Synthesis and complexation of well-defined labeled poly(N,N-dimethylaminoethyl methacrylate)s (PDMAEMA)

: We present the synthesis and characterization of well-deﬁned polycationic copolymers containing thiazole dyes in the side chain. Atom transfer radical polymerization (ATRP) was used for the copolymerization of 3-azidopropyl methacrylate (AzPMA) and N , N -dimethylaminoethyl methacrylate (DMAEMA) of different composition. Thiazole-based alkyne-functionalized dyes (e.g., 5-methyl-4-(prop-2-yn-1-yloxy)-2-(pyridin-2-yl)thiazole, (MPPT)) were afterwards covalently attached using copper catalyzed azide alkyne cycloadditions (CuAAC) reaching contents of up to 9 mol % dye. Subsequent quaternization of the tertiary nitrogen of DMAEMA with strong methylation agents (e.g., methyl iodide) led to permanently charged polyelectrolytes. The materials were characterized by size exclusion chromatography, as well as NMR- and UV/VIS-spectroscopy. Particular attention is paid to the spectroscopic properties of the dyes in the side chain upon environmental changes such as pH and salinity. We anticipate the application of such precisely functionalized polyelectrolytes as temperature- and pH-responsive sensors in biomedical applications, e.g., within interpolyelectrolyte complexes. Concerning the latter, ﬁrst complex formation results are demonstrated.


Introduction
Complex and well-defined macromolecular architectures can nowadays be realized by various living and controlled polymerization techniques [1,2].Owing to increased tolerance of controlled radical polymerizations, a great variety of functional groups can be directly incorporated into materials with narrow molecular weight distributions, predetermined molecular weight, and the possibility of quantitative chain end modification [3,4].
As an alternative, post polymerization modification remains a viable tool to incorporate functional groups, which are incompatible even with moderately tolerant controlled radical polymerization (CRP) techniques [3].Among those, so-called "click" reactions have gained increasing attention due to their high specificity, often quantitative yields, and good tolerance towards other functional groups being present [3].Since introduction of this term by Fokin, Finn and Sharpless in 2001, "Click chemistry" has been frequently exploited both in applied and fundamental research [30,31].In that respect, probably the most often used type are copper(I) catalyzed Huisgen-1,3-dipolar cycloadditions between an azide and an alkyne, resulting in 1,4-disubstituted 1,2,3-triazoles [16,32,33].This reaction could be exploited for the preparation of a variety of different macromolecular architectures [30].
As an example for dye-labeled polycationic polymers, poly(4-vinylbenzyl chloride) was covalently attached to a coumarin dye by Baussard et al. [34].Besides coumarin, additionally aniline-based chromophores were introduced by azo-coupling reactions [35].Another interesting class of dyes are 1,3-thiazoles.Characterized by their blue emission, high room-temperature fluorescence, large Stokes shifts, and high quantum yields they are a promising class of dyes for a wide field of applications [36][37][38].Additionally, the facile introduction of various functional groups and their influence on both absorption and emission enables their application as sensors [36,39,40].In further studies, it was shown that 4-hydroxy-1,3-thiazoles could be incorporated into various polymeric backbones [9,36,41,42].This simple synthetic access in combination with enhanced photo-stability also enabled their use in blue emitting polymers [41,43] as well as in light harvesting experiments using Ru(II) polypyridylcomplexes [43,44].Further, these materials have been employed as sensors for the detection of fluoride [40,45], or as sensitizers in Grätzel-type dye-sensitized solar cells (DSSCs).
Here, we extend the application field of 4-hydroxy-thiazole dyes as side chain chromophores in stimuli-responsive copolymers.Linear copolymers of DMAEMA and AzPMA were synthesized using ATRP and the materials were subsequently labeled using alkyne-functionalized 4-hydroxy-1,3-thiazole dyes via CuAAC.Afterwards, the DMAEMA part of the resulting P(DMAEMA-co-AzPMA) copolymers was quaternized and the materials were used as polycations in micellar interpolyelectrolyte complexes (IPECs) [21].

Experimental Section
All starting materials were purchased from Sigma-Aldrich (Munich, Germany), Merck (Darmstadt, Germany), or ABCR GmbH (Karlsruhe, Germany) and were used as received if not mentioned otherwise.Tetrahydrofuran, dichloromethane and toluene were purified using a PureSolv-EN™ Solvent purification System (Innovative Technology, Garching, Germany).If necessary, THF and toluene were further dried by refluxing over sodium/benzophenone, while triethylamine (TEA) was distilled over calcium hydride and stored under argon.Any glassware was cleaned in a KOH/iso-propanol bath and dried at 110 ˝C.All deuterated solvents were obtained from Euriso-Top GmbH (Saarbrücken, Germany) and ABCR.The thiazole dye (MPPT) was synthesized according to literature protocols [46].For dialysis, a Spectra/Por Dialysis membrane with a molecular weight cut-off (MWCO) of 1000 g¨mol ´1 was used.

Nuclear Magnetic Resonance Spectroscopy (NMR)
Proton nuclear magnetic resonance ( 1 H NMR) spectra were recorded in CDCl 3 (or D 2 O, CD 2 Cl 2 ) on a Bruker (Bruker, Karlsruhe, Germany) AC 300-MHz spectrometer at 298 K.Chemical shifts are given in parts per million (ppm, δ scale) relative to the residual signal of the deuterated solvent.

Solvent CHCl 3
Size exclusion Chromatography was performed on a Shimadzu (Kyoto, Japan) system equipped with a SCL-10A system controller, a LC-10AD pump, and a RID-10A refractive index detector using a solvent mixture containing chloroform (CHCl 3 ), triethylamine (TEA), and iso-propanol (i-PrOH) (94:4:2) at a flow rate of 1 mL¨min ´1 on a PSS SDV linear M 5-µm column at 40 ˝C.The system was calibrated with PMMA (410-88,000 g¨mol ´1) standards.

Solvent DMAc
Size-exclusion chromatography was performed on an Agilent (Santa Clara, CA, USA) system equipped with a G1310A pump, a G1362A refractive index detector, and both a PSS Gram30 and a PSS Gram1000 column in series.N,N-Dimethylacetamide with 2.1 g¨L ´1 LiCl was applied as eluent at 1 mL¨min ´1 flow rate and the column oven was set to 40 ˝C.The system was calibrated with PMMA (102-981,000 g¨mol ´1) standards.

Solvent Water
Size-exclusion chromatography was performed on a Jasco (Groß-Umstadt, Germany) system equipped with a PU-980 pump, a RI-930 refractive index detector, a UV-975 UV/VIS-detector and both a AppliChrom ABOA CatPhil guard 200 Å and an AppliChrom ABOA CatPhil guard 350 Å column in series.Water with 0.1% TFA and 0.1 M NaCl was applied as eluent at 1 mL¨min ´1 flow rate and the column oven was set to 30 ˝C.The system was calibrated with Dextran (180-277,000 g¨mol ´1) standards.

Dynamic Light Scattering (DLS)
DLS measurements were performed using an ALV laser CGS3 Goniometer equipped with a 633 nm HeNe Laser (ALV GmbH, Langen, Germany).DLS measurements were performed at 25 ˝C and at a detection angle of 90 ˝.The CONTIN analysis of the obtained correlation functions was performed using the ALV 7002 FAST Correlator Software.

Zeta-Potential Measurements
The ζ-potentials were measured using a Zetasizer Nano ZS from Malvern (Malvern Instruments Ltd, Worcestershire, UK) via M3-PALS technique with a He-Ne laser operating at 633 nm.The detection angle was 13 ˝.The electrophoretic mobilities (u) were converted into ζ-potentials via the Smoluchowski equation: where η denotes the viscosity and ε the permittivity of the solution.

Transmission Electron Microscopy (TEM)
TEM measurements were performed on a Zeiss-CEM 902A (Zeiss, Oberkochen, Germany) operated at 80 kV.Images were recorded using a 1 k TVIPS FastScan CCD camera.TEM samples were prepared by applying a drop of an aqueous sample solution onto the surface of a plasma-treated carbon coated copper grid (Quantifoil Micro-Tools GmbH, Jena, Germany).

Infrared Spectroscopy (IR)
IR spectra were measured on an Affinity-1 ATR FT-IR (Shimadzu, Kyoto, Japan).Dry samples were placed directly on the ATR unit and measured in the range of 600 to 4000 cm ´1.

Synthesis of 3-Azidopropanol
3-Chloropropanol (6 g, 63.47 mmol) was added to a mixture of water (7 mL), sodium azide (8.24 g, 127 mmol), and tetrabutylammonium hydrogen sulfate (0.18 g, 0.53 mmol).The mixture was stirred at 80 ˝C for 24 h and then at room temperature for 14 h.The product was extracted with diethyl ether three times, the organic phase was dried over sodium sulfate, and the solvent removed under reduced pressure.The final product was obtained as yellow oil in a yield of 76% (4.86 g).

Synthesis of 3-Azidopropyl Methacrylate (AzPMA)
A solution of 3-azidopropanol (6 g, 59.3 mmol), triethylamine (7.66 g, 10.5 mL, 75.7 mmol), hydroquinone (150 mg), and methylene chloride (24 mL) was cooled in an ice-bath to 0 ˝C.Methacryloyl chloride (7.4 g, 6.9 mL, 70.3 mmol) dissolved in methylene chloride (12 mL) was added dropwise over a period of 20 min, and the mixture was stirred for 1 h at 0 ˝C.Afterwards the solution was allowed to warm to room temperature and stirred for further 14 h.Methylene chloride (25 mL) was added, and the mixture was extracted with an aqueous solution of hydrochloric acid (1/10 v/v, 2 ˆ25 mL), water (2 ˆ25 mL), 10 wt % aqueous NaOH (2 ˆ25 mL), and again with water.The organic phase was mixed with hydroquinone (0.1 g), dried over sodium sulfate, and the solvent was removed under reduced pressure.The crude oil (10 g) was purified by silica gel column chromatography (methylene chloride) resulting in a colorless oil (6.5 g, 38.6 mmol, 65%, Caution: due to its shock sensitive character at higher temperatures special care should be taken).
2.11.General Procedure for the CuAAC Cycloaddition between P(AzPMA x -co-DMAEMA y ) Copolymers and an Alkyne-Functionalized Thiazole-Dye and Cu(I)Br were dissolved in THF (30 mL) (Feed ratio: After four freeze-pump-thaw cycles the reaction mixture was stirred at room temperature for 48 h.After removal of copper by an aluminum oxide column the polymers were further purified via dialysis (molecular weight cut off [MWCO]: 1000 g¨mol ´1).After drying, a slightly yellow solid was obtained.
2.12.General Procedure for the Quaternization of the Functionalized P(AzPMA x -co-DMAEMA y ) Copolymers Exemplarily, P(AzPMA 0.09 -co-DMAEMA 0.91 ) and methyl iodide (MeI; 30 fold-excess with respect to the DMAEMA units in the corresponding copolymer) were dissolved in water/dioxane (0.45 mL/0.45 mL; c copolymer = 2.9 ˆ10 ´3 mol¨L ´1) and stirred for two days at 38 ˝C.Afterwards, the excess MeI was removed under reduced pressure.The resulting solution was freeze dried, resulting in a yellow solid.
).The polymerization was carried out at 50 ˝C for 4 days.Then, the reaction was terminated by cooling down in liquid nitrogen.After removal of copper by a silica gel column, the block copolymer was further purified via dialysis against THF.After removal of the solvent under reduced pressure, the polymer was precipitated in hexane and freeze dried.The composition was determined using 1 H NMR spectroscopy.
PEO 118 -b-PtBMA 63 : Ð = 1.05, determined using SEC (CHCl 3 /i-PrOH/TEA): PMMA-calibration).PEO 118 -b-PtBuAA 63 (200 mg) was dissolved in dichloromethane (20 mL) and trifluoracetic acid (TFA, 0.93 mL, 20 fold excess with respect to the tBA units) was added and stirred at room temperature for two days.After removal of the solvent in vacuum, the crude product was further purified via dialysis (Spectra/Por Dialysis Membrane, MWCO: 1000 g¨mol ´1).After freeze drying, a solid block copolymer could be obtained (109 mg). 1  After stirring overnight, the solutions were filtered (Target (Nylon), 5 µm).Different Z ´{`v alues were obtained by mixing the solutions in the required ratios.The prepared interpolyelectrolyte complexes (IPEC)-solutions were mixed in small glass vials (5 mL) and stirred at room temperature for at least 15 h.
Variation of the ionic strength at IPEC Z ´{`= 1.0: The prepared IPEC-solutions were mixed stepwise with a stock solution of sodium chloride at room temperature until the desired molarities were reached.After the addition, the solutions were allowed to stir 24 h at room temperature.

Results and Discussion
Herein, we focus on the synthesis of linear, fluorescently labeled polycations and their potential use in the formation of well-defined micellar IPECs.Therefore, P(AzPMA x -co-DMAEMA y ) copolymers of different composition were synthesized by atom transfer radical polymerization (ATRP) and subsequently labeled using an alkyne-functionalized thiazole dye (Scheme 1).3-Azidopropyl methacrylate (AzPMA) was prepared as reported by Sumerlin and coworkers starting from 3-chloropropanol but with slightly altered workup conditions (Figures S1 and S2) [3].

Preparation of Micellar Interpolyelectrolyte Complexes (IPEC)
P(AzPMA*0.05-co-METAI0.95) and PEO118-b-PAA63 were dissolved in buffer solution pH 10 (Merck, borate buffer) with concentrations of c = 1.0 g•L −1 .After stirring overnight, the solutions were filtered (Target (Nylon), 5 µm).Different Z−/+ values were obtained by mixing the solutions in the required ratios.The prepared interpolyelectrolyte complexes (IPEC)-solutions were mixed in small glass vials (5 mL) and stirred at room temperature for at least 15 h.
Variation of the ionic strength at IPEC Z−/+ = 1.0: The prepared IPEC-solutions were mixed stepwise with a stock solution of sodium chloride at room temperature until the desired molarities were reached.After the addition, the solutions were allowed to stir 24 h at room temperature.
After attachment of MPPT, the copolymer elution traces from the UV/VIS-detector are a first indication for the success of the reaction.All SEC curves were monomodal and the characteristics of the labeled copolymers are listed in Table 2.The effective degree of functionalization was estimated via NMR (Table 2).Further, the absence of the azide functionality in FT-IR measurements afterwards hints towards complete consumption of AzPMA (Figure S8).
To transform the PDMAEMA part of the copolymers into a strong polycation, quaternization using methyl iodide as strong methylation agent was carried out [49].Therefore, the respective copolymer P(AzPMA* x -co-DMAEMA y ) and methyl iodide (30 fold excess) were dissolved in 1,4-dioxane/water (v/v 1/1) and stirred for 48 h at 38 ˝C and afterwards P(AzPMA* x -co-METAI y ) (poly{ [2-(methacryloyloxy)ethyl] trimethylammonium iodide}) copolymers with iodide as counter ion could be isolated.SEC in aqueous media confirmed that these copolymers still are UV-active (Figure S9).We attribute the increased Ð in this case to the combination of eluent and column material.According to NMR, a nearly quantitative quaternization was reached (>98%, Figure 2 and Figure S11) [24].Due to the different NMR solvents used (CDCl 3 /CD 2 Cl 2 ) and electronic changes by quaternization, a strong shift of some copolymer signals occurs.For calculation of the quaternization efficiency, the signals marked as c and d were used (Figure 2) [47].UV/VIS investigations for all intermediate stages were carried out in water (Figure 3 and Figure S12-S14, Table 2).For all three co-monomer ratios prior to the attachment of the thiazole dye only the absorption of the υ azide 265 nm can be observed (Figure S15).After covalent attachment of the thiazole dye, its characteristic absorption band at 340 nm can be found, even in case of the lowest dye content, P(AzPMA* 0.01 -co-DMAEMA 0.99 ).Regarding this, no difference between the free and covalently bound dye was observed during our investigations (Figures S6 and S12-S14).
Polymers 2015, 7, page-page 9 UV/VIS investigations for all intermediate stages were carried out in water (Figures 3 and S12-S14, Table 2).For all three co-monomer ratios prior to the attachment of the thiazole dye only the absorption of the υazide 265 nm can be observed (Figure S15).After covalent attachment of the thiazole dye, its characteristic absorption band at 340 nm can be found, even in case of the lowest dye content, P(AzPMA*0.01-co-DMAEMA0.99).Regarding this, no difference between the free and covalently bound dye was observed during our investigations (Figures S6 and S12-S14).After quaternization, the copolymers show different absorption spectra: first, an additional signal at 290 nm can be seen which, according to literature, can be attributed to the presence of I 3 (absorption maxima at 290 and 360 nm) [50][51][52][53][54][55].Second, the absorption band of the dye is shifted to higher λ max .By taking a closer look at the absorption maxima (λ max2 ), a stronger shift in wavelength with decreasing amount of dye can be observed (9%: ∆(λ max2 ) = 11 5%: ∆(λ max2 ) = 18 nm; and 1%: ∆(λ max2 ) = 25 nm).This effect might be explained by the interaction of adjacent dye molecules.After methylation, a rather elongated copolymer conformation due to electrostatic repulsion can be anticipated.
To investigate whether MPPT itself is affected by the quaternization reaction, we also subjected the pristine dye to comparable reaction conditions and compared the resulting UV/VIS spectra (Figure 4, Table 3) with those of P(AzPMA* 0.09 -co-DMAEMA 0.91 ) under both neutral conditions and at pH 10 (the conditions where interpolyelectrolyte complex formation will take place later on).Due to its rather low solubility in aqueous media, UV/VIS spectra of MPPT were measured in THF both before and after quaternization.After quaternization, MPPT displays absorption bands at 299 nm and 349 nm, comparable to the absorption spectra obtained for the labeled copolymers after methylation.Nevertheless, no indication of a successful quaternization of MPPT could be observed by 1 H NMR, and therefore we attribute the appearance of a second UV/VIS band to remaining I 3 ´.
Surprisingly, at pH 10 the first absorption band for the copolymer vanishes and only the absorption at 349 nm can be observed.Further, the absorption band for MPPT broadens and decreases in intensity, which we at this point attribute to the used borate buffer.Further, also the triazole ring will be quaternized under these conditions, but the stability of this moiety after quaternization was previously confirmed by Mishra et al. by NMR studies [56].
To investigate whether MPPT itself is affected by the quaternization reaction, we also subjected the pristine dye to comparable reaction conditions and compared the resulting UV/VIS spectra (Figure 4, Table 3) with those of P(AzPMA*0.09-co-DMAEMA0.91)under both neutral conditions and at pH 10 (the conditions where interpolyelectrolyte complex formation will take place later on).Due to its rather low solubility in aqueous media, UV/VIS spectra of MPPT were measured in THF both before and after quaternization.After quaternization, MPPT displays absorption bands at 299 nm and 349 nm, comparable to the absorption spectra obtained for the labeled copolymers after methylation.Nevertheless, no indication of a successful quaternization of MPPT could be observed by 1 H NMR, and therefore we attribute the appearance of a second UV/VIS band to remaining I3 − .Surprisingly, at pH 10 the first absorption band for the copolymer vanishes and only the absorption at 349 nm can be observed.Further, the absorption band for MPPT broadens and decreases in intensity, which we at this point attribute to the used borate buffer.Further, also the triazole ring will be quaternized under these conditions, but the stability of this moiety after quaternization was previously confirmed by Mishra et al. by NMR studies [56].

Interpolyelectrolyte Complex Formation
In order to use the above described labeled polycations for the formation of micellar interpolyelectrolyte complexes (IPECs) [57], poly(ethylene oxide)-block-poly(acrylic acid) (PEO118-b-PAA63) was prepared via deprotection of poly(ethylene oxide)-block-poly(tert-butyl acrylate) (PEO118b-PtBuAA63) with trifluoroacetic acid (TFA) at room temperature in dichloromethane (Figure S10).The most prominent 1 H NMR signals of PEO118-b-PtBuAA63 in CDCl3 can be observed at 3.34-4.19ppm (PEO backbone), 2.31-2.15ppm (PAA backbone) and 1.39-1.95ppm (tert-butyl-group).Successful hydrolysis is indicated by the complete disappearance of the signal for the tert-butyl-group.For IPEC formation, P(AzPMA*0.05-co-MEATI0.95) as polycation and PEO118-b-PAA63 as polyanionic block copolymer were chosen (Scheme 2).Using these components a good comparability to previously investigated IPEC systems can be achieved [58].The Z-value represents the mixing ratio according to the used charges and is defined as: We were interested in whether the dye can be spectroscopically detected after encapsulation within the IPEC core and how this can be influenced by variation of the Z−/+-value.For all IPEC solutions only a slight change in turbidity was observed after mixing.All mixtures were prepared in a basic buffer (pH 10) solution, to ensure the complete deprotonation of PEO118-b-PAA63.
For IPECs with Z−/+-values of 1.5, 1.0 and 0.5 both dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements were carried out, whereas in (intensity-weighted) DLS experiments, the samples showed the presence of larger aggregates (Figures 5 and S16, Table 4), number-weighted CONTIN plots depicted monomodal size distributions.Here, values of <Rh>n,app = 5 nm (Z−/+ = 1.5, Figure 5A), and 10 nm (Z−/+ = 0.5, 1.0) are found, respectively.In case of Z−/+ = 1.5 most probably mainly block copolymer unimers are detected.Also, TEM measurements for all micellar IPECs confirmed these results as two size distributions were observed, which fit to the values obtained by DLS (Figure 5 and Table 4).In both cases, the IPEC core can be detected and the PEO corona can be ascribed to the grey shadow surrounding the particles.Both single micellar IPECs and clusters thereof are displayed in Figure 5 (and the corresponding insets).
Zeta-potential measurements were further used to evaluate the overall net charge of the formed micellar IPECs and the constituting polyelectrolytes (Table S2), whereas PEO118-b-PAA63 exhibited −38 mV and P(AzPMA*0.05-co-METAI0.95) +37 mV, the zeta-potentials for the IPECs at all Z−/+ ratios were close to charge neutrality.We tentatively explain this finding with the presence of a neutral PEO-shell.The slightly positive value in case of Z−/+ = 0.25 can be explained by the excess of polycation.Using these components a good comparability to previously investigated IPEC systems can be achieved [58].The Z-value represents the mixing ratio according to the used charges and is defined as: Z " p´q p`q " overall amount o f negative charge overall amount o f positive charge We were interested in whether the dye can be spectroscopically detected after encapsulation within the IPEC core and how this can be influenced by variation of the Z ´{`-value.For all IPEC solutions only a slight change in turbidity was observed after mixing.All mixtures were prepared in a basic buffer (pH 10) solution, to ensure the complete deprotonation of PEO 118 -b-PAA 63.
For IPECs with Z ´{`-values of 1.5, 1.0 and 0.5 both dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements were carried out, whereas in (intensity-weighted) DLS experiments, the samples showed the presence of larger aggregates (Figure 5 and Figure S16, Table 4), number-weighted CONTIN plots depicted monomodal size distributions.Here, values of <R h > n,app = 5 nm (Z ´{`= 1.5, Figure 5A), and 10 nm (Z ´{`= 0.5, 1.0) are found, respectively.In case of Z ´{`= 1.5 most probably mainly block copolymer unimers are detected.Also, TEM measurements for all micellar IPECs confirmed these results as two size distributions were observed, which fit to the values obtained by DLS (Figure 5 and Table 4).In both cases, the IPEC core can be detected and the PEO corona can be ascribed to the grey shadow surrounding the particles.Both single micellar IPECs and clusters thereof are displayed in Figure 5 (and the corresponding insets).
Zeta-potential measurements were further used to evaluate the overall net charge of the formed micellar IPECs and the constituting polyelectrolytes (Table S2), whereas PEO 118 -b-PAA 63 exhibited ´38 mV and P(AzPMA* 0.05 -co-METAI 0.95 ) +37 mV, the zeta-potentials for the IPECs at all Z ´{`r atios were close to charge neutrality.We tentatively explain this finding with the presence of a neutral PEO-shell.The slightly positive value in case of Z ´{`= 0.25 can be explained by the excess of polycation.We further investigated the formed micellar IPECs by UV/VIS spectroscopy and compared the results with the previously investigated polycationic copolymers.As can be seen, complex formation seems to induce a slight shift to higher wavelengths for the absorption maxima, depending on charge stoichiometry (Figure S17, Table 4).

Scheme 1 .
Scheme 1.Copolymerization of DMAEMA and AzPMA, followed by post-polymerization modification via CuAAC between the azide functionalized copolymer and MPPT.

Table 4 .
Evaluation of TEM, dynamic light scattering (DLS) and UV/VIS measurements of micellar interpolyelectrolyte complexes (IPECs) in buffer solution at pH 10. a determined via TEM by counting 50 individual IPECs; b determined by DLS.

Table 3 .
Absorption maxima for the herein used thiazole dye (MPPT) prior and after quaternization as well as P(AzPMA* 0.05 -co-DMAEMA 0.95 ) under different conditions.Determined in THF solution using a Specord 250 spectrometer (Analytik Jena) in Suprasil quartz glass cuvettes 104-QS (Hellma Analytics) with a thickness of 10 mm.