DOI:
10.1039/C6RA25648A
(Paper)
RSC Adv., 2017,
7, 1101-1109
A strategy for preparing spirobichroman dianhydride from bisphenol A and its resulting polyimide with low dielectric characteristic†
Received
22nd October 2016
, Accepted 29th October 2016
First published on 3rd November 2016
Abstract
A spirobichroman dianhydride (SBCDA) was prepared through oxidation of an octamethyl spirobichroman (OMSBC), which was synthesized from acid-fragmentation of bisphenol A by 3,4-dimethylphenol, followed by Diels–Alder reaction. The reaction mechanism was proposed, and the optimal reaction conditions were discussed. Based on a high temperature solution polymerization of SBCDA and 4,4′-diaminodiphenylmethane (DDM), a spirobichroman-containing polyimide, SBC-DDM, was successfully prepared. Because of the contorted spiro-structure and rigid polymer backbone, SBC-DDM exhibits a large free volume, leading to outstanding organo-solubility and a low dielectric constant. In addition, the resulting film of SBC-DDM shows foldability, a high glass transition temperature, and good thermal stability.
Introduction
Because of the rigid main chain and strong intermolecular interactions, aromatic polyimides (PIs) exhibit many attractive properties, such as outstanding high-temperature stability,1–3 good chemical and solvent resistance,4 and excellent mechanical properties.4,5 Based on their advantages, PIs have been applied in electronics,6,7 optics, and membranes.8,9 However, the rigid chain characteristics of PIs also lead to poor organo-solubility and high melting points, leading to limited processability. Thus, the processing of most commercial PIs was carried out with their precursors, poly(amic acid)s (PAAs), followed by thermal imidization. Unfortunately, it is difficult to store PAAs for a long period of time because of their thermal and hydrolytic instability.
To overcome the limitation of processability, increasing the free volume in PI matrix by introducing bulky groups, and non-coplanar structures into polymer chains has received much attention.9–11 For example, Liou et al. introduced propeller-shaped triphenylamine (TPA) structures into polyimide backbones.12,13 The non-coplanar TPA units effectively disrupt inter-chain packing, and the PIs were soluble in many aprotic solvents with good film-forming capability. In addition, the incorporation of spiroskeletons along the polymer backbones is also regarded as a successful approach to improve the organo-solubility without sacrificing much in thermal properties due to the non-coplanar and rigid characteristic of spiroskeletons.14 Thomas et al. prepared an organo-soluble PI (soluble even in chloroform and dichloromethane) based on spirobifluorene diamine.15 Hsiao et al. extended two kinds of spirobichroman diol (1)–(2) to spirobichroman dietheramines (3)–(4) and dietheranhydride (5), respectively (Scheme 1).16–18 Spirobichroman and diether-containing polyetherimides (PEIs) were further prepared, showing excellent organo-solubility.16–18 However, the Tg values of these PEIs are in the range of 175–280 °C. Obviously, the diether linkages reduced the rigidity of polymer chains, leading to only moderate Tgs.
![image file: c6ra25648a-s1.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-s1.gif) |
| Scheme 1 Structure of (1)–(5). | |
Generally, increasing the free volume in polymer matrix is also an effective approach for reducing dielectric constant. For example, Nagai et al. prepared 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA)-based PIs to investigate the relationship of fractional free volume (FFV) and dielectric constant of PIs, concluding that the larger FFV of polymer brought about lower dielectric constant.19 Zhang et al. prepared a (E)-N1-(4-aminophenyl)-N1-(4′-(2-phenyl-2-(4′-(trifluoromethyl)biphenyl-4-yl)vinyl)-biphenyl-4-yl)benzene-1,4-diamine-based polyimide, FPTTPI, containing a large nonplanar conjugated side chain.20 In addition to the improvement of organo-solubility, the large free volume in FPTTPI film also led to excellent electrical properties, with a dielectric constant (Dk) of 1.52 at a frequency of 10 kHz.
On the concept of polymers of intrinsic microporosity (PIMs), contorted molecular structures combined with highly rigid polymer backbones can prevent the molecular packing efficiently, leading to larger free volume.21 Pinnau and Han et al. reported that spiroskeleton-containing polyimides without the presence of flexible diether linkage could be prepared from a spiroindane diamine (7), which was synthesized by nitration of spiroindane bisphenol (6), followed by reduction (Scheme 2).22 Apart from that, the resulting PIs exhibited large FFV (around 0.20), leading to excellent organo-solubility. However, the incorporation of polar hydroxyl groups enhanced the affinity of PIs to water. This would sacrifice the dielectric properties. For the purpose of obtaining a high-performance, organo-soluble, and low-dielectric polyimide, we provided a strategy for preparing a less polar spirobichroman dianhydride, SBCDA, for polyimide synthesis (Scheme 2).
![image file: c6ra25648a-s2.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-s2.gif) |
| Scheme 2 Structure of (6)–(7), OMSBC, and SBCDA. | |
The key for successfully synthesizing SBCDA is the derivatization from its precursor, octamethyl spirobichroman (OMSBC, Scheme 2). To the best of our knowledge, OMSBC has not been synthesized. However, the work done by Caruso et al.23 gives us a light for OMSBC preparation. An acid-fragmentation of bisphenol A (BPA) by a exogenous phenol, such as m-cresol was attempted.23 The phenol units of BPA were substituted by two exogenous phenols, and a tetramethyl xanthene derivative (see compound 2 in that work) with 72% yield was obtained (Scheme S1† lists the detailed mechanism for the transformation of compound 2). According to gas chromatography-mass spectrometry (GCMS), a spiroketal compound (see compound 24 in that work) was observed in the initially formed product. Compound 24 afforded tetramethyl xanthene 2 when re-subjected to the reaction conditions. Apparently, compound 24 is a kinetic product for the reaction. To explain the formation of compound 24, a reaction mechanism including the acid fragmentation of BPA and twice Diels–Alder reactions was proposed.20 However, the optimized reaction condition for compound 24 was not further elaborated. Moreover, spiro compound was not observed from the acid-fragmentation of BPA by 3,4-dimethylphenol. According to researches on Diels–Alder reaction,24–26 retro Diels–Alder reaction will be occurred at high temperatures. Based on the above, we prepared OMSBC through acid-fragmentation of BPA by 3,4-dimethylphenol at low temperatures (Scheme 3). After oxidizing the tetramethyl of OMSBC, followed by condensation of diacid to dianhydride, the spirobichroman dianhydride, SBCDA, was obtained. Through a high temperature solution polymerization of SBCDA and 4,4′-diaminodiphenylmethane (DDM), a spirobichroman-containing polyimide, SBC-DDM, was successfully prepared. With the presence of spiroskeletons, rigid backbone, and hydrophobic aliphatic units (chroman and methylene groups), the polyimide, SBC-DDM exhibited outstanding organo-solubility and low dielectric constant. Detailed synthesis including optimal reaction conditions, characterizations, and properties were reported.
![image file: c6ra25648a-s3.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-s3.gif) |
| Scheme 3 Proposed synthetic route of X-2 (Route a) and OMSBC (Route b). | |
Experimental
Materials
Bisphenol A (BPA), manganese(II) acetate (Mn(OAc)2), and cobalt(II) acetate (Co(OAc)2) were purchased from Alfa. 3,4-Dimethylphenol and t-butyl cumyl peroxide (TBCP) were purchased from Acros. Sodium bromide (NaBr) and sodium hydroxide (NaOH) were purchased from Showa. Methane sulfonic acid (MSA) and isoquinoline were purchased from Fluka. 4,4′-Diaminodiphenylmethane (DDM) was purchased from Chriskev and recrystallized from methanol. Acetic acid glacial and m-cresol were purchased from Scharlau. All solvents are HPLC grade and were used without any further purification.
Characterization
NMR measurements were performed using a Varian Inova 400 NMR in DMSO-d6 or CDCl3. The chemical shift of 1H NMR was calibrated by setting the chemical shift of trace amount of DMSO-d5 in DMSO-d6 as 2.49 ppm. Melting point measurements were performed by a Fargo Melting Point Apparatus MP-2D. Thermogravimetric analysis (TGA) was performed at a heating rate of 20 °C min−1 in flowing nitrogen or air (20 mL min−1) by a Perkin-Elmer Pyris1. Thermomechanical analysis (TMA) was performed with a sample size of 10 mm × 5 mm using a SII TMA/SS6100. The analysis was performed at a heating rate of 5 °C min−1 from 40 to 350 °C without N2 or air flow. The coefficient of thermal expansion (CTE) was recorded from the second-run in three kinds of temperature ranges. IR spectra were obtained from at least 32 scans in the standard wavenumber range of 650–4000 cm−1 using a PerkinElmer RX1 infrared spectrophotometer. Gel permeation chromatography (GPC) was carried out on a Hitachi LaChrom Elite using N-methyl-2-pyrrolidone (NMP) as the eluent at 60 °C with a flow rate of 0.6 mL min−1. The molecular weights were calibrated with polystyrene standard. Elemental analysis was performed on an Elementar Vario EL III (CHN-OS Rapid, German). The accuracy and precision of this instrument are 0.1% and 0.2%, respectively. Acetanilide and benzoic acid were used as standards and the data of them as follows: N 10.36%, C 71.09%, H 6.71% for acetanilide; O 26.20% for benzoic acid. The X-ray crystallographic data were collected on a Bruker D8 VENTURE. High resolution mass (HRMS) measurements were performed by a Finnigan/Thermo Quest MAT 95XL mass spectrometer by electron impact ionization. The dielectric constant of the polymer film was measured without any preprocess at a frequency of 100 MHz and 1 GHz, using Agilent E4991A RF impedance/material analyzer with a sample size of 1 cm × 1 cm × 150 μm. Experimental data was obtained from at least 5 times for each test.
Synthesis of octamethyl spirobichroman (OMSBC)
BPA 20.60 g (0.09 mol) and 3,4-dimethylphenol 77.14 g (0.63 mol) were introduced into a 500 mL round-bottom glass flask equipped with a nitrogen inlet, and a magnetic stirrer. The reaction mixture was stirred continuously at 80 °C until the reagents melted completely. MSA 4.12 g (20 wt% based on BPA) was then added to the reaction mixture, which was further stirred at 80 °C for 4 h. Subsequently, the reaction temperature was cooled to room temperature. The mixture was dissolved in toluene, washed with 10 wt% NaOH solution, and rinsed with water. Toluene was removed using a rotary evaporator and then the crude product was washed with hot methanol to remove xanthene derivatives (will be discussed in 3.1). The purified product was collected by filtration and dried in vacuum at 60 °C. White powders (20% yield) were obtained with a melting point of 180 °C. HR-MS (EI) m/z: calcd for C25H32O2 364.2402; anal., for 364.2393. Elem. anal. calcd C, 82.37%; H, 8.85%; O, 8.78%. Found: C, 82.60%; H, 9.05%; O, 8.32%. 1H-NMR (DMSO-d6), δ = 7.1 ppm (s, 2H, H4), 6.3 ppm (s, 2H, H7), 2.1 ppm (s, 6H, H5), 2.0 ppm (s, 6H, H6), 1.8–2.1 ppm (d–d, 4H, H1), 1.5 ppm (s, 6H, H3), 1.2 ppm (s, 6H, H2).
Synthesis of spirobichroman dianhydride (SBCDA)
To a Parr reactor equipped with a oxygen inlet, OMSBC 5.00 g (0.014 mol), Mn(OAc)2 0.10 g, Co(OAc)2 0.10 g, NaBr 0.10 g, TBCP 0.20 g, and acetic anhydride 40 mL were added. After the reaction system was purged with oxygen eight times, the pressure of the Parr reactor was kept at 250–300 psi under oxygen atmosphere. The reaction mixture was stirred at 170–180 °C for 11 h. After the reaction was complete and the reactor was cooled to room temperature, the solution was filtered. The filtrate was poured into 500 mL water and filtered again. The raw product was refluxed in acetic anhydride for 5 h. After cooling to room temperature, the crystalline product was filtered and dried in vacuum at 80 °C. Yellow green crystals (11% yield) were obtained. HR-MS (EI) m/z: calcd for C25H20O8 448.1158; anal., for 448.1154. Elem. anal. calcd C, 66.96%; H, 4.50%; O, 28.54%. Found: C, 65.01%; H, 4.38%; O, 29.30%. 1H-NMR (DMSO-d6), δ = 8.3 ppm (s, 2H, H4), 7.3 ppm (s, 2H, H5), 2.2–2.4 ppm (d–d, 4H, H1), 1.7 ppm (s, 6H, H3), 1.4 ppm (s, 6H, H2). FTIR (KBr): 1839 and 1770 cm−1 (C
O stretch).
Preparation of SBC-DDM
DDM 0.4342 g (2.19 mmol) and m-cresol 8.02 g were introduced into a 100 mL round-bottom glass flask equipped with a nitrogen inlet, and a magnetic stirrer. After the diamine was dissolved completely, SBCDA 0.9821 g (2.19 mmol) and 2 drops of isoquinoline were added. The mixture was reacted at 170 °C for 12 h. Subsequently, the viscous solution was poured into methanol giving rise to a brown fibrous precipitate (90% yield) that was collected by filtration, and dried in vacuum at 70 °C. 1H-NMR (CDCl3), δ = 8.0 ppm (s, 2H, H5), 7.3 ppm (d, 8H, H6 and H7), 7.1 ppm (s, 2H, H1), 4.1 ppm (s, 2H, H8), 2.2 ppm (d–d, 4H, H4), 1.8 ppm (s, 6H, H2), 1.4 ppm (s, 6H, H3).
Preparation of the polyimide film
A solution of the polymer was prepared by dissolving 0.4 g of SBC-DDM in 2 mL of NMP. The homogeneous solution was cast onto a glass substrate and heated in an oven at 80 °C for 12 h to remove most of the solvent; then the semi-dried film was further dried in vacuum at 100 °C (1 h), followed by 200 °C (1 h). An automatic film applicator BRAIVE/B-4300 was used for coating procedure. The solution was cast on glass by setting a controlling gap thickness of 200 μm. The resulting thin film was around 10 μm thick and sectioned to controlled geometries for TMA and dielectric measurement.
Results and discussion
Synthesis of OMSBC
To prepare OMSBC, the acid-fragmentation of BPA by 3,4-dimethylphenol was performed at various reaction conditions (Table 1).
Table 1 Reaction conditions for the synthesis of OMSBC
Runa |
Molar ratio (BPA/3,4-dimethylphenol) |
Temperature (°C) |
Product |
Isolated OMSBC yield (%) |
Reaction time is 24 h; the acid catalyst is methanesulfonic acid (20 wt% based on BPA). |
1 |
1/20 |
100 |
X-2 |
0 |
2 |
1/10 |
100 |
X-2 |
0 |
3 |
1/5 |
100 |
X-2 |
0 |
4 |
1/20 |
80 |
X-2 + OMSBC |
3 |
5 |
1/10 |
80 |
X-2 + OMSBC |
10 |
6 |
1/7 |
80 |
X-2 + OMSBC |
14 |
7 |
1/5 |
80 |
X-2 + OMSBC |
10 |
Firstly, we followed Caruso's work,23 using 100 °C as reaction temperature. But a xanthene derivative, X-2 (the structure was shown in Scheme 3), was the only product (Run 1). The assignment in 1H NMR spectrum (Fig. S1, ESI†) supports the structure of X-2. Based on the mechanism reported by Caruso et al.,23 we proposed a possible mechanism as shown in Scheme 3. Initially, the acid fragmentation of BPA by 3,4-dimethylphenol leads to 2-isopropenylene-4,5-dimethylphenol (1b). Two possible routes for further reactions of (1b) were proposed. Route a explains the formation of X-2, while Route b explains the formation of OMSBC. In Route a, an electrophilic substitution between 3,4-dimethylphenol and (1b) occurred, leading to the formation of X-2. On the concept of this mechanism, we reduced the amount of 3,4-dimethylphenol to decrease the probability of electrophilic addition between (1b) and 3,4-dimethylphenol, avoiding the formation of X-2. However, the results of both entries are the same as that of Run 1 (only xanthene X-2 was obtained in Run 2–3). Changing the ratio of BPA/3,4-dimethylphenol has no effect on the outcome of products. Furthermore, we reduced reaction temperature to 80 °C, leading to a mixture of OMSBC and X-2. The result agrees with our speculation that a high temperature reaction conditions favors X-2, while low temperature reaction condition leads to the formation of OMSBC. The yield of OMSBC was improved by reducing the amount of 3,4-dimethylphenol added to the reaction. However, the yield was decreased when much less amount of 3,4-dimethylphenol was added to the reaction. Therefore, a highest isolated yield occurred in Run 6 was established. We suggest that the formation of the key intermediate (1b) became more difficult in Run 7, leading to the reduced yield of OMSBC. The 1H-NMR spectrum of OMSBC was shown in Fig. 1(a), and the assignment supports its structure. In Route b, a Diels–Alder reaction between (1b) and its tautomer (1b′) leads to (2b). Then, a presumed chroman (3b) would be generated by leaving one 3,4-dimethylphenol. Chroman (3b) acts as a dienophile for the second Diels–Alder reaction with (1b′), leading to the formation of OMSBC. Since high temperatures favor retro Diels–Alder reaction, Route b is not a preferred route at high temperatures.
![image file: c6ra25648a-f1.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f1.gif) |
| Fig. 1 1H NMR spectrum of (a) OMSBC and (b) SBCDA. | |
This mechanism explains the result in Table 1 that reacting at above 100 °C leads to only X-2, while reacting at 80 °C leads to mixture of X-2 and OMSBC. However, an attempt to enhance the yield of OMSBC via further reducing the reaction temperature to 60 °C was failed due to the fact that the melting point of 3,4-dimethylphenol was 68 °C.
To discuss the influence of reaction time, we used the best reaction condition in Table 1 (Run 6) to perform 1H NMR trace at various stages of reaction. Fig. S2 (ESI†) shows 1H NMR trace for OMSBC synthesis after 24 h and 48 h of reaction, respectively. The benzene signals of OMSBC at 7.1 and 6.3 ppm decreased; on the other hand, the benzene signals of X-2 at 7.2 and 6.8 ppm increased with increasing reaction time. This implies that retro Diels–Alder reaction still occurred in the presence of acid catalyst at low temperatures (80 °C), leading to the transformation of OMSBC to X-2. Scheme S2† shows the proposed mechanism on retro Diels–Alder reaction of OMSBC in the presence of methanesulfonic acid (MsOH). The first retro Diels–Alder reaction was initiated by protonation on the oxygen of OMSBC and releasing of (1b′), leading to the formation of intermediate (3b). Subsequently, the intermediate (2b) was generated by acid-catalyzed electrophilic addition of (3b) with 3,4-dimethylphenol. After protonation on the oxygen of (2b), the second retro Diels–Alder reaction was carried out, leading to the formation of (1b) and its tautomer (1b′).
To avoid the retro Diels–Alder reaction, we shortened the reaction time and further monitored the reaction by 1H NMR trace (Fig. S3†). The benzene signals of OMSBC at 7.1 and 6.3 ppm were observed after 1 h, and reached a maximum after 4 h. After that, the benzene signals slightly decreased, and the impurity signals (around 6–7 ppm in Fig. S3†) increased with increasing reaction time, demonstrating that the retro Diels–Alder reaction occurred after 5 h. After optimizing the reaction conditions, a maximum yield around 20% of synthesizing OMSBC was achieved in this work.
Synthesis of SBCDA
As shown in Scheme 4, a spirobichroman dianhydride (SBCDA) was prepared by the oxidation of the ortho-dimethyl groups of OMSBC, followed by chemical cyclodehydration with acetic anhydride. As mentioned earlier, retro Diels–Alder reaction of OMSBC would occur in the presence of acid catalyst (Scheme S2†). Therefore, acetic anhydride was used as solvent for the oxidation procedure instead of acetic acid.27,28 Experimental data show that the methyl groups of OMSBC were transferred to carboxylic acids incompletely under standard pressure. Fig. 1(b) shows 1H NMR spectrum of SBCDA. As compared with the spectrum of OMSBC, the characteristic peaks of benzene shifted from 7.1 to 8.3 ppm and 6.3 to 7.3 ppm. The chemical shifts are more downfield due to the formation of carbonyl groups, which exhibit strong electron-withdrawing characteristic. In addition, the characteristic peaks of methyl group on benzene disappeared in Fig. 1(b), confirming the structure of SBCDA. Fig. 2 shows FTIR spectra of OMSBC and SBCDA. The characteristic absorptions at 1839 (C
O asymmetric stretch) and 1770 cm−1 (C
O symmetric stretch) further confirm the structure of SBCDA.
![image file: c6ra25648a-s4.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-s4.gif) |
| Scheme 4 Synthesis of SBCDA and its derived polyimide SBC-DDM. | |
![image file: c6ra25648a-f2.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f2.gif) |
| Fig. 2 FTIR spectra of OMSBC and SBCDA. | |
The structural configuration of SBCDA was confirmed by single crystal diffractogram, as shown in Fig. 3. The detailed diffraction data of SBCDA is listed in Tables S1–S5 (ESI†). As seen in Fig. 3, the non-coplanar SBCDA compound provides a site of contortion due to the presence of spirobichroman unit, demonstrating that the molecular packing of its derived polymers can be restricted.21,22 The spectroscopic data in Fig. 1–3 support the synthesis of SBCDA through the high-temperature (170–180 °C) and high-pressure (250–300 psi) procedure.
![image file: c6ra25648a-f3.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f3.gif) |
| Fig. 3 Single crystal diffractogram of SBCDA. | |
Polyimide synthesis
SBC-DDM was prepared by the one-pot, high temperature solution polymerization of SBCDA with 4,4′-diaminodiphenylmethane (DDM) in m-cresol in the presence of isoquinoline (Scheme 4). After reaction was completed, the polymer solution became highly viscous and fiber-like product could be precipitated in methanol. Due to the outstanding organo-solubility (to be discussed later), SBC-DDM can be dissolved in CDCl3 for 1H NMR spectroscopic analysis (Fig. 4). The assignment of each peak is detailed in the figure, confirming the structure of SBC-DDM. GPC data of SBC-DDM was measured using N-methyl-2-pyrrolidinone (NMP) as eluent. The number-average molecular weight (Mn) and weight-average molecular weight (Mw) are 7.0 × 104 and 17.2 × 104 g mol−1, respectively. Fig. 5 shows the photos of SBC-DDM film via solution casting. As seen in the figure, the transparent and foldable film further supports the high molecular weight of SBC-DDM.
![image file: c6ra25648a-f4.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f4.gif) |
| Fig. 4 1H NMR spectrum of SBC-DDM in CDCl3. | |
![image file: c6ra25648a-f5.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f5.gif) |
| Fig. 5 Photo of SBC-DDM film. | |
Physical and electric properties
The fractional free volume (FFV) was calculated by using the following relationship:29–31 |
![image file: c6ra25648a-t1.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-t1.gif) | (2) |
where V is the molar volume (cm3 mol−1) of the polymer, M is the molar mass (g mol−1) of the polymer, and ρ is the density (g cm−3) of the polymer, which was measured experimentally (determined by measurements of the weight in air and in deionized water). Vw is the van der Waals volume (cm3 mol−1) of polymer. According to literature,29–31 Vw is often calculated from Bondi's group contribution method.32–34 However, it is very time-consuming and easy to make a miscalculation for complex compounds. To simplify the calculation of Vw, a fast method has been reported by Abraham.35 Eqn (3) based on Bondi radii was used to calculate Vw in this work: |
Vvdw (Å3 per molecule) = Σall atom contributions − 5.92NB − 14.7RA − 3.8RNA
| (3) |
where N is the total number of atoms, RA and RNA are the number of aromatic and nonaromatic rings, respectively. All atomic volume contributions are referred to literature35 (see Table 2 of this literature). Herein, we converted the unit from Å3 per molecule to cm3 mol−1 by multiplying by 0.602. The results are listed in Table 2. To investigate the relationship of free volume and chemical structure, a commercial polyimide, PMDA-ODA, was used for comparison. The FFV of SBC-DDM (0.20) is higher than that of PMDA-ODA (0.05), demonstrating that the molecular packing can be disrupted effectively by introducing a spirobichroman into polymer backbone. Further comparison with spiroindane-containing polyimides which prepared by Han et al.,22 the FFV of SBC-DDM is the same as that of PIM-PMDA–OH (0.20), supporting that the introduction of spirobichroman unit into rigid polymer backbones would enhance the FFV of polymer. However, the FFV of SBC-DDM is slightly lower than that of PIM-6FDA–OH (0.23) due to the absence of bulky trifluoromethyl (–CF3) groups.
Table 2 Physical properties of SBC-DDM
Sample ID |
ρ (g cm−3) |
V (cm3 mol−1) |
M (g mol−1) |
Vw (cm3 mol−1) |
FFV |
Prepared from pyromellitic dianhydride (PMDA) and 4,4′-diaminodiphenylether (ODA). Data from ref. 22. Not available. |
SBC-DDM |
1.13 |
538.98 |
610.67 |
333.1 |
0.20 |
PMDA–ODAa |
1.39 |
275.0 |
382.3 |
194.8 |
0.05 |
PIM-PMDA–OHb |
1.18 |
NAc |
NA |
NA |
0.20 |
PIM-6FDA–OHb |
1.22 |
NA |
NA |
NA |
0.23 |
The solubility properties of SBC-DDM are listed in Table 3. Owing to the large FFV, SBC-DDM exhibited outstanding organo-solubility. Different from many organo-soluble polyimides, SBC-DDM can be more easily dissolved in borderline polar and nonpolar aprotic solvents such as THF, CHCl3 and CH2Cl2 than in polar aprotic solvents (such as DMF and DMSO). This is due to the incorporation of hydrophobic chroman and methylene units in SBC-DDM. When compared with the diether and spirobichroman-containing polyetherimide 7f (the structure is shown in Table 3),16 diether-free SBC-DDM exhibits superior organo-solubility (Table 3).
Table 3 Solubility properties of SBC-DDM and referenced PEI 7f16
Sample ID |
Solventa |
NMP |
DMF |
DMSO |
m-Cresol |
CH2Cl2 |
CHCl3 |
THF |
Solubility was tested with a 5 mg sample in 0.5 mL of solvent. +, soluble at room temperature; +h, soluble on heating; −, insoluble on heating. Not available. Structure of 7f: . |
SBC-DDM |
+b |
+h |
+h |
+ |
+ |
+ |
+ |
7fd |
+ |
+ |
− |
+ |
NAc |
+ |
+ |
To study the influence of conformational changes in polymers, molecular modeling analysis of SBC-DDM with two spirobichroman units were performed by using ChemBio3D Ultra software as shown in Fig. 6. It is postulated that the rigid backbone combined with the contorted spiro-structure in SBC-DDM prevent an efficient packing and entanglement in polymer chain, contributing to the organo-solubility.
![image file: c6ra25648a-f6.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f6.gif) |
| Fig. 6 Molecular models of SBC-DDM as calculated with energy minimization. | |
The dielectric constant of SBC-DDM was 2.451 ± 0.001 and 2.342 ± 0.001 at a frequency of 100 MHz and 1 GHz, respectively. Owing to the large FFV and hydrophobic aliphatic structures, SBC-DDM exhibited much lower dielectric constant than did PMDA–ODA (around 3.1–3.5),36 showing the low dielectric characteristic. As a result, the introduction of spiroskeleons into rigid polymer backbone is beneficial to increase the free volume in polymer matrix, improve the organo-solubility and reduce dielectric constant.
Thermal properties
Fig. 7(a) shows the TMA thermogram of SBC-DDM. The Tg value, defined by on onset temperature of the TMA thermogram, is 343 °C. On the other hand, the Tg value of the referenced PEI 7f is 235 °C,16 demonstrating that the higher rigidity of diether-free SBC-DDM contributes to the improved thermal properties. The coefficient of thermal expansion (CTE) of SBC-DDM in the temperature range of 50–150 °C is around 41 ppm °C−1, suggesting a remarkable dimensional stability at low temperature. However, the CTE decreased to a negative value (−130 ppm °C−1) in the temperature range of 200–300 °C. According to Hasegawa's report,37 we suggested that the high rigidity backbone and contorted spiro-structure in SBC-DDM contributes to a high level of in-plane orientation of PI main chains and a decrease in crystallinity, leading to thermal contraction in SBC-DDM. Furthermore, the CTE value increased rapidly with further increasing temperature due to the softening of the polyimide film under the tension mode. The 10 wt% decomposition temperature (Td10) in air atmosphere (467 °C) is higher than in a nitrogen atmosphere (457 °C) because of the oxidation of aliphatic segments as reported in literature.16 As compared with the Td10 of referenced PEI 7f (457 and 454 °C in air and N2, respectively),16 SBC-DDM exhibits somewhat better thermal stability due to the absence of diether linkage. In addition, the char yield of SBC-DDM at 800 °C in a nitrogen atmosphere is around 38%, which is similar to that of 7f (41%).16 Indeed, SBC-DDM exhibits good thermal stability, suggesting that the spirobichroman unit is stable at high temperatures without the presence of acid catalyst.
![image file: c6ra25648a-f7.tif](/image/article/2017/RA/c6ra25648a/c6ra25648a-f7.gif) |
| Fig. 7 (a) TMA and (b) TGA thermogram of SBC-DDM. | |
Conclusions
We have successfully synthesized an octamethyl spirobichroman (OMSBC) through the acid-fragmentation of BPA by 3,4-dimethylphenol. The synthesis is sensitive to the reaction temperatures. A reaction mechanism was proposed in Scheme 1 to explain the fact that reacting at above 100 °C leads to only X-2, while reacting at 80 °C leads to mixture of X-2 and OMSBC. Through high pressure oxidation of OMSBC at high temperatures, a spirobichroman dianhydride (SBCDA) was newly developed. SBCDA was used to prepare a high performance polyimide (SBC-DDM) by a high temperature solution polymerization with DDM. After solution casting, a transparent and foldable film was obtained. Due to the contorted spirobichroman units leading to large free volume (Table 2), the polyimide, SBC-DDM possessed outstanding organo-solubility (Table 3) and a low-dielectric constant (2.34 at 1 GHz). SBC-DDM exhibits much higher thermal properties (Fig. 7) than did a spirobichroman dietheranhydride-based polyetherimide (7f in Hsiao's work16). The combination of organosolubility, high-Tg and low-dielectric properties make SBC-DDM attractive for electronic applications.
Acknowledgements
Financial support on this work from the Ministry of Science and Technology, Taiwan is highly appreciated.
References
- J. P. Gao and Z. Y. Wang, J. Polym. Sci., Part A: Polym. Chem., 1995, 33, 1627–1635 CrossRef CAS
. - A. Kausar, S. Zulfiqar, Z. Ahmad and M. I. Sarwar, Polym. Degrad. Stab., 2010, 95, 1826–1833 CrossRef CAS
. - H.-L. Lin, T.-Y. Juang, L.-H. Chan, R.-H. Lee, S. A. Dai, Y.-L. Liu, W.-C. Su and R.-J. Jeng, Polym. Chem., 2011, 2, 685–693 RSC
. - M. G. Dhara and S. Banerjee, Prog. Polym. Sci., 2010, 35, 1022–1077 CrossRef CAS
. - D. M. Stoakley, A. K. S. Clair and C. I. Croall, J. Appl. Polym. Sci., 1994, 51, 1479–1483 CrossRef CAS
. - O. J. Dautel, G. Wantz, D. Flot, J.-P. Lere-Porte, J. J. E. Moreau, J.-P. Parneix, F. Serein-Spirau and L. Vignau, J. Mater. Chem., 2005, 15, 4446–4452 RSC
. - X. Jia, D. Chao, H. Liu, L. He, T. Zheng, X. Bian and C. Wang, Polym. Chem., 2011, 2, 1300–1306 RSC
. - Y. Xiao, B. T. Low, S. S. Hosseini, T. S. Chung and D. R. Paul, Prog. Polym. Sci., 2009, 34, 561–580 CrossRef CAS
. - H.-J. Yen and G.-S. Liou, Polym. Chem., 2012, 3, 255–264 RSC
. - A. Ghosh, S. K. Sen, S. Banerjee and B. Voit, RSC Adv., 2012, 2, 5900–5926 RSC
. - X. Ma, O. Salinas, E. Litwiller and I. Pinnau, Polym. Chem., 2014, 5, 6914–6922 RSC
. - H.-J. Yen, J.-H. Wu, Y.-H. Huang, W.-C. Wang, K.-R. Lee and G.-S. Liou, Polym. Chem., 2014, 5, 4219–4226 RSC
. - C.-W. Chang, H.-J. Yen, K.-Y. Huang, J.-M. Yeh and G.-S. Liou, J. Polym. Sci., Part A: Polym. Chem., 2008, 46, 7937–7949 CrossRef CAS
. - S. Zhang, Y. Li, T. Ma, J. Zhao, X. Xu, F. Yang and X.-Y. Xiang, Polym. Chem., 2010, 1, 485–493 RSC
. - J. Weber, Q. Su, M. Antonietti and A. Thomas, Macromol. Rapid Commun., 2007, 28, 1871–1876 CrossRef CAS
. - S.-H. Hsiao and C.-Y. Yang, J. Polym. Sci., Part A: Polym. Chem., 1997, 35, 2801–2809 CrossRef CAS
. - S.-H. Hsiao, C.-P. Yang and C.-Y. Yang, J. Polym. Sci., Part A: Polym. Chem., 1997, 35, 1487–1497 CrossRef CAS
. - S.-H. Hsiao and C.-Y. Yang, Macromol. Chem. Phys., 1997, 198, 2181–2195 CrossRef CAS
. - S. Miyata, S. Sato, K. Nagai, T. Nakagawa and K. Kudo, J. Appl. Polym. Sci., 2008, 107, 3933–3944 CrossRef CAS
. - Y. Liu, C. Qian, L. Qu, Y. Wu, Y. Zhang, X. Wu, B. Zou, W. Chen, Z. Chen, Z. Chi, S. Liu, X. Chen and J. Xu, Chem. Mater., 2015, 27, 6543–6549 CrossRef CAS
. - P. M. Budd, B. S. Ghanem, S. Makhseed, N. B. McKeown, K. J. Msayib and C. E. Tattershall, Chem. Commun., 2004, 230–231 RSC
. - X. Ma, R. Swaidan, Y. Belmabkhout, Y. Zhu, E. Litwiller, M. Jouiad, I. Pinnau and Y. Han, Macromolecules, 2012, 45, 3841–3849 CrossRef CAS
. - A. J. Caruso and J. L. Lee, J. Org. Chem., 1997, 62, 1058–1063 CrossRef CAS
. - N. Kuramoto, K. Hayashi and K. Nagai, J. Polym. Sci., Part A: Polym. Chem., 1994, 32, 2501–2504 CrossRef CAS
. - Y.-L. Liu, C.-Y. Hsieh and Y.-W. Chen, Polymer, 2006, 47, 2581–2586 CrossRef CAS
. - E. Goiti, M. B. Huglin and J. M. Rego, Macromol. Rapid Commun., 2003, 24, 692–696 CrossRef CAS
. - C. H. Lin, C. M. Huang, M. W. Wang, S. A. Dai, H. C. Chang and T. Y. Juang, J. Polym. Sci., Part A: Polym. Chem., 2014, 52, 424–434 CrossRef CAS
. - M.-C. Kuo, Y.-C. Tung, C.-L. Yeh, H.-Y. Chang, R.-J. Jeng and S. A. Dai, Macromolecules, 2008, 41, 9637–9642 CrossRef CAS
. - N. Du, G. P. Robertson, I. Pinnau and M. D. Guiver, Macromolecules, 2009, 42, 6023–6030 CrossRef CAS
. - N. Du, G. P. Robertson, J. Song, I. Pinnau, S. Thomas and M. D. Guiver, Macromolecules, 2008, 41, 9656–9662 CrossRef CAS
. - N. Du, G. P. Robertson, I. Pinnau, S. Thomas and M. D. Guiver, Macromol. Rapid Commun., 2009, 30, 584–588 CrossRef CAS PubMed
. - W. M. Lee, Polym. Eng. Sci., 1980, 20, 65–69 CAS
. - A. Bondi, J. Phys. Chem., 1964, 68, 441–451 CrossRef CAS
. - H.-l. Lv, B.-G. Wang and Y. Kong, Polym. J., 2009, 41, 1049–1054 CrossRef CAS
. - Y. H. Zhao, M. H. Abraham and A. M. Zissimos, J. Org. Chem., 2003, 68, 7368–7373 CrossRef CAS PubMed
. - C. E. Sroog, Prog. Polym. Sci., 1991, 16, 561–694 CrossRef CAS
. - J. Ishii, A. Takata, Y. Oami, R. Yokota, L. Vladimirov and M. Hasegawa, Eur. Polym. J., 2010, 46, 681–693 CrossRef CAS
.
Footnote |
† Electronic supplementary information (ESI) available. CCDC 1498507. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6ra25648a |
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