DOI QR코드

DOI QR Code

Modification of Poly(methylsilene) Catalyzed by Group 4 and 6 Transition Metal Complexes and Its Pyrolysis

  • Published : 1997.12.20

초록

The poly(methylsilene) (1) was modified with the group 4 metallocene Cp2MCl2/Red-Al (M = Ti, Zr, Hf) combination catalyst and with the group 6 metal carbonyl M(CO)6 (M = Cr, Mo, W) catalyst, producing the highly cross-linked isoluble polymer and the lowly cross-linked soluble polymer, respectively. An interrelationship between molecular weight and percent ceramic residue yield with metal within the respective group was not found. The polymers modified with the group 4 metallocene combination catalysts have higher molecular weight and lower percent ceramic residue yield than the polymers modified with the group 6 metal carbonyl catalysts do. The catalytic activity of group 4 metallocene combinations appears to be higher at ∼100 ℃, but to be lower at very high temperature than those of group 6 metal carbonyls. The pyrolysis of the modified 1 yielded SiC ceramic.

키워드

참고문헌

  1. Chem. Rev. v.90 Hench, L. L.;West, J. K.
  2. Gmellin Handbook of Inorganic Chemistry(8th ed.) v.Supplement volume B2
  3. Preparation and Properties of Solid-State Materials v.7 Messier, D. R.;Croft, W. J.;Wilcox, W. R.(Ed.)
  4. Am. Ceram. Soc. Bull. v.65 Fizer, E.;Gadow, R.
  5. Am. Ceram. Soc. Bull. v.69 Sheppard, L. M.
  6. Chem. Lett. Yajima, S.;Hayashi, J.;Omori, M.
  7. J. Am. Ceram. Soc. v.59 Yajima, S.;Okamura, K.;Hayashi, J.;Omori, M.
  8. Compos. Sci. Technol. v.51 Lipowitz, J.;Barnard, T.;Bujalski, D.;Rade, J.;Zank, G.;Zangvil, A.;Xu, Y.
  9. Polym. Prepr. (Am. Chem. Soc., Div. Polym. Chem.) v.31 Toreki, W.;Creed, N. M.;Batich, C. D.
  10. J. Am. Ceram. Soc. v.75 Seyferth, D.;Wood, T. G.;Tracy, H. J.;Robison, J. L.
  11. Can. J. Chem. v.65 Aitken, C.;Harrod, J. F.;Yun, S. S.
  12. Organometallics v.6 Harrod, J. F.;Yun, S. S.
  13. Organometallics v.8 Aitken, C.;Barry, J.-P.;Gauvin, F.;Harrod, J. F.;Malek, A.;Rousseau, D.
  14. Organometallics v.9 Harrod, J. F.;Ziegler, T.;Tschinke, V.
  15. Oraganometallics v.12 Woo, H.-G.;Harrod, J. F.;Henique, J.;Samuel, E.
  16. Organomatallics v.12 Britten, J.;Mu, Y.;Harrod, J. F.;Polowin, J.;Baird, M. C.;Samuel, E.
  17. J. Am. Chem. Soc. v.111 Woo, H.-G.;Tilley, T. D.
  18. J. Am. Chem. Soc. v.111 Woo, H.-G.;Tilley, T. D.
  19. J. Am. Chem. Soc. v.114 Woo, H.-G.;Heyn, R. H.;Tilley, T. D.
  20. Macromolecules v.24 Woo, H.-G.;Walzer, J. F.;Tilley, T. D.
  21. Chem. Mater. v.5 Imori, T.;Woo, H.-G.;Walzer, J. F.;Tilley, T. D.
  22. Acc. Chem. Res. v.26 Tilley, T. D.
  23. Organomatallics v.14 Woo, H.-G.;Kim, S.-Y.;Han, M.-K.;Cho, E. J.;Jung, I. N.
  24. Bull. Korean Chem. Soc. v.16 Woo, H.-G.;Kim, S.-Y.;Kim, W.-G.;Cho, E. J.;Yeon, S. H.;Jung, I. N.
  25. Bull. Korean Chem. Soc. v.17 Woo, H.-G.;Song, S.-J.;You, H.;Cho, E. J.;Jung, I. N.
  26. Bull. Korean Chem. Soc. v.17 Woo, H.-G.;Song, S.-J.
  27. New J. Chem. v.14 Seyferth, D.;Sobon, C. A.;Borm, J.
  28. Korean J. Mater. Res. v.6 Kim, D.-P.;Lee, J.-D.
  29. Modern Powder Diffraction Smith, D. K.;Bish, D. L.(ed.);Post, J. E.(ed.)
  30. Am. Ceram. Soc. Bull. v.56 Yajima, S.;Shishido, T.;Okamura, K.
  31. J. Am. Ceram. Soc. v.58 Yajima, S.;Okamura, K.;Hayashi, J.
  32. NMR and the Periodic Table Harris, R. K.;Kennedy, J. D.;McFarlane, W.;Harris, R. K.(ed.);Mann, B. E.(ed.)
  33. Bull. Korean Chem. Soc. v.17 Woo, H.-G.;Song, S.-J.;Cho, E. J.;Jung, I. N.
  34. Organometallics v.10 Seyferth, D.;Lang, H.
  35. Silicon-containing Polymers Wiseman, A. I.;Jones, R. G.;Swain, A. C.;Went, M. J.;Jones, R. G.(Ed.)
  36. Principles and Applications of Organotransition Metal Chemistry Collman, J. P.;Hegedus, L. S.;Norton, J. R.;Finke, R. G.
  37. J. Am. Chem. Soc. v.119 Ley, K. D.;Whittle, C. E.;Bartberger, M. D.;Schanze, K. S.
  38. Unpublished results Woo, H.-G.;Song, S.-J.