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Synthesis and Characterization of Soluble, High Temperature 3-Phenylethynyl Aniline Functionalized Polyimides via the Ester-Acid Route

Published online by Cambridge University Press:  15 February 2011

G. W. Meyer
Affiliation:
Virginia Polytechnic Institute and State University Department of Chemistry and NSF Science and Technology Center: High Performance Polymeric Adhesives and Composites Blacksburg, VA 24061-0344
S. Jayaraman
Affiliation:
Virginia Polytechnic Institute and State University Department of Chemistry and NSF Science and Technology Center: High Performance Polymeric Adhesives and Composites Blacksburg, VA 24061-0344
Y. J. Lee
Affiliation:
Virginia Polytechnic Institute and State University Department of Chemistry and NSF Science and Technology Center: High Performance Polymeric Adhesives and Composites Blacksburg, VA 24061-0344
G. D. Lyle
Affiliation:
Virginia Polytechnic Institute and State University Department of Chemistry and NSF Science and Technology Center: High Performance Polymeric Adhesives and Composites Blacksburg, VA 24061-0344
T. E. Glass
Affiliation:
Virginia Polytechnic Institute and State University Department of Chemistry and NSF Science and Technology Center: High Performance Polymeric Adhesives and Composites Blacksburg, VA 24061-0344
J. E. McGrath*
Affiliation:
Virginia Polytechnic Institute and State University Department of Chemistry and NSF Science and Technology Center: High Performance Polymeric Adhesives and Composites Blacksburg, VA 24061-0344
*
*To whom correspondence should be addressed
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Abstract

The synthesis of soluble imide oligomers of controlled molecular weight endcapped with the 3-phenylethynyl aniline endcapping agent is described. The 3-phenylethynyl aniline was employed to afford a higher curing temperature (380 - 420°C) which widens the processing window compared to commercially available acetylene endcapped polyimides. The polyimides were synthesized via solution imidization techniques, using the ester-acid of various dianhydrides and various aromatic diamines. The “one pot” procedure utilizes NMP as the solvent and o-dichlorobenzene as the azeotroping agent, and reproducibly exhibit fully imidized soluble polyimides with Mw/Mn values of ∼2.0 determined by gel permeation chromatography. Thermally cured samples display good solvent resistance and exhibit glass transition temperatures comparable to their high molecular weight linear analogs. These polyimides show excellent thermal stability at 700°F aged in air up to 100 hours. Mechanical testing has been performed on a pyromellitic dianhydride (PMDA) and a phosphine oxide-based system. The flow properties have been studied by parallel plate rheology and the cure cycle has been monitored using 13CNMR.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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References

1. Feger, C., Khojasteh, M. and McGrath, J. E., Editors Polyimides: Materials. Chemistry and Characterization, Elsevier, 1989.Google Scholar
2. Wilson, D., Hergenrother, P. and Stenzenberger, H. Editors, Polyimides, Chapman and Hall, 1990.Google Scholar
3. Scola, D. A. and Vontell, J. H. Chemtech, February, 112, 1989.Google Scholar
4.Polyimides,’ Mittal, K. L., Editor, Vol 1 & 2, Plenum Press, 1984.Google Scholar
5. Arnold, C. A., Summers, J. D., Chen, Y. P., Yoon, T. H., McGrath, B. E., Chen, D. and McGrath, J. E., Proceedings from the Third International Conference on Polyimides, Ellenvile, NY 1988, 69.Google Scholar
6. Bilow, N., Landis, A. L. and Miller, L. J. US Patent 3845018, 1974 (Hughes Aircraft).Google Scholar
7. Landis, A. L., Bilow, N., Boschan, R. H., Lawrence, R. E. and Aponyi, T. J.. Polym. Prepr., 15, 537, 1974.Google Scholar
8. Harris, F. W., Podaki, S. M. and Varaprath, S. Poly. Prepr., 21 (1), 3, 1980.Google Scholar
9. Sarfaraz, A., Kandpal, L. D. and Varma, I. K. J.M.S. - Rev. Macromol. Chem. Phys., C33 (3), 291320, 1993.Google Scholar
10. Shantarovich, P. S. and Shlyapnikova, I. A. Polym. Sci. USSR, 3, 103, 1961.Google Scholar
11. Bantsyrev, G. N., Scherbakova, I. M., Cherkashin, M. I., Kalikhman, I. D., Chigir, A. N. and Berlin, A. A. Izv. Akad. Nauk. SSSR Ser. Khim, 8, 1762, 1970.Google Scholar
12. Pickard, J. M., Jones, E. G. and Goldfarb, I. J. Macromolecules, 12, 895, 1979.Google Scholar
13. Pickard, J. M., Jones, E. G. and Goldfarb, I. J. Polym. Prepr., 20, 370, 1979.Google Scholar
14. Moy, T. M., DePorter, C. D. and McGrath, J. E. Poly. Prep., 33 (2), 489490, 1992; Polymer (London), 34 (4), 819–825 1993.Google Scholar
15. Nosova, V. V., Kudryavtsev, Y. M., Gasilova, E. P., Lukasov, S. V., Galaktionova, E. F. and Zhukova, T. I., Polymer Science, 34, 6, 1992.Google Scholar
16. Paul, C. W., Schultz, R. A. and Fenelli, S. P. National Starch and ChemicalCompany presented at the Fourth International Conference on Polyimides, Ellenville, NY, 1991.Google Scholar
17. Hergenrother, P. M. Macromolecules, 14, 898, 1981.Google Scholar
18. Jayaraman, S., Meyer, G., Moy, T. M., Srinivasan, R. and McGrath, J. E. Polym. Prep., 34, 11, 1993.Google Scholar
19. Harris, F. W., Pamidimukkala, A., Gupta, R., Das, S., Wu, T. and Mock, G. J. Macromol. Sci.-Chem., A21, (8&9), 11171135, 1984.Google Scholar
20. Gungor, A., Smith, C. D., Wescott, J., Srinivasan, S. and McGrath, J. E. Polym. Prepr., 32, 1, 1991.Google Scholar
21. Wescott, J. Ph.D. Dissertation, Virginia Polytechnic Institute and State University, 1993.Google Scholar
22. Swanson, S. A., Fleming, W. W. and Hofer, D. C. Macromolecules, 25, 582588, 1992.Google Scholar
23. Konas, M., Rogers, M. E., Moy, T. M., Schultz, A. R., Ward, T. C. and McGrath, J. E. J. Poly. Sci. Physics, in press (1993).Google Scholar