Lewis Acid-Base Pair-Regulated Ring-Opening Copolymerization of Succinic Anhydride and Tetrahydrofuran†

Lewis Acid-Base Pair-Regulated Ring-Opening Copolymerization of Succinic Anhydride and Tetrahydrofuran† | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article Lewis Acid-Base Pair-Regulated Ring-Opening Copolymerization of Succinic Anhydride and Tetrahydrofuran† Wenjun Lu, Hongjun Yin, Ting Li, Jing Huang, Xuhui Zhang, Yang Wang, and 3 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-8152611/v1 This work is licensed under a CC BY 4.0 License Status: Published Journal Publication published 23 Mar, 2026 Read the published version in Journal of Polymer Research → Version 1 posted 5 You are reading this latest preprint version Abstract The cationic ring-opening copolymerization (ROCOP) of succinic anhydride (SA) and tetrahydrofuran (THF) was conducted using aluminium trifluoromethanesulfonate (Al(OTf) 3 ) via bulk polymerization to synthesize poly(butylene succinate) (PBS). The molecular weight and ester content of products were regulated by constructing Lewis acid-base pairs through the introduction of co-catalysts. Compared with the control group without co-catalysts, the resulting products exhibited significant enhancements in molecular weight. The polyester product with 99.38% ester content was achieved by incorporating gallic acid as co-catalyst. When sodium dihydrogen phosphate (NaH 2 PO 4 ) was employed as co-catalyst, a product with molecular weight of 4.008 kDa was obtained. The employment of Lewis base as a co-catalyst yielded products with 85.93% ester content and molecular weight of 4.570 kDa. The regulatory mechanism of Lewis acid-base pairs in this system was systematically investigated based on experimental results, demonstrating potential application prospects in industrial-scale production. ring-opening copolymerization Lewis acid-base pairs succinic anhydride tetrahydrofuran Figures Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 Introduction The widespread use of polymer materials has brought tremendous convenience to society while simultaneously posing increasingly severe environmental pollution challenges. With social development, environmentally friendly polymer materials have attracted increasing attention. Among these, aliphatic polyesters have emerged as promising biodegradable alternatives to petroleum-based polymers, and their research and applications have continuously achieved new progress in recent years[1, 2]. Poly(butylene succinate) (PBS) represents a significant biodegradable material[3-5]. As a biodegradable polyester, PBS exhibits excellent biodegradability, being decomposable into harmless substances such as water and carbon dioxide in composting or natural environments, thereby mitigating white pollution[6]. It demonstrates cost advantages compared to similar biodegradable materials while maintaining favourable physical properties that balance flexibility and strength. Its thermal resistance (melting point approximately 100-120°C) surpasses that of biopolymers like polylactic acid, making it suitable for daily necessities and agricultural films. PBS also offers excellent processability, compatible with conventional plastic processing techniques such as injection moulding, blow moulding, and extrusion, enabling adaptation to existing production equipment and reduced application costs. Its advantages are particularly pronounced in scenarios requiring short-term utilization[7]. Ring-opening copolymerization (ROCOP) is a polymerization methodology involving the ring-opening of cyclic monomers under catalytic conditions to form linear polymers through homopolymerization or copolymerization with other monomers[8-18]. This technique is commonly employed in the copolymerization of epoxides and cyclic anhydrides for polyester synthesis. ROCOP demonstrates high flexibility in monomer selection, allowing precise control over polymer chain structures through strategic selection of cyclic monomers with varying architectures[19-22]. It enables molecular weight and molecular weight distribution regulation via adjustment of monomer feed ratios and catalyst design[23]. The reaction conditions of ROCOP are relatively mild, typically conducted at lower temperatures and pressures. Notably, the absence of small molecule by-products (e.g., water) during the process reduces side reactions and simplifies post-processing, exhibiting atom economy that aligns with green chemistry principles. ROCOP exhibits a propensity for alternating copolymerization, facilitating the formation of alternating structures that enhance ester group content in products. Many ROCOP systems demonstrate characteristics of living polymerization, enabling production of high molecular weight polymers with narrow molecular weight distributions[24]. As a promising polymerization strategy, ROCOP has naturally been applied to PBS synthesis research following extensive investigation. Tetrahydrofuran (THF), a polymer producible through furfural hydrogenation or 1,4-butanediol dehydration, holds significant potential for environmentally sustainable production due to its biomass-derived origin. As a five-membered cyclic ether with low ring strain, THF maintains chemical stability under standard conditions, facilitating transportation and storage. It demonstrates high selectivity for catalysts and undergoes controllable ring-opening reactions under cationic initiators with mild reaction conditions and high efficiency[25-32]. Succinic anhydride (SA), featuring a five-membered cyclic structure and relatively low melting point, enables solvent-free bulk polymerization in its molten state, thereby minimizing post-processing requirements[33-39]. SA exhibits no homopolymerization tendency after ring-opening, effectively suppressing side reactions. Leveraging these advantages, this study employs THF and SA as monomers for the direct synthesis of PBS via ROCOP, investigating the effects of Lewis acid-base pair systems and multifunctional chain terminators on polymerization outcomes[40-45]. Experimental methods Instruments and reagents A JWZFG-100ml mechanical high-pressure reactor (Xi’an Tai-Kang Biotechnology Co., Ltd., China), Nicolet iS50 Fourier-transform infrared spectrometer (FT-IR, Thermo Fisher Scientific, USA), TGA2 thermogravimetric analyser (TGA, Mettler-Toledo, Switzerland), DSC3 differential scanning calorimeter (DSC, Mettler-Toledo, Switzerland), AVANCE NEO 600 MHz nuclear magnetic resonance spectrometer (NMR, Bruker, Switzerland), and LC-20ADXR gel permeation chromatograph (GPC, Shimadzu Corporation, Japan) were utilized. Succinic anhydride (SA, ≥ 99.5%) was purchased from Xu-Ke New Materials (Shandong) Co., Ltd. Tetrahydrofuran (THF, ≥ 99.5%), calcium hydride (CaH 2 , ≥ 99.7%), calcium hydroxide (Ca(OH)2, ≥ 99.7%), benzyl alcohol (BnOH, ≥ 99.7%), ethylene glycol (EG, ≥ 99.5%), glycerol (GLY, ≥ 99.5%), pentaerythritol (PER, ≥ 99.5%), absolute ethanol (≥ 99.5%), and chloroform (≥ 99.7%) were obtained from Sinopharm Chemical Reagent Co., Ltd. Aluminium trifluoromethanesulfonate (Al(OTf) 3 , ≥ 98%), anhydrous sodium dihydrogen phosphate (NaH 2 PO 4 , ≥ 99%), anhydrous calcium dihydrogen phosphate (Ca(H 2 PO 4 ) 2 , ≥ 99%), magnesium dihydrogen phosphate (Mg(H 2 PO 4 ) 2 , ≥ 98%), aluminium dihydrogen phosphate (Al(H 2 PO 4 ) 3 , ≥ 98%), and gallic acid (GA, ≥ 98%) were sourced from Macklin Inc. Petroleum ether (≥ 99.7%) was purchased from General-Reagent. Experimental procedure SA was dried in a vacuum oven at 40°C for 48 hours, and THF was dehydrated using 2–3 mm molecular sieves for 72 hours. All materials were weighed in a glovebox. After removing the reactor from the glovebox, nitrogen was purged for 10 minutes. The reactor was then pressurized to 1.0 MPa with nitrogen at a stirring rate of 200 rpm, and the reaction temperature and time were set according to experimental requirements. Upon reaction completion, the reactor was rapidly cooled in a water bath at ambient temperature, and the product was collected. An ethanol-water solution (2:3 v/v) was prepared and acidified to pH 3 using hydrochloric acid. The crude product was washed with this acidified solution to remove residual catalysts and unreacted small molecules. After filtration, the product was rinsed with deionized water until the pH reached 7. The filtered solid was dissolved in chloroform under stirring, and the solution was rapidly poured into petroleum ether (three times the solution volume) to precipitate potential polyether by-products. The settled solid was filtered and dried in a vacuum oven at 40°C for 24 hours. The reaction pathway shown in Fig. 1 suggests two distinct initiation mechanisms. In Fig. 1 (a) , initiation starts with SA where Al(OTf) 3 , as a strong Lewis acid, preferentially coordinates to the carbonyl oxygen of SA. This coordination polarizes and enhances its electrophilicity, leading to ring-opening. The activated terminal then attacks the oxygen atom of THF, inducing its ring-opening and subsequent polymerization to form ester linkages. The newly formed active terminal may react with either SA or THF. When reacting with THF, ether segments are generated, resulting in a copolymer containing both ester and ether segments. In Fig. 1 (b) , initiation begins with THF, which undergoes ring-opening under Al³⁺ activation to form an oxonium ion. This species acts as an active centre to attack the carbonyl group of SA, generating ester linkages and propagating the polymerization. Given the lack of homopolymerization propensity in SA, when its chain end becomes an active centre, it can only undergo ring-opening polymerization with THF. The activated THF terminal retains dual reactivity for both homopolymerization and copolymerization. Despite the distinct initiation pathways, the final polymer structure under both scenarios contains both ester and ether segments, demonstrating analogous compositional features. Characterization FT-IR analysis: Samples were pressed into thin films and analysed in attenuated total reflectance (ATR) mode. Spectra were recorded over 32 scans at a resolution of 4 cm -1 , covering a wavenumber range of 500–4000 cm -1 . TGA analysis: Conducted under nitrogen atmosphere, samples were heated from 25°C to 600°C at 10°C/min. Decomposition temperatures and maximum decomposition rate temperatures were derived from the thermogravimetric curves. DSC analysis: Performed under nitrogen atmosphere, samples were heated from 25°C to 150°C at 10°C/min, held for 5 minutes, cooled to 0°C at 10°C/min, held for 5 minutes, and reheated to 150°C at 10°C/min. Crystallization temperatures were determined from the first cooling curve, while melting temperatures were obtained from the second heating curve. GPC analysis: Number-average molecular weight (Mn), weight-average molecular weight (Mw), and polydispersity index (PDI, Mw/Mn) were measured using a tetrahydrofuran-based gel permeation chromatograph. Polystyrene standards and THF as the mobile phase were employed, with samples filtered through a 0.22 µm syringe filter prior to analysis. NMR analysis: Proton nuclear magnetic resonance ( 1 H NMR) spectra were acquired to elucidate molecular structures. Ester content and molecular weight were calculated based on peak area ratios proportional to hydrogen atom counts. Results and discussion Effects of Lewis acid-base Pair systems on polymerization Through a series of preliminary exploratory experiments, aluminum trifluoromethanesulfonate (Al(OTf) 3 ) was selected as the catalyst, with Lewis acids such as sodium dihydrogen phosphate (NaH 2 PO 4 ) serving as co-catalysts. The optimal molar ratio of catalyst, co-catalyst, SA, and THF was determined to be 3:3:1000:1100. The polymerization was conducted under a nitrogen atmosphere at 1.0 MPa, with a reaction temperature of 120°C maintained for 2 hours. As illustrated in Fig. 2 , a comparative analysis of the infrared spectra among the product synthesized with co-catalyst, the product without co-catalyst, and commercially available PBS are presented in Fig. 2 (a) . The product exhibits characteristic peaks consistent with PBS: C-H stretching vibration of methylene groups at 2945 cm -1 , C = O stretching vibration of ester linkages at 1712 cm -1 , and C-O-C stretching vibration of ester bonds at 1155 cm -1 . Notably, all major absorption bands align with those of commercial PBS, and the overall spectral pattern demonstrates analogous features. The 1 H NMR spectrum of the polymer product synthesized at 120°C with co-catalyst is shown in Fig. 2 (b) . Peaks are observed at 4.12 ppm, assigned to the -R-CH 2 -COO- group, 2.64 ppm attributed to the -COO-CH 2 CH 2 -COO- group, and 1.72 ppm corresponding to the -CH 2 -R-COO- group. The peak area ratios of these signals were calculated to be approximately 1:1:1, consistent with the predicted 1 H NMR pattern of PBS. Combined with prior characterization results, this confirms the successful synthesis of PBS. Additionally, a resonance peak at 3.44 ppm is assigned to the -O-R-CH 2 -CH 2 -R-O- group. A distinct peak near 3.70 ppm corresponds to the chain-terminal HO-CH 2 -R- group, indicative of residual hydroxyl end groups. These characterization results demonstrate the successful synthesis of PBS through ring-opening polymerization of SA and THF under a Lewis acid-base pair catalytic system. Further experiments were subsequently conducted based on the synthesized PBS. Co-catalysts with weaker Lewis acidity (Lewis acids) or Lewis basicity were employed to preserve the activity of the primary catalyst. The reaction products were characterized through 1 H NMR and GPC analyses, as summarized in Table 1 . The data reveal that under equivalent co-catalyst loadings, NaH 2 PO 4 significantly enhanced the molecular weight of the product while moderately reducing ester content, accompanied by a noticeable narrowing of molecular weight distribution. Mg(H 2 PO 4 ) 2 and Ca(H 2 PO 4 ) 2 induced marginal reductions in ester content and slight increases in molecular weight, though the variations were less pronounced. Notably, Ca(H 2 PO 4 ) 2 exhibited a broadening of molecular weight distribution. Al(H 2 PO 4 ) 3 demonstrated minimal catalytic efficacy, showing negligible effects on both molecular weight and ester content. Gallic acid slightly increased the molecular weight while concurrently enhancing the ester content. CaH 2 , functioning as a Lewis base, provided limited enhancement in molecular weight but substantially elevated the ester content of the product. Ca(OH) 2 , while reducing ester content moderately, achieved remarkable molecular weight augmentation. Based on these experimental findings, further investigations were conducted on gallic acid, NaH 2 PO 4 , CaH 2 , and Ca(OH) 2 to systematically examine the influence of co-catalyst loading on reaction outcomes. Table 1 Effects of Lewis acid-base pair types on the ROCOP of SA and THF a Co-Catalyst Ester (%) b Ether (%) b Mn (kDa) c Mw/Mn c TON (g/mol) d Blank 98.89 1.11 1.829 1.43 31325.77 NaH 2 PO 4 95.69 4.31 2.791 1.36 35168.01 Mg(H 2 PO 4 ) 2 96.85 3.15 2.408 1.42 36139.82 Al(H 2 PO 4 ) 3 98.64 1.36 1.789 1.45 41555.40 Ca(H 2 PO 4 ) 2 94.45 5.55 2.075 1.97 38215.10 Gallic acid 99.13 0.87 2.274 1.43 35806.12 CaH 2 96.39 3.61 2.836 1.41 32987.27 Ca(OH) 2 85.93 14.07 4.570 1.52 37438.43 a The molar ratio of other substances was set as SA: THF: Al(OTf) 3 : co-catalyst = 1000: 1100: 3: 3, with nSA = 100 mmol. The reaction pressure was 0.9 MPa, and the reaction time was 2 h. A control experiment without any co-catalyst under identical conditions for 2 h was conducted for comparison. b Ester Unit and Ether Unit were determined via 1H NMR analysis. c Number-average molecular weight (Mn) and molecular weight distribution (Mw/Mn) were characterized by GPC. d Turnover Number (TON) was calculated as the ratio of the mass of the product to the amount of substance of the primary catalyst Al(OTf) 3 . Effects of Gallic Acid on Lewis acid-base pair systems Polymerization reactions were conducted with varying gallic acid loadings while maintaining other parameters constant. As shown in Table 2 and Fig. 3 , when the additive amount ranged between 0.1 and 0.4 mmol, the ester content exhibited an initial increase followed by a gradual decline, yet consistently remained above 99%—surpassing the performance observed in the absence of a co-catalyst—with the maximum ester content of 99.38% achieved at 0.2 mmol. When the additive amount reached 0.5 mmol, the ester content demonstrated a pronounced downward trend, while the TON increased substantially. The molecular weight of the product displayed an overall upward trajectory with increasing gallic acid dosage, showing minor fluctuations within the 0.1–0.4 mmol range and rising to 2.513 kDa at 0.5 mmol. Table 2 Effects of Gallic Acid Input Amount on Polymerization Catalyst : Co-Catalyst Ester (%) Ether (%) Mn (kDa) Mw/Mn TON (g/mol) Blank 98.89 1.11 1.829 1.43 31325.77 3:1 99.22 0.78 2.214 1.33 35864.25 3:2 99.38 0.62 2.069 1.27 37370.07 3:3 99.13 0.87 2.274 1.43 35806.12 3:4 99.26 0.74 2.166 1.38 37598.36 3:5 98.04 1.96 2.513 1.53 41058.31 This phenomenon arises because gallic acid contains three adjacent phenolic hydroxyl groups and one carboxylic acid group, demonstrating strong coordination capacity. Its functional groups can form stable polynuclear complexes with Al 3+ , partially replacing the original coordination structure. The formation of these complexes reduces the concentration of free Al 3+ and weakens the Lewis acidity. Although the initial initiation efficiency was decelerated, the lifespan of active chains was prolonged. Moreover, these complexes may synergistically catalyze with Al(OTf) 3 to promote polymerization, thereby enhancing molecular weight. The phenolic hydroxyl groups in gallic acid partially neutralize the strongly acidic triflate ions in the system, reducing free proton concentration and consequently inhibiting chain transfer and termination reactions, extending chain propagation duration. The bulky aromatic structure of gallic acid generates spatial effects that hinder local aggregation of active chains and reduce cyclization side reactions, further facilitating linear chain growth. However, excessive gallic acid input creates a weakly acidic environment where partial SA hydrolysis leads to polycondensation participation, decreasing ester bond formation rate. This may transform the original ring-opening polymerization into a combined ring-opening-polycondensation process. The proton acid provided by gallic acid promotes ester bond hydrolysis. THF exhibits Lewis basicity and demonstrates higher susceptibility to co-catalyzed ring-opening by Lewis acid systems compared to SA. With increased input of gallic acid, a competitive relationship emerges between gallic acid and SA, leading to enhanced probability of chain transfer from the active chains of ring-opened THF to gallic acid. These factors collectively promote the propensity of THF toward homopolymerization within the reaction system, ultimately resulting in a decrease in ester content. Effects of NaHPO on Lewis acid-base pair systems Polymerization reactions were performed with adjusted NaH 2 PO 4 loadings while maintaining other parameters constant. The products were analyzed via 1 H NMR and GPC, as summarized in Table 3 and Fig. 4 . The data indicate that at low loadings (0.1–0.2 mmol), the ester content of the products showed no significant variation, whereas the molecular weight exhibited a pronounced upward trend, with molecular weight distribution remaining around 1.30. Upon increasing the loading to 0.3 mmol, the ester content displayed a marked reduction, while molecular weight continued to rise. At a loading of 0.5 mmol, the ester content remained above 94%, and the molecular weight increased to 3.421 kDa. Further increasing the loading to 0.7 mmol resulted in a molecular weight of 4.008 kDa, albeit with a decline in ester content below 90%. Notably, the molecular weight distribution consistently remained below 1.5, and the TON exceeded 35000 across all conditions. Table 3 The Effect of NaH 2 PO 4 Input Amount on Polymerization Catalyst : Co-Catalyst Ester (%) Ether (%) Mn (kDa) Mw/Mn TON (g/mol) Blank 98.89 1.11 1.829 1.43 31325.77 3:1 99.08 0.92 2.249 1.31 37447.93 3:2 99.11 0.89 2.570 1.26 40681.68 3:3 95.69 4.31 2.791 1.36 35168.01 3:5 94.45 5.55 3.421 1.37 39604.48 3:7 88.50 11.50 4.008 1.47 35960.49 As can be seen from Fig. 4 (a) , the NMR spectra of products obtained using NaH 2 PO 4 as a co-catalyst at different loadings. The spectra reveal that after adding NaH 2 PO 4 , the resonance peak area of the terminal methylene group at approximately 3.70 ppm significantly diminishes, while the resonance peak of the polyether segment methylene group at 3.44 ppm becomes more pronounced with increasing NaH 2 PO 4 loading. Correspondingly, as shown in Fig. 4 (b) , the aforementioned trend becomes more evident: the ester content of the product decreases with increasing input amount, exhibiting distinct inflection points, while the molecular weight increase curve demonstrates a smoother and more stable progression. The underlying reason for this phenomenon may be attributed to the establishment of a Lewis acid-base pair system between NaH 2 PO 4 (weak Lewis acid) and Al(OTf) 3 , generating synergistic catalytic effects. The molecular weight enhancement mechanism is as follows: During the reaction, the coordination between Al 3+ and PO 4 3- forms a dynamic equilibrium, continuously releasing free Al 3+ and PO 4 3- to activate SA and stabilize oxonium ions, respectively. Al 3+ from Al(OTf) 3 coordinates with H 2 PO 4 - (dissociated from NaH 2 PO 4 ) via oxygen atoms, forming a bimetallic complex (Al-O- PO 4 -Al). The Al 3+ retains its coordination capability toward SA's carbonyl oxygen, with enhanced coordination strength due to PO 4 3- bridging. The synergistic effect of Al 3+ and PO 4 3- in the complex promotes more efficient polarization of SA's carbonyl oxygen, resulting in a highly polarized C = O bond that lowers activation energy for nucleophilic attack, thereby accelerating THF ring-opening and ester bond formation. This increases chain propagation rate and molecular weight. PO 4 3- acts as an electron buffer to modulate Al 3+ acidity, preventing over-polarization-induced side reactions while modifying Al 3+ coordination environment and enhancing stability. The ester content reduction mechanism involves nucleophilic attack by H 2 PO 4 - on ester bonds, triggering both intramolecular and intermolecular ester exchange reactions (Fig. 5 ). As shown in Fig. 5 (a) , partial ester bond cleavage under H 2 PO 4 - generates carboxylic acid and hydroxyl groups, which may act as new initiators. The carboxylic acid's proton activates THF to form oxonium ions, whose reactive termini further polymerize with SA and THF to extend the main chain. However, polyether segments exhibit lower hydrolysis susceptibility compared to polyester segments under H 2 PO 4 - influence, leading to preferential ether segment formation and reduced total ester content. As illustrated in Fig. 5 (b) , intermolecular ester exchange redistributes ester groups across chains, forming longer main chains. While this elevates molecular weight, it concurrently decreases overall ester content. Simultaneously, as a Lewis acid, NaH 2 PO 4 forms a competitive relationship with SA for the active sites on THF chain segments with increasing dosage, thereby driving the reaction toward THF homopolymerization. The addition of NaH 2 PO 4 enhances the molecular weight and reduces ester content in the product through dual mechanisms of synergistic catalysis and ester bond reorganization. This result holds potential application value in PBS synthesis, as molecular weight and ester content can be modulated by adjusting NaH 2 PO 4 dosage, thereby regulating the material's mechanical properties and degradation rate. Effects of Ca(OH) on Lewis acid-base pair systems Polymerization reactions were conducted by adjusting the Ca(OH) 2 input amount under otherwise constant conditions, with results characterized by 1 H NMR and GPC analyses as presented in Table 4 and Fig. 6 . The data demonstrate that even a minor Ca(OH) 2 input (0.1 mmol) significantly enhances molecular weight. As the Ca(OH) 2 dosage increases, the molecular weight exhibits a stable improvement, ultimately reaching 4.570 kDa. Concurrently, the ester content decreases, having already declined to 85.93% at 0.3 mmol input. The molecular weight distribution also displays a broadening trend. As shown in Fig. 6 (a) , upon addition of 0.1 mmol calcium hydroxide, a distinct resonance peak emerges at 3.44 ppm, with further amplification of this ether segment-associated peak area observed at higher dosages. Correspondingly, As shown in Fig. 6 (b) , the data illustrates a pronounced increase in product molecular weight and reduction in ester content with escalating Ca(OH) 2 quantities. Table 4 The Effect of Ca(OH) 2 Input Amount on Polymerization Catalyst : Co-Catalyst Ester (%) Ether (%) Mn (kDa) Mw/Mn TON (g/mol) Blank 98.89 1.11 1.829 1.43 31325.77 3:1 98.40 1.60 2.948 1.30 36461.02 3:2 94.45 5.55 3.519 1.42 38152.81 3:3 85.93 14.07 4.570 1.52 37438.43 Upon addition of Ca(OH) 2 , both OH - and Ca 2+ may react with Al(OTf) 3 to form Al-OH or Al-O-Ca structures, reducing the concentration of free Al 3+ ions. The formation of these complexes diminishes chain termination and prolongs chain propagation duration. As a Lewis base, Ca(OH) 2 establishes a Lewis acid-base pair system with the strong Lewis acid Al(OTf) 3 , enabling synergistic catalysis of SA and THF, thereby enhancing the overall catalytic activity. Even at low Ca(OH) 2 dosages, its catalytic effect on SA ring-opening becomes pronounced, with efficacy further improving as dosage increases. This significantly accelerates SA initiation rates, manifesting as a sharp increase in molecular weight. Additionally, Ca(OH) 2 rapidly neutralizes acidic byproducts generated during the reaction, creating an alkaline environment. This alkalinity induces competitive interactions with THF, reducing ester bond formation between THF and SA. Consequently, even minimal Ca(OH) 2 addition leads to a rapid decline in ester content of the product. Effects of CaH 2 on Lewis acid-base pair systems Polymerization reactions were conducted by adjusting the CaH 2 input amount under otherwise constant conditions, with results characterized by 1 H NMR and GPC as shown in Table 5 and Fig. 7 . The data indicate that ester content decreases progressively with increasing CaH 2 dosage. The dosage of the co-catalyst in the range of 0.1–0.3 mmol induced a gradual decrease in ester content, whereas a precipitous decline in ester content occurred when the dosage exceeded 0.4 mmol. The molecular weight demonstrated an ascending trend, exhibiting a moderate increase at CaH 2 dosages of 0.1–0.3 mmol, followed by a pronounced enhancement reaching a maximum value of 3.782 kDa at 0.4 mmol. Further increases in CaH 2 dosage resulted in a decline in molecular weight. The molecular weight distribution displayed negligible variation with minimal calcium hydride addition, fluctuating around 1.45. However, excessive CaH 2 loading caused significant broadening of the molecular weight distribution. Table 5 The Effect of CaH 2 Input Amount on Polymerization Catalyst : Co-Catalyst Ester (%) Ether (%) Mn (kDa) Mw/Mn TON (g/mol) Blank 98.89 1.11 1.829 1.43 31325.77 3:1 97.92 2.08 2.349 1.55 35256.84 3:2 97.32 2.68 2.674 1.34 33962.26 3:3 96.39 3.61 2.836 1.41 32987.27 3:4 93.13 6.87 3.782 1.73 31711.46 3:5 87.24 12.76 3.152 2.05 38821.87 This is likely attributable to altered acid-base conditions induced by the strongly basic CaH 2 . As CaH 2 dosage increased, the system transitioned progressively from acidic to neutral. Both H - and Ca 2+ may react with Al(OTf) 3 , forming Al-H or Al-O-Ca structures, which reduce free Al 3+ concentration and active site availability. Although the chain propagation rate decreased due to fewer active sites, the lifetime of individual active sites may have been extended. Additionally, trace Ca 2+ might synergize with Al 3+ to stabilize propagating chain ends, suppressing chain transfer and termination, ultimately yielding higher molecular weights. When CaH 2 input ranged from 0.1–0.4 mmol, the propensity for ester exchange reactions increased with dosage. Concurrently, dominant chain extension resulted in elevated molecular weight with minimal ester content reduction. However, excessive CaH 2 input (≥ 0.5 mmol) caused complete neutralization and structural alteration of Al(OTf) 3 , severely diminishing or even eliminating catalytic activity. Under such conditions, side reactions proliferated, with Ca 2+ likely dominating to promote ester exchange-induced bond rearrangement or cleavage. For instance, β-elimination occurred, where β-hydrogen abstraction from ester bonds generated carboxylic acid and alkene. Under such conditions, the occurrence of side reactions becomes significantly intensified. Calcium ions (Ca 2+ ) in the system may assume a dominant role, promoting ester exchange reactions that induce rearrangement or cleavage of ester bonds, exemplified by β-elimination processes. Compared with Ca(OH) 2 , although CaH 2 exhibits stronger Lewis acidity in anhydrous organic solutions, OH - can directly undergo neutralization reactions with acidic intermediates generated during polymerization, rapidly reducing system acidity and thus decreasing ester bond formation. In contrast, H - must first react with free protons or active centers in the system to eliminate acidic species, resulting in a longer reaction pathway. Therefore, CaH 2 only induces a significant reduction in the ester content of the product when its dosage reaches 0.5 mmol. Conclusions Upon adding a Lewis acid catalyst, the ester content of the polymeric product exceeded 99%, but higher catalyst dosages decreased ester content while increasing molecular weight, ultimately producing a 4.008 kDa product. The reaction mechanisms of gallic acid and NaH 2 PO 4 as cocatalysts were elucidated. Gallic acid stabilized the reaction system via coordination effects while suppressing cyclization through steric hindrance, promoting linear chain growth. NaH 2 PO 4 enhanced molecular weight and reduced ester content through dual mechanisms: synergistic catalysis and ester bond rearrangement. When Lewis acids served as cocatalysts, they competed with SA for active centers on ring-opened THF chains, thereby inhibiting SA-THF polymerization and lowering ester content. Introducing Lewis bases to construct Lewis acid-base pair catalytic systems further reduced ester content and elevated molecular weight, achieving a 4.570 kDa product. Ca(OH) 2 significantly increased molecular weight by forming extensive complexes with the primary catalyst, while its rapid OH - neutralization minimized acidic byproducts, drastically reducing ester content. When CaH 2 was employed as a cocatalyst, it acted as a desiccant to eliminate residual water in reagents. Limited complexation with the primary catalyst and partial promotion of transesterification resulted in only marginal molecular weight gains and a gradual ester content reduction below 0.3 mmol. Although Lewis bases enhanced SA ring-opening efficiency and substantially increased molecular weight, their strong basicity induced competitive interactions with THF, ultimately decreasing ester content by impeding SA-THF polymerization. In summary, PBS was synthesized via cationic ring-opening polymerization. By constructing Lewis acid-base pair catalytic systems with cocatalysts and adjusting the molar ratios of acid-base pairs and catalyst-to-monomer, precise control over product molecular weight and ester content was achieved. This approach provides a viable pathway for industrial-scale ring-opening polymerization processes. Declarations Supplementary Information The online version contains supplementary material available at https://osf.io/mz6b4/?view_only=744a40c3d34b4059ab841eec7de327f0 Competing interests The authors declare no competing financial interests. Funding This work was supported by Key Technology for Preparation of Biobased Degradable Packaging Materials from Cheap Biomass (2022YFC2104602). Author contributions: Wenjun Lu: Formal analysis and investigation, Writing-original draft preparation, Writing-review and editing; Hongjun Yin: Writing-Supervision; Ting Li: Resources; Jing Huang, Xu-Hui Zhang, Yang Wang, Bihua Xia: Writing-review; Shibo Wang: Writing-review and editing; Weifu Dong: Supervision Data availability The data that support the findings of this study are available from the corresponding author upon reasonable request. 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10:07:42","extension":"html","order_by":22,"title":"","display":"","copyAsset":false,"role":"acdc-reference","size":143057,"visible":true,"origin":"","legend":"","description":"","filename":"earlyproof.html","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/6f932ac7dd462d4d83c88778.html"},{"id":97141954,"identity":"959e1ba7-10c5-45cb-9aa5-8688c1c39cb5","added_by":"auto","created_at":"2025-12-01 10:07:12","extension":"jpg","order_by":1,"title":"Figure 1","display":"","copyAsset":false,"role":"figure","size":62697,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003e(a)\u003c/strong\u003e SA-initiated plausible reaction pathway for ring-opening copolymerization; \u003cstrong\u003e(b)\u003c/strong\u003e THF-initiated plausible reaction pathway for ring-opening copolymerization.\u003c/p\u003e","description":"","filename":"1.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/f40e2d06562b35c22e5d4fb6.jpg"},{"id":97142431,"identity":"cf0d31a1-ec2d-47e5-bc0b-2944e0baa6ba","added_by":"auto","created_at":"2025-12-01 10:07:37","extension":"jpg","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":63018,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003e(a) \u003c/strong\u003eFT-IR spectra of the product with co-catalyst, product without co-catalyst, and commercially available PBS; \u003cstrong\u003e(b)\u003c/strong\u003e ¹H NMR spectrum of the product obtained at a polymerization temperature of 120°C.\u003c/p\u003e","description":"","filename":"2.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/2852ad5ce38b2fe64fe365c8.jpg"},{"id":97112131,"identity":"f90abf83-6422-4d45-90f6-79bfebec7fb4","added_by":"auto","created_at":"2025-12-01 06:42:17","extension":"jpg","order_by":3,"title":"Figure 3","display":"","copyAsset":false,"role":"figure","size":46019,"visible":true,"origin":"","legend":"\u003cp\u003ePlots of ester content and molecular weight versus Gallic Acid loading.\u003c/p\u003e","description":"","filename":"3.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/352c3e206cb17d79dad93fac.jpg"},{"id":97112128,"identity":"987c9e43-093a-4f23-8b77-f6bdda9ebceb","added_by":"auto","created_at":"2025-12-01 06:42:17","extension":"jpg","order_by":4,"title":"Figure 4","display":"","copyAsset":false,"role":"figure","size":63434,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003e(a) \u003c/strong\u003e\u003csup\u003e1\u003c/sup\u003eH NMR spectra in the range of 3.2-4.0 ppm for products with NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e as a co-catalyst; \u003cstrong\u003e(b)\u003c/strong\u003e Plots of ester content and molecular weight versus NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e loading.\u003c/p\u003e","description":"","filename":"4.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/bde5e0da548a67ac65f2718a.jpg"},{"id":97112125,"identity":"a7f89944-9d30-473d-823c-660c11dfcaf3","added_by":"auto","created_at":"2025-12-01 06:42:17","extension":"jpg","order_by":5,"title":"Figure 5","display":"","copyAsset":false,"role":"figure","size":47517,"visible":true,"origin":"","legend":"\u003cp\u003e(a) Hydrolysis reaction after NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e addition; (b) Ester exchange reaction after NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e addition.\u003c/p\u003e","description":"","filename":"5.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/d3d84b97ea024a686d7efcd8.jpg"},{"id":97112135,"identity":"fc583990-a5ae-44ae-9c5a-93893f98b56d","added_by":"auto","created_at":"2025-12-01 06:42:17","extension":"jpg","order_by":6,"title":"Figure 6","display":"","copyAsset":false,"role":"figure","size":52579,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003e(a) \u003c/strong\u003e\u003csup\u003e1\u003c/sup\u003eH NMR spectra in the range of 3.2-4.0 ppm for products with Ca(OH)\u003csub\u003e2\u003c/sub\u003e as a co-catalyst; \u003cstrong\u003e(b)\u003c/strong\u003e Plots of ester content and molecular weight versus Ca(OH)\u003csub\u003e2\u003c/sub\u003e loading.\u003c/p\u003e","description":"","filename":"6.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/206d794bf1e17425743fc533.jpg"},{"id":97141162,"identity":"3397f94e-5f31-4f73-94da-a995c4bbc9e8","added_by":"auto","created_at":"2025-12-01 10:06:20","extension":"jpg","order_by":7,"title":"Figure 7","display":"","copyAsset":false,"role":"figure","size":51208,"visible":true,"origin":"","legend":"\u003cp\u003ePlots of ester content and molecular weight versus CaH\u003csub\u003e2\u003c/sub\u003e loading.\u003c/p\u003e","description":"","filename":"7.jpg","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/812c7855ee31837ea1ffa885.jpg"},{"id":105756062,"identity":"590ac594-38be-403c-be9a-d49f3a61f74f","added_by":"auto","created_at":"2026-03-30 16:34:58","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":1371448,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-8152611/v1/1406270c-c7d8-43bd-9c4b-576798046da7.pdf"}],"financialInterests":"","formattedTitle":"Lewis Acid-Base Pair-Regulated Ring-Opening Copolymerization of Succinic Anhydride and Tetrahydrofuran†","fulltext":[{"header":"Introduction","content":"\u003cp\u003eThe widespread use of polymer materials has brought tremendous convenience to society while simultaneously posing increasingly severe environmental pollution challenges. With social development, environmentally friendly polymer materials have attracted increasing attention. Among these, aliphatic polyesters have emerged as promising biodegradable alternatives to petroleum-based polymers, and their research and applications have continuously achieved new progress in recent years[1, 2]. Poly(butylene succinate) (PBS) represents a significant biodegradable material[3-5]. As a biodegradable polyester, PBS exhibits excellent biodegradability, being decomposable into harmless substances such as water and carbon dioxide in composting or natural environments, thereby mitigating white pollution[6]. It demonstrates cost advantages compared to similar biodegradable materials while maintaining favourable physical properties that balance flexibility and strength. Its thermal resistance (melting point approximately 100-120\u0026deg;C) surpasses that of biopolymers like polylactic acid, making it suitable for daily necessities and agricultural films. PBS also offers excellent processability, compatible with conventional plastic processing techniques such as injection moulding, blow moulding, and extrusion, enabling adaptation to existing production equipment and reduced application costs. Its advantages are particularly pronounced in scenarios requiring short-term utilization[7].\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eRing-opening copolymerization (ROCOP) is a polymerization methodology involving the ring-opening of cyclic monomers under catalytic conditions to form linear polymers through homopolymerization or copolymerization with other monomers[8-18]. This technique is commonly employed in the copolymerization of epoxides and cyclic anhydrides for polyester synthesis. ROCOP demonstrates high flexibility in monomer selection, allowing precise control over polymer chain structures through strategic selection of cyclic monomers with varying architectures[19-22]. It enables molecular weight and molecular weight distribution regulation via adjustment of monomer feed ratios and catalyst design[23]. The reaction conditions of ROCOP are relatively mild, typically conducted at lower temperatures and pressures. Notably, the absence of small molecule by-products (e.g., water) during the process reduces side reactions and simplifies post-processing, exhibiting atom economy that aligns with green chemistry principles. ROCOP exhibits a propensity for alternating copolymerization, facilitating the formation of alternating structures that enhance ester group content in products. Many ROCOP systems demonstrate characteristics of living polymerization, enabling production of high molecular weight polymers with narrow molecular weight distributions[24]. As a promising polymerization strategy, ROCOP has naturally been applied to PBS synthesis research following extensive investigation.\u003c/p\u003e\n\u003cp\u003eTetrahydrofuran (THF), a polymer producible through furfural hydrogenation or 1,4-butanediol dehydration, holds significant potential for environmentally sustainable production due to its biomass-derived origin. As a five-membered cyclic ether with low ring strain, THF maintains chemical stability under standard conditions, facilitating transportation and storage. It demonstrates high selectivity for catalysts and undergoes controllable ring-opening reactions under cationic initiators with mild reaction conditions and high efficiency[25-32]. Succinic anhydride (SA), featuring a five-membered cyclic structure and relatively low melting point, enables solvent-free bulk polymerization in its molten state, thereby minimizing post-processing requirements[33-39]. SA exhibits no homopolymerization tendency after ring-opening, effectively suppressing side reactions. Leveraging these advantages, this study employs THF and SA as monomers for the direct synthesis of PBS via ROCOP, investigating the effects of Lewis acid-base pair systems and multifunctional chain terminators on polymerization outcomes[40-45].\u003c/p\u003e"},{"header":"Experimental methods","content":"\u003cdiv id=\"Sec3\" class=\"Section2\"\u003e\u003ch2\u003eInstruments and reagents\u003c/h2\u003e\u003cp\u003eA JWZFG-100ml mechanical high-pressure reactor (Xi\u0026rsquo;an Tai-Kang Biotechnology Co., Ltd., China), Nicolet iS50 Fourier-transform infrared spectrometer (FT-IR, Thermo Fisher Scientific, USA), TGA2 thermogravimetric analyser (TGA, Mettler-Toledo, Switzerland), DSC3 differential scanning calorimeter (DSC, Mettler-Toledo, Switzerland), AVANCE NEO 600 MHz nuclear magnetic resonance spectrometer (NMR, Bruker, Switzerland), and LC-20ADXR gel permeation chromatograph (GPC, Shimadzu Corporation, Japan) were utilized.\u003c/p\u003e\u003cp\u003eSuccinic anhydride (SA, \u0026ge;\u0026thinsp;99.5%) was purchased from Xu-Ke New Materials (Shandong) Co., Ltd. Tetrahydrofuran (THF, \u0026ge;\u0026thinsp;99.5%), calcium hydride (CaH\u003csub\u003e2\u003c/sub\u003e, \u0026ge;\u0026thinsp;99.7%), calcium hydroxide (Ca(OH)2, \u0026ge;\u0026thinsp;99.7%), benzyl alcohol (BnOH, \u0026ge;\u0026thinsp;99.7%), ethylene glycol (EG, \u0026ge;\u0026thinsp;99.5%), glycerol (GLY, \u0026ge;\u0026thinsp;99.5%), pentaerythritol (PER, \u0026ge;\u0026thinsp;99.5%), absolute ethanol (\u0026ge;\u0026thinsp;99.5%), and chloroform (\u0026ge;\u0026thinsp;99.7%) were obtained from Sinopharm Chemical Reagent Co., Ltd. Aluminium trifluoromethanesulfonate (Al(OTf)\u003csub\u003e3\u003c/sub\u003e, \u0026ge;\u0026thinsp;98%), anhydrous sodium dihydrogen phosphate (NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e, \u0026ge;\u0026thinsp;99%), anhydrous calcium dihydrogen phosphate (Ca(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e, \u0026ge;\u0026thinsp;99%), magnesium dihydrogen phosphate (Mg(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e, \u0026ge;\u0026thinsp;98%), aluminium dihydrogen phosphate (Al(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e3\u003c/sub\u003e, \u0026ge;\u0026thinsp;98%), and gallic acid (GA, \u0026ge;\u0026thinsp;98%) were sourced from Macklin Inc. Petroleum ether (\u0026ge;\u0026thinsp;99.7%) was purchased from General-Reagent.\u003c/p\u003e\u003c/div\u003e\n\u003ch3\u003eExperimental procedure\u003c/h3\u003e\n\u003cp\u003eSA was dried in a vacuum oven at 40\u0026deg;C for 48 hours, and THF was dehydrated using 2\u0026ndash;3 mm molecular sieves for 72 hours.\u003c/p\u003e\u003cp\u003eAll materials were weighed in a glovebox. After removing the reactor from the glovebox, nitrogen was purged for 10 minutes. The reactor was then pressurized to 1.0 MPa with nitrogen at a stirring rate of 200 rpm, and the reaction temperature and time were set according to experimental requirements. Upon reaction completion, the reactor was rapidly cooled in a water bath at ambient temperature, and the product was collected.\u003c/p\u003e\u003cp\u003eAn ethanol-water solution (2:3 v/v) was prepared and acidified to pH 3 using hydrochloric acid. The crude product was washed with this acidified solution to remove residual catalysts and unreacted small molecules. After filtration, the product was rinsed with deionized water until the pH reached 7. The filtered solid was dissolved in chloroform under stirring, and the solution was rapidly poured into petroleum ether (three times the solution volume) to precipitate potential polyether by-products. The settled solid was filtered and dried in a vacuum oven at 40\u0026deg;C for 24 hours.\u003c/p\u003e\u003cp\u003eThe reaction pathway shown in Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003e suggests two distinct initiation mechanisms. In Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003e \u003cb\u003e(a)\u003c/b\u003e, initiation starts with SA where Al(OTf)\u003csub\u003e3\u003c/sub\u003e, as a strong Lewis acid, preferentially coordinates to the carbonyl oxygen of SA. This coordination polarizes and enhances its electrophilicity, leading to ring-opening. The activated terminal then attacks the oxygen atom of THF, inducing its ring-opening and subsequent polymerization to form ester linkages. The newly formed active terminal may react with either SA or THF. When reacting with THF, ether segments are generated, resulting in a copolymer containing both ester and ether segments. In Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003e \u003cb\u003e(b)\u003c/b\u003e, initiation begins with THF, which undergoes ring-opening under Al\u0026sup3;⁺ activation to form an oxonium ion. This species acts as an active centre to attack the carbonyl group of SA, generating ester linkages and propagating the polymerization. Given the lack of homopolymerization propensity in SA, when its chain end becomes an active centre, it can only undergo ring-opening polymerization with THF. The activated THF terminal retains dual reactivity for both homopolymerization and copolymerization. Despite the distinct initiation pathways, the final polymer structure under both scenarios contains both ester and ether segments, demonstrating analogous compositional features.\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\n\u003ch3\u003eCharacterization\u003c/h3\u003e\n\u003cp\u003eFT-IR analysis: Samples were pressed into thin films and analysed in attenuated total reflectance (ATR) mode. Spectra were recorded over 32 scans at a resolution of 4 cm\u003csup\u003e-1\u003c/sup\u003e, covering a wavenumber range of 500\u0026ndash;4000 cm\u003csup\u003e-1\u003c/sup\u003e.\u003c/p\u003e\u003cp\u003eTGA analysis: Conducted under nitrogen atmosphere, samples were heated from 25\u0026deg;C to 600\u0026deg;C at 10\u0026deg;C/min. Decomposition temperatures and maximum decomposition rate temperatures were derived from the thermogravimetric curves.\u003c/p\u003e\u003cp\u003eDSC analysis: Performed under nitrogen atmosphere, samples were heated from 25\u0026deg;C to 150\u0026deg;C at 10\u0026deg;C/min, held for 5 minutes, cooled to 0\u0026deg;C at 10\u0026deg;C/min, held for 5 minutes, and reheated to 150\u0026deg;C at 10\u0026deg;C/min. Crystallization temperatures were determined from the first cooling curve, while melting temperatures were obtained from the second heating curve.\u003c/p\u003e\u003cp\u003eGPC analysis: Number-average molecular weight (Mn), weight-average molecular weight (Mw), and polydispersity index (PDI, Mw/Mn) were measured using a tetrahydrofuran-based gel permeation chromatograph. Polystyrene standards and THF as the mobile phase were employed, with samples filtered through a 0.22 \u0026micro;m syringe filter prior to analysis.\u003c/p\u003e\u003cp\u003eNMR analysis: Proton nuclear magnetic resonance (\u003csup\u003e1\u003c/sup\u003eH NMR) spectra were acquired to elucidate molecular structures. Ester content and molecular weight were calculated based on peak area ratios proportional to hydrogen atom counts.\u003c/p\u003e"},{"header":"Results and discussion","content":"\u003cdiv id=\"Sec7\" class=\"Section2\"\u003e\u003ch2\u003eEffects of Lewis acid-base Pair systems on polymerization\u003c/h2\u003e\u003cp\u003eThrough a series of preliminary exploratory experiments, aluminum trifluoromethanesulfonate (Al(OTf)\u003csub\u003e3\u003c/sub\u003e) was selected as the catalyst, with Lewis acids such as sodium dihydrogen phosphate (NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e) serving as co-catalysts. The optimal molar ratio of catalyst, co-catalyst, SA, and THF was determined to be 3:3:1000:1100. The polymerization was conducted under a nitrogen atmosphere at 1.0 MPa, with a reaction temperature of 120\u0026deg;C maintained for 2 hours. As illustrated in Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e, a comparative analysis of the infrared spectra among the product synthesized with co-catalyst, the product without co-catalyst, and commercially available PBS are presented in Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e \u003cb\u003e(a)\u003c/b\u003e. The product exhibits characteristic peaks consistent with PBS: C-H stretching vibration of methylene groups at 2945 cm\u003csup\u003e-1\u003c/sup\u003e, C\u0026thinsp;=\u0026thinsp;O stretching vibration of ester linkages at 1712 cm\u003csup\u003e-1\u003c/sup\u003e, and C-O-C stretching vibration of ester bonds at 1155 cm\u003csup\u003e-1\u003c/sup\u003e. Notably, all major absorption bands align with those of commercial PBS, and the overall spectral pattern demonstrates analogous features. The \u003csup\u003e1\u003c/sup\u003eH NMR spectrum of the polymer product synthesized at 120\u0026deg;C with co-catalyst is shown in Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e \u003cb\u003e(b)\u003c/b\u003e. Peaks are observed at 4.12 ppm, assigned to the -R-CH\u003csub\u003e2\u003c/sub\u003e-COO- group, 2.64 ppm attributed to the -COO-CH\u003csub\u003e2\u003c/sub\u003e CH\u003csub\u003e2\u003c/sub\u003e-COO- group, and 1.72 ppm corresponding to the -CH\u003csub\u003e2\u003c/sub\u003e-R-COO- group. The peak area ratios of these signals were calculated to be approximately 1:1:1, consistent with the predicted \u003csup\u003e1\u003c/sup\u003eH NMR pattern of PBS. Combined with prior characterization results, this confirms the successful synthesis of PBS. Additionally, a resonance peak at 3.44 ppm is assigned to the -O-R-CH\u003csub\u003e2\u003c/sub\u003e-CH\u003csub\u003e2\u003c/sub\u003e-R-O- group. A distinct peak near 3.70 ppm corresponds to the chain-terminal HO-CH\u003csub\u003e2\u003c/sub\u003e-R- group, indicative of residual hydroxyl end groups. These characterization results demonstrate the successful synthesis of PBS through ring-opening polymerization of SA and THF under a Lewis acid-base pair catalytic system.\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\u003cp\u003eFurther experiments were subsequently conducted based on the synthesized PBS. Co-catalysts with weaker Lewis acidity (Lewis acids) or Lewis basicity were employed to preserve the activity of the primary catalyst. The reaction products were characterized through \u003csup\u003e1\u003c/sup\u003eH NMR and GPC analyses, as summarized in Table\u0026nbsp;\u003cspan refid=\"Tab1\" class=\"InternalRef\"\u003e1\u003c/span\u003e. The data reveal that under equivalent co-catalyst loadings, NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e significantly enhanced the molecular weight of the product while moderately reducing ester content, accompanied by a noticeable narrowing of molecular weight distribution. Mg(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e and Ca(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e induced marginal reductions in ester content and slight increases in molecular weight, though the variations were less pronounced. Notably, Ca(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e exhibited a broadening of molecular weight distribution. Al(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e3\u003c/sub\u003e demonstrated minimal catalytic efficacy, showing negligible effects on both molecular weight and ester content. Gallic acid slightly increased the molecular weight while concurrently enhancing the ester content. CaH\u003csub\u003e2\u003c/sub\u003e, functioning as a Lewis base, provided limited enhancement in molecular weight but substantially elevated the ester content of the product. Ca(OH)\u003csub\u003e2\u003c/sub\u003e, while reducing ester content moderately, achieved remarkable molecular weight augmentation. Based on these experimental findings, further investigations were conducted on gallic acid, NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e, CaH\u003csub\u003e2\u003c/sub\u003e, and Ca(OH)\u003csub\u003e2\u003c/sub\u003e to systematically examine the influence of co-catalyst loading on reaction outcomes.\u003c/p\u003e\u003cp\u003e\u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab1\" border=\"1\"\u003e\u003ccaption language=\"En\"\u003e\u003cdiv class=\"CaptionNumber\"\u003eTable 1\u003c/div\u003e\u003cdiv class=\"CaptionContent\"\u003e\u003cp\u003eEffects of Lewis acid-base pair types on the ROCOP of SA and THF \u003csup\u003e\u003cb\u003ea\u003c/b\u003e\u003c/sup\u003e\u003c/p\u003e\u003c/div\u003e\u003c/caption\u003e\u003ccolgroup cols=\"6\"\u003e\u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c5\" colnum=\"5\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c6\" colnum=\"6\"\u003e\u003c/div\u003e\u003cthead\u003e\u003ctr\u003e\u003cth align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCo-Catalyst\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c2\"\u003e\u003cp\u003eEster\u003c/p\u003e\u003cp\u003e(%) \u003csup\u003e\u003cem\u003eb\u003c/em\u003e\u003c/sup\u003e\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c3\"\u003e\u003cp\u003eEther\u003c/p\u003e\u003cp\u003e(%) \u003csup\u003e\u003cem\u003eb\u003c/em\u003e\u003c/sup\u003e\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c4\"\u003e\u003cp\u003eMn\u003c/p\u003e\u003cp\u003e(kDa)\u003csup\u003e\u003cem\u003ec\u003c/em\u003e\u003c/sup\u003e\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c5\"\u003e\u003cp\u003eMw/Mn \u003csup\u003e\u003cem\u003ec\u003c/em\u003e\u003c/sup\u003e\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c6\"\u003e\u003cp\u003eTON\u003c/p\u003e\u003cp\u003e(g/mol) \u003csup\u003e\u003cem\u003ed\u003c/em\u003e\u003c/sup\u003e\u003c/p\u003e\u003c/th\u003e\u003c/tr\u003e\u003c/thead\u003e\u003ctbody\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eBlank\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.89\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.11\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e1.829\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e31325.77\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eNaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e95.69\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e4.31\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.791\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.36\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35168.01\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eMg(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e96.85\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e3.15\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.408\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.42\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e36139.82\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eAl(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e3\u003c/sub\u003e\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.64\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.36\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e1.789\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.45\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e41555.40\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCa(H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e)\u003csub\u003e2\u003c/sub\u003e\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e94.45\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e5.55\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.075\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.97\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e38215.10\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eGallic acid\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.13\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.87\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.274\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35806.12\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCaH\u003csub\u003e2\u003c/sub\u003e\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e96.39\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e3.61\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.836\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.41\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e32987.27\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCa(OH)\u003csub\u003e2\u003c/sub\u003e\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e85.93\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e14.07\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e4.570\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.52\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e37438.43\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003c/tbody\u003e\u003c/colgroup\u003e\u003c/table\u003e\u003c/div\u003e\u003c/p\u003e\u003cp\u003e\u003csup\u003e\u003cb\u003ea\u003c/b\u003e\u003c/sup\u003e The molar ratio of other substances was set as SA: THF: Al(OTf)\u003csub\u003e3\u003c/sub\u003e : co-catalyst\u0026thinsp;=\u0026thinsp;1000: 1100: 3: 3, with nSA\u0026thinsp;=\u0026thinsp;100 mmol. The reaction pressure was 0.9 MPa, and the reaction time was 2 h. A control experiment without any co-catalyst under identical conditions for 2 h was conducted for comparison. \u003csup\u003e\u003cb\u003eb\u003c/b\u003e\u003c/sup\u003e Ester Unit and Ether Unit were determined via 1H NMR analysis. \u003csup\u003e\u003cb\u003ec\u003c/b\u003e\u003c/sup\u003e Number-average molecular weight (Mn) and molecular weight distribution (Mw/Mn) were characterized by GPC. \u003csup\u003e\u003cb\u003ed\u003c/b\u003e\u003c/sup\u003e Turnover Number (TON) was calculated as the ratio of the mass of the product to the amount of substance of the primary catalyst Al(OTf)\u003csub\u003e3\u003c/sub\u003e.\u003c/p\u003e\u003c/div\u003e\u003cdiv id=\"Sec8\" class=\"Section2\"\u003e\u003ch2\u003eEffects of Gallic Acid on Lewis acid-base pair systems\u003c/h2\u003e\u003cp\u003ePolymerization reactions were conducted with varying gallic acid loadings while maintaining other parameters constant. As shown in Table\u0026nbsp;\u003cspan refid=\"Tab2\" class=\"InternalRef\"\u003e2\u003c/span\u003e and Fig.\u0026nbsp;\u003cspan refid=\"Fig3\" class=\"InternalRef\"\u003e3\u003c/span\u003e, when the additive amount ranged between 0.1 and 0.4 mmol, the ester content exhibited an initial increase followed by a gradual decline, yet consistently remained above 99%\u0026mdash;surpassing the performance observed in the absence of a co-catalyst\u0026mdash;with the maximum ester content of 99.38% achieved at 0.2 mmol. When the additive amount reached 0.5 mmol, the ester content demonstrated a pronounced downward trend, while the TON increased substantially. The molecular weight of the product displayed an overall upward trajectory with increasing gallic acid dosage, showing minor fluctuations within the 0.1\u0026ndash;0.4 mmol range and rising to 2.513 kDa at 0.5 mmol.\u003c/p\u003e\u003cp\u003e\u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab2\" border=\"1\"\u003e\u003ccaption language=\"En\"\u003e\u003cdiv class=\"CaptionNumber\"\u003eTable 2\u003c/div\u003e\u003cdiv class=\"CaptionContent\"\u003e\u003cp\u003eEffects of Gallic Acid Input Amount on Polymerization\u003c/p\u003e\u003c/div\u003e\u003c/caption\u003e\u003ccolgroup cols=\"6\"\u003e\u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c5\" colnum=\"5\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c6\" colnum=\"6\"\u003e\u003c/div\u003e\u003cthead\u003e\u003ctr\u003e\u003cth align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCatalyst : Co-Catalyst\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c2\"\u003e\u003cp\u003eEster\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c3\"\u003e\u003cp\u003eEther\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c4\"\u003e\u003cp\u003eMn\u003c/p\u003e\u003cp\u003e(kDa)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c5\"\u003e\u003cp\u003eMw/Mn\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c6\"\u003e\u003cp\u003eTON\u003c/p\u003e\u003cp\u003e(g/mol)\u003c/p\u003e\u003c/th\u003e\u003c/tr\u003e\u003c/thead\u003e\u003ctbody\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eBlank\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.89\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.11\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e1.829\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e31325.77\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:1\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.22\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.78\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.214\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.33\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35864.25\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:2\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.38\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.62\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.069\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.27\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e37370.07\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:3\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.13\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.87\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.274\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35806.12\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:4\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.26\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.74\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.166\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.38\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e37598.36\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:5\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.04\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.96\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.513\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.53\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e41058.31\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003c/tbody\u003e\u003c/colgroup\u003e\u003c/table\u003e\u003c/div\u003e\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\u003cp\u003eThis phenomenon arises because gallic acid contains three adjacent phenolic hydroxyl groups and one carboxylic acid group, demonstrating strong coordination capacity. Its functional groups can form stable polynuclear complexes with Al\u003csup\u003e3+\u003c/sup\u003e, partially replacing the original coordination structure. The formation of these complexes reduces the concentration of free Al\u003csup\u003e3+\u003c/sup\u003e and weakens the Lewis acidity. Although the initial initiation efficiency was decelerated, the lifespan of active chains was prolonged. Moreover, these complexes may synergistically catalyze with Al(OTf)\u003csub\u003e3\u003c/sub\u003e to promote polymerization, thereby enhancing molecular weight. The phenolic hydroxyl groups in gallic acid partially neutralize the strongly acidic triflate ions in the system, reducing free proton concentration and consequently inhibiting chain transfer and termination reactions, extending chain propagation duration. The bulky aromatic structure of gallic acid generates spatial effects that hinder local aggregation of active chains and reduce cyclization side reactions, further facilitating linear chain growth. However, excessive gallic acid input creates a weakly acidic environment where partial SA hydrolysis leads to polycondensation participation, decreasing ester bond formation rate. This may transform the original ring-opening polymerization into a combined ring-opening-polycondensation process. The proton acid provided by gallic acid promotes ester bond hydrolysis. THF exhibits Lewis basicity and demonstrates higher susceptibility to co-catalyzed ring-opening by Lewis acid systems compared to SA. With increased input of gallic acid, a competitive relationship emerges between gallic acid and SA, leading to enhanced probability of chain transfer from the active chains of ring-opened THF to gallic acid. These factors collectively promote the propensity of THF toward homopolymerization within the reaction system, ultimately resulting in a decrease in ester content.\u003c/p\u003e\u003c/div\u003e\n\u003ch3\u003eEffects of NaHPO on Lewis acid-base pair systems\u003c/h3\u003e\n\u003cp\u003ePolymerization reactions were performed with adjusted NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e loadings while maintaining other parameters constant. The products were analyzed via \u003csup\u003e1\u003c/sup\u003eH NMR and GPC, as summarized in Table\u0026nbsp;\u003cspan refid=\"Tab3\" class=\"InternalRef\"\u003e3\u003c/span\u003e and Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003e. The data indicate that at low loadings (0.1\u0026ndash;0.2 mmol), the ester content of the products showed no significant variation, whereas the molecular weight exhibited a pronounced upward trend, with molecular weight distribution remaining around 1.30. Upon increasing the loading to 0.3 mmol, the ester content displayed a marked reduction, while molecular weight continued to rise. At a loading of 0.5 mmol, the ester content remained above 94%, and the molecular weight increased to 3.421 kDa. Further increasing the loading to 0.7 mmol resulted in a molecular weight of 4.008 kDa, albeit with a decline in ester content below 90%. Notably, the molecular weight distribution consistently remained below 1.5, and the TON exceeded 35000 across all conditions.\u003c/p\u003e\u003cp\u003e\u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab3\" border=\"1\"\u003e\u003ccaption language=\"En\"\u003e\u003cdiv class=\"CaptionNumber\"\u003eTable 3\u003c/div\u003e\u003cdiv class=\"CaptionContent\"\u003e\u003cp\u003eThe Effect of NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e Input Amount on Polymerization\u003c/p\u003e\u003c/div\u003e\u003c/caption\u003e\u003ccolgroup cols=\"6\"\u003e\u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c5\" colnum=\"5\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c6\" colnum=\"6\"\u003e\u003c/div\u003e\u003cthead\u003e\u003ctr\u003e\u003cth align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCatalyst : Co-Catalyst\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c2\"\u003e\u003cp\u003eEster\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c3\"\u003e\u003cp\u003eEther\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c4\"\u003e\u003cp\u003eMn\u003c/p\u003e\u003cp\u003e(kDa)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c5\"\u003e\u003cp\u003eMw/Mn\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c6\"\u003e\u003cp\u003eTON\u003c/p\u003e\u003cp\u003e(g/mol)\u003c/p\u003e\u003c/th\u003e\u003c/tr\u003e\u003c/thead\u003e\u003ctbody\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eBlank\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.89\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.11\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e1.829\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e31325.77\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:1\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.08\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.92\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.249\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.31\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e37447.93\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:2\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e99.11\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e0.89\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.570\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.26\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e40681.68\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:3\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e95.69\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e4.31\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.791\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.36\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35168.01\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:5\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e94.45\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e5.55\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e3.421\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.37\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e39604.48\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:7\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e88.50\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e11.50\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e4.008\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.47\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35960.49\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003c/tbody\u003e\u003c/colgroup\u003e\u003c/table\u003e\u003c/div\u003e\u003c/p\u003e\u003cp\u003eAs can be seen from Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003e \u003cb\u003e(a)\u003c/b\u003e, the NMR spectra of products obtained using NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e as a co-catalyst at different loadings. The spectra reveal that after adding NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e, the resonance peak area of the terminal methylene group at approximately 3.70 ppm significantly diminishes, while the resonance peak of the polyether segment methylene group at 3.44 ppm becomes more pronounced with increasing NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e loading. Correspondingly, as shown in Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003e \u003cb\u003e(b)\u003c/b\u003e, the aforementioned trend becomes more evident: the ester content of the product decreases with increasing input amount, exhibiting distinct inflection points, while the molecular weight increase curve demonstrates a smoother and more stable progression.\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\u003cp\u003eThe underlying reason for this phenomenon may be attributed to the establishment of a Lewis acid-base pair system between NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e (weak Lewis acid) and Al(OTf)\u003csub\u003e3\u003c/sub\u003e, generating synergistic catalytic effects. The molecular weight enhancement mechanism is as follows: During the reaction, the coordination between Al\u003csup\u003e3+\u003c/sup\u003e and PO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e3-\u003c/sup\u003e forms a dynamic equilibrium, continuously releasing free Al\u003csup\u003e3+\u003c/sup\u003e and PO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e3-\u003c/sup\u003e to activate SA and stabilize oxonium ions, respectively. Al\u003csup\u003e3+\u003c/sup\u003e from Al(OTf)\u003csub\u003e3\u003c/sub\u003e coordinates with H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e-\u003c/sup\u003e (dissociated from NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e) via oxygen atoms, forming a bimetallic complex (Al-O- PO\u003csub\u003e4\u003c/sub\u003e-Al). The Al\u003csup\u003e3+\u003c/sup\u003e retains its coordination capability toward SA's carbonyl oxygen, with enhanced coordination strength due to PO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e3-\u003c/sup\u003e bridging. The synergistic effect of Al\u003csup\u003e3+\u003c/sup\u003e and PO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e3-\u003c/sup\u003e in the complex promotes more efficient polarization of SA's carbonyl oxygen, resulting in a highly polarized C\u0026thinsp;=\u0026thinsp;O bond that lowers activation energy for nucleophilic attack, thereby accelerating THF ring-opening and ester bond formation. This increases chain propagation rate and molecular weight. PO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e3-\u003c/sup\u003e acts as an electron buffer to modulate Al\u003csup\u003e3+\u003c/sup\u003e acidity, preventing over-polarization-induced side reactions while modifying Al\u003csup\u003e3+\u003c/sup\u003e coordination environment and enhancing stability.\u003c/p\u003e\u003cp\u003eThe ester content reduction mechanism involves nucleophilic attack by H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e-\u003c/sup\u003e on ester bonds, triggering both intramolecular and intermolecular ester exchange reactions (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003e). As shown in Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003e \u003cb\u003e(a)\u003c/b\u003e, partial ester bond cleavage under H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e-\u003c/sup\u003e generates carboxylic acid and hydroxyl groups, which may act as new initiators. The carboxylic acid's proton activates THF to form oxonium ions, whose reactive termini further polymerize with SA and THF to extend the main chain. However, polyether segments exhibit lower hydrolysis susceptibility compared to polyester segments under H\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e\u003csup\u003e-\u003c/sup\u003e influence, leading to preferential ether segment formation and reduced total ester content. As illustrated in Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003e \u003cb\u003e(b)\u003c/b\u003e, intermolecular ester exchange redistributes ester groups across chains, forming longer main chains. While this elevates molecular weight, it concurrently decreases overall ester content. Simultaneously, as a Lewis acid, NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e forms a competitive relationship with SA for the active sites on THF chain segments with increasing dosage, thereby driving the reaction toward THF homopolymerization.\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\u003cp\u003eThe addition of NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e enhances the molecular weight and reduces ester content in the product through dual mechanisms of synergistic catalysis and ester bond reorganization. This result holds potential application value in PBS synthesis, as molecular weight and ester content can be modulated by adjusting NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e dosage, thereby regulating the material's mechanical properties and degradation rate.\u003c/p\u003e\n\u003ch3\u003eEffects of Ca(OH) on Lewis acid-base pair systems\u003c/h3\u003e\n\u003cp\u003ePolymerization reactions were conducted by adjusting the Ca(OH)\u003csub\u003e2\u003c/sub\u003e input amount under otherwise constant conditions, with results characterized by \u003csup\u003e1\u003c/sup\u003eH NMR and GPC analyses as presented in Table\u0026nbsp;\u003cspan refid=\"Tab4\" class=\"InternalRef\"\u003e4\u003c/span\u003e and Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003e. The data demonstrate that even a minor Ca(OH)\u003csub\u003e2\u003c/sub\u003e input (0.1 mmol) significantly enhances molecular weight. As the Ca(OH)\u003csub\u003e2\u003c/sub\u003e dosage increases, the molecular weight exhibits a stable improvement, ultimately reaching 4.570 kDa. Concurrently, the ester content decreases, having already declined to 85.93% at 0.3 mmol input. The molecular weight distribution also displays a broadening trend. As shown in Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003e \u003cb\u003e(a)\u003c/b\u003e, upon addition of 0.1 mmol calcium hydroxide, a distinct resonance peak emerges at 3.44 ppm, with further amplification of this ether segment-associated peak area observed at higher dosages. Correspondingly, As shown in Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003e \u003cb\u003e(b)\u003c/b\u003e, the data illustrates a pronounced increase in product molecular weight and reduction in ester content with escalating Ca(OH)\u003csub\u003e2\u003c/sub\u003e quantities.\u003c/p\u003e\u003cp\u003e\u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab4\" border=\"1\"\u003e\u003ccaption language=\"En\"\u003e\u003cdiv class=\"CaptionNumber\"\u003eTable 4\u003c/div\u003e\u003cdiv class=\"CaptionContent\"\u003e\u003cp\u003eThe Effect of Ca(OH)\u003csub\u003e2\u003c/sub\u003e Input Amount on Polymerization\u003c/p\u003e\u003c/div\u003e\u003c/caption\u003e\u003ccolgroup cols=\"6\"\u003e\u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c5\" colnum=\"5\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c6\" colnum=\"6\"\u003e\u003c/div\u003e\u003cthead\u003e\u003ctr\u003e\u003cth align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCatalyst : Co-Catalyst\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c2\"\u003e\u003cp\u003eEster\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c3\"\u003e\u003cp\u003eEther\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c4\"\u003e\u003cp\u003eMn\u003c/p\u003e\u003cp\u003e(kDa)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c5\"\u003e\u003cp\u003eMw/Mn\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c6\"\u003e\u003cp\u003eTON\u003c/p\u003e\u003cp\u003e(g/mol)\u003c/p\u003e\u003c/th\u003e\u003c/tr\u003e\u003c/thead\u003e\u003ctbody\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eBlank\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.89\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.11\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e1.829\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e31325.77\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:1\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.40\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.60\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.948\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.30\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e36461.02\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:2\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e94.45\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e5.55\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e3.519\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.42\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e38152.81\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:3\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e85.93\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e14.07\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e4.570\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.52\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e37438.43\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003c/tbody\u003e\u003c/colgroup\u003e\u003c/table\u003e\u003c/div\u003e\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\u003cp\u003eUpon addition of Ca(OH)\u003csub\u003e2\u003c/sub\u003e, both OH\u003csup\u003e-\u003c/sup\u003e and Ca\u003csup\u003e2+\u003c/sup\u003e may react with Al(OTf)\u003csub\u003e3\u003c/sub\u003e to form Al-OH or Al-O-Ca structures, reducing the concentration of free Al\u003csup\u003e3+\u003c/sup\u003e ions. The formation of these complexes diminishes chain termination and prolongs chain propagation duration. As a Lewis base, Ca(OH)\u003csub\u003e2\u003c/sub\u003e establishes a Lewis acid-base pair system with the strong Lewis acid Al(OTf)\u003csub\u003e3\u003c/sub\u003e, enabling synergistic catalysis of SA and THF, thereby enhancing the overall catalytic activity. Even at low Ca(OH)\u003csub\u003e2\u003c/sub\u003e dosages, its catalytic effect on SA ring-opening becomes pronounced, with efficacy further improving as dosage increases. This significantly accelerates SA initiation rates, manifesting as a sharp increase in molecular weight. Additionally, Ca(OH)\u003csub\u003e2\u003c/sub\u003e rapidly neutralizes acidic byproducts generated during the reaction, creating an alkaline environment. This alkalinity induces competitive interactions with THF, reducing ester bond formation between THF and SA. Consequently, even minimal Ca(OH)\u003csub\u003e2\u003c/sub\u003e addition leads to a rapid decline in ester content of the product.\u003c/p\u003e\u003cdiv id=\"Sec11\" class=\"Section2\"\u003e\u003ch2\u003eEffects of CaH\u003csub\u003e2\u003c/sub\u003e on Lewis acid-base pair systems\u003c/h2\u003e\u003cp\u003ePolymerization reactions were conducted by adjusting the CaH\u003csub\u003e2\u003c/sub\u003e input amount under otherwise constant conditions, with results characterized by \u003csup\u003e1\u003c/sup\u003eH NMR and GPC as shown in Table\u0026nbsp;\u003cspan refid=\"Tab5\" class=\"InternalRef\"\u003e5\u003c/span\u003e and Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003e. The data indicate that ester content decreases progressively with increasing CaH\u003csub\u003e2\u003c/sub\u003e dosage. The dosage of the co-catalyst in the range of 0.1\u0026ndash;0.3 mmol induced a gradual decrease in ester content, whereas a precipitous decline in ester content occurred when the dosage exceeded 0.4 mmol. The molecular weight demonstrated an ascending trend, exhibiting a moderate increase at CaH\u003csub\u003e2\u003c/sub\u003e dosages of 0.1\u0026ndash;0.3 mmol, followed by a pronounced enhancement reaching a maximum value of 3.782 kDa at 0.4 mmol. Further increases in CaH\u003csub\u003e2\u003c/sub\u003e dosage resulted in a decline in molecular weight. The molecular weight distribution displayed negligible variation with minimal calcium hydride addition, fluctuating around 1.45. However, excessive CaH\u003csub\u003e2\u003c/sub\u003e loading caused significant broadening of the molecular weight distribution.\u003c/p\u003e\u003cp\u003e\u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab5\" border=\"1\"\u003e\u003ccaption language=\"En\"\u003e\u003cdiv class=\"CaptionNumber\"\u003eTable 5\u003c/div\u003e\u003cdiv class=\"CaptionContent\"\u003e\u003cp\u003eThe Effect of CaH\u003csub\u003e2\u003c/sub\u003e Input Amount on Polymerization\u003c/p\u003e\u003c/div\u003e\u003c/caption\u003e\u003ccolgroup cols=\"6\"\u003e\u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c5\" colnum=\"5\"\u003e\u003c/div\u003e\u003cdiv align=\"char\" char=\".\" class=\"colspec\" colname=\"c6\" colnum=\"6\"\u003e\u003c/div\u003e\u003cthead\u003e\u003ctr\u003e\u003cth align=\"left\" colname=\"c1\"\u003e\u003cp\u003eCatalyst : Co-Catalyst\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c2\"\u003e\u003cp\u003eEster\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c3\"\u003e\u003cp\u003eEther\u003c/p\u003e\u003cp\u003e(%)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c4\"\u003e\u003cp\u003eMn\u003c/p\u003e\u003cp\u003e(kDa)\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c5\"\u003e\u003cp\u003eMw/Mn\u003c/p\u003e\u003c/th\u003e\u003cth align=\"left\" colname=\"c6\"\u003e\u003cp\u003eTON\u003c/p\u003e\u003cp\u003e(g/mol)\u003c/p\u003e\u003c/th\u003e\u003c/tr\u003e\u003c/thead\u003e\u003ctbody\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003eBlank\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e98.89\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e1.11\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e1.829\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.43\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e31325.77\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:1\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e97.92\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e2.08\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.349\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.55\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e35256.84\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:2\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e97.32\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e2.68\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.674\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.34\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e33962.26\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:3\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e96.39\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e3.61\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e2.836\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.41\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e32987.27\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:4\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e93.13\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e6.87\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e3.782\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e1.73\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e31711.46\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003ctr\u003e\u003ctd align=\"left\" colname=\"c1\"\u003e\u003cp\u003e3:5\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c2\"\u003e\u003cp\u003e87.24\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c3\"\u003e\u003cp\u003e12.76\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c4\"\u003e\u003cp\u003e3.152\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c5\"\u003e\u003cp\u003e2.05\u003c/p\u003e\u003c/td\u003e\u003ctd align=\"char\" char=\".\" colname=\"c6\"\u003e\u003cp\u003e38821.87\u003c/p\u003e\u003c/td\u003e\u003c/tr\u003e\u003c/tbody\u003e\u003c/colgroup\u003e\u003c/table\u003e\u003c/div\u003e\u003c/p\u003e\u003cp\u003e\u003c/p\u003e\u003cp\u003eThis is likely attributable to altered acid-base conditions induced by the strongly basic CaH\u003csub\u003e2\u003c/sub\u003e. As CaH\u003csub\u003e2\u003c/sub\u003e dosage increased, the system transitioned progressively from acidic to neutral. Both H\u003csup\u003e-\u003c/sup\u003e and Ca\u003csup\u003e2+\u003c/sup\u003e may react with Al(OTf)\u003csub\u003e3\u003c/sub\u003e, forming Al-H or Al-O-Ca structures, which reduce free Al\u003csup\u003e3+\u003c/sup\u003e concentration and active site availability. Although the chain propagation rate decreased due to fewer active sites, the lifetime of individual active sites may have been extended. Additionally, trace Ca\u003csup\u003e2+\u003c/sup\u003e might synergize with Al\u003csup\u003e3+\u003c/sup\u003e to stabilize propagating chain ends, suppressing chain transfer and termination, ultimately yielding higher molecular weights. When CaH\u003csub\u003e2\u003c/sub\u003e input ranged from 0.1\u0026ndash;0.4 mmol, the propensity for ester exchange reactions increased with dosage. Concurrently, dominant chain extension resulted in elevated molecular weight with minimal ester content reduction. However, excessive CaH\u003csub\u003e2\u003c/sub\u003e input (\u0026ge;\u0026thinsp;0.5 mmol) caused complete neutralization and structural alteration of Al(OTf)\u003csub\u003e3\u003c/sub\u003e, severely diminishing or even eliminating catalytic activity. Under such conditions, side reactions proliferated, with Ca\u003csup\u003e2+\u003c/sup\u003e likely dominating to promote ester exchange-induced bond rearrangement or cleavage. For instance, β-elimination occurred, where β-hydrogen abstraction from ester bonds generated carboxylic acid and alkene. Under such conditions, the occurrence of side reactions becomes significantly intensified. Calcium ions (Ca\u003csup\u003e2+\u003c/sup\u003e) in the system may assume a dominant role, promoting ester exchange reactions that induce rearrangement or cleavage of ester bonds, exemplified by β-elimination processes.\u003c/p\u003e\u003cp\u003eCompared with Ca(OH)\u003csub\u003e2\u003c/sub\u003e, although CaH\u003csub\u003e2\u003c/sub\u003e exhibits stronger Lewis acidity in anhydrous organic solutions, OH\u003csup\u003e-\u003c/sup\u003e can directly undergo neutralization reactions with acidic intermediates generated during polymerization, rapidly reducing system acidity and thus decreasing ester bond formation. In contrast, H\u003csup\u003e-\u003c/sup\u003e must first react with free protons or active centers in the system to eliminate acidic species, resulting in a longer reaction pathway. Therefore, CaH\u003csub\u003e2\u003c/sub\u003e only induces a significant reduction in the ester content of the product when its dosage reaches 0.5 mmol.\u003c/p\u003e\u003c/div\u003e"},{"header":"Conclusions","content":"\u003cp\u003eUpon adding a Lewis acid catalyst, the ester content of the polymeric product exceeded 99%, but higher catalyst dosages decreased ester content while increasing molecular weight, ultimately producing a 4.008 kDa product. The reaction mechanisms of gallic acid and NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e as cocatalysts were elucidated. Gallic acid stabilized the reaction system via coordination effects while suppressing cyclization through steric hindrance, promoting linear chain growth. NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e enhanced molecular weight and reduced ester content through dual mechanisms: synergistic catalysis and ester bond rearrangement. When Lewis acids served as cocatalysts, they competed with SA for active centers on ring-opened THF chains, thereby inhibiting SA-THF polymerization and lowering ester content.\u003c/p\u003e\u003cp\u003eIntroducing Lewis bases to construct Lewis acid-base pair catalytic systems further reduced ester content and elevated molecular weight, achieving a 4.570 kDa product. Ca(OH)\u003csub\u003e2\u003c/sub\u003e significantly increased molecular weight by forming extensive complexes with the primary catalyst, while its rapid OH\u003csup\u003e-\u003c/sup\u003e neutralization minimized acidic byproducts, drastically reducing ester content. When CaH\u003csub\u003e2\u003c/sub\u003e was employed as a cocatalyst, it acted as a desiccant to eliminate residual water in reagents. Limited complexation with the primary catalyst and partial promotion of transesterification resulted in only marginal molecular weight gains and a gradual ester content reduction below 0.3 mmol. Although Lewis bases enhanced SA ring-opening efficiency and substantially increased molecular weight, their strong basicity induced competitive interactions with THF, ultimately decreasing ester content by impeding SA-THF polymerization.\u003c/p\u003e\u003cp\u003eIn summary, PBS was synthesized via cationic ring-opening polymerization. By constructing Lewis acid-base pair catalytic systems with cocatalysts and adjusting the molar ratios of acid-base pairs and catalyst-to-monomer, precise control over product molecular weight and ester content was achieved. This approach provides a viable pathway for industrial-scale ring-opening polymerization processes.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003ch2\u003eSupplementary Information\u003c/h2\u003e\u003cp\u003eThe online version contains supplementary material available at \u003cspan class=\"ExternalRef\"\u003e\u003cspan class=\"RefSource\"\u003ehttps://osf.io/mz6b4/?view_only=744a40c3d34b4059ab841eec7de327f0\u003c/span\u003e\u003cspan address=\"https://osf.io/mz6b4/?view_only=744a40c3d34b4059ab841eec7de327f0\" targettype=\"URL\" class=\"RefTarget\"\u003e\u003c/span\u003e\u003c/span\u003e\u003c/p\u003e\u003cp\u003e\u003cstrong\u003eCompeting interests\u003c/strong\u003e\u003cp\u003eThe authors declare no competing financial interests.\u003c/p\u003e\u003c/p\u003e\u003ch2\u003eFunding\u003c/h2\u003e\u003cp\u003eThis work was supported by Key Technology for Preparation of Biobased Degradable Packaging Materials from Cheap Biomass (2022YFC2104602).\u003c/p\u003e\u003ch2\u003eAuthor contributions:\u003c/h2\u003e\u003cp\u003eWenjun Lu: Formal analysis and investigation, Writing-original draft preparation, Writing-review and editing; Hongjun Yin: Writing-Supervision; Ting Li: Resources; Jing Huang, Xu-Hui Zhang, Yang Wang, Bihua Xia: Writing-review; Shibo Wang: Writing-review and editing; Weifu Dong: Supervision\u003c/p\u003e\u003ch2\u003eData availability\u003c/h2\u003e\u003cp\u003eThe data that support the findings of this study are available from the corresponding author upon reasonable request.\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\u003cli\u003e\u003cspan\u003eZhang X, Zhang C, Zhang X (2022) A Facile and Unprecedented Route to a Library of Thermostable Formaldehyde-Derived Polyesters: Highly Active and Selective Copolymerization of Cyclic Acetals and Anhydrides. 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CCS Chem 5(5):1233\u0026ndash;1241. \u003cspan class=\"ExternalRef\"\u003e\u003cspan class=\"RefSource\"\u003e10.31635/ccschem.022.202202072\u003c/span\u003e\u003cspan address=\"10.31635/ccschem.022.202202072\" targettype=\"DOI\" class=\"RefTarget\"\u003e\u003c/span\u003e\u003c/span\u003e\u003c/span\u003e\u003c/li\u003e\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":false,"highlight":"","institution":"","isAcceptedByJournal":true,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"journal-of-polymer-research","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":false,"externalIdentity":"jpol","sideBox":"Learn more about [Journal of Polymer Research](https://www.springer.com/journal/10965)","snPcode":"10965","submissionUrl":"https://www.editorialmanager.com/jpol/","title":"Journal of Polymer Research","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"em","reportingPortfolio":"Springer Hybrid","inReviewEnabled":true,"inReviewRevisionsEnabled":false},"keywords":"ring-opening copolymerization, Lewis acid-base pairs, succinic anhydride, tetrahydrofuran","lastPublishedDoi":"10.21203/rs.3.rs-8152611/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-8152611/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003cp\u003eThe cationic ring-opening copolymerization (ROCOP) of succinic anhydride (SA) and tetrahydrofuran (THF) was conducted using aluminium trifluoromethanesulfonate (Al(OTf)\u003csub\u003e3\u003c/sub\u003e) via bulk polymerization to synthesize poly(butylene succinate) (PBS). The molecular weight and ester content of products were regulated by constructing Lewis acid-base pairs through the introduction of co-catalysts. Compared with the control group without co-catalysts, the resulting products exhibited significant enhancements in molecular weight. The polyester product with 99.38% ester content was achieved by incorporating gallic acid as co-catalyst. When sodium dihydrogen phosphate (NaH\u003csub\u003e2\u003c/sub\u003ePO\u003csub\u003e4\u003c/sub\u003e) was employed as co-catalyst, a product with molecular weight of 4.008 kDa was obtained. The employment of Lewis base as a co-catalyst yielded products with 85.93% ester content and molecular weight of 4.570 kDa. The regulatory mechanism of Lewis acid-base pairs in this system was systematically investigated based on experimental results, demonstrating potential application prospects in industrial-scale production.\u003c/p\u003e","manuscriptTitle":"Lewis Acid-Base Pair-Regulated Ring-Opening Copolymerization of Succinic Anhydride and Tetrahydrofuran†","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2025-12-01 06:42:12","doi":"10.21203/rs.3.rs-8152611/v1","editorialEvents":[{"type":"communityComments","content":0},{"type":"reviewerAgreed","content":"","date":"2025-12-10T01:20:15+00:00","index":0,"fulltext":""},{"type":"reviewersInvited","content":"","date":"2025-11-26T06:00:43+00:00","index":"","fulltext":""},{"type":"editorInvited","content":"Journal of Polymer Research","date":"2025-11-23T17:46:42+00:00","index":"","fulltext":""},{"type":"editorAssigned","content":"","date":"2025-11-19T13:02:54+00:00","index":"","fulltext":""},{"type":"submitted","content":"Journal of Polymer Research","date":"2025-11-19T03:10:58+00:00","index":"","fulltext":""}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"journal-of-polymer-research","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":false,"externalIdentity":"jpol","sideBox":"Learn more about [Journal of Polymer Research](https://www.springer.com/journal/10965)","snPcode":"10965","submissionUrl":"https://www.editorialmanager.com/jpol/","title":"Journal of Polymer Research","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"em","reportingPortfolio":"Springer Hybrid","inReviewEnabled":true,"inReviewRevisionsEnabled":false}}],"origin":"","ownerIdentity":"6b00ef1b-4afb-4feb-a19a-02cc64084fe2","owner":[],"postedDate":"December 1st, 2025","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"published-in-journal","subjectAreas":[],"tags":[],"updatedAt":"2026-03-30T16:31:32+00:00","versionOfRecord":{"articleIdentity":"rs-8152611","link":"https://doi.org/10.1007/s10965-026-04847-0","journal":{"identity":"journal-of-polymer-research","isVorOnly":false,"title":"Journal of Polymer Research"},"publishedOn":"2026-03-23 16:09:24","publishedOnDateReadable":"March 23rd, 2026"},"versionCreatedAt":"2025-12-01 06:42:12","video":"","vorDoi":"10.1007/s10965-026-04847-0","vorDoiUrl":"https://doi.org/10.1007/s10965-026-04847-0","workflowStages":[]},"version":"v1","identity":"rs-8152611","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-8152611","identity":"rs-8152611","version":["v1"]},"buildId":"XKTyCvWXoU3ODBz1xrDgd","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}