Dergiler / Turkish Journal of Chemistry / 2009 / Cilt: 33 - Sayı: 1

Rapid Synthesis of New Poly(amide-imide)s Based on N-(4-Carboxy phenyl) trimellitimide and Hydantoin Derivatives under Microwave Irradiation

Sayfa
87–97
Yayın Tarihi
2009-01-01
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Then diacid (3) was converted to N-(4-chlorocarbonyl phenyl) trimellitimide acid chloride (4) by reaction with thionyl chloride in the presence of pyridine.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Six new poly (amide-imide)s (6a-f) were prepared under microwave irradiation by polycondensation reaction of diacid chloride (4) with 6 different derivatives of hydantoins (5a-f) using O-cresol as a microwave absorbent.
📊
Temel Bulgular & Veri:These new PAIs were obtained in high yield and with inherent viscosities between 0.15 and 0.25 dL/g.
💡
Sonuç & Katkı:Then diacid (3) was converted to N-(4-chlorocarbonyl phenyl) trimellitimide acid chloride (4) by reaction with thionyl chloride in the presence of pyridine.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Thermally stable polymers · icrowave irradiation · Poly (amide-imide

Özet

Six new poly (amide-imide)s (6a-f) were prepared under microwave irradiation by polycondensation reaction of diacid chloride (4) with 6 different derivatives of hydantoins (5a-f) using O-cresol as a microwave absorbent. These new PAIs were obtained in high yield and with inherent viscosities between 0.15 and 0.25 dL/g. The resulting poly(amide-imide)s were characterized by elemental analysis, viscosity measurements, thermal gravimetric analysis (TGA & DTG), solubility test, and FT-IR spectroscopy. N-(4-chlorocarbonyl phenyl) trimellitimide acid chloride (4) was prepared by a 2-step reaction. First trimellitic anhydride (1) was reacted with 4-amino benzoic acid (2) in acetic acid solution and the resulting imide-acid [N-(4-carboxy phenyl) trimellitimide] (3) was obtained in high yield. Then diacid (3) was converted to N-(4-chlorocarbonyl phenyl) trimellitimide acid chloride (4) by reaction with thionyl chloride in the presence of pyridine.

Abstract

Six new poly (amide-imide)s (6a-f) were prepared under microwave irradiation by polycondensation reaction of diacid chloride (4) with 6 different derivatives of hydantoins (5a-f) using O-cresol as a microwave absorbent. These new PAIs were obtained in high yield and with inherent viscosities between 0.15 and 0.25 dL/g. The resulting poly(amide-imide)s were characterized by elemental analysis, viscosity measurements, thermal gravimetric analysis (TGA & DTG), solubility test, and FT-IR spectroscopy. N-(4-chlorocarbonyl phenyl) trimellitimide acid chloride (4) was prepared by a 2-step reaction. First trimellitic anhydride (1) was reacted with 4-amino benzoic acid (2) in acetic acid solution and the resulting imide-acid [N-(4-carboxy phenyl) trimellitimide] (3) was obtained in high yield. Then diacid (3) was converted to N-(4-chlorocarbonyl phenyl) trimellitimide acid chloride (4) by reaction with thionyl chloride in the presence of pyridine.

🔖

Bu Makaleye Atıf Yap

GHOLIZADEH, K. F. A. M. (2009). Rapid Synthesis of New Poly(amide-imide)s Based on N-(4-Carboxy phenyl) trimellitimide and Hydantoin Derivatives under Microwave Irradiation. Turkish Journal of Chemistry, Cilt: 33 - Sayı: 1, 87–97. https://ajindex.com/articles/185080

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (15)

  1. K. L. Mittal, Polyimides: Synthesis Characterization and Application, Plenum Press,
  2. New York (1984).
  3. M. J. M. Abade and B. Silicon, Polyimides and Other High Temperature Polymers, Elsevier, New York (1991).
  4. H. Bai and. W. S. Winston Ho, J. Memb. Sci. 313, 75 (2008).
  5. S. J. Park, K. Li and F. L. Jin, Mater. Chem. and Phys., 108, 214 (2008).
  6. Z. Ge, L Fan and S. Yang, Eur. Polym. J. 44, 1252 (2008).
  7. N. S. Choi, K. H. Yew, W. U. Choi and S. S. Kim, J. Power Sources, 177, 590, (2008).
  8. Y. Wang, S. H. Goh and T. S. Chung, Polymer, 48, 2901 (2007).
  9. C. J. Brillerbeck, S. J. Henke and J. M. Margolis, Engineering Thermoplastic. Marcel Dekker, New York (1985). Kirk-Othmer Encyclopedia of Chemical Technology, John Wiley and Sons, New York, 3rdEd, 12, 692 (1983).
  10. R. A. Abramovich, Org. Prep. Proceed. Int. 23, 683 (1991).
  11. S. Chatti, M. Bortolussi, A. Loupy, J. C. Blais, D. Bogdal and M. Majdoub, Eur. Polym. J. 38, 1851 (2002).
  12. A. R. Hajipour, S. E. Mallakpour and S. Khoee, Synlett. 5, 740 (2000).
  13. Kh. Faghihi, Kh. Zamani and A. Mobinikhaledi, Turk. J. Chem., 28, 345 (2004).
  14. Kh. Faghihi, Polym. J. 37, 449 (2005).
  15. Kh. Faghihi and Kh. Zamani, J. Appl. Polym. Sci, 101, 4263 (2006).