Synthesis and Properties of Novel Photosensitive Poly(amide-imide)s Containing Chalcone Moiety and Aromatic Diamines in the Main Chain

Six new poly(amide-imide)s were synthesized by the polycondensation reaction of 1,3-bis[4,4'-bis(trimellityimido) phenyl]-2-propenone (6) with 3,3'-diamino diphenyl sulfone (7a), 4,4'-diamino diphenyl sulfone (7b), 4,4'-diamino diphenyl ether (7c), 1,5-diamino naphthalene (7d), 6-phenyl-1,3,5-triazine (7e), and 6-choloro-1,3-diazine (7f) in a medium consisting of N-methyl-2- pyrrolidone, triphenyl phosphite, calcium chloride, and pyridine. The polycondensation reaction produced a series of novel poly(amide-imide)s (8a-f) in high yield and with inherent viscosities between 0.42 and 0.62 dL/g. The resulting polymers were characterized by elemental analysis, viscosity measurement, solubility testing, thermo-gravimetric analysis (TGA & DTG), FT-IR, and UV-VIS spectroscopy.

Synthesis and Properties of Novel Photosensitive Poly(amide-imide)s Containing Chalcone Moiety and Aromatic Diamines in the Main Chain

Six new poly(amide-imide)s were synthesized by the polycondensation reaction of 1,3-bis[4,4'-bis(trimellityimido) phenyl]-2-propenone (6) with 3,3'-diamino diphenyl sulfone (7a), 4,4'-diamino diphenyl sulfone (7b), 4,4'-diamino diphenyl ether (7c), 1,5-diamino naphthalene (7d), 6-phenyl-1,3,5-triazine (7e), and 6-choloro-1,3-diazine (7f) in a medium consisting of N-methyl-2- pyrrolidone, triphenyl phosphite, calcium chloride, and pyridine. The polycondensation reaction produced a series of novel poly(amide-imide)s (8a-f) in high yield and with inherent viscosities between 0.42 and 0.62 dL/g. The resulting polymers were characterized by elemental analysis, viscosity measurement, solubility testing, thermo-gravimetric analysis (TGA & DTG), FT-IR, and UV-VIS spectroscopy.

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  • P. E. Cassidy, “Thermally Stable Polymers”, Dekker, New York (1980).
  • C. J. Billerbeck and S. J. Henke, “Engineering Thermoplastics” Dekker, New York (1985).
  • Y. Imai, N. N. Malder and M. Kakimoto, J. Polym. Sci. Part A: Polym. Chem. 30, 2189 (1989).
  • M. Yamada, M. Kusama, T. Matsumoto and T. Kurosaki, J. Polym. Sci. Part A: Polym. Chem. 35, 1027 (1997).
  • G. C. Eastmond and J. Paprotny, Macromolecules 28, 2140 (1995).
  • G. C. Eastmond and J. Paprotny, Polym. 35, 5148 (1994).
  • C. P. Yang, R. S. Chen and C. D. Chen, J. Polym. Sci. Part A: Polym. Chem. 39, 775 (2001).
  • C. P. Yang and R. S. Chen, J. Polym. Sci. Part A: Polym. Chem. 38, 2082 (2000).
  • Y. Imai, N. N. Malder and M. Kakimoto, J. Polym. Sci. Part A: Polym. Chem. 23, 2077 (1985).
  • J. L. Nieto, J. G. de la Campa and J. de Abjo, Makromol. Chem. 183, 557 (1982).
  • M. K. Ghosh and K. L. Mittal, “Polyimides”, Marcel, Dekker, New York (1996).
  • J. de Abajo, J. P. Gabardaand J. Fontan, Angew. Makromol. Chem. 71, 143 (1978).
  • A. V. R. Reddy, P. R. Sreenivasulu and P. S. Anand, Eur. Polym. J. 34, 1441 (1998).
  • D. Fritsch and K. V. Peinemann, J. Membrane. Sci. 99, 29 (1995).
  • J. W. Simmons and O. K. Ekiner, US Patent 5,232,472 (1993).
  • Kh. Faghihi, Polym. J. 37, 449 (2005).
  • Kh. Faghihi, J. of Appl. Polym. Sci. 102, 5062 (2006).
  • Kh. Faghihi and M. Hajibeygi, Tur. J. of Chem. 31, 65 (2007).
  • K. Feng, T. Tsushima, T. Matsumoto and T. Kurosaki, J. of Appl. Polym. Sci. 36, 685 (1998).
  • A. V. R. Redy, K. Subramania, V. Krishnasamy and J. Ravichandran, Eur. Polym. J. 32, 919 (1996).
  • H. R. Allocock and C. G. Cameron, Macromol. 27, 3131 (1994).
  • A. Akelah, A. Selim and N. S. El Deen, Polym. Adv. Technol. 4, 393 (1993).
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
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