Intrinsic self-healing polymers with a high E -modulus based on dynamic reversible urea bonds

The straightforward synthesis of a urea polymer network is presented. Commercially available monomers are polymerized using light-induced polymerization, resulting in networks crosslinked by hindered urea molecules. These moieties are reversible and, thus, can be converted into the starting compounds (that is, isocyanate and amine) by a simple thermal treatment. This process is monitored using differential scanning calorimetry as well as Raman and infrared spectroscopy. Furthermore, the self-healing ability of these polymer networks is investigated using scratch-healing tests as well as bulk-healing investigations using tensile testing. The resultant materials have a high E -modulus, are able to heal scratches at temperatures above 70 °C multiple times and their mechanical properties can be partially regenerated. The underlying healing mechanism is based on the reversible opening of the urea bonds and exchange reactions between two functional groups, which were con ﬁ rmed from a spectroscopic analysis. In summary, these new materials are a new type of intrinsically healable polymers and provide a ﬁ rst step toward hard and healable polymers.


INTRODUCTION
The limited availability of natural resources is gradually causing modern society to develop more sustainable uses of oil-based materials. In particular, healing abilities in damaged materials such as polymers can increase the lifetime of such systems as these materials are able to recover their original (mechanical) properties. 1,2 However, special polymer designs are required to obtain this behavior. Generally, self-healing polymers can be divided into extrinsic and intrinsic self-healing polymers. Extrinsic self-healing materials are based on the encapsulation of a healing agent (for example, in microcapsules) within the polymer matrix, which is released after cracking. [3][4][5] In contrast, intrinsic self-healing materials can recover their properties due to the presence of specific reversible chemical bonds, which is beneficial due to the possibility of multiple healing steps at the same location. 6 These binding motifs can be composed of either dynamic covalent bonds, [7][8][9] for example, the Diels-Alder reaction [10][11][12] or radical-based systems, 13 or supramolecular interactions, such as hydrogen or halogen bonds, [14][15][16] ionic interactions, 17 π-π interactions, 18 host-guest interactions 19 or metal-ligand interactions. [20][21][22][23] Often there is a trade-off between the mechanical properties and the healing efficiency (Figure 1). High healing efficiencies are mostly only possible for low E-moduli; for E-moduli above 10 7 -10 8 Pa, the number of reported examples decreases significantly, as well as the achieved healing efficiencies.
Two interesting industrial polymer classes are polyurethanes and polyureas. Those materials can be easily produced by the reaction of an isocyanate with an alcohol or amine. Thus, imparting those polymers with healing abilities is a highly relevant industrial topic. Consequently, polyurethanes and polyureas have already been utilized for designing self-healing polymers. 15 Polyurethanes and polyureas can also be applied for designing intrinsically healable polymers as those polymers feature hydrogen bonds. [24][25][26] These weak bonds are highly dynamic 27 and, thus, can be utilized for designing intrinsic self-healing materials. 10 In particular, Leibler and his group demonstrated the self-healing effects caused by dynamic hydrogen bonds. 15 Furthermore, the shape-memory effect of polyurethanes can be utilized to enhance the self-healing behaviors of polymers, which has been described as shape-memory-assisted selfhealing. [28][29][30] One intriguing feature of sterically hindered ureas is the reversibility of the formed urea bonds. 31,32 During thermal treatment or exposure to water, reversible reactions can be observed in which the isocyanate and its corresponding co-reactant are reformed. 33,34 This reversibility has been well investigated in solution but has, to the best of our knowledge, only been utilized once for designing a self-healing material. In that case, Cheng and co-workers presented a poly (urea-urethane) that was able to self-heal due to the reversibility of the dynamic urea bonds. 35 Nevertheless, the investigated substances were soft materials with poor mechanical properties (a Young's modulus of ca. 1 MPa at room temperature). The follow-up study by the same authors described an improvement in the mechanical properties by using a denser polymer network, which could be completely depolymerized under thermal treatment, resulting in the formation of the educts. 36 Consequently, remendability as well as recyclability of the polymer network was possible. However, this behavior was associated with the nearly complete depolymerization of the network and, thus, a (partial) decrease in the mechanical integrity of the material.
In the present study, we investigate the reversibility of dynamic poly (methacrylate) systems crosslinked with dynamic urea moieties and their corresponding self-healing properties. The networks consist of commercially available substances. Furthermore, a sterically hindered amine is utilized during polymerization due to its ability to open urea bonds during thermal treatment. The polymer network is obtained after a simple photopolymerization procedure. The mechanical properties are investigated using tensile testing. Hard materials with improved mechanical and self-healing properties are obtained (Figure 1), which are novel properties for an intrinsically healable polymer. Compared to other known intrinsic self-healing polymers, a relatively high E-modulus is obtained combined with a rather high healing efficiency, which has not been described in the literature so far. For the first time, the dynamic character of the urea bonds in the solid state is confirmed using differential scanning calorimetry (DSC) and Raman and infrared (IR) spectroscopy. These results enable new mechanistic insights into the self-healing behavior of these materials.

MATERIALS AND METHODS
All used chemicals were purchased from VWR (Darmstadt, Germany), Aldrich (Taufkirchen, Germany) and TCI (Zwijndrecht, Belgium). They were used without further purification. Butyl methacrylate (BMA) was passed over a short aluminum oxide plug. Toluene was dried by refluxing over sodium/benzophenone. The reaction progress was monitored using thin-layer chromatography with aluminum sheets precoated with silica gel 60 F 254 (Merck, Darmstadt, Germany).
One-dimensional ( 1 H, 13 C) nuclear magnetic resonance spectra were recorded using a Bruker (Rheinstetten, Germany) AC 300 (300 MHz) at 298 K. The chemical shifts are reported in parts per million (p.p.m., δ scale) relative to the residual signal of the solvent. The coupling constants are given in hertz.
Elemental analyses were performed using a Vario El III (Elementar, Langensebold, Germany) elemental analyzer.
A thermogravimetric analysis was carried out under nitrogen using a Netzsch (Selb, Germany) TG 209 F1 Iris, and DSC was performed using a DSC 204 F1 Phoenix from Netzsch under a nitrogen atmosphere with a heating rate of 10 or 20 K min − 1 .
The scratch-healing experiments were carried out using the optical microscope of an atomic force microscopy setup. The scratches in the material were created using a Feather disposable scalpel no. 11 (stainless steel). The investigation of the self-healing behavior started at 100°C. If the material revealed self-healing properties, multiple scratch-healing tests at the same temperature and position were performed. Afterwards, the temperature was reduced in 10 K intervals until no further self-healing was observed. The bulk healing was performed at 100°C (P1 and P2) and at 120°C (P3) for 72 h. Afterwards, annealing at the same temperature was performed for 72 h.
Tensile tests were performed using a standard tensile machine (Z020, Zwick/Roell, Ulm, Germany) at room temperature or at 100°C (error ± 10 K) with a speed of 2 mm min − 1 . The specimens were 5 mm high, 30 mm long and 5 mm wide. For each measurement condition, five different specimens were synthesized, and the average values were determined and listed in Table 3 due to the variations in each specimen.
All dynamic mechanical thermal analysis experiments were performed using an MCR 301 rheometer from Anton Paar (Ostfildern-Scharnhausen, Germany) with a convection temperature device (CTD 450) that covered a broad temperature range from − 100 to 450°C. The test specimens were 12.5 mm × 28.5 mm × 4 mm, which were polymerized in a special Teflon mold and mounted into the solid rectangular fixture of the device for dynamic mechanical thermal analysis measurements under torsion. The instrument was operated with a sample gap of 20 mm and a frequency of 1 Hz with a 0.1% strain. The sample was cooled to 25°C, and the measurements were conducted during a warm-up cycle to 140°C. Furthermore, the frequency dependency was investigated by keeping the temperature constant at 80, 100 and 120°C. The frequency was varied from 0.1 to 100 Hz.
The Fourier transform-IR (FT-IR) spectra of polymer P2 on a sodium chloride crystal and of compound 1 (a potassium bromide pellet) were  The FT-IR spectra were recorded between 400 (P2) or 700 (1) and 4000 cm − 1 with a spectral resolution of 4 cm − 1 . The sample temperature was adjusted using a Linkam stage LTS 350 (Linkam, Tadworth, UK). The FT-IR spectra of 1 were recorded at room temperature and at 100°C, while the FT-IR spectra of P2 were recorded at 30, 50, 75, 100, 125, 150 and 175°C. The heating rate was 30°C min − 1 . The FT-IR spectra of a pure sodium chloride crystal and a pure potassium bromide pellet were recorded at the measurement temperatures and utilized as background spectra. The FT-IR spectra consist of 32 (1) or 64 (P2) single spectra, respectively. The sodium chloride crystal contained small amounts of liquid water on the surface, which evaporated at elevated temperatures. Thus, the FT-IR spectra slightly changed in the region betweeñ 1600 and 3400 cm − 1 due to the evaporating water. The raw FT-IR data were preprocessed using R 3.3.2 software. 37 First, the FT-IR spectra were restricted to the wavenumber region of interest, that is, the region between 700 and 3125 cm − 1 . Subsequently, the FT-IR data were baseline corrected using a SNIP algorithm 38 (iterations = 150, order = 2 and smoothing window = 3) and the area normalized to the IR peaks between 2750 and 3100 cm − 1 (1).
To determine whether Raman spectroscopy was suited to follow the polymerization and crosslinking process, the wavenumber-restricted and background-corrected spectra of BMA, PBMA, 1, the nine BMA-PBMA mixtures and the five mixtures of 1 with PBMA were area-normalized to the peak at 1451 cm − 1 (integrated from 1420 to 1490 cm − 1 ). This peak was attributed to CH deformation vibrations, which should have been similar for all studied substances. To follow the polymerization process, three Raman peaks were monitored: the C = C stretching vibration stemming from BMA at 1641 cm − 1 (integrated from 1610 to 1667 cm − 1 ), the = C-H stretching vibration stemming from BMA at 3107 cm − 1 (integrated from 3080 to 3140 cm − 1 ) and the = C-H deformation vibration also stemming from BMA at 1404 cm − 1 (integrated from 1385 to 1420 cm − 1 ). To monitor the urea content, the C = O stretching vibration at 1631 cm − 1 (integrated from 1614 to 1654 cm − 1 ) was used. Linear models were built using the mole fractions of BMA or compound 1 and the corresponding integrated band area (Supplementary Information; Supplementary Figures S39-S41). Using the described approach, the limit of detection for the BMA inside PBMA was~5 mol%, while the limit of detection for compound 1 inside PBMA was~2 mol%. The limit of detection was calculated using the respective peak area+3 × the s.d. of the peak area extracted from the Raman spectra of the pure PBMA. It is important to note that the simultaneous identification of BMA and 1 inside PBMA was possible. First, the BMA mole fraction was evaluated using the peak at 3107 cm − 1 , and after, the urea mole fraction was analyzed by integrating the overlapped peak at~1635 cm − 1 and subtracting the contribution of the afore-calculated BMA mole fraction (Supplementary Figures S39-S41).
To further investigate the self-healing mechanism of the present class of polymers and to validate the band assignments, quantum chemical calculations were performed. To reduce the computational demand, only the monomers N,N'-di-tert-butylethylenediamine, hexyl isocyanate, 2-isocyanatoethyl methacrylate, 1 and 2 were considered. All quantum chemical simulations were performed using DFT with the global hybrid functional B3LYP 39,40 and the 6-31+G(d,p) double-ζ basis set 41,42 implemented in the Gaussian 09 program. 43 The fully relaxed equilibrium structures of N,N'-di-tert-butyl-ethylenediamine, hexyl isocyanate, 2-isocyanatoethyl methacrylate, 1 and 2 were obtained, while the subsequent vibrational analysis determined the minima of the 3N − 6 dimensional potential energy (hyper)surfaces as well as the vibrational frequencies and IR and Raman intensities. To account for anharmonicity and the lack of electronic correlation, the frequencies were scaled by a factor of 0.964. 44,45 The calculated IR and Raman spectra were preprocessed (wavenumber region restriction, baseline/background correction and normalization) to make them comparable to the experimental IR and Raman spectra.

Experimental procedures
Synthesis of the model compound and the monomer. 1-1′-(Ethane-1,2-diybis (1-tert-butyl)-3-hexylurea) (1): Hexyl isocyanate (2.30 ml; 15.79 mmol) and 0.1 ml of dibutyltin dilaurate (0.17 mmol) were dissolved in 20 ml of dry toluene under nitrogen atmosphere. Subsequently, 1.7 ml of N,N'-di-tert-butylethylenediamine (7.88 mmol) was added slowly over 15 min. Afterwards, the reaction mixture was stirred at room temperature for 18 h. The solvent was removed, and the residual solid was dissolved in 200 ml of chloroform. The organic layer was washed with water (2 × 200 ml) and dried over sodium sulfate. After filtration and evaporation of the solvent, a white product was obtained.
The polymer network P4 was prepared according to the literature. 23 The pure PBMA, which was only utilized as a model substance for the Raman measurements, was also synthesized according to the previous literature reports. 16 Dissolution experiments of P1 in aniline. In a 20 ml microwave vial, 96 mg of P1 was suspended in 5 ml of freshly distilled aniline. Subsequently, the mixture was heated to 100°C for 48 h, and the complete dissolution of the polymer was observed. An size exclusion chromatography of the solution was measured.
As a control experiment, 113 mg of P1 was suspended in 5 ml of freshly distilled aniline and stirred for 48 h at room temperature. In that case, polymer dissolution was not observed, and soluble polymers were not present during the SEC measurement.

RESULTS AND DISCUSSION
To obtain dynamic networks based on urea bonds, a specific monomer was synthesized. In addition, a model substance was prepared to understand the mechanism of healing. For this purpose, N,N'-di-tert-butylethylenediamine, as a sterically hindered amine, was converted with either hexyl isocyanate, resulting in model compound 1, or with 2-isocyanate ethyl methacrylate, resulting in monomer 2-the reversible crosslinker. Both compounds were characterized via NMR and Raman spectroscopy ( Supplementary  Information; Supplementary Figures S4) to confirm the formation of urea bonds.
The prepared monomer was utilized to prepare the polymer networks. To obtain a sufficiently crosslinked system, an additional comonomer was required. Moreover, a comonomer with a relatively low glass transition temperature was desired to achieve sufficient mobility during the healing process. For this purpose, the solubility of 2 was evaluated in different commercially available comonomers. The synthesized crosslinker was not soluble in the methacrylates tested, such as BMA or lauryl methacrylate or even more polar monomers such as di(ethylene glycol) methyl ether methacrylate. Consequently, the bulk polymerization of 2 with the aforementioned comonomers was impossible. Thus, a different approach was utilized to obtain urea-crosslinked copolymers. 2-Isocyanatoethyl methacrylate and N,N'-di-tert-butylethylenediamine were directly mixed with the corresponding comonomer, that is, BMA and benzoin methyl ether (as initiator), as shown in Scheme 1. The homogeneous mixture was polymerized, resulting in a urea-crosslinked poly(methacrylate) network. The photopolymerization process included radical polymerization of the methacrylate moieties, as well as crosslinking via the formation of reversible urea bonds. Using this procedure, three different copolymer networks were prepared. The resulting copolymers featured different concentrations of reversible urea crosslinks (P1, P2 and P3 featured 5%, 10% and 50% urea crosslinks, respectively).
The presence of urea bonds, which were formed during polymerization, and the conversion of methacrylate were confirmed using Raman spectroscopy. The Raman spectrum of P2 is depicted in the supporting information (Supplementary Figure S35). In this context, the full conversion of the monomers (both urea formation and methacrylate polymerization) was evident from these spectra by monitoring the C = C double bond or the C-H stretching of the methacrylate as well as the C = O double bond of the urea. To prove the suitability of this method, a series of concentrations of either compound 1 or BMA in PBMA was analyzed ( Supplementary  Information; Supplementary Figures S39-S41). Thus, the limits of detection for the nonpolymerized methacrylate and urea bonds were 5% and 2%, respectively (for details of the characterization, see the experimental section; the graphs are depicted in the Supplementary  Information; Supplementary Figures S39-S41). In addition, the analysis of P2 revealed the full conversion of the methacrylate polymerization, and furthermore, the expected urea content of 10% was also found.
Moreover, the thermal properties were measured using DSC and thermogravimetric analysis. The copolymer networks P1 and P2 featured a glass transition temperature (T g ) of ca. 30-35°C, whereas no T g was observed for P3. Furthermore, the copolymers were thermally stable up to 190°C. However, the thermogravimetric analysis measurements revealed a two-step degradation process, which was presumably associated with the evaporation of the amine at  Supplementary Figures S14 and S15). These data revealed softening of the polymers at temperatures above 70 (P1) and 80°C (P2), respectively, which present comparable behavior with vitrimers. 46 In addition to the urea-crosslinked copolymers, a polymer network featuring no reversible crosslinker was prepared (P4). This material was obtained after the bulk polymerization of BMA and 1,6-hexanediol dimethacrylate according to procedures reported in the literature. 23 The degree of crosslinking was 5% and, thus, was comparable with P1.
The synthesized copolymer networks were investigated with respect to their self-healing behavior. For this purpose, scratch-healing tests, which are the standard technique for evaluating the healing behavior of coatings, 47 were performed. These experiments revealed that copolymer network P3 did not have self-healing abilities ( Supplementary Information; Supplementary Figure S3). Owing to its high crosslinking density, the flexibility of the network was significantly reduced, preventing crack closure. In contrast, the other two networks, P1 and P2, were capable of self-healing. The self-healing ability of P1 was higher (Figure 2; Supplementary Figure S1) than that of P2 (Supplementary Information; Supplementary Figure S2). In the case of P1, the scratch was healed within 10 min at 100°C. To undergo scratch healing, temperatures higher than 70°C were required. In contrast, P2 required longer self-healing times (60 min at 100°C) and higher temperatures (480°C) ( Supplementary Information; Supplementary Figure S2) due to the higher crosslinking density, which reduced the overall flexibility of the polymer network. Furthermore, P4, the reference polymer without any reversible moiety, featured no scratch-healing ability, as reported in the literature. 23 In addition to the scratch-healing tests, tensile testing was performed. For this purpose, the above-described bulk polymerization was performed in a Teflon mold to obtain dog bone-shaped specimens ( Supplementary Information; Supplementary Figure S22). First, the mechanical properties of the three virgin polymers were studied (see Supplementary Information for the diagrams; Supplementary  Figures S23-S26). The obtained average values are summarized in Table 3. The resulting materials were rather hard compared to many other self-healing polymers ( Figure 1) and featured excellent mechanical properties (E-moduli between 0.34 and 0.97 GPa). Such values are not obtained often for intrinsic self-healing systems, and the current materials are among the hardest intrinsically healable polymers, to the best of our knowledge, described in the literature (Figure 1). One other example of a self-healing material with a high E-modulus was described by Wudl and co-workers, who utilized a highly crosslinked polymer network (E-modulus: 3 GPa). 10,11 Subsequently, the polymers were cut into two pieces and brought back into contact. Afterwards, the specimens were heated to 100°C to initiate the healing process. Compared to the scratch-healing process, much longer healing times were required, which was due to the poor contact between the surfaces of the cut pieces, representing a general problem during tensile testing of self-healing polymers. 47 This behavior also limited the overall self-healing performance. In addition, the hardness of the material had a negative impact that could lead to reduced contact between the surfaces. To prove this assumption, the hardness of P1 was measured at 100°C using tensile testing ( Supplementary Information; Supplementary Figure S23). Even at high temperatures, E-modulus values 41 MPa were observed, which is a standard value of many other intrinsically healable polymers at room temperature ( Figure 1). Thus, this material still featured sufficient hardness at high temperatures compared to other self-healing systems. 10,36 These results indicate that neither depolymerization of the whole polymer nor complete decrosslinking occurred, which was further proven by testing the P4 reference, which featured comparable mechanical performance at both temperatures. Consequently, the mechanical integrity of the specimen was ensured. However, the mobility of the polymer network was lower compared to other very hard intrinsic self-healing polymers, indicating depolymerization behavior. As an example, the Diels-Alder polymer networks reported by Wudl and co-workers depolymerized completely during thermal treatment, resulting in a very mobile phase and, consequently, in efficient self-healing behavior. 10 However, during depolymerization and formation of the educts, the mechanical integrity was (partially) lost.
Thus, these novel urea-based materials became hard materials at room temperature, and even under the healing conditions, the residual mechanical performance was good (comparable to the mechanical properties of other reported self-healing polymers at room Scheme 1 Schematic representation of the synthesis of model compound 1 and copolymers P1-P3 using a photopolymerization process with benzoin methyl ether (BME) as the initiator and light between 320 and 520 nm.
Fabrication of intrinsic self-healing materials S Zechel et al temperature). Thus, the materials presented here are among the few intrinsically healable polymers with very good mechanical properties ( Figure 1).
Nevertheless, the healing efficiency of the bulk materials was not optimal. In contrast, the E-modulus could be regenerated nearly completely. However, the healing efficiency based on the maximal stress values was 50% for P1, which is quite high for such a hard material (Table 1). Comparable hard materials were reported by Wudl et al., and the authors reported a healing efficiency of~50% even under nearly complete depolymerization of the network. 10 Furthermore, there were differences in the self-healing abilities of the different copolymer networks. The highest efficiency was obtained for P1 and the lowest efficiency was obtained for the highly crosslinked P3 material. For P3, higher temperatures were required to enable bulk healing, that is, 120°C. Furthermore, the higher degree of crosslinking also led to a harder material and thus the contact between the broken specimen was reduced, as mentioned above. 47 In addition to both healing tests (the scratch-healing and tensile tests), the molecular mechanism was investigated. For this purpose, different techniques were utilized, such as DSC and Raman and IR spectroscopy. All corresponding spectra are depicted in the Supplementary Information. The polymers and model compound 1 were investigated regarding the thermal behavior. This compound featured a melting point at 98°C, which was confirmed from the DSC measurement during the first heating run ( Supplementary  Information; Supplementary Figure S7). Furthermore, the compound was analyzed using FT-IR spectroscopy at different temperatures, and the urea bonds opened during thermal treatment at 100°C. This observation was confirmed by the appearance of the specific signal of the isocyanate moiety at 2300 cm − 1 , proving the reversibility of the urea bonds (Figure 3). Thus, the melting of the compound at 98°C was associated with the opening of the reversible bonds.
The same experiment was performed with P2, and the resulting spectra are depicted in the Supplementary Information. In addition,  Fabrication of intrinsic self-healing materials S Zechel et al temperature-dependent Raman spectroscopy measurements were performed. However, both analytical methods revealed no structural changes, and the spectra did not change during thermal treatment under the healing conditions. Thus, the isocyanate band was not observed. The urea-isocyanate equilibrium did not shift significantly during heating to 100°C, as opposed to the equilibrium found for model compound 1. As a result, the self-healing mechanism of these systems was based on reversible exchange reactions between the urea crosslinks in the copolymer network. Presumably, a small number of reversible bonds were opened during thermal treatment, but the exchange and rebinding process to other amine functionalities was too fast to detect using steady-state spectroscopic measurements. Furthermore, the absence of any changes within the Raman spectra also revealed the molecular integrity of the polymer network. However, at much higher temperatures (150°C), slight bond opening was also observed in the FT-IR spectroscopy results for polymer P2 (Supplementary Information; Supplementary Figure S38). Furthermore, frequency-dependent rheology measurements were performed at three different temperatures using polymers P1 and P2 (80, 100 and 120°C; Supplementary Information; Supplementary  Figures S16-S21). In all cases, a crossover between Gʹ and Gʺ was observed within in the range of 0.90-24.13 Hz (Supplementary  Information; Supplementary Table S1). Consequently, these materials featured sufficient flow at these temperatures and still revealed reversible network properties. In case of the supramolecular systems, the crossover between Gʹ and Gʺ in a certain frequency regime could be correlated to the supramolecular bond lifetime and the self-healing properties. Thus, times in the range of 1 μs ⩽ τ ⩽ 60 s (the corresponding frequencies were 0.02-1.000.000 Hz) could be correlated to the excellent healing properties. 17  Moreover, the Gʹ value at very low frequencies was greater than the Gʺ value. Both findings revealed the presence of the network structure at the healing temperatures, indicating that dynamic exchange reactions provided the healing mechanism. 48 In addition, these findings could also be observed within the DSC measurements. In contrast to model compound 1, an endothermic signal at 100°C was not observed for polymers P1-P3. Furthermore, the temperature-dependent mechanical performance of P1 (in particular, compared to P4) proves this hypothesis, as complete opening of the bonds would have resulted in an enormous loss in the mechanical performance. Thus, the self-healing mechanism was presumably based on exchange reactions between the dynamic urea bonds. Final evidence of the exchange reactions was revealed by stirring polymer P2 for 24 h in aniline at 100°C. Afterwards, the polymer was completely dissolved, which allowed us to perform SEC measurements (Supplementary Information; Supplementary Figure S6), which revealed a soluble polymer with a molar mass of M n = 5300 g mol − 1 .

CONCLUSION
In conclusion, the fabrication of new intrinsic self-healing materials with excellent mechanical properties was reported. The systems are based on crosslinked methacrylates featuring dynamic urea bonds as reversible crosslinking moieties. These functional units can be reversibly opened during thermal treatment due to the utilization of sterically hindered amine groups. To obtain these copolymer networks, urea bonds were formed in situ during photopolymerization. The structural changes in the model compound (opening of the reversible urea bonds) and the corresponding healing mechanism were analyzed using Raman and IR spectroscopy. The self-healing behavior was studied using scratch and bulk-healing tests. Much better scratch-healing behavior compared to the bulk-healing behavior was revealed, which was associated with the reduced contact between sections of the broken specimen during the bulk-healing experiments. Furthermore, the crosslinking density was a crucial parameter for the self-healing performance. Thus, using 5% crosslinker produced hard materials (E-modulus: 0.34 GPa) with excellent scratch-healing and acceptable bulk-healing properties at temperatures above 70°C.
The investigated system is a new representative for smart and stimuli-responsive materials, and further work will be directed toward an application driven investigation. In addition, additional analysis of the molecular behavior will be performed to obtain a detailed overview of the structural changes in the system during external stimulation. The results presented here are the first step toward hard and intrinsically healable polymers, which are usually considered to be an oxymoron. 49