Journals / Turkish Journal of Chemistry / 2008 / Cilt: 32 - Sayı: 2

Synthesis and Properties of New Polyamides Based on 4-Phenylenediacrylic Acid and Hydantoin Derivatives in the Main Chain

Pages
191–200
Publication Date
2008-02-01
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

The resulting polyamides were characterized by elemental analysis, viscosity measurements, thermal gravimetric analysis (TGA and DTG), solubility test, and FT-IR and UV-vis spectroscopy. 4-Phenylenediacrylic acid (3) was prepared by the reaction of terephthal aldehyde (1) with malonic acid (2) in the presence of pyridine.

📌 3 Key Takeaways

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Objective & Hypothesis:Six new polyamides (5a-f) containing p-phenylenediacrylic and hydantoin moieties in the main chain were prepared by direct polycondensation reaction of 4-phenylenediacrylic acid (3) with 6 different hydantoin derivatives (4a-f) using thionyl chloride and pyridine as condensing agents and N-methyl-2-pyrolidone as solvent.
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Key Findings & Data:These new polymers (5a-f) were obtained in high yield and inherent viscosity between 0.35-0.55 dL/g.
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Conclusion & Impact:The resulting polyamides were characterized by elemental analysis, viscosity measurements, thermal gravimetric analysis (TGA and DTG), solubility test, and FT-IR and UV-vis spectroscopy. 4-Phenylenediacrylic acid (3) was prepared by the reaction of terephthal aldehyde (1) with malonic acid (2) in the presence of pyridine.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Polyamides · 4-phenylenediacrylic acid · hydantoin derivatives

Abstract

Six new polyamides (5a-f) containing p-phenylenediacrylic and hydantoin moieties in the main chain were prepared by direct polycondensation reaction of 4-phenylenediacrylic acid (3) with 6 different hydantoin derivatives (4a-f) using thionyl chloride and pyridine as condensing agents and N-methyl-2-pyrolidone as solvent. These new polymers (5a-f) were obtained in high yield and inherent viscosity between 0.35-0.55 dL/g. The resulting polyamides were characterized by elemental analysis, viscosity measurements, thermal gravimetric analysis (TGA and DTG), solubility test, and FT-IR and UV-vis spectroscopy. 4-Phenylenediacrylic acid (3) was prepared by the reaction of terephthal aldehyde (1) with malonic acid (2) in the presence of pyridine.

Özet

Six new polyamides (5a-f) containing p-phenylenediacrylic and hydantoin moieties in the main chain were prepared by direct polycondensation reaction of 4-phenylenediacrylic acid (3) with 6 different hydantoin derivatives (4a-f) using thionyl chloride and pyridine as condensing agents and N-methyl-2-pyrolidone as solvent. These new polymers (5a-f) were obtained in high yield and inherent viscosity between 0.35-0.55 dL/g. The resulting polyamides were characterized by elemental analysis, viscosity measurements, thermal gravimetric analysis (TGA and DTG), solubility test, and FT-IR and UV-vis spectroscopy. 4-Phenylenediacrylic acid (3) was prepared by the reaction of terephthal aldehyde (1) with malonic acid (2) in the presence of pyridine.

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Cite This Article

FAGHIHI, K. (2008). Synthesis and Properties of New Polyamides Based on 4-Phenylenediacrylic Acid and Hydantoin Derivatives in the Main Chain. Turkish Journal of Chemistry, Cilt: 32 - Sayı: 2, 191–200. https://ajindex.com/articles/193102

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References (27)

  1. P. E. Cassidy, Thermally Stable Polymers, Dekker, New York (1980).
  2. H. H. Yang, Aromatic High-Strength Fibers, Wiley, New York (1989).
  3. S. H. Hsiao, C. P. Yang and K. Y. Chu, J. Polym. Sci. Part A: Polym. Chem. 35, 1469 (1997)
  4. S. H. Hsiao and K. Y. Chu, J. Polym. Sci. Part A: Polym. Chem. 35, 3385 (1997).
  5. P. W. Morgan, Chemtech. 9, 316 (1979).
  6. K. P. Park, M. A. Kakimoto and Y. Imai, J. Polym. Sci. Part A: Polym. Chem. 33, 1031 (1995).
  7. C. P. Yang, S. H. Hsiao and C. C. Yang, J. Polym. Sci. Part A: Polym. Chem. 35, 2147 (1997).
  8. J. A. Mikroyannidis, J. Polym. Sci. Part A: Polym. Chem. 35, 1353 (1997).
  9. S. H. Hsiao and K. Y. Chu, J. Polym. Sci. Part A: Polym. Chem. 35, 3385 (1997).
  10. Y. L. Liu and S. H. Tsai, Polym. 43, 5757 (2002).
  11. Z. Ge, S. Yang, Z. Tao, J. Liu and I. Fan, Polym. 45, 3627 (2004).
  12. S. A. Mehdipour, Y. SarraŞ, M. Hatami and L. F. Akbarian, Eur. Polym. J. 41, 491 (2005).
  13. N. Avella, G. Maglio, R.; Palumbo, F. Russo and M. C. Vignola, Makromol. Chem. Rapid Commun. 14, (1993).
  14. H. J. Jeong, Y. Oishi, M. Kakimoto and Y.Imai, J. Polym. Sci. Part A: Polym. Chem. 28, 3293 (1990).
  15. H. J. Jeong, M. A. Kakimoto and Y. Imai, J. Polym. Sci. Polym. Chem. 29, 767 (1991).
  16. A. L. Cimecioglu and R. A. Weiss, J. Polym. Sci. Polym. Chem. 30, 1051 (1992).
  17. Y. Delaviz, A. Gungor, J. E. McGrath and H. W. Gibson, Polym. 34, 210 (1993).
  18. M. Takayanagi and T. Katayose, J. Polym. Sci. Polym. Chem. Ed. 19, 1133 (1981).
  19. H. G. Rogers, R. A. Gaudiana, W. C. Hollinsed, P. S. Kalyanaraman, J. S. Manello, C. McGowan, R. A. Minns and R. Sahatjian, Macromol. 18, 1058 (1985).
  20. N. Yamazaki, F. Higashi and J. Kawabata, J. Polym. Sci. Polym. Chem. Ed. 12, 2149 (1974).
  21. N. Yamazaki, M. Matsumoto and F. Higashi, J. Polym. Sci. Polym. Chem. Ed. 13, 1373 (1975).
  22. P. L. Egertone, J. Trigg, E. M. Hyde and A. Reiser, Macromol. 14, 100 (1984).
  23. L. Chienhui, C. Tehchou and H. Kehying, J. Polym. Sci. Polym. Chem. Ed. 31, 1119 (1993).
  24. H. Kehying, L. Chienhui, C. Tehchou and C. Tsuyao, J. Polym. Sci. Polym. Chem. Ed. 31, 971 (1993).
  25. H. Tanaka, K. Sasai, T. Sato and O. Tadatoshi, Macromol. 21, 3536 (1988).
  26. Kh. Faghihi and M. Hajibeygi, Eur. Polym. J. 2003. 39, 2307 (2003).
  27. M. Lamothe, M. Lannuzel and M. Perez, J. Comb. Chem. 4, 73 (2002). Kirk-Othmer Encyclopedia of Chemical Technology, John Wiley and Sons, New York, 3rdEd, 12, 692 (1983).