2008
DOI: 10.1016/j.eurpolymj.2008.05.022
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Synthesis and characterization of novel polyamides from new aromatic phosphonate diamine monomer

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Cited by 12 publications
(5 citation statements)
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“…The resulting mixture was stirred at room temperature for 24 h and was then taken to dryness in vacuo, and the residue was washed with water and diethyl ether successively to afford the yellow crude product, which was further recrystallized in CH 2 Cl 2 / petroleum ether, and the desired yellow crystalline product 2 was obtained in 62% yield (0.078 g). IR (KBr): 3053 m, 2961 w, 2926 w, 1635 w, 1604 s, 1582 s, 1544 m, 1519 s, 1453 s, 1439 s, 1411 s, 1305 m, 1264 m, 1226 m, 1159 m, 1059 m, 1030 m, 1007 m, 964 m, 756 s, 732 m, 697 m, 670 m. 1 H NMR (in CDCl 3 ): δ 2.17 (s, 3H), δ 2.09 (s, 3H), 5.29 (s, 1H), 5.83 (s, 1H), 5.90 (d,J = 8 Hz,2H),6.52 (m,2H),6.72 (m,4H),7.02 (m,2H),7.45 (d,J = 7.6 Hz,2H),3H),7.78 (d,J = 8 Hz,2H),7.85 (d,J = 7.2 Hz,2H),8.88 (d,J = 7.6 Hz,2H). Anal.…”
Section: Methodsmentioning
confidence: 99%
“…The resulting mixture was stirred at room temperature for 24 h and was then taken to dryness in vacuo, and the residue was washed with water and diethyl ether successively to afford the yellow crude product, which was further recrystallized in CH 2 Cl 2 / petroleum ether, and the desired yellow crystalline product 2 was obtained in 62% yield (0.078 g). IR (KBr): 3053 m, 2961 w, 2926 w, 1635 w, 1604 s, 1582 s, 1544 m, 1519 s, 1453 s, 1439 s, 1411 s, 1305 m, 1264 m, 1226 m, 1159 m, 1059 m, 1030 m, 1007 m, 964 m, 756 s, 732 m, 697 m, 670 m. 1 H NMR (in CDCl 3 ): δ 2.17 (s, 3H), δ 2.09 (s, 3H), 5.29 (s, 1H), 5.83 (s, 1H), 5.90 (d,J = 8 Hz,2H),6.52 (m,2H),6.72 (m,4H),7.02 (m,2H),7.45 (d,J = 7.6 Hz,2H),3H),7.78 (d,J = 8 Hz,2H),7.85 (d,J = 7.2 Hz,2H),8.88 (d,J = 7.6 Hz,2H). Anal.…”
Section: Methodsmentioning
confidence: 99%
“…The obtained metal consists of Co 0 with a cubic structure as revealed by XRD analysis presented in Fig. 5-A Para-aminoaniline is an aromatic diamine used in many application including the synthesis of Kevlar [59] and dyes matrices [60], [61], while aminophenols are biologically active and are used in the pharmaceutical industry [62].…”
Section: A Aerogels Characterizationmentioning
confidence: 99%
“…However, they are generally insoluble and infusible after conversion from their poly(amic-acid) precursors to polyimdes (3)(4)(5). Replacement of polyimides by copolyimides such as poly(amide-imide)s (PAIs) may be useful to tackle the intractability of polyimides (6)(7)(8)(9). PAIs are also expected to have the advantages of polyamides and polyimides, such as solvent resistance.…”
Section: Introductionmentioning
confidence: 99%