Using aromatic bis(4-bromophenyl) ether and various aromatic diamines as the monomers, a series of novel poly(amine ether)s (PAEs) have been synthesized via palladium-catalyzed aryl amination, which is the Hartwig-Buchwald polycondensation reaction. Their structures were characterized by means of elemental analysis, FT-IR, 1^H NMR and UV-Vis spectroscopy. The results show a good agreement with the proposed structures. Their general properties were studied by DSC and TG and it's obvious that they show high glass transition temperatures (Tg〉200 ℃), good thermal stability with high decomposition temperatures (TD〉500℃) and excellent solubility. The mechanical behavior of these polymers suggested that they could be considered a new class of high-performance polymers. 相似文献
A series of novel benzimidazole-containing aromatic polyimides with precise structures in high yields were synthesized by the catalyst-free nucleophilic substitution polycondensation of 4,4’-bis(4-fluorophthalimido) diphenyl ether with different molar ratios of 1,4-bis(2-benzimidazolyl) benzene to 4,4’-dihydroxydiphenyl sulfone via a C–N/C–O coupling reaction process. The reaction was carried out at 210°C in the presence of anhydrous potassium carbonate. The structures of the resulting polymers were characterized by means of FTIR, 1H NMR spectroscopy, and elemental analysis, and the results were largely consistent with the proposed structure. DSC and TG measurements showed that the polymers had high glass transition temperatures (Tg > 215°C), good thermostability, and high decomposition temperatures (Td5% > 456°C). These novel polymers also showed easy solubility. In addition, the obtained films have good optical transparency, and the mechanical properties exhibited tension strength of 48.2–74.8 MPa and tensile moduli of 1.3–1.9 GPa without any stretching. 相似文献
A series of poly(aryl ether sulfone ketone)s containing phthalazinone and biphenyl moieties were synthesized by aromatic nucleophilic
displacement polycondensation of 4-(4-hydroxylphenyl)(2H)-phthalazin-1-one (DHPZ), 4,4′-dichlorobenzophenone (DCB), 4,4′-dichlorodiphenyl
sulfone (DCS) and 4,4′-biphenol (BP) in different molar ratios. The obtained copolymers were characterized by different instrumental
techniques (FTIR, TGA, DSC, WAXD, etc.). The inherent viscosities of these polymers were in the range of 0.43–0.56 dL g−1. They were amorphous and had good solubility in polar aprotic organic solvents. The copolymers exhibited high glass transition
temperatures (Tgs) between 225°C and 256°C and excellent thermal stability up to 517–526°C (thermal decomposition temperatures for 5% weight
loss, Td, 5%) in nitrogen. The tensile strength and elongation at break of the polymers ranged from 63 MPa to 71 MPa and from 18% to 21%,
respectively. The processability of the material was effectively improved by the introduction of biphenyl group into polymer
backbone. 相似文献
Summary: Poly(arylene ether amine)s were synthesized by a nucleophilic aromatic substitution polycondensation of bis[4‐fluoro‐3‐(trifluoromethyl)phenyl]amine with several bisphenols. Even though the monomer has an electron‐donating diphenylamine moiety, which normally deactivates a nucleophilic aromatic substitution (SNAr) reaction, the polymerization proceeded by a SNAr reaction to give high‐molecular‐weight polymers. The polymers show good solubility in common organic solvents and have Tgs in the range of 123 °C to 177 °C.
High‐molecular‐weight poly(arylene ether amine)s synthesized by a SNAr reaction with the monomer containing an electron‐donating diphenylamine moiety. 相似文献
Two series of novel alternating copolyoxamides (PAnT-alt-n2 and PAn2-alt-62) are synthesized via solution/solid-state polycondensation (SSP). The alternating structures are analyzed carefully with 1H NMR and 13C NMR spectra. The melting behaviors, thermal stabilities, crystal structures and crystallinities are systematically evaluated by DSC, TGA and WAXD. The results reveal that these alternating copolyoxamides possess almost perfect alternating chain structures and have high melting temperature (Tm > 270 °C), high crystallinity (Xc > 32%) and high decomposition temperature (T5 > 405 °C) as well as low saturated water absorption (<3.5 wt%), which suggests that they have high potential as engineering plastic of high heat resistant. 相似文献
Using 4,4′‐dibromobenzophenone and 4,4′‐diaminoazobenzene as monomers, poly(aryl imino) containing azobenzene unit (PAI‐A) was synthesized via palladium‐catalyzed amination, and structurally characterized by means of FT‐IR, 1H NMR spectra and elemental analysis, the results of which show an agreement with the proposed structure. The UV absorption spectra were tested under different conditions. Additionally, differential scanning calorimetry (DSC) and thermogravimetric (TG) measurements show that PAI‐A possesses high glass transition temperature (Tg>176°C) and good thermal stability with high decomposition temperatures in nitrogen atmosphere (TD>410°C). 相似文献
New aromatic polyimides containing triphenylamine unit were prepared by two different methods, i.e., a conventional two-step method starting from 4,4′-diaminotriphenylamine and aromatic tetracarboxylic dianhydrides and the one-step thioanhydride method starting from the aromatic diamine and aromatic tetracarboxylic dithioanhydrides. Both procedures yielded high-molecular-weight polyimides with inherent viscosities of 0.47–1.17 dL/g. Some of these polymers were soluble in organic solvents such as N,N-dimethylacetamide, N-methyl-2-pyrrolidone, m-cresol, and pyridine. All the polyimides afforded transparent, flexible, and tough films, and the color varied from pale yellow to dark red, depending markedly on the tetracarboxylic acid components. The glass transition temperatures (Tgs) of these polyimides were in the range of 287–331°C and the 10% weight loss temperatures were above 520°C in air. The polyimides prepared by the one-step method exhibited better solubility in organic solvents and had somewhat lower Tgs than the polymers prepared by a conventional two-step method. 相似文献
Based on the 9,9-di(4-anilinyl)fluorene, structurally different fluorene-polyimino ketones have been obtained by the Buchwald-Hartwig cross coupling reaction. Their structure and performance have been characterized by FT-IR, 1H NMR, UV-vis and thermal analysis. The results show an agreement with the proposed structure, which possesses high glass transition temperature (Tg>250 ℃) and good thermal stability with high decomposition temperatures in nitrogen atmosphere (TD>520 ℃). Additionally, the polymers synthesized showed good solubility, which can be dissolved in common organic solvent CHCl3 at room temperature. 相似文献