Role of Functional Monomers upon the Properties of Bisphenol A Molecularly Imprinted Silica Films

: In this study, two types of bisphenol A molecularly imprinted ﬁlms (BPA-MIP) were successfully prepared via sol-gel derived methods using two different organosilane functional monomers N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (DAMO-T) or (3-mercaptopropyl)trimethoxysilane (MPTES). The physical-chemical characterization of ﬁlms, in terms of morphology, structure, thermal analysis, and optical features, suggested that thinner ﬁlms with a homogenous porous structure were more likely to retain BPA molecules. The MIP ﬁlms revealed the rapid and quantitative adsorption of BPA, registering the most speciﬁc binding in the ﬁrst ﬁve minutes of contact with the BPA-MIP ﬁlm. Silica ﬁlms were effectively regenerated for further usage for at least ﬁve times, demonstrating their high stability and reusability. Even if the performance of ﬁlms for BPA uptake dropped dramatically after the third adsorption/reconditioning cycle, this synthesis method for BPA-MIP ﬁlms has proven to be a reliable and cheap way to prepare sensitive ﬁlms with potential application for re-usable optical sensors. the provides a simpler more reproducible procedure to prepare BPA-MIPs, the use of MI and sol-gel techniques. The methodology is original and consisted of casting the BPA-MIP layer on top degreased glass support. the present combined procedure of BPA imprinting has been used to prepare MIP ﬁlms.


Introduction
Bisphenol A (BPA) [2,2-bis (4-hydroxyphenyl)propane], an endocrine disruptor chemical (EDC), is known as the most widely used and toxic additive in the production of plastic together with polycarbonates, epoxy and polyester resins, and others (flame retardants, polyacrylate, polysulfone resins, polyetherimide). Many studies revealed that BPA leaches out from plastic products used for food packaging such as: plastic (baby) bottles, industrial supplies, dental sealant, medical devices, or sport equipment [1][2][3][4]. Despite the ongoing COVID-19 pandemic that has affected the sales of paints and coatings in 2020, the global volume consumption of BPA is growing dynamically and is estimated to reach more than ten million metric tons by 2022 [5]. In 2019, the European Commission decided to form a research cluster namely EURION to find novel testing and screening methods to identify EDC [6]. BPA is easily released into the atmosphere and the natural environment through direct discharge, landfill leachate, is and frequently found in food and water sources [7,8]. Long-term exposure to BPA alters endocrine function, causing many diseases as diabetes, obesity, cardiovascular diseases, chronic respiratory, thyroid and immune systems diseases, and even cancer [9][10][11]. Exposure to BPA occurs mostly via the oral route (approximately 90%) meaning dietary contamination and non-dietary sources such as sea water and cosmetics [12]. So far, several analytical methods have been established and Thereby, the aim of this work was to prepare and characterize two types of BPA-MIP films, based on two different organosilane monomers, meaning N-(2-aminoethyl)-3aminopropyltrimethoxysilane (DAMO-T) and (3-mercaptopropyl)trimethoxysilane (MPTES). The films BPA-MIP DAMOT and BPA-MIP MPTES were obtained by spraying the sol-gel precursor solutions directly on previously degreased glass slides. The proposed sol-gel approach for BPA-MIP preparation seemed to be suitable due to the low temperature processing conditions (for polycondensation at 25 • C and for the maturation of films at 60 • C). The prepared BPA-MIP films were well characterized by Fourier-Transform Infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and Atomic Force Microscopy (AFM), as well as thermogravimetric analysis (TGA). The optical behavior of films was investigated by ellipsometry, to establish the imprinting effect over the final properties of the obtained BPA-MIPs. The BPA-MIP films were further tested in terms of rebinding measurements in liquid state via spectrophotometric techniques, to assess their potential as sensing elements for optic sensors. The reusability and stability of the sol-gel films were also discussed.

Instruments and Characterization
All measurements were performed at room temperature (RT considered 25 • C). The prepared BPA-MIP and NIP films were analyzed morpho-structurally and thermally using various equipment and techniques. Fourier Transform Infrared Spectroscopy (FTIR) of films was performed on Bruker Tensor 37 (ATR) in 400-4000 cm −1 domenium, a resolution of 4 cm −1 and 16 scans. Thermogravimetric analysis (TGA) was carried out under nitrogen atmosphere at a 10 • C/min heating rate with TA Q2000 IR Instrument with auto-sampler. The thermal stability of sol-gel films was investigated in order to underline the effect of imprinting upon the organosilica materials, as complementary results to FTIR measurements. Estimation of films thickness was made by ellipsometry with UV-VIS-NIR Ellipsometer VASE ® model (J.A. Woollam Co, Inc., Lincoln, NE, USA), in the 300-1000 nm wavelength range at 70 o AOI with a 2 nm wavelength step and 20 scans/measurement (microspot). It is relevant to note that a translucent scotch tape was fixed on the glass slides back in order to prevent the effect of 'backside reflection'. The surface morphology of the films deposited on glass slides was investigated with an Environmental Scanning Electron Microscope (ESEM) FEI Quanta 200 from Philips, equipped with gaseous secondary electron detector (GSED). Topography was performed by Atomic Force Microscopy using XE 100 instrument from Park Systems, in non-contact tapping mode at resonance frequency of Z-scanner: 5 kHz. All AFM measurements were recorded using silicon tips with a scan range of XY-scanner of (max) 50 µm, and a working distance of Z-scanner: 12 µm. The AFM images were elaborated with the XEI program (v 1.8.0-Park Systems) for exhibiting roughness evaluation. The UV-2501-PC spectrometer (Shimadzu Co., Tokyo, Japan) was used to perform the BPA batch re-binding experiments and the washing procedures for BPA removal in the 200-1000 nm wavelength range, with a 10 mm quartz cuvette.

Synthesis of Bisphenol A-Molecularly Imprinted Polymer (BPA-MIP) Films
Two types of BPA-imprinted organosilica films (i.e., BPA-MIP MPTES and BPA-MIP DAMOT ) were successfully prepared by directly spraying the precursor solutions on glass supports, according to a similar one-step procedure described by our group, with slight modifications [34]. In a typical batch for BPA-MIP preparation, two solutions were prepared separately at room temperature (RT considered 25 • C), the catalyst and the precursor solution. The catalyst consisted of an aqueous solution of 25% ammonia hydroxide (0.565 mL NH 4 OH/0.225 mL H 2 O). The precursor solution was prepared by dissolving the functional monomer DAMO-T or MPTES and the template BPA in 1 mL of ethanol under stirring (molar ratio monomer: BPA = 10:1). After stirring for 30 min at 200 rpm, in the precursor solution containing DAMO-T a structural monomer (0.13 mL TEOS) was also added to ensure the adhesion to the glass support. The precursor monomer solution was magnetically stirred for 1 h after which it was gradually added in the catalytic medium and mechanically stirred at 200 rpm, for 2 h (sol-gel time, tsg), when the partial hydrolysis reaction occurs, generating sols. The resulted solution was applied by directly spraying it onto cleaned glass supports to form crosslinked networks by alcohol/aldol polycondensation of sols. The obtained films were maturated for 48 h at 25 • C (until complete polycondensation), followed by curing for 48 h at 60 • C in an oven.
The cured films were then washed two times according to the following procedure: step 1-washing with ethanol, for 8 h at room temperature, for removing unreacted monomers and step 2-extraction of BPA molecules with ethanol-acetic acid (9:1, v/v) for 4 h assisted by ultrasound (at 35 kHz frequency). As shown in Figure S1, a rigorous control of the supernatant solutions was performed by UV-Visible spectroscopy in order to assess the efficiency of the washing/extraction procedures. It can be observed in the second washing/extraction cycle that BPA was successfully extracted from the imprinted films (as confirmed by the absence of specific absorption peaks of BPA). Afterward, all films were dried at 60 • C overnight until constant weight and stored in dried conditions until use. By contrast, non-imprinted control films (noted by analogy NIP) were synthesized, conditioned, and washed respecting the same procedures as for the MIPs; the only difference was the absence of BPA from the synthesis.

Batch Binding Measurements and Regeneration of BPA Films
Binding experiments were performed to investigate the specificity of MIP films by measuring the adsorbed amount of BPA onto MIPs and NIPs. The binding tests referred to contacting the MIP and NIP films with 35 mL BPA solution of a known concentration (experiments conducted in batch conditions in duplicate) and measuring the initial and the final concentration of BPA. Due to BPA poor solubility in water, organic solvent-based assays were employed. The UV-visible absorption spectrum of bisphenol A in ethanol is given in Figure S2. The specific wavelengths of bisphenol A were registered at 229 nm and 278 nm. Since the value at 229 nm is susceptible to the influence of the solvent, the quantification of BPA was performed against the value at 278 nm as characteristic wavelength for BPA adsorption [35]. Thus, the calibration of BPA at λ = 278 nm was obtained in ethanol using a series of standard solutions containing BPA in the 0.2-0.008 g/L concentration range. The concentration of BPA was found to have a good linear relationship with r 2 = 0.997 (according to Figure S3). Herein, the concentration limits chosen for the study, meaning 0.008 and 0.2 g/L, represented the lowest and the highest quantity of BPA that can be detected by UV.
The kinetic of BPA rebinding was studied in the first 120 min of contact with 0.2 g/L BPA solution in ethanol. Afterward, using various concentrations of BPA (i.e., 0.2, 0.15, 0.1, and 0.08 g BPA/L in ethanol), the adsorbed amount of BPA was measured after a period of only 5 min, considered proper for specificity.
The reusability of the BPA-MIPs and NIPs deposited on glass slides was also investigated by using the same batch of films through the adsorption-desorption studies in five consecutive cycles. The re-binding capacities, Q (mg BPA g −1 polymer film), of BPA-MIP and NIP films were calculated using Equation (1); where C N,i (g/L) and C N,f (g/L) are the initial and final concentration of BPA in the feed solution, m p (mg) the films weight (m p = 40 ± 1 mg) and V S (L) is the volume of the feed solution (i.e., 35 mL).
Imprinting factors, F, expressed by Equation (2), quantified the specificity with which BPA-MIP films re-bind BPA, compared to their corresponding NIPs, where Q MIP and Q NIP are the re-binding capacities of BPA-MIP and NIP, respectively.

Preparation of the BPA-MIP Films
This work was aimed at obtaining BPA-MIP films having two different organosilane functional monomers i.e., DAMO-T and MPTES. It is worth to mention that sol-gel hybrid films have attracted attention due to their efficient immobilization on various substrates, their enhanced stability and, in this case, easy access to the recognition cavities thus created. In this respect, the MPTES organosilane monomer was chosen for its adhesive properties and the ability to interact with the template, whereas DAMO-T monomer was expected to create stronger interactions with the template due to its diamino functionalities. For the later formulation, the adhesive properties to the substrate were compensated by addition of TEOS. Furthermore, the preparation method of films via sol-gel was very simple, quick, and did not require expensive chemicals or instrumentation.
The synthesis recipes for the precursor solutions used to obtain BPA-MIP and NIP films are given in Table 1. Previously reported results showed that aromatic templates are difficult to extract from MIP films with over 4-5 µm thickness and thinner films under 100 nm detach from the glass slide after multiple washing procedures [21]. Therefore, the monomer(s)/solvent/catalyst ratios were similar to the ones reported previously. The schematic representation for BPA imprinting in sol-gel films and deposition on glass substrates is given in Figure 1. An alkaline solution (1 N NaOH) was used to clean the surface of the glass substrates before film casting. The cleaning per glass slide was carried out in triplicate by immersing it in 10 mL of alkaline solution for 30 min. Finally, it was dried in a vacuum oven at 60 • C for 2 h. Herein, monolayers of polymeric films were prepared by spraying the obtained precursor solutions directly on cleaned glass substrates. In the first step, following the MI principle, a polymerizable complex between the organosilane precursors DAMO-T or MPTES and BPA molecules is formed in ethanol and, further on, a partial hydrolysis of this assembly takes place in basic medium (NH 4 OH, H 2 O) [22]. The second step consists of sols formation [34]. Non-hydrolyzed and partially hydrolyzed DAMO-T/MPTES-BPA molecules undergo a polycondensation reaction to form cross-linked and homogeneous tridimensional networks in the third step [14,36]. After a suitable maturation/curing protocol [28], the hybrid MIP films were washed several times and BPA was properly extracted with the formation of specific imprints. prepared by spraying the obtained precursor solutions directly on cleaned glass substrates. In the first step, following the MI principle, a polymerizable complex between the organosilane precursors DAMO-T or MPTES and BPA molecules is formed in ethanol and, further on, a partial hydrolysis of this assembly takes place in basic medium (NH4OH, H2O) [22]. The second step consists of sols formation [34]. Non-hydrolyzed and partially hydrolyzed DAMO-T/MPTES-BPA molecules undergo a polycondensation reaction to form cross-linked and homogeneous tridimensional networks in the third step [14,36]. After a suitable maturation/curing protocol [28], the hybrid MIP films were washed several times and BPA was properly extracted with the formation of specific imprints.

Structure of BPA-MIP and NIP Films
FTIR spectroscopy was used to characterize the films and specifically to prove the presence of BPA molecules upon the organosilica matrix. In Figure 2a

Structure of BPA-MIP and NIP Films
FTIR spectroscopy was used to characterize the films and specifically to prove the presence of BPA molecules upon the organosilica matrix. In Figure 2a In the spectrum of BPA (Figure 2a,b), we can distinguish the characteristic band of the aromatic ring νC = C (Ar-C=C) recorded at 1603 cm −1 and bands recorded at 1508, 1437, and 1360 cm −1 assigned to the C-H bending. The stretching vibrations from 3319 cm −1 (very intense band) and 2970/3030 cm −1 were assigned to the νOH (Ar-OH) and ν-CH3-(C-CH3) bonds, respectively. The band recorded at 1223 cm −1 is due to C-O stretching. Figure 2a also revealed the characteristic bands of BPA in the spectrum of BPA-MIPMPTES film, meaning the aromatic rings vibration at 1601 cm −1 , the bands for C-H bending at 1510 cm −1 , 1437, and 1354 cm −1 and the stretching of C-O bonds given by the spiked intensity of the band at 1234 cm −1 , indicating that BPA molecules were successfully imprinted in the matrix [37,38]. For BPA-MIPDAMOT, Figure 2b, these bands overlap with  (Figure 2a), the band at 2552 cm −1 revealed the presence of mercapto group (-SH) in the organosilica matrix. In addition to mercapto band, other characteristic bands in the BPA-MIP MPTES spectrum were distinguished as follos: the bands of the methoxy groups, asymmetric ν asym (Si-OCH 3 ) and symmetric ν sym (Si-OCH 3 ) stretching vibrations at 2924 and 2864 cm −1 . In Figure 2b, spectra of films with DAMO-T, some of the characteristic bands of N-H bonds form DAMO-T were spotted at 3381 cm −1 (ν N-H ) and the bending vibrations at 1652 cm −1 (δ N-H ). The results indicate that the organosilica functional monomers were quantitatively incorporated into the hybrid crosslinked networks by alcohol/aldol polycondensation of DAMO-T or MPTES.
In the spectrum of BPA (Figure 2a,b), we can distinguish the characteristic band of the aromatic ring ν C = C (Ar-C=C) recorded at 1603 cm −1 and bands recorded at 1508, 1437, and 1360 cm −1 assigned to the C-H bending. The stretching vibrations from 3319 cm −1 (very intense band) and 2970/3030 cm −1 were assigned to the ν OH (Ar-OH) and ν -CH3-(C-CH 3 ) bonds, respectively. The band recorded at 1223 cm −1 is due to C-O stretching. Figure 2a also revealed the characteristic bands of BPA in the spectrum of BPA-MIP MPTES film, meaning the aromatic rings vibration at 1601 cm −1 , the bands for C-H bending at 1510 cm −1 , 1437, and 1354 cm −1 and the stretching of C-O bonds given by the spiked intensity of the band at 1234 cm −1 , indicating that BPA molecules were successfully imprinted in the matrix [37,38]. For BPA-MIP DAMOT , Figure 2b, these bands overlap with those of DAMO-T. Yet, a hint to BPA imprinting was given by the significant shifting of bands from 1652 and 1565 cm −1 (in the spectrum of NIP) to 1665 and 1593 cm −1 (in the spectrum of BPA-MIP DAMOT ) and the presence of a band assigned to C-H bending at 1441 cm −1 .
The bands at 3335 cm −1 (sharp band) and 3032 cm −1 in BPA-MIP MPTES and 3272 cm −1 (wide band) in BPA-MIP DAMOT spectra were attributed to the stretching and bending mode of O-H groups from BPA implied in the monomer-template interactions through hydrogen bonding. When comparing the spectra of the two imprinted films, it is important to point out that a more visible imprinting effect was highlighted for BPA-MIP MPTES (as compared to BPA-MIP DAMOT ).

Morphology of BPA-MIP and NIP Films
The surface morphology evaluation of prepared sol-gel films was firstly explored by scanning electron microscopy (SEM, Figure 3) and, afterwards, with atomic force microscopy (AFM, Figure 4). The SEM images of BPA-MIP MPTES and BPA-MIP DAMOT and their corresponding NIP MPTES and NIP DAMOT , respectively, are presented in Figure 3, where significant changes of surface morphology can be noticed. The micrographs of BPA-MIPs and NIPs films clearly indicated morphological differences even though the main network is chemically resemblant (Si-O-Si).
Comparing the morphology of the NIPs with that of BPA-MIPs, the difference was striking. NIP films presented smoother surfaces with little visible asperities or pores, ascribed to the absence of imprinted sites. An overview at lower scales revealed an aggregated structure of the NIP MPTES film (Figure 3b) with rather large gaps instead of pores. Interestingly, BPA-MIP MPTES exhibited a dense structure of pores consisting of aggregated sols, in which case it can be due to the presence of monomer-template assemblies that clearly influenced the growth mode of the entire sol-gel network (Figure 3a). This porous structure of BPA-MIP MPTES films is very beneficial for the mass transfer, BPA rebinding, and may lead to shorter periods for equilibrium adsorption [39]. For BPA-MIP DAMOT films, an interesting, elongated structure (like pine branches) was observed in Figure 3c, unveiling again the result of a preferential arrangement and growth of the network in the presence of monomer-template assemblies. Unlike BPA-MIP MPTES , the surface of BPA-MIP DAMOT seemed to be more compact, which may be caused by the addition of TEOS that conferred rigidity to the whole structure. structure of BPA-MIPMPTES films is very beneficial for the mass transfer, BPA rebinding, and may lead to shorter periods for equilibrium adsorption [39]. For BPA-MIPDAMOT films, an interesting, elongated structure (like pine branches) was observed in Figure 3c, unveiling again the result of a preferential arrangement and growth of the network in the presence of monomer-template assemblies. Unlike BPA-MIPMPTES, the surface of BPA-MIPDAMOT seemed to be more compact, which may be caused by the addition of TEOS that conferred rigidity to the whole structure. The topography and roughness of both BPA-MIP films and their corresponding NIPs were investigated by AFM (Figure 4), as well. The surface roughness of the sol-gel films was evaluated using the root-mean-square roughness (RMSR) function of XEI AFM software. As shown in Figure 4b, five different topographic images were chosen to calculate the arithmetic average leading to the RMSR results. The AFM images of NIPs and BPA-MIP films emphasized again the changes that occur in surface topography due to the presence of monomer-template assemblies. In agreement with the SEM analysis, the 3D images of the BPA-MIPMPTES/NIPMPTES films (Figure 4a) pair displayed a fully different porous architecture compared to the flatter and smoother surface of the other pair, BPA-MIPDAMOT/NIPDAMOT (Figure 4a). Compared to SEM, the AFM footage revealed a very dense porous structure for the BPA-MIPDAMOT film, as well. Yet, in this case the pore sizes are much smaller than the ones observed on the surface of BPA-MIPMPTES, which may lead to a slow diffusion of BPA during rebinding trials and low binding efficiency [40]. The presence of BPA led to higher surface roughness values for BPA-MIPMPTES and BPA-MIPDAMOT (with a RMSR of 1.7 nm and 0.6 nm, respectively) compared to those of

Thermal Stability of BPA-MIP and NIP Films
Thermogravimetric analysis, performed under nitrogen gas at a 10 °C/min heating rate, indicated similar decomposition trends for the two types of sol-gel films ( Figure 5). The thermal degradations of BPA-MIPDAMOT and BPA-MIPMPTES and their non-imprinted NIPDAMOT and NIPMPTES revealed that all films were thermally stable. Three main degra- The topography and roughness of both BPA-MIP films and their corresponding NIPs were investigated by AFM (Figure 4), as well. The surface roughness of the sol-gel films was evaluated using the root-mean-square roughness (RMSR) function of XEI AFM software.
As shown in Figure 4b, five different topographic images were chosen to calculate the arithmetic average leading to the RMSR results. The AFM images of NIPs and BPA-MIP films emphasized again the changes that occur in surface topography due to the presence of monomer-template assemblies. In agreement with the SEM analysis, the 3D images of the BPA-MIP MPTES /NIP MPTES films (Figure 4a) pair displayed a fully different porous architecture compared to the flatter and smoother surface of the other pair, BPA-MIP DAMOT /NIP DAMOT (Figure 4a). Compared to SEM, the AFM footage revealed a very dense porous structure for the BPA-MIP DAMOT film, as well. Yet, in this case the pore sizes are much smaller than the ones observed on the surface of BPA-MIP MPTES , which may lead to a slow diffusion of BPA during rebinding trials and low binding efficiency [40]. The presence of BPA led to higher surface roughness values for BPA-MIP MPTES and BPA-MIP DAMOT (with a RMSR of 1.7 nm and 0.6 nm, respectively) compared to those of the corresponding NIPs (1.4 nm and 0.4 nm, respectively). The differences of RMSR values can be explained by the presence of template molecules that exert a steric effect during the growth of the sol-gel network. Meaning, the physical volume occupied by the template molecules, which translates later into imprinted cavities, is responsible for the formation of small gaps between the neighboring SiO 2 chains.
Thereby, from the morphological analysis, one conclusion may be drawn with regard to the type of organosilane monomer (or better yet the organic functionalities of the monomer), i.e., the nature of the functionalities influenced the films morphology and the growth pattern of the sol-gel network.

Thermal Stability of BPA-MIP and NIP Films
Thermogravimetric analysis, performed under nitrogen gas at a 10 • C/min heating rate, indicated similar decomposition trends for the two types of sol-gel films ( Figure 5). The thermal degradations of BPA-MIP DAMOT and BPA-MIP MPTES and their non-imprinted NIP DAMOT and NIP MPTES revealed that all films were thermally stable. Three main degradation steps were observed for all the samples. For DAMO-T-based films, a higher mass loss was observed between 50 and 150 • C and it was attributed to the evaporation of intrinsic water, hence confirming the FTIR spectroscopy results where significant amount of water was retained in the structure of DAMO-T-based film.
Appl. Sci. 2021, 11, x FOR PEER REVIEW 10 of 17 loss was also registered for the NIP based on DAMO-T in this same region and may be linked with the loss of amino fragments from DAMO-T. The second degradation stage occurred between 300 and 500 °C and was generally attributed with the total degradation/fragmentation of the pendant groups (i.e., methyl/ethyl fragment types, amino-ethyl/methyl, mercaptopropyl). The degradation of the polymer backbone occurred in the last degradation step, between 500-800 °C, [34]. It should be underlined that for both BPA-MIPs the residues were up to 57 wt.% and slightly lower compared to their corresponding NIPs, up to 61 wt.%, confirming a similar behavior between them but also their good thermal stability considering their structural differences.

Optical Properties of BPA-MIP and NIP Films
The spectroscopic ellipsometry (SE) measurements were performed to highlight the effect of imprinting on the optical properties of films, in terms of refractive index and The first degradation step was recorded in the 200-300 • C temperature range, with maximums registered at 273 • C and 223 • C for BPA-MIP DAMOT and BPA-MIP MPTES , respectively, and attributed to BPA degradation according to the thermogram of BPA provided in Figure S4 (Tmax = 268 • C). The shift to lower or higher maximum decomposition temperatures is not unusual and this observation can help explain two interesting phenomena that may occur during imprinting in soft and rigid sol-gel networks [21,36,41]. For instance, in the case of BPA-MIP MPTES films (Figure 5b), the low stability of BPA indicated that interactions between the template and the functional SH groups of the monomer, potentially weaken the (C-CH 3 ) bonds from BPA which led to the fragmentation of the molecule. On the other hand, the BPA imprinted in the BPA-MIP DAMOT film (Figure 5a) degraded at higher temperatures due to the inherent rigidity of the sol-gel network, given by the addition of TEOS. It should also be mentioned that a small mass loss was also registered for the NIP based on DAMO-T in this same region and may be linked with the loss of amino fragments from DAMO-T.
The second degradation stage occurred between 300 and 500 • C and was generally attributed with the total degradation/fragmentation of the pendant groups (i.e., methyl/ethyl fragment types, amino-ethyl/methyl, mercaptopropyl). The degradation of the polymer backbone occurred in the last degradation step, between 500-800 • C, [34]. It should be underlined that for both BPA-MIPs the residues were up to 57 wt.% and slightly lower compared to their corresponding NIPs, up to 61 wt.%, confirming a similar behavior between them but also their good thermal stability considering their structural differences.

Optical Properties of BPA-MIP and NIP Films
The spectroscopic ellipsometry (SE) measurements were performed to highlight the effect of imprinting on the optical properties of films, in terms of refractive index and transmittance. The refractive index of the films was measured in the 200-1000 nm wavelength domenium and the transmittance profiles were evaluated up to 900 nm spectral range, respectively, in different points of the films surface. In this respect, the Cauchy dispersion model was used for modelling the ellipsometric experimental data (Figures S5.1-S5.4, SM) which delivered reliable values for the films thickness and surface roughness.
The thickness and surface roughness for both prepared sets of films, summarized in Table 2, revealed major differences as function of the various employed monomers. For MPTES-based films the thickness varied between 230 and 290 nm, while for the DAMO-Tbased films was 10-fold higher. A similar trend was registered for the roughness, as well. The thickness and roughness discrepancy between the two types of films was attributed to the different growth mechanism of the organosilica matrix upon BPA addition and to the presence of TEOS, supporting the results attained in the morphological assessment.  Figure 6 shows the refractive index, n, and the transmittance spectra of BPA-MIP DAMOT and BPA-MIP MPTES films against their corresponding NIPs. Pronounced modifications of the optical features (transmittance and refractive index) for both type of films were recorded particularly in the 300-550 nm wavelength region. The variance of refractive index and transmittance presented similar profiles for both MIP films, indicating the presence of BPA in both film structures. The refractive index (Figure 6a) showed great fluctuations for both types of films. For example, the n values registered for the MIP/NIP films with DAMO-T were affected by thickness and, thus, their whole profile is shifted towards higher n values compared to the MIP/NIP pair with MPTES. However, the same trend is maintained between the imprinted and non-imprinted films suggesting that light travels faster through the non-imprinted material (as lower n values were registered in both cases compared to the ones of MIPs).

Batch Rebinding of BPA on BPA-MIP and NIP Films
The rebinding studies of BPA consisted of adsorption kinetics analysis and isotherm batch adsorption assays, carried out for the two types of BPA-MIP films (i.e., BPA-MIPMPTES and BPA-MIPDAMOT) and their corresponding blank NIPMPTES and NIPDAMOT as references. The specificity for BPA uptake was assessed by calculating the adsorption capacities, Q (mg/g) and imprinting factors, F of films (Figure 7a,b). From this point of view, the quantification of bonded BPA was conducted indirectly by determining the un-bonded BPA from the supernatants at 278 nm (characteristic wavelength for BPA absorbance). Figure 7a shows the adsorption kinetics of the two BPA-MIP films and their corresponding blank NIPs from a 0.20 g/L BPA solution. The adsorption capacity of all films increased rapidly in the first 20 min, especially for the BPA-MIP films. This trend was followed by a plateau after which the binding equilibrium (Qe) was attained, at 60 min. The NIP films presented similar adsorption profiles over time compared to BPA-MIP films and attained lower values for the adsorption capacity due to the lack of specific binding sites. More importantly, the imprinting factor (F) of BPA-MIPMPTES (Figure 7b) was 3.03 in the first 5 min, indicating not only excellent imprinting of BPA but also the recommended time of contact for attaining the most specific adsorption of BPA. In accordance with the refractive index, the transmittance profiles of the BPA-MIP films registered a drop of about 25% T compared to the NIPs (Figure 6b). This sudden decrease from 90% T to around 66% T was again attributed to the presence of BPA. Yet, the BPA-MIP DAMOT film led to a more obvious decrease of transmittance as the film thickness is 10-fold higher than the one of BPA-MIP MPTES .
Both the refractive index and transmittance profiles are consistent with the findings from previous studies [22,34]. These results strengthen the belief that ellipsometric data may better underline the effect of imprinting and the presence of the template when preparing thin and transparent MIP films. Hence, it can be used as a complementary method to characterize the optical features of MIP films and decide upon the potential of such films to be used as sensitive elements for building optical sensors. In addition, the small values of the roughness for the MPTES-based films obtained in this work are considered suitable for optical sensing applications [42].

Batch Rebinding of BPA on BPA-MIP and NIP Films
The rebinding studies of BPA consisted of adsorption kinetics analysis and isotherm batch adsorption assays, carried out for the two types of BPA-MIP films (i.e., BPA-MIP MPTES and BPA-MIP DAMOT ) and their corresponding blank NIP MPTES and NIP DAMOT as references. The specificity for BPA uptake was assessed by calculating the adsorption capacities, Q (mg/g) and imprinting factors, F of films (Figure 7a,b). From this point of view, the quantification of bonded BPA was conducted indirectly by determining the un-bonded BPA from the supernatants at 278 nm (characteristic wavelength for BPA absorbance). Figure 7a shows the adsorption kinetics of the two BPA-MIP films and their corresponding blank NIPs from a 0.20 g/L BPA solution. The adsorption capacity of all films increased rapidly in the first 20 min, especially for the BPA-MIP films. This trend was followed by a plateau after which the binding equilibrium (Qe) was attained, at 60 min. The NIP films presented similar adsorption profiles over time compared to BPA-MIP films and attained lower values for the adsorption capacity due to the lack of specific binding sites. More importantly, the imprinting factor (F) of BPA-MIP MPTES (Figure 7b) was 3.03 in the first 5 min, indicating not only excellent imprinting of BPA but also the recommended time of contact for attaining the most specific adsorption of BPA. As a result, the following isothermal adsorption of BPA in ethanol was determined after only 5 min of contact with the two types of films, in a concentration range varying from 0.08 to 0.2 g/L. As shown in Figure 8, the rebinding amounts of BPA increased gradually with the increasing BPA concentration. The rebinding of BPA, for both BPA-MIP films, exhibited an incremental increase of the adsorption capacity values [28]. As expected, the bonded amount of BPA to the MIP was higher than the one bonded to the NIP. Considering that the concentration of BPA feed solution (Ci) was varied between 0.08-0.20 g/L, the maximum adsorption capacity values were registered at 0.20 g/L, for both the BPA-MIPMPTES and NIPMPTES (Qmax 11.98 and 3.96 mg g −1 , respectively). This high difference in BPA binding affinity to the BPA-MIP and NIP clearly indicated the role of the imprinting in the formation of specific binding sites. Moreover, comparing the adsorption capacity values of the two imprinted films, it was observed that BPA-MIPDAMOT registered a maximum adsorption capacity of 8.78 mg/g for the same BPA feed solution (Ci = 0.20 g/L). These results highlighted the impact of the film thickness and the discrete porous structure of BPA-MIPDAMOT film upon the rebinding performance. Chang et al. [2] reported a maximum BPA adsorption of silica MIPs nanospheres of 444.6 μmol g −1 and Yang and Park [31] reported a Qmax of 170 mg g −1 . Hence, in this case, it seems like thinner films are more efficient for rebinding BPA and the maximum capacities are in good agreement with other reported values.
Considering that the best results were obtained for thinner BPA-MIPMPTES films, it was expected to have better performances for NIPMPTES vs. NIPDAMOT films. Thereby, it seemed like the different growth mechanism of the organosilica matrix upon BPA addition somehow affected the following binding properties of BPA-MIPDAMOT films as compared to the MIP/NIP system with MPTES. As a result, the following isothermal adsorption of BPA in ethanol was determined after only 5 min of contact with the two types of films, in a concentration range varying from 0.08 to 0.2 g/L. As shown in Figure 8, the rebinding amounts of BPA increased gradually with the increasing BPA concentration. The rebinding of BPA, for both BPA-MIP films, exhibited an incremental increase of the adsorption capacity values [28]. As expected, the bonded amount of BPA to the MIP was higher than the one bonded to the NIP. Considering that the concentration of BPA feed solution (Ci) was varied between 0.08-0.20 g/L, the maximum adsorption capacity values were registered at 0.20 g/L, for both the BPA-MIP MPTES and NIP MPTES (Qmax 11.98 and 3.96 mg g −1 , respectively). This high difference in BPA binding affinity to the BPA-MIP and NIP clearly indicated the role of the imprinting in the formation of specific binding sites. Moreover, comparing the adsorption capacity values of the two imprinted films, it was observed that BPA-MIP DAMOT registered a maximum adsorption capacity of 8.78 mg/g for the same BPA feed solution (Ci = 0.20 g/L). These results highlighted the impact of the film thickness and the discrete porous structure of BPA-MIP DAMOT film upon the rebinding performance. Chang et al. [2] reported a maximum BPA adsorption of silica MIPs nanospheres of 444.6 µmol g −1 and Yang and Park [31] reported a Qmax of 170 mg g −1 . Hence, in this case, it seems like thinner films are more efficient for rebinding BPA and the maximum capacities are in good agreement with other reported values.
Considering that the best results were obtained for thinner BPA-MIP MPTES films, it was expected to have better performances for NIP MPTES vs. NIP DAMOT films. Thereby, it seemed like the different growth mechanism of the organosilica matrix upon BPA addition somehow affected the following binding properties of BPA-MIP DAMOT  Nevertheless, both imprinted films, BPA-MIPMPTES and BPA-MIPDAMOT, exhibited higher affinity for BPA than the corresponding non-imprinted films leading to the maximum imprinting factors of 3.03 and 1.37, respectively (Figure 8b). Therefore, it can be seen that BPA-MIPMPTES films were more efficient for BPA recognition concluding that the imprinting effect was clearly distinguished by these preliminary batch rebinding tests. The higher values of the imprinting factor and of the binding capacity registered for BPA-MIPMPTES, compared to BPA-MIPDAMOT were in agreement with the conclusions drawn from the morpho-structural evaluation of films. According to other reported values for the imprinting factor, such as the one reported for nylon nanofibers (3.4 [32]) and the one reported by Yang and Park (2.15 [31]), the maximum F value of 3.03 found in this study is quite adequate.

Reusability and Stability of Films
The reusability and stability of the prepared BPA-MIP and NIP films were also evaluated. Reusability and, implicitly, stability are some of the most important features of MIPs due to the fact that are decisive factors for establishing the whole cost-effectiveness of the process. Thereby, in order to evaluate the performance at repeated use, the films were subjected to 5 reutilization cycles. As shown in Figure 9, all the films can be effectively regenerated for further usage with only around 35% loss of the initial rebinding capacity after three cycles, demonstrating high stability and reusability in BPA recognition. After the 4th cycle the binding capacity drops dramatically, up to 65% in the final cycle. Therefore, the BPA-MIP films proved to maintain their structure after several reuse. Yet, it is recommended to use the films only for 3 cycles as the specificity is also altered after the 4th and 5 th cycles; the binding capacities of the NIP presented a much lower binding capacity loss. The relative standard deviation (RSD) value of 2.1% ascribed to the good repeatability of the films. It is relevant to mention that all the films were able to withstand the conditions for reconditioning and rebinding for at least five cycles without detaching from the glass support. In terms of long-term stability, the films were kept in dry conditions for several months at room temperature when not in use. Nevertheless, both imprinted films, BPA-MIP MPTES and BPA-MIP DAMOT , exhibited higher affinity for BPA than the corresponding non-imprinted films leading to the maximum imprinting factors of 3.03 and 1.37, respectively (Figure 8b). Therefore, it can be seen that BPA-MIP MPTES films were more efficient for BPA recognition concluding that the imprinting effect was clearly distinguished by these preliminary batch rebinding tests. The higher values of the imprinting factor and of the binding capacity registered for BPA-MIP MPTES , compared to BPA-MIP DAMOT were in agreement with the conclusions drawn from the morpho-structural evaluation of films. According to other reported values for the imprinting factor, such as the one reported for nylon nanofibers (3.4 [32]) and the one reported by Yang and Park (2.15 [31]), the maximum F value of 3.03 found in this study is quite adequate.

Reusability and Stability of Films
The reusability and stability of the prepared BPA-MIP and NIP films were also evaluated. Reusability and, implicitly, stability are some of the most important features of MIPs due to the fact that are decisive factors for establishing the whole cost-effectiveness of the process. Thereby, in order to evaluate the performance at repeated use, the films were subjected to 5 reutilization cycles. As shown in Figure 9, all the films can be effectively regenerated for further usage with only around 35% loss of the initial rebinding capacity after three cycles, demonstrating high stability and reusability in BPA recognition. After the 4th cycle the binding capacity drops dramatically, up to 65% in the final cycle. Therefore, the BPA-MIP films proved to maintain their structure after several reuse. Yet, it is recommended to use the films only for 3 cycles as the specificity is also altered after the 4th and 5th cycles; the binding capacities of the NIP presented a much lower binding capacity loss. The relative standard deviation (RSD) value of 2.1% ascribed to the good repeatability of the films. It is relevant to mention that all the films were able to withstand the conditions for reconditioning and rebinding for at least five cycles without detaching from the glass support. In terms of long-term stability, the films were kept in dry conditions for several months at room temperature when not in use.

Conclusions
The study provides significant information regarding the role of functional monomers in the molecular imprinting process of BPA in silica networks. The two sets of BPA molecularly imprinted films (i.e., BPA-MIPDAMOT and BPA-MIPMPTES) were successfully prepared via sol-gel derived methods using N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (DAMO-T) and (3-mercaptopropyl)trimethoxysilane (MPTES) as functional organosilane monomers.
Morpho-structural, thermal, and optical studies were undertaken to assess the influence of the monomers' functionalities upon the overall features of films but also to highlight the meaningful changes brought by the addition of BPA. Ellipsometry results suggested that there is much potential for application of such BPA-MIP films in optical sensing applications. An evaluation of specificity for BPA was conducted and the relevant results on adsorption capacities and imprinting factors for both types of films-were in agreement with their morpho-structural properties.
The overall results have shown that thinner films with better-defined porous morphology, meaning BPA-MIPMPTES were more likely to retain BPA molecules. In this case, the most specific binding of BPA was registered in the first five minutes after contact (F = 3.03). BPA-MIP films were effectively regenerated for further usage 5 times and the adsorption capacity of films decreased only by 35% after three cycles, demonstrating high stability and reusability.
In order to ascertain the real application potential of the prepared sol-gel imprinted films for BPA detection, the next challenges will assume an investigation of the selective adsorption of BPA-MIP films using compounds with similar structure and application of the methodology for real samples contaminated with BPA. Considering that the BPA-MIPs films enable stability and reusability, the real-time response can be estimated in terms of quantification limit (LOQ) in the range of ng-μg in aqueous samples. Although further investigations are required, this work is a step forward to develop simple and cost-effective molecularly imprinted silica films for optical sensors.

Conclusions
The study provides significant information regarding the role of functional monomers in the molecular imprinting process of BPA in silica networks. The two sets of BPA molecularly imprinted films (i.e., BPA-MIP DAMOT and BPA-MIP MPTES ) were successfully prepared via sol-gel derived methods using N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (DAMO-T) and (3-mercaptopropyl)trimethoxysilane (MPTES) as functional organosilane monomers.
Morpho-structural, thermal, and optical studies were undertaken to assess the influence of the monomers' functionalities upon the overall features of films but also to highlight the meaningful changes brought by the addition of BPA. Ellipsometry results suggested that there is much potential for application of such BPA-MIP films in optical sensing applications. An evaluation of specificity for BPA was conducted and the relevant results on adsorption capacities and imprinting factors for both types of films-were in agreement with their morpho-structural properties.
The overall results have shown that thinner films with better-defined porous morphology, meaning BPA-MIP MPTES were more likely to retain BPA molecules. In this case, the most specific binding of BPA was registered in the first five minutes after contact (F = 3.03). BPA-MIP films were effectively regenerated for further usage 5 times and the adsorption capacity of films decreased only by 35% after three cycles, demonstrating high stability and reusability.
In order to ascertain the real application potential of the prepared sol-gel imprinted films for BPA detection, the next challenges will assume an investigation of the selective adsorption of BPA-MIP films using compounds with similar structure and application of the methodology for real samples contaminated with BPA. Considering that the BPA-MIPs films enable stability and reusability, the real-time response can be estimated in terms of quantification limit (LOQ) in the range of ng-µg in aqueous samples. Although further investigations are required, this work is a step forward to develop simple and cost-effective molecularly imprinted silica films for optical sensors.