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Synthesis, Characterization, and Environmental Applications of Novel Per-Fluorinated Organic Polymers with Azo- and Azomethine-Based Linkers via Nucleophilic Aromatic Substitution

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13 October 2023

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17 October 2023

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Abstract
This study reports the synthesis and characterization of novel per-fluorinated organic polymers with azo- and azomethine-based linkers using nucleophilic aromatic substitution. The polymers reveal variations in the fluorine content via the incorporation of decafluorobiphenyl and hexafluorobenzene linkers, which enhanced their hydrophobic nature. The rich fluorine polymers were slightly soluble in THF and have shown molecular weights between 4886 to 11948 g/mol. All polymers exhibit thermal stability in the range of 350-500°C, with varying thermal stability depending on the fluorine and nitrogen content. Conjugation of the polymers was confirmed through changes in the UV-Vis spectra, with a hypsochromic shift observed in all cases, more pronounced in azo-based fluorinated chains due to H-bonding on the nitrogen sites, chain conformations, and planarity. The optical band gap (Eg) of the polymers was determined from the UV-Vis data, with the Eg values of the azo-based fluorinated polymers being 1 eV higher than those of their corresponding linkers. The cross-linking formation was characterized by porosity measurements, with the azo-based polymer exhibiting the highest surface area of 770 m²/g with a pore volume of 0.35 cm³/g, while the open-chain azomethine-based polymer exhibited the lowest surface area of 285 m²/g with a pore volume of 0.0872 cm³/g. Porous structures with varied hydrophobicities were investigated as adsorbents for separating water-benzene and water-phenol mixtures and selectively binding methane/carbon dioxide gases from the air. The most hydrophobic polymers containing the decafluorbiphenyl linker were suitable for benzene separation, while the best methane uptake values were 6.14 and 3.46 mg/g for DAB-Z-1O and DAB-A-1O, respectively. DAB-Z-1h, with the highest surface area and rich in nitrogen sites, exhibited the highest CO₂ uptake at 298 K (17.25).
Keywords: 
Subject: Chemistry and Materials Science  -   Polymers and Plastics

1. Introduction

Perfluorinated organic polymers (PFPs) with extended ether bonds are a widely recognized type of multi-functional, open-chain organic polymers. They are synthesized by introducing fluorinated linkers into the polymer chains [1]. The C-F bond exhibits strong polarization and has a high bond energy (approximately 480 kJ/mol), which makes PFPs suitable for various applications [2]. PFPs find extensive use in various fields such as medicine, biomedical research, electronics, optoelectronics, high-quality coatings, sensors, and environmental applications [3,4,5,6]. The synthesis of PFPs has been utilized in the polymer industry to produce novel materials with several desirable properties such as high-temperature stability, high glass transition temperature, resistance to solvents, and applicability for gas separation. PFPs also exhibit an anti-flammable nature, making them useful in various applications [7,8]. PFPs possess tunable properties such as thermal and oxidative stability, hydrophobicity, lipophobicity, dielectric properties, and adjustable polarity. This enables their utilization in a diverse array of applications [9,10].
PFPs have been utilized in the synthetic modification of insoluble organic polymers by incorporating perfluorinated chains into their frameworks. This approach has improved the processability (e.g., solubility) of various insoluble organic polymers such as poly(chains), ether, imine, azo-based, imide, ketone, and sulfone, in non-polar media. This is achieved by introducing fluorinated linkers known for their hydrophobic nature (immiscibility in water) and very low dipole [4,5,9,11].
This approach has been employed to enhance the casting and moldability of various polyethers. For instance, NORYL™, a popular polyether polymer composed of polyphenylene oxide, features high aromatic content and polymer aggregation chains that restrict its solubility. To improve the moldability of NORYL™ for numerous applications, plasticizing additives such as polystyrene have been compounded with it [12]. Nevertheless, improving the processability of the polymer is often accompanied by a decrease in its thermal stability and resistance to oxidation [13]. To address this limitation, PPO was modified by selectively introducing hexafluorobenzene, decafluorobiphenyl, and bisphenol AF into its polymer backbone. This approach enriched the polymer chain with fluorine substituents, thereby enhancing its solubility and thermal stability.
Recent developments in PFPs have focused on the class of fluorinated ether-based polymers. These polymers have been synthesized through metal-catalyzed coupling reactions and nucleophilic aromatic substitution (NAS) reactions between diols and fluorinated linkers (refer to the general NAS mechanism illustrated in Scheme S1) [14,15,16]. In the NAS synthetic methodology, successful substitution of the C-F bond is achieved by using strong nucleophiles containing oxygen, such as aromatic phenoxide or aliphatic alkoxides. This approach is employed with various small-molecules or polymer chains such as fluorinated poly(aryl ether), poly(aliphatic ethers), poly(ether ketone)s, poly(ether sulfone)s, and poly(ether nitrile)s [11,17,18,19,20,21]. The above-mentioned principle is also employed in the preparation of fluorinated polyamines or fluorinated poly(sulfide) using diamines and dithiols. Furthermore, hybrid chains have been reported in the literature that demonstrate the presence of conjugated chains composed of poly(aryl ether)s alternating with poly(imide)s, poly(azomethine), or poly(diazo-based) units [4,20,22,23].
It is worth noting that the synthesis of para-connected, open-chain fluorinated polymers with optimal solubility was achieved using mild polymerization conditions. This involved the use of a weak base, optimized monomer ratio, low feeding order, and low reaction temperatures [22]. Nonetheless, these mild polymerization conditions are associated with low formation yield and long polymerization times for the polymers [13]. In contrast, utilizing harsher polymerization conditions results in optimal yield and time while producing random agglomerated frameworks with high cross-linking rates and minimal solubility. These cross-linked frameworks are created due to the rapid rate of NAS at high temperatures, leading to the substitution of C-F bonds at both para- and ortho-positions of the aromatic linkers. This results in the formation of randomly branched chains [24].
Most of the existing literature has primarily focused on the synthesis of perfluorinated organic polymers as open chains and their potential applications, with limited studies on the advantageous formation of cross-linked fluorinated polymers. However, recent work has reported the development of new cross-linked fluorinated poly(aryl ether) (C-FPAE) films. These films exhibit excellent thermal stability up to 495 °C, dimensional stability, hydrophobic properties, and a high storage modulus in high-temperature environments. Additionally, they serve as a low dielectric material [16]. Another recent study reported the synthesis of new cross-linked fluorinated polymers that functioned as a supporting skeleton for controlling the structural integrity of Al/oxidizer microspheres in the production process of composite propellants [25].
After conducting a thorough review of the literature, we have observed a limited number of reports emphasizing the potential advantages of synthesizing fluorinated cross-linked frameworks. Furthermore, there is a lack of research on the opportunity to create high-surface-area and porous frameworks through cross-linking, which would enhance their potential for environmental applications such as separation.
The absence of sufficient research in this area has motivated us to focus on synthesizing a new series of fluorinated organic polymers and investigating the factors that impact their solubility, polarity, and porosity after cross-linking formation. Our initial phase involves incorporating diol-based linkers, specifically nitrogen-rich organic linkers such as azomethine and azo-based compounds, connected with fluorinated linkers into the new polymers. These combinations were specifically chosen to study the impact of fluorine content on the solubility of poly(imine)s and poly(diazo-based) polymers. Additionally, we investigated the influence of factors such as the size of the fluorinated linker, the connection site (ortho or para), and the cross-linking polymerization conditions. The newly synthesized polymers were then tested as solid sorbents for phenol, benzene, carbon dioxide, and methane. By testing polar and non-polar adsorbates, we aimed to fine-tune the polarity of the polymers during cross-linking formation. The confirmation of successful polymer preparation through the NAS reaction was achieved using the 19F-NMR technique. Additionally, we utilized various characterization techniques to verify the synthesis of the polymers and establish their porosity. This study also presents the environmental applications of these polymers in separating the selected adsorbates.

2. Material and Methods

2.1. Materials

All chemicals used in this study were purchased from Sigma-Aldrich and used without additional purification, except where specified. The polymer synthesis was conducted using the Schlenk line technique, in the presence of a Dean-Stark trap and under a nitrogen atmosphere. The structures of both the linkers and polymers were confirmed using 1H-NMR and 13C-NMR techniques. Meanwhile, 19F-NMR was only utilized for the analysis of polymers. These measurements were conducted using a Bruker 500 MHz-Avance III spectrometer in deuterated DMSO (DMSO-d6). Additionally, the FTIR spectra of all structures were recorded using a Shimadzu FTIR-8300, employing KBr pellets in the range of 4000-600 cm-1. The thermogravimetric analysis (TGA) of the polymers was performed using a Perkin Elmer TGA800 device. The samples were heated under air from 30 to 850°C, with a heating rate of 10°C/min. UV-Vis measurements were conducted using a Shimadzu UV spectrometer UV-1800. Molecular weight measurements were done by gel permeation chromatography (GPC) using a Waters 510 system equipped with a UV detector set at 254 nm. THF was used as eluent and the calibration was made with polystyrene standards. The surface area, argon sorption isotherms at 87 K, methane and carbon dioxide uptakes at 298 K were obtained using a by using a TriStar II 3020 surface area and porosity analyzer (Micromeritics, USA). The argon isotherm was obtained at a temperature of 87 K and used to determine the pore size distribution and Brunauer-Emmett-Teller (BET) surface area. Prior to conducting the porosity measurements, the samples were degassed under vacuum at a temperature of 150°C for a duration of 12 hours.

2.2. Synthesis of Organic linkers

2.2.1. Synthesis of 4,4-(diazomethine phenyl)-o-diphenol (DAB-A-OH)

DAB-A-OH was synthesized using a Schiff-base condensation reaction, following the procedures described in previous literature [26]. In the synthetic protocol, a solution of aromatic diamine (2.0 mmol) in 10.0 mL of absolute ethanol was added gradually over a 15-minute period to a separate solution containing salicylaldehyde (4.0 mmol) dissolved in 10.0 mL of absolute ethanol. A catalytic amount of glacial acetic acid (1.0 mL) was then added to the solution, resulting in a yellow-colored mixture, which was refluxed for a duration of 6 hours. The resulting precipitate was filtered, washed multiple times using water and diethyl ether, and dried under a vacuum. The final product was a yellow solid that showed solubility in DMF, DMSO, and CHCl3. The yield obtained was 87%, and the melting point was recorded to be between 127-129°C. The 1H-NMR analysis of the product showed a chemical shift of δ 6.98 (s, 1H, Ar-H), 7.02-7.69 (m, 11H, Ar-OH, Ar-H), 9.06 (s, 2H, HC=N-), and 13.04 (s, 2H, Ar-OH) at a temperature of 298 K. The 13C-NMR spectrum revealed chemical shifts of δ 114.33, 117.11, 119.72, 120.66, 130.83, 133.11, 133.94 (Ar-C), 149.73 (N-C-Ar), 160.79 (-C=N-), and 164.64 (ArC-OH) at the same temperature (Figure S1-S2).

2.2.2. Synthesis of 4,4-(diazophenyl)-p-diphenol (DAB-Z-OH)

The synthesis of DAB-Z-OH involved a diazotization reaction as per previously reported literature [27]. To synthesize DAB-Z-OH, 1,3-Diaminobenzene (DAB) (3.0 mmol) was dissolved in 30 mL of distilled water and stirred for 15 minutes. Next, concentrated hydrochloric acid (9 mmol) was added dropwise to the solution while maintaining a temperature of 0-4°C. Solution 2, which contained sodium nitrite (6 mmol) in 10 mL of distilled water, was then added dropwise to Solution 1. Once the diazotization process was complete, the mixture was stirred for an hour while the temperature was kept around 4°C. The solution was slowly added to a mixture of 6 mmol of phenol, 10 mL of ethanol, and a buffer solution containing acetic acid and sodium acetate with a pH of 6.5. The final mixture was then stirred in an ice bath for two hours to produce the dye. Afterward, the dye was filtered, washed with cold water, and dried under a vacuum. The final product obtained was a lustrous red crystalline solid that could dissolve in methanol, DMSO, and DMF. The yield of the product was 85%, and the melting point was below 300°C, beyond which it decomposed. The 1H-NMR spectrum, recorded at 500 MHz in DMSO-d6 at 298 K, showed peaks at δ 6.92 (d, 4H, Ar-OH), 7.73 (d, 4H, Ar-OH), 7.74 (q, 1H, Ar-H), 7.79 (d, 2H, Ar-H), 8.16 (s, 1H, Ar-H), and 10.43(s, 2H, Ar-OH). Likewise, the 13C-NMR spectrum, recorded at 500 MHz in DMSO-d6 at 298 K, displayed peaks at δ 115.99, 124.55, 125.12, 130.27, 145.11 (Ar-C), 161.32 (ArC-OH), and 152.86 (C-N=N-) (Figure S3-S4).

2.3. General synthesis of per-fluorinated polymers

To start the synthesis process, we dissolved di-phenol linkers (0.44 mmol) of either DAB-A-OH or DAB-Z-OH and potassium carbonate (0.52 mmol) in 10 mL of toluene and 50 mL of dimethylacetamide (DMAc) inside a 250 mL Schlenk flask. We then connected a Dean-Stark trap and reflux setup to the flask and purged the system with an inert nitrogen flow to create an oxygen-free environment. The solution containing di-phenol linkers and potassium carbonate underwent six hours of reflux to collect most of the produced water in the trap and remove it. The excess toluene was then distilled off to produce the phenoxide anion. The cooled solution was combined with DMAc and gradually added to a solution of hexaflourobenzene (HFB) or decaflourobiphenyl (DFB) monomers (0.44 mmol). The resulting solution was then stirred for three hours at room temperature and heated to 60 °C for 48 hours. We carefully poured the solution into a 1000 mL beaker that contained a concentrated mixture of HCl, water, and methanol (0.5:1:1). After forming a precipitate, we filtered, washed it with water, and dried it under a vacuum. The resulting pale to dark-brown solid showed slight solubility in THF, diethyl ether, DMSO, and CHCl3. The physical and spectral data of the product are as follows:

2.3.1. Poly(4,4-(diazomethine phenyl)-o-diphenoxy-tetrafluorbenzene) (DAB-A-1h):

DAB-A-1h was synthesized by the polymerization of (DAB-A-OH) and (HFB), resulting in brown solid with a yield (0.22 g, 82%); FTIR (KBr) ν cm-1: 3600-3000 (Ar-OH), 2800-3000 Ar(-C-H), 1600 (-C=N-), 1475-1505 Ar(-C=C-), 1216 Ar(C-O-C), 1007 (C-F); 1H-NMR (500 MHz, DMSO-d6, ppm, 298 K): weak broad signals in the range δ (7.21- 7.82) and the asymmetric protons of (H-C=N-) appears at two positions (9.67, 10.49); 13C-NMR (500 MHz, DMSO-d6, ppm, 298 K): Ar-C appeared in the ranges δ (115.49-130.9), C-F appeared at δ (139.42, 141.05, 140.94, 144.0), (-C=N) at δ 170.17, Ar(C-N) at δ 156.04 and Ar(C-O) at δ 158.71. 1H-NMR and 13C-NMR are shown in Figure S5-S6. 19F NMR (500MHz, DMSO-d6, ppm, 298 K) (Figure 2A): Peak at -154.66 corresponding to the chemical shift of the (fluoro group–sites) after the polymerization that takes place on the para-sites of HFB. The peaks at -155.05, -157.89, -157.93, -160.81, -161.25, -166.77, -167.66, and -168.67 are related the random polymerization (on ortho and para) of HFB.

2.3.2. Poly(4,4-(diazomethine phenyl)-o-diphenoxy-octafluorobiphenyl) (DAB-A-1O):

DAB-A-1O was produced by polymerizing (DAB-A-OH) and (DFB), resulting in a brown and solid polymer with a weight of 0.20 g and a yield of 69%. The FT-IR spectrum (KBr) revealed peaks at 3600-3000 cm-1 (Ar-OH), 2800-3000 cm-1 (Ar(-C-H)), 1608 cm-1 (-C=N-), 1488-1505 cm-1 (Ar(-C=C-)), 1194 cm-1 (Ar(C-O-C)), and 979 cm-1 (C-F). The 1H-NMR spectrum, measured at 500 MHz in DMSO-d6 at 298 K, showed weak broad signals in the δ range (6.51-8.63). The 13C-NMR spectrum, also recorded at 500 MHz in DMSO-d6 at 298 K, displayed the appearance of Ar-C in the δ range (119.66-129.68), C-F at δ (136.73-145.80), (-C=N) at δ 170.03, Ar(C-N) at δ 162.24, and Ar(C-O) at δ 160.0. Both the 1H-NMR and 13C-NMR spectra are included in Figure S7-S8. Additionally, the 19F NMR spectrum was recorded at 500 MHz in DMSO-d6 at 298 K (Figure 2B), which exhibited peaks at -140.69 and -148.2, indicating para-polymerization of DFB with no further random polymerization peaks.

2.3.3. Poly(4,4-(diazophenyl)-p-diphenoxy-tetrafluorbenzene) (DAB-Z-1h):

DAB-Z-1h was obtained by polymerizing (DAB-Z-OH) and (HFB), resulting in a brown and solid polymer with a weight of 0.22 g and a yield of 88%. The FTIR spectrum (KBr) showed peaks at 3600-3000 cm-1 (Ar-OH), 2800-3000 cm-1 (Ar(-C-H)), 1518 cm-1 (-N=N-), 1500-1560 cm-1 (Ar(-C=C-)), 1211 cm-1 (Ar(C-O-C)), and 997 cm-1 (C-F). The 1H-NMR spectrum, recorded at 500 MHz in DMSO-d6 at 298 K, exhibited weak broad signals in the δ range (6.51-8.63). Similarly, the 13C-NMR spectrum, measured at 500 MHz in DMSO-d6 at 298 K, showed the appearance of Ar-C in the δ range (116.15-116.94, 122.88-137.44), Ar(C-O-C) at δ 170.0, and (C-N=N-) at δ 155.0 and 160.0. C-F appeared at δ (139.42, 140.05, 140.94, 143.00, 143.75, 148.60, 153.0). Both 1H-NMR and 13C-NMR are displayed in Figure S9-S10. The 19F NMR spectrum, recorded at 500 MHz in DMSO-d6 at 298 K (Figure 3A), displayed the peak at -154.95 corresponding to the polymerization at the para-positions of HFB, while the peaks at -140.70, -147.97, -148.21, -157.93, -160.62, -161.35, and -162.25 were related to further random connections at the ortho- and para-positions of HFB.

2.3.4. Poly(4,4-(diazophenyl)-p-diphenoxy-octafluorobiphenyl) (DAB-Z-1O):

DAB-Z-1O was synthesized by polymerizing (DAB-Z-OH) and (DFB), resulting in a brown and solid polymer with a weight of 0.26 g and a yield of 70%. The FTIR spectrum (KBr) displayed peaks at 3600-3000 cm-1 (Ar-OH), 2800-3000 cm-1 (Ar(-C-H)), 1491 cm-1 (-N=N-), 1500-1560 cm-1 (Ar(-C=C-)), 1211 cm-1 (Ar(C-O-C)), and 972 cm-1 (C-F). The 1H-NMR spectrum, recorded at 500 MHz in DMSO-d6 at 298 K, showed weak broad signals in the δ range (7.43-8.85). Similarly, the 13C-NMR spectrum, measured at 500 MHz in DMSO-d6 at 298 K, revealed the appearance of Ar-C in the δ range (119.9-129.0), δ (C-F) at δ (143.42, 144.05, 144.94, 146.00), Ar(C-O-C) at 180.0, and (C-N=N-) at 170.0 and 155.0. Both 1H-NMR and 13C-NMR are shown in Figure S11-S12. The 19F NMR spectrum, recorded at 500 MHz in DMSO-d6 at 298 K, displayed peaks at -138.88 and -153.97 related to the polymerization on the para-position of DFB, while the peaks at -138.64, -141.30, -160.34, and -160.38 were attributed to random polymerization.

3. Results and Discussion

3.1. Synthesis of organic linkers

The aim of our study was to synthesize a fresh set of open-chain organic polymers that are fully fluorinated. To achieve this, we utilized the nucleophilic aromatic substitution (NAS) reaction method, which involves the reaction between di-phenols and aromatic fluorinated linkers as outlined in existing literature [5,14]. The di-phenols used in our study were DAB-A-OH and DAB-Z-OH, which are azomethine-based and diazo-based, respectively. DAB-A-OH was obtained through the condensation reaction of salicylaldehyde with 1,3-diaminobenzene (DAB) under reflux conditions for 24 hours in an acid-catalyzed medium (acetic acid) as shown in Scheme 1A. The final product was a yellow solid with good solubility in various solvents such as DMSO, DMAc, DMF, methanol, and ethanol. The authenticity of the product was confirmed through 1H, 13C-NMR, and FTIR analysis. Confirmation of linker formation was achieved through 1H-NMR analysis, where the proton of an imine bond (-HC=N-) was observed at δ 9.06, and the incorporation of the phenol group (proton of OH) was seen at δ 13.04, as demonstrated in Figure S1. Similarly, 13C-NMR analysis of DAB-A-OH displayed distinct carbon regions (Figure S2), with two prominent carbons of the imine bond (-C=N-) and (C-OH), observed at δ 160.79 and 164.64, respectively. Additionally, the FTIR spectrum within the range of 4000–600 cm-1 and expanded area of 2500–700 cm-1 (Figure 1 A-B) allowed for identification of the hydroxyl of Ar-OH and the imine bond (-C=N-) at 3600–3000 and 1622 cm-1, respectively.
The diazo-based linker DAB-Z-OH was synthesized through the diazotization reaction of the appropriate 1,3-diaminobenzene (DAB), followed by coupling of the bis(diazonium salt) with di-phenol, as shown in Scheme 1B. The final product obtained was a dark brown solid, soluble in polar solvents such as DMAc and DMSO. Analysis through 1H-NMR revealed all protons appearing in the aromatic region, while the OH- group proton was determined at δ 10.43. Notably, the prominent carbons related to phenol-C and (C-N=N-) were observed at δ 161.3 and 152.9, respectively (Figure S3–S4). The FTIR spectrum covering the full range of 4000–600 cm-1 and expanded area of 2500–700 cm-1 (Figure 2 A-B) allowed for the identification of bands corresponding to (Ar-OH), Ar(-C-N), and (-N=N-) at 3600–3000, 1590, and 1500 cm-1, respectively.

3.2. Synthesis of perfluorinated polymers

Following the successful characterization of the di-phenol organic linkers, we synthesized four new fluorinated polymers by coupling (1: 2.5 mmol) of the linkers DAB-A-OH and DAB-Z-OH with HFB and DFB, respectively, as illustrated in Scheme 2. The newly produced series of polymers were named DAB-A-1h, DAB-A-1O, DAB-Z-1h, and DAB-Z-1O, where the symbols (h) and (O) signify hexa- and octa- groups, respectively, and (A) and (Z) correspond to azomethine and azo-based groups, respectively. The polymers were synthesized using a one-step polycondensation reaction between di-phenols and fluorinated linkers in the presence of potassium carbonate as a base through the nucleophilic aromatic substitution (NAS) reaction. The formation of the bis-phenoxide basic sites was followed by a nucleophilic substitution reaction at the C-F bond, resulting in the anticipated extended ether (C-O-C) chains. The general mechanism for this reaction is depicted in Scheme S1.
As outlined in the synthetic methodology, the polymers were precipitated in an acidic solution, filtered, and washed with water several times to eliminate any residual potassium fluoride salt. The final products obtained were pale to dark brown solids, with good yields (Table 1). While all the polymers exhibited slight solubility in DMSO, DMAc, and THF the polymer DAB-A-1O was completely soluble in diethyl ether and THF, as demonstrated in Figure S14. The slight to good solubility of the polymers in THF has allowed us to determine their molecular weight by applying gel permeation chromatography (GPC) measurements. As summarized in Table 1, DAB-A-1O is soluble in THF and has shown the highest number and weight average molecular weights (Mn = 4068, Mwt = 11948 g/mol). The other polymers have shown lower values due to the slight solubility during the measurements. DAB-Z-1h is insoluble in THF, thus we couldn’t apply the measurement. Confirmation of the formation of ether bonds in all the polymers was achieved through 1H- and 13C-NMR analysis, as shown in Figures S5-S12.
In the 1H-NMR spectra of DAB-A-1h and DAB-A-1O, the disappearance of the terminal hydroxyl group (OH) proton, which appears around 13 ppm in the spectrum of the linker DAB-A-OH (Figure S5, S7), was observed. Similarly, in the polymers DAB-Z-1h and DAB-Z-1O, the disappearance of the terminal hydroxyl group proton, located around 11 ppm as seen in the 1H-NMR spectrum of the linker DAB-Z-OH (Figure S9, S11), was detected. The 13C-NMR spectra of the polymers validated the integration of the fluoro-aromatic linkers, evident from the C-F chemical shifts appearing within the range of 137–144 ppm. Additionally, the disappearance of the OH group and the subsequent formation of the C-O-C ether linker occurred around 170 ppm, while the inclusion of phenyl-N and C=N was observed at 155–159 ppm (Figure S6, S8). In contrast, the presence of phenyl-N=N was confirmed at 155–160 ppm in the 13C-NMR spectra of polymers DAB-Z-1h and DAB-Z-1O (Figure S10, S12). The limited resolution of the peaks observed in the 1H- and 13C-NMR spectra of the polymers may be attributed to the slight solubility of the polymers in the polar solvent DMSO. Moreover, the cross-linking formation of the polymer chains could have contributed to the enhanced aggregation, further impacting the resolution of the peaks.
The FTIR spectra of the polymers in the range of 4000–600 cm-1, along with the expanded area of 2500–700 cm-1, demonstrated significant changes due to the integration of fluorinated benzene (HFB) and (DFB) in the polymer chains. Notably, the broad area of the OH group around 3000 cm-1 gradually decreased upon polymerization, and the observed broadening may be attributed to the presence of un-polymerized terminals of the linkers DAB-Z-OH or DAB-A-OH. Alternatively, the broadening may be due to the presence of agglomerated water molecules. Confirmation of the successful NAS reaction at the fluoro-sites was established through the formation of the C-O-C bond around 1250 cm-1 and the integration of the C-F bond around 1000 cm-1. The inclusion of the di-azo (N=N) and azomethine (C=N) groups was evident in the range of 2500–500 cm-1, appearing at 1500 and 1630 cm-1, respectively. The FTIR spectra of the polymers, along with their corresponding monomers, are presented within the range of 4000–600 cm-1 and the expanded area of 2500–700 cm-1, as demonstrated in Figure 1.
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Figure 1. FTIR in the full and expanded ranges: (A-B) DAB-A-OH and the corresponding polymers; (C–D) DAB-Z-OH and corresponding polymers.
Figure 1. FTIR in the full and expanded ranges: (A-B) DAB-A-OH and the corresponding polymers; (C–D) DAB-Z-OH and corresponding polymers.
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3.3. Nucleophilic aromatic substitution (NAS) and cross-linking formation

As mentioned earlier, the synthesis of novel ether-linked perfluorinated polymers was achieved through the NAS mechanism. The polymerization process involved the deprotonation of DAB-A-OH and DAB-Z-OH to generate bis-phenoxide anion (Nu:), followed by the nucleophilic attack of the fluorine positions of the fluorinated linkers such as HFB and DFB. The nucleophilic attack occurred at the (C-F) bond, which was ortho or para to another C-F bond, thereby facilitating the substitution reaction. The detailed steps of the reaction mechanism are presented in Scheme S1. The polymerization technique employed in this study has been utilized in the preparation of numerous previously reported perfluorinated organic polymers [1,4,10,21]. As stated in the literature, the preparation of polymers containing HFB or DFB linkers was conducted under mild conditions, with relatively low temperatures that did not exceed 80 °C, along with a prolonged stirring time [22]. In this instance, the polymers were created as para-connected extended open chains, exhibiting low formation yield, and displaying good solubility in non-polar solvents [28,29]. In contrast, performing the polymerization at high temperatures resulted in the formation of polymers with good yield but limited solubility. For instance, a collection of perfluorocyclobutyl-based polymers were synthesized at polymerization temperatures ranging from 160–200 °C. These polymers exhibited limited solubility in most organic solvents and appeared as random-agglomerated chains referred to as cross-linked frameworks [30]. In this regard, we have focused on obtaining extended cross-linked chains that exhibit a porosity nature. To reach this target, we have repeated the experimental protocol with optimal conditions, where the temperature did not exceed 60 °C with gradual heating over 48 hrs.
To identify the possibility of forming open-chains or cross-linked polymers, we conducted an analysis of the polymers using 19F-NMR. Given that the polymerization temperature reached 60 °C, random NAS and the formation of agglomerated chains were anticipated. The 19F-NMR spectra of the polymers were acquired using DMSO-d6 solvent, and the chemical shifts of the fluorine groups were determined and compared with J-coupled spectroscopy (JCS) calculations (Table S1) [31]. In this study, we investigated the 19F-NMR spectra of the new polymers and propose their formation based on the following two aspects:

3.3.1. Azomethine-based fluorinated polymers

The azomethine-based polymers (DAB-A-1h and DAB-A-1O) were synthesized through the polymerization of HFB or DFB with DAB-A-OH, respectively (Scheme 2). According to the NAS mechanism, the anticipated structure of DAB-A-1h should exhibit one type of 19F located at the -155 ppm position, which corresponds to the fluorine of the C-F bonds labeled (a) in Figure 2A. However, the 19F-NMR spectrum of DAB-A-1h exhibited three additional peaks at positions -157.8, -160.8, and -167 ppm, which can be attributed to the formation of side products resulting from the polymerization on the ortho-sides labeled (*). In contrast, the 19F-NMR spectrum of DAB-A-1O confirmed the successful and controlled para-substituted open chain through the presence of two distinctive peaks at -141 and -148 ppm, as shown in Figure 2B. These peaks were assigned to the two different types of fluorine in the C-F bonds on the biphenyl linker, labeled (a) and (b) in Figure 2B.
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Figure 2. 19F-NMR spectra of the polymers: (A) DAB-A-1h and (B) DAB-A-1O in DMSO.
Figure 2. 19F-NMR spectra of the polymers: (A) DAB-A-1h and (B) DAB-A-1O in DMSO.
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The formation of the polymers can also be influenced by the size and type of linkers used, in addition to the polymerization conditions. In this case, both DFB and HFB were linked to the phenoxide group, which was located ortho to the -C=N- group. The steric factor that resulted from connecting DFB and HFB to the phenoxide group, which was ortho to the -C=N- group, played a role in the formation of the polymers. This connection contributed to further structural collapse. Due to the steric effect and the large size of DFB, the accessible sites for further NAS were limited, resulting in an open-chain polymer (DAB-A-1O). On the other hand, even though DAB-A-1h was synthesized under the same conditions, the small size of HFB facilitated random NAS. The higher reactivity of HFB was due to the flexible rotation of the linker, which provided more available fluorine sites for nucleophilic substitution during the polymerization process. DAB-A-1O, which had a larger size DFB linker, had limited sites for further NAS, leading to the formation of an open-chain polymer. DAB-A-1O had good solubility in non-polar solvents, such as THF and diethyl ether, owing to its hydrophobic nature and high fluorine content (Figure S14). On the other hand, the limited solubility of DAB-A-1h and DAB-A-1O in polar solvents, such as DMAc, DMSO, and chloroform, was attributed to the presence of the nitrogen atom in the C=N group [9,11,46].

3.3.2. Diazo-Based Fluorinated Polymers

Fluorinated polymers with diazo-based linkers (DAB-Z-1h and DAB-Z-1O) were prepared by coupling DAB-Z-OH with HFB and DFB, respectively. The 19F-NMR spectra of both polymers indicated the formation of cross-linked structures in addition to the expected open chains. The linker DAB-Z-OH contained hydroxyl groups para to the azo group, unlike DAB-A-OH (Scheme 1B). The presence of hydroxyl groups para to the azo group in DAB-Z-OH increased the accessibility of the fluorine atoms for the NAS during polymerization. The free rotation of the fluorinated linkers allowed for random substitution of the phenoxide on the C-F sites, which led to the elimination of steric factors and facilitated the NAS. As a result, cross-linking occurred, forming both expected open chains and cross-linked structures in DAB-Z-1h and DAB-Z-1O, as confirmed by their 19F-NMR spectra. The 19F-NMR spectrum of DAB-Z-1h indicated a peak at -154.95 ppm labeled (a) in Figure 3A, which was assigned to the fluorine of C-F bonds of the para-connected polymer. However, the other peaks at -140.70, -147.97, -148.21, -157.93, -160.62, -161.35, and -162.25 ppm were attributed to C-F bonds that were formed due to the random polymerization, as shown in Figure 3A. Similarly, in the 19F-NMR spectrum of DAB-Z-1O, two peaks at -138.88 and -153.97 ppm were observed, labeled (a) and (b) in Figure 3B, corresponding to the C-F bonds of para-connected chains. Other peaks around -138.64, -141.3, and -160.34 ppm were related to C-F bonds after random polymerization. The presence of asymmetric structures due to the flexible rotation of the chains was indicated by the observed duplication of peaks.
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Figure 3. 19F-NMR spectra of the polymers (A) DAB-Z-1h and (B) DAB-Z-1O in DMSO.
Figure 3. 19F-NMR spectra of the polymers (A) DAB-Z-1h and (B) DAB-Z-1O in DMSO.
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3.4. Thermal stability of the polymers

The thermal stability of organic polymers is a crucial factor that determines their potential applications in various fields, including electronic and environmental applications. Perfluorinated polymers (PFPs) have shown promising properties in terms of thermal stability under both air and inert conditions, making them an attractive option for such applications [32]. A widely recognized fact is that the presence of a significant amount of heteroatoms in polymer structures increases their thermal stability [33]. The newly synthesized polymers contain a high amount of fluorine and nitrogen functional groups, which make them potentially thermally stable. Therefore, it was important to investigate the thermal stability of these polymers.
The thermal stability of the newly synthesized polymers was investigated using TGA with a heating rate of 10 °C/min from 30 to 850 °C under air atmosphere, as shown in Figure 4A. The TGA results indicate that DAB-Z-1h and DAB-Z-1O exhibit significantly higher thermal stability when compared to DAB-A-1h and DAB-A-1O. The higher thermal stability observed in the diazo-based polymers could be attributed to their high nitrogen content, as well as the para-connections between the linkers and cross-linking formation. It has been suggested in several studies that para-connected polymers exhibit greater thermal stability than their meta- or ortho-connected counterparts [34]. In contrast, DAB-A-1O exhibited higher thermal stability than DAB-A-1h, possibly due to its high fluorine content and linear chain formation, as verified by the 19F-NMR analysis. This finding is consistent with a previously reported series of linear and para-connected dibenzoxane-fluorinated chains, where the most stable chains were rigid-rod polymer chains [11].
To investigate the thermal stability of the polymers, DTG curves were generated (Figure 4B). The curves showed several distinct stages of decomposition varied in the range of 450-600 °C, which represents the peak temperature at which the materials decompose at the maximum rate (Ts). At 100°C, there are no indication of the presence water and accumulated solvents, except an obvious trace in the case of DAB-A-1O, which might be removed with adequate time of drying. The Ts value was found to be approximately 500°C for DAB-Z-1h, DAB-Z-1O, and 484 °C for DAB-A-1O, while it was around 461°C for DAB-A-1h. These results suggest that the high nitrogen content in the diazo-based polymers contributes to their superior thermal stability. Furthermore, the higher Ts value observed for DAB-A-1O compared to DAB-A-1h further supports the role of fluorine in enhancing thermal stability.
Table 2 summarizes the temperatures of decomposition at 50% and 100% weight loss, as well as the Ts values, for all the polymers studied. At 100% weight loss, DAB-A-1h and DAB-A-1O were completely decomposed, leaving only residual ash due to the oxidative process. On the other hand, DAB-Z-1h and DAB-Z-1O were decomposed down to 95% of the contents, leaving non-oxidized sample, which might be attributed to the high nitrogen load when compared with the 100% decomposed samples. The TGA/DTG data indicated that the diazo-based polymers exhibited higher thermal stability than the azomethine-based polymers, which could be attributed to their high nitrogen content. Additionally, the higher thermal stability of DAB-A-1O compared to DAB-A-1h may be due to the linear chain formation and high fluorine content.
The optical properties of the polymers, their extended conjugation, and band gap determinations were investigated and the results are shown in the supplementary information section part 2.

3.5. Porosity measurements

Based on the 19F-NMR spectra, it was observed that DAB-A-1h, DAB-Z-1h, and DAB-Z-1O were formed as cross-linked chains, whereas DAB-A-1O was formed as an open chain, as summarized in Scheme 3. The formation of cross-linked chains is significant as it allows for the expansion of chains in two dimensions, resulting in an increased surface area and the formation of pores and cavities within the polymer chains.
To assess the potential formation of porous chains, the textural properties of the materials were analyzed using argon sorption measurements at 87 K (as shown in Figure 7A). The isotherms show physisorption (adsorption–desorption) process, where the closed and the open symbols represent the adsorption and desorption steps, respectively. The adsorption shows the affinity of the gas molecules to cover the surface and enter inside the pores of the porous material, while the desorption represents a reversible departure of the gas from the surface and pores of solid adsorbent. Thus, the feasibility of the gas removal from the surface and pores is practically known as a sample regeneration step. The pore volume and pore size distributions were obtained using nonlocal density functional theory (NLDFT). The argon adsorption-desorption isotherms showed large uptake at low relative pressure (0-0.1 bar), indicating permanent microporosity, and the isotherms were fully reversible.
The microporous nature of the porosity of the polymers was confirmed by the pore size distribution (PSD) curve obtained from the nonlocal density functional theory (NLDFT), which showed a peak centered in the range of 5-10 Å (Figure 7B) [38]. The pore volume of the polymers was measured at a relative pressure of P/P0 = 0.98 atm. The pore volume of each polymer was rationalized based on its surface area. Higher surface area values were associated with greater pore volumes. Since all polymers are conjugated chains, they are characterized by π-π stacking and tight packing, which decrease the measured porosity and limit the available free volume.
The surface area was determined using the Brunauer-Emmett-Teller (BET) method, and by applying the multi-point BET calculations. The calculations were performed on the gas adsorbed at low pressure range P/P0 between 0.025-0.30 [35,36,37]. The results of BET determination are shown in Figure 8A along with one sample calculations Figure 8B and summarized in Table S3. Further explanation of the calculations and the raw data are shown in supplementary part 3 and Figure S15.
As stated previously, the cross-linking formation in the polymers can create branching and increase their surface area. The open-chain polymer, DAB-A-1O, has the lowest surface area, measuring at 285 m2g-1, due to its lack of cross-linking. The low surface area of DAB-A-1O can be attributed to the steric effect, resulting in a partial structural collapse that limits the accessible sites for argon gas interactions. However, the surface areas of DAB-A-1h, DAB-Z-1h, and DAB-Z-1O were higher, determined as 403, 494, and 770 m2g-1, respectively. The observed surface area values for the synthesized polymers were considered reasonable due to the formation of random cross-linked chains. It was observed that the HFB-based polymers had higher surface area values than the DFB-based polymers, which could be attributed to the presence of flexible and smaller HFB linkers that facilitate extended branching. However, it is noteworthy that the fluorinated polymers had higher surface area values compared to their non-fluorinated counterparts, as reported in a previous study on a series of fluorinated and non-fluorinated polyaminal polymers, which also showed higher N2, CH4 and CO2 uptake [39].

3.6. Environmental Applications

The newly synthesized polymers exhibit a range of desirable properties such as hydrophobicity and porosity, as described in the previous sections. These properties make them promising candidates for various environmental applications. Therefore, this section will assess their potential for use in specific environmental applications. In this study, we investigate the ability of the synthesized polymers to separate carbon dioxide, methane, phenol, and benzene from their media. These pollutants are of concern as carbon dioxide and methane are air pollutants, while phenol and benzene are water pollutants. The experimental procedures and the results obtained for these pollutants will be discussed in the following sections.

3.6.1. Methane and Carbon Dioxide Adsorption

The increasing release of carbon dioxide, commonly known as "green gas," into the atmosphere is a significant global environmental concern [40]. Approximately 80% of CO2 emissions originate from the combustion of oil, coal, and natural gas, particularly in developing countries due to their economic and industrial growth [41]. Therefore, addressing this issue and mitigating the contribution of CO2 to global warming is of utmost importance. Methods used to control CO2 emissions include ethanol amine technology and solid sorbents, such as MOFs. However, these methods have limitations, such as the high energy required for CO2 recovery from ethanol amine solutions and the air sensitivity of MOFs. Porous organic polymers (POPs) are a well-established category of materials designed for this purpose, owing to their air stability, high gas capture and storage capacity, and physisorption mechanism for CO2 desorption [42].
Methane (CH4) is a constituent of natural gas and is the second most significant greenhouse gas after CO2 [43]. Due to its abundance and lower carbon emissions, methane is considered as an alternative to petroleum fuel. Therefore, there is significant interest in replacing gasoline and petroleum with methane, and many energy agencies and research groups are developing porous adsorbents capable of capturing it from the environment or gas mixtures. Zeolites, activated carbon, and metal organic frameworks (MOFs) are some examples of these adsorbents that require high pressure for methane capture but can be performed at room temperature, providing economic benefits, convenience, and high safety [44].
The primary challenge in achieving efficient methane uptake is the need for a suitable surface area with an optimal pore size and functionalized surface that facilitates physical adsorption processes. Due to methane's lack of a dipole moment, high pressure is required to pack the gas molecules within the pores of high-surface-area polymers. This high-pressure requirement presents safety challenges, making it crucial to design and develop materials that can safely and effectively capture methane. In this section, we investigate the potential of the fluorinated polymers' hydrophobicity and porosity for the separation of non-polar CH4 and polarizable CO2 gases (Figure 9), as an alternative to high-pressure methods. The gas uptake isotherms for CH4 and CO2 were measured at 298 K, which corresponds to real-world environmental conditions.
Based on the CH4 uptake values presented in Table 3 and Figure 9, DAB-Z-1O and DAB-A-1O exhibit uptake values of 6.14 and 3.46 mg/g, respectively. Both polymers have a high content of fluorine and lower surface areas compared to DAB-Z-1h and DAB-A-1h. The higher CH4 uptake of DAB-Z-1O is attributed to the presence of fluorine and smaller pores, which provide more accessible interaction sites for CH4. Other studies have also confirmed that fluorinated materials have superior CH4 uptake, such as the fluorinated MOF NOTT-108a, which shows higher CH4 uptake compared to non-fluorinated MOF NOTT-101a [45].
The CO2 uptake values of the polymers were also investigated and the results showed that DAB-Z-1h exhibited the highest uptake (17.21 mg/g) due to its higher porosity and nitrogen content compared to the other polymers. The other polymers showed similar uptake values, which can be attributed to their moderate surface areas. Therefore, controlling the hydrophobicity and porosity of the polymers are crucial factors that determine their gas uptake capabilities. Fluorine-rich polymers with low surface areas are preferred for CH4 uptake, while nitrogen-rich polymers with high surface areas are preferred for CO2 uptake.
To assess the ability of the new polymers as adsorbents for CO2 or CH4, we calculated a selectivity parameter. Various calculation methods can be used to determine the selective binding of CO2/CH4 at 298 K, such as (1) initial slope calculations, (2) Henry’s Law constants, and (3) ideal adsorbed solution theory (IAST) [46]. In this study, we utilized the initial slope method to determine the selectivity parameter for CO2 or CH4 adsorption. This method involves the calculation of the slope of the linear relationship between the low-pressure range and gas uptake (mmol g-1) in the pressure range of 0-0.1 bar. The slope ratio between the pure gas isotherms of CO2 and CH4 at 298 K provides the numerical selectivity value. Figure 10 illustrates the calculation process by taking the slope of each CO2 and CH4 pure gas isotherm at 298 K in the low-pressure range and then computing the slope ratio between the pure gas isotherms [47]. The selectivity results for CO2/CH4 are presented in Table 3, which shows that the polymers with the highest CO2 uptake are also the most selective for CO2. Conversely, DAB-A-1O and DAB-Z-1O, which are rich in fluorine, exhibit a higher binding selectivity for CH4 than CO2.

3.6.2. Separation of benzene–water and phenol–water mixtures

The fluorine and nitrogen contents, as well as the tailored polarity of the polymers, are crucial factors in facilitating the separation of polar/polarizable CO2 and non-polar CH4 molecules from the air. The potential of these polymers for separating other organic molecules from water was also examined. The selected solvents were benzene (non-polar) and phenol (polar), and the separation process was carried out. In line with the aforementioned hypothesis, the polymers with a high fluorine loading exhibited a significant hydrophobic nature, which makes them promising adsorbents for benzene. Similar study has used fluorinated polyethers supported with graphene oxide surface for separation of oil-water [48]. Conversely, the cross-linked polymers with low fluorine contents contain reactive C-F bonds and high nitrogen contents, making them potentially effective adsorbents for phenol as a polar solvent. To perform qualitative adsorption experiments, the polymers were submerged in benzene-water or phenol-water saturated solutions for a certain period. UV-Vis absorption measurements of the solutions were then conducted over a 90-minute period to track the amount of organic solvents adsorbed onto the polymer surfaces.
Figure 11A shows the UV-Vis absorption of the benzene-water solution. DAB-A-1h displayed a consistent trend for benzene adsorption throughout the measurement time. This behavior can be attributed to its hydrophilic nature due to free C-F and nitrogen. Additionally, the ortho-connected structure of DAB-A-1h facilitated the formation of an agglomerated and collapsed structure, which led to a reduction in surface area and a subsequent limitation in the ability of benzene to be adsorbed on the surface or within the pores. DAB-A-1O exhibited a more distinct trend for benzene separation from water in the initial measurement after 10 minutes, as shown in Figure 11B. This behavior suggests that the adsorption of benzene on the octaflourobiphenyl linker occurred as a one-layer adsorption with time. The para-open extended chain and the ortho-para-branched framework of the diazo-based polymers (DAB-Z-1h and DAB-Z-1O) were confirmed to form cross-linked structures through the 19F-NMR spectra. Moreover, the azo-groups in these polymers were found to be para-related to the ether C-O-C bond (as depicted in Scheme 3), which facilitated the rate of nucleophilic aromatic substitution (NAS) and promoted the flexible rotation of the chains. This, in turn, increased the rate of interaction with the solvent as demonstrated in Figure 11 C-D. The initial response of these polymers towards benzene adsorption during the first 30 minutes can be attributed to the presence of accessible C-F sites that possess a diminished dipole moment.
Phenol is a harmful polar organic pollutant commonly found in water, posing a significant threat to both humans and aquatic life. Thus, its presence in water must be restricted. Sources of phenol pollution in water include industrial waste from oil refineries, coal tar, and plastics, as well as waste from olive farming and agricultural activities, in addition to its natural occurrence [49,50]. The impact of connection sites, cross-linking, and flexibility on the polarities of the polymers DAB-A-1h, DAB-A-1O, DAB-Z-1h, and DAB-Z-1O enabled us to explore their potential in adsorbing benzene. To provide a comparative study, we also evaluated the ability of these polymers to separate phenol from water through similar experimental procedures used in the benzene adsorption experiments. As previously demonstrated, DAB-A-1O exhibited a highly hydrophobic nature and showed potential for adsorbing benzene, as seen in the previous experiment. This observation was further confirmed by the decrease in adsorption of phenol on the polymer surface, as shown in Figure 12A. Additionally, the presence of octafluorobiphenyl in DAB-Z-1O supports the observation of low response to phenol adsorption, as shown in Figure 12B. In contrast, DAB-A-1h and DAB-Z-1h, which were formed through the reactive NAS and have low fluorine and high nitrogen contents, moderate surface area, and flexible chains, showed improved interactions with phenol, as depicted in Figure 12C and D.

4. Conclusions

In this study, we synthesized four new fluorinated organic polymers using the nucleophilic aromatic substitution (NAS) reaction and characterized them fully. The possibility of forming a porous analog of these polymers due to the NAS reaction was confirmed by 19F-NMR. The surface area of the polymers, as measured by nitrogen sorption, ranged from 285 to 770 m2/g. Due to their characteristics, including the presence of fluorine, nitrogen, pores, and cavities, along with a reasonable surface area, this new series of polymers shows promise for separation applications. Polymers with a high concentration of fluorine are more hydrophobic, making them suitable for separating methane gas and benzene from media. The combination of hydrophobicity and controlled cross-linking in the design of fluorinated polymers makes this class of polymers a very promising candidate for environmental remediation. The high-surface-area polymers with high nitrogen contents are suitable for CO2 capture and phenol separation from media, while polymers with high fluorine concentration are applicable for separating methane gas and benzene from media. Based on the findings of this study, several future research directions and potential applications can be explored. Further research could focus on modifying the composition and structure of the polymers, such as incorporating different functional groups or altering the connectivity of the monomers, to enhance their adsorption capacities and selectivity for specific gases or pollutants. The adsorption capacities of these polymers can be studied under various temperature and pressure conditions to better understand their potential for real-world applications, such as carbon capture and storage (CCS) or gas separation in industrial settings. The synthesized polymers could be tested for the separation of other air and water pollutants, including volatile organic compounds (VOCs), heavy metals, and particulate matter, to evaluate their applicability in a broader range of environmental applications. Combining the synthesized polymers with other materials, such as metal-organic frameworks (MOFs), zeolites, or carbon-based materials, could lead to the development of novel composite materials with enhanced adsorption properties and potential applications in various industries, including energy storage, catalysis, and sensors. The long-term stability and recyclability of these polymers should be investigated to determine their suitability for large-scale applications. By assessing their performance after multiple adsorption-desorption cycles, researchers can better understand their potential for sustainable and cost-effective environmental remedy.

Supplementary Materials

The following supporting information can be downloaded at the website of this paper posted on Preprints.org.

Author Contributions

S. T and O.A wrote the manuscript, analyzed all the data, and prepared all the figures, schemes, and tables; H. E and A.J gathered porosity data and revised the manuscript; M.A performed measurement of 19F-, 1H- and 13C-NMR; T.A and L.A performed the methane and carbon dioxide measurements and GPC measurements; I. Y and R.A performed all the UV–Vis measurements.

Funding

Funding was provided by Tafila Technical University, Tafila-Jordan (grant no. 122/2020).

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

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Preprints 87770 sch001
Scheme 1. Synthetic routes of linkers (A) DAB-A-OH and (B) DAB-Z-OH.
Scheme 1. Synthetic routes of linkers (A) DAB-A-OH and (B) DAB-Z-OH.
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Scheme 2. Synthesis protocol of (A) DAB-A-1O and DAB-A-1h; (B) DAB-Z-1O and DAB-Z-1h (m = the number of fluorinated phenyls, the present structure of each polymer represents one repeating units).
Scheme 2. Synthesis protocol of (A) DAB-A-1O and DAB-A-1h; (B) DAB-Z-1O and DAB-Z-1h (m = the number of fluorinated phenyls, the present structure of each polymer represents one repeating units).
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Figure 4. (A) Thermal gravimetric analysis (TGA) thermograms of the polymers; (B) first derivative (DTG) of the polymers.
Figure 4. (A) Thermal gravimetric analysis (TGA) thermograms of the polymers; (B) first derivative (DTG) of the polymers.
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Scheme 3. Possible structures of the polymers.
Scheme 3. Possible structures of the polymers.
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Figure 7. (A)Argon uptake isotherms at 87 K; (closed symbols: adsorption, empty symbols: desorption); (B) pore size distribution.
Figure 7. (A)Argon uptake isotherms at 87 K; (closed symbols: adsorption, empty symbols: desorption); (B) pore size distribution.
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Figure 8. (A) BET multi-point fitting; and (B)determination of BET of DAB-Z-1h. (X is the weight of gas adsorbed at relative pressure (P/P0)).
Figure 8. (A) BET multi-point fitting; and (B)determination of BET of DAB-Z-1h. (X is the weight of gas adsorbed at relative pressure (P/P0)).
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Figure 9. (A) CH4 gas uptake by the polymers at 298 K; (B) CO2 gas uptake by the polymers at 298 K.
Figure 9. (A) CH4 gas uptake by the polymers at 298 K; (B) CO2 gas uptake by the polymers at 298 K.
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Figure 10. The initial slope calculations for DAB-A-1h (A), DAB-A-1O (B), DAB-Z-1h (C), and DAB-Z-1O at 298 K.
Figure 10. The initial slope calculations for DAB-A-1h (A), DAB-A-1O (B), DAB-Z-1h (C), and DAB-Z-1O at 298 K.
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Figure 11. The UV–visible spectra of benzene adsorption by polymers over a period of time.
Figure 11. The UV–visible spectra of benzene adsorption by polymers over a period of time.
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Figure 12. The UV–visible spectra of phenol adsorption by polymers over a period of time.
Figure 12. The UV–visible spectra of phenol adsorption by polymers over a period of time.
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Table 1. physical properties of the polymers.
Table 1. physical properties of the polymers.
Polymer Appearance Solubility %yield Mn (g/mol) Mwt (g/mol)
DAB-Z-1h Dark brown (DMSO, DMAc)a , THFc 88 In soluble in THF
DAB-Z-1O Dark brown DMSO, DMAc, THF a 70 3106 7328
DAB-A-1h Pale brown DMSO, DMAc, THF a 82 1381 4886
DAB-A-1O Pale brown THFb, (DMSO, DMAc )c 69 4068 11948
(a) slightly soluble; (b) completely soluble; (c) insoluble; Mn: number average molecular weight; Mwt: weight average molecular weight
Table 2. Data extrapolated from TGA and DTA.
Table 2. Data extrapolated from TGA and DTA.
Polymer Decomposition (°C) Ts (DTA) T (°C) 50% T (°C) 100% T (°C) 95%
DAB-Z-1h 420 498 500 - 590
DAB-Z-1O 423 521 493 - 566
DAB-A-1h 230 461 471 649 -
DAB-A-1O 283 484 544 661 -
DTA: first derivative of TGA; Ts: the peak temperature derived from the DTA curve; (-): no data
Table 3. BET surface area, pore volume, and CH4 and CO2 uptake values of the polymers.
Table 3. BET surface area, pore volume, and CH4 and CO2 uptake values of the polymers.
Polymer Surface area (BET)
m2 g-1 		Total pore volume (cm3/g) CH4 uptake (mg/g) CO2 uptake (mg/g) Selectivity CO2/CH4
DAB-A-1h 403 0.2103 2.86 6.0 4.19
DAB-A-1O 285 0.0872 3.46 2.6 1.2
DAB-Z-1h 494 0.3524 2.19 17.2 14.9
DAB-Z-1O 770 0.2587 6.14 7.98 1.64
BET: Brunauer–Emmett–Teller/Total pore volume calculated at p/p0 = 0.98; CH4 and CO2 uptake at 298 K. Selectivity (CO2/CH4) determined from slope ratios (see Figure 10).
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