DOI QR코드

DOI QR Code

Modification of Thermal Degradation of Oligo(methylsilene) Catalyzed by Group 4 and 6 Transition Metal Complexes

  • Published : 1998.12.20

Abstract

The oligo(methylsilene) (1) was treated with the group 4 metallocene Cp2MCl2/Red-Al (M = Ti, Zr, Hf) combination catalysts and with the group 6 metal carbonyl M(CO)6 (M = Cr, W) catalysts, producing the modified, cross-linked polymers. The average molecular weights and percent ceramic residue yields of modified polymers increase as the catalyst goes down from Ti to Hf and similarly as the catalyst goes down from Cr to W. An interrelationship between average molecular weights and percent ceramic residue yield is found within the respective group of catalysts, but is not observed as the catalyst goes down from Ti to W. The polymers modified with the group 4 metallocene combination catalysts have higher molecular weights and similar percent ceramic residue yields as compared to the polymers modified with the group 6 metal carbonyl catalysts. The catalytic activities of group 4 metallocene combinations appear to be higher -100 ℃, but to be lower at very high temperature than those of group 6 metal carbonyls.

Keywords

References

  1. Chem. Rev. v.90 Hench, L.L.;West, J.K.
  2. Better Ceramics Through Chemistry Ⅵ Cheetham, A.K.(ed.);Brinker, C.J.(ed.);Mecartney, M.L.(ed.);Sanchez, C.(ed.)
  3. Introduction to Ceramics(2nd ed.) Kingery, W.D.;Bowen, H.K.;Uhlmann, D.R.
  4. Ultrastructure Processing of Advanced Ceramics Mackenzie, J.D(ed.);Ulrich, D.R.(ed.)
  5. Gmelin Handbook of Inorganic Chemistry(8th ed.)
  6. In Perparation and Properties of Solid-State Materials(Volume 7) Messier, D.R.;Croft, W.J.;Wilcos, W.R.(ed.)
  7. Science v.277 Lieber, C.M.;Wong, E.W.;Sheehan, P.E.
  8. Am. Ceram. Soc. Bull. v.65 Fizer, E.;Gadow, R.
  9. Am. Ceram. Soc. Bull. v.69 Sheppard, L.M.
  10. Chem. Lett. Yajima, S.;Hayashi, J.;Omori, M.
  11. Am. Ceram. Soc. Bull. v.59 Yajima, S.;Okamira, K.;Hayashi, J.;Omori, M.
  12. Compos. Sci. Technol. v.51 Lipowitz, J.;Barnard, T.;Bujalski, D.;Rade, J.;Zank, G.;Zangvil, A.;Xu, Y.
  13. Polym. Prepr.(Am. Chem. Soc., Div. Polym. Chem) v.31 Toreki, W.;Creed, N.M.;Batich, C.D.
  14. Can. J. Chem. v.65 Aitken, C.;Harrod, J.F.;Gill, U.S.
  15. Organometallics v.6 Harrod, J.F.;Yun, S.S.
  16. Organometallics v.8 Aitken, C.;Barry, J.P.;Gauvin, F.;Harrod, J.F.;Malek, A.;Rousseau, D.
  17. Organometallics v.9 Harrod, J.F.;Ziegler, T.;Tschinke, V.
  18. Oraganometllics v.12 Woo, H.G.;Harrod, J.F.;Henique, J.;Samuel, E.
  19. Organometallics v.12 Britten, J.;Mu, Y.;Harrod, J.F.;Polowin, J.;Baird, M.C.;Samuel, E.
  20. J. Am. Chem. Soc. v.119 Xin, S.;Woo, H.G.;Harrod, J.F.;Samuel, E.;Lebuis, A.M.
  21. Adv. Organomet. Chem. Gauvin, F.;Harrod, J.F.;Woo, H.G.
  22. J. Am. Chem. Soc. v.111 Woo, H.G.;Tilley, T.D.
  23. J. Am. Chem. Soc. v.111 Woo, H.G.;Tilley, T.D.
  24. J. Am. Chem. Soc. v.114 Woo, H.G.;Heyn, R.H.;Tilleym T.D.
  25. J. Am. Chem. Soc. v.114 Woo, H.G.;Walzer, J.F.;Tilleym T.D.
  26. Macromolecules v.24 Woo, H.G.;Walzer, J.F.;Tilley, T.D.
  27. Chem. Mater. v.5 Imori, T.;Woo, H.G.;Walzer, J.F.;Tilley, T.D.
  28. Acc. Chem. Res. v.26 Tilley, T.D.
  29. Organometallics v.14 Woo, H.G.;Kim, S.Y.;Han, M.K.;Cho, E.J.;Jung, I.N.
  30. Bull. Korean Chem. Soc. v.16 Woo, H.G.;Kim, S.Y.;Kim, W.G.;Cho, E.J.;Yeon, S.H.;Jung, I.N.
  31. Bull. Korean Chem. Soc. v.17 Woo, H.G.;Song, S.J.;You, H.;Cho, E.J.;Jung, I.N.
  32. Bull. Korean Chem. Soc. v.17 Woo. H.G.;Song, S.J.
  33. J. Am. Ceram. Soc. v.75 Seyferth, D.;Wood, T.G.;Tracy, H.J.;Robinson, J.L.
  34. New J. Chem. v.14 Seyferth, D.;Sobon, C.A.;Borm, J.
  35. Korean J. Mater. Res. v.6 Kim, D.P.;Lee, J.D.
  36. Am. Ceram. Soc. Bull. v.56 Yajima, S.;Shishido, T.;Okamura, K.
  37. Basic Liquid Chromatography; Varian Aerography Hadden, N.;Baumann, F.;MacDonald, F.;Munk, M.;Stevenson, R.;Gere, D.;Zamaroni, F.;Magors, R.
  38. Reversed-Phase High Performance Liquid Chromatography Krstulovic, A.M.;Brown, P.R.
  39. J. Am. Ceram. Soc. v.58 Yajima, S.;Okamura, K.;Hayashi, J.
  40. In NMR and the Periodic Table Harris, R.K.;Kennedy, J.D.;McFarlane, W.;Harris, R.K.(ed.);Mann, B.E.(ed.)
  41. Bull. Korean Chem. Soc. v.17 Woo, H.G.;Song, S.J.;Cho, E.J.;Jung, I.N.
  42. Organometallics v.10 Seyferth, D.;Lang, H.
  43. In Silicon-Containing Polymers Wiseman, A.I.;Jones, R.G.;Swain, A.C.;Went, M.J.;Jones, R.G.(ed.)
  44. Principles and Applications of Oragnotransition Metal Chemistry Collman, J.P.;Hegedus, L.S.;Norton, J.R.;Finke, R.G.
  45. Manuscript in preparation Song, S.J.;Woo, H.G.