Greta
Becker
ab,
Zhuoling
Deng
c,
Maria
Zober
c,
Manfred
Wagner
a,
Karen
Lienkamp
*c and
Frederik R.
Wurm
*a
aMax-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany. E-mail: wurm@mpip-mainz.mpg.de
bGraduate School Materials Science in Mainz, Staudinger Weg 9, 55128 Mainz, Germany
cBioactive Polymer Synthesis and Surface Engineering Group, Department of Microsystems Engineering (IMTEK) and Freiburg Center for Interactive Materials and Bioinspired Technologies (FIT), Georges-Köhler-Allee 105, 79110 Freiburg, Germany. E-mail: lienkamp@imtek.uni-freiburg.de
First published on 19th December 2017
Photo-reactive poly(phosphoester)s (PPEs) forming surface-attached PPE-networks and hydrogels are presented. These contain benzophenone groups, which can photochemically cross-link polymer films via a C,H-insertion cross-linking (CHiC) reaction. To make the target polymers, a benzophenone-functionalized cyclic phosphate monomer was synthesized and copolymerized with ethylene ethyl phosphate (EEP). Polymerization with EEP and further cyclic phosphates gave terpolymers with additional chemical functionality (e.g. furfuryl or alkene groups). The resulting PPE copolymers and terpolymers were water-soluble and UV-reactive. Copolymerization kinetics of up to three different comonomers were studied by real-time 31P NMR, indicating a gradient-like structure of the copolymers and terpolymers. Cross-linked, surface-attached PPE-networks were formed by spin-coating these polymers onto pre-functionalized substrates, followed by UV irradiation. The resulting surface-attached polymer networks were smooth and hydrophilic (static contact angles of 20–26°). Since PPEs are biocompatible, these networks might be potential anti-fouling coatings for biomedical devices as implants or catheters. The furan and alkenyl groups in two of the terpolymers present a selectively addressable chemical function to further tune the surface properties of PPE-films.
Examples for substance classes that resist biofilm formation are hydrophobic poly(dimethylsiloxane) (PDMS)-based5 or fluorinated6 polymers, which might be used for coating of ship hulls or pipelines. They are classified as “fouling release” coatings: while they have a high interfacial energy with water, which enables amphiphilic proteins to attach to them, these biofoulants can be easily removed by shear stress, e.g. by stress due to hydrodynamic flow.7
“Non-fouling” coatings, on the other hand are typically hydrophilic polymers and have a low interfacial energy with water, leading to lower protein adsorption.7 Prominent protein-repellent examples include poly(ethylene glycol) (PEG)-based polymers, amphiphilic polymer coatings (including those with heterogeneities on the nanoscale prepared from block copolymers), oligosaccharide-containing polymers mimicking the glycocalyx of blood vessels, and zwitterionic polymers.4,7 PEG is particularly well-known to suppress protein adhesion on nanocarriers (“stealth effect”), which led to several PEGylated nanocarriers already in clinical use, and is also the gold standard for macroscopic surfaces with low protein adsorption.8,9 Polyzwitterionic surface-attached networks are also strongly protein-repellent;10–12 a polyzwitterion surface with protein repellency, cell-compatibility, and antimicrobial activity was also recently reported.13
The aim of this study was to explore the potential of poly(phosphoester) (PPE)-based surface-attached networks as potentially protein-repellent coatings. These form hydrogels when immersed into aqueous media. Many PPEs have been reported to be biocompatible and to have low cytotoxicity.14 In particular, poly(ethyl ethylene phosphate) (PEEP), which is hydrophilic15 and protein-repellent, can be considered as a degradable analog of PEG. For example, PPEylated nanoparticles or proteins that were obtained by grafting PPE chains exhibited reduced protein adsorption and low interaction with human immune cells and were thus very similar to PEGylated nanocarriers.9,16,17
To study the bioactivity of PPEs on macroscopic planar surfaces, we designed PPE-copolymers and terpolymers that can form surface-attached polymer networks by simultaneous photo-induced inter-chain crosslinking and surface attachment (Scheme 1). The advantage of this method of surface functionalization is that it is straightforward, efficient and that the thickness of the coating can be tuned over a wider range than when using other methods (e.g. grafting-from or grafting-onto methods, where the coating thickness depends on the molecular weight of the polymer used).
Scheme 1 (a) Terpolymers used in this study to form surface-attached PPE-networks; (b) CHiC process for UV-activated cross-linking and surface-attachment of PPEs using benzophenone. |
The target polymers consist of the EEP repeat units, repeat units carrying a UV-cross-linkable benzophenone group, higher homologous of EEP, and optionally functional repeat units (Scheme 1a). To be able to make these polymers, we synthesized a novel monomer consisting of a cyclic phosphate and a benzophenone side chain (BeEP, Scheme 2). The BeEP monomer (1) was copolymerized with the protein-repellent EEP monomer (2), its homologs (3 and 4) and optionally other cyclic phosphates carrying functional groups (5 and 6) by ring-opening polymerization (ROP). The resulting copolymers are water-soluble and can be cross-linked by a UV-activated C,H-insertion cross-linking reaction (the so-called CHiC process, Scheme 1b and Scheme S1†).18–20
Scheme 2 (a) Synthesis of 4-(2-hydroxyethoxy) benzophenone; (b) synthesis of cyclic phosphate monomers; (c) cyclic phosphate monomers used in this study. |
As has been described previously for other polymeric systems,18–20 the benzophenone groups in these polymers form a biradical upon UV irradiation, leading to the abstraction of a proton from a nearby alkyl group. When this radical on the former carbonyl C atom of benzophenone collapses with the C radical on the alkyl chain, a covalent bond and thus an inter-chain cross-link is formed (Scheme 1b). Advantageously, the benzophenone group does not need a specific reaction partner but can react with most aliphatic CH groups, so that a polymeric network is formed.20–23 This concept was introduced by Rühe and coworkers into polymer chemisty; they used copolymers containing covalently attached benzophenone to prepare surface-attached polymer networks and hydrogels, e.g. made from dimethylacrylamide and methacryloyloxybenzophenone.23
We here report the synthesis, copolymerization kinetics, and characterization of several benzophenone-containing PPE-copolymers with various pendant groups with different overall hydrophilicity and number of reactive C–H-bonds for the ChiC process. We further present films made from these polymers on silicon surfaces, as well as their characterization. First results of surface modification of these films by Diels–Alder reactions, give an idea how to build up more complex surface architectures from these materials.
P1: EEP (993 mg, 6.53 mmol, 142 eq.), BeEP (128 mg, 368 μmol, 8 eq.), DBU (56 mg, 368 μmol, 8 eq.), TU (136 mg, 368 μmol, 8 eq.), initiator (7 mg, 46 μmol, 1 eq.). Yield: 921 mg, 80%. Mn(NMR): 38600 g mol−1. 1H-NMR (300 MHz, DMSO-d6): δ [ppm] 7.76–7.53 (m, 86H Ar–C(O)–Ar–O–CH2–CH2–O–P–), 7.33 (m, 5H, Ar–, initiator), 7.14–7.08 (m, 22H, Ar–C(O)–Ar–O–CH2–CH2–O–P–), 4.47–3.84 (m, 1450H, Ar–C(O)–Ar–O–CH2–CH2–O–P–, –P–O–CH2–CH3, –O–CH2–CH2–O–, backbone), 1.26 (t, 676, –CH3).31P{H} NMR (121 MHz, DMSO-d6): δ [ppm] −1.24, −0.99.
P2: EEP (881 mg, 5.80 mmol, 126 eq.), BeEP (128 mg, 368 μmol, 8 eq.), PEP (143 mg, 736 μmol, 16 eq.), DBU (56 mg, 368 μmol, 8 eq.), TU (136 mg, 368 μmol, 8 eq.), initiator (7 mg, 46 μmol, 1 eq.). Yield: 1002 mg, 83%. Mn(NMR): 21000 g mol−1. 1H-NMR (300 MHz, DMSO-d6): δ [ppm] 7.76–7.52 (m, 58H Ar–C(O)–Ar–O–CH2–CH2–O–P–), 7.33 (m, 5H, Ar–, initiator), 7.14–7.05 (m, 16H, Ar–C(O)–Ar–O–CH2–CH2–O–P–), 4.47–3.87 (m, 847H, Ar–C(O)–Ar–O–CH2–CH2–O–P–, –P–O–CH2–CH3, –P–O–CH2–CH2–CH2–CH2–CH3, –O–CH2–CH2–O–, backbone), 1.70–1.51 (m, 30H, –P–O–CH2–CH2–CH2–CH2–CH3), 1.35–1.16 (m, 404H, –P–O–CH2–CH2–CH2–CH2–CH3, –P–O–CH2–CH3), 0.87 (t, 42H, –P–O–CH2–CH2–CH2–CH2–CH3). 31P{H} NMR (121 MHz, DMSO-d6): δ [ppm] −1.24, −1.14, −0.98, −0.89.
P3: EEP (268 mg, 1.76 mmol, 134 eq.), BeEP (37 mg, 105 μmol, 8 eq.), EBP (22 mg, 105 μmol, 8 eq.), DBU (16 mg, 105 μmol, 8 eq.), TU (39 mg, 105 μmol, 8 eq.), initiator (2 mg, 13 μmol, 1 eq.). Yield: 269 mg, 82%. Mn(NMR): 28600 g mol−1. 1H-NMR (500 MHz, DMSO-d6): δ [ppm] 7.78–7.51 (m, 48H Ar–C(O)–Ar–O–CH2–CH2–O–P–), 7.33 (m, 5H, Ar–, initiator), 7.16–7.06 (m, 13H, Ar–C(O)–Ar–O–CH2–CH2–O–P–), 4.42–3.99 (m, 1051H, Ar–C(O)–Ar–O–CH2–CH2–O–P–, –P–O–CH2–CH3, –O–CH2–CH2–O–, backbone), 3.99–3.87 (m, 34H, –P–O–CH2–CH–(CH2–CH3)2), 1.36–1.29 (m, 17H, –P–O–CH2–CH–(CH2–CH3)2), 1.26 (m, 479H, –P–O–CH2–CH–(CH2–CH3)2, –P–O–CH2–CH3), 0.86 (t, 72H, –P–O–CH2–CH–(CH2–CH3)). 31P{H} NMR (202 MHz, DMSO-d6): δ [ppm] −1.25, −1.01, −0.99.
P4: EEP (881 mg, 5.80 mmol, 126 eq.), BeEP (128 mg, 368 μmol, 8 eq.), FEP (183 mg, 736 μmol, 16 eq.), DBU (56 mg, 368 μmol, 8 eq.), TU (136 mg, 368 μmol, 8 eq.), initiator (7 mg, 46 μmol, 1 eq.). Yield: 907 mg, 76%. Mn(NMR): 34500 g mol−1. 1H-NMR (300 MHz, DMSO-d6): δ [ppm] 7.76–7.52 (m, 108H Ar–C(O)–Ar–O–CH2–CH2–O–P–, –P–CH2–CH2–O–CH2–C–O–CHCH–CH), 7.33 (m, 5H, Ar–, initiator), 7.14–7.05 (m, 22H, Ar–C(O)–Ar–O–CH2–CH2–O–P–), 6.43 (s, 44H, –P–CH2–CH2–O–CH2–C–O–CHCH–CH), 4.45 (s, 53H, –P–CH2–CH2–O–CH2–C–O–CHCH–CH), 4.27–3.88 (m, 1167H, Ar–C(O)–Ar–O–CH2–CH2–O–P–, –P–O–CH2–CH3, –P–CH2–CH2–O–CH2–C–O–CHCH–CH, –O–CH2–CH2–O–, backbone), 3.59 (s, 107H, –P–CH2–CH2–O–CH2–C–O–CHCH–CH), 1.26 (t, 494H, –P–O–CH2–CH3). 31P{H} NMR (121 MHz, DMSO-d6): δ [ppm] −1.29 to −1.18, −0.98, −0.89.
P5: EEP (881 mg, 5.80 mmol, 126 eq.), BeEP (128 mg, 368 μmol, 8 eq.), BuEP (131 mg, 736 μmol, 16 eq.), DBU (56 mg, 368 μmol, 8 eq.), TU (136 mg, 368 μmol, 8 eq.), initiator (7 mg, 46 μmol, 1 eq.). Yield: 1048 mg, 84%. Mn(NMR): 46300 g mol−1. 1H-NMR (300 MHz, DMSO-d6): δ [ppm] 7.79–7.49 (m, 95H Ar–C(O)–Ar–O–CH2–CH2–O–P–), 7.33 (m, 5H, Ar–, initiator), 7.16–7.05 (m, 25H, Ar–C(O)–Ar–O–CH2–CH2–O–P–), 5.87–5.72 (m, 20H, –P–O–CH2–CH2–CHCH2), 5.17–5.06 (m, 51H, –P–O–CH2–CH2–CHCH2), 4.46–3.88 (m, 1720H, Ar–C(O)–Ar–O–CH2–CH2–O–P–, –P–O–CH2–CH3, –P–O–CH2–CH2–CHCH2, –O–CH2–CH2–O–, backbone), 2.44–2.32 (m, 61H, –P–O–CH2–CH2–CHCH2), 1.26 (t, 729H, –P–O–CH2–CH3). 31P{H} NMR (121 MHz, DMSO-d6): δ [ppm] −1.28, −1.24, −0.99.
P6: EEP (937 mg, 6.16 mmol, 134 eq.), BuEP (131 mg, 736 μmol, 16 eq.), DBU (56 mg, 368 μmol, 8 eq.), TU (136 mg, 368 μmol, 8 eq.), initiator (7 mg, 46 μmol, 1 eq.). Yield: 942 mg, 85%. Mn(NMR): 28100 g mol−1. 1H-NMR (300 MHz, DMSO-d6): δ [ppm] 7.34 (m, 5H, Ar–, initiator), 5.87–5.72 (m, 24H, –P–O–CH2–CH2–CHCH2), 5.20–5.05 (m, 43H, –P–O–CH2–CH2–CHCH2), 4.51 (s, 2H, Ar–CH2–O–, initiator), 4.26–3.98 (m, 1058H, –P–O–CH2–CH3, –P–O–CH2–CH2–CHCH2, –O–CH2–CH2–O–, backbone), 2.42–2.38 (q, 46H, –P–O–CH2–CH2–CHCH2), 1.26 (t, 468H, –P–O–CH2–CH3). 31P{H} NMR (121 MHz, DMSO-d6): δ [ppm] −1.27, −1.24, −0.98.
P1, P2, P4, P5: FTIR (cm−1): 3660–3358 (O–H stretching), 2983 (–CH2– and –CH3 stretching), 2957 (–CH2– and –CH3 stretching), 2911 (–CH2– and –CH3 stretching), 1652 (diaryl-CO), 1601 (CC stretching), 1508 (CC stretching), 1454 (–CH2– deformation), 1394 (O–CH2– deformation), 1372 (–CH3 deformation), 1267 (PO stretching), 1167 (–CH3 rocking), 1123 (–CH3 rocking), 1015 (P–O–C stretching), 958 (P–O–C stretching), 797 (O–CH2– stretching), 742 (–CH2– rocking), 704, 683.
P6: FTIR (cm−1): 3660–3358 (O–H stretching), 2983 (–CH2– and –CH3 stretching), 2957 (–CH2– and –CH3 stretching), 2911 (–CH2– and –CH3 stretching), 1642 (CC stretching), 1454 (–CH2– deformation), 1394 (O–CH2– deformation), 1372 (–CH3 deformation), 1267 (PO stretching), 1167 (–CH3 rocking), 1123 (–CH3 rocking), 1015 (P–O–C stretching), 958 (P–O–C stretching), 797 (O–CH2– stretching), 738 (–CH2– rocking), 704, 683.
For pre-functionalization with trimethox(propyl)silane and (3-aminopropyl)triethoxysilane, ethanol solutions with a total concentration of 50 mM were prepared: (a) propyl/amine ratio of 5:1, 20.5 mg (0.125 mmol, 5 eq.) trimethox(propyl)silane and 5.5 mg (0.0249 mmol, 1 eq.) (3-aminopropyl)triethoxysilane in 3 mL ethanol; (b) propyl/amine ratio of 2:1, 16.4 mg (0.099 mmol, 2 eq.) trimethox(propyl)silane and 11.1 mg (0.050 mmol, 1 eq.) (3-aminopropyl)triethoxysilane in 3 mL ethanol; (c) propyl/amine ratio of 1:1, 12.3 mg (0.075 mmol, 1 eq.) trimethox(propyl)silane and 16.6 mg (0.075 mmol, 1 eq.) (3-aminopropyl)triethoxysilane in 3 mL ethanol. The Si wafer was cut in 1.5 × 1.5 cm sized substrates and a solution of (a), (b) or (c) was spin coated on the substrates at 1000 rpm, 1000 rpm/sec for 30 s. The substrates were cured for 45 min at 120 °C on a hot plate, washed with DCM, and dried under a continuous nitrogen flow.
Pre-functionalization with 3-butenyltriethoxysilane and (3-aminopropyl) triethoxysilane was achieved in the same way with a total silane concentration of 50 mM in ethanol. The butenyl/amine ratios were 5:1, 2:1, or 1:1, respectively.
Fig. 1 (a) SEC elugrams of all co- and terpolymers (in DMF, RI signal), (b) DSC thermograms of all co- and terpolymers (heating and cooling rate 10 K min−1, 1st run). |
2-Ethoxy-2-oxo-1,3,2-dioxaphospholane EEP (2) was synthesized as a second monomer (Scheme 2). EEP forms the water-soluble polymer PEEP, which is usually used as hydrophilic building block in PPE-based drug delivery systems,29,30 and was the major comonomer in the polymers synthesized herein. Further cyclic comonomers used in this study were 2-pentyloxy-2-oxo-1,3,2-dioxaphospholane (PEP, 3), 2-(2-ethyl butoxy)-2-oxo-1,3,2-dioxaphospholane (EBP, 4),31 2-(2-(furan-2-ylmethoxy)ethoxy)-2-oxo-1,3,2-dioxaphospholane (FEP, 5)32 and 2-(but-3-en-1-yloxy)-2-oxo-1,3,2-dioxaphospholane (BuEP, 6).24 Monomers 3 and 4 were used because they contained a larger number of aliphatic CH– groups than EEP and thus served as reaction partner for the benzophenone moieties. FEP (5) and BuEP (6) additionally carry functional groups that are inert under ROP conditions but reactive in Diels–Alder or thiol–ene reactions. These groups can be used for the post-polymerization functionalization of either the polymer or polymer networks.
Scheme 3 (a) Copolymerization of cyclic phosphates by ROP, (b) co- and terpolymers P1–P6 obtained herein. |
[I]/[1]/[2]/ [3/4/5/6] | DPtha | 1/DPb | 1/%c | 2/DPb | 2/% c | 3/4/5/6/DPb | 3/4/5/6/% | M n b (kg mol−1) | M w/Mnd | T g / °C | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|
a DPth = theoretical degree of polymerization. b DP = degree of polymerization of monomer 1 or 2 determined from the 1H-NMR spectra. c Percentage of comonomer 1 or 2 (determined from NMR). d Determined by SEC in DMF, PEO standard, RI-signal. e Determined by DSC. | ||||||||||||
P1 | 1-co-2 | 1/8/142/— | 150 | 12 | 5 | 225 | 95 | — | 38.6 | 1.16 | −48 | |
P2 | 1-co-2-co-3 | 1/8/126/16 | 150 | 8 | 6 | 115 | 83 | 15 | 11 | 21.0 | 1.16 | −58 |
P3 | 1-co-2-co-4 | 1/8/134/8 | 150 | 7 | 4 | 160 | 91 | 8 | 5 | 28.6 | 1.19 | −56 |
P4 | 1-co-2-co-5 | 1/8/126/16 | 150 | 11 | 6 | 165 | 83 | 22 | 11 | 34.5 | 1.15 | −51 |
P5 | 1-co-2-co-6 | 1/8/126/16 | 150 | 13 | 5 | 243 | 86 | 26 | 9 | 46.3 | 1.16 | −50 |
P6 | 2-co-6 | 1/-/134/16 | 150 | — | — | 156 | 87 | 23 | 13 | 28.1 | 1.10 | −57 |
All polymerizations were carried out with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and N-cyclohexyl-N‘-(3,5-bis(trifluoromethyl)phenyl) thiourea (TU) as catalyst system24 at 0 °C in dry DCM, at a total monomer concentration of 4 mol L−1. The polymers were soluble in non-polar organic solvents such as dichloromethane and chloroform, or polar solvents such as THF, ethanol, methanol, and DMSO. They were insoluble in hexane or diethyl ether. Successful copolymerization and formation of copolymers was proven by size exclusion chromatography (SEC) and 31P{H} NMR measurements. An overview of the analytical data thus obtained is given in Table 1. It demonstrates that the PPE-based polymers had narrow molecular weight distributions (Đ = 1.10–1.19, Fig. 1, Table 1) and relatively high monomer conversions (76–84%). This indicates the controlled nature of the polymerization using the DBU/TU catalyst system. The shift of the phosphorus signals in the 31P{H} NMR spectra (16.83 to 17.90 ppm for the monomers, −0.89 to −1.28 ppm for the polymers) also confirmed that polymer was obtained (see ESI for details†).
Additional 1H DOSY spectra were used to confirm that the polymers obtained were indeed copolymers and not a mixture of different homopolymers (see ESI for details†). Additionally, the aromatic protons of the initiator 2-(benzyloxy)ethanol were used for molecular weight calculations by end group analysis from 1H NMR spectra. End group analysis revealed that the degree of polymerization varied from 138–282 for the polymers, i.e. molecular weights of 21000 to 46300 g mol−1 were obtained under these conditions. 1H NMR spectra of P2 and P4 show the resonances of the aromatic protons in the initiator at 7.33 ppm (signal b in Fig. 2), which were compared with distinct resonances of the three different repeat units in the polymer: the doublet signal at 7.10 ppm (c in Fig. 2) of the BeEP repeat units, the signal at 1.60 ppm (e in Fig. 2) of the PEP units in P2, the singlet at 6.43 ppm (d in Fig. 2) of FEP units in P4, and the triplet signal at 1.26 ppm (f or h in Fig. 2) which belongs to the EEP repeat unit. The signal of the backbone and the methylene groups in the side chains neighboring the P–O bond at 4.50–3.80 ppm (d or f in Fig. 2) gives the degree of polymerization compared to the initiator resonances and coincides with the total number of monomer repeat units (Fig. 2). This 1H NMR analysis shows that the initial feed ratios of the comonomers matched the repeat unit composition of the copolymers. All copolymers exhibited glass transition temperatures (Tg) of −57 to −48 °C, which is typical for PPEs obtained via ROP (Fig. 1).27
Fig. 2 1H NMR spectra (300 MHz, DMSO-d6) of (a) the BeEP monomer (1), (b) terpolymer P2, and (c) terpolymer P4. |
In all cases, the statistical copolymerization of the above monomers gave a significantly faster incorporation of BeEP than of EEP, while the consumption of FEP and PEP was, within the limit of the method, comparable to that of EEP (with FEP being only slightly faster incorporated, Fig. 3b–d). For example, for P1 at 40% total conversion, 60% of BeEP was consumed, while 80% of EEP monomer remained in the reaction mixture (Fig. 3b). Likewise, for P2 at 40% conversion, 70% of BeEP was consumed, while 75% of EEP and PEP, respectively, remained in the reaction mixture. In P4, 62% of BeEP was consumed after 40% conversion, while 78% EEP remained. Reactivity ratios were also determined from the thus obtained data. For the copolymerization of BeEP and EEP (P1), the reactivity ratios obtained were r1 = 3.5 and r2 = 0.3 (from the current dataset). These indicate a repeat unit gradient in P1 with BeEP being the preferred comonomer (details and further can be found in the ESI†). Care must be taken not to over-interpret the values. They show a reactivity trend but should not be taken as absolute values, because the reaction rates in ROP, as in most anionic polymerization reactions, are high. Fitting of the curves for the other polymer systems (Fig. 3) also indicated that these were gradient copolymers. They were benzophenone-rich up to about 30% total conversion (50% BeEP conversion), and then rich in non-crosslinkable repeat units. The relative reactivity of the comonomers during the copolymerization was thus BeEP ≫ FEP > PEP ≈ EEP. This means that there was also a polarity gradient in these polymers since BeEP is more hydrophobic than EEP. This fact was not further considered in this study of film formation, but will be analyzed in future work.
Additionally, when attempting to prepare networks from polymer P1, the films obtained could be washed off after UV-irradiation, indicating insufficient cross-links inside the network. Apparently, polymer P1, with 95% PEE repeat units, did not contain a sufficient amount of C–H bonds to which productive cross-links could be formed. The terpolymers P2 to P4, on the other hand, with 5% 2-ethyl butyl, 10% pentyl or furfuryl side chains, had significantly more aliphatic C–H groups. P2 and P4 accordingly formed stable surface-attached networks on substrates pre-functionalized with benzophenone and amine (ratio of 1:1) after UV-irradiation. After washing to remove unbound polymer, the layer thicknesses were 164 ± 1 nm for P4, and 78 ± 1 nm for P2 (determined by ellipsometry). P3 (containing EBP units) formed a smooth layer on these pre-functionalized substrates, but after washing the layer was removed completely. This was unexpected because this polymer also contained many aliphatic CH groups and is not yet fully understood. It is possible that the benzophenone cross-linker, which was previously reported to cause polymer main chain cleavage as a side reaction for several polymer backbones,33,34 also had this effect on the poly(phosphoester) backbone. Thus, overall, the functionalization of surfaces with PEE copolymers using benzophenone as cross-linker is far from trivial, and the substrate and polymer structures need to be carefully matched to avoid surface dewetting and/or insufficient cross-linking during network formation.
Since the PPE-networks were intended as surface-coatings for biomedical devices, it would be advantageous if they could be used on polymer surfaces without a substrate pre-functionalization step. Many polymeric materials (e.g. PMMA, poly(amides)- or -poly(urethanes)) contain a high amount of aliphatic CH groups, and are thus accessible for the CHiC reaction, as shown by Rühe and coworkers.35,36 However, technical polymer substrates cannot be studied with many of the surface analytical techniques used herein (which either need reflective, IR-transparent or very smooth substrates). Therefore, this situation was modeled on silicon wafers by pre-functionalizing them with propyl silanes (to imitate the aliphatic the C–H groups of a polymer substrate) and 3-aminopropyl silanes (to make the surface more hydrophilic). Different ratios of propyl silane to 3-aminopropyl silane (5:1, 2:1 and 1:1) were used.
Polymers P2 and P4 indeed formed surface-attached networks on these substrates, which demonstrated that these PPE polymers can be used to react with substrates that do not carry benzophenones. As is well known, the thickness obtained by spin-coating depends, among other parameters, on the concentration of the polymer solution. The here used polymers complied with this rule, and a “master curve” of layer thickness vs. polymer concentration for P4 is shown in Fig. S50.† Additionally, an influence of hydrophilicity on the thickness of the polymer layers obtained was noticed (Fig. 4): with increasing hydrophilicity of the pre-functionalized substrates, the layer thickness of these coatings increased from 132 ± 2 to 199 ± 2 nm for P4, and from 56 ± 1 to 104 ± 1 nm for P2 (Table S3,†Fig. 4). Thus, PPE-films can spread more easily on the more hydrophilic substrates. This is not only important in the context of spin-coating, which is rarely used to make biomaterials, but also when using these polymers in combination with other coating techniques. It indicates that the surface of the biomaterial must be hydrophilized prior to applying these coatings. A layer thickness of 263 ± 1 nm was observed for P5-networks. When multilayers of two or three films were prepared from P2 and P4, an increase of thicknesses was observed with each layer added (Table S3†). However, these multilayers became visibly less homogeneous and were therefore not further considered in this study.
The physical properties of the surface-attached polymer networks made from P2, P4 and P5 on Si wafers that had been pre-functionalized with a propyl/amine silanes at a ratio of 1:1 were thoroughly characterized. Besides the thickness measured by ellipsometry (Fig. 4 and Table 2), contact angle measurements were performed. These revealed that the materials were highly hydrophilic, with static contact angels of 21, 26 and 26° for P2, P4, and P5, respectively (Fig. 5, Table 2, and Table S2†). This is in line with the expectations since the main comonomer EEP is known to produce hydrophilic PPEs. Atomic force microscopy (AFM) was used to investigate the morphology of the P2 and P4 networks. Height images (Fig. 5) showed a homogeneous morphology of the networks with an average roughness of 0.40 nm for P2, 0.68 nm for P4, and 0.59 nm for P4. Networks of P4 showed nanometer-sized pinholes, probably to minimize the contact area with the comparatively hydrophobic substrate surface. Additional AFM images are shown in the ESI (Fig. S52†). The film morphology was further characterized by scanning electron microscopy (SEM, Fig. S53 of the ESI†). For this, a wafer piece with a P4 coating was frozen in liquid nitrogen and freeze-fractured. The fracture location (i.e. a cross-section perpendicular to the wafer surface) was then investigated by SEM. The images show that the polymer film is very dense. Even at the highest magnification, no internal pores were visible.
Fig. 5 AFM height images of PPE-networks, photographs of the coated silicon substrates and photographs their static contact angle with water: (a) P2 networks and (b) P4 networks. |
Polymer | Dry layer thickness on silicon/nm | Static contact angle/° | Roughness (Rq)/nm |
---|---|---|---|
P2 | 104 ± 1 | 21 ± 1 | 0.40 |
P4 | 199 ± 2 | 26 ± 3 | 0.68 |
P5 | 263 ± 1 | 26 ± 1 | 0.59 |
The PPE networks were further analyzed by FT-IR spectroscopy and compared with spectra of the monomers and polymers. All spectra are shown in the ESI.† These spectra confirmed that the expected IR bands were present. The dominant bands in the monomer spectra (PO stretching at 1282–1285 cm−1 and P–O–C stretching at 831–884, 980–1005 and 1016–1025 cm−1) could be retrieved in the polymer spectra at 1267, 797, 958 and 1015 cm−1, respectively.37,38 They all exhibited a shift and broadening of the band because of the formation of a linear backbone containing the phosphate groups compared to the strained rings of monomers. Characteristic bands of –CH2, O–CH2 and –CH3 stretching and rocking of EEP monomer at 752, 1100, 1166, 1369, 1393, 1445, 2915 and 2985 cm−1, respectively, could also be observed in all polymer spectra, albeit with slight wavenumber shifts. Further characteristic bands for the pentyl, furfuryl or butenyl groups in the side chains from the comonomers PEP, FEP, and BuEP in P2, P4 and P5 could not be observed because the above-mentioned signals were dominant and all polymers contained the latter repeat units only in small amounts. Characteristic bands of the BeEP monomer could be observed in polymers P1 to P5: a carbonyl band at 1601 cm−1 (at 1601 cm−1 in the monomer spectrum of BeEP) and aromatic CC stretching signals at 704, 1508 and 1652 cm−1 (703, 1505 and 1643 cm−1 in the monomer BeEP). In polymer P6 (only containing EEP and BuEP), a CC stretching band of an alkene group at 1641 cm−1 could be retrieved, in which was also found for the BuEP monomer. In IR spectra of the PPE-networks of P2, P4 and P5 on Si substrates, the dominant signals for PO stretching at 1275 cm−1 and P–O–C stretching at 822, 984 and 1026 cm−1 could be also retrieved, again with a slight shift (around 10 cm−1) to higher wavenumbers. Additionally, stretching bands of –CH2–, –CH3 and CC were visible again at 741, 1398 and 1456 cm−1 (–CH2– stretching) or 1130, 1167, and 1371 cm−1 (–CH3 stretching), as well as 2900–3000 cm−1 or 1506 and 1653 cm−1 again (CC stretching), respectively. Most importantly, the CO stretching band of the benzophenone residue at 1601 cm−1 disappeared because its carbonyl group was transferred into an OH group upon irradiation with UV-light.
To qualitatively test the strength of the surface adhesion of the polymer networks, the so-called tape test was conducted. For this test, regular office tape was glued on top of the surface-attached polymer network (in this case P2), and it was then peeled off at right angles to the surface. The thickness before this treatment and after this treatment was measured by ellipsometry. This data as well as photographs of the wafer before and after the tape test are shown in Fig. S51 in the ESI.† The data shows that only a few nanometers thin layer of polymer was removed. This, in combination with the fact that the polymer did not delaminate from the substrate, demonstrates substantial adhesion to the functionalized silicon substrate.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c7py01777d |
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