w/Mna | [η]b |
---|---|---|---|---|
a Determined by GPC analysis using THF–TEA 95 : 5 (v/v) as the mobile phase and PMMA as calibrants. b Intrinsic viscosities were measured for polymer 10 and its cleaved/reformed derivatives. | ||||
9 | 5.40 | 5.99 | 1.11 | — |
Cleaved | 2.76 | 3.25 | 1.18 | — |
Reformed | 4.10 | 4.96 | 1.21 | — |
10 | 12.0 | 13.5 | 1.12 | 0.072 |
Cleaved | 6.5 | 7.81 | 1.21 | 0.041 |
Reformed | 8.9 | 11.0 | 1.24 | 0.052 |
11 | 54.7 | 62.9 | 1.15 | — |
Cleaved | 28.4 | 34. 7 | 1.22 | — |
Reformed | 42.0 | 52.0 | 1.24 | — |
Fig. 3 GPC data of (i) polymer 10 (black), (ii) cleaved polymer (red), and (iii) the reformed polymer (blue), under the conditions described in Fig. 2. |
Polymers prepared from the difunctional initiator DA1 (7) showed excellent cleavage/re-healing properties. Polymer 12, prepared from the difunctional initiator DA2 (8), was introduced as maleimide–anthracene molecules which are known to undergo Diels–Alder process in a facile manner. Aydan et al. showed that star polymers could be synthesised via a Diels–Alder click reaction.24 An arm first core was grown first with an anthracene-based initiator. Subsequently, a protected maleimide functional polymer was introduced, and a highly efficient deprotection followed by click reaction to the anthracene core in one pot occurred.24 However, subsequent deprotection of these polymers was not reported. This suggested either that the retro-Diels–Alder did not occur or that the process did occur to a certain extent, but the Diels–Alder linkers subsequently did reform, upon cooling or directly at the temperature employed for the deprotection, which is common in self-healing systems.9 The polymers formed from DA1 (7) did not exhibit reformation upon cooling.
In order to investigate whether the anthracene–maleimide linker was cleaving and then reforming upon cooling, an excess of a dienophile was added to capture any cleaved anthracene-terminated polymer (Fig. 4). For this purpose, we synthesised a maleimide-containing rhodamine B probe (Fig. 5). Retro-Diels–Alder cleavage was attempted in the presence of 50-fold molar excess of the rhodamine tag, in refluxing DMSO. The tag was introduced as its furan adduct which released the desired maleimide-containing fluorophore in situ, upon heating. Complete cleavage, as in the case of polymers 9–11, should halve the Mn. In this case the Mn decreased by only 20%, suggesting that approximately a fifth of the linker had effectively cleaved throughout the process. Evidence that exchange has taken place came from GPC with UV-Vis detection at λ = 550 nm, the resulting material was now clearly seen (Fig. 6). The starting material (12) has no absorption at this wavelength. This suggests that the anthracene–maleimide linker in 12 has a higher thermal stability than the furan–maleimide present in 9–11, and that any cleaved materials formed upon heating 12 at 200 °C were able to undergo Diels–Alder cycloaddition upon slow cooling back to ambient temperature.
Fig. 4 Attempted deprotection of 12 in DMSO at 200 °C: (i) reaction scheme, (ii) GPC data, and (iii) partial 1H NMR spectra before and after the attempted retro-Diels–Alder polymer cleavage. |
Fig. 5 The expected product 12 cleaved during the heating process. This product could then be detected by UV GPC. |
Fig. 6 Cleavage of DA2 polymer monitored by GPC with (i) DRI detection and (ii) UV detection showing no absorbance in the original polymer, and a peak following cleavage and addition to the rhodamine tag, retention time is given for the UV trace as this detector was not calibrated. |
In order to investigate the applicability of the approach the study was extended to star polymers. A difunctional cross-linker monomer containing a substituted furan–maleimide Diels–Alder adduct was synthesised for this purpose. Due to structural similarities with polymers 9–11 obtained from the initiator DA1 (7) we expected the retro-Diels–Alder cleavage of the cross-linker to occur to a relatively large extent.
Refluxing 13 (Fig. 7) in toluene for 24 h suggested that a small amount of cleavage takes place with a shoulder corresponding to a lower molecular weight material detected in the GPC chromatogram, Fig. 8. As polymers 9–11 were easily cleaved under analogous reaction conditions, it was suspected that a significant proportion of the star cleaves and reforms within the cooling cycle. In this system complete cleavage of the star was expected to afford lower molecular weight materials with narrower PDI's. One possible explanation for this behaviour was that in a cross-linked network a less than quantitative retro-Diels–Alder process would caused the diene/dienophile cleaved moieties to remain spatially close to each other which would favour the reformation of the Diels–Alder linkers.
Fig. 7 Synthesis of star polymer (13). |
Fig. 8 GPC data before and after attempted cleavage of the star polymer. Evidence that some cleavage has occurred is seen from the appearance of low molecular shoulder in the cleaved product. |
In order to investigate this the maleimide functionalised rhodamine trapping agent was added in the reaction mixture. In this case the Mn and Mw of the star polymer were reduced dramatically, and the PDI decreased from 1.78 to 1.26 indicating that the majority of the cross-linker units was effectively cleaving under these conditions (Fig. 9).
Fig. 9 GPC data before and after cleavage with the rhodamine tag, showing a vast reduction in the polydispersity and Mw data. |
At this stage it is still not clear whether this system did reheal upon cooling or whether the Diels–Alder linkers were constantly cleaving and reforming. The cleaving and reforming throughout the heating cycle were confirmed by high temperature GPC at 140 °C, with 1,2,4-trichlorobenzene as eluent, which showed little change from the original polymer (see ESI†).
Footnote |
† Electronic supplementary information (ESI) available: Full experimental details and additional characterisation data. See DOI: 10.1039/b9py00316a |
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