Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Synthesis of Poly(p-xylylene) from α,α'-Bis(alkoxy or aryloxy)-p-xylenes by Chemical Vapor Deposition Polymerization

  • Tung, Ngo Trinh (Division of Chemistry and Molecular Engineering and Center for Electro- and Photo-Responsive Molecules, Korea University) ;
  • Yu, Young-Jun (Division of Chemistry and Molecular Engineering and Center for Electro- and Photo-Responsive Molecules, Korea University) ;
  • Kim, Kyung-Kon (Division of Chemistry and Molecular Engineering and Center for Electro- and Photo-Responsive Molecules, Korea University) ;
  • Joo, Sung-Hoon (Division of Chemistry and Molecular Engineering and Center for Electro- and Photo-Responsive Molecules, Korea University) ;
  • Jin, Jung-Il (Division of Chemistry and Molecular Engineering and Center for Electro- and Photo-Responsive Molecules, Korea University)
  • Published : 2004.01.20
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Abstract

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References

  1. Vedula, R.; Kaza, S.; Desu, S. B. In Chemical Vapor Deposition;Park, J.-H., Ed.; ASM International: Ohio, 2001, Chapter 8.
  2. Szwarc, M. Nature 1947, 160, 403.
  3. Gorham, W. F. J. Polym. Sci. 1966, A-1(4), 3027.
  4. Gorham, W. F. U S Patent 3, 342, 754 (1967).
  5. Greiner, A.; Mang, S.; Schaefer, O.; Simon, P. Acta Polymer 1997,48, 1. https://doi.org/10.1002/actp.1997.010480101
  6. Lang, C. L.; Yang, G. R.; Moore, J. A.; Lu, T. M. Proc. Mater. Res. Symp. 1995, 381, 45.
  7. Moore, J. A.; Lang, C. L.; Lu, T. M.; Yang, G. R. ACS. Sym. Ser.1995, 614, 449. https://doi.org/10.1021/bk-1995-0614.ch030
  8. Iwatsuki, S. Adv. Polym. Sci. 1984, 58, 93. https://doi.org/10.1007/3-540-12793-3_8
  9. Simon, P.; Mang, S.; Hasenhindl, A.; Gronski, W.; Greiner, A.Macromolecules 1998, 31, 8775. https://doi.org/10.1021/ma9808070
  10. Kim, K.; Jin, J.-I. Nano Letter 2001, 1, 631. https://doi.org/10.1021/nl010055e
  11. Lee, K.-R.; Jeong, S.-H.; Kim, K.; Jin, J.-I. Macromol. Symp. In press.
  12. Schaefer, O.; Greiner, A.; Pommerehme, J.; Guss, W.; Vestweber,H.; Tak, H. Y.; Bassler, H.; Schmidt, C.; Lussem, G.; Schartel, B.;Stumpflen, V.; Wensdorff, J. H.; Spiegel, S.; Moller, C.; Spiess, H.W. Synth. Met. 1996, 82, 1. https://doi.org/10.1016/S0379-6779(97)80001-X
  13. Morgan, M.; Rhee, S.-H.; Zhao, J.-H.; Malik, I.; Ryan, T.; Ho, H.-M.; Plano, M. A.; Ho, P. Macromolecules 1999, 32, 7555. https://doi.org/10.1021/ma991049w
  14. Isoda, S.; Tsuji, M.; Ohara, M.; Kawaguchi, A.; Katayama, K.Polymer 1983, 24, 1155. https://doi.org/10.1016/0032-3861(83)90248-3
  15. Miller, K. J.; Hollinger, H. B.; Grebowicz, J.; Wunderlich, B.Macromolecules 1990, 23, 3855. https://doi.org/10.1021/ma00218a022
  16. Beach, W. F. Macromolecules 1978, 11, 72. https://doi.org/10.1021/ma60061a014
  17. The solid NMR investigation was performed at the Korea Basic Science Institute-Seoul Branch, Korea University, by using MSL200 Bruker Spectrometer at a 13 C resonance frequency of 50.36 MHz and rotor frequency of about 3.5 kHz.

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