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1.
Tsuyoshi Kiyotsukuri Naoto Tsutsumi Kazuya Okada Kunihiko Asai Minoru Nagata 《Journal of polymer science. Part A, Polymer chemistry》1988,26(8):2225-2234
A new series of 16 aramids and 16 polyarylates having perfluoro-substituents on the benzene ring was prepared by a low temperature solution or an interfacial polycondensation. The effects of fluorine substituents on the structure and properties of polymers were examined. Fluorinated aramids exhibited higher crystallinity, while fluorinated polyarylates show lower crystallinity. The melting point (Tm) of aramids decreased with fluorine substitution, whereas Tm of polyarylates from fluorinated aromatic diols was higher than that of those from unfluorinated ones. The temperature of 10% weight loss and the residue at 900°C decreased with fluorine substitution except for the aramids from fluorinated diamines. Solubility and contact angle also increased with fluorine substitution. Some polyarylates were found to exhibit an optical anisotropy. 相似文献
2.
Sheng-Huei Hsiao Perng-Chih Huang 《Journal of polymer science. Part A, Polymer chemistry》1997,35(12):2421-2429
Two ether-sulfone-dicarboxylic acids, 4,4′-[sulfonylbis(2,6-dimethyl-1,4-phenylene)dioxy]dibenzoic acid (Me- III ) and 4,4′-[sulfonylbis(1,4-phenylene)dioxy]-dibenzoic acid ( III ), were prepared by the fluorodisplacement of 4,4′-sulfonylbis(2,6-dimethylphenol) and 4,4′-sulfonyldiphenol with p-fluorobenzonitrile, and subsequent alkaline hydrolysis of intermediate dinitriles. Using triphenyl phosphite (TPP) and pyridine as condensing agents, aromatic polyamides containing ether and sulfone links were prepared by the direct polycondensation of the dicarboxylic acids with various aromatic diamines in the N-methyl-2-pyrrolidone (NMP) solution containing dissolved calcium chloride. The inherent viscosities of the resulting polymers were above 0.4 dL/g and up to 1.01 dL/g. Most of the polyamides were readily soluble in polar solvents such as NMP, N,N-dimethylacetamide (DMAc), N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO), and afforded tough and transparent films by solution-casting. Most of the polymers showed distinct glass transition on their differential scanning calorimetry (DSC) curves, and their glass transition temperatures (Tg) were recorded between 212–272°C. The methyl-substituted polyamides showed slightly higher Tgs than the corresponding unsubstituted ones. The results of the thermogravimetry analysis (TGA) revealed that all the polyamides showed no significant weight loss before 400°C, and the methyl-substituted polymers showed lower initial decomposition temperatures than the unsubstituted ones. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35 : 2421–2429, 1997 相似文献
3.
Hung‐Ju Yen Kun‐Ying Lin Guey‐Sheng Liou 《Journal of polymer science. Part A, Polymer chemistry》2012,50(1):61-69
Two novel series of ambipolar and near‐infrared electrochromic aromatic polyamides with electroactive anthraquinone group were synthesized from new aromatic diamines, 2‐(bis(4‐aminophenyl)amino)anthracene‐9,10‐dione and 2‐(4‐(bis(4‐aminophenyl)amino)phenoxy)anthracene‐9,10‐dione, respectively, via low‐temperature solution polycondensation reaction. These polymers were readily soluble in many polar solvents and showed useful levels of thermal stability associated with high glass‐transition temperatures (Tg) (285–360 °C). Electrochemical studies of these electrochromic polyamides revealed ambipolar behavior with reversible redox couples and high contrast ratio both in the visible range and near‐infrared region. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
4.
Teruaki Hayakawa Takashi Morishita Masaki Okazaki Mitsuru Ueda Kazuhiro Takeuchi Michihiko Asai 《Journal of polymer science. Part A, Polymer chemistry》2000,38(21):3875-3882
A convenient method for the synthesis of polyamides containing hydroxyl and amino substituents on the aromatic rings of the backbones was developed. These polymers were prepared readily by the chemoselective polycondensation of dicarboxylic acids with diamines with hydroxyl and amino functional groups via the activating agent diphenyl(2,3‐dihydro‐2‐thioxo‐3‐bezoxazolyl)phosphonate. The model reactions were studied in detail to demonstrate the feasibility of chemoselective polycondensation. The direct polycondensation of 5‐hydroxy or 5‐aminoisophthalic acid with 4,4′‐diamino‐4″‐hydroxytriphenylmethane proceeded smoothly under mild conditions and produced the desired polyamides with inherent viscosities up to 0.73 dL · g−1. The polymers obtained were characterized by IR, 1H NMR, and 13C NMR spectroscopies. The polymers were readily soluble in aprotic polar solvents such as N‐methyl‐2‐pyrrolidinone, N,N‐dimethyl formamide, and dimethyl sulfoxide. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 3875–3882, 2000 相似文献
5.
Zhirong Fan Klaus Jaehnichen Philippe Desbois Liane Haeussler Roland Vogel Brigitte Voit 《Journal of polymer science. Part A, Polymer chemistry》2009,47(14):3558-3572
To explore the possible applications of hyperbranched polymers for modifying linear polyamides, two hyperbranched aromatic polyesters characterized as high Tg polymers possessing phenolic end groups were used in melt mixing with partly aromatic polyamide and commercially available aliphatic polyamide‐6, respectively. Different amounts of both hyperbranched polyesters (from 1 wt % up to 20 wt %) were added to the polyamides, and the influence of these hyperbranched polyesters on the properties of the polyamides was investigated. The hyperbranched polyester based on an AB2 approach was found to be the most effective modifier. A significant increase of the glass transition temperature of the final blend was detected. However, a remarkable reduction of crystallinity as well as complex melt viscosity of those blends was also observed. The use of an A2+B3 hyperbranched polyester as melt modifier for the polyamides was less effective for changing the thermal properties, and the complex melt viscosity of the final material increased since heterogeneous blends were formed. In contrast to that, generally, the addition of the AB2 hyperbranched polyester to the polyamides resulted in homogeneous blends with improved Tg and processability. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3558–3572, 2009 相似文献
6.
Der-Jang Liaw Pei-Nan Hsu Jao-Jin Chen Been-Yang Liaw Chieh-Ying Hwang 《Journal of polymer science. Part A, Polymer chemistry》2001,39(10):1557-1563
A dicarboxylic acid monomer, 5-phthalimidoisophthalic acid, containing a phthalimide pendent group was prepared by the condensation of 5-aminoisophthalic acid and phthalic anhydride in glacial acetic anhydride. The monomer was reacted with various aromatic diamines to produce polyamides using triphenyl phosphite and pyridine as condensing agents. These polyamides were produced with inherent viscosities of 0.64–1.14 dL · g−1. All the polymers, characterized by wide-angle X-ray diffraction, revealed an amorphous nature resulting from the presence of the bulky pendent group. These polyamides exhibited excellent solubility in a variety of solvents such as N- methyl-2-pyrrolidinone, N,N-dimethylacetamide (DMAc), N,N-dimethylformamide, dimethyl sulfoxide, pyridine, and cyclohexanone. These polyamides showed glass-transition temperatures (Tg's) between 247 and 273 °C (by DSC) and 248 and 337 °C (by a dynamic mechanical analyzer). The thermogravimetric analytic measurement revealed the decomposition temperature at 10% weight-loss temperatures (Td10) ranging from 442 to 530 °C in nitrogen. The polyamides containing phthalimide groups exhibited higher Tg and Td10 values than those having no phthalimide groups. Transparent, tough, and flexible films of these polyamides could be cast from the DMAc solutions. These casting films had tensile strengths ranging from 81 to 126 MPa, elongations at break ranging from 7 to 13%, and tensile moduli ranging from 2.0 to 2.9 GPa. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1557–1563, 2001 相似文献
7.
Jorge F. Espeso Ángel E. Lozano José G. de la Campa Íñigo García‐Yoldi Javier de Abajo 《Journal of polymer science. Part A, Polymer chemistry》2010,48(8):1743-1751
A new diacid monomer containing a pendent adamantyl ring was reacted with various aromatic diamines to prepare novel aromatic polyisophthalamides (PIPAs). The polymers were obtained in high yield and high molecular weight by the Yamazaki‐Higashi phosphorylation method of polycondensation. Inherent viscosities ranged from 0.40 to 0.82 dL/g, which corresponds to weight‐average and number‐average molecular weights (GPC) in the range 21,000–63,000 g/mol and 9000–31,000 g/mol, respectively. The polymers were essentially amorphous and soluble in a variety of polar aprotic solvents, and they afforded transparent, creasable films by the solution‐casting method. The great size of the polyhedral adamantyl moiety brought about a significant restriction of segmental mobility, which translated into a strong increase of Tg, so that very high glass transition temperatures were observed, in the range 335–370 °C (DSC), which are 70–90 °C above the glass transition temperatures of homologous PIPAs without pendent groups. Thus, it can be stated that these adamantyl containing polyamides are among the soluble aromatic PIPAs with highest Tg ever described. Conversely, the initial decomposition temperature, as measured by thermogravimetric analysis, was about 400 °C, which is lower by 40–70° than that of unsubstituted counterparts. Polymer films exhibited good mechanical properties, with tensile strengths over 65 MPa and tensile moduli between 2.0 and 2.6 GPa. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1743–1751, 2010 相似文献
8.
Francesco A. Bottino Giovanna Di Pasquale Nicoletta Leonardi Antonino Pollicino 《Journal of polymer science. Part A, Polymer chemistry》1996,34(7):1305-1310
High molecular-weight aromatic polyamides were obtained from 1,5- and 2,6-bis-(4′-carboxy-4-phenylenoxy-sulfonyl)naphthalene by direct polycondensation reaction in N-methyl-2-pyrrolidone with various aromatic diamines, using triphenyl phosphite and pyridine as condensing agents. The polymers were characterized by elemental analysis, thermogravimetric analysis, differential scanning calorimetry, and infrared analysis. The polyamides, obtained in quantitative yield, possessed inherent viscosities in the range 0.42–1.70 dL/g, glass transition temperatures between 245–310°C, and 10% weight loss temperatures in nitrogen and air above 435 and 424°C, respectively. Most of the polymers were soluble in aprotic solvents. The effect of the structure on properties, such as solubility, Tg, and thermal behavior, were also studied. © 1996 John Wiley & Sons, Inc. 相似文献
9.
Sheng‐Huei Hsiao Wei‐Tsun Chen 《Journal of polymer science. Part A, Polymer chemistry》2003,41(3):420-431
Two series of novel fluorinated aromatic polyamides were prepared from 1,1‐bis[4‐(4‐carboxyphenoxy)phenyl]‐1‐phenyl‐2,2,2‐trifluoroethane with various aromatic diamines or from 1,1‐bis[4‐(4‐aminophenoxy)phenyl]‐1‐phenyl‐2,2,2‐trifluoroethane with various aromatic dicarboxylic acids with the phosphorylation polyamidation technique. These polyamides had inherent viscosities ranging from 0.51 to 1.54 dL/g that corresponded to weight‐average and number‐average molecular weights (by gel permeation chromatography) of 36,200–80,000 and 17,200–64,300, respectively. All polymers were highly soluble in aprotic polar solvents, such as N‐methyl‐2‐pyrrolidone and N,N‐dimethylacetamide, and some could even be dissolved in less‐polar solvents like tetrahydrofuran. The flexible and tough films cast from the polymer solutions possessed tensile strengths of 76–94 MPa and initial moduli of 1.70–2.22 GPa. Glass‐transition temperatures (Tg's) and softening temperatures of these polyamides were observed in the range of 185–268 °C by differential scanning calorimetry or thermomechanical analysis. Decomposition temperatures (Td's) for 10% weight loss all occurred above 500 °C in both nitrogen and air atmospheres. Almost all the fluorinated polyamides displayed relatively higher Tg and Td values than the corresponding nonfluorinated analogues. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 420–431, 2003 相似文献
10.
Aromatic polyamides were synthesized from 4,5-bis(4-aminophenyl)-2-phenyloxazole (APO) or 4,5-bis[4(4-aminophenoxy)phenyl]-2-phenyloxazole (APPO) containing 2-phenyl-4,5-oxazolediyl units with several aromatic carboxylic dichlorides by a low-temperature solution polycondensation method. The polyamides were obtained quantitatively, and their inherent viscosities ranged from 0.48 to 1.25 dL g?1. The glass transition temperatures (T gs) were displayed between 234 to 311°C, and the residual weight at 600°C (Res.wt600) exceeded 52% in nitrogen atmosphere. The polyamides showed good solubility in several aprotic polar solvents, such as N,N-dimethylacetoamide (DMAc), N-methyl-2-pyrrolidone (NMP), and dimethyl sulfoxide (DMSO). Aromatic polyimides were derived from APO or APPO with aromatic carboxylic dianhydrides through polyamic acids. The inherent viscosities of the polyamic acids, which were 0.53 to 1.02 dL g?1, T gs of the polyimides were observed between 259 to 361°C and their Res.wts600 were above 70%. The polyamides and polyimides were amorphous and afforded thin, flexible and tough films. We also prepared a nanocomposite of the polyamide derived from APPO with organophilic montmorillonite clay. 相似文献
11.
New types of polyamides containing pendent triaryl pyridine groups were successfully synthesized by direct polycondensation of a symmetry diamine,(4-(4-(2,6-diphenylpyridin-4yl)phenoxy)phenyl)-3,5-diaminobezamide(DPDAB), and various aromatic and aliphatic dicarboxylic diacids in NMP using triphenyl phosphate(TPP) and pyridine as catalyst. The diamine and all the prepared polyamides were fully characterized by using FT-IR,1H-NMR,UV-Vis spectroscopy, fluorimetry and elemental analysis.The inherent viscosity of polyamides ranged from 0.45 dL/g to 0.68 dL/g.All the polymers exhibited solubility in common polar aprotic solvents such as NMP,DMAc,DMF,DMSO,pyridine,HMPA,and even in less polar solvents such as THF and m-cresol at room temperature.Thermal properties of polyamides were evaluated by means of DSC,DMTA and TGA.These polymers showed glass transition temperatures(Tg) in the range of 138-210℃. Their initial decomposition temperature(Ti) varied from 265℃to 310℃under N2.The dilute solution(0.2 g/dL) of polyamides in DMF exhibited fluorescence emission withλmax in the range of 470-550 nm. 相似文献
12.
A series of novel aromatic diamines ( 2 – 4 ) containing the alkyl‐, aryl, or chloro‐substituted group of phthalazinone segments were synthesized via two synthetic steps starting from 4‐(3‐R‐4‐hydroxyphenyl)‐2,3‐phthalazinone‐1 (R = Ph, CH3, Cl). Three series of aromatic polyamides containing phthalazinone moieties were prepared through diamines 2 – 4 reacting with different aromatic dicarboxylic acids via a direct Yamazaki–Higashi phosphorylation polycondensation reaction. The resulting aromatic polyamides had inherent viscosities in the range of 0.40–0.76 dL/g. The thermal property of the polyamides was examined with DSC and thermogravimetric analysis. The glass‐transition temperatures of these polyamides ranged from 298 to 340 °C. The 10% mass‐loss temperature was above 405 °C under nitrogen. Structures of monomers 2 – 4 and the polymers were confirmed by Fourier transform infrared spectroscopy, 1H NMR, and mass spectrometry. Good solubility of these polymers in polar solvents such as N‐methylpyrrolidone, dimethylformamide, dimethylacetamide (DMAc), and m‐cresol was observed, and tough, flexible films were obtained from the polymer's DMAc solutions. The effect of the substituted group on the physical property of polymers was also investigated. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2026–2030, 2004 相似文献
13.
Masa-Aki Kakimoto Masaru Yoneyama Yoshio Imai 《Journal of polymer science. Part A, Polymer chemistry》1988,26(1):149-157
New soluble aramids having pendant phenoxy and phenylthio groups were prepared in high molecular weights by the polycondensation of aromatic diacids with 4-phenoxy-m-phenylenediamine and 4-phenylthio-m-phenylenediamine, respectively. Glass transition temperatures (Tg) of these aramids were in the range 195–255°C, where Tgs of phenoxy pendant aramids were higher than those of phenylthio substituted aramids. These properties were compared with those of the parent aramids derived from m-phenylenediamine and aromatic diacids. Aromatic-aliphatic polyamides were also prepared by the reaction of these three diamines with aliphatic diacids having 4–10 methylene groups and were characterized in detail. 相似文献
14.
《高分子科学杂志,A辑:纯化学与应用化学》2013,50(5):425-435
Novel aromatic polyamides were prepared from aromatic diamine containing 4,5-imidazolediyl unit, either by low temperature solution polycondensation or by direct polycondensation. Used diamines were 4,5-bis(4-aminophenyl)-2-phenylimidazole 1, 4,5-bis[4-(4-aminophenyl)]-2-(4-methylphenyl)imidazole 2 and 4,5-bis[4-(4-aminophenoxy)phenyl]-2-phenylimidazole 3. The obtained aromatic polyamides were produced with moderate to high inherent viscosity and soluble in polar aprotic solvents such as N,N-dimethylacetamide (DMAc), 1-methyl-2-pyrrolidone (NMP), N,N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO). Thermogravimetric analysis showed those polymers were stable up to 422°C in nitrogen atmosphere. The glass transition temperature (T g)s of the polymers derived from diamine 3 were in the range between 243 and 275°C, and these values were approximately 120–160°C lower than those analogue polyamide I series containing no phenoxy units. The properties of polyamide I series are also compared with those of analogue polymers that order of aromatic nuclei and amide linkage is reversible. 相似文献
15.
A chiral diacid monomer containing L ‐phenylalanine‐9,10‐dihydro‐9,10‐ethanoanthracene‐11,12‐dicarboximido unit was successfully synthesized in four steps and used in the preparation of a series of novel optically active polyamides by direct polycondensation with diverse aromatic diamines using 1,3‐dipropylimidazolium bromide under microwave dielectric heating. Ionic liquids (ILs) efficiently absorb microwave energy and thus are employed as solvent. By controlling the concentration of 1,3‐dipropylimidazolium bromide, reaction time and power level, high yield and moderate inherent viscosity polymers could be achieved in a very short period of time. All the resulting polymers exhibited excellent solubility in various organic solvents. The polyamides were found to have inherent viscosities in the range of 0.54–0.85 dL g?1. These polyamides had glass‐transition temperatures (Tg) above 180°C, and a 10% weight‐loss temperatures in excess of 340°C with char yield at 800°C in nitrogen higher than 40%. A comparative study on effects exerted by microwave technique with conventional method is also presented. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
16.
A new series of blue photoluminescent aromatic polyesters (polyarylates) were synthesized from 1-[N,N-di(4-carboxyphenyl)amino]naphthalene with various bisphenols by the diphenylchlorophosphate (DPCP) activated direct polycondensation in a medium of pyridine and lithium chloride. The synthesis, basic characterizations, photoluminescence and electrochemical properties of this series of novel polyarylates bearing pendent naphthylamine chromophores were investigated. All polymers not only had good solubility in many polar aprotic solvents and excellent thin-film-forming ability, but also exhibited high Tg values, good thermal stability and lower highest occupied molecular orbital (HOMO) level. Thus, these naphthylamine-containing polyarylates may be widely applied in P-LED as hole-transporting layer and blue light-emitting materials due to their proper HOMO level, excellent thermal stability and fluorescence quantum efficiency. 相似文献
17.
Hung‐ju Yen Guey‐Sheng Liou 《Journal of polymer science. Part A, Polymer chemistry》2008,46(22):7354-7368
A series of novel polyamides with pendent anthrylamine units were prepared via the direct phosphorylation polycondensation from various diamines and the anthrylamine‐based aromatic dicarboxylic acid, 9‐[N,N‐di(4‐carboxyphenyl)amino]anthracene (4). The aromatic polyamides had useful levels of thermal stability associated with relatively high softening temperatures (Ts) (290–300 °C), 10% weight‐loss temperatures (Td10) nearly in excess of 550 °C, and char yields at 800 °C in nitrogen higher than 60%. These aromatic polyamides I exhibited highly photoluminescence quantum yield in NMP solution ranges from 55% for Ia to 74% for Ie due to the introduction of anthrylamine chromophores. Cyclic voltammograms of the polyamide films cast onto an indium‐tin oxide (ITO)‐coated glass substrate exhibited one oxidation and reduction couples (Eonset) around 1.10 and ?1.50 V versus Ag/AgCl in acetonitrile (CH3CN) and DMF solutions, respectively. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7354–7368, 2008 相似文献
18.
Sheng-Huei Hsiao Chin-Ping Yang Sheng-Wen Wang Ming-Hung Chuang 《Journal of polymer science. Part A, Polymer chemistry》1999,37(18):3575-3583
1,1-Bis[4-(4-carboxyphenoxy)phenyl]cyclohexane (III) and 1,1-bis[4-(4-aminophenoxy)phenyl]cyclohexane (V) were prepared in two main steps starting from the aromatic nucleophilic substitution of p-fluorobenzonitrile and p-chloronitrobenzene, respectively, with 1,1-bis(4-hydroxyphenyl)cyclohexane in the presence of potassium carbonate in N,N-dimethylformamide (DMF). Using triphenyl phosphite and pyridine as condensing agents, two series of polyamides with cyclohexylidene cardo groups were directly polycondensated from dicarboxylic acid III with various aromatic diamines or from diamine V with various aromatic dicarboxylic acids in an N-methyl-2-pyrrolidone (NMP) solution containing dissolved calcium chloride. The polyamides exhibited inherent viscosities in the range of 0.45 to 1.78 dL/g. Almost all of the polymers were readily soluble in polar aprotic solvents such as NMP and N,N-dimethylacetamide (DMAc) and could afford transparent, flexible, and tough films by solution casting. The glass transition temperatures (Tg) of these aromatic polyamides were in the range of 180–243°C by DSC, and the 10% weight loss temperatures in nitrogen and air were all above 450°C. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 3575–3583, 1999 相似文献
19.
A series of rigid‐rod polyamides and polyimides containing p‐terphenyl or p‐quinquephenyl moieties in backbone as well as naphthyl pendent groups were synthesized from two new aromatic diamines. The polymers were characterized by inherent viscosity, elemental analysis, FT‐IR, 1H‐NMR, 13C‐NMR, X‐ray, differential scanning calorimetry (DSC), thermomechanical analysis (TMA), thermal gravimetric analysis (TGA), isothermal gravimetric analysis, and moisture absorption. All polymers were amorphous and displayed Tg values at 304–337°C. Polyamides dissolved upon heating in polar aprotic solvents containing LiCl as well as CCl3COOH, whereas polyimides were partially soluble in these solvents. No weight loss was observed up to 377–422°C in N2 and 355–397°C in air. The anaerobic char yields were 57–69% at 800°C. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 15–24, 1999 相似文献
20.
Der‐Jang Liaw Been‐Yang Liaw Chao‐Min Yang Pei‐Nan Hsu Chieh‐Ying Hwang 《Journal of polymer science. Part A, Polymer chemistry》2001,39(8):1156-1161
A new dicarboxylic acid containing a diphenylmethylene linkage, bis[4‐(4‐carboxyphenoxy)phenyl]diphenylmethane (BCAPD), was prepared from bis(4‐hydroxphenyl)diphenylmethane and p‐fluorobenzonitrile via an aromatic nucleophilic substitution reaction followed by hydrolysis. A series of novel polyamides were prepared by the direct polycondensation of BCAPD and various aromatic diamines. The polymers were produced with moderate to high inherent viscosities of 0.80–0.85 dL g?1. Nearly all the polymers were readily soluble in polar solvents such as N‐methyl‐2‐pyrrolidinone, N,N‐dimethylacetamide, N,N‐dimethylformamide, and dimethyl sulfoxide, in less polar solvents such as pyridine and cyclohexanone, and in tetrahydrofuran. All the polymers were amorphous, and the polyamide films had a tensile strength and a tensile modulus greater than 80 MPa and 2.0 GPa, respectively. These polyamides had glass‐transition temperatures between 249 and 274 °C, and their temperatures at a 10% weight loss were 477–538 and 483–540 °C in nitrogen and air atmospheres, respectively. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1156–1161, 2001 相似文献