Bulletin of the Korean Chemical Society

  • 제30권9호
  • /
  • Pages.2161-2164
  • /
  • 2009
  • /
  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

An Efficient Synthetic Method for 3,3',4,4'-Biphenyltetracarboxylic Anhydride

  • Hu, Yu Lin (Chemical Engineering College, Nanjing University of Science and Technology) ;
  • Lu, Ming (Chemical Engineering College, Nanjing University of Science and Technology) ;
  • Liu, Xiang (Chemical Engineering College, Nanjing University of Science and Technology) ;
  • Wang, Peng Cheng (Chemical Engineering College, Nanjing University of Science and Technology)
  • 발행 : 2009.09.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  1. Malay, K. G.; Mittal, K. L. Polyimides: Fundamentals and Applications; Marcel Dekker Inc: New York, 1996; pp 1-470
  2. Farr, I. V.; Glass, T. E.; Ji, Q.; McGrath, J. E. High Perform. Polym. 1997, 9, 345 https://doi.org/10.1088/0954-0083/9/3/012
  3. Tong, Y. J.; Huang, W. X.; Luo, J.; Ding, M. X. J. Polym. Sci. Part A 1999, 37, 1425 https://doi.org/10.1002/(SICI)1099-0518(19990515)37:10<1425::AID-POLA4>3.0.CO;2-G
  4. Ding, M. X.; He, T. B. Polyimide Material; Chemical Industry Press: Beijing, 1998; pp 283- 294
  5. Richard, R. A. S.; David, F. M. Mater. Today 2002, 5, 26
  6. Mitsumasa, K.; Yoshio, K.; Shigenori, K. U. S. Patent 4900843, 1990
  7. Xie, K. L.; Wang, X. Z.; Dai, L. Y.; Chen, Y. Q. Chin. J. Chem. Ind. Eng. 2005, 56, 1085-1089
  8. Kataoka, F.; Shoji, F. J. P. Patent 61167642, 1986
  9. Shoji, F.; Kataoka, F. J. P. Patent 63072649, 1988
  10. Ding, M. X.; Wang, X. Q.; Zhang, J. C. N. Patent 1041754, 1990
  11. Ding, M. X.; Wang, X. Q.; Zhang, J. U. S. Patent 5081281, 1992
  12. Hiroshi, I.; Hataaki, Y. J. Org. Chem. 1973, 38, 76-79 https://doi.org/10.1021/jo00941a014
  13. Ishikawa, A.; Mitsui, H.; Tanaka, Y. J. P. Patent 2001302654, 2001
  14. Kraft, T. E.; Rich, J. D.; McDermott, P. J. J. Org. Chem. 1990, 55, 5430-5432 https://doi.org/10.1021/jo00307a005
  15. Allum, K. G.; Hancock, R. D.; Howell, I. V. J. Organomet. Chem. 1987, 7, 203-216 https://doi.org/10.1016/S0022-328X(00)91068-4
  16. Tsukamoto, J.; Yamashita, T. J. P. Patent 2001290023, 2001
  17. Yang, J. G.; Duan, Q. W.; He, M. Y. Advancs in Fine Petrohemicals 2002, 3, 1-4
  18. Rich, J. D.; Kraft, T. E.; McDermott, P. J. E. P. Patent 339455, 1989
  19. Antonio, M.; Echavarren, J. K. S. J. Am. Chem. Soc. 1987, 109, 5478-5486 https://doi.org/10.1021/ja00252a029
  20. Bumagin, N. A.; Gulevich, Y. V.; Beletskaya, I. P. J. Organomet. Chem. 1985, 282, 421-425 https://doi.org/10.1016/0022-328X(85)87200-4
  21. Nishida, T.; Tashiro, Y.; Yamamoto, M. J. Fluorine Chem. 2003, 120, 135 https://doi.org/10.1016/S0022-1139(02)00322-6
  22. Lou, W. Y.; Zong, M. H.; Wu, H.; Xu, R. Chin. J. Chem. Eng. 2004, 12, 543-549
  23. Wasserscheid, P.; Keim, W. Angew. Chem. Int. Ed. 2000, 39, 3772-3789 https://doi.org/10.1002/1521-3773(20001103)39:21<3772::AID-ANIE3772>3.0.CO;2-5
  24. Wasserscheid, P.; Welton, T. Ionic Liquids in Synthesis; Wiley-VCH: Weinheim, 2003
  25. Jorapur, Y. R.; Lee, C. H.; Chi, D. Y. Org. Lett. 2005, 7, 1231 https://doi.org/10.1021/ol047446v
  26. March, J. Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 4 ed.; John Wiley & Sons: New York, 1992
  27. Park, H. J.; Oh Kim, Y. H.; Shim, J. A.; Choi, S. N. Bull. Korean Chem. Soc. 1993, 14, 444-449
  28. Vasylyev, M.; Neumann, R. Chem. Mater. 2006, 18, 2781 https://doi.org/10.1021/cm0603506
  29. Steinhoff, B. A.; Fix, S. A.; Stahl, S. S. J. Am. Chem. Soc. 2002, 124, 766 https://doi.org/10.1021/ja016806w
  30. Hou, Z.; Theyseeen, N.; Leitner, W. Green Chem. 2007, 9, 127 https://doi.org/10.1039/b606740a
  31. Kirihara, M.; Ochiai, Y.; Takizawa, S.; Takahata, H.; Nemoto, H. Chem. Commun. 1999, 1387
  32. Ligtenbarg, A. G. J.; Hage, R.; Feringa, B. L. Coord. Chem. Rev. 2003, 237, 89-101 https://doi.org/10.1016/S0010-8545(02)00308-9
  33. Reddy, S. R.; Das, S.; Punniyamurthy, T. Tetrahedron Lett. 2004, 45, 3561 https://doi.org/10.1016/j.tetlet.2004.03.056
  34. Radosevich, A. T.; Musich, C.; Toste, F. D. J. Am. Chem. Soc. 2005, 127, 1090 https://doi.org/10.1021/ja0433424
  35. Bekkum, H.; Lichtenthaler, F. W. Carbohydrates as Organic Raw Meterials; Wiley-VCH: Weinheim, 1990.
  36. Jiang, N.; Ragauskas, A. J. Tetrahedron Lett. 2007, 48, 273 https://doi.org/10.1016/j.tetlet.2006.11.032
  37. Jiang, N.; Ragauskas, A. J. J. Org. Chem. 2007, 72, 7030-7033 https://doi.org/10.1021/jo0707737
  38. Li, J. H.; Liu, W. J.; Xie, Y. X. J. Org. Chem. 2005, 70, 5409-5412 https://doi.org/10.1021/jo050353m
  39. Shi, Y. L.; Shi, M. Org. Biomol. Chem. 2005, 3, 1620-1621 https://doi.org/10.1039/b501942g
  40. Valnes, K.; Brandtzaeg, P. J. Histochem. Cytochem. 1985, 33, 755-761 https://doi.org/10.1177/33.8.3926864
  41. Wang, J.; Wang, H.; Zhang, S.; Zhang, H.; Zhao, Y. J. Phys. Chem. B 2007, 111, 6181-6188 https://doi.org/10.1021/jp068798h
  42. Dzyuba, S. V.; Bartsch, R. A. J. Heterocyclic Chem. 2001, 38, 265-268 https://doi.org/10.1002/jhet.5570380139
  43. Dong, W. K.; Hwan, J. J.; Seok, T. L.; Myung, H. S.; Dae, Y. C. Tetrahedron 2008, 64, 4209-4214 https://doi.org/10.1016/j.tet.2008.02.094
  44. Galan, M. C.; Brunet, C.; Fuensanta, M. Tetrahedron Lett. 2009, 50, 442-445 https://doi.org/10.1016/j.tetlet.2008.11.042
  45. Fang, Y. X.; Deng, Y. Q.; Ren, Q. G.; Huang, J. P. Chin. J. Chem. Eng. 2008, 16, 357-360 https://doi.org/10.1016/S1004-9541(08)60087-7
  46. Kenneth, R. S.; Annegret, S. Green Chem. 2002, 4, 119-123 https://doi.org/10.1039/b111160b
  47. Yi, S. X.; Men, J.; Ma, X. Y.; Jiang, Y.; Gao, G. W. Chin. Chem. Lett. 2009, 20, 306-309 https://doi.org/10.1016/j.cclet.2008.11.008

피인용 문헌

  1. Towards Halomethylated Benzene-Bearing Monomeric and Polymeric Substrates vol.14, pp.3, 2011, https://doi.org/10.1163/138577211X557495
  2. ChemInform Abstract: An Efficient Synthetic Method for 3,3′,4,4′-Biphenyltetracarboxylic Anhydride. vol.41, pp.5, 2010, https://doi.org/10.1002/chin.201005071