Synthesis of Sulfonated Polyphenylene Block Copolymers via In Situ Generation of Ni(0)

Proton exchange membranes (PEMs) fabricated from sulfonated polyphenylenes (sPP) exhibit superior proton conductivity and electrochemical performance. However, the Ni(0) catalyst required for Colon’s cross-coupling reaction for the synthesis of sPP block copolymers is expensive. Therefore, in this study, we generated Ni(0) in situ from an inexpensive Ni(II) salt in the presence of the reducing metal Zn and NaI. The sPP block copolymers were synthesized from neopentyl-protected 3,5- and 2,5-dichlorobenzenesulfonates and oligo(arylene ether ketone) using the catalyst NiBr2(PPh3)2. The block copolymers synthesized using our strategy and the Ni(0) catalyst exhibited comparable polydispersity index values and high molecular weights. Thin, transparent, and bendable PEMs fabricated using selected high-molecular-weight sPP block copolymers synthesized via our strategy exhibited similar proton conductivities to those of the block copolymers synthesized using the Ni(0) catalyst. We believe that our strategy will promote the synthesis of similar multifunctional block copolymers.


Introduction
Proton exchange membranes (PEMs) are essential components of energy storage and conversion devices. The performance and cost of these devices are highly dependent on the properties and costs of PEMs. Perfluorosulfonic acid (PFSA) membranes have received considerable attention owing to their excellent electrochemical performance and durability; however, these membranes have several drawbacks such as high cost, poor environmental compatibility, narrow operating temperature range, and high gas permeability [1][2][3]. In order to overcome these limitations, research efforts should be directed toward the development of high-performance and low-cost alternative polymer electrolytes.
Aromatic polymers can overcome the limitations of PFSA ionomers because of their diverse molecular structures, facile synthesis, and low cost. Several sulfonated aromatic polymers have been investigated as membrane materials and outperformed PFSA membranes in terms of electrochemical performance [4][5][6]. However, statistical sulfonated aromatic copolymers exhibit chemical instability, dependence of relative humidity (RH) on the proton conductivity, and excessive swelling behavior [7,8]. Hence, multiblock copolymers have been designed by incorporating rigid hydrophilic blocks such as sulfonated polyphenylenes to overcome the shortcomings of existing aromatic ionomers [2,3,9,10]. Polyphenylenes are the most promising alternative candidates for the development of PEMs. Sulfonated polyphenylene exhibits chemical stability and mechanical toughness in the polymer backbone [1,4,11,12]. The structure of polyphenylene guarantees appreciable chemical stability even at elevated temperatures because of the absence of vulnerable heteroatoms in the backbone and the high aromatic C-C bond dissociation energy. Block copolymers are self-assembled, structurally interesting materials in which the morphology and domain size are harmonized at the nanoscale level. This is because ionic and nonionic blocks facilitate ion transport in a reliable order.
Colon's Ni-catalyzed cross-coupling reactions are one of the most promising approaches for synthesizing polyphenylenes and can be applied to various polymers using various starting materials [13,14]. The zerovalent Ni complex Ni(COD) 2 is one of the best catalysts for the synthesis of polyphenylenes, but its high cost could undermine the economic benefits of hydrocarbon-based membranes. In contrast, inexpensive Ni(II) complexes have been proven effective in catalyzing polymerization to obtain high-molecular-weight polymers [15]. In situ generation of Ni(0) from Ni(II) is a key limitation associated with the use of Ni(II) complexes. The use of a strong reducing metal in Colon's C-C coupling reaction system promotes the reduction in Ni(II) to Ni(0). In addition, the metal can act as an acceptor in the presence of halides. Therefore, using the right reducing metal is important. Furthermore, an alkali metal salt such as NaI would act as a chaotropic agent and an additive weak ligand that neutralizes the acidity generated in Colon's C-C coupling reaction and would supply iodide ions for a halide exchange [16,17].
Therefore, we synthesized sulfonated polyphenylene-based multiblock copolymers using a Ni(II) salt in the presence of the strong reducing metal Zn and the alkali metal salt NaI. Furthermore, we investigated the effect of the Ni(II) equivalents in relation to those of total chlorine and optimized the polymerization conditions. We also observed the effect of the sulfonated monomer ratio under the optimized polymerization conditions on the resultant polymer molecular weight. Moreover, the resultant polymers and membranes were compared with those produced by Ni(0)-complex-catalyzed polymerization.

Synthesis of Neopentyl 2,5-Dichlorobenzenesulfonate and Neopentyl 3,5-Dichlorobenzenesulfonate
Neopentyl 2,5-dichlorobenzene sulfonate (pNDCBS) and neopentyl 3,5-dichlorobenzene sulfonate (mNDCBS) were synthesized according to a previously reported method [3]. The 1 H NMR spectra of pNDCBS and mNDCBS, along with those of the starting materials, are presented in Figure S1. The chemical shift values were in good agreement with the predicted values for the proposed structure. 1

Synthesis of Hydrophobic Cl-End-Capped OAEK Oligomer
The hydrophobic block of oligo(arylene ether ketone) (OAEK) with a repeating unit length of five (X5) units was prepared using 4,4-dichlorobenzophenone and 2,2-bis(4-hydroxyphenyl)hexafluoropropane monomers. Briefly, a 100-mL four-neck doublejacketed flask (Radleys, Essex, UK) equipped with a reflux condenser, overhead stirrer, and argon inlet/outlet was charged with 6F-BP (5.0 g, 14.87 mmol) and DCBP (4.84 g, 17.85 mmol) at 120 • C. The required DMAc was added to the mixture to obtain a 20 wt% transparent homogeneous solution. CaCO 3 (8.93 g, 89.23 mmol) was added to this solution and the temperature was increased to 150 • C, following which K 2 CO 3 (3.08 g, 22.31 mmol) was added to initiate the reaction. The reaction progress was examined by periodic gel permeation chromatography (GPC). Next, the Cl-end-capping agent DCBP (0.45 g, 1.78 mmol) was added to the reaction mixture, and the reaction was allowed to proceed for 6 h to ensure full end-capping. The mixture was filtered through a 0.45-µm membrane (Merck Millipore, Burlington, MA, USA) under reduced pressure, and the filtrate was precipitated in methyl alcohol. The white precipitate was washed several times with ethyl alcohol and vacuum-dried for 12 h at 80 • C.

Synthesis of sPP Block Copolymers via Ni(II)-Catalyzed Colon's Cross-Coupling Reaction
The block copolymerization reaction of neopentyl-protected monomers (2,5/3,5-dichlorobenzene sulfonate) and hydrophobic OAEK oligomer (X5) (Scheme 1) in the presence of the NiBr 2 (PPh 3 ) 2 catalyst was investigated under different conditions. The length of the hydrophilic block (Y) was determined by adjusting the molar equivalents of neopentyl-protected dichlorobenzene sulfonate monomers to afford a 2.50 meq/g IEC of the final block copolymer. The equivalents of NiBr 2 (PPh 3 ) 2 were varied in relation to the total chlorine equivalents. A 1:1 ratio of mNDCBS and pNDCBS, along with 0.030, 0.050, 0.065, and 0.075 equivalents of NiBr 2 (PPh 3 ) 2 , were used to afford sPP30@1:1, sPP50@1:1, sPP65@1:1, and sPP75@1:1, respectively. Similarly, a 1:4 ratio of pNDCBS to mNDCBS and 0.065 equivalents of NiBr 2 (PPh 3 ) 2 afforded sPP65@1:4. In all the experiments, the molar ratios of catalyst to ligand (1:10), catalyst to Zn (1:30), and catalyst to NaI (1:1) were kept constant, and the solution concentration was adjusted to 10 wt% considering the theoretical yield of the polymer. sPP30@1:1 refers to sulfonated polyphenylene, which was prepared in the presence of 0.030 equivalents of NiBr 2 (PPh 3 ) 2 to the total terminal chlorine and a hydrophilic phenylene ratio (pNDCBS: mNDCBS) of 1:1. In the case of sPP(COD)@1:1, 1.25 equivalents of Ni(COD) 2 to the total terminal chlorine were used. Considering the polymerization of sPP65@1:1 as an example, the typical polymerization process is as follows: To a previously dried 100-mL four-neck double-jacketed flask fitted with an oil circulator and overhead mechanical stirrer, a mixture of NiBr 2 (PPh 3 ) 2 (0.22 g, 0.30 mmol), PPh 3 (0.79 g, 3.00 mmol), Zn (0.59 g, 9.00 mmol), and NaI (0.05 g, 0.30 mmol) was added at 80 • C under continuous Ar flow (40 cc/min). DMAc (6.58 g) was added to this mixture. Next, a solution of pNDCBS (0.63 g, 2.12 mmol), mNDCBS (0.63 g, 2.12 mmol), and the OAEK oligomer (1.23 g, 0.38 mmol) in DMAc (11.39 g) was injected into the flask using a syringe. The reaction mixture was allowed to react at the same temperature for 12 h. Then, the reaction mixture was diluted and precipitated into a large excess of 6 M HCl/MeOH. The obtained white fibrous precipitate was washed with methanol, 1 M NaHCO 3 , DI water, and methanol and vacuum-dried at 80 • C. this mixture. Next, a solution of pNDCBS (0.63 g, 2.12 mmol), mNDCBS (0.63 g, 2.12 mmol), and the OAEK oligomer (1.23 g, 0.38 mmol) in DMAc (11.39 g) was injected into the flask using a syringe. The reaction mixture was allowed to react at the same temperature for 12 h. Then, the reaction mixture was diluted and precipitated into a large excess of 6 M HCl/MeOH. The obtained white fibrous precipitate was washed with methanol, 1 M NaHCO3, DI water, and methanol and vacuum-dried at 80 C. Scheme 1. Schematic of the synthesis of an sPP block copolymer using in-situ-generated Ni(0).

Synthesis of sPP Block Copolymers via Ni(0)-Catalyzed Colon's Cross-Coupling Reaction
For a comparative study, the two polymers sPP(COD)@1:1 and sPP(COD)@1:4 were synthesized with a target IEC of 2.50 meq/g using the Ni(COD)2 catalyst. The molar equivalents of pNDCBS and mNDCBS used for sPP(COD)@1:1 was 1:1, whereas that for sPP(COD)@1:4 was 1:4. Other reaction conditions were similar in both cases: The catalyst equivalents were 1.25 to those of total chlorine, the catalyst to ligand ratio was 1:2, and the solution concentration was adjusted to 20 wt% using the theoretical yield of the polymer. A typical polymerization procedure for sPP(COD)@1:1 is as follows: To a previously dried four-neck double-jacketed flask connected to an oil circulator and overhead mechanical stirrer, OAEK oligomer (1.43 g, 0.47 mmol), pNDCBS (0.794 g, 2.67 mmol), and mNDCBS (0.79 g, 2.67 mmol) were added at 80 C under Ar flow (40 cc/min), following which NMP (7.28 g) was added. To this mixture, BPy (2.55 g, 14.54 mmol), 2.76 g of NMP, and Ni(COD)2 (2.00 g, 7.27 mmol) were successively added, following which the reaction was allowed to proceed at the same temperature for 4 h. The viscous solution was diluted by adding NMP (4 g). After the mixture was cooled, it was poured into a 6 M HCl/MeOH solution, filtered, and washed with methanol. The obtained brown reddish precipitate was washed with 1 M NaHCO3, water, and methanol and vacuum-dried at 80 C.

Deprotection and Protonation of sPP Block Copolymers
sPP block copolymers with reasonable molecular weights were considered for deprotection and protonation reactions. Briefly, a solution of sPP block copolymer (2.00 g, 0.38 mmol) in DMAc (18.00 g) was added to a 50-mL round-bottom flask fitted with a reflux condenser, magnetic stirrer, and Ar inlet/outlet at 80 C. NaI (4.07 g, 27.13 mmol) was added to this solution, and the reaction mixture was allowed to react at the same temperature for 12 h under Ar flow. Next, the reaction mixture was poured into excess ethanol, filtered, and washed with ethanol. The filtrate was then washed with chloroform to remove any unprotected sPP block copolymer. The samples were washed with ethanol and vacuum-dried at 80 C.
The dried precipitate was further treated with 3 M HCl/H2O in a closed vessel equipped with a magnetic stirrer and thermometer at 80 C for 12 h to ensure the complete protonation of the deprotected polymer. Subsequently, the polymer was washed with DI water until a neutral pH was reached and then vacuum-dried at 80 C. Scheme 1. Schematic of the synthesis of an sPP block copolymer using in-situ-generated Ni(0).

Synthesis of sPP Block Copolymers via Ni(0)-Catalyzed Colon's Cross-Coupling Reaction
For a comparative study, the two polymers sPP(COD)@1:1 and sPP(COD)@1:4 were synthesized with a target IEC of 2.50 meq/g using the Ni(COD) 2 catalyst. The molar equivalents of pNDCBS and mNDCBS used for sPP(COD)@1:1 was 1:1, whereas that for sPP(COD)@1:4 was 1:4. Other reaction conditions were similar in both cases: The catalyst equivalents were 1.25 to those of total chlorine, the catalyst to ligand ratio was 1:2, and the solution concentration was adjusted to 20 wt% using the theoretical yield of the polymer. A typical polymerization procedure for sPP(COD)@1:1 is as follows: To a previously dried four-neck double-jacketed flask connected to an oil circulator and overhead mechanical stirrer, OAEK oligomer (1.43 g, 0.47 mmol), pNDCBS (0.794 g, 2.67 mmol), and mNDCBS (0.79 g, 2.67 mmol) were added at 80 • C under Ar flow (40 cc/min), following which NMP (7.28 g) was added. To this mixture, BPy (2.55 g, 14.54 mmol), 2.76 g of NMP, and Ni(COD) 2 (2.00 g, 7.27 mmol) were successively added, following which the reaction was allowed to proceed at the same temperature for 4 h. The viscous solution was diluted by adding NMP (4 g). After the mixture was cooled, it was poured into a 6 M HCl/MeOH solution, filtered, and washed with methanol. The obtained brown reddish precipitate was washed with 1 M NaHCO 3 , water, and methanol and vacuum-dried at 80 • C.

Deprotection and Protonation of sPP Block Copolymers
sPP block copolymers with reasonable molecular weights were considered for deprotection and protonation reactions. Briefly, a solution of sPP block copolymer (2.00 g, 0.38 mmol) in DMAc (18.00 g) was added to a 50-mL round-bottom flask fitted with a reflux condenser, magnetic stirrer, and Ar inlet/outlet at 80 • C. NaI (4.07 g, 27.13 mmol) was added to this solution, and the reaction mixture was allowed to react at the same temperature for 12 h under Ar flow. Next, the reaction mixture was poured into excess ethanol, filtered, and washed with ethanol. The filtrate was then washed with chloroform to remove any unprotected sPP block copolymer. The samples were washed with ethanol and vacuum-dried at 80 • C.
The dried precipitate was further treated with 3 M HCl/H 2 O in a closed vessel equipped with a magnetic stirrer and thermometer at 80 • C for 12 h to ensure the complete protonation of the deprotected polymer. Subsequently, the polymer was washed with DI water until a neutral pH was reached and then vacuum-dried at 80 • C.

Preparation of sPP Block Copolymer Membranes
The sPP block copolymer solution was prepared using DMAc, and the resultant homogeneous transparent solution was filtered through a 0.45-µm membrane and degassed. The degassed solution was cast onto a flat glass plate, dried at 70 • C for 24 h, and then further vacuum-dried at 100 • C for 12 h to ensure the complete evaporation of DMAc. The membranes were treated with 3 M HCl/H 2 O for 12 h at 80 • C in a closed vessel, washed with DI water until a neutral pH was achieved, and then dried at 30 • C for 24 h. The thicknesses of the membranes were adjusted to 35 µm.

Molecular Weight Measurements
The molecular weights of the oligomer and the prepared block copolymers were analyzed using a gel permeation chromatography (GPC) instrument equipped with a Younglin YL 9112 isocratic pump and YL 9120 UV-visible detector (Younglin Instruments, Anyang, Republic of Korea). Shodex SB-803HQ and Shodex KF-805L columns were used for polymer and oligomer analyses, respectively. DMAc containing 0.01 M LiBr was used as the eluent. Molecular weights were confirmed using standard polystyrene samples.

Structural Analysis
1 H NMR spectra were recorded on an AVANCE III (600 MHz) spectrometer (Bruker BioSpin, Billerica, MA, USA) in CDCl 3 or d 6 -DMSO using tetramethylsilane (TMS) as the internal reference standard.

Water Uptake, Swelling Ratio, and Conductivity Measurements for Membranes
For the measurements, the membrane samples were dried at 120 • C for 24 h. Then, the dried membrane samples were immersed in DI water for 24 h at 25 • C and 3 h at 80 • C. The water uptake, as well as the in-plane and through-plane swelling behavior of the membranes in protonated form, were analyzed in DI water using the following equations: where W wet and W dry are the weights of the membrane samples in wet and dry states, respectively; A wet and A dry are the areas of the membrane under wet and dry conditions, respectively; and T wet and T dry are the wet and dry membrane thicknesses, respectively. Water vapor uptake was recorded on a TGA Q5000 instrument at 30, 50, and 70% RH conditions at 80 • C. In-plane proton conductivity was measured in four-probe conductivity cells (WonATech, Seoul, Republic of Korea) using an electrochemical impedance analyzer. The analysis was conducted in the frequency range of 10 −1 -10 5 Hz at an amplitude of 100 mV using a Solartron 1287 electrochemical interface and Solartron 1260 impedance/gain-phase analyzer. Proton conductivity was calculated using the following equation: where D, L, and T are the distance between the electrodes, width of the sample, and thickness of the sample, respectively, and R is the resistance obtained by extrapolating the Nyquist plot to the x-intercept in the frequency range of 10 −1 -10 5 Hz.

Synthesis of Hydrophobic Cl-End-Capped OAEK Oligomer
A Cl-end-capped OAEK was synthesized by a polycondensation reaction at elevated temperatures. The end-group functionality and the number of repeating units were controlled by adjusting the feed monomer ratio. However, the ether-ether exchange reaction during the polycondensation at elevated temperatures is a serious limitation [18]. During the nucleophilic step of oligomerization at high reaction temperatures, randomization of repeating unit sequences occurs via ether-ether exchange reactions. The GPC profile of the OAEK oligomer with a length of X5 and the corresponding 1 H NMR spectra are presented in Figure 1. The chemical shift values were in good agreement with the predicted values for the proposed structure, suggesting the absence of side reactions such as ether-ether exchange reactions. Here, the use of CaCO 3 functioned well in inhibiting the ether-ether exchange reaction [19]. In addition, the number of repeating units calculated from the integral ratio of protons of the repeating units and protons of the end group was nearly five.

Synthesis of Hydrophobic Cl-End-Capped OAEK Oligomer
A Cl-end-capped OAEK was synthesized by a polycondensation reaction at elevated temperatures. The end-group functionality and the number of repeating units were controlled by adjusting the feed monomer ratio. However, the ether-ether exchange reaction during the polycondensation at elevated temperatures is a serious limitation [18]. During the nucleophilic step of oligomerization at high reaction temperatures, randomization of repeating unit sequences occurs via ether-ether exchange reactions. The GPC profile of the OAEK oligomer with a length of X5 and the corresponding 1 H NMR spectra are presented in Figure 1. The chemical shift values were in good agreement with the predicted values for the proposed structure, suggesting the absence of side reactions such as etherether exchange reactions. Here, the use of CaCO3 functioned well in inhibiting the etherether exchange reaction [19]. In addition, the number of repeating units calculated from the integral ratio of protons of the repeating units and protons of the end group was nearly five.

Block Copolymer Synthesis Using NiBr2(PPh3)2 with the Reducing Metal Zn
Among the various parameters affecting the polycondensation, the following factors are crucial: (i) anhydrous conditions must be maintained in the presence of Ni(0) as water reduces the aryl halide to arene, thereby inhibiting polymerization and deactivating the catalyst; (ii) oxygen in the presence of triphenylphosphine deactivates the catalyst. Nevertheless, the reaction system is highly reducing in nature, but nickel oxide is highly stable and cannot be reduced under these conditions; and (iii) the quality and surface area of Zn.
The choice of the catalyst is important for a high polymeric yield and high molecular weight. Here, the Ni(II) catalyst acts as a color indicator. The catalytic mixture turns red from green upon Ni(II) reduction. The reaction mixture turns greenish yellow upon the addition of polycondensation monomers, which then turn red in color. This phenomenon confirms the progress of the reaction, whereas a persistent greenish color indicates that the Ni complex is not reduced to Ni(0), and a greyish color indicates total catalyst deactivation. Moreover, the ligand system is critical. Aryl transfer from triphenylphosphine (PPh3) to Ni is a serious limitation during polymerization [17,20]. The reaction temperature and ligand concentration also have profound effects on this phenomenon [21]. Tonozuka et al. used bipyridyl as a co-ligand with PPh3 to suppress such reactions and reported a high polymerization yield and high-molecular-weight polymer by finely tuning the ratio

Block Copolymer Synthesis Using NiBr 2 (PPh 3 ) 2 with the Reducing Metal Zn
Among the various parameters affecting the polycondensation, the following factors are crucial: (i) anhydrous conditions must be maintained in the presence of Ni(0) as water reduces the aryl halide to arene, thereby inhibiting polymerization and deactivating the catalyst; (ii) oxygen in the presence of triphenylphosphine deactivates the catalyst. Nevertheless, the reaction system is highly reducing in nature, but nickel oxide is highly stable and cannot be reduced under these conditions; and (iii) the quality and surface area of Zn.
The choice of the catalyst is important for a high polymeric yield and high molecular weight. Here, the Ni(II) catalyst acts as a color indicator. The catalytic mixture turns red from green upon Ni(II) reduction. The reaction mixture turns greenish yellow upon the addition of polycondensation monomers, which then turn red in color. This phenomenon confirms the progress of the reaction, whereas a persistent greenish color indicates that the Ni complex is not reduced to Ni(0), and a greyish color indicates total catalyst deactivation. Moreover, the ligand system is critical. Aryl transfer from triphenylphosphine (PPh 3 ) to Ni is a serious limitation during polymerization [17,20]. The reaction temperature and ligand concentration also have profound effects on this phenomenon [21]. Tonozuka et al. used bipyridyl as a co-ligand with PPh 3 to suppress such reactions and reported a high polymerization yield and high-molecular-weight polymer by finely tuning the ratio of the ligand and co-ligand with respect to the catalyst [12]. In this study, the NiBr 2 (PPh 3 ) 2 catalyst with the PPh 3 ligand produced high-molecular-weight polymers in high polymerization yields without any co-ligands. A large excess of PPh 3 is recommended to achieve a high polymerization yield and high molecular weight [21]. Even moderate equivalents of PPh 3 afforded good yields. Consequently, polymerization under optimized conditions not only provided a high-molecular-weight block copolymer, but also high reproducibility.

Effect of the Equivalents of the Catalyst and Monomers on the Polymer Molecular Weight
The effects of the equivalents of NiBr 2 (PPh 3 ) 2 on the polymerization of neopentylprotected dichlorobenzene sulfonate monomers and Cl-end-capped OAEK were investigated. The molar equivalents of the feed comonomers (pNDCBS and mNDCBS) were kept constant at 1:1. The poly(para-phenylene) structure is highly rigid with a linear main chain, which lowers the solvent solubility, thereby inhibiting the molecular weight buildup. Feeding an equivalent molar ratio of meta-monomers is an effective and promising approach to improve solvent solubility and the molecular weight of the polymer. The reaction conditions and GPC results are summarized in Table 1, and the corresponding GPC profiles are shown in Figure S2. The dependence of the NiBr 2 (PPh 3 ) 2 equivalents on the resultant polymer molecular weight is shown in Figure 2. Using 0.03 NiBr 2 (PPh 3 ) 2 equivalents afforded the block copolymer sPP30@1:1 with the lowest molecular weight (M w = 20 kDa). The molecular weight of the polymer increased with increasing catalyst equivalent weight. The use of 0.065 equivalents afforded 55 kDa of the resultant block copolymer sPP65@1:1 in 92% yield; this polymer had good solubility in polar organic solvents. Therefore, we used higher equivalents to obtain a higher-M w block copolymer. However, when 0.075 equivalents were used, the M w of sPP75@1:1 (M w = 26 kDa) decreased. This result is consistent with the results of a study by Colon and Kwiatkowski, where they observed that both high and low catalyst equivalents do not yield high-molecular-weight polymers [22]. Low-molecular-weight block copolymers are obtained because when most aryl chlorides react with Ni(0), the remaining Ni(0) forms aryl-nickel species without further reaction. We observed that 0.065 equivalents of NiBr 2 (PPh 3 ) 2 is the optimal amount of catalyst for the polymerization of sulfonated polyphenylenes to yield a high-molecular-weight block copolymer, considering the abovementioned monomers and oligomer.  The effect of the feed monomer ratio on the molecular weight of the block copolymers was also investigated. Polymerization was conducted under previously optimized conditions using a 1:4 ratio of pNDCBS and mNDCBS monomers. The GPC profiles of the sPP65@1:1 and sPP655@1:4 block copolymers are shown in Figure 3, and the quantitative GPC results are summarized in Table 1. The reactivity of less-sterically hindered compounds is much higher than that of sterically hindered compounds. When high equivalents of para-substituted monomer are used in block copolymerization, the resultant block The effect of the feed monomer ratio on the molecular weight of the block copolymers was also investigated. Polymerization was conducted under previously optimized conditions using a 1:4 ratio of pNDCBS and mNDCBS monomers. The GPC profiles of the sPP65@1:1 and sPP655@1:4 block copolymers are shown in Figure 3, and the quantitative GPC results are summarized in Table 1. The reactivity of less-sterically hindered compounds is much higher than that of sterically hindered compounds. When high equivalents of para-substituted monomer are used in block copolymerization, the resultant block copolymer has a linear and rigid main chain, which lowers the solubility and limits the molecular weight [23]. The flexibility of the main chain in the sPP65@1:4 block copolymer is the governing factor in achieving a high molecular weight. Generally, Ni-catalyzed coupling block copolymers exhibit a high polydispersity index (PDI) [24]; however, in this study, both sPP65@1:1 and sPP65@1:4 block copolymers had relatively low PDI values, which implies that the in-situ-generated Ni(0) was highly reactive in the block copolymer synthesis. Figure 2. Effect of NiBr2(PPh3)2 equivalents on the sPP block copolymer molecular weight, when catalyst to ligand, zinc, and NaI ratios were maintained at 1:10, 1:30, and 1:1, respectively.
The effect of the feed monomer ratio on the molecular weight of the block copolymers was also investigated. Polymerization was conducted under previously optimized conditions using a 1:4 ratio of pNDCBS and mNDCBS monomers. The GPC profiles of the sPP65@1:1 and sPP655@1:4 block copolymers are shown in Figure 3, and the quantitative GPC results are summarized in Table 1. The reactivity of less-sterically hindered compounds is much higher than that of sterically hindered compounds. When high equivalents of para-substituted monomer are used in block copolymerization, the resultant block copolymer has a linear and rigid main chain, which lowers the solubility and limits the molecular weight [23]. The flexibility of the main chain in the sPP65@1:4 block copolymer is the governing factor in achieving a high molecular weight. Generally, Ni-catalyzed coupling block copolymers exhibit a high polydispersity index (PDI) [24]; however, in this study, both sPP65@1:1 and sPP65@1:4 block copolymers had relatively low PDI values, which implies that the in-situ-generated Ni(0) was highly reactive in the block copolymer synthesis.  Table 1.

Role of Zn and NaI in the Polymerization Reaction
The mechanism of our reaction system is as follows: in-situ-generated Ni(0) from the Ni(II) salt in the presence of Zn actively reacts with Cl-end-capped OAEK and neopentyl-  Table 1.

Role of Zn and NaI in the Polymerization Reaction
The mechanism of our reaction system is as follows: in-situ-generated Ni(0) from the Ni(II) salt in the presence of Zn actively reacts with Cl-end-capped OAEK and neopentylprotected dichloro monomers to yield an oxidative addition adduct (a) (Scheme 2). In the presence of NaI, adduct (a) undergoes metathetical displacement to yield another oxidative adduct (b). Subsequently, adduct (b) readily produces adducts (c) and (d). In addition, disproportionation of adduct (b) yields adduct (d), which subsequently produces a highmolecular-weight polymer. The polymerization reaction involves a sequence of oxidative addition, metathesis, and reductive elimination steps, which are well known in transitionmetal-catalyzed chemistry. To guarantee efficient Ni(0)-catalyzed polymerization, Ni(0) must be regenerated from the Ni(II) species formed during the reaction; in this reaction, Zn and NaI aid in the regeneration of the Ni(0) species. The use of NaI has a positive effect on polymerization [16,20]. Earlier studies on biaryl synthesis postulated that the presence of alkali metal salt additives (iodide or bromide salts) accelerates the coupling reaction [17,25]. However, these studies focused only on synthesizing biaryl compounds, rather than high-molecular-weight polyphenylenes.
addition, metathesis, and reductive elimination steps, which are well known in transitionmetal-catalyzed chemistry. To guarantee efficient Ni(0)-catalyzed polymerization, Ni(0) must be regenerated from the Ni(II) species formed during the reaction; in this reaction, Zn and NaI aid in the regeneration of the Ni(0) species. The use of NaI has a positive effect on polymerization [16,20]. Earlier studies on biaryl synthesis postulated that the presence of alkali metal salt additives (iodide or bromide salts) accelerates the coupling reaction [17,25]. However, these studies focused only on synthesizing biaryl compounds, rather than high-molecular-weight polyphenylenes. Scheme 2. Reaction path demonstrating the role of Zn and NaI in Ni-catalyzed polymerization.

Block Copolymer Synthesis Using Ni(COD)2
For comparison, sPP(COD)@1:1 and sPP(COD)@1:4 block copolymers were synthesized using the Ni(COD)2 catalyst using the molar equivalents of 1:1 and 1:4 of pNDCBS to mNDCBS, respectively. To catalyze polymerization with Ni(COD)2, a very large amount of 1.25 equivalents to those of total chlorine was used. This is because the Ni(II) species formed in the oxidative addition step could not be reduced to Ni(0) in situ. The GPC profiles of sPP(COD)@1:1 and sPP(COD)@1:4 are shown in Figure S2, and the properties associated with the data are listed in Table 1. Although the molecular weights of the block copolymers synthesized with the Ni(COD)2 catalyst were slightly lower than those of the block copolymers synthesized with the NiBr2(PPh3)2 catalyst, all polymers not only had high molecular weights, which were sufficient for casting membranes, but also demonstrated good solubility in polar organic solvents.

Structural Characterization of the Synthesized Block Copolymers
The 1 H NMR spectra of the block copolymers synthesized in this study are shown in Figures S3 and 4. The chemical shift values for all block copolymers were consistent with the predicted values of the proposed structures. Moreover, the chemical shifts of the neopentyl group indicated that it was preserved after block copolymerization. The 1 H NMR spectra in Figure 4 suggests a complete deprotection step because the neopentyl group was not observed. Furthermore, the solubility of the block copolymers remained unchanged even after deprotection. The 1 H NMR spectra also shows that the chemical shifts corresponding to the aromatic region remained intact. However, the chemical shifts of the OAEK repeating unit remained identical to those of the sPP block copolymers, whereas those of the end group protons shifted downfield in the block copolymer. Scheme 2. Reaction path demonstrating the role of Zn and NaI in Ni-catalyzed polymerization.

Block Copolymer Synthesis Using Ni(COD) 2
For comparison, sPP(COD)@1:1 and sPP(COD)@1:4 block copolymers were synthesized using the Ni(COD) 2 catalyst using the molar equivalents of 1:1 and 1:4 of pNDCBS to mNDCBS, respectively. To catalyze polymerization with Ni(COD) 2 , a very large amount of 1.25 equivalents to those of total chlorine was used. This is because the Ni(II) species formed in the oxidative addition step could not be reduced to Ni(0) in situ. The GPC profiles of sPP(COD)@1:1 and sPP(COD)@1:4 are shown in Figure S2, and the properties associated with the data are listed in Table 1. Although the molecular weights of the block copolymers synthesized with the Ni(COD) 2 catalyst were slightly lower than those of the block copolymers synthesized with the NiBr 2 (PPh 3 ) 2 catalyst, all polymers not only had high molecular weights, which were sufficient for casting membranes, but also demonstrated good solubility in polar organic solvents.

Structural Characterization of the Synthesized Block Copolymers
The 1 H NMR spectra of the block copolymers synthesized in this study are shown in Figure S3 and Figure 4. The chemical shift values for all block copolymers were consistent with the predicted values of the proposed structures. Moreover, the chemical shifts of the neopentyl group indicated that it was preserved after block copolymerization. The 1 H NMR spectra in Figure 4 suggests a complete deprotection step because the neopentyl group was not observed. Furthermore, the solubility of the block copolymers remained unchanged even after deprotection. The 1 H NMR spectra also shows that the chemical shifts corresponding to the aromatic region remained intact. However, the chemical shifts of the OAEK repeating unit remained identical to those of the sPP block copolymers, whereas those of the end group protons shifted downfield in the block copolymer.

Fabrication of PEMs from the Synthesized sPP Block Copolymers
The block copolymers sPP65@1:1 and sPP65@1:4, which had the highest molecular weights, were selected for membrane casting. Thin, transparent, and bendable membranes were obtained from these copolymers using the solution-casting technique. Digital

Fabrication of PEMs from the Synthesized sPP Block Copolymers
The block copolymers sPP65@1:1 and sPP65@1:4, which had the highest molecular weights, were selected for membrane casting. Thin, transparent, and bendable membranes were obtained from these copolymers using the solution-casting technique. Digital photographs of the fabricated membranes are shown in Figure 5. These results imply that the polymerization catalyzed by the in-situ-generated Ni(0) species from the Ni(II) salt in the presence of Zn was successful. For comparison, we also prepared membranes from the block copolymers synthesized using the Ni(COD) 2 catalyst.

Fabrication of PEMs from the Synthesized sPP Block Copolymers
The block copolymers sPP65@1:1 and sPP65@1:4, which had the highest molecular weights, were selected for membrane casting. Thin, transparent, and bendable membranes were obtained from these copolymers using the solution-casting technique. Digital photographs of the fabricated membranes are shown in Figure 5. These results imply that the polymerization catalyzed by the in-situ-generated Ni(0) species from the Ni(II) salt in the presence of Zn was successful. For comparison, we also prepared membranes from the block copolymers synthesized using the Ni(COD)2 catalyst.

Ion Exchange Capacity, Proton Conductivity, Water Uptake, and Dimension Stability of Membranes
A feed IEC of 2.50 meq/g and a hydrophobic-hydrophilic block structural composition of X5Y11.3 were used for the block copolymer synthesis. The calculated IEC values for block copolymer membranes are listed in Table 2, and these values are in good agreement with the feed IEC values.

Ion Exchange Capacity, Proton Conductivity, Water Uptake, and Dimension Stability of Membranes
A feed IEC of 2.50 meq/g and a hydrophobic-hydrophilic block structural composition of X 5 Y 11.3 were used for the block copolymer synthesis. The calculated IEC values for block copolymer membranes are listed in Table 2, and these values are in good agreement with the feed IEC values. Table 2. Measured ion exchange capacity, water uptake (Φ w ), and in-plane (∆l) and through-plane (∆t) swelling ratios for block copolymers selected for membrane casting. Proton transport in PEMs occurs through water-filled percolating hydrophilic domains surrounding the acid functionalities, i.e., water uptake (Φ w ) is a key property of protonconducting membranes and directly influences proton conductivity. However, excessive water uptake under hydration conditions negatively impacts the mechanical and dimensional properties of the membrane. Table 2 lists the Φ w values, which range between 61% and 71%. The water uptake consistently followed an increasing trend with an increase in relative humidity ( Figure S4). Anisotropic dimensional variations were observed for all block copolymer membranes, where the ∆t values were greater than ∆l values (Table 2). This is attributed to the difference in chain alignment between the hydrophobic and hydrophilic segments in the block copolymer main backbone [8]. The rigid hydrophobic segment aligned in the in-plane direction, whereas the hydrophilic segment aligned in the through-plane direction. Hydrophilic moieties are solely responsible for membrane swelling under hydration conditions. Figure 6 shows the proton conductivities of the block copolymer membranes, which are in accordance with their IEC values. The conductivity values for the sPP65@1:4 copolymer membrane surpassed the conductivity value of sPP65@1:1 despite the low IEC value. This is attributed to the more flexible hydrophilic segment in sPP65@1:4, where the molar equivalent for the meta-comonomer is 4 equivalents to the para-comonomer. This is attributed to the difference in chain alignment between the hydrophobic and hydrophilic segments in the block copolymer main backbone [8]. The rigid hydrophobic segment aligned in the in-plane direction, whereas the hydrophilic segment aligned in the through-plane direction. Hydrophilic moieties are solely responsible for membrane swelling under hydration conditions. Figure 6 shows the proton conductivities of the block copolymer membranes, which are in accordance with their IEC values. The conductivity values for the sPP65@1:4 copolymer membrane surpassed the conductivity value of sPP65@1:1 despite the low IEC value. This is attributed to the more flexible hydrophilic segment in sPP65@1:4, where the molar equivalent for the meta-comonomer is 4 equivalents to the para-comonomer.

Conclusions
In this study, we highlighted the potential of in-situ-generated Ni(0) in the presence of the strong reducing metal Zn and the weak additive ligand NaI as the polycondensation promoter in the synthesis of sulfonated polyphenylenes. The effects of Ni(II) complex equivalents to those of total chlorine and the hydrophilic monomer feed ratio of the resultant polymer were investigated. The in-situ-generated Ni(0) from Ni(II)Br2(PPh3)2 in the presence of Zn successfully catalyzed the synthesis of sulfonated polyphenylene block copolymers in catalytic equivalents. An increase in the NiBr2(PPh3)2 equivalents up to 0.065 equivalents afforded high-molecular-weight block copolymers. The resultant block copolymers synthesized using NiBr2(PPh3)2 had comparable physical properties and chemical structures to those synthesized using Ni(COD)2. The water sorption parameters and ion transport properties of the block copolymers sPP65@1:1 and sPP65@1:4, which had the highest molecular weights, were studied in detail. We believe that our approach will open new avenues for the synthesis of other functional block copolymers.

Conclusions
In this study, we highlighted the potential of in-situ-generated Ni(0) in the presence of the strong reducing metal Zn and the weak additive ligand NaI as the polycondensation promoter in the synthesis of sulfonated polyphenylenes. The effects of Ni(II) complex equivalents to those of total chlorine and the hydrophilic monomer feed ratio of the resultant polymer were investigated. The in-situ-generated Ni(0) from Ni(II)Br 2 (PPh 3 ) 2 in the presence of Zn successfully catalyzed the synthesis of sulfonated polyphenylene block copolymers in catalytic equivalents. An increase in the NiBr 2 (PPh 3 ) 2 equivalents up to 0.065 equivalents afforded high-molecular-weight block copolymers. The resultant block copolymers synthesized using NiBr 2 (PPh 3 ) 2 had comparable physical properties and chemical structures to those synthesized using Ni(COD) 2 . The water sorption parameters and ion transport properties of the block copolymers sPP65@1:1 and sPP65@1:4, which had the highest molecular weights, were studied in detail. We believe that our approach will open new avenues for the synthesis of other functional block copolymers.